1-Naphthaldehyde [C11H8O]

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Reaxys ID 386082 View in Reaxys

1/1 CAS Registry Number: 66-77-3 Chemical Name: 1-naphthaldehyde; 1 -naphthaldehyde; 1napthaldehyde Linear Structure Formula: CHOC10H7 Molecular Formula: C11H8O Molecular Weight: 156.184 Type of Substance: isocyclic InChI Key: SQAINHDHICKHLX-UHFFFAOYSA-N Note:

O

Substance Label (521) Label References 3

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Shuang-Hong; Dong, Guang-Ping; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 189; nb.

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Khurana, Jitender M.; Dawra, Kiran; Sharma, Purnima; RSC Advances; vol. 5; nb. 16; (2015); p. 12048 12051, View in Reaxys

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N3

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16B

Xia, Xuanshu; Toy, Patrick H.; Synlett; vol. 26; nb. 12; (2015); p. 1737 - 1743; Art.No: ST-2015-W0209-L, View in Reaxys

S-4o

Zhang, Jian; Wang, Heng; Ren, Shaobo; Zhang, Wei; Liu, Yunkui; Organic Letters; vol. 17; nb. 12; (2015); p. 2920 - 2923, View in Reaxys

27f

Schneider, Angelika E.; Manolikakes, Georg; Journal of Organic Chemistry; vol. 80; nb. 12; (2015); p.

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Kaur, Ramandeep; Naaz, Fatima; Sharma, Sahil; Mehndiratta, Samir; Gupta, Manish Kumar; Bedi, Preet Mohinder Singh; Nepali, Kunal; Medicinal Chemistry Research; vol. 24; nb. 8; (2015); p. 3334 - 3349, View in Reaxys

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2{6}

Yugandhar; Srivastava, Ajay Kumar; ACS Combinatorial Science; vol. 17; nb. 8; (2015); p. 474 - 481, View in Reaxys

3{13}

Park, Sujin; Kwon, Dah In; Lee, Jeeyeon; Kim, Ikyon; ACS Combinatorial Science; vol. 17; nb. 8; (2015); p. 459 - 469, View in Reaxys

10r

Hamasaka, Go; Tsuji, Hiroaki; Uozumi, Yasuhiro; Synlett; vol. 26; nb. 14; (2015); p. 2037 - 2041; Art.No: ST-2015-B0414-L, View in Reaxys

1S

Billamboz, Muriel; Len, Christophe; ChemSusChem; vol. 8; nb. 10; (2015); p. 1664 - 1675, View in Reaxys

14e

Skvorcova, Marija; Grigorjeva, Liene; Jirgensons, Aigars; Organic Letters; vol. 17; nb. 12; (2015); p.

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9j

Dogan, Özdemir; Bulut, Adnan; Tecimer, M. Ali; Tetrahedron Asymmetry; vol. 26; nb. 17; (2015); p. 966 969; Art.No: 59338, View in Reaxys

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46b

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3c

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Np-1CHO

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6g

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9e

Morimoto, Haruki; Harada, Toshiro; European Journal of Organic Chemistry; vol. 2015; nb. 33; (2015); p.

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13b

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129a

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1l

Goto, Akihiro; Endo, Kohei; Ukai, Yu; Irle, Stephan; Saito, Susumu; Chemical Communications; nb. 19; (2008); p. 2212 - 2214, View in Reaxys; Kidwai, Mazaahir; Chauhan, Ritika; Bhatnagar, Divya; Singh, Abhay K.; Mishra, Biswajit; Dey, Sharmistha; Monatshefte fur Chemie; vol. 143; nb. 12; (2012); p. 1675 1680, View in Reaxys; Mita, Tsuyoshi; Higuchi, Yuki; Sato, Yoshihiro; Chemistry - A European Journal; vol. 19; nb. 3; (2013); p. 1123 - 1128, View in Reaxys; Yadav, Arvind K.; Yadav, Lal Dhar S.; Tetrahedron Letters; vol. 55; nb. 13; (2014); p. 2065 - 2069, View in Reaxys; Yadav, Veena D.; Dighe, Shashikant U.; Batra, Sanjay; RSC Advances; vol. 4; nb. 101; (2014); p. 57587 - 57590, View in Reaxys

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2M

Yu, Bo; Zhao, Yanfei; Zhang, Hongye; Xu, Jilei; Hao, Leiduan; Gao, Xiang; Liu, Zhimin; Chemical Communications; vol. 50; nb. 18; (2014); p. 2330 - 2333, View in Reaxys

2w

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1aB

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11i

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Rasouli, Mohammad Ali; Mahdavi, Mohammad; Firoozpour, Loghman; Shafiee, Abbas; Foroumadi, Alireza; Tetrahedron; vol. 70; nb. 25; (2014); p. 3931 - 3934, View in Reaxys

4o

Liu, Chengwei; Qian, Qinqin; Nie, Kun; Wang, Yaorong; Shen, Qi; Yuan, Dan; Yao, Yingming; Dalton Transactions; vol. 43; nb. 22; (2014); p. 8355 - 8362, View in Reaxys

7w

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5N

Natarajan, Palani; Vagicherla, Vinuta Devi; Vijayan, Muthana Thevar; Tetrahedron Letters; vol. 55; nb.

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8d

Karami; Eskandari; Khodabakhshi; Journal of the Iranian Chemical Society; vol. 11; nb. 3; (2014); p. 631 637, View in Reaxys

12b

Jiang, Xiao; Wang, Jin-Mei; Zhang, Ying; Chen, Zhong; Zhu, Yong-Ming; Ji, Shun-Jun; Organic Letters; vol. 16; nb. 13; (2014); p. 3492 - 3495, View in Reaxys

4{9}

Mobaraki, Akbar; Movassagh, Barahman; Karimi, Babak; ACS Combinatorial Science; vol. 16; nb. 7; (2014); p. 352 - 358, View in Reaxys

8o

Pandey, Anand Kumar; Sharma, Rashmi; Singh, Awantika; Shukla, Sanjeev; Srivastava, Kumkum; Puri, Sunil K.; Kumar, Brijesh; Chauhan, Prem M. S.; RSC Advances; vol. 4; nb. 51; (2014); p. 26757 26770, View in Reaxys

2j; 5m

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10p

Wolińska, Ewa; Tetrahedron Asymmetry; vol. 25; nb. 15; (2014); p. 1122 - 1128, View in Reaxys

XIg

Babak; Gella; Semenenko; Shishkina; Shishkin; Musatov; Lipson; Russian Journal of Organic Chemistry; vol. 50; nb. 7; (2014); p. 1048 - 1055; Zh. Org. Khim.; vol. 50; nb. 7; (2014); p. 1048 - 1055,7, View in Reaxys

37b; 4h

Denmark, Scott E.; Wilson, Tyler W.; Burk, Matthew T.; Chemistry - A European Journal; vol. 20; nb. 30; (2014); p. 9268 - 9279, View in Reaxys

8r

Pi, Danwei; Jiang, Kun; Zhou, Haifeng; Sui, Yuebo; Uozumi, Yasuhiro; Zou, Kun; RSC Advances; vol. 4; nb. 101; (2014); p. 57875 - 57884, View in Reaxys

7l

Cai, Hao; Zhou, Yu; Zhang, Dong; Xu, Jinyi; Liu, Hong; Chemical Communications; vol. 50; nb. 94; (2014); p. 14771 - 14774, View in Reaxys

9N

Natarajan, Palani; Vagicherla, Vinuta Devi; Vijayan, Muthana Thevar; Tetrahedron Letters; vol. 55; nb.

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17o

Woliska, Ewa; Tetrahedron Asymmetry; vol. 25; nb. 22; (2014); p. 1478 - 1487, View in Reaxys

S-2f

Kiruthika, Selvarangam E.; Nandakumar, Avanashiappan; Perumal, Paramasivan Thirumalai; Organic Letters; vol. 16; nb. 17; (2014); p. 4424 - 4427, View in Reaxys

9q

Li, Jin-Liang; Liu, Li; Pei, Yu-Ning; Zhu, Hua-Jie; Tetrahedron; vol. 70; nb. 47; (2014); p. 9077 - 9083, View in Reaxys

18b

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S1k

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VIIIk

Galeta, Juraj; Man, Stanislav; Potacek, Milan; Chemical Papers; vol. 67; nb. 1; (2013); p. 29 - 39, View in Reaxys

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11d

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4m

Zhao, Jiannan; Liu, Xiaohua; Luo, Weiwei; Xie, Mingsheng; Lin, Lili; Feng, Xiaoming; Angewandte Chemie - International Edition; vol. 52; nb. 12; (2013); p. 3473 - 3477; Angew. Chem.; vol. 125; nb. 12; (2013); p. 3557 - 3561,5, View in Reaxys

6a; 1-NaphCHO

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Biswas, Kallolmay; Kumar, Arvind; Das Sarma, Koushik; ACS Combinatorial Science; vol. 15; nb. 5; (2013); p. 255 - 260, View in Reaxys

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11a

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Sharma, Moni; Chauhan, Kuldeep; Shivahare, Rahul; Vishwakarma, Preeti; Suthar, Manish K.; Sharma, Abhisheak; Gupta, Suman; Saxena, Jitendra K.; Lal, Jawahar; Chandra, Preeti; Kumar, Brijesh; Chauhan, Prem M. S.; Journal of Medicinal Chemistry; vol. 56; nb. 11; (2013); p. 4374 - 4392, View in Reaxys

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8c

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14p

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3s

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AL18

Kumar, Sarvesh; Thornton, Paul D.; Santini, Conrad; ACS Combinatorial Science; vol. 15; nb. 11; (2013); p. 564 - 571, View in Reaxys

1'o

Bhanuchandra; Kuram, Malleswara Rao; Sahoo, Akhila K.; Journal of Organic Chemistry; vol. 78; nb. 23; (2013); p. 11824 - 11834, View in Reaxys

3{19}

Kanchithalaivan, Selvaraj; Sivakumar, Sathiyamoorthi; Ranjith Kumar, Raju; Elumalai, Palani; Ahmed, Qazi Naveed; Padala, Anil K.; ACS Combinatorial Science; vol. 15; nb. 12; (2013); p. 631 - 638, View in Reaxys

5i

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7h

Wang, Xiang; Li, Pei; Li, Zhining; Yin, Juan; He, Ming; Xue, Wei; Chen, Zhiwei; Song, Baoan; Journal of Agricultural and Food Chemistry; vol. 61; nb. 40; (2013); p. 9575 - 9582, View in Reaxys

6B

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2B

Noroozi Pesyan, Nader; Shokr, Alireza; Behroozi, Mohammad; Sahin, Ertan; Journal of the Iranian Chemical Society; vol. 10; nb. 3; (2013); p. 565 - 575, View in Reaxys

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Hanyu, Naoto; Mino, Takashi; Sakamoto, Masami; Fujita, Tsutomu; Tetrahedron Letters; vol. 41; nb. 23; (2000); p. 4587 - 4590, View in Reaxys; Sharma, Vishal; Gupta, Vivek; Anthal, Sumati; Saxena, Ajit K.; Ishar, Mohan Paul S.; Tetrahedron Letters; vol. 53; nb. 42; (2012); p. 5649 - 5651, View in Reaxys

3d

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Morana, Fabio; Basso, Andrea; Bella, Marco; Riva, Renata; Banfi, Luca; Advanced Synthesis and Catalysis; vol. 354; nb. 11-12; (2012); p. 2199 - 2210, View in Reaxys

53a

Boobalan, Ramalingam; Lee, Gene-Hsian; Chen, Chinpiao; Advanced Synthesis and Catalysis; vol. 354; nb. 13; (2012); p. 2511 - 2520, View in Reaxys

20l

Agarwal, Jyoti; Peddinti, Rama Krishna; European Journal of Organic Chemistry; nb. 32; (2012); p. 6390 6406,17, View in Reaxys; Agarwal, Jyoti; Peddinti, Rama Krishna; European Journal of Organic Chemistry; nb. 32; (2012); p. 6390 - 6406, View in Reaxys

4, Ar=1-naphthyl

Hasaninejed, Alireza; Kazerooni, Maryam Rasekhi; Zare, Abdolkarim; Catalysis Today; vol. 196; nb. 1; (2012); p. 148 - 155, View in Reaxys

SM to 2i

Ashok; Vijaya Lakshmi; Indian Journal of Heterocyclic Chemistry; vol. 21; nb. 4; (2012); p. 337 - 340, View in Reaxys

1-1

Patent; MERCK and CO., INC.; WO2009/78934; (2009); (A1) English, View in Reaxys

8-1

Patent; LINK MEDICINE CORPORATION; WO2009/36275; (2009); (A1) English, View in Reaxys

Tab.2, entry.7: educt

Dong, Zhi-Bing; Liu, Bing; Fang, Cao; Li, Jin-Shan; Journal of Organometallic Chemistry; vol. 693; nb. 1; (2008); p. 17 - 22, View in Reaxys

1-Nald

Basu, Aditya; Phale, Prashant S.; Biodegradation; vol. 19; nb. 1; (2008); p. 83 - 92, View in Reaxys

aldehyde, k

Wuennemann, Stefan; Froehlich, Roland; Hoppe, Dieter; European Journal of Organic Chemistry; nb. 4; (2008); p. 684 - 692, View in Reaxys

3, R = 1-naphthyl

Zhou, Xin; Liu, Xiaohua; Yang, Xu; Shang, Deju; Xin, Junguo; Feng, Xiaoming; Angewandte Chemie International Edition; vol. 47; nb. 2; (2008); p. 392 - 394, View in Reaxys

Substrate, Tab.2, run 5

Matsukawa, Satoru; Kitazaki, Eri; Tetrahedron Letters; vol. 49; nb. 18; (2008); p. 2982 - 2984, View in Reaxys

aldehyde, entry 9

Maiti, Gourhari; Kundu, Pradip; Guin, Chandrani; Tetrahedron Letters; vol. 44; nb. 13; (2003); p. 2757 2758, View in Reaxys; Bedford, Robin B.; Pilarski, Lukasz T.; Tetrahedron Letters; vol. 49; nb. 27; (2008); p. 4216 - 4219, View in Reaxys

NAL

Krishnakumar; Prabavathi; Muthunatesan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 69; nb. 2; (2008); p. 528 - 533, View in Reaxys

tab 3. entr. 7

Tzeng, Zheng-Hao; Chen, Hung-Yao; Huang, Ching-Ting; Chen, Kwunmin; Tetrahedron Letters; vol. 49; nb. 26; (2008); p. 4134 - 4137, View in Reaxys

5n

Martinez, R. Fernando; Avalos, Martin; Babiano, Reyes; Cintas, Pedro; Jimenez, Jose L.; Light, Mark E.; Palacios, Juan C.; Perez, Esther M.S.; Tetrahedron; vol. 64; nb. 27; (2008); p. 6377 - 6386, View in Reaxys

RCHO, c

Aouf, Chahinez; Abed, Douniazad El; Giorgi, Michel; Santelli, Maurice; Tetrahedron Letters; vol. 49; nb.

31; (2008); p. 4630 - 4632, View in Reaxys

1s

Ismail, Tabasum; Shafi, Syed; Singh, Parvinder Pal; Qazi, Naveed Ahmed; Sawant, Sanghapal D.; Ali, Intzar; Khan, Inshad Ali; Kumar; Qazi, Ghulam Nabi; Alam, M. Sarwar; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 47; nb. 5; (2008); p. 740 - 747, View in Reaxys

aldehyde for 4d

Maccari, Rosanna; Ottana, Rosaria; Ciurleo, Rosella; Rakowitz, Dietmar; Matuszczak, Barbara; Laggner, Christian; Langer, Thierry; Bioorganic and Medicinal Chemistry; vol. 16; nb. 11; (2008); p. 5840 - 5852, View in Reaxys

1-naphthyl-CHO

Yanagisawa, Akira; Kageyama, Hiromi; Nakatsuka, Yoshinari; Asakawa, Kenichi; Matsumoto, Yukari; Yamamoto, Hisashi; Angewandte Chemie - International Edition; vol. 38; nb. 24; (1999); p. 3701 - 3703, View in Reaxys; Yanagisawa; Nakatsuka; Asakawa; Kageyama; Yamamoto; Synlett; nb. 1; (2001); p. 69 72, View in Reaxys; Nyerges; Fejes; Viranyi; Groundwater; Toeke; Synthesis; nb. 10; (2001); p. 1479 1482, View in Reaxys; Hayakawa, Ryuuichirou; Makino, Hiroaki; Shimizu, Makoto; Chemistry Letters; nb.

8; (2001); p. 756 - 757, View in Reaxys; Sarvary, Ian; Wan, Yiqian; Frejd, Torbjoern; Journal of the Chemical Society. Perkin Transactions 1; nb. 5; (2002); p. 645 - 651, View in Reaxys; Wadamoto, Manabu; Ozasa, Nobuko; Yanagisawa, Akira; Yamamoto, Hisashi; Journal of Organic Chemistry; vol. 68; nb. 14; (2003); p.

5593 - 5601, View in Reaxys; Kiec-Kononowicz; Szymanska; Farmaco; vol. 57; nb. 11; (2003); p. 909 916, View in Reaxys; Itoh, Takashi; Nagata, Kazuhiro; Ishikawa, Hiroyuki; Ohsawa, Akio; Heterocycles; vol. 63; nb. 12; (2004); p. 2769 - 2783, View in Reaxys; Wei, Han-Xun; Timmons, Cody; Farag, Mohamed Ali; Pare, Paul W.; Li, Guigen; Organic and Biomolecular Chemistry; vol. 2; nb. 20; (2004); p. 2893 - 2896, View in Reaxys; Wang, Libo; Nakamura, Shuichi; Toru, Takeshi; Organic and Biomolecular Chemistry; vol.

2; nb. 15; (2004); p. 2168 - 2169, View in Reaxys; Sarvari, Mona Hosseini; Synthesis; nb. 5; (2005); p. 787 790; Art.No: Z18204SS, View in Reaxys; Lee, Byoung Se; Mahajan, Suresh; Janda, Kim D.; Synlett; nb. 8;

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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(2005); p. 1325 - 1327; Art.No: S01705ST, View in Reaxys; Pan, Chongfeng; Ma, Zhixiong; Yu, Jie; Zhang, Zuhui; Hui, Ailing; Wang, Zhiyong; Synlett; nb. 12; (2005); p. 1922 - 1926; Art.No: U14105ST, View in Reaxys; Bhatt, Pralav V.; Wadia, Devang N.; Patel, Rajni M.; Patel, Pravin M.; Heterocyclic Communications; vol. 12; nb. 1; (2006); p. 79 - 82, View in Reaxys; Ohkubo, Mutsumi; Hayashi, Daisuke; Oikawa, Daisuke; Fukuhara, Kouki; Okamoto, Sentaro; Sato, Fumie; Tetrahedron Letters; vol. 47; nb. 35; (2006); p. 6209 - 6212, View in Reaxys; Tokuda, Ryoh; Matsunaga, Hirofumi; Ishizuka, Tadao; Nakajima, Makoto; Kunieda, Takehisa; Heterocycles; vol. 66; nb. 1; (2005); p. 135 - 141, View in Reaxys; Matsuya, Yuji; Hayashi, Kousuke; Nemoto, Hideo; Chemistry - A European Journal; vol. 11; nb. 18; (2005); p. 5408 5418, View in Reaxys; Xue, Song; He, Lin; Liu, Yong-Kang; Han, Kai-Zhen; Guo, Qing-Xiang; Synthesis; nb. 4; (2006); p. 666 - 674, View in Reaxys; Zhong, Jiangchun; Wang, Mingan; Guo, Hongchao; Yin, Mingming; Bian, QingHua; Wang, Min; Synlett; nb. 11; (2006); p. 1667 - 1670, View in Reaxys; Kumar, Atul; Maurya, Ram Awatar; Tetrahedron Letters; vol. 48; nb. 26; (2007); p. 4569 - 4571, View in Reaxys; Yanagisawa, Akira; Aoki, Takahiro; Arai, Takayoshi; Synlett; nb. 13; (2006); p. 2071 - 2074, View in Reaxys; Ishihara, Midori; Togo, Hideo; Synthesis; nb. 13; (2007); p. 1939 - 1942, View in Reaxys; Takahashi, Hiroshi; Arai, Takayoshi; Yanagisawa, Akira; Synlett; nb. 17; (2006); p. 2833 - 2835, View in Reaxys; Li, Ma; Jin, Rin-Zhe; Lue, Guang-Hua; Bian, Zhen; Ding, Meng-Xian; Gao, Lian-Xun; Synthesis; nb. 16; (2007); p.

2461 - 2470, View in Reaxys; Jiang, Fu-Yong; Liu, Bing; Dong, Zhi-Bing; Li, Jin-Shan; Journal of Organometallic Chemistry; vol. 692; nb. 20; (2007); p. 4377 - 4380, View in Reaxys; Park, Soon Bong; Alper, Howard; Chemical Communications; nb. 10; (2005); p. 1315 - 1317, View in Reaxys; Li, Hongwang; Huang, Yongbo; Jin, Wei; Xue, Feng; Wan, Boshun; Tetrahedron Letters; vol. 49; nb. 10; (2008); p. 1686 - 1689, View in Reaxys; Kumar, Atul; Maurya, Ram Awatar; Synlett; nb. 6; (2008); p. 883 - 885, View in Reaxys ald., Tab. 1, entry 22

Kumar, Dinesh; Kumar, Raj; Chakraborti, Asit K.; Synthesis; nb. 8; (2008); p. 1249 - 1256, View in Reaxys

4k

Li, Yan; He, Bin; Qin, Bo; Feng, Xiaoming; Zhang, Guolin; Journal of Organic Chemistry; vol. 69; nb. 23; (2004); p. 7910 - 7913, View in Reaxys; Xiong, Yan; Wang, Fei; Huang, Xiao; Wen, Yuehong; Feng, Xiaoming; Chemistry - A European Journal; vol. 13; nb. 3; (2007); p. 829 - 833, View in Reaxys

2, n

Varala, Ravi; Nasreen, Aayesha; Enugala, Ramu; Adapa, Srinivas R.; Tetrahedron Letters; vol. 48; nb. 1; (2007); p. 69 - 72, View in Reaxys

educt to 8

Kiyooka, Syun-ichi; Hosokawa, Satomi; Tsukasa, Sayaka; Tetrahedron Letters; vol. 47; nb. 23; (2006); p.

3959 - 3962, View in Reaxys; Downey, C. Wade; Johnson, Miles W.; Tetrahedron Letters; vol. 48; nb. 20; (2007); p. 3559 - 3562, View in Reaxys

Tab 2, aldehyde, run 14

Iwanami, Katsuyuki; Yano, Kentaro; Oriyama, Takeshi; Chemistry Letters; vol. 36; nb. 1; (2007); p. 38 39, View in Reaxys

3; Ar=1-naphthyl

Jin, Jian; Wang, Yonghui; Wang, Feng; Kerns, Jeffery K.; Vinader, Victoria M.; Hancock, Ashley P.; Lindon, Matthew J.; Stevenson, Graeme I.; Morrow, Dwight M.; Rao, Parvathi; Nguyen, Cuc; Barrett, Victoria J.; Browning, Chris; Hartmann, Guido; Andrew, David P.; Sarau, Henry M.; Foley, James J.; Jurewicz, Anthony J.; Fornwald, James A.; Harker, Andy J.; Moore, Michael L.; Rivero, Ralph A.; Belmonte, Kristen E.; Connor, Helen E.; Bioorganic and Medicinal Chemistry Letters; vol. 17; nb. 6; (2007); p.

1722 - 1725, View in Reaxys

T. 3-8, aldehyde

Lin, Li; Jiang, Xianxing; Liu, Weixia; Qiu, Li; Xu, Zhaoqing; Xu, Jiangke; Chan, Albert S. C.; Wang, Rui; Organic Letters; vol. 9; nb. 12; (2007); p. 2329 - 2332, View in Reaxys

Tab 2, substrate, run11

Oriyama, Takeshi; Aoyagi, Masaru; Iwanami, Katsuyuki; Chemistry Letters; vol. 36; nb. 5; (2007); p. 612 613, View in Reaxys

Tab. 2, entry 6

Fujisawa, Hidehiko; Nakagawa, Takashi; Mukaiyama, Teruaki; Advanced Synthesis and Catalysis; vol.

346; nb. 9-10; (2004); p. 1241 - 1246, View in Reaxys; Matsumoto, Tsutomu; Ueno, Masaharu; Kobayashi, Juta; Miyamura, Hiroyuki; Mori, Yuichiro; Kobayashi, Shue; Advanced Synthesis and Catalysis; vol.

349; nb. 4-5; (2007); p. 531 - 534, View in Reaxys

Tab1, aldehyde, entry 5

Eom, Deok Ki; Choi, Seong Jib; An, Duk Keun; Heterocycles; vol. 71; nb. 5; (2007); p. 1141 - 1146, View in Reaxys

6k

Paraskar, Abhimanyu S.; Sudalai, Arumugam; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 46; nb. 2; (2007); p. 331 - 335, View in Reaxys

7k

Liu, Kegang; Haeussinger, Daniel; Woggon, Wolf-D.; Synlett; nb. 14; (2007); p. 2298 - 2300, View in Reaxys

table 2, entry 6

Heravi, Majid M.; Sabaghiani, Ali J.; Bakavoli, Mehdi; Ghassemzadeh, Mitra; Bakhtiari, Khadijeh; Journal of the Chinese Chemical Society; vol. 54; nb. 1; (2007); p. 123 - 126, View in Reaxys

1-C10H7CHO

Casper, David M.; Burgeson, James R.; Esken, Joel M.; Ferrence, Gregory M.; Hitchcock, Shawn R.; Organic Letters; vol. 4; nb. 21; (2002); p. 3739 - 3742, View in Reaxys; Yanagisawa, Akira; Takahashi, Hiroshi; Arai, Takayoshi; Chemical Communications; nb. 5; (2004); p. 580 - 581, View in Reaxys; Yanagisawa, Akira; Okitsu, Shogo; Arai, Takayoshi; Synlett; nb. 11; (2005); p. 1679 - 1682; Art.No: U11505ST, View in Reaxys; Gullickson, Glen C.; Khan, Mushtaq A.; Walters, Jessica A.; Baughman, Russell G.; Lewis, David E.; Synthesis; nb. 17; (2005); p. 2906 - 2912; Art.No: M09104SS, View in Reaxys; Yanagisa-

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wa, Akira; Ichikawa, Toshikazu; Arai, Takayoshi; Journal of Organometallic Chemistry; vol. 692; nb. 1-3; (2007); p. 550 - 553, View in Reaxys; Trifonov; Goncharov; Aksenov; Chemistry of Heterocyclic Compounds; vol. 42; nb. 7; (2006); p. 955 - 956, View in Reaxys; Kamble, Vinod T.; Bandgar, Babasaheb P.; Joshi, Neeta S.; Jamode, Vasant S.; Synlett; nb. 17; (2006); p. 2719 - 2722, View in Reaxys Table 1, entry 11

Brennfuhrer, Anne; Neumann, Helfried; Beller, Matthias; Synlett; nb. 16; (2007); p. 2537 - 2540, View in Reaxys

ArCHO

Igarashi, Tetsutaro; Shimokawa, Masaru; Iwasaki, Miyuki; Nagata, Kensaku; Fujii, Masato; Sakurai, Tadamitsu; Synlett; nb. 9; (2007); p. 1436 - 1440, View in Reaxys

educt to 1c

Idzik, Krzysztof R.; Cabaj, Joanna; Soloducho, Jadwiga; Abdel-Fattah, Ashraf A. A.; Helvetica Chimica Acta; vol. 90; nb. 9; (2007); p. 1672 - 1680, View in Reaxys

1, entry 12

Kamble; Tayade; Davane; Kadam; Australian Journal of Chemistry; vol. 60; nb. 8; (2007); p. 590 - 594, View in Reaxys

1, Table 1, Entry 6-7

Bigdeli, Mohammad A.; Nemati, Firouzeh; Mahdavinia, Gholam Hossien; Tetrahedron Letters; vol. 48; nb. 38; (2007); p. 6801 - 6804, View in Reaxys

Tab. 2, Ent. 1, RCHO

Dumas, Aaron M.; Seed, Adam; Zorzitto, Alexander K.; Fillion, Eric; Tetrahedron Letters; vol. 48; nb. 40; (2007); p. 7072 - 7074, View in Reaxys

Ar'=1-naphthyl

Karthikeyan, Subramanian Vedhanarayanan; Perumal, Subbu; Balasubramanian; Tetrahedron Letters; vol. 48; nb. 35; (2007); p. 6133 - 6136, View in Reaxys

educt to 1j

Hatano, Bunpei; Nagahashi, Keita; Habaue, Shigeki; Chemistry Letters; vol. 36; nb. 12; (2007); p. 1418 1419, View in Reaxys

21-C16

Castellano, Sabrina; Fiji, Hannah D. G.; Kinderman, Sape S.; Watanabe, Masaru; De Leon, Pablo; Tamanoi, Fuyuhiko; Kwon, Ohyun; Journal of the American Chemical Society; vol. 129; nb. 18; (2007); p. 5843 - 5845, View in Reaxys

Ar-CHO (e)

Maccari, Rosanna; Paoli, Paolo; Ottana, Rosaria; Jacomelli, Michela; Ciurleo, Rosella; Manao, Giampaolo; Steindl, Theodora; Langer, Thierry; Vigorita, Maria Gabriella; Camici, Guido; Bioorganic and Medicinal Chemistry; vol. 15; nb. 15; (2007); p. 5137 - 5149, View in Reaxys

7f

Nemoto, Hisao; Ma, Rujian; Moriguchi, Hideki; Kawamura, Tomoyuki; Kamiya, Masaki; Shibuya, Masayuki; Journal of Organic Chemistry; vol. 72; nb. 25; (2007); p. 9850 - 9853, View in Reaxys

28

Li, Qun; Woods, Keith W.; Wang, Weibo; Lin, Nan-Horng; Claiborne, Akiyo; Gu, Wen-Zhen; Cohen, Jerry; Stoll, Vincent S.; Hutchins, Charles; Frost, David; Rosenberg, Saul H.; Sham, Hing L.; Bioorganic and Medicinal Chemistry Letters; vol. 15; nb. 8; (2005); p. 2033 - 2039, View in Reaxys; Ekoue-Kovi, Kekeli; Wolf, Christian; Organic Letters; vol. 9; nb. 17; (2007); p. 3429 - 3432, View in Reaxys; Hashimoto, Toru; Shiomi, Takushi; Ito, Jun-ichi; Nishiyama, Hisao; Tetrahedron; vol. 63; nb. 52; (2007); p. 12883 - 12887, View in Reaxys

ArCHO, Ar=1naphthyl

Achard, Thierry; Belokon', Yuri N.; Fuentes, Jose A.; North, Michael; Parsons, Teresa; Tetrahedron; vol.

60; nb. 28; (2004); p. 5919 - 5930, View in Reaxys; Hassan; Hegab; Hashem; Abdel-Motti; Hebah; AbdelMegeid; Journal of Heterocyclic Chemistry; vol. 44; nb. 4; (2007); p. 775 - 782, View in Reaxys

2b, R = 1-naphthyl

Kaboudin, Babak; Haruki, Terumitsu; Yamagishi, Takehiro; Yokomatsu, Tsutomu; Synthesis; nb. 20; (2007); p. 3226 - 3232, View in Reaxys

4h

Simion, Alina; Simion, Cristian; Kanda, Tadeshige; Nagashima, Satoko; Mitoma, Yoshiharu; Yamada, Tomoko; Mimura, Keisuke; Tashiro, Masashi; Journal of the Chemical Society. Perkin Transactions 1; nb.

17; (2001); p. 2071 - 2078, View in Reaxys; Denmark, Scott E.; Wilson, Tyler W.; Burk, Matthew T.; Heemstra Jr., John R.; Journal of the American Chemical Society; vol. 129; nb. 48; (2007); p. 14864 - 14865, View in Reaxys

9a

Banerjee; Mandal; Roy; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 46; nb. 4; (2007); p. 669 - 673, View in Reaxys

1-naphthylCHO

Li, Lian-Hai; Chan, Tak Hang; Tetrahedron Letters; vol. 41; nb. 26; (2000); p. 5009 - 5012, View in Reaxys; Li, Lian-Hai; Chan, Tak Hang; Organic Letters; vol. 2; nb. 8; (2000); p. 1129 - 1131, View in Reaxys; Blaszczyk, Edyta; Krawczyk, Henryk; Janecki, Tomasz; Synlett; nb. 15; (2004); p. 2685 - 2688, View in Reaxys; Harada, Toshiro; Kanda, Kousou; Organic Letters; vol. 8; nb. 17; (2006); p. 3817 - 3819, View in Reaxys; Sydnes, Leiv K.; Pedersen, Gry S.; Holmelid, Bjarte; Sandberg, Marcel; Synthesis; nb.

23; (2007); p. 3692 - 3696, View in Reaxys

R1CHO, R1=1naphthyl

Kobayashi, Shu; Akiyama, Ryo; Tetrahedron Letters; vol. 39; nb. 50; (1998); p. 9211 - 9214, View in Reaxys; Sprout, Christopher M.; Richmond, Meaghan L.; Seto, Christopher T.; Journal of Organic Chemistry; vol. 70; nb. 18; (2005); p. 7408 - 7417, View in Reaxys; Pedrosa, Rafael; Andres, Celia; Mendiguchia, Pilar; Nieto, Javier; Journal of Organic Chemistry; vol. 71; nb. 14; (2006); p. 5388 - 5391, View in Reaxys

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4f

Basavaiah; Sreenivasulu; Reddy; Muthukumaran; Synthetic Communications; vol. 31; nb. 19; (2001); p.

2987 - 2995, View in Reaxys; Marcelli, Tommaso; Van Der Haas, Richard N. S.; Van Maarseveen, Jan H.; Hiemstra, Henk; Angewandte Chemie - International Edition; vol. 45; nb. 6; (2006); p. 929 - 931, View in Reaxys

13e

Nakano, Ayako; Kawahara, Sakie; Akamatsu, Saori; Morokuma, Kenji; Nakatani, Mari; Iwabuchi, Yoshiharu; Takahashi, Keisuke; Ishihara, Jun; Hatakeyama, Susumi; Tetrahedron; vol. 62; nb. 2-3; (2006); p.

381 - 389, View in Reaxys

product 14

Farhadi, Saeid; Zaringhadam, Parisa; Sahamieh, Reza Zarei; Tetrahedron Letters; vol. 47; nb. 12; (2006); p. 1965 - 1968, View in Reaxys

RCHO, Tab.2. run Guo, Qun-Sheng; Lu, Yong-Na; Liu, Bing; Xiao, Jian; Li, Jin-Shan; Journal of Organometallic Chemistry; 6 vol. 691; nb. 6; (2006); p. 1282 - 1287, View in Reaxys Ed. to VIf

Kazemeini; Azizi; Saidi; Russian Journal of Organic Chemistry; vol. 42; nb. 1; (2006); p. 48 - 51, View in Reaxys

7a

Duan, Hai-Feng; Xie, Jian-Hua; Shi, Wen-Jian; Zhang, Qi; Zhou, Qi-Lin; Organic Letters; vol. 8; nb. 7; (2006); p. 1479 - 1481, View in Reaxys

T.4, Entry 9, Prod- Shirini; Esm-Hosseini; Hejazi; Mohammadpoor-Baltork; Journal of Chemical Research; nb. 1; (2006); p. uct 29 - 31, View in Reaxys Tab 2/10 Educt

Mukaiyama, Teruaki; Kitazawa, Takayuki; Fujisawa, Hidehiko; Chemistry Letters; vol. 35; nb. 3; (2006); p.

328 - 329, View in Reaxys

Educt, Tab.1, run 7

Xi, Bixia; Nevalainen, Vesa; Tetrahedron Letters; vol. 47; nb. 15; (2006); p. 2561 - 2564, View in Reaxys

carbonyl comp. tab 2/15

Iwanami, Katsuyuki; Aoyagi, Masaru; Oriyama, Takeshi; Tetrahedron Letters; vol. 47; nb. 27; (2006); p.

4741 - 4744, View in Reaxys

Tab. 5, entry 8

Xu, Zhaoqing; Lin, Li; Xu, Jiangke; Yan, Wenjin; Wang, Rui; Advanced Synthesis and Catalysis; vol. 348; nb. 4-5; (2006); p. 506 - 514, View in Reaxys

7i

Matsunaga, Shigeki; Qin, Hongbo; Sugita, Mari; Okada, Shigemitsu; Kinoshita, Tomofumi; Yamagiwa, Noriyuki; Shibasaki, Masakatsu; Tetrahedron; vol. 62; nb. 28; (2006); p. 6630 - 6639, View in Reaxys

27

Nakanishi, Jun; Tatamidani, Hiroto; Fukumoto, Yoshiya; Chatani, Naoto; Synlett; nb. 6; (2006); p. 869 872, View in Reaxys

2, R1=1-naphthyl

Rafiee, Ezzat; Jafari, Hadi; Bioorganic and Medicinal Chemistry Letters; vol. 16; nb. 9; (2006); p. 2463 2466, View in Reaxys

entry 22

Farhadi, Saeid; Afshari, Mozhgan; Journal of Chemical Research; nb. 3; (2006); p. 188 - 191, View in Reaxys

educt to 20

Philipova; Dobrikov; Krumova; Kaneti; Journal of Heterocyclic Chemistry; vol. 43; nb. 4; (2006); p. 1057 1063, View in Reaxys

Substrate,Tab.1, run 5a

Kamble, Vinod T.; Jamode, Vasant S.; Joshi, Neeta S.; Biradar, Ankush V.; Deshmukh, Rameshchandra Y.; Tetrahedron Letters; vol. 47; nb. 31; (2006); p. 5573 - 5576, View in Reaxys

educt to 4i

Lombardo, Marco; Pasi, Filippo; Trombini, Claudio; European Journal of Organic Chemistry; nb. 14; (2006); p. 3061 - 3063, View in Reaxys

entry 11 in Table 2

Hui, Ailing; Zhang, Jintang; Fan, Jinmin; Wang, Zhiyong; Tetrahedron Asymmetry; vol. 17; nb. 14; (2006); p. 2101 - 2107, View in Reaxys

Table 3, entry 8

Liu, Bing; Jiang, Fu-Yong; Song, Hai-Bin; Li, Jin-Shan; Tetrahedron Asymmetry; vol. 17; nb. 14; (2006); p. 2149 - 2153, View in Reaxys

1, R1=1-naphthyl

Lin, Chunchi; Fang, Hulin; Tu, Zhijay; Liu, Ju-Tsung; Yao, Ching-Fa; Journal of Organic Chemistry; vol.

71; nb. 17; (2006); p. 6588 - 6591, View in Reaxys

4 (R = 1-naphthyl) Wu, Yongyong; Zhang, Yazhu; Yu, Menglong; Zhao, Gang; Wang, Shaowu; Organic Letters; vol. 8; nb.

20; (2006); p. 4417 - 4420, View in Reaxys 14b

Rao, P. N. Praveen; Chen, Qiao-Hong; Knaus, Edward E.; Journal of Medicinal Chemistry; vol. 49; nb. 5; (2006); p. 1668 - 1683, View in Reaxys

subst., Table 2, run 11

Iwanami, Katsuyuki; Oriyama, Takeshi; Synlett; nb. 1; (2006); p. 112 - 114; Art.No: U28505ST, View in Reaxys

Chart S1/44

Wang, Shenliang; Chang, Young-Tae; Journal of the American Chemical Society; vol. 128; nb. 32; (2006); p. 10380 - 10381, View in Reaxys

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2018-02-14 08:04:49

educt to 12

Kiyooka, Syun-ichi; Takeshita, Yushi; Tanaka, Yoshinori; Higaki, Takafumi; Wada, Yosuke; Tetrahedron Letters; vol. 47; nb. 26; (2006); p. 4453 - 4456, View in Reaxys

Tab3, col 1, entry 5

Gosiewska, Silvia; Martinez, Sara Herreras; Lutz, Martin; Spek, Anthony L.; Van Koten, Gerard; Gebbink, Robertus J. M. Klein; European Journal of Inorganic Chemistry; nb. 22; (2006); p. 4600 - 4607, View in Reaxys

28 (Ar = 1-naphthyl)

Lloyd-Jones, Guy C.; Wall, Philip D.; Slaughter, Jennifer L.; Parker, Alexandra J.; Laffan, David P.; Tetrahedron; vol. 62; nb. 49; (2006); p. 11402 - 11412, View in Reaxys

R1-CE

Habashita, Hiromu; Kokubo, Masaya; Hamano, Shin-ichi; Hamanaka, Nobuyuki; Toda, Masaaki; Shibayama, Shiro; Tada, Hideaki; Sagawa, Kenji; Fukushima, Daikichi; Maeda, Kenji; Mitsuya, Hiroaki; J. Med. Chem.; vol. 49; nb. 14; (2006); p. 4145 - 4152, View in Reaxys

3, Ar=naphthalen-1-yl

Hassani, Zahra; Islami, Mohammad Reza; Kalantari, Maryam; Bioorganic and Medicinal Chemistry Letters; vol. 16; nb. 17; (2006); p. 4479 - 4482, View in Reaxys

Educt, Tab.2, run 8

Shimizu, Makoto; Kurokawa, Hiroshi; Nishiura, Shuji; Heterocycles; vol. 70; (2006); p. 57 - 64, View in Reaxys

product, tab 3/19

Farhadi, Saeid; Zabardasti, Abedien; Babazadeh, Zaynab; Tetrahedron Letters; vol. 47; nb. 50; (2006); p.

8953 - 8957, View in Reaxys

tab. 1, entry 2, ald.

Wolf, Christian; Liu, Shuanglong; Journal of the American Chemical Society; vol. 128; nb. 34; (2006); p.

10996 - 10997, View in Reaxys

7 R1=1-C10H7

Heynekamp, Justin J.; Weber, Waylon M.; Hunsaker, Lucy A.; Gonzales, Amanda M.; Orlando, Robert A.; Deck, Lorraine M.; Vander Jagt, David L.; Journal of Medicinal Chemistry; vol. 49; nb. 24; (2006); p.

7182 - 7189, View in Reaxys

RCHO, R=1naphthyl

Andrus, Merritt B.; Sekhar, B. B. V. Soma; Meredith, Erik L.; Dalley, N. Kent; Organic Letters; vol. 2; nb.

19; (2000); p. 3035 - 3037, View in Reaxys; Xu, Jianjun; Burton, Donald J.; Journal of Organic Chemistry; vol. 71; nb. 10; (2006); p. 3743 - 3747, View in Reaxys

1-Naphthyl-CHO

Praveen Kumar, K; Muthiah, C; Kumaraswamy, Sudha; Kumara Swamy; Tetrahedron Letters; vol. 42; nb.

18; (2001); p. 3219 - 3221, View in Reaxys; Ogawa, Chikako; Sugiura, Masaharu; Kobayashi, Shu; Chemical Communications; nb. 2; (2003); p. 192 - 193, View in Reaxys; Nakamura, Yutaka; Takeuchi, Seiji; Ohgo, Yoshiaki; Journal of Fluorine Chemistry; vol. 120; nb. 2; (2003); p. 121 - 129, View in Reaxys; Denmark, Scott E.; Heemstra Jr., John R.; Synlett; nb. 13; (2004); p. 2411 - 2416, View in Reaxys; Lombardo, Marco; Pasi, Filippo; Tiberi, Caterina; Trombini, Claudio; Synthesis; nb. 15; (2005); p. 2609 - 2614; Art.No: C04005SS, View in Reaxys; Gan, Changsheng; Chen, Xing; Lai, Guoyin; Wang, Zhiyong; Synlett; nb. 3; (2006); p. 387 - 390, View in Reaxys

1-Np-CHO

Tse, Man Kin; Bhor, Santosh; Klawonn, Markus; Anilkumar, Gopinathan; Jiao, Haijun; Doebler, Christian; Spannenberg, Anke; Magerlein, Wolfgang; Hugl, Herbert; Beller, Matthias; Chemistry - A European Journal; vol. 12; nb. 7; (2006); p. 1855 - 1874, View in Reaxys

subs., Tab. 1, entry 30

Rudrawar, Santosh; Besra, Ram C.; Chakraborti, Asit K.; Synthesis; nb. 16; (2006); p. 2767 - 2771, View in Reaxys

C10H7-1-CHO

Hsieh, Sheng-Hsiang; Gau, Han-Mou; Synlett; nb. 12; (2006); p. 1871 - 1874, View in Reaxys

tbl.1, ent.2, aldehyde

Lerebours, Rachel; Wolf, Christian; Journal of the American Chemical Society; vol. 128; nb. 40; (2006); p.

13052 - 13053, View in Reaxys

RCHO Table 2, entry 11

Wu, Kuo-Hui; Gau, Han-Mou; Journal of the American Chemical Society; vol. 128; nb. 46; (2006); p. 14808 - 14809, View in Reaxys

1-NaphCHO

Chernick, Erin T; Eisler, Sara; Tykwinski, Rik R; Tetrahedron Letters; vol. 42; nb. 49; (2001); p. 8575 8578, View in Reaxys; Ogoshi, Sensuke; Kamada, Hirohumi; Kurosawa, Hideo; Tetrahedron; vol. 62; nb.

32; (2006); p. 7583 - 7588, View in Reaxys; Harada, Toshiro; Nakatsugawa, Masashi; Synlett; nb. 2; (2006); p. 321 - 323, View in Reaxys; Shiomi, Takushi; Ito, Jun-Ichi; Yamamoto, Yoshihiko; Nishiyama, Hisao; European Journal of Organic Chemistry; nb. 24; (2006); p. 5594 - 5600, View in Reaxys; Katritzky, Alan R.; Idzik, Krzysztof R.; Abdel-Fattah, Ashraf A. A.; Soloducho, Jadwiga; Steel, Peter J.; Synthesis; nb. 20; (2006); p. 3377 - 3388, View in Reaxys

6j

Cheng, Chuanling; Wei, Siyu; Sun, Jian; Synlett; nb. 15; (2006); p. 2419 - 2422, View in Reaxys

Tab. 3, entry 9, subst.

Zhu, Bingchun; Jiang, Xuanzhen; Synlett; nb. 17; (2006); p. 2795 - 2798, View in Reaxys

educt table 2, entry 9

Kitazawa, Takayuki; Mukaiyama, Teruaki; Heterocycles; vol. 69; nb. 1; (2006); p. 417 - 427, View in Reaxys

subst., Tab.2, entry 14

Setamdideh, Davood; Zeynizadeh, Behzad; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 61; nb. 10; (2006); p. 1275 - 1281, View in Reaxys

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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1, R=1-naphthyl

Gangadasu, Banda; Palaniappan, Srinivasan; Rao, Vaidya Jayathirtha; Synlett; nb. 7; (2004); p. 1285 1287, View in Reaxys; De, Surya K.; Gibbs, Richard A.; Synthesis; nb. 11; (2005); p. 1748 - 1750; Art.No: M00305SS, View in Reaxys

tab. 3, entry 4, ald.

Nakajima, Makoto; Kotani, Shunsuke; Ishizuka, Tadao; Hashimoto, Shunichi; Tetrahedron Letters; vol.

46; nb. 1; (2005); p. 157 - 159, View in Reaxys

tab1, col2, entry7

Hunsen, Mo; Tetrahedron Letters; vol. 46; nb. 10; (2005); p. 1651 - 1653, View in Reaxys

Substrate,Tab. 1,run4/24

Lin, Yu-Sheng; Liu, Chih-Wei; Tsai, Thomas Y. R.; Tetrahedron Letters; vol. 46; nb. 11; (2005); p. 1859 1861, View in Reaxys

Tab.2. col.2 run 8

Nishiyama, Yutaka; Kakushou, Fujio; Sonoda, Noboru; Tetrahedron Letters; vol. 46; nb. 5; (2005); p. 787 - 789, View in Reaxys

5 Table 1, Entry 14

Mahajan, Vishal A.; Shinde, Popat D.; Borate, Hanumant B.; Wakharkar, Radhika D.; Tetrahedron Letters; vol. 46; nb. 6; (2005); p. 1009 - 1012, View in Reaxys

30,R=1-naphthyl

Tsou, Hwei-Ru; Overbeek-Klumpers, Elsebe G.; Hallett, William A.; Reich, Marvin F.; Floyd, M. Brawner; Johnson, Bernard D.; Michalak, Ronald S.; Nilakantan, Ramaswamy; Discafani, Carolyn; Golas, Jonathan; Rabindran, Sridhar K.; Shen, Ru; Shi, Xiaoqing; Wang, Yu-Fen; Upeslacis, Janis; Wissner, Allan; Journal of Medicinal Chemistry; vol. 48; nb. 4; (2005); p. 1107 - 1131, View in Reaxys

aldehyde, entry 10

Wang, Jun-Ke; Zong, Ying-Xiao; An, Hong-Gang; Xue, Guo-Qing; Wu, Dong-Qing; Wang, Yong-Sheng; Tetrahedron Letters; vol. 46; nb. 22; (2005); p. 3797 - 3799, View in Reaxys

Tab.2.col.2.run 7

Shen, Zhi-Liang; Ji, Shun-Jun; Loh, Teck-Peng; Tetrahedron Letters; vol. 46; nb. 17; (2005); p. 3137 3139, View in Reaxys

Tab. col.2 run 11

Srilakshmi Krishnaveni; Surendra; Pavan Kumar; Srinivas; Suresh Reddy; Rama Rao; Tetrahedron Letters; vol. 46; nb. 25; (2005); p. 4299 - 4301, View in Reaxys

1-naphhyl-CHO

Swamy, K. C. Kumara; Kumaraswamy, Sudha; Kumar, K. Senthil; Muthiah; Tetrahedron Letters; vol. 46; nb. 19; (2005); p. 3347 - 3351, View in Reaxys

7g

Dubbaka, Srinivas Reddy; Vogel, Pierre; Tetrahedron; vol. 61; nb. 6; (2005); p. 1523 - 1530, View in Reaxys; Uenaldi, Seda; Froehlich, Roland; Hoppe, Dieter; Synthesis; nb. 15; (2005); p. 2507 2520; Art.No: T03305SS, View in Reaxys

starting comp. to 5i

Farghaly; Vanelle; El-Kashef; Heterocyclic Communications; vol. 11; nb. 3-4; (2005); p. 255 - 262, View in Reaxys

educt tabl 1, entr.

16

Besra, Ram C.; Rudrawar, Santosh; Chakraborti, Asit K.; Tetrahedron Letters; vol. 46; nb. 37; (2005); p.

6213 - 6217, View in Reaxys

Table 2, RCHO, entry 7

Iwanami, Katsuyuki; Hinakubo, Yumi; Oriyama, Takeshi; Tetrahedron Letters; vol. 46; nb. 35; (2005); p.

5881 - 5883, View in Reaxys

aldehyde f

Shagufta; Raghunandan, Resmi; Maulik, Prakas R.; Panda, Gautam; Tetrahedron Letters; vol. 46; nb. 32; (2005); p. 5337 - 5341, View in Reaxys

11g

Nair, Vijay; Sreekumar; Bindu; Suresh, Eringathodi; Organic Letters; vol. 7; nb. 12; (2005); p. 2297 2300, View in Reaxys

12e

Zhu, Shou-Fei; Yang, Yun; Wang, Li-Xin; Liu, Bin; Zhou, Qi-Lin; Organic Letters; vol. 7; nb. 12; (2005); p.

2333 - 2335, View in Reaxys

aldehyde for 2

Azzena, Ugo; Dettori, Giovanna; Lubinu, Caterina; Mannu, Alberto; Pisano, Luisa; Tetrahedron; vol. 61; nb. 36; (2005); p. 8663 - 8668, View in Reaxys

RCHO for 22

Swamy; Min, Sun Park; Su, Jung Han; Sook, Kyung Kim; Ju, Hee Kim; Lee, Chongmok; Bang, Hyunjin; Kim, Youngmee; Kim, Sung-Jin; Yoon, Juyoung; Tetrahedron; vol. 61; nb. 43; (2005); p. 10227 10234, View in Reaxys

10l

Normand-Bayle, Marie; Benard, Christophe; Zouhiri, Fatima; Mouscadet, Jean-Francois; Leh, Herve; Thomas, Claire-Marie; Mbemba, Gladys; Desmaele, Didier; D'Angelo, Jean; Bioorganic and Medicinal Chemistry Letters; vol. 15; nb. 18; (2005); p. 4019 - 4022, View in Reaxys

tab1, ald/ket, entry8

Kumar, Raj; Chakraborti, Asit K.; Tetrahedron Letters; vol. 46; nb. 48; (2005); p. 8319 - 8323, View in Reaxys

2(vi)

Quesada, Ernesto; Taylor, Richard J.K.; Tetrahedron Letters; vol. 46; nb. 38; (2005); p. 6473 - 6476, View in Reaxys

substrate to (+/-)-19k

Lysek, Robert; Schuetz, Catherine; Vogel, Pierre; Helvetica Chimica Acta; vol. 88; nb. 10; (2005); p. 2788 - 2811, View in Reaxys

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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2, Tab. 1, entry 13 List, Benjamin; Doehring, Arno; Hechavarria Fonseca, Maria T.; Wobser, Kathrin; Van Thienen, Hendrik; Torres, Ramon Rios; Galilea, Pedro Llamas; Advanced Synthesis and Catalysis; vol. 347; nb. 11-13; (2005); p. 1558 - 1560, View in Reaxys 1j, Tab. 1, entry 10

Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Advanced Synthesis and Catalysis; vol. 347; nb.

11-13; (2005); p. 1561 - 1568, View in Reaxys

Tab. 2, entry 12

Ni, Ming; Wang, Rui; Han, Zhi-Jian; Mao, Bin; Da, Chao-Shan; Liu, Lei; Chen, Chao; Advanced Synthesis and Catalysis; vol. 347; nb. 11-13; (2005); p. 1659 - 1665, View in Reaxys

sch.2, aldehyde k

Baskar; Pandian; Priya; Chadha, Anju; Tetrahedron; vol. 61; nb. 52; (2005); p. 12296 - 12306, View in Reaxys

17f

Itsuno, Shinichi; Arima, Shinnosuke; Haraguchi, Naoki; Tetrahedron; vol. 61; nb. 51; (2005); p. 12074 12080, View in Reaxys

2; Tab.1, entry 2

Lu, Jun; Hong, Mei-Ling; Ji, Shun-Jun; Loh, Teck-Peng; Chemical Communications; nb. 8; (2005); p.

1010 - 1012, View in Reaxys

37

Master, Hoshang E.; Khan, Shabana I.; Poojari, Krishna A.; Bioorganic and Medicinal Chemistry; vol. 13; nb. 16; (2005); p. 4891 - 4899, View in Reaxys

Table 1, entry f

Rajaram, Sridhar; Sigman, Matthew S.; Organic Letters; vol. 7; nb. 24; (2005); p. 5473 - 5475, View in Reaxys

2, Tab. 1, entry 7

Quesada, Ernesto; Taylor, Richard J. K.; Synthesis; nb. 19; (2005); p. 3193 - 3195; Art.No: C04705SS, View in Reaxys

Tab. 1, entry 5, prod.

Hunsen, Mo; Journal of Fluorine Chemistry; vol. 126; nb. 9-10; (2005); p. 1356 - 1360, View in Reaxys

subst., Tab.1, entry 9

Zeynizadeh, Behzad; Behyar, Tarifen; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 60; nb. 4; (2005); p. 453 - 457, View in Reaxys

b

Denmark; Fujimori; Synlett; nb. SPEC. ISS; (2001); p. 1024 - 1029, View in Reaxys; Denmark, Scott E.; Fujimori, Shinji; Organic Letters; vol. 4; nb. 20; (2002); p. 3473 - 3476, View in Reaxys; Denmark, Scott E.; Fujimori, Shinji; Pham, Son M.; Journal of Organic Chemistry; vol. 70; nb. 26; (2005); p. 10823 - 10840, View in Reaxys

8a

Liu, Xiaodong; Verkade, John G.; Journal of Organic Chemistry; vol. 65; nb. 15; (2000); p. 4560 - 4564, View in Reaxys; Chandrasekhar; Prakash, S. Jaya; Shyamsunder; Ramachandar; Synthetic Communications; vol. 35; nb. 24; (2005); p. 3127 - 3131, View in Reaxys

R3M7

Su, Jing; McKittrick, Brian A.; Tang, Haiqun; Czarniecki, Michael; Greenlee, William J.; Hawes, Brian E.; O'Neill, Kim; Bioorganic and Medicinal Chemistry; vol. 13; nb. 5; (2005); p. 1829 - 1836, View in Reaxys

α-naphthyl-CHO

Kaboudin, Babak; Tetrahedron Letters; vol. 41; nb. 17; (2000); p. 3169 - 3171, View in Reaxys; Akiyama, Ryo; Sagae, Takahiro; Sugiura, Masaharu; Kobayashi, Shu; Journal of Organometallic Chemistry; vol.

689; nb. 23; (2004); p. 3806 - 3809, View in Reaxys; Schleth, Florian; Vogler, Thomas; Harms, Klaus; Studer, Armido; Chemistry - A European Journal; vol. 10; nb. 17; (2004); p. 4171 - 4185, View in Reaxys

α-naphthylCHO

Kaboudin, Babak; Nazari, Rahman; Tetrahedron Letters; vol. 42; nb. 46; (2001); p. 8211 - 8213, View in Reaxys; He, Ke; Zhou, Zhenghong; Wang, Lixin; Li, Kangying; Zhao, Guofeng; Zhou, Qilin; Tang, Chuchi; Synlett; nb. 9; (2004); p. 1521 - 1524, View in Reaxys

RCHO, entry 2

Ranu, Brindaban C.; Jana, Ranjan; Dey, Suvendu S.; Chemistry Letters; vol. 33; nb. 3; (2004); p. 274 275, View in Reaxys

Table 2, entry 6

Li, Ming; Zhu, Xia-Zhen; Yuan, Ke; Cao, Bo-Xun; Hou, Xue-Long; Tetrahedron Asymmetry; vol. 15; nb. 2; (2004); p. 219 - 222, View in Reaxys

10i

Matsunaga, Shigeki; Kinoshita, Tomotumi; Okada, Shigemitsu; Harada, Shinji; Shibasaki, Masakatsu; Journal of the American Chemical Society; vol. 126; nb. 24; (2004); p. 7559 - 7570, View in Reaxys

subst.,Tab. 1, entry 11

Chakraborti, Asit K.; Thilagavathi, Ramasamy; Kumar, Raj; Synthesis; nb. 6; (2004); p. 831 - 833, View in Reaxys

2, R2=1-naphthyl

Behnke, Dirk; Taube, Roswitha; Illgen, Katrin; Nerdinger, Sven; Herdtweck, Eberhardt; Synlett; nb. 4; (2004); p. 688 - 692, View in Reaxys

aldehyde, educt of 3

Chen, Dianjun; Timmons, Cody; Liu, Junying; Headley, Allan; Li, Guigen; European Journal of Organic Chemistry; nb. 15; (2004); p. 3330 - 3335, View in Reaxys

starting to 3 Tab. 1run9

Ooi, Takashi; Ohmatsu, Kohsuke; Uraguchi, Daisuke; Maruoka, Keiji; Tetrahedron Letters; vol. 45; nb.

23; (2004); p. 4481 - 4484, View in Reaxys

table 2, entry 8

Zhou, Yi-Feng; Wang, Rui; Xu, Zhao-Qing; Yan, Wen-Jin; Liu, Lei; Gao, Yan-Feng; Da, Chao-Shan; Tetrahedron Asymmetry; vol. 15; nb. 4; (2004); p. 589 - 591, View in Reaxys

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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E5

Therkelsen, Frans D.; Rottlaender, Mario; Thorup, Niels; Pedersen, Erik Bjerregaard; Organic Letters; vol. 6; nb. 12; (2004); p. 1991 - 1994, View in Reaxys

Table 1, entry 10

Habibi, Mohammad H.; Farhadi, Saeid; Journal of Chemical Research; nb. 4; (2004); p. 296 - 297, View in Reaxys

Tab.1, entry 6, substr.

Xu, Xiaolan; Zha, Zhenggen; Miao, Qian; Wang, Zhiyong; Synlett; nb. 7; (2004); p. 1171 - 1174, View in Reaxys

Tab. 3, entry 7c

Hosseinzadeh, Rahman; Tajbakhsh, Mahmood; Shakoori, Alireza; Niaki, Mohammad Yazdani; Monatshefte fur Chemie; vol. 135; nb. 10; (2004); p. 1243 - 1249, View in Reaxys

RCHO, R=1Naphthyl

Wang, Libo; Nakamura, Shuichi; Ito, Yuji; Toru, Takeshi; Tetrahedron Asymmetry; vol. 15; nb. 19; (2004); p. 3059 - 3072, View in Reaxys

aldeh., Tab.3, entry 4

Abiko, Yumi; Yamagiwa, Noriyuki; Sugita, Mari; Tian, Jun; Matsunaga, Shigeki; Shibasaki, Masakatsu; Synlett; nb. 13; (2004); p. 2434 - 2436, View in Reaxys

IIIt

Kozlov; Gusak; Tereshko; Firgang; Shashkov; Russian Journal of Organic Chemistry; vol. 40; nb. 8; (2004); p. 1181 - 1186, View in Reaxys

starting to 2

Ackermann, Damian; Haener, Robert; Helvetica Chimica Acta; vol. 87; nb. 11; (2004); p. 2790 - 2804, View in Reaxys

Ih

Nenaidenko; Golubinskii; Lenkova; Shastin; Balenkova; Russian Journal of Organic Chemistry; vol. 40; nb. 10; (2004); p. 1518 - 1520, View in Reaxys

44

Li, Qian; Lee, Jun-Seok; Ha, Chanki; Chan, Beum Park; Yang, Guang; Wen, Biao Gan; Chang, YoungTae; Angewandte Chemie - International Edition; vol. 43; nb. 46; (2004); p. 6331 - 6335, View in Reaxys

Ar-CHO, Ar=1naphthyl

Kise, Naoki; Ohya, Kengo; Arimoto, Kie; Yamashita, Yutaka; Hirano, Yuuki; Ono, Tadahiro; Ueda, Nasuo; Journal of Organic Chemistry; vol. 69; nb. 22; (2004); p. 7710 - 7719, View in Reaxys

Table 2, entry 7

Tian, Fengshou; Lu, Shiwei; Journal of Chemical Research; nb. 9; (2004); p. 632 - 633, View in Reaxys

subs. Tab. 2, entry 7

Wong, Wing-Leung; Lee, Chi-Sing; Leung, Hon-Kit; Kwong, Hoi-Lun; Organic and Biomolecular Chemistry; vol. 2; nb. 14; (2004); p. 1967 - 1969, View in Reaxys

Table 2, entry 8

Mao, Jincheng; Wan, Boshun; Wang, Rongliang; Wu, Fan; Lu, Shiwei; Journal of Organic Chemistry; vol. 69; nb. 26; (2004); p. 9123 - 9127, View in Reaxys

16, R2 = α-naphthyl

Biava, Mariangela; Porretta, Giulio Cesare; Deidda, Delia; Pompei, Raffaello; Tafi, Andrea; Manetti, Fabrizio; Bioorganic and Medicinal Chemistry; vol. 12; nb. 6; (2004); p. 1453 - 1458, View in Reaxys

tab. 1, entry 8, ald.

Narsaiah, A. Venkat; Basak; Visali; Nagaiah; Synthetic Communications; vol. 34; nb. 16; (2004); p. 2893 2901, View in Reaxys

Tab. 1, Ent. 5, ald. Zhong, Yu-Wu; Jiang, Chang-Sheng; Xu, Ming-Hua; Lin, Guo-Qiang; Tetrahedron; vol. 60; nb. 40; (2004); p. 8861 - 8868, View in Reaxys 6r

Tanaka, Hirotaka; Hashimoto, Kentaro; Suzuki, Kyosuke; Kitaichi, Yasunori; Sato, Mitsuo; Ikeno, Taketo; Yamada, Tohru; Bulletin of the Chemical Society of Japan; vol. 77; nb. 10; (2004); p. 1905 - 1914, View in Reaxys

subs., Tab. 1, entry 6

Zeynizadeh, Behzad; Yahyaei, Saiedeh; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 59; nb. 6; (2004); p. 704 - 710, View in Reaxys

educt of 1f

Suresh, Surisetti; Periasamy, Mariappan; Tetrahedron Letters; vol. 45; nb. 33; (2004); p. 6291 - 6293, View in Reaxys

educt to 7

Flowers II, Robert A.; Xu, Xin; Timmons, Cody; Li, Guigen; European Journal of Organic Chemistry; nb.

14; (2004); p. 2988 - 2990, View in Reaxys

Tab.1.col.1 run 9

Sun, Wei; Kuehn, Fritz E.; Tetrahedron Letters; vol. 45; nb. 40; (2004); p. 7415 - 7418, View in Reaxys

educt to 5f

Chung, Woo Jin; Ngo, Silvana C.; Higashiya, Seiichiro; Welch, John T.; Tetrahedron Letters; vol. 45; nb.

28; (2004); p. 5403 - 5406, View in Reaxys

2c, R=1-naphthyl

Arai, Shigeru; Hasegawa, Kazuya; Nishida, Atsushi; Tetrahedron Letters; vol. 45; nb. 5; (2004); p. 1023 1026, View in Reaxys

27b

Mulzer, Johann; Strecker, Achim R.; Kattner, Lars; Tetrahedron Letters; vol. 45; nb. 48; (2004); p. 8867 8870, View in Reaxys

10g

Shimada, Toyoshi; Kina, Asato; Hayashi, Tamio; Journal of Organic Chemistry; vol. 68; nb. 16; (2003); p.

6329 - 6337, View in Reaxys; Suzuki, Yumiko; Sato, Masayuki; Tetrahedron Letters; vol. 45; nb. 8; (2004); p. 1679 - 1681, View in Reaxys

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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2018-02-14 08:04:49

byproduct T. 1, e.

12

Mohajer, Daryoush; Iranpoor, Nasser; Rezaeifard, Abdolreza; Tetrahedron Letters; vol. 45; nb. 3; (2004); p. 631 - 634, View in Reaxys

1. educt to 6m

Song, Aimin; Marik, Jan; Lam, Kit S.; Tetrahedron Letters; vol. 45; nb. 13; (2004); p. 2727 - 2730, View in Reaxys

t.1,substr.,entry 4

Choi, Matthew Kwok Wai; Toy, Patrick H.; Tetrahedron; vol. 60; nb. 12; (2004); p. 2875 - 2879, View in Reaxys

8g

Palmieri, Gianni; Tetrahedron Asymmetry; vol. 11; nb. 16; (2000); p. 3361 - 3373, View in Reaxys; Blanchet, Jerome; Zhu, Jieping; Tetrahedron Letters; vol. 45; nb. 23; (2004); p. 4449 - 4452, View in Reaxys

1, R=α-naphthyl

Ding, Kuiling; Ishii, Akihiro; Mikami, Koichi; Angewandte Chemie - International Edition; vol. 38; nb. 4; (1999); p. 497 - 501, View in Reaxys; Yadav; Reddy; Krishnam Raju; Synthesis; nb. 6; (2003); p. 883 - 886, View in Reaxys

Tab.1. subst., entry 14

Sharghi, Hashem; Sarvari, Mona Hosseini; Synthesis; nb. 2; (2003); p. 243 - 246, View in Reaxys

7, R1 = 1-naphthyl

Casey, Mike; Smyth, Martin P.; Synlett; nb. 1; (2003); p. 102 - 106, View in Reaxys

product, tab 1, e 4 Das, Sasmita; Panigrahi; Maikap, Golak C.; Tetrahedron Letters; vol. 44; nb. 7; (2003); p. 1375 - 1377, View in Reaxys α-naphthaleneCHO

Karolak-Wojciechowska, Janina; Mrozek, Agnieszka; Kiec-Kononowicz, Katarzyna; Handzlik, Jadwiga; Journal of Molecular Structure; vol. 649; nb. 1-2; (2003); p. 25 - 36, View in Reaxys

fluorophore ald. d

Arimori, Susumu; Consiglio, Giuseppe A.; Phillips, Marcus D.; James, Tony D.; Tetrahedron Letters; vol. 44; nb. 25; (2003); p. 4789 - 4792, View in Reaxys

substr. entry 8

Sonavane, Sachin U.; Mohapatra, Susanta K.; Jayaram, Radha V.; Selvam, Parasuraman; Chemistry Letters; vol. 32; nb. 2; (2003); p. 142 - 143, View in Reaxys

NA-CHO

Tzing, Shin-Hwa; Ghule, Anil; Chang, Jia-Yaw; Ling, Yong-Chien; Journal of Mass Spectrometry; vol. 38; nb. 4; (2003); p. 401 - 408, View in Reaxys

5, P1=1-naphthyl

Lam, Patrick Y. S.; Adams, Jessica J.; Clark, Charles G.; Calhoun, W. Jason; Luettgen, Joseph M.; Knabb, Robert M.; Wexler, Ruth R.; Bioorganic and Medicinal Chemistry Letters; vol. 13; nb. 10; (2003); p.

1795 - 1799, View in Reaxys

1 (Table 1, run 6)

Sampath Kumar; Rao, M. Shesha; Joyasawal, Sipak; Yadav; Tetrahedron Letters; vol. 44; nb. 22; (2003); p. 4287 - 4289, View in Reaxys

starting to 3

Jursic, Branko S.; Neumann, Donna M.; Journal of Heterocyclic Chemistry; vol. 40; nb. 3; (2003); p. 465 474, View in Reaxys

educt to 6g

Kamitori, Yasuhiro; Heterocycles; vol. 60; nb. 5; (2003); p. 1185 - 1190, View in Reaxys

Table 1, Entry 8, subs.

Cordoba, Ruben; Plumet, Joaquin; Tetrahedron Letters; vol. 44; nb. 32; (2003); p. 6157 - 6159, View in Reaxys

8b

Okuyama, Yuko; Nakano, Hiroto; Igarashi, Mayumi; Kabuto, Chizuko; Hongo, Hiroshi; Heterocycles; vol. 59; nb. 2; (2003); p. 635 - 643, View in Reaxys

13f

Jimeno, Ciril; Pasto, Mireia; Riera, Antoni; Pericas, Miquel A.; Journal of Organic Chemistry; vol. 68; nb.

8; (2003); p. 3130 - 3138, View in Reaxys

chart 1, b

Denmark, Scott E.; Pham, Son M.; Journal of Organic Chemistry; vol. 68; nb. 13; (2003); p. 5045 - 5055, View in Reaxys

20b

Kitahara, Yoshiyasu; Mochii, Masaaki; Mori, Masakazu; Kubo, Akinori; Tetrahedron; vol. 59; nb. 16; (2003); p. 2885 - 2891, View in Reaxys

Tab.1, substr., en- Palaniappan, Srinivasan; Narender, Puli; Saravanan, Chandrasekaran; Rao, Vaidya Jayathirtha; Syntry 9 lett; nb. 12; (2003); p. 1793 - 1796, View in Reaxys educt to 3d

Sener, Ahmet; Genc, Hasan; Sener, M. Kasim; Journal of Heterocyclic Chemistry; vol. 40; nb. 4; (2003); p.

697 - 700, View in Reaxys

Product, Tab.1, run 13

Shirini; Zolfigol; Safari; Mohammadpoor-Baltork; Mirjalili; Tetrahedron Letters; vol. 44; nb. 40; (2003); p.

7463 - 7465, View in Reaxys

aldehyde for 8h

Sonda, Shuji; Kawahara, Toshio; Murozono, Takahiro; Sato, Noriko; Asano, Kiyoshi; Haga, Keiichiro; Bioorganic and Medicinal Chemistry; vol. 11; nb. 19; (2003); p. 4225 - 4234, View in Reaxys

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16b

Wang, Chaojie; Delcros, Jean-Guy; Cannon, Laura; Konate, Fanta; Carias, Horacio; Biggerstaff, John; Gardner, Richard Andrew; Phanstiel IV, Otto; Journal of Medicinal Chemistry; vol. 46; nb. 24; (2003); p.

5129 - 5138, View in Reaxys

Tab. I, entry 17

Zolfigol, Mohammad Ali; Poor-Baltork, Iraj Mohammad; Mirjalili, Bibi Fatemeh; Shirini, Farhad; Salehzadeh, Sadegh; Keypour, Hassan; Ghorbani-Choghamarani, Arash; Zebarjadian, Mohammad Hassan; Mohammadi, Kamal; Hazar, Azizeh; Phosphorus, Sulfur and Silicon and the Related Elements; vol.

178; nb. 12; (2003); p. 2735 - 2743, View in Reaxys

1, R4=1-naphthyl

Abdel-Fattah, Ashraf A. A.; Synthesis; nb. 15; (2003); p. 2358 - 2362, View in Reaxys

Tab. 1; entry 10-11

Azizi, Najmedin; Saidi, Mohammad R.; European Journal of Organic Chemistry; nb. 23; (2003); p. 4630 4633, View in Reaxys

subst., Tab.1, entry 7

Zeynizadeh, Behzad; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 58; nb.

12; (2003); p. 1220 - 1226, View in Reaxys

A35

Lee, Jae Wook; Jung, Michelle; Rosania, Gustavo R.; Chang, Young-Tae; Chemical Communications; nb.

15; (2003); p. 1852 - 1853, View in Reaxys

32

Rosania, Gustavo R.; Lee, Jae Wook; Ding, Liang; Yoon, Hai-Shin; Chang, Young-Tae; Journal of the American Chemical Society; vol. 125; nb. 5; (2003); p. 1130 - 1131, View in Reaxys; Velcheva, Evelina A.; Juchnovski, Ivan N.; Binev, Ivan G.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 59; nb. 8; (2003); p. 1745 - 1749, View in Reaxys

Tab.1, starting, entry1

Wang, Chun-Jiang; Shi, Min; European Journal of Organic Chemistry; nb. 15; (2003); p. 2823 - 2828, View in Reaxys

1-NaphthylCHO

Bandini, Marco; Cozzi, Pier Giorgio; Morganti, Stefano; Umani-Ronchi, Achille; Tetrahedron Letters; vol.

40; nb. 10; (1999); p. 1997 - 2000, View in Reaxys; Shimizu, Makoto; Iwata, Atsushi; Makino, Hiroaki; Synlett; nb. 9; (2002); p. 1538 - 1540, View in Reaxys

Table, entry 7

Desai; Swami; Nandurdikar; Synthetic Communications; vol. 32; nb. 6; (2002); p. 931 - 933, View in Reaxys

educt to 6b

Arai, Sadao; Yoda, Hiroe; Sato, Kiyoshi; Yamagishi, Takamichi; Journal of Heterocyclic Chemistry; vol.

39; nb. 2; (2002); p. 425 - 428, View in Reaxys

aldehyde, Table 1, e4

Liu, Junjie; Wong, Chi-Huey; Tetrahedron Letters; vol. 43; nb. 21; (2002); p. 3915 - 3917, View in Reaxys

Ar=1-naphthyl

Nakamura, Yutaka; Takeuchi, Seiji; Okumura, Kazuo; Ohgo, Yoshiaki; Curran, Dennis P; Tetrahedron; vol. 58; nb. 20; (2002); p. 3963 - 3969, View in Reaxys

educt to 5c

Taka, Hideo; Fujita, Ken-Ichi; Oishi, Akihiro; Taguchi, Yoichi; Heterocycles; vol. 57; nb. 8; (2002); p. 1487 - 1493, View in Reaxys

t.1, 1, entry 7

Bose, D. Subhas; Goud, P. Ravinder; Synthetic Communications; vol. 32; nb. 23; (2002); p. 3621 - 3624, View in Reaxys

Tab.1, entry 10, subst.

Roy, Subhas Chandra; Banerjee, Biplab; Synlett; nb. 10; (2002); p. 1677 - 1678, View in Reaxys

j, Ar

Shi, Min; Zhao, Gui-Ling; Tetrahedron Letters; vol. 43; nb. 50; (2002); p. 9171 - 9174, View in Reaxys

educt of 5

Mukaiyama, Teruaki; Fujisawa, Hidehiko; Nakagawa, Takashi; Helvetica Chimica Acta; vol. 85; nb. 12; (2002); p. 4518 - 4531, View in Reaxys

1-NpCHO

Fujisawa, Hidehiko; Mukaiyama, Teruaki; Chemistry Letters; nb. 8; (2002); p. 858 - 859, View in Reaxys

tab1, aldehyde, entry12

Morohashi, Naoya; Hattori, Tetsutaro; Yokomakura, Katsuya; Kabuto, Chizuko; Miyano, Sotaro; Tetrahedron Letters; vol. 43; nb. 43; (2002); p. 7769 - 7772, View in Reaxys

Product, Tab.2, run 27

Ganchegui, Benjamin; Bouquillon, Sandrine; Henin, Francoise; Muzart, Jacques; Tetrahedron Letters; vol. 43; nb. 37; (2002); p. 6641 - 6644, View in Reaxys

table 2, entry 10

Xu, Ming-Hua; Pu, Lin; Organic Letters; vol. 4; nb. 25; (2002); p. 4555 - 4557, View in Reaxys

entry 10, table 2

Nishiyama, Yutaka; Kajimoto, Hiroyuki; Kotani, Kazuya; Nishida, Takuma; Sonoda, Noboru; Journal of Organic Chemistry; vol. 67; nb. 16; (2002); p. 5696 - 5700, View in Reaxys

1-Naph-CHO

Asis, Silvia E.; Bruno, Ana M.; Martinez, Andrea R.; Sevilla, Maria V.; Gaozza, Carlos H.; Romano, Alejandra M.; Coussio, Jorge D.; Ciccia, Graciela; Farmaco; vol. 54; nb. 8; (1999); p. 517 - 523, View in Reaxys; Dai, Wei-Min; Wu, Anxin; Hamaguchi, Wataru; Tetrahedron Letters; vol. 42; nb. 25; (2001); p. 4211 - 4214, View in Reaxys

Substrate, Tab.1, run 4

Basu, Manas K.; Banik, Bimal K.; Tetrahedron Letters; vol. 42; nb. 2; (2001); p. 187 - 189, View in Reaxys

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4(15)

Uozumi, Yasuhiro; Mizutani, Kanako; Nagai, Shin-ichi; Tetrahedron Letters; vol. 42; nb. 3; (2001); p. 407 410, View in Reaxys

aldehyde to 6

Kawase; Varu; Shah; Motohashi; Tani; Saito; Debnath; Mahapatra; Dastidar; Chakrabarty; ArzneimittelForschung/Drug Research; vol. 51; nb. 1; (2001); p. 67 - 71, View in Reaxys

2, Ar=1-naphthyl

Hirao, Toshikazu; Morimoto, Chihiro; Takada, Takashi; Sakurai, Hidehiro; Tetrahedron Letters; vol. 42; nb. 10; (2001); p. 1961 - 1963, View in Reaxys

1, R1,R2=benzo, R3=H

Nair, Vijay; Bindu; Balagopal, Lakshmi; Tetrahedron Letters; vol. 42; nb. 10; (2001); p. 2043 - 2044, View in Reaxys

aldehyde for 3Ae

Mantani; Shiomi; Konno; Ishihara; Yamanaka; Journal of Organic Chemistry; vol. 66; nb. 10; (2001); p.

3442 - 3448, View in Reaxys

2, R2=1-C10H7

Ramalinga; Vijayalakshmi; Kaimal; Synlett; nb. 6; (2001); p. 863 - 865, View in Reaxys

Substrate, Tab.2, run 7

Xu, Qianyong; Wang, Hui; Pan, Xinfu; Chan, Albert S.C; Yang, Teng-Kuei; Tetrahedron Letters; vol. 42; nb. 35; (2001); p. 6171 - 6173, View in Reaxys

R'CHO Tab. 2, entry 9

Teng, Xin; Wada, Takeshi; Okamoto, Sentaro; Sato, Fumie; Tetrahedron Letters; vol. 42; nb. 32; (2001); p.

5501 - 5503, View in Reaxys

RCHO R=1-naph- Shimizu, Makoto; Takeuchi, Yuka; Sahara, Tetsuya; Chemistry Letters; nb. 11; (2001); p. 1196 - 1197, thyl View in Reaxys product, Tab2, en- Hashimoto, Kentaro; Kitaichi, Yasunori; Tanaka, Hirotaka; Ikeno, Taketo; Yamada, Tohru; Chemistry try 17 Letters; nb. 9; (2001); p. 922 - 923, View in Reaxys 11, Table 5, entry 34

Nagayama; Shimizu; Yamamoto; Bulletin of the Chemical Society of Japan; vol. 74; nb. 10; (2001); p. 1803 - 1815, View in Reaxys

α-Naph-CHO

Maruoka, Keiji; Journal of Fluorine Chemistry; vol. 112; nb. 1; (2001); p. 95 - 99, View in Reaxys

aldehyde to LI

Gusak; Tereshko; Kozlov; Russian Journal of Organic Chemistry; vol. 37; nb. 10; (2001); p. 1495 - 1502, View in Reaxys

2, R = 1-naphthyl

Schneider; Hansch; Chemical Communications; nb. 13; (2001); p. 1218 - 1219, View in Reaxys

f

Denmark, Scott E.; Pham, Son M.; Organic Letters; vol. 3; nb. 14; (2001); p. 2201 - 2204, View in Reaxys

16a

Laali, Kenneth K.; Herbert, Mark; Cushnyr, Brad; Bhatt, Anand; Terrano, David; Journal of the Chemical Society. Perkin Transactions 1; nb. 6; (2001); p. 578 - 583, View in Reaxys

1-NA

Fukuzumi; Satoh; Okamoto; Yasui; Suenobu; Seko; Fujitsuka; Ito; Journal of the American Chemical Society; vol. 123; nb. 32; (2001); p. 7756 - 7766, View in Reaxys

Note 10

Nakamura, Yutaka; Takeuchi, Seiji; Ohgo, Yoshiaki; Curran, Dennis P.; Tetrahedron Letters; vol. 41; nb.

1; (2000); p. 57 - 60, View in Reaxys

α-Np-CHO

Ooi, Takashi; Takaya, Keisuke; Miura, Tomoya; Maruoka, Keiji; Synlett; nb. 1; (2000); p. 69 - 70, View in Reaxys

1(entry 14)

Ali, Sayyed Iliyas; Nikalje, Milind D.; Dewkar, Gajanan K.; Paraskar, Abhimanyu S.; Jagtap; Sudalai; Journal of Chemical Research - Part S; nb. 1; (2000); p. 30 - 31, View in Reaxys

Table 1 Entry 10 subst.

Kabalka, George W.; Wu, Zhongzhi; Ju, Yuhong; Tetrahedron Letters; vol. 41; nb. 27; (2000); p. 5161 5164, View in Reaxys

educt of 5b

Shimizu, Masaki; Hata, Takeshi; Hiyama, Tamejiro; Heterocycles; vol. 52; nb. 2; (2000); p. 707 - 717, View in Reaxys

educt of 4c

Dudot, Bruno; Royer, Jacques; Sevrin, Mireille; George, Pascal; Tetrahedron Letters; vol. 41; nb. 22; (2000); p. 4367 - 4371, View in Reaxys

26

Kantlehner, Willi; Vettel, Markus; Gissel, Alexander; Haug, Erwin; Ziegler, Georg; Ciesielski, Michael; Scherr, Oliver; Haas, Richard; Advanced Synthesis and Catalysis; vol. 342; nb. 3; (2000); p. 297 - 310, View in Reaxys

ArCHO (Ar=1naphthyl)

Santa Deepthi; Sahadeva Reddy; Reddy; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 39; nb. 3; (2000); p. 220 - 222, View in Reaxys

educt, tab 2, entry Hayakawa, Ryuuichirou; Shimizu, Makoto; Chemistry Letters; nb. 7; (2000); p. 724 - 725, View in Reaxys 6 RCHO (table 1 entry 2)

Li, Jianke; Li, Chao-Jun; Heterocycles; vol. 53; nb. 8; (2000); p. 1691 - 1695, View in Reaxys

RCHO to 2f (E)

Cristau; Pirat; Drag; Kafarski; Tetrahedron Letters; vol. 41; nb. 50; (2000); p. 9781 - 9785, View in Reaxys

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A, CHO

Castellano, Sabrina; Stefancich, Giorgio; Musiu, Chiara; La Colla, Paolo; Archiv der Pharmazie; vol.

333; nb. 9; (2000); p. 299 - 304, View in Reaxys

ald.for 2r

Sackus; Amankaviciene; Martynaitis; Chemistry of Heterocyclic Compounds; vol. 36; nb. 6; (2000); p. 663 - 671, View in Reaxys

ald.for 14d

Muthiah; Praveen Kumar; Aruna Mani; Kumara Swamy; Journal of Organic Chemistry; vol. 65; nb. 12; (2000); p. 3733 - 3737, View in Reaxys

Tab.1,aldehyde,entry 3

Nair, Vijay; Vinod; Chemical Communications; nb. 12; (2000); p. 1019 - 1020, View in Reaxys

C10H7CHO

Kamimura, Akio; Omata, Yoji; Mitsudera, Hiromasa; Kakehi, Akikazu; Journal of the Chemical Society, Perkin Transactions 1; nb. 24; (2000); p. 4499 - 4504, View in Reaxys

d

Denmark; Stavenger; Journal of the American Chemical Society; vol. 122; nb. 37; (2000); p. 8837 - 8847, View in Reaxys

Table 4 Entry 7 Ald.

Keller, Felix; Rippert, Andreas Johannes; Helvetica Chimica Acta; vol. 82; nb. 1; (1999); p. 125 - 137, View in Reaxys

RCHO, R = c

Ivanova, Diana; Kolev, Vilen; Lazarova, Tzvetana; Padros, Esteve; Tetrahedron Letters; vol. 40; nb. 13; (1999); p. 2645 - 2648, View in Reaxys

t.1, entry 8

Venkatachalapathy; Rajarajan; Shayira Banu; Pitchumani; Tetrahedron; vol. 55; nb. 13; (1999); p. 4071 4076, View in Reaxys

16d

Denmark, Scott E.; Su, Xiping; Nishigaichi, Yutaka; Coe, Diane M.; Wong, Ken-Tsung; Winter, Stephen B. D.; Choi, Jun Young; Journal of Organic Chemistry; vol. 64; nb. 6; (1999); p. 1958 - 1967, View in Reaxys

Aldehyde, entry 4

Falck; Barma; Mioskowski, Charles; Schlama, Thierry; Tetrahedron Letters; vol. 40; nb. 11; (1999); p.

2091 - 2094, View in Reaxys

Scheme 3

Torun, Lokman; Mohammad, Taj; Morrison, Harry; Tetrahedron Letters; vol. 40; nb. 29; (1999); p. 5279 5282, View in Reaxys

to 13a

Hoffmann, Douglas; Reinke, Helmut; Oehme, Hartmut; Journal of Organometallic Chemistry; vol. 585; nb.

1; (1999); p. 189 - 197, View in Reaxys

entry 13

Mohammadpoor-Baltork; Aliyan; Synthetic Communications; vol. 29; nb. 16; (1999); p. 2741 - 2746, View in Reaxys

1-naphthaldehyde Welch, John T.; Gregor, Tamas; Kornilov, Andrei; Israel Journal of Chemistry; vol. 39; nb. 2; (1999); p. 171 - 178, View in Reaxys RCHO, Table 1, entry 6

Kuroki, Yoshichika; Iseki, Katsuhiko; Tetrahedron Letters; vol. 40; nb. 47; (1999); p. 8231 - 8234, View in Reaxys

R'COR", Table 1, run 8

Marchi, Caroline; Buono, Gerard; Tetrahedron Letters; vol. 40; nb. 52; (1999); p. 9251 - 9254, View in Reaxys

1-NaphthCHO

Millot, Nicolas; Knochel, Paul; Tetrahedron Letters; vol. 40; nb. 44; (1999); p. 7779 - 7782, View in Reaxys

ArCHO to compound 14

Altas, Yesim; Safak, Cihat; Batu, Oezlem S.; Erol, Kevser; Arzneimittel-Forschung/Drug Research; vol.

49; nb. 10; (1999); p. 824 - 829, View in Reaxys

aldehyde 18

Leonel, Eric; Paugam, Jean-Paul; Heintz, Monique; Nedelec, Jean-Yves; Synthetic Communications; vol.

29; nb. 22; (1999); p. 4015 - 4024, View in Reaxys

product 4

Nair, Vijay; Nair, Latha G.; Balagopal, Lakshmi; Rajan, Roshini; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 38; nb. 11; (1999); p. 1234 - 1236, View in Reaxys

9g

Deng, Wei-Ping; Hou, Xue-Long; Dai, Li-Xin; Tetrahedron Asymmetry; vol. 10; nb. 24; (1999); p. 4689 4693, View in Reaxys

NaphCHO

Nakanishi, Ikuo; Itoh, Shinobu; Fukuzumi, Shunichi; Chemistry - A European Journal; vol. 5; nb. 10; (1999); p. 2810 - 2818, View in Reaxys

Table 4, Entry 7

Mohammadpoor-Baltork, Iraj; Hajipour, Abdol Reza; Mohammadi, Hasan; Bulletin of the Chemical Society of Japan; vol. 71; nb. 7; (1998); p. 1649 - 1653, View in Reaxys

1-naphthyl-CH=O

Pagenkopf, Brian L.; Carreira, Erick M.; Tetrahedron Letters; vol. 39; nb. 52; (1998); p. 9593 - 9596, View in Reaxys

R=1-naphthyl

Aspinall, Helen C.; Greeves, Nicholas; McIver, Edward G.; Tetrahedron Letters; vol. 39; nb. 50; (1998); p.

9283 - 9286, View in Reaxys

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20i

Vyskocil, Stepn; Jaracz, Stanislav; Smrcina, Martin; Sticha, Martin; Hanus, Vladimir; Miroslav Poldsek; Kocovsky, Pavel; Journal of Organic Chemistry; vol. 63; nb. 22; (1998); p. 7727 - 7737, View in Reaxys

C10H7-CHO

Curran, Dennis P.; Luo, Zhiyong; Medicinal Chemistry Research; vol. 8; nb. 4-5; (1998); p. 261 - 265, View in Reaxys

educt to 14(a-d)

Fioravanti, Rossella; Biava, Mariangela; Porretta, Giulio Cesare; Artico, Marino; Lampis, Giorgio; Deidda, Delia; Pompei, Raffaello; Medicinal Chemistry Research; vol. 7; nb. 2; (1997); p. 87 - 97, View in Reaxys

α-C10H7-CHO

Cha, Jin Soon; Lee, Jae Cheol Lee; Lee, Sung Eun; Organic Preparations and Procedures International; vol. 24; nb. 3; (1992); p. 327 - 330, View in Reaxys

Patent-Specific Data (23) Prophetic ComLocation in Patent References pound Patent; Hangzhou Normal University; Yang, Limin; Zhong, Guofu; Jiang, Shengsheng; Yan, Jun; (24 pag.); CN106336384; (2017); (A) Chinese, View in Reaxys Patent; Nanjing University of Science and Technology; LI, Feng; LU, Lei; MA, Juan; CHENG, Rui; (18 pag.); CN106518789; (2017); (A) Chinese, View in Reaxys Patent; Xihua University; Wang, Zhouyu; Ma, Xiaobo; Ai, Wensi; Xu, Zhihong; He, Tao; (21 pag.); CN104529784; (2017); (B) Chinese, View in Reaxys Patent; Huaqiao University; Cheng Guolin; Weng Yunxiang; (17 pag.); CN106883241; (2017); (A) Chinese, View in Reaxys Patent; Zhejiang University of Technology; Zhang Guofu; Zhao Yiyong; Zhang Guihua; Ding Chengrong; Lv Jinghui; Yu Yidong; (10 pag.); CN106905097; (2017); (A) Chinese, View in Reaxys Patent; Dalian University of Technology; Wang Baomin; Zhang Huanrui; Qu Jingping; (26 pag.); CN105037386; (2017); (B) Chinese, View in Reaxys Patent; SANKO TEKSTIL ISLETMELERI SAN. VE TIC. A.S.; Aker, Acelya; Ocal, Nuket; Ergindemir, Hikmet Nil; Hamitbeyli, Agamirze; (31 pag.); US9834524; (2017); (B2) English, View in Reaxys Patent; Zhejiang University; Gu, Haorui; Jin, Enze; Lin, Xufeng; (7 pag.); CN105418611; (2016); (A) Chinese, View in Reaxys Patent; Beijing Institute of Technology; LI, JIARONG; YANG, JUNJUAN; SHI, DAXIN; ZHANG, QI; (12 pag.); CN103980193; (2016); (B) Chinese, View in Reaxys Patent; Henan Normal University; Fan, Xuesen; Li, Bin; Zhang, Xinying; Chen, Nana; Guo, Shenghai; (9 pag.); CN105601480; (2016); (A) Chinese, View in Reaxys Patent; Henan Normal University; Zhang, Xinying; Wang, Qianqian; Fan, Xuesen; Wang, Zhangxin; Xu, Yuanshuang; (15 pag.); CN106220503; (2016); (A) Chinese, View in Reaxys Page/Page column

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Patent; AstraZeneca AB; US6342601; (2002); (B1) English, View in Reaxys Patent; Mitsui Chemicals, Inc.; US6369269; (2002); (B2) English, View in Reaxys Patent; MITSUI CHEMICALS, INC.; EP1193264; (2002); (A1) English, View in Reaxys Patent; ELI LILLY AND COMPANY; EP1266897; (2002); (A2) English, View in Reaxys prophetic product

Patent; Ciba-Geigy Corporation; US3987023; (1976); (A1) English, View in Reaxys; Patent; Smith Kline and French Laboratories Limited; US4185103; (1980); (A1) English, View in Reaxys; Patent; Petrolite Corporation; US4311841; (1982); (A1) English, View in Reaxys; Patent; Basu; Amaresh; Gahman; Timothy C.; Girten; Beverly E.; Griffith; Michael C.; Hecht; Curtis C.; Kiely; John S.; Slivka; Sandra R.; US6127381; (2000); (A1) English, View in Reaxys; Patent; Ethyl Corporation; US4837327; (1989); (A1) English, View in Reaxys

Druglikeness (1) 1 of 1

LogP

2.984

H Bond Donors

0

H Bond Acceptors

1

Rotatable Bonds

1

TPSA

17.07

Lipinski Number

4

Veber Number

2

Related Structure (2) Related Structure References . The author has doubts about the constitution/ configuration of the title compound.

Skoczynska, Ewa; Korytar, Peter; De Boer, Jacob; Environmental Science and Technology; vol. 42; nb.

17; (2008); p. 6611 - 6618, View in Reaxys

Suzuki et al. al.; Journal of Molecular Spectroscopy; vol. 57; (1975); p. 490, View in Reaxys Derivative (41) Comment (Derivative)

Derivative

References

1-naphthaldehyde Card,P.J.; Friedli,F.E.; Shechter,H.; Journal of the American Chemical Society; vol. 105; 2,4-dinitrophenyl- (1983); p. 6104, View in Reaxys hydrazone By formation of compound with 2,4-dinitrophenylhydrazine

Walther, H.; Haase, L.; Gross, H.; Costisella, B.; Keitel, I.; Journal fuer Praktische Chemie (Leipzig); vol. 322; nb. 6; (1980); p. 902 - 908, View in Reaxys

Pikrat: Bildungsgroessen der Komplexbildung in CDCl3: ΔH0,ΔG0, ΔS0

Abdel-Rehiem et al.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 71; (1975); p. 1762,1765, View in Reaxys

2,4-DNPH: F: 228-230grad

Gurudutt,K.N.; Seshadri,T.R.; Phytochemistry (Elsevier); vol. 13; (1974); p. 2845 2847, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 262-264gradgelb

Wege,D.; Wilkinson,S.P.; Australian Journal of Chemistry; vol. 26; (1973); p. 1751 1762, View in Reaxys

Phenylhydrazon: F: 76grad

Kremlev et al.; Voprosy Khimii i Khimicheskoi Tekhnologii; vol. 25; (1972); p. 32,33-36; Chem.Abstr.; vol. 78; nb. 110775z; Chem. Zentralbl.; Ref.Zh.Khim. No 16 <1972> Zh 217, View in Reaxys

Oxim, F: 98-99grad

Kreutzberger; Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft; vol. 304; (1971); p. 362,363, 365, View in Reaxys

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Pikrat-Komplex: Assoz.-Konst.

(Tab.1)

Farrell; Westwood; Journal of the Chemical Society [Section] B: Physical Organic; (1970); p. 1518, View in Reaxys

Komplex mit TCNE: UV; LCAO-Ber. d. Energieniveaus

Figeys; Wilmet-Devos; Bulletin des Societes Chimiques Belges; vol. 79; (1970); p.

459,460, View in Reaxys

DNP; mp: 257-258grad

Watkins; Phytochemistry (Elsevier); vol. 8; (1969); p. 979,981, View in Reaxys

Komplex m. ICl: CO-Valenzschwingungsfrequenz

Chauning; Wells; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1887, View in Reaxys

2-Chlor-<5>thienylsulfonylhydrazon: F: 147grad

Munshi; Trivedi; Journal of the Indian Chemical Society; vol. 40; (1963); p. 1039, View in Reaxys

2-Brom-<5>thienylsulfonylhydrazon: F: 156-157grad

Munshi; Trivedi; Journal of the Indian Chemical Society; vol. 40; (1963); p. 1039, View in Reaxys

Charge-TransferKomplex m. IBr: spektroskop.

Nachw.

Augdahl; Klaeboe; Acta Chemica Scandinavica (1947-1973); vol. 16; (1962); p.

1647,1649, View in Reaxys

Charge-TransferKomplex m. ICl: spektroskop.

Nachw.

Augdahl; Klaeboe; Acta Chemica Scandinavica (1947-1973); vol. 16; (1962); p.

1647,1649, View in Reaxys

Charge-TransferKomplex m. Iod: spektroskop.

Nachw.

Augdahl; Klaeboe; Acta Chemica Scandinavica (1947-1973); vol. 16; (1962); p.

1647,1649, View in Reaxys

Thiobenzoylhydrazon: F: 126grad

Jensen,K.A.; Pedersen,C.; Acta Chemica Scandinavica (1947-1973); vol. 15; (1961); p.

1097 - 1103, View in Reaxys

Phenylthioacetylhydrazon: F: 160grad

Jensen,K.A.; Pedersen,C.; Acta Chemica Scandinavica (1947-1973); vol. 15; (1961); p.

1097 - 1103, View in Reaxys

2,4-Dinitro-phenylhydrazon: F: 256-257grad

Stiles,M.; Sisti,A.J.; Journal of Organic Chemistry; vol. 25; nb. 10; (1960); p. 1691 1693, View in Reaxys

compound with 2,4,7-trinitro-fluoren-9-one (mp: 155 degree , yellow green); Further Data see Handbook

Laskowski; McCrone; Analytical Chemistry; vol. 30; (1958); p. 542, View in Reaxys

thiobenzoylhydrazone (mp: 126 degree )

Jensen; Jensen; Acta Chemica Scandinavica (1947-1973); vol. 6; (1952); p. 957, View in Reaxys

2-phenyl-thioacetylhydrazone (mp: 160 degree )

Jensen; Jensen; Acta Chemica Scandinavica (1947-1973); vol. 6; (1952); p. 957, View in Reaxys

methyl-phenyl-hydrazone (mp: 92 degree )

Jensen; Dynesen; Acta Chemica Scandinavica (1947-1973); vol. 4; (1950); p. 692,699, View in Reaxys

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4-phenyl semicarbazone (mp: 205-206 degree )

Jensen; Dynesen; Acta Chemica Scandinavica (1947-1973); vol. 4; (1950); p. 692,699, View in Reaxys

3-nitro-benzoylhydrazone (mp: 217-218 degree )

Jensen; Dynesen; Acta Chemica Scandinavica (1947-1973); vol. 4; (1950); p. 692,699, View in Reaxys

2,4-dinitro-phenylhydrazone (mp: 260-262 degree )

Jensen; Dynesen; Acta Chemica Scandinavica (1947-1973); vol. 4; (1950); p. 692,699, View in Reaxys

semicarbazone (mp: 219 degree )

Coles; Dodds; Journal of the American Chemical Society; vol. 60; (1938); p. 853, View in Reaxys

phenylhydrazone (mp: 82 degree )

Coles; Dodds; Journal of the American Chemical Society; vol. 60; (1938); p. 853, View in Reaxys

thiosemicarbazone (mp: 217 degree )

Coles; Dodds; Journal of the American Chemical Society; vol. 60; (1938); p. 853, View in Reaxys

4-nitro-phenylhydrazone (mp: 237 degree )

Coles; Dodds; Journal of the American Chemical Society; vol. 60; (1938); p. 853, View in Reaxys

N.N-diphenyl-hydrazone (mp: 100,5 degree )

Coles; Dodds; Journal of the American Chemical Society; vol. 60; (1938); p. 853, View in Reaxys

naphthyl-(2)-hydrazone (mp: 174-175 degree )

Coles; Dodds; Journal of the American Chemical Society; vol. 60; (1938); p. 853, View in Reaxys

4.4-diphenyl semicarbazone (mp: 197 degree )

Coles; Dodds; Journal of the American Chemical Society; vol. 60; (1938); p. 853, View in Reaxys

4-bromo-phenylhydrazone (mp: 136-137 degree )

Coles; Dodds; Journal of the American Chemical Society; vol. 60; (1938); p. 853, View in Reaxys

2.4-dinitro-phenylhydrazone (mp: 254 degree )

Coles; Dodds; Journal of the American Chemical Society; vol. 60; (1938); p. 853, View in Reaxys

2.5-dichloro-phenylhydrazone (mp: 114 degree )

Coles; Dodds; Journal of the American Chemical Society; vol. 60; (1938); p. 853, View in Reaxys

oxime (mp: 98,5 degree )

Wuyts; Bulletin des Societes Chimiques Belges; vol. 39; (1930); p. 58,63, View in Reaxys

azine (mp: 156-157 degree )

Wuyts; Bulletin des Societes Chimiques Belges; vol. 39; (1930); p. 58,63, View in Reaxys

semicarbazone (mp: 228 degree )

Wuyts; Bulletin des Societes Chimiques Belges; vol. 39; (1930); p. 58,63, View in Reaxys

4-nitro-phenylhydrazone (mp: 233-235 degree )

Shoesmith; Guthrie; Journal of the Chemical Society; (1928); p. 2332, View in Reaxys

4-nitro-phenylhydrazone (mp: 234 degree )

Stephen; Journal of the Chemical Society; vol. 127; (1925); p. 1877, View in Reaxys

Melting Point (4) 1 of 4

Melting Point [°C]

33

Sitkin,A.I. et al.; Zhurnal Organicheskoi Khimii; vol. 11; (1975); p. 452,443 - 444, View in Reaxys; Patent; Jagupolskij et al.; SU387962; (1973); Ref. Zh., Khim.; vol. 15; nb. N175P; (1974), View in Reaxys 2 of 4

Melting Point [°C]

2.5

Angyal; Tetaz; Wilson; Organic Syntheses; vol. Coll. Vol. IV; (1963); p. 690, View in Reaxys

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3 of 4

Melting Point [°C]

2.5

Comment (Melting Point)

der E II 335 angegebene Schmelzpunkt (33-34grad) ist unrichtig.

Angyal et al.; Journal of the Chemical Society; (1950); p. 2141,2142,2144, View in Reaxys 4 of 4

Melting Point [°C]

33 - 34

Stephen; Journal of the Chemical Society; vol. 127; (1925); p. 1877, View in Reaxys Boiling Point (32) Boiling Point [°C] Pressure (Boiling Point) [Torr] 161

Location

Comment (Boiling References Point)

supporting information

Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 - 595, View in Reaxys

160 - 162

15

Hajipour, Abdol R.; Adibi, Hadi; Ruoho, Arnold E.; Journal of Organic Chemistry; vol. 68; nb. 11; (2003); p. 4553 - 4555, View in Reaxys

97

0.5

Kantlehner, Willi; Vettel, Markus; Gissel, Alexander; Haug, Erwin; Ziegler, Georg; Ciesielski, Michael; Scherr, Oliver; Haas, Richard; Advanced Synthesis and Catalysis; vol.

342; nb. 3; (2000); p. 297 - 310, View in Reaxys

140 - 143

3

Banik, Bimal K.; Ghatak, Anjan; Venkatraman; Becker, Frederick F.; Synthetic Communications; vol. 30; nb. 15; (2000); p. 2701 - 2705, View in Reaxys

160 - 161

12

Hirano, Masao; Ukawa, Ken; Yakabe, Sigetaka; Clark, James H.; Morimoto, Takashi; Synthesis; nb. 8; (1997); p. 858 - 860, View in Reaxys; Hirano, Masao; Ukawa, Ken; Yakabe, Shigetaka; Morimoto, Takashi; Organic Preparations and Procedures International; vol. 29; nb. 4; (1997); p. 480 - 484, View in Reaxys

155

12

Blanc; Bulletin de la Societe Chimique de France; vol. <4> 33; (1923); p. 317; Chem. Zentralbl.; vol. 94; nb. I; (1923); p. 1571, View in Reaxys; Niestroj, Michael; Neumann, Wilhelm P.; Chemische Berichte; vol. 129; nb. 1; (1996); p. 45 - 51, View in Reaxys

115 - 116

0.2

Olah, George A.; Surya Prakash, G. K.; Arvanaghi, Massoud; Synthesis; nb. 3; (1984); p.

228 - 230, View in Reaxys

142

6

Olah, George A.; Arvanaghi, Massoud; Angewandte Chemie; vol. 93; nb. 10; (1981); p. 925 926, View in Reaxys

100

1.5

Gupton, John T.; Polk, Dale E.; Synthetic Communications; vol. 11; nb. 7; (1981); p. 571 - 578, View in Reaxys

84 - 89

0.05

Comins; Meyers; Synthesis; (1978); p. 403, View in Reaxys

147 - 149

12

Schoenberg,A.; Heck,R.F.; Journal of the American Chemical Society; vol. 96; nb. 25; (1974); p.

7761 - 7764, View in Reaxys; Patent; Univ. of Delaware; US3960932; (1976); Chem.Abstr.; vol. 85; nb. 108421, View in Reaxys

141 - 142

7

Kreutzberger; Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesell-

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schaft; vol. 304; (1971); p. 362,363, 365, View in Reaxys 114 - 116

2

Horiie; Masomura; Kogyo Kagaku Zasshi; vol.

72; (1969); p. 686,687; Chem.Abstr.; vol. 72; nb.

66154; (1970), View in Reaxys

140 - 142

8

Price; Voong; Journal of Organic Chemistry; vol.

14; (1949); p. 111,114, View in Reaxys; Oda; Hayashi; Nippon Kagaku Zasshi; vol. 87; (1966); p. 291,292, View in Reaxys

162 - 164

18

Angyal; Tetaz; Wilson; Organic Syntheses; vol.

Coll. Vol. IV; (1963); p. 690, View in Reaxys; Ol'dekop; Kalinina; J. Gen. Chem. USSR (Engl.

Transl.); vol. 34; (1964); p. 3473,3515, View in Reaxys

112 - 115

1

Gross,H.; Matthey,G.; Chemische Berichte; vol.

97; (1964); p. 2606 - 2613, View in Reaxys

105 - 107

0.2

Angyal; Tetaz; Wilson; Organic Syntheses; vol.

Coll. Vol. IV; (1963); p. 690, View in Reaxys

101

1

Bell; Linschitz; Journal of the American Chemical Society; vol. 85; (1963); p. 528, View in Reaxys

165

20

Gaiffe; Pallaud; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 252; (1961); p. 1339,1340, View in Reaxys

105

0.5

Stiles,M.; Sisti,A.J.; Journal of Organic Chemistry; vol. 25; nb. 10; (1960); p. 1691 - 1693, View in Reaxys

150

9

Rousset; Bulletin de la Societe Chimique de France; vol. <3> 17; (1897); p. 309, View in Reaxys; Price; Voong; Journal of Organic Chemistry; vol. 14; (1949); p. 111,114, View in Reaxys

156 - 157

14

Ruggli; Preuss; Helvetica Chimica Acta; vol. 24; (1941); p. 1345,1354, View in Reaxys

150

13

Badger; Journal of the Chemical Society; (1941); p. 535,537, View in Reaxys

291 - 292

Hinkel; Ayling; Beynon; Journal of the Chemical Society; (1936); p. 339,342, View in Reaxys

156

15

Shoppee; Journal of the Chemical Society; (1933); p. 37,39, View in Reaxys

169 - 170

30

Schlenk; Bergmann; Justus Liebigs Annalen der Chemie; vol. 479; (1930); p. 58,74, View in Reaxys

173 - 174

35

Shoesmith; Guthrie; Journal of the Chemical Society; (1928); p. 2332, View in Reaxys

152

12

Rupe; Becherer; Helvetica Chimica Acta; vol. 6; (1923); p. 882, View in Reaxys

158.6 - 159

15

Krollpfeiffer; Justus Liebigs Annalen der Chemie; vol. 430; (1923); p. 199, View in Reaxys

164

20

Hebert; Bulletin de la Societe Chimique de France; vol. <4> 27; (1920); p. 50, View in Reaxys

291

760

Hebert; Bulletin de la Societe Chimique de France; vol. <4> 27; (1920); p. 50, View in Reaxys

291.6

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Fluessigkeit.

46/91

Bamberger; Lodter; Chemische Berichte; vol.

21; (1888); p. 258, View in Reaxys

2018-02-14 08:04:49

Refractive Index (6) Refractive Index Wavelength (Refractive Index) [nm]

Temperature (Refractive Index) [°C]

References

1.65

589

25

Ol'dekop; Kalinina; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 3473,3515, View in Reaxys

1.6503

589

25

Angyal; Tetaz; Wilson; Organic Syntheses; vol. Coll. Vol. IV; (1963); p. 690, View in Reaxys

1.644

656.3

19.3

Krollpfeiffer; Justus Liebigs Annalen der Chemie; vol. 430; (1923); p. 199, View in Reaxys

1.6546

589

19.3

Krollpfeiffer; Justus Liebigs Annalen der Chemie; vol. 430; (1923); p. 199, View in Reaxys

1.6849

486.1

19.3

Krollpfeiffer; Justus Liebigs Annalen der Chemie; vol. 430; (1923); p. 199, View in Reaxys

1.7162

434

19.3

Krollpfeiffer; Justus Liebigs Annalen der Chemie; vol. 430; (1923); p. 199, View in Reaxys

Density (2) 1 of 2

Density [g·cm-3]

1.1503

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Wuyts; Berman; Lacourt; Bulletin des Societes Chimiques Belges; vol. 40; (1931); p. 665,669, View in Reaxys 2 of 2

Density [g·cm-3]

1.149

Reference Temperature [°C]

4

Measurement Temperature [°C]

19.3

Krollpfeiffer; Justus Liebigs Annalen der Chemie; vol. 430; (1923); p. 199, View in Reaxys Adsorption (MCS) (1) 1 of 1

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

silica-SnO2

Kodakari, Nobuaki; Katada, Naonobu; Niwa, Miki; Journal of the Chemical Society, Chemical Communications; nb. 6; (1995); p. 623 - 624, View in Reaxys Association (MCS) (10) 1 of 10

Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

24.84

Partner (Association (MCS))

trimethylsilyl trifluoromethanesulfonate

Fukuzumi; Satoh; Okamoto; Yasui; Suenobu; Seko; Fujitsuka; Ito; Journal of the American Chemical Society; vol. 123; nb. 32; (2001); p. 7756 - 7766, View in Reaxys 2 of 10

Description (Association Formation constant of a complex (MCS)) Solvent (Association (MCS))

acetonitrile

Temperature (Association (MCS)) [°C]

24.84

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Partner (Association (MCS))

Mg(ClO4)2

Fukuzumi; Satoh; Okamoto; Yasui; Suenobu; Seko; Fujitsuka; Ito; Journal of the American Chemical Society; vol. 123; nb. 32; (2001); p. 7756 - 7766, View in Reaxys 3 of 10

Description (Association Formation constant of a complex (MCS)) Solvent (Association (MCS))

acetonitrile

Temperature (Association (MCS)) [°C]

24.84

Partner (Association (MCS))

Sc(OTf)3

Fukuzumi; Satoh; Okamoto; Yasui; Suenobu; Seko; Fujitsuka; Ito; Journal of the American Chemical Society; vol. 123; nb. 32; (2001); p. 7756 - 7766, View in Reaxys 4 of 10

Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

acetonitrile

Temperature (Association (MCS)) [°C]

24.84

Partner (Association (MCS))

Sc(OTf)3

Fukuzumi; Satoh; Okamoto; Yasui; Suenobu; Seko; Fujitsuka; Ito; Journal of the American Chemical Society; vol. 123; nb. 32; (2001); p. 7756 - 7766, View in Reaxys 5 of 10

Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

acetonitrile

Temperature (Association (MCS)) [°C]

24.84

Partner (Association (MCS))

Mg(ClO4)2

Fukuzumi; Satoh; Okamoto; Yasui; Suenobu; Seko; Fujitsuka; Ito; Journal of the American Chemical Society; vol. 123; nb. 32; (2001); p. 7756 - 7766, View in Reaxys 6 of 10

Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

acetonitrile

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

Mg(ClO4)2

Fukuzumi, Shunichi; Okamoto, Toshihiko; Otera, Junzo; Journal of the American Chemical Society; vol. 116; nb.

12; (1994); p. 5503 - 5504, View in Reaxys 7 of 10

Description (Association Stability constant of the complex with ...

(MCS)) Solvent (Association (MCS))

acetonitrile

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

Mg(ClO4)2

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2018-02-14 08:04:49

Fukuzumi, Shunichi; Okamoto, Toshihiko; Otera, Junzo; Journal of the American Chemical Society; vol. 116; nb.

12; (1994); p. 5503 - 5504, View in Reaxys 8 of 10

Description (Association Dipole moment of the complex (MCS)) Temperature (Association (MCS)) [°C]

20

Partner (Association (MCS))

cyclohexane

Grosse, Constantino; Mechetti, Magdalena; Brito, Pedro; Canadian Journal of Chemistry; vol. 63; (1985); p.

1031 - 1034, View in Reaxys 9 of 10

Description (Association Stability constant of the complex with ...

(MCS)) Solvent (Association (MCS))

CDCl3

Partner (Association (MCS))

trifluoroacetic acid

Schuster, Ingeborg I.; Journal of Organic Chemistry; vol. 50; nb. 10; (1985); p. 1656 - 1662, View in Reaxys 10 of 10

Description (Association NMR spectrum of the complex (MCS)) Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

28

Partner (Association (MCS))

trifluoroacetic acid

Schuster, Ingeborg I.; Journal of Organic Chemistry; vol. 50; nb. 10; (1985); p. 1656 - 1662, View in Reaxys Chromatographic Data (4) Chromatographic Location data HPLC (High performance liquid chromatography)

References

supporting information

Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 595, View in Reaxys; Zheng, Yu-Cong; Xu, Jian-He; Wang, Hui; Lin, Guo-Qiang; Hong, Ran; Yu, Hui-Lei; Advanced Synthesis and Catalysis; vol. 359; nb. 7; (2017); p.

1185 - 1193, View in Reaxys

GC (Gas chroma- supporting infortography) mation

Borah, Suchibrata; Bhattacharyya, Bagmita; Deka, Jumi; Borah, Aditya; Devi, Anuchaya; Deka, Dhanapati; Mishra, Shashank; Raidongia, Kalyan; Gogoi, Nayanmoni; Dalton Transactions; vol. 46; nb. 26; (2017); p. 8664 - 8672, View in Reaxys

TLC (Thin layer chromatography)

Khumraksa, Bannarak; Phakhodee, Wong; Pattarawarapan, Mookda; Tetrahedron Letters; vol. 54; nb. 15; (2013); p. 1983 - 1986, View in Reaxys

supporting information

TLC (Thin layer chromatography)

Krane Thvedt, Thor H.; Kaasa, Kristin; Sundby, Eirik; Charnock, Colin; Hoff, Bard Helge; European Journal of Medicinal Chemistry; vol. 68; (2013); p. 482 - 496, View in Reaxys

Conformation (1) Object of Investi- References gation Conformation

Drakenberg,T.; Sandstroem,J.; Seita,J.; Organic Magnetic Resonance; vol. 11; (1978); p. 246, View in Reaxys; Narayanan; Shukla; Current Science; vol. 42; (1973); p. 329, View in Reaxys; Lunazzi, Lodovico; Placucci, Giuseppe; Macciantelli, Dante; Tetrahedron; vol. 47; nb. 43; (1991); p. 9125 - 9128, View in Reaxys; Benassi, Rois; Iarossi, Dario; Folli, Ugo; Schenetti, Luisa; Taddei, Ferdinando; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1981); p. 228 232, View in Reaxys; Abraham, Raymond J.; Chadwick, Derek J.; Sancassan, Fernando; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1988); p. 169 - 177, View in Reaxys; Dean, Francis M.; El-Kass, Gassan; Prakash, Lalit; Journal of the Chemical Society, Chemical Communications; nb. 8; (1985); p. 502 - 503, View in Reaxys; Boykin, D. W.; Balakrishnan, P.; Baumstark, A. L.; Magnetic Resonance in Chemistry; vol. 25; (1987); p. 248 - 250, View in Reaxys; Salman, Salman R.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 3; (1984); p.

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229 - 232, View in Reaxys; Salman, Salman R.; Organic Magnetic Resonance; vol. 21; nb. 11; (1983); p.

672 - 674, View in Reaxys Crystal Property Description (9) Colour & Other Location Properties yellow

References Ahmad, Jahir Uddin; Raeisaenen, Minna T.; Kemell, Marianna; Heikkilae, Mikko J.; Leskelae, Markku; Repo, Timo; Applied Catalysis A: General; vol. 449; (2012); p. 153 162, View in Reaxys; Liu, Xiaolong; Xia, Qinqin; Zhang, Yuejiao; Chen, Congyan; Chen, Wanzhi; Journal of Organic Chemistry; vol. 78; nb. 17; (2013); p. 8531 - 8536, View in Reaxys; Chen, Congyan; Liu, Bo; Chen, Wanzhi; Synthesis (Germany); vol.

45; nb. 24; (2013); p. 3387 - 3391; Art.No: SS-2013-H0531-OP, View in Reaxys; Feng, Qiang; Song, Qiuling; Journal of Organic Chemistry; vol. 79; nb. 4; (2014); p. 1867 1871, View in Reaxys; Tabata, Masayuki; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 16; (2014); p. 3402 - 3410, View in Reaxys; Wang, Lianyue; Bie, Zhixing; Shang, Sensen; Lv, Ying; Li, Guosong; Niu, Jingyang; Gao, Shuang; RSC Advances; vol. 6; nb. 41; (2016); p. 35008 35013, View in Reaxys; Buxaderas, Eduardo; Graziano-Mayer, Marilyn; Volpe, María Alicia; Radivoy, Gabriel; Synthesis (Germany); vol. 49; nb. 6; (2017); p. 1387 - 1393; Art.No: SS-2016-M0473-OP, View in Reaxys; Hu, Guang; Ramakumar, Kinthada; Brenner-Moyer, Stacey E.; Journal of Organic Chemistry; vol. 82; nb. 13; (2017); p.

6972 - 6977, View in Reaxys

yellow

supporting information

Zhu, Yingguang; Zhao, Baoguo; Shi, Yian; Organic Letters; vol. 15; nb. 5; (2013); p.

992 - 995, View in Reaxys; Zhang, Lin; Bi, Xihe; Guan, Xiaoxue; Li, Xingqi; Liu, Qun; Barry, Badru-Deen; Liao, Peiqiu; Angewandte Chemie - International Edition; vol. 52; nb. 43; (2013); p. 11303 - 11307; Angew. Chem.; vol. 125; nb. 43; (2013); p. 11513 11517,5, View in Reaxys; Jiang, Xiao; Wang, Jin-Mei; Zhang, Ying; Chen, Zhong; Zhu, Yong-Ming; Ji, Shun-Jun; Organic Letters; vol. 16; nb. 13; (2014); p. 3492 - 3495, View in Reaxys; Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb.

9; (2015); p. 591 - 595, View in Reaxys; Huang, He; Li, Xiangmin; Yu, Chenguang; Zhang, Yueteng; Mariano, Patrick S.; Wang, Wei; Angewandte Chemie - International Edition; vol. 56; nb. 6; (2017); p. 1500 - 1505; Angew. Chem.; vol. 129; nb. 6; (2017); p.

1522 - 1527,6, View in Reaxys; Yan, Qi; Fang, Ye Chen; Jia, Yun Xue; Duan, Xin Hong; New Journal of Chemistry; vol. 41; nb. 6; (2017); p. 2372 - 2377, View in Reaxys; Han, Wei; Liu, Binbin; Chen, Junjie; Zhou, Qing; Synlett; vol. 28; nb. 7; (2017); p. 835 - 840, View in Reaxys; Khodaei, Mohammad M.; Alizadeh, Abdolhamid; Hezarkhani, Hadis Afshar; Chemistry Letters; vol. 46; nb. 6; (2017); p. 840 - 843, View in Reaxys; Huang, He; Yu, Chenguang; Li, Xiangmin; Zhang, Yongqiang; Zhang, Yueteng; Chen, Xiaobei; Mariano, Patrick S.; Xie, Hexin; Wang, Wei; Angewandte Chemie - International Edition; vol. 56; nb. 28; (2017); p. 8201 - 8205; Angew. Chem.; vol. 129; nb.

28; (2017); p. 8313 - 8317,5, View in Reaxys

colourless

supporting information

Ueda, Tsuyoshi; Konishi, Hideyuki; Manabe, Kei; Angewandte Chemie - International Edition; vol. 52; nb. 33; (2013); p. 8611 - 8615; Angew. Chem.; vol. 125; nb. 33; (2013); p. 8773 - 8777,5, View in Reaxys; Liu, Dongwang; Zhou, Hongxia; Gu, Xiangyong; Shen, Xiaoqin; Li, Pixu; Chinese Journal of Chemistry; vol. 32; nb. 2; (2014); p. 117 122, View in Reaxys; Gowrisankar, Saravanan; Neumann, Helfried; Goerdes, Dirk; Thurow, Kerstin; Jiao, Haijun; Beller, Matthias; Chemistry - A European Journal; vol.

19; nb. 47; (2013); p. 15979 - 15984, View in Reaxys; Wang, Yuanxun; Wang, Chao; Sun, Jian; Synthetic Communications; vol. 44; nb. 20; (2014); p. 2961 - 2965, View in Reaxys; Natte, Kishore; Dumrath, Andreas; Neumann, Helfried; Beller, Matthias; Angewandte Chemie - International Edition; vol. 53; nb. 38; (2014); p. 10090 10094; Angew. Chem.; vol. 126; nb. 38; (2015); p. 10254 - 10258,5, View in Reaxys; Shil, Arun K.; Kumar, Sandeep; Reddy, C. Bal; Dadhwal, Sumit; Thakur, Vandna; Das, Pralay; Organic Letters; vol. 17; nb. 21; (2015); p. 5352 - 5355, View in Reaxys; Too, Pei Chui; Chan, Guo Hao; Tnay, Ya Lin; Hirao, Hajime; Chiba, Shunsuke; Angewandte Chemie - International Edition; vol. 55; nb. 11; (2016); p. 3719 - 3723; Angew.

Chem.; vol. 128; nb. 11; (2016); p. 3783 - 3787,5, View in Reaxys; Mete, Trimbak B.; Khopade, Tushar M.; Bhat, Ramakrishna G.; Tetrahedron Letters; vol. 58; nb. 29; (2017); p. 2822 - 2825, View in Reaxys; Sakai, Norio; Minato, Kohei; Ogiwara, Yohei; Tetrahedron Letters; vol. 58; nb. 48; (2017); p. 4563 - 4567, View in Reaxys

white

supporting information

Moore, Peter W.; Mirzayans, Paul M.; Williams, Craig M.; Chemistry - A European Journal; vol. 21; nb. 9; (2015); p. 3567 - 3571, View in Reaxys; Haraguchi, Ryosuke; Tanazawa, Sho-Go; Tokunaga, Naoya; Fukuzawa, Shin-Ichi; Organic Letters; vol. 19; nb. 7; (2017); p. 1646 - 1649, View in Reaxys

colourless

Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p.

427 - 431, View in Reaxys; Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol.

4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys; Ogiwara, Yohei; Ono, Yuji; Sakai,

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Norio; Synthesis (Germany); vol. 48; nb. 23; (2016); p. 4143 - 4148; Art.No: SS-2016F0462-OP, View in Reaxys yellow

Paragraph 0010; Patent; Henan Normal University; Fan, Xuesen; Li, Bin; Zhang, Xinying; Chen, Na0011; 0012; 0013; na; Guo, Shenghai; (9 pag.); CN105601480; (2016); (A) Chinese, View in Reaxys 0014; 0015; 0016; 0017

white

Luo, Qun-Li; Nan, Wen-Hui; Li, Yu; Chen, Xiang; Arkivoc; vol. 2014; nb. 4; (2014); p.

350 - 361, View in Reaxys

yellow

Mamros, Audrey N.; Sharrow, Phillip R.; Weller, William E.; Luderer, Mark R.; Fair, Justin D.; Pazehoski, Kristina O.; Luderer, Matthew R.; Arkivoc; vol. 2011; nb. 5; (2011); p. 23 - 33, View in Reaxys

light-yellow

Kesharwani, Tanay; Larock, Richard C.; Tetrahedron; vol. 64; nb. 26; (2008); p. 6090 6102, View in Reaxys

Dielectric Constant (1) References Lakshmi et al.; Journal of Physical Chemistry; vol. 82; (1978); p. 1091, View in Reaxys Dissociation Exponent (3) 1 of 3

Comment (Dissociation Exponent)

(pk')pK, pK*

Kovi et al.; Spectroscopy Letters; vol. 6; (1973); p. 7,11, 13, View in Reaxys 2 of 3

Comment (Dissociation Exponent)

(pk')pK(A)-Best. in wss. H2SO4, UV-spektrometr.

Greig; Johnson; Journal of the American Chemical Society; vol. 90; (1968); p. 6453, View in Reaxys 3 of 3

Comment (Dissociation Exponent)

(pk')pK: -6.34 (wss. H2SO4, spektrophotometr.)

Culbertson; Pettit; Journal of the American Chemical Society; vol. 85; (1963); p. 741, View in Reaxys Electrical Data (2) 1 of 2

Description (Electrical Data)

Dielectric relaxation time

Lakshmi et al.; Journal of Physical Chemistry; vol. 82; (1978); p. 1091, View in Reaxys; Hanna; Abdel-Nour; Indian Journal of Physics (1926-1976); vol. 44; (1970); p. 367, View in Reaxys 2 of 2

Description (Electrical Data)

Electrical properties

Makhija; Dawar; Indian Journal of Pure and Applied Physics; vol. 16; (1978); p. 92, View in Reaxys; Makhija; Dawar; Indian Journal of Pure and Applied Physics; vol. 15; (1977); p. 542, View in Reaxys Electrical Moment (4) 1 of 4

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

SCF-CI (S.323)

Tjutjulkow; Neikow; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 10; (1977); p. 313,318,319,323, View in Reaxys 2 of 4

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ (Tab.6)

Fratew et al.; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 3; (1970); p.

579,585,587,590, View in Reaxys 3 of 4

Description (Electrical Moment)

Dipole moment

Hanna; Abdel-Nour; Indian Journal of Physics (1926-1976); vol. 44; (1970); p. 367, View in Reaxys 4 of 4

Description (Electrical Moment)

Dipole moment

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Comment (Electrical Moment)

Dipolmoment (ε, CCl4): 2.87 D

Le Fevre; Sundaram; Journal of the Chemical Society; (1962); p. 4756,4760, View in Reaxys Electrochemical Behaviour (2) Description (Elec- References trochemical Behaviour) Polarography

Galpern et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 26; (1971); p. 1206,1080, View in Reaxys; Anthoine et al.; Bulletin des Societes Chimiques Belges; vol. 78; (1969); p. 465, View in Reaxys

Basicity

Hopkinson; Wyatt; Journal of the Chemical Society [Section] B: Physical Organic; (1967); p. 1333, View in Reaxys

Electrochemical Characteristics (9) 1 of 9

Description (Electrochemical Characteristics)

oxidation potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

21.84

Vasilieva; Irtegova; Vaganova; Shteingarts; Journal of Physical Organic Chemistry; vol. 21; nb. 1; (2008); p. 73 78, View in Reaxys 2 of 9

Description (Electrochemical Characteristics)

oxidation potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

21.84

Vasilieva; Irtegova; Vaganova; Shteingarts; Journal of Physical Organic Chemistry; vol. 21; nb. 1; (2008); p. 73 78, View in Reaxys 3 of 9

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

21.84

Vasilieva; Irtegova; Vaganova; Shteingarts; Journal of Physical Organic Chemistry; vol. 21; nb. 1; (2008); p. 73 78, View in Reaxys 4 of 9

Description (Electrochemical Characteristics)

Electrochemical characteristics given

Sioda, Roman E.; Frankowska, Barbara; Monatshefte fur Chemie; vol. 139; nb. 8; (2008); p. 881 - 886, View in Reaxys 5 of 9

Description (Electrochemical Characteristics)

redox potential

Fukuzumi, Shunichi; Okamoto, Toshihiko; Otera, Junzo; Journal of the American Chemical Society; vol. 116; nb.

12; (1994); p. 5503 - 5504, View in Reaxys 6 of 9

Description (Electrochemical Characteristics)

polarographic half-wave potential

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Galpern et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 26; (1971); p. 1206,1080, View in Reaxys 7 of 9

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochem- in wss. Aethanol vom pH 2,2-12.0. ical Characteristics) Powers; Day; Journal of the American Chemical Society; vol. 80; (1958); p. 808,810, View in Reaxys 8 of 9

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochem- in wss. Aethanol vom pH 2,9-10.3. ical Characteristics) Imoto et al.; Bl. Naniwa Univ.; vol. <A> 3; (1955); p. 203,205, View in Reaxys; Imoto et al.; Nippon Kagaku Zasshi; vol. 77; (1956); p. 804,807; Chem.Abstr.; (1958); p. 9066, View in Reaxys 9 of 9

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochem- in wss. Aethanol vom pH 2,35-12,80. ical Characteristics) Schmid; Heilbronner; Helvetica Chimica Acta; vol. 37; (1954); p. 1453,1458, View in Reaxys Electron Binding (1) Description (Elec- References tron Binding) Electron affinity

Wentworth; Chen; Journal of Physical Chemistry; vol. 71; (1967); p. 1929, View in Reaxys; Heinis, Thomas; Chowdhury, Swapan; Kebarle, Paul; Organic Mass Spectrometry; vol. 28; nb. 4; (1993); p. 358 - 365, View in Reaxys; Chowdhury, Swapan; Heinis, Thomas; Kebarle, Paul; Journal of the American Chemical Society; vol. 108; nb. 15; (1986); p. 4662 - 4663, View in Reaxys

Energy Barriers (1) References Drakenberg,T.; Sandstroem,J.; Seita,J.; Organic Magnetic Resonance; vol. 11; (1978); p. 246, View in Reaxys Further Information (17) Description (Fur- References ther Information) Further information

Szabo et al.; Justus Liebigs Annalen der Chemie; (1977); p. 747,758, View in Reaxys

Further information

Kanamaru; Lim; Journal of Chemical Physics; vol. 65; (1976); p. 4055, View in Reaxys

Further information

Lin et al.; Journal of Chemical Physics; vol. 60; (1974); p. 4994,4997, View in Reaxys

Further information

Farrell; Westwood; Journal of the Chemical Society [Section] B: Physical Organic; (1970); p. 1518, View in Reaxys

Further information

Lim et al.; Journal of Chemical Physics; vol. 53; (1970); p. 2443, View in Reaxys

Further information

Filipescu; Mushrush; Journal of Physical Chemistry; vol. 72; (1968); p. 3516,3519,3522, View in Reaxys

Further information

Chauning; Wells; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1887, View in Reaxys

Further information

Nakaya et al.; Bulletin of the Chemical Society of Japan; vol. 40; (1967); p. 691, View in Reaxys

Further information

Morcillo et al.; Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica; vol. 63; (1967); p. 639,640-660, View in Reaxys

Further information

Figeys; Nasielski; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 23; (1967); p. 465, View in Reaxys

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Further information

Herkstroeter; Hammond; Journal of the American Chemical Society; vol. 88; (1966); p. 4769, View in Reaxys

Further information

Porter; Suppan; Transactions of the Faraday Society; vol. 61; (1965); p. 1664,1666, View in Reaxys

Further information

Claverie; Garrigou-Lagrange; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 61; (1964); p. 889,896-902, View in Reaxys

Further information

Martin et al.; Tetrahedron; vol. 20; (1964); p. 1505,1513, 1514, View in Reaxys

Further information

Augdahl; Klaeboe; Acta Chemica Scandinavica (1947-1973); vol. 16; (1962); p. 1647,1649, View in Reaxys

Further information

Epstein,M.; Buckler,S.A.; Tetrahedron; vol. 18; (1962); p. 1231 - 1242, View in Reaxys

Further information

Beattie et al.; Analytical Chemistry; vol. 33; (1961); p. 1890, View in Reaxys

Interatomic Distances and Angles (1) Description References Electron distribution

Tjutjulkow; Neikow; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol.

10; (1977); p. 313,318,319,323, View in Reaxys

Ionization Potential (1) References Fratew et al.; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 3; (1970); p.

579,585,587,590, View in Reaxys Liquid/Liquid Systems (MCS) (3) 1 of 3

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 and solvent 2

Comment (Liquid/Liquid Systems (MCS))

phase 1= hexadecane; phase 2= water/diacetyl phosphatidylcholine; distribution coefficient = 1.36

Partner (Liquid/Liquid Systems (MCS))

Hexadecane; water; diacetyl phosphatidylcholine

Natesan, Senthil; Lukacova, Viera; Peng, Ming; Subramaniam, Rajesh; Lynch, Sandra; Wang, Zhanbin; Tandlich, Roman; Balaz, Stefan; Molecular Pharmaceutics; vol. 11; nb. 10; (2014); p. 3577 - 3595, View in Reaxys 2 of 3

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 and solvent 2

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25

Comment (Liquid/Liquid Systems (MCS))

phase 1= hexadecane; phase 2= water/diacetyl phosphatidylcholine; distribution coefficient = 1.36

Partner (Liquid/Liquid Systems (MCS))

Hexadecane; water; diacetyl phosphatidylcholine

Lukacova, Viera; Natesan, Senthil; Peng, Ming; Tandlich, Roman; Wang, Zhanbin; Lynch, Sandra; Subramaniam, Rajesh; Balaz, Stefan; Molecular Pharmaceutics; vol. 10; nb. 10; (2013); p. 3684 - 3696, View in Reaxys 3 of 3

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

27

Partner (Liquid/Liquid Systems (MCS))

sodium dodecyl-sulfate

Bonar-Law, Richard P.; Journal of Organic Chemistry; vol. 61; nb. 11; (1996); p. 3623 - 3634, View in Reaxys Mechanical Properties (1)

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Description (Mechanical Properties)

References

Molar volume

Carlson, Rolf; Prochazka, Michal P.; Lundstedt, Torbjoern; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 42; nb. 3; (1988); p. 145 - 156, View in Reaxys

Molecular Deformation (1) Description (MoReferences lecular Deformation) Force constants Optics (2) Description (Optics)

Paul et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1969); p.

1849,1851, View in Reaxys References

Magnetic circular dichroism

Whipple et al.; Journal of the American Chemical Society; vol. 100; (1978); p. 6844,6849, View in Reaxys

Electric birefringence (Kerr effect)

Le Fevre; Sundaram; Journal of the Chemical Society; (1962); p. 4756,4760, View in Reaxys

Other Thermochemical Data (3) Description (Oth- References er Thermochemical Data) Thermodynamic properties

Lakshmi et al.; Journal of Physical Chemistry; vol. 82; (1978); p. 1091, View in Reaxys; Fratew et al.; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 3; (1970); p.

579,585,587,590, View in Reaxys

Entropy

Hanna; Abdel-Nour; Indian Journal of Physics (1926-1976); vol. 44; (1970); p. 367, View in Reaxys

Enthalpy

Dewar,M.J.S. et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 6321 - 6325, View in Reaxys; Hanna; Abdel-Nour; Indian Journal of Physics (1926-1976); vol. 44; (1970); p. 367, View in Reaxys

Solubility (MCS) (1) 1 of 1

Comment (Solubility (MCS))

poorly soluble in water

Yang, Zhanhui; Zhu, Zhongpeng; Luo, Renshi; Qiu, Xiang; Liu, Ji-Tian; Yang, Jing-Kui; Tang, Weiping; Green Chemistry; vol. 19; nb. 14; (2017); p. 3296 - 3301, View in Reaxys Transport Phenomena (MCS) (1) 1 of 1

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

chloroform

Jaccard, Guy; Lauterwein, Juergen; Helvetica Chimica Acta; vol. 69; (1986); p. 1469 - 1485, View in Reaxys NMR Spectroscopy (90) 1 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Han, Mikyoung; Jeong, Ku Sun; Lee, Jong Chan; Bulletin of the Korean Chemical Society; vol. 33; nb. 7; (2012); p. 2405 - 2406, View in Reaxys; Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 - 431, View in Reaxys; Buxaderas, Eduardo; Graziano-Mayer, Marilyn; Volpe, María Alicia; Radivoy, Gabriel; Synthesis (Germany); vol. 49; nb. 6; (2017); p. 1387 - 1393; Art.No: SS-2016-M0473-OP, View in Reaxys

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2 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Location

supporting information

Zhang, Guofu; Han, Xingwang; Luan, Yuxin; Wang, Yong; Wen, Xin; Ding, Chengrong; Chemical Communications; vol. 49; nb. 72; (2013); p. 7908 - 7910, View in Reaxys; Zhang, Guofu; Lei, Jie; Han, Xingwang; Luan, Yuxin; Ding, Chengrong; Shan, Shang; Synlett; vol. 26; nb. 6; (2015); p. 779 - 784, View in Reaxys; Haraguchi, Ryosuke; Tanazawa, Sho-Go; Tokunaga, Naoya; Fukuzawa, Shin-Ichi; Organic Letters; vol. 19; nb. 7; (2017); p.

1646 - 1649, View in Reaxys; Hu, Guang; Ramakumar, Kinthada; Brenner-Moyer, Stacey E.; Journal of Organic Chemistry; vol. 82; nb. 13; (2017); p. 6972 - 6977, View in Reaxys 3 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

125

Location

supporting information

Zhang, Guofu; Han, Xingwang; Luan, Yuxin; Wang, Yong; Wen, Xin; Ding, Chengrong; Chemical Communications; vol. 49; nb. 72; (2013); p. 7908 - 7910, View in Reaxys; Zhang, Guofu; Lei, Jie; Han, Xingwang; Luan, Yuxin; Ding, Chengrong; Shan, Shang; Synlett; vol. 26; nb. 6; (2015); p. 779 - 784, View in Reaxys; Hu, Guang; Ramakumar, Kinthada; Brenner-Moyer, Stacey E.; Journal of Organic Chemistry; vol. 82; nb. 13; (2017); p. 6972 6977, View in Reaxys 4 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Liu, Xiaolong; Xia, Qinqin; Zhang, Yuejiao; Chen, Congyan; Chen, Wanzhi; Journal of Organic Chemistry; vol.

78; nb. 17; (2013); p. 8531 - 8536, View in Reaxys; Chen, Congyan; Liu, Bo; Chen, Wanzhi; Synthesis (Germany); vol. 45; nb. 24; (2013); p. 3387 - 3391; Art.No: SS-2013-H0531-OP, View in Reaxys; Yu, Bo; Zhao, Yanfei; Zhang, Hongye; Xu, Jilei; Hao, Leiduan; Gao, Xiang; Liu, Zhimin; Chemical Communications; vol. 50; nb. 18; (2014); p.

2330 - 2333, View in Reaxys; Feng, Qiang; Song, Qiuling; Journal of Organic Chemistry; vol. 79; nb. 4; (2014); p.

1867 - 1871, View in Reaxys; Liu, Dongwang; Zhou, Hongxia; Gu, Xiangyong; Shen, Xiaoqin; Li, Pixu; Chinese Journal of Chemistry; vol. 32; nb. 2; (2014); p. 117 - 122, View in Reaxys; Tabata, Masayuki; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 16; (2014); p. 3402 - 3410, View in Reaxys; Jiang, Xiao; Wang, Jin-Mei; Zhang, Ying; Chen, Zhong; Zhu, Yong-Ming; Ji, Shun-Jun; Organic Letters; vol. 16; nb. 13; (2014); p. 3492 - 3495, View in Reaxys; Wang, Yuanxun; Wang, Chao; Sun, Jian; Synthetic Communications; vol. 44; nb. 20; (2014); p. 2961 - 2965, View in Reaxys; Gong, Jin-Long; Qi, Xinxin; Wei, Duo; Feng, Jian-Bo; Wu, Xiao-Feng; Organic and Biomolecular Chemistry; vol. 12; nb. 38; (2014); p. 7486 - 7488, View in Reaxys; Moore, Peter W.; Mirzayans, Paul M.; Williams, Craig M.; Chemistry - A European Journal; vol.

21; nb. 9; (2015); p. 3567 - 3571, View in Reaxys; Gu, Lijun; Jin, Cheng; Chemical Communications; vol. 51; nb.

30; (2015); p. 6572 - 6575, View in Reaxys; Yu, Bo; Yang, Zhenzhen; Zhao, Yanfei; Hao, Leiduan; Zhang, Hongye; Gao, Xiang; Han, Buxing; Liu, Zhimin; Chemistry - A European Journal; vol. 22; nb. 3; (2016); p. 1097 1102, View in Reaxys; Qi, Xinxin; Li, Chong-Liang; Wu, Xiao-Feng; Chemistry - A European Journal; vol. 22; nb.

17; (2016); p. 5835 - 5838, View in Reaxys; Ray, Ritwika; Chandra, Shubhadeep; Maiti, Debabrata; Lahiri, Goutam Kumar; Chemistry - A European Journal; vol. 22; nb. 26; (2016); p. 8814 - 8822, View in Reaxys; Ye, Xiaojing; Fu, Hongliang; Ma, Jiahao; Zhong, Weihui; Synthetic Communications; vol. 46; nb. 10; (2016); p. 885 - 892, View in Reaxys; Yan, Qi; Fang, Ye Chen; Jia, Yun Xue; Duan, Xin Hong; New Journal of Chemistry; vol. 41; nb. 6;

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(2017); p. 2372 - 2377, View in Reaxys; Han, Wei; Liu, Binbin; Chen, Junjie; Zhou, Qing; Synlett; vol. 28; nb. 7; (2017); p. 835 - 840, View in Reaxys; Mete, Trimbak B.; Khopade, Tushar M.; Bhat, Ramakrishna G.; Tetrahedron Letters; vol. 58; nb. 29; (2017); p. 2822 - 2825, View in Reaxys 5 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Liu, Xiaolong; Xia, Qinqin; Zhang, Yuejiao; Chen, Congyan; Chen, Wanzhi; Journal of Organic Chemistry; vol.

78; nb. 17; (2013); p. 8531 - 8536, View in Reaxys; Chen, Congyan; Liu, Bo; Chen, Wanzhi; Synthesis (Germany); vol. 45; nb. 24; (2013); p. 3387 - 3391; Art.No: SS-2013-H0531-OP, View in Reaxys; Yu, Bo; Zhao, Yanfei; Zhang, Hongye; Xu, Jilei; Hao, Leiduan; Gao, Xiang; Liu, Zhimin; Chemical Communications; vol. 50; nb. 18; (2014); p.

2330 - 2333, View in Reaxys; Feng, Qiang; Song, Qiuling; Journal of Organic Chemistry; vol. 79; nb. 4; (2014); p.

1867 - 1871, View in Reaxys; Tabata, Masayuki; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 16; (2014); p. 3402 - 3410, View in Reaxys; Gu, Lijun; Jin, Cheng; Chemical Communications; vol. 51; nb. 30; (2015); p. 6572 - 6575, View in Reaxys; Yu, Bo; Yang, Zhenzhen; Zhao, Yanfei; Hao, Leiduan; Zhang, Hongye; Gao, Xiang; Han, Buxing; Liu, Zhimin; Chemistry - A European Journal; vol. 22; nb. 3; (2016); p. 1097 - 1102, View in Reaxys; Ye, Xiaojing; Fu, Hongliang; Ma, Jiahao; Zhong, Weihui; Synthetic Communications; vol. 46; nb. 10; (2016); p. 885 - 892, View in Reaxys; Han, Wei; Liu, Binbin; Chen, Junjie; Zhou, Qing; Synlett; vol. 28; nb. 7; (2017); p. 835 - 840, View in Reaxys; Mete, Trimbak B.; Khopade, Tushar M.; Bhat, Ramakrishna G.; Tetrahedron Letters; vol. 58; nb. 29; (2017); p. 2822 - 2825, View in Reaxys 6 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Gowrisankar, Saravanan; Neumann, Helfried; Goerdes, Dirk; Thurow, Kerstin; Jiao, Haijun; Beller, Matthias; Chemistry - A European Journal; vol. 19; nb. 47; (2013); p. 15979 - 15984, View in Reaxys; Natte, Kishore; Dumrath, Andreas; Neumann, Helfried; Beller, Matthias; Angewandte Chemie - International Edition; vol. 53; nb. 38; (2014); p. 10090 - 10094; Angew. Chem.; vol. 126; nb. 38; (2015); p. 10254 - 10258,5, View in Reaxys; Huang, He; Li, Xiangmin; Yu, Chenguang; Zhang, Yueteng; Mariano, Patrick S.; Wang, Wei; Angewandte Chemie - International Edition; vol. 56; nb. 6; (2017); p. 1500 - 1505; Angew. Chem.; vol. 129; nb. 6; (2017); p. 1522 - 1527,6, View in Reaxys; Huang, He; Yu, Chenguang; Li, Xiangmin; Zhang, Yongqiang; Zhang, Yueteng; Chen, Xiaobei; Mariano, Patrick S.; Xie, Hexin; Wang, Wei; Angewandte Chemie - International Edition; vol. 56; nb. 28; (2017); p.

8201 - 8205; Angew. Chem.; vol. 129; nb. 28; (2017); p. 8313 - 8317,5, View in Reaxys; Sakai, Norio; Minato, Kohei; Ogiwara, Yohei; Tetrahedron Letters; vol. 58; nb. 48; (2017); p. 4563 - 4567, View in Reaxys 7 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

75

Location

supporting information

Gowrisankar, Saravanan; Neumann, Helfried; Goerdes, Dirk; Thurow, Kerstin; Jiao, Haijun; Beller, Matthias; Chemistry - A European Journal; vol. 19; nb. 47; (2013); p. 15979 - 15984, View in Reaxys; Natte, Kishore; Dumrath, Andreas; Neumann, Helfried; Beller, Matthias; Angewandte Chemie - International Edition; vol. 53; nb. 38; (2014); p. 10090 - 10094; Angew. Chem.; vol. 126; nb. 38; (2015); p. 10254 - 10258,5, View in Reaxys; Huang, He; Li, Xiangmin; Yu, Chenguang; Zhang, Yueteng; Mariano, Patrick S.; Wang, Wei; Angewandte Chemie - International Edition; vol. 56; nb. 6; (2017); p. 1500 - 1505; Angew. Chem.; vol. 129; nb. 6; (2017); p. 1522 - 1527,6,

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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View in Reaxys; Huang, He; Yu, Chenguang; Li, Xiangmin; Zhang, Yongqiang; Zhang, Yueteng; Chen, Xiaobei; Mariano, Patrick S.; Xie, Hexin; Wang, Wei; Angewandte Chemie - International Edition; vol. 56; nb. 28; (2017); p.

8201 - 8205; Angew. Chem.; vol. 129; nb. 28; (2017); p. 8313 - 8317,5, View in Reaxys; Sakai, Norio; Minato, Kohei; Ogiwara, Yohei; Tetrahedron Letters; vol. 58; nb. 48; (2017); p. 4563 - 4567, View in Reaxys 8 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

75

Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 - 431, View in Reaxys; Buxaderas, Eduardo; Graziano-Mayer, Marilyn; Volpe, María Alicia; Radivoy, Gabriel; Synthesis (Germany); vol. 49; nb. 6; (2017); p. 1387 - 1393; Art.No: SS-2016-M0473-OP, View in Reaxys 9 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

Paragraph 0094

Patent; Institute of Chemistry, Chinese Academy of Sciences; Liu, Zhimin; Yu, Bo; Zhang, Hongye; Zhao, Yanfei; Yang, Zhenzhen; Yang, Guanying; (10 pag.); CN104803835; (2017); (B) Chinese, View in Reaxys 10 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Location

Paragraph 0094

Patent; Institute of Chemistry, Chinese Academy of Sciences; Liu, Zhimin; Yu, Bo; Zhang, Hongye; Zhao, Yanfei; Yang, Zhenzhen; Yang, Guanying; (10 pag.); CN104803835; (2017); (B) Chinese, View in Reaxys 11 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

125

Location

supporting information

Haraguchi, Ryosuke; Tanazawa, Sho-Go; Tokunaga, Naoya; Fukuzawa, Shin-Ichi; Organic Letters; vol. 19; nb.

7; (2017); p. 1646 - 1649, View in Reaxys 12 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

Paragraph 0066

Patent; Soochow University; Li, Hongxi; Tan, Dawei; Li, Haiyan; Lang, Jianping; (15 pag.); CN106588957; (2017); (A) Chinese, View in Reaxys 13 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Frequency (NMR Spectroscopy) [MHz]

151

Location

Paragraph 0066

Patent; Soochow University; Li, Hongxi; Tan, Dawei; Li, Haiyan; Lang, Jianping; (15 pag.); CN106588957; (2017); (A) Chinese, View in Reaxys 14 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

600

Location

supporting information

Jing, Xiaobi; Yuan, Dandan; Yu, Lei; Advanced Synthesis and Catalysis; vol. 359; nb. 7; (2017); p. 1194 - 1201, View in Reaxys 15 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Location

Paragraph 0099

Patent; Zhejiang University of Technology; Zhang Guofu; Zhao Yiyong; Zhang Guihua; Ding Chengrong; Lv Jinghui; Yu Yidong; (10 pag.); CN106905097; (2017); (A) Chinese, View in Reaxys 16 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

125

Location

Paragraph 0100

Patent; Zhejiang University of Technology; Zhang Guofu; Zhao Yiyong; Zhang Guihua; Ding Chengrong; Lv Jinghui; Yu Yidong; (10 pag.); CN106905097; (2017); (A) Chinese, View in Reaxys

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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17 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

21.94

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Khodaei, Mohammad M.; Alizadeh, Abdolhamid; Hezarkhani, Hadis Afshar; Chemistry Letters; vol. 46; nb. 6; (2017); p. 840 - 843, View in Reaxys 18 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

22.54

Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Khodaei, Mohammad M.; Alizadeh, Abdolhamid; Hezarkhani, Hadis Afshar; Chemistry Letters; vol. 46; nb. 6; (2017); p. 840 - 843, View in Reaxys 19 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Moghadam, Majid; Tangestaninejad, Shahram; Mirkhani, Valiollah; Mohammadpoor-baltork, Iraj; Sirjanian, Narges; Parand, Somayeh; Bioorganic and Medicinal Chemistry; vol. 17; nb. 9; (2009); p. 3394 - 3398, View in Reaxys; Chu, Guobiao; Li, Chunbao; Organic and Biomolecular Chemistry; vol. 8; nb. 20; (2010); p. 4716 4719, View in Reaxys; Too, Pei Chui; Chan, Guo Hao; Tnay, Ya Lin; Hirao, Hajime; Chiba, Shunsuke; Angewandte Chemie - International Edition; vol. 55; nb. 11; (2016); p. 3719 - 3723; Angew. Chem.; vol. 128; nb. 11; (2016); p. 3783 - 3787,5, View in Reaxys 20 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Hamasaki, Akiyuki; Yasutake, Yutaro; Norio, Takafumi; Ishida, Tamao; Akita, Tomoki; Ohashi, Hironori; Yokoyama, Takushi; Honma, Tetsuo; Tokunaga, Makoto; Applied Catalysis A: General; vol. 469; (2014); p. 146 152, View in Reaxys; Jiang, Jianwen; Wang, Pingping; Cai, Mingzhong; Journal of Chemical Research; vol. 38; nb. 4; (2014); p. 218 - 222, View in Reaxys; Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys; Li, Bin; Shen, Nana; Fan, Xuesen; Zhang, Xinying; Tetrahedron Let-

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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ters; vol. 57; nb. 17; (2016); p. 1843 - 1846, View in Reaxys; Wang, Lianyue; Bie, Zhixing; Shang, Sensen; Lv, Ying; Li, Guosong; Niu, Jingyang; Gao, Shuang; RSC Advances; vol. 6; nb. 41; (2016); p. 35008 - 35013, View in Reaxys 21 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Hamasaki, Akiyuki; Yasutake, Yutaro; Norio, Takafumi; Ishida, Tamao; Akita, Tomoki; Ohashi, Hironori; Yokoyama, Takushi; Honma, Tetsuo; Tokunaga, Makoto; Applied Catalysis A: General; vol. 469; (2014); p. 146 152, View in Reaxys; Jiang, Jianwen; Wang, Pingping; Cai, Mingzhong; Journal of Chemical Research; vol. 38; nb. 4; (2014); p. 218 - 222, View in Reaxys; Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys; Li, Bin; Shen, Nana; Fan, Xuesen; Zhang, Xinying; Tetrahedron Letters; vol. 57; nb. 17; (2016); p. 1843 - 1846, View in Reaxys 22 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

101

Location

supporting information

Liu, Dongwang; Zhou, Hongxia; Gu, Xiangyong; Shen, Xiaoqin; Li, Pixu; Chinese Journal of Chemistry; vol. 32; nb. 2; (2014); p. 117 - 122, View in Reaxys; Jiang, Xiao; Wang, Jin-Mei; Zhang, Ying; Chen, Zhong; Zhu, YongMing; Ji, Shun-Jun; Organic Letters; vol. 16; nb. 13; (2014); p. 3492 - 3495, View in Reaxys; Qi, Xinxin; Li, Chong-Liang; Wu, Xiao-Feng; Chemistry - A European Journal; vol. 22; nb. 17; (2016); p. 5835 - 5838, View in Reaxys 23 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Too, Pei Chui; Chan, Guo Hao; Tnay, Ya Lin; Hirao, Hajime; Chiba, Shunsuke; Angewandte Chemie - International Edition; vol. 55; nb. 11; (2016); p. 3719 - 3723; Angew. Chem.; vol. 128; nb. 11; (2016); p. 3783 - 3787,5, View in Reaxys 24 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

101

Wang, Lianyue; Bie, Zhixing; Shang, Sensen; Lv, Ying; Li, Guosong; Niu, Jingyang; Gao, Shuang; RSC Advances; vol. 6; nb. 41; (2016); p. 35008 - 35013, View in Reaxys 25 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy)

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Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

Ray, Ritwika; Chandra, Shubhadeep; Maiti, Debabrata; Lahiri, Goutam Kumar; Chemistry - A European Journal; vol. 22; nb. 26; (2016); p. 8814 - 8822, View in Reaxys 26 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Loman, Jacob J.; Pistritto, Vincent A.; Kelly, Christopher B.; Leadbeater, Nicholas E.; Synlett; vol. 27; nb. 16; (2016); p. 2372 - 2377; Art.No: ST-2016-R0295-L, View in Reaxys 27 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Loman, Jacob J.; Pistritto, Vincent A.; Kelly, Christopher B.; Leadbeater, Nicholas E.; Synlett; vol. 27; nb. 16; (2016); p. 2372 - 2377; Art.No: ST-2016-R0295-L, View in Reaxys 28 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Original Text (NMR Spectroscopy)

1H

NMR (400 MHz, CDCl3): δ=7.55-7.64 (m, 2H), 7.68 (t, J=7.3 Hz, 1H), 7.90 (d, J=8.2 Hz, 1H), 7.96 (d, J=7.0 Hz, 1H), 8.07 (d, J=8.2 Hz, 1H), 9.25 (d, J=8.6 Hz, 1H), 10.38 (s, 1H)

Location

supporting information

Signals [ppm]

7.55 - 7.64; 7.68; 7.9; 7.96; 8.07; 9.25; 10.38

Kind of signal

m, 2H; t, J=7.3 Hz, 1H; d, J=8.2 Hz, 1H; d, J=7.0 Hz, 1H; d, J=8.2 Hz, 1H; d, J=8.6 Hz, 1H; s, 1H

Imai, Sho; Togo, Hideo; Tetrahedron; vol. 72; nb. 44; (2016); p. 6948 - 6954, View in Reaxys 29 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy)

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Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Original Text (NMR Spectroscopy)

13C NMR (100 MHz, CDCl ): δ=124.82 (2C), 126.90, 128.42, 129.01, 130.46, 131.32, 3 133.65, 135.24, 136.65, 193.51

Location

supporting information

Signals [ppm]

124.82; 126.9; 128.42; 129.01; 130.46; 131.32; 133.65; 135.24; 136.65; 193.51

Kind of signal

2C

Imai, Sho; Togo, Hideo; Tetrahedron; vol. 72; nb. 44; (2016); p. 6948 - 6954, View in Reaxys 30 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

Paragraph 0010

Patent; Henan Normal University; Fan, Xuesen; Li, Bin; Zhang, Xinying; Chen, Nana; Guo, Shenghai; (9 pag.); CN105601480; (2016); (A) Chinese, View in Reaxys 31 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Location

Paragraph 0010

Patent; Henan Normal University; Fan, Xuesen; Li, Bin; Zhang, Xinying; Chen, Nana; Guo, Shenghai; (9 pag.); CN105601480; (2016); (A) Chinese, View in Reaxys 32 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

500.2

Location

supporting information

Ogiwara, Yohei; Ono, Yuji; Sakai, Norio; Synthesis (Germany); vol. 48; nb. 23; (2016); p. 4143 - 4148; Art.No: SS-2016-F0462-OP, View in Reaxys 33 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy)

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Frequency (NMR Spectroscopy) [MHz]

125.8

Location

supporting information

Ogiwara, Yohei; Ono, Yuji; Sakai, Norio; Synthesis (Germany); vol. 48; nb. 23; (2016); p. 4143 - 4148; Art.No: SS-2016-F0462-OP, View in Reaxys 34 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 - 595, View in Reaxys 35 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Original Text (NMR Spectroscopy)

1H NMR (400 MHz, CDCl ): δ=10.41 (s, 1H), 9.26 (d, J=8.4 Hz, 1H), 8.11 (d, J=8.4 Hz, 3 1H), 8.00 (d, J=7.2 Hz, 1H), 7.93 (d, J=8.0 Hz, 1H), 7.72-7.58 (m, 3H)

Location

supporting information

Zhao, Hong; Chen, Qiurong; Wei, Li; Jiang, Yuanyuan; Cai, Mingzhong; Tetrahedron; vol. 71; nb. 46; (2015); p.

8725 - 8731; Art.No: 27151, View in Reaxys 36 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Original Text (NMR Spectroscopy)

13C NMR (100 MHz, CDCl ): δ=193.3, 136.3, 135.2, 133.8, 131.6, 130.6, 129.0, 128.4, 3 126.9, 124.9, 124.8

Location

supporting information

Signals [ppm]

193.3; 136.3; 135.2; 133.8; 131.6; 130.6; 129; 128.4; 126.9; 124.9; 124.8

Zhao, Hong; Chen, Qiurong; Wei, Li; Jiang, Yuanyuan; Cai, Mingzhong; Tetrahedron; vol. 71; nb. 46; (2015); p.

8725 - 8731; Art.No: 27151, View in Reaxys 37 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectroscopy) [MHz]

600

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Location

supporting information

Shil, Arun K.; Kumar, Sandeep; Reddy, C. Bal; Dadhwal, Sumit; Thakur, Vandna; Das, Pralay; Organic Letters; vol. 17; nb. 21; (2015); p. 5352 - 5355, View in Reaxys 38 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectroscopy) [MHz]

150

Location

supporting information

Shil, Arun K.; Kumar, Sandeep; Reddy, C. Bal; Dadhwal, Sumit; Thakur, Vandna; Das, Pralay; Organic Letters; vol. 17; nb. 21; (2015); p. 5352 - 5355, View in Reaxys 39 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

19.84

Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Luo, Qun-Li; Nan, Wen-Hui; Li, Yu; Chen, Xiang; Arkivoc; vol. 2014; nb. 4; (2014); p. 350 - 361, View in Reaxys 40 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

19.84

Frequency (NMR Spectroscopy) [MHz]

75

Location

supporting information

Luo, Qun-Li; Nan, Wen-Hui; Li, Yu; Chen, Xiang; Arkivoc; vol. 2014; nb. 4; (2014); p. 350 - 361, View in Reaxys 41 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

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Khumraksa, Bannarak; Phakhodee, Wong; Pattarawarapan, Mookda; Tetrahedron Letters; vol. 54; nb. 15; (2013); p. 1983 - 1986, View in Reaxys 42 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Zhu, Yingguang; Zhao, Baoguo; Shi, Yian; Organic Letters; vol. 15; nb. 5; (2013); p. 992 - 995, View in Reaxys 43 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

75

Location

supporting information

Zhu, Yingguang; Zhao, Baoguo; Shi, Yian; Organic Letters; vol. 15; nb. 5; (2013); p. 992 - 995, View in Reaxys 44 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

22.5

Frequency (NMR Spectroscopy) [MHz]

500

Location

supporting information

Ueda, Tsuyoshi; Konishi, Hideyuki; Manabe, Kei; Angewandte Chemie - International Edition; vol. 52; nb. 33; (2013); p. 8611 - 8615; Angew. Chem.; vol. 125; nb. 33; (2013); p. 8773 - 8777,5, View in Reaxys 45 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

22.9

Frequency (NMR Spectroscopy) [MHz]

125

Location

supporting information

Ueda, Tsuyoshi; Konishi, Hideyuki; Manabe, Kei; Angewandte Chemie - International Edition; vol. 52; nb. 33; (2013); p. 8611 - 8615; Angew. Chem.; vol. 125; nb. 33; (2013); p. 8773 - 8777,5, View in Reaxys 46 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy)

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Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectroscopy) [MHz]

500

Location

supporting information

Zhang, Lin; Bi, Xihe; Guan, Xiaoxue; Li, Xingqi; Liu, Qun; Barry, Badru-Deen; Liao, Peiqiu; Angewandte Chemie - International Edition; vol. 52; nb. 43; (2013); p. 11303 - 11307; Angew. Chem.; vol. 125; nb. 43; (2013); p.

11513 - 11517,5, View in Reaxys 47 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- dimethyl sulfoxide scopy) Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectroscopy) [MHz]

125

Location

supporting information

Zhang, Lin; Bi, Xihe; Guan, Xiaoxue; Li, Xingqi; Liu, Qun; Barry, Badru-Deen; Liao, Peiqiu; Angewandte Chemie - International Edition; vol. 52; nb. 43; (2013); p. 11303 - 11307; Angew. Chem.; vol. 125; nb. 43; (2013); p.

11513 - 11517,5, View in Reaxys 48 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Anisur, Rahman Md; Shin, Jongmin; Choi, Hyung Ho; Yeo, Kyung Min; Kang, Eun Joo; Lee, In Su; Journal of Materials Chemistry; vol. 20; nb. 47; (2010); p. 10615 - 10621, View in Reaxys; Lee, Kyung Sig; Anisur, Rahman Md; Kim, Ki Woong; Kim, Won Sun; Park, Tae-Joon; Kang, Eun Joo; Lee, In Su; Chemistry of Materials; vol. 24; nb. 4; (2012); p. 682 - 687, View in Reaxys 49 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

200

Original Text (NMR Spectroscopy)

1H

Signals [ppm]

1.19; 1.83; 2.07; 2.31; 2.6; 3.95; 4.27; 5.09; 7.7

Kind of signal

dd, 6H, J = 8 Hz; q, 1H, J = 12 Hz; q, 1H, J = 12 Hz; m, 1H; m, 2H; m, 1H; m, 1H; d, 1H, J = 12 Hz; m, 7H

NMR (CDCl3, 200 MHz): δ 1.19 (dd, 6H, J = 8 Hz), 1.83 (q, 1H, J = 12 Hz), 2.07 (q, 1H, J = 12 Hz), 2.31 (m, 1H), 2.60 (m, 2H), 3.95 (m, 1H), 4.27 (m, 1H), 5.09 (d, 1H, J = 12 Hz), 7.7 (m, 7H)

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Capim, Saulo L.; Carneiro, Paulo H.P.; Castro, Paloma C.; Barros, Maithê R.M.; Marinho, Bruno G.; Vasconcellos, Mário L.A.A.; European Journal of Medicinal Chemistry; vol. 58; (2012); p. 1 - 11, View in Reaxys 50 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

50

Original Text (NMR Spectroscopy)

13C

Signals [ppm]

18.97; 33.89; 38.6; 42.72; 55.2; 66.08; 75.16; 75.81; 123.02; 123.29; 125.42; 125.52; 126.09; 128.49; 128.9; 130.31; 133.77; 136.06; 176.85

NMR (CDCl3 50 MHz): 18.97, 33.89, 38.60, 42.72, 55.20, 66.08, 75.16, 75.81, 123.02, 123.29, 125.42, 125.52, 126.09, 128.49, 128.90, 130.31, 133.77, 136.06, 176.85

Capim, Saulo L.; Carneiro, Paulo H.P.; Castro, Paloma C.; Barros, Maithê R.M.; Marinho, Bruno G.; Vasconcellos, Mário L.A.A.; European Journal of Medicinal Chemistry; vol. 58; (2012); p. 1 - 11, View in Reaxys 51 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

200

Original Text (NMR Spectroscopy)

δH: 7.57-7.71 (m, 3H, Ar-H), 7.87-7.97 (m, 2H, Ar-H), 8.06 (d, 1H, J = 8.0 Hz, Ar-H), 9.24 (d, 1H, J = 8.4 Hz, Ar-H), 10.37 (s, 1H, CH=O) ppm

Ahmad, Jahir Uddin; Raeisaenen, Minna T.; Kemell, Marianna; Heikkilae, Mikko J.; Leskelae, Markku; Repo, Timo; Applied Catalysis A: General; vol. 449; (2012); p. 153 - 162, View in Reaxys 52 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

50

Original Text (NMR Spectroscopy)

δC: 124.7, 126.8, 128.3, 128.9, 130.4, 131.2, 133.5, 135.1, 136.6, 193.4 ppm

Ahmad, Jahir Uddin; Raeisaenen, Minna T.; Kemell, Marianna; Heikkilae, Mikko J.; Leskelae, Markku; Repo, Timo; Applied Catalysis A: General; vol. 449; (2012); p. 153 - 162, View in Reaxys 53 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Mamros, Audrey N.; Sharrow, Phillip R.; Weller, William E.; Luderer, Mark R.; Fair, Justin D.; Pazehoski, Kristina O.; Luderer, Matthew R.; Arkivoc; vol. 2011; nb. 5; (2011); p. 23 - 33, View in Reaxys 54 of 90

Description (NMR Spec- Chemical shifts troscopy)

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Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Mamros, Audrey N.; Sharrow, Phillip R.; Weller, William E.; Luderer, Mark R.; Fair, Justin D.; Pazehoski, Kristina O.; Luderer, Matthew R.; Arkivoc; vol. 2011; nb. 5; (2011); p. 23 - 33, View in Reaxys 55 of 90

Description (NMR Spec- NOESY (Nuclear Overhauser Enhanced Spectroscopy) troscopy) Nucleus (NMR Spectroscopy)

1H; 1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

600.1

Busacca, Carl A.; Campbell, Scot; Gonnella, Nina C.; Senanayake, Chris H.; Magnetic Resonance in Chemistry; vol. 48; nb. 1; (2010); p. 74 - 79, View in Reaxys 56 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Zhang, Li; Zha, Zhenggen; Wang, Zhiyong; Synlett; nb. 13; (2010); p. 1915 - 1918, View in Reaxys 57 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

75

Location

supporting information

Zhang, Li; Zha, Zhenggen; Wang, Zhiyong; Synlett; nb. 13; (2010); p. 1915 - 1918, View in Reaxys 58 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Frequency (NMR Spectroscopy) [MHz]

75

Location

supporting information

Zhang, Li; Zha, Zhenggen; Wang, Zhiyong; Synlett; nb. 13; (2010); p. 1915 - 1918, View in Reaxys 59 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

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Zhang, Li; Zha, Zhenggen; Wang, Zhiyong; Synlett; nb. 13; (2010); p. 1915 - 1918, View in Reaxys 60 of 90

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Chu, Guobiao; Li, Chunbao; Organic and Biomolecular Chemistry; vol. 8; nb. 20; (2010); p. 4716 - 4719, View in Reaxys 61 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- [D3]acetonitrile scopy) Watanabe, Asako; Matsushita, Maya; Masuda, Aya; Igarashi, Tetsutaro; Sakurai, Tadamitsu; Heterocycles; vol.

78; nb. 10; (2009); p. 2431 - 2437, View in Reaxys 62 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) Benassi, Rois; Iarossi, Dario; Folli, Ugo; Schenetti, Luisa; Taddei, Ferdinando; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1981); p. 228 - 232, View in Reaxys; Dean, Francis M.; El-Kass, Gassan; Prakash, Lalit; Journal of the Chemical Society, Chemical Communications; nb. 8; (1985); p. 502 - 503, View in Reaxys; Cerfontain, Hans; Zou, Yousi; Bakker, Bert H.; Recueil des Travaux Chimiques des Pays-Bas; vol. 113; nb. 9; (1994); p. 403 - 410, View in Reaxys; Gupton, John T.; Polk, Dale E.; Synthetic Communications; vol. 11; nb. 7; (1981); p. 571 - 578, View in Reaxys; Niestroj, Michael; Neumann, Wilhelm P.; Chemische Berichte; vol. 129; nb. 1; (1996); p. 45 - 51, View in Reaxys; Baudin, Jean-Bernard; Commenil, MarieGabrielle; Julia, Sylvestre A.; Lome, Robert; Ruel, Odile; Bulletin de la Societe Chimique de France; vol. 133; nb. 11; (1996); p. 1127 - 1141, View in Reaxys; Kesharwani, Tanay; Larock, Richard C.; Tetrahedron; vol. 64; nb.

26; (2008); p. 6090 - 6102, View in Reaxys 63 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Lee, Kyoungsoo; Maleczka Jr., Robert E.; Organic Letters; vol. 8; nb. 9; (2006); p. 1887 - 1888, View in Reaxys; Kumar, Dinesh; Kumar, Raj; Chakraborti, Asit K.; Synthesis; nb. 8; (2008); p. 1249 - 1256, View in Reaxys 64 of 90

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Lee, Kyoungsoo; Maleczka Jr., Robert E.; Organic Letters; vol. 8; nb. 9; (2006); p. 1887 - 1888, View in Reaxys

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65 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

75

Lee, Kyoungsoo; Maleczka Jr., Robert E.; Organic Letters; vol. 8; nb. 9; (2006); p. 1887 - 1888, View in Reaxys 66 of 90

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

75

Lee, Kyoungsoo; Maleczka Jr., Robert E.; Organic Letters; vol. 8; nb. 9; (2006); p. 1887 - 1888, View in Reaxys 67 of 90

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Lee, Kyoungsoo; Maleczka Jr., Robert E.; Organic Letters; vol. 8; nb. 9; (2006); p. 1887 - 1888, View in Reaxys 68 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Yi, Wen-Bin; Yin, Ya-Qing; Cai, Chun; Canadian Journal of Chemistry; vol. 84; nb. 11; (2006); p. 1563 - 1566, View in Reaxys 69 of 90

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Yi, Wen-Bin; Yin, Ya-Qing; Cai, Chun; Canadian Journal of Chemistry; vol. 84; nb. 11; (2006); p. 1563 - 1566, View in Reaxys 70 of 90

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CDCl3 scopy) Comment (NMR Spectroscopy)

1H-1H

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Baudin, Jean-Bernard; Commenil, Marie-Gabrielle; Julia, Sylvestre A.; Lome, Robert; Ruel, Odile; Bulletin de la Societe Chimique de France; vol. 133; nb. 11; (1996); p. 1127 - 1141, View in Reaxys 71 of 90

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) Lunazzi, Lodovico; Placucci, Giuseppe; Macciantelli, Dante; Tetrahedron; vol. 47; nb. 43; (1991); p. 9125 9128, View in Reaxys 72 of 90

Description (NMR Spec- NOE troscopy) Lunazzi, Lodovico; Placucci, Giuseppe; Macciantelli, Dante; Tetrahedron; vol. 47; nb. 43; (1991); p. 9125 9128, View in Reaxys

73 of 90

Description (NMR Spec- NMR with shift reagents troscopy) Hatano; Nippon Kagaku Kaishi; (1975); p. 1917,1918,1919, View in Reaxys; Benassi, Rois; Iarossi, Dario; Folli, Ugo; Schenetti, Luisa; Taddei, Ferdinando; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1981); p. 228 - 232, View in Reaxys; Abraham, Raymond J.; Chadwick, Derek J.; Sancassan, Fernando; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1988); p. 169 - 177, View in Reaxys

74 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

30

Abraham, Raymond J.; Chadwick, Derek J.; Sancassan, Fernando; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1988); p. 169 - 177, View in Reaxys 75 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

30

Abraham, Raymond J.; Chadwick, Derek J.; Sancassan, Fernando; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1988); p. 169 - 177, View in Reaxys 76 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- acetonitrile scopy) Temperature (NMR Spectroscopy) [°C]

75

Boykin, D. W.; Balakrishnan, P.; Baumstark, A. L.; Magnetic Resonance in Chemistry; vol. 25; (1987); p. 248 250, View in Reaxys 77 of 90

Description (NMR Spec- Chemical shifts troscopy)

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Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

40

Jaccard, Guy; Lauterwein, Juergen; Helvetica Chimica Acta; vol. 69; (1986); p. 1469 - 1485, View in Reaxys 78 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

28

Schuster, Ingeborg I.; Journal of Organic Chemistry; vol. 50; nb. 10; (1985); p. 1656 - 1662, View in Reaxys 79 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- benzene-d6 scopy) Dean, Francis M.; El-Kass, Gassan; Prakash, Lalit; Journal of the Chemical Society, Chemical Communications; nb. 8; (1985); p. 502 - 503, View in Reaxys 80 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Temperature (NMR Spectroscopy) [°C]

31.9

Salman, Salman R.; Organic Magnetic Resonance; vol. 21; nb. 11; (1983); p. 672 - 674, View in Reaxys 81 of 90

Description (NMR Spec- Spin-spin coupling constants troscopy) Temperature (NMR Spectroscopy) [°C]

31.9

Comment (NMR Spectroscopy)

1H-1H.

Salman, Salman R.; Organic Magnetic Resonance; vol. 21; nb. 11; (1983); p. 672 - 674, View in Reaxys 82 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CCl4 scopy) Barton, Derek H. R.; Hui, Raymond A. H. F.; Ley, Steven V.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); nb. 9; (1982); p. 2179 - 2186, View in Reaxys 83 of 90

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CCl4 scopy) Comment (NMR Spectroscopy)

1H-1H

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Barton, Derek H. R.; Hui, Raymond A. H. F.; Ley, Steven V.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); nb. 9; (1982); p. 2179 - 2186, View in Reaxys 84 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Schuster,I.I.; Journal of Organic Chemistry; vol. 46; (1981); p. 5110, View in Reaxys 85 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3; trifluoroacetic acid scopy) Schuster,I.I.; Journal of Organic Chemistry; vol. 46; (1981); p. 5110, View in Reaxys 86 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- acetone-d6 scopy) Salman, S. R.; Journal of Molecular Structure; vol. 77; (1981); p. 277 - 282, View in Reaxys 87 of 90

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- acetone-d6 scopy) Salman, S. R.; Journal of Molecular Structure; vol. 77; (1981); p. 277 - 282, View in Reaxys 88 of 90

Description (NMR Spec- NMR troscopy) Wege,D.; Wilkinson,S.P.; Australian Journal of Chemistry; vol. 26; (1973); p. 1751 - 1762, View in Reaxys; Menger,F.M. et al.; Journal of the American Chemical Society; vol. 100; nb. 15; (1978); p. 4676 - 4678, View in Reaxys; Gurudutt,K.N.; Seshadri,T.R.; Phytochemistry (Elsevier); vol. 13; (1974); p. 2845 - 2847, View in Reaxys; Hansen,P.E.; Poulsen,O.K.; Berg,A.; Organic Magnetic Resonance; vol. 9; (1977); p. 649, View in Reaxys; Drakenberg,T.; Sandstroem,J.; Seita,J.; Organic Magnetic Resonance; vol. 11; (1978); p. 246, View in Reaxys; Comins; Meyers; Synthesis; (1978); p. 403, View in Reaxys; Klinck; Stothers; Canadian Journal of Chemistry; vol. 40; (1962); p. 1071,1073, View in Reaxys; Stothers; Lauterbur; Canadian Journal of Chemistry; vol. 42; (1964); p.

1563,1572, View in Reaxys; Narayanan; Shukla; Current Science; vol. 42; (1973); p. 329, View in Reaxys; Seita et al.; Organic Magnetic Resonance; vol. 11; (1978); p. 239,243, View in Reaxys; Emsley et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 611,613, View in Reaxys; Adcock et al.; Australian Journal of Chemistry; vol. 27; (1974); p. 1817,1819, View in Reaxys; Emsley et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1970); p. 1513, View in Reaxys; Forsyth et al.; Journal of the American Chemical Society; vol. 98; (1976); p. 2512,2513, View in Reaxys

89 of 90

Description (NMR Spec- Spin-spin coupling constants troscopy) Yamamoto et al.; Molecular Physics; vol. 17; (1969); p. 249,252, View in Reaxys

90 of 90

Description (NMR Spec- Spectrum troscopy) Martin et al.; Tetrahedron; vol. 20; (1964); p. 1505,1513, 1514, View in Reaxys

IR Spectroscopy (29) 1 of 29

Description (IR Spectroscopy)

Bands

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Solvent (IR Spectroscopy)

neat liquid

Location

supporting information

Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 - 595, View in Reaxys; Mete, Trimbak B.; Khopade, Tushar M.; Bhat, Ramakrishna G.; Tetrahedron Letters; vol. 58; nb. 29; (2017); p. 2822 - 2825, View in Reaxys 2 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Buxaderas, Eduardo; Graziano-Mayer, Marilyn; Volpe, María Alicia; Radivoy, Gabriel; Synthesis (Germany); vol. 49; nb. 6; (2017); p. 1387 - 1393; Art.No: SS-2016-M0473-OP, View in Reaxys 3 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Original Text (IR Spectroscopy)

IR (neat): 2725, 1683 cm-1

Signals [cm-1]

2725; 1683

Imai, Sho; Togo, Hideo; Tetrahedron; vol. 72; nb. 44; (2016); p. 6948 - 6954, View in Reaxys 4 of 29

Description (IR Spectroscopy)

Bands

Original Text (IR Spectroscopy)

IR (film, cm-1): 1689, 1573, 1217, 1170, 909

Comment (IR Spectroscopy)

film

Signals [cm-1]

1689; 1573; 1217; 1170; 909

Zhao, Hong; Chen, Qiurong; Wei, Li; Jiang, Yuanyuan; Cai, Mingzhong; Tetrahedron; vol. 71; nb. 46; (2015); p.

8725 - 8731; Art.No: 27151, View in Reaxys 5 of 29

Description (IR Spectroscopy)

Bands; Spectrum

Location

supporting information

Bansal, Deepak; Pandey, Saurabh; Hundal, Geeta; Gupta, Rajeev; New Journal of Chemistry; vol. 39; nb. 12; (2015); p. 9772 - 9781, View in Reaxys 6 of 29

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

film

Jiang, Jianwen; Wang, Pingping; Cai, Mingzhong; Journal of Chemical Research; vol. 38; nb. 4; (2014); p. 218 222, View in Reaxys 7 of 29

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands

Tabata, Masayuki; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb.

16; (2014); p. 3402 - 3410, View in Reaxys 8 of 29

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

film

Zhu, Yingguang; Zhao, Baoguo; Shi, Yian; Organic Letters; vol. 15; nb. 5; (2013); p. 992 - 995, View in Reaxys; Khumraksa, Bannarak; Phakhodee, Wong; Pattarawarapan, Mookda; Tetrahedron Letters; vol. 54; nb. 15; (2013); p. 1983 - 1986, View in Reaxys

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9 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Original Text (IR Spectroscopy)

IR (KBr, cm-1): 779 and 732 (C-H aromatic), 1246 and 1157 (C-O ester), 1597 and 1465 (C=C aromatic), 1735 (C=O ester), 2873 (C-H sp3), 3051 (=C-H aromatic) cm-1

Signals [cm-1]

779; 732; 1246; 1157; 1597; 1465; 1735; 2873; 3051

Intensity

m (medium); s (strong); m (medium); s (strong); s (strong); m (medium)

Capim, Saulo L.; Carneiro, Paulo H.P.; Castro, Paloma C.; Barros, Maithê R.M.; Marinho, Bruno G.; Vasconcellos, Mário L.A.A.; European Journal of Medicinal Chemistry; vol. 58; (2012); p. 1 - 11, View in Reaxys 10 of 29

Description (IR Spectroscopy)

Bands

Original Text (IR Spectroscopy)

IR (cm-1): 1684 (υC=O)

Signals [cm-1]

1684

Intensity

s (strong)

Ahmad, Jahir Uddin; Raeisaenen, Minna T.; Kemell, Marianna; Heikkilae, Mikko J.; Leskelae, Markku; Repo, Timo; Applied Catalysis A: General; vol. 449; (2012); p. 153 - 162, View in Reaxys 11 of 29

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

film

Zhang, Li; Zha, Zhenggen; Wang, Zhiyong; Synlett; nb. 13; (2010); p. 1915 - 1918, View in Reaxys 12 of 29

Description (IR Spectroscopy)

Mid IR (MIR); Bands

Location

supporting information

Comment (IR Spectroscopy)

neat (no solvent)

Moghadam, Majid; Tangestaninejad, Shahram; Mirkhani, Valiollah; Mohammadpoor-baltork, Iraj; Sirjanian, Narges; Parand, Somayeh; Bioorganic and Medicinal Chemistry; vol. 17; nb. 9; (2009); p. 3394 - 3398, View in Reaxys 13 of 29

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

film

Krishnakumar; Prabavathi; Muthunatesan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 69; nb. 2; (2008); p. 528 - 533, View in Reaxys 14 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

film

Krishnakumar; Prabavathi; Muthunatesan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 69; nb. 2; (2008); p. 528 - 533, View in Reaxys 15 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

Yi, Wen-Bin; Yin, Ya-Qing; Cai, Chun; Canadian Journal of Chemistry; vol. 84; nb. 11; (2006); p. 1563 - 1566, View in Reaxys

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16 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

solid Ar

Temperature (IR Spectroscopy) [°C]

-263.15

Inui, Hiroshi; Murata, Shigeru; Chemical Physics Letters; vol. 359; nb. 3-4; (2002); p. 267 - 272, View in Reaxys; Inui, Hiroshi; Murata, Shigeru; Journal of the American Chemical Society; vol. 127; nb. 8; (2005); p. 2628 - 2636, View in Reaxys 17 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

dimethylsulfoxide

Velcheva, Evelina A.; Juchnovski, Ivan N.; Binev, Ivan G.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 59; nb. 8; (2003); p. 1745 - 1749, View in Reaxys 18 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

3060 - 771 cm**(-1)

Niestroj, Michael; Neumann, Wilhelm P.; Chemische Berichte; vol. 129; nb. 1; (1996); p. 45 - 51, View in Reaxys 19 of 29

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1685 cm**(-1)

Doepp, Dietrich; Memarian, Hamid Reza; Chemische Berichte; vol. 123; nb. 2; (1990); p. 315 - 319, View in Reaxys 20 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1689 cm**(-1)

Kolb, Vera M.; Stupar, Joseph W.; Janota, Timothy E.; Duax, William L.; Journal of Organic Chemistry; vol. 54; nb. 10; (1989); p. 2341 - 2346, View in Reaxys 21 of 29

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1690 cm**(-1)

Doepp, Dietrich; Memarian, Hamid Reza; Krueger, Carl; Raabe, Eleonore; Chemische Berichte; vol. 122; (1989); p. 585 - 588, View in Reaxys 22 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

3040 - 1700 cm**(-1)

Barton, Derek H. R.; Hui, Raymond A. H. F.; Ley, Steven V.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); nb. 9; (1982); p. 2179 - 2186, View in Reaxys 23 of 29

Description (IR Spectroscopy)

Bands

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Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1675 cm**(-1)

Gupton, John T.; Polk, Dale E.; Synthetic Communications; vol. 11; nb. 7; (1981); p. 571 - 578, View in Reaxys 24 of 29

Description (IR Spectroscopy)

Bands

Reimlinger,H. et al.; Chemische Berichte; vol. 97; (1964); p. 349 - 362, View in Reaxys; Ferrari et al.; Journal of the American Chemical Society; vol. 87; (1965); p. 1247,1251, View in Reaxys; Laurence et al.; Journal of the American Chemical Society; vol. 101; (1979); p. 4793,4795, View in Reaxys; Zadorozhnyi; Ishchenko; Optics and Spectroscopy; vol. 19; (1965); p. 306; ; p. 551, View in Reaxys; Morcillo et al.; Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica; vol. 63; (1967); p. 639,640-660, View in Reaxys; Cogrossi; Annali di Chimica (Rome, Italy); vol. 56; (1966); p. 270,278, 279, 282, View in Reaxys 25 of 29

Description (IR Spectroscopy)

IR

Gurudutt,K.N.; Seshadri,T.R.; Phytochemistry (Elsevier); vol. 13; (1974); p. 2845 - 2847, View in Reaxys; Comins; Meyers; Synthesis; (1978); p. 403, View in Reaxys; Watkins; Phytochemistry (Elsevier); vol. 8; (1969); p. 979,981, View in Reaxys; Yang et al.; Tetrahedron Letters; (1964); p. 3657,3658-3659, View in Reaxys; Yukhnovskii; Theoretical and Experimental Chemistry; vol. 3; (1967); p. 67; ; p. 123, View in Reaxys; Sharma et al.; Indian Journal of Physics (1926-1976); vol. 48; (1974); p. 494, View in Reaxys; Morcillo et al.; Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica; vol. 63; (1967); p. 639,640-660, View in Reaxys 26 of 29

Description (IR Spectroscopy)

Spectrum

Powers et al.; Analytical Chemistry; vol. 32; (1960); p. 1287, View in Reaxys; Fratew et al.; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 3; (1970); p. 579,585,587,590, View in Reaxys; Cox et al.; Spectrochimica Acta; vol. 21; (1965); p. 1663, View in Reaxys 27 of 29

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

1800 - 1600 cm**(-1)

Hunsberger; Journal of the American Chemical Society; vol. 72; (1950); p. 5626,5630, View in Reaxys 28 of 29

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

3700 - 2600 cm**(-1)

Hunsberger; Journal of the American Chemical Society; vol. 72; (1950); p. 5626,5630, View in Reaxys 29 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

durch UV-Licht erregt bei -183grad.

Lewis; Kasha; Journal of the American Chemical Society; vol. 66; (1944); p. 2100,2107; Journal of the American Chemical Society; vol. 67; (1945); p. 994,1000, View in Reaxys Mass Spectrometry (18) Description (Mass Location Spectrometry) high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); timeof-flight mass

supporting information

References Zhang, Lin; Bi, Xihe; Guan, Xiaoxue; Li, Xingqi; Liu, Qun; Barry, Badru-Deen; Liao, Peiqiu; Angewandte Chemie - International Edition; vol. 52; nb. 43; (2013); p. 11303 11307; Angew. Chem.; vol. 125; nb. 43; (2013); p. 11513 - 11517,5, View in Reaxys; Mete, Trimbak B.; Khopade, Tushar M.; Bhat, Ramakrishna G.; Tetrahedron Letters; vol. 58; nb. 29; (2017); p. 2822 - 2825, View in Reaxys

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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spectra (TOFMS); spectrum electron impact (EI); spectrum

supporting information

Gu, Lijun; Jin, Cheng; Chemical Communications; vol. 51; nb. 30; (2015); p. 6572 6575, View in Reaxys; Sakai, Norio; Minato, Kohei; Ogiwara, Yohei; Tetrahedron Letters; vol. 58; nb. 48; (2017); p. 4563 - 4567, View in Reaxys

gas chromatography mass spectrometry (GCMS); electron impact (EI); spectrum

Buxaderas, Eduardo; Graziano-Mayer, Marilyn; Volpe, María Alicia; Radivoy, Gabriel; Synthesis (Germany); vol. 49; nb. 6; (2017); p. 1387 - 1393; Art.No: SS-2016-M0473OP, View in Reaxys

high resolution mass spectrometry (HRMS); electron impact (EI); spectrum

Hu, Guang; Ramakumar, Kinthada; Brenner-Moyer, Stacey E.; Journal of Organic Chemistry; vol. 82; nb. 13; (2017); p. 6972 - 6977, View in Reaxys

spectrum

supporting information

Borah, Suchibrata; Bhattacharyya, Bagmita; Deka, Jumi; Borah, Aditya; Devi, Anuchaya; Deka, Dhanapati; Mishra, Shashank; Raidongia, Kalyan; Gogoi, Nayanmoni; Dalton Transactions; vol. 46; nb. 26; (2017); p. 8664 - 8672, View in Reaxys

spectrum

Akimoto, Yoshio; Aoki, Tadamitu; Nito, Shin'ichi; Inouye, Yoshio; Chemosphere; vol.

34; nb. 2; (1997); p. 263 - 273, View in Reaxys; Li, Bin; Shen, Nana; Fan, Xuesen; Zhang, Xinying; Tetrahedron Letters; vol. 57; nb. 17; (2016); p. 1843 - 1846, View in Reaxys

gas chromatogra- supporting inforphy mass specmation trometry (GCMS); electron impact (EI); spectrum

Gong, Jin-Long; Qi, Xinxin; Wei, Duo; Feng, Jian-Bo; Wu, Xiao-Feng; Organic and Biomolecular Chemistry; vol. 12; nb. 38; (2014); p. 7486 - 7488, View in Reaxys; Qi, Xinxin; Li, Chong-Liang; Wu, Xiao-Feng; Chemistry - A European Journal; vol. 22; nb. 17; (2016); p. 5835 - 5838, View in Reaxys

electron impact (EI); spectrum

Ogiwara, Yohei; Ono, Yuji; Sakai, Norio; Synthesis (Germany); vol. 48; nb. 23; (2016); p. 4143 - 4148; Art.No: SS-2016-F0462-OP, View in Reaxys

gas chromatogra- supporting inforphy mass specmation trometry (GCMS); spectrum

Khumraksa, Bannarak; Phakhodee, Wong; Pattarawarapan, Mookda; Tetrahedron Letters; vol. 54; nb. 15; (2013); p. 1983 - 1986, View in Reaxys; Moore, Peter W.; Mirzayans, Paul M.; Williams, Craig M.; Chemistry - A European Journal; vol. 21; nb. 9; (2015); p. 3567 - 3571, View in Reaxys

electrospray ioni- supporting inforsation (ESI); time- mation of-flight mass spectra (TOFMS); high resolution mass spectrometry (HRMS); spectrum

Gu, Lijun; Jin, Cheng; Chemical Communications; vol. 51; nb. 30; (2015); p. 6572 6575, View in Reaxys

electrospray ionisation (ESI); spectrum

supporting information

Banerjee, Shibdas; Goyal, Sandeep; Mazumdar, Shyamalava; Bioorganic Chemistry; vol. 62; (2015); p. 94 - 105, View in Reaxys

electron impact (EI); gas chromatography mass spectrometry (GCMS); spectrum

supporting information

Liu, Dongwang; Zhou, Hongxia; Gu, Xiangyong; Shen, Xiaoqin; Li, Pixu; Chinese Journal of Chemistry; vol. 32; nb. 2; (2014); p. 117 - 122, View in Reaxys

liquid chromatog- supporting inforraphy mass spec- mation trometry (LCMS); electrospray ionisation (ESI); timeof-flight mass spectra (TOFMS); spectrum

Jiang, Xiao; Wang, Jin-Mei; Zhang, Ying; Chen, Zhong; Zhu, Yong-Ming; Ji, ShunJun; Organic Letters; vol. 16; nb. 13; (2014); p. 3492 - 3495, View in Reaxys

high resolution mass spectrometry (HRMS); elec-

Natte, Kishore; Dumrath, Andreas; Neumann, Helfried; Beller, Matthias; Angewandte Chemie - International Edition; vol. 53; nb. 38; (2014); p. 10090 - 10094; Angew. Chem.; vol. 126; nb. 38; (2015); p. 10254 - 10258,5, View in Reaxys

supporting information

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tron impact (EI); spectrum high resolution mass spectrometry (HRMS); timeof-flight mass spectra (TOFMS); liquid chromatography mass spectrometry (LCMS); IT (ion trap); spectrum

Capim, Saulo L.; Carneiro, Paulo H.P.; Castro, Paloma C.; Barros, Maithê R.M.; Marinho, Bruno G.; Vasconcellos, Mário L.A.A.; European Journal of Medicinal Chemistry; vol. 58; (2012); p. 1 - 11, View in Reaxys

ESI (Electrospray ionisation); Spectrum

Wang, Lin; Chai, Yunfeng; Tu, Peijun; Sun, Cuirong; Pan, Yuanjiang; Journal of Mass Spectrometry; vol. 46; nb. 12; (2011); p. 1203 - 1210, View in Reaxys

spectrum; chemical ionization (CI); positive secondary ions

Tzing, Shin-Hwa; Ghule, Anil; Chang, Jia-Yaw; Ling, Yong-Chien; Journal of Mass Spectrometry; vol. 38; nb. 4; (2003); p. 401 - 408, View in Reaxys

Hadjiantoniou et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 69; (1973); p. 1704,1705, View in Reaxys; Szabo et al.; Justus Liebigs Annalen der Chemie; (1977); p. 747,758, View in Reaxys UV/VIS Spectroscopy (18) 1 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

chloroform

Location

supporting information

Das, Paramita; Kumar, Atul; Howlader, Prodip; Mukherjee, Partha Sarathi; Chemistry - A European Journal; vol.

23; nb. 51; (2017); p. 12565 - 12574, View in Reaxys 2 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

water

Location

supporting information

Das, Paramita; Kumar, Atul; Howlader, Prodip; Mukherjee, Partha Sarathi; Chemistry - A European Journal; vol.

23; nb. 51; (2017); p. 12565 - 12574, View in Reaxys 3 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Location

supporting information

Ravelli, Davide; Zema, Michele; Mella, Mariella; Fagnoni, Maurizio; Albini, Angelo; Organic and Biomolecular Chemistry; vol. 8; nb. 18; (2010); p. 4158 - 4164, View in Reaxys; Kool, Eric T.; Park, Do-Hyoung; Crisalli, Pete; Journal of the American Chemical Society; vol. 135; nb. 47; (2013); p. 17663 - 17666, View in Reaxys 4 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Location

supporting information

Okamoto, Hideki; Yamaji, Minoru; Gohda, Shin; Kubozono, Yoshihiro; Komura, Noriko; Sato, Kaori; Sugino, Hisako; Satake, Kyosuke; Organic Letters; vol. 13; nb. 10; (2011); p. 2758 - 2761, View in Reaxys 5 of 18

Description (UV/VIS Spectroscopy)

UV excited state absorption

Fukuzumi; Satoh; Okamoto; Yasui; Suenobu; Seko; Fujitsuka; Ito; Journal of the American Chemical Society; vol. 123; nb. 32; (2001); p. 7756 - 7766, View in Reaxys 6 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

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Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ 485 VIS) [nm] Clark, K. B.; Bhattacharyya, K.; Das, P. K.; Scaiano, J. C.; Schaap, A. P.; Journal of Organic Chemistry; vol. 57; nb. 13; (1992); p. 3706 - 3712, View in Reaxys 7 of 18

Description (UV/VIS Spectroscopy)

Singlet-triplet band

Clark, K. B.; Bhattacharyya, K.; Das, P. K.; Scaiano, J. C.; Schaap, A. P.; Journal of Organic Chemistry; vol. 57; nb. 13; (1992); p. 3706 - 3712, View in Reaxys; Boldridge,, David W.; Justus, Brian L.; Scott, Gary W.; Journal of Chemical Physics; vol. 80; nb. 7; (1984); p. 3179 - 3184, View in Reaxys 8 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

methanol

Absorption Maxima (UV/ 242; 247; 312 VIS) [nm] Ext./Abs. Coefficient [l·mol-1cm-1]

6026; 6026; 2455

Pozharskii, A.F.; Alexandrov, G.G; Vistorobskii N.V.; Journal of Organic Chemistry USSR (English Translation); vol. 27; nb. 7; (1991); p. 1347 - 1352; Zhurnal Organicheskoi Khimii; vol. 27; nb. 7; (1991); p. 1536 - 1543, View in Reaxys 9 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol; H2O

Comment (UV/VIS Spectroscopy)

Ratio of solvents: 50percent

Absorption Maxima (UV/ 369 VIS) [nm] Somera, Neusa M.; Stachissini, Antonia S.; Amaral, Antonia T. do; Amaral, Luciano do; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1987); p. 1717 - 1722, View in Reaxys 10 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

methanol

Comment (UV/VIS Spectroscopy)

375 - 525 nm

Boldridge,, David W.; Justus, Brian L.; Scott, Gary W.; Journal of Chemical Physics; vol. 80; nb. 7; (1984); p.

3179 - 3184, View in Reaxys 11 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

375 - 525 nm

Boldridge,, David W.; Justus, Brian L.; Scott, Gary W.; Journal of Chemical Physics; vol. 80; nb. 7; (1984); p.

3179 - 3184, View in Reaxys 12 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

various solvent(s)

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Comment (UV/VIS Spectroscopy)

375 - 525 nm

Boldridge,, David W.; Justus, Brian L.; Scott, Gary W.; Journal of Chemical Physics; vol. 80; nb. 7; (1984); p.

3179 - 3184, View in Reaxys 13 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

toluene; various solvent(s)

Comment (UV/VIS Spectroscopy)

375 - 525 nm

Boldridge,, David W.; Justus, Brian L.; Scott, Gary W.; Journal of Chemical Physics; vol. 80; nb. 7; (1984); p.

3179 - 3184, View in Reaxys 14 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Belaits et al.; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 480; ; p. 869, View in Reaxys; Proskuryakova; Nurmuknametov; Optics and Spectroscopy; vol. 27; (1969); p. 119; ; p. 224, View in Reaxys; Suzuki et al. al.; Journal of Molecular Spectroscopy; vol. 57; (1975); p. 490, View in Reaxys; Kitamura; Baba; Bulletin of the Chemical Society of Japan; vol. 48; (1975); p. 1191,1192, 1193, View in Reaxys; Treinin; Hayon; Journal of the American Chemical Society; vol. 98; (1976); p. 3884,3885, 3887, View in Reaxys; Whipple et al.; Journal of the American Chemical Society; vol. 100; (1978); p. 6844,6849, View in Reaxys; Nurmukhametov; Optics and Spectroscopy; vol. 23; (1967); p. 209; ; p. 389, View in Reaxys; Prot; Roczniki Chemii; vol. 45; (1971); p. 247, View in Reaxys; Warwick; Wells; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 589,590, View in Reaxys 15 of 18

Description (UV/VIS Spectroscopy)

Triplet-triplet band

Nouchi; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 548, View in Reaxys; Tjutjulkow; Neikow; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 10; (1977); p. 313,318,319,323, View in Reaxys 16 of 18

Description (UV/VIS Spectroscopy)

UV/VIS

Yang et al.; Tetrahedron Letters; (1964); p. 3657,3658-3659, View in Reaxys; Hatano; Nippon Kagaku Kaishi; (1975); p. 1917,1918,1919, View in Reaxys; Grammaticakis; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 269; (1969); p. 248, View in Reaxys; Figeys; Wilmet-Devos; Bulletin des Societes Chimiques Belges; vol. 79; (1970); p. 459,460, View in Reaxys; Bell; Linschitz; Journal of the American Chemical Society; vol. 85; (1963); p. 528, View in Reaxys; Gompper; Wagner; Tetrahedron Letters; (1968); p. 165, View in Reaxys; Tjutjulkow; Neikow; Izvestiya na Otdelenieto za Khimicheski Nauki (Bulgarska Akademiya na Naukite); vol. 10; (1977); p. 313,318,319,323, View in Reaxys 17 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Kovi et al.; Spectroscopy Letters; vol. 6; (1973); p. 7,11, 13, View in Reaxys; Nagai; Nippon Kagaku Zasshi; vol.

91; (1970); p. 362,367-369; Chem.Abstr.; vol. 73; nb. 55442h; (1970), View in Reaxys 18 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

240 - 375 nm

Ramart-Lucas; Hoch; Bulletin de la Societe Chimique de France; (1952); p. 422,424, View in Reaxys ESR Spectroscopy (1) 1 of 1

Description (ESR Spectroscopy)

Spectrum

Hatano; Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan; vol. 93; nb. 7; (1973); p. 910 - 915, View in Reaxys Raman Spectroscopy (2) Description (Ram- Solvent (Raman an Spectroscopy) Spectroscopy) Spectrum

film

References Krishnakumar; Prabavathi; Muthunatesan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 69; nb. 2; (2008); p. 528 - 533, View in Reaxys

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Bands

film

Luminescence Spectroscopy (5) Description (LuComment (Lumiminescence nescence SpecSpectroscopy) troscopy)

Krishnakumar; Prabavathi; Muthunatesan; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 69; nb. 2; (2008); p. 528 - 533, View in Reaxys References

Luminescence lifetime

Akagi et al.; Nippon Kagaku Zasshi; vol. 87; (1966); p. 689,693, View in Reaxys; Kitamura; Baba; Bulletin of the Chemical Society of Japan; vol. 48; (1975); p. 1191,1192, 1193, View in Reaxys; Boldridge,, David W.; Justus, Brian L.; Scott, Gary W.; Journal of Chemical Physics; vol. 80; nb. 7; (1984); p. 3179 - 3184, View in Reaxys

Luminescence quantum yield

Kitamura; Baba; Bulletin of the Chemical Society of Japan; vol. 48; (1975); p.

1191,1192, 1193, View in Reaxys

Luminescence

Li; Lim; Journal of Chemical Physics; vol. 57; (1972); p. 605,606, View in Reaxys; Belaits et al.; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 480; ; p. 869, View in Reaxys; Ermolaev et al.; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 24; (1960); p. 499; ; p. 492, View in Reaxys

Luminescence quantum yield

Quantenausbeute Ermolaew; Switaschew; Optika i Spektroskopiya; vol. 7; (1959); p. 664; engl. Ausg. S. der Phosphores- 399, View in Reaxys cenz (A. + Ae.) bei -196grad.

Lasing properties

Abklingzeit der Phosphorescenz (A. + Ae.) bei -196grad.

Ermolaew; Switaschew; Optika i Spektroskopiya; vol. 7; (1959); p. 664; engl. Ausg. S. 399, View in Reaxys

Fluorescence Spectroscopy (4) Description (Fluo- Temperature (Flu- Location rescence Specorescence Spectroscopy) troscopy) [°C]

Comment (Fluorescence Spectroscopy)

References

Maxima; Spectrum

supporting information

Mase, Nobuyuki; Ando, Taishi; Shibagaki, Fumiya; Sugita, Atsushi; Narumi, Tetsuo; Toda, Mitsuo; Watanabe, Naoharu; Tanaka, Fujie; Tetrahedron Letters; vol. 55; nb. 11; (2014); p.

1946 - 1948, View in Reaxys

Fluorescence

supporting information

Hu, Shenshen; Li, Jiuyuan; Xiang, Junfeng; Pan, Jie; Luo, Sanzhong; Cheng, Jin-Pei; Journal of the American Chemical Society; vol.

132; nb. 20; (2010); p. 7216 - 7228, View in Reaxys; Bandela, Anilkumar; Prakash Chinta, Jugun; Kumar Hinge, Vijaya; Dikundwar, Amol G.; Row Guru, Tayur N.; Rao, Chebrolu P.; Journal of Organic Chemistry; vol. 76; nb. 6; (2011); p. 1742 - 1750, View in Reaxys

Fluorescence intensity

24.84

in the presence of Fukuzumi; Satoh; Okamoto; Yasui; Suenobu; inorganic comSeko; Fujitsuka; Ito; Journal of the American pounds Chemical Society; vol. 123; nb. 32; (2001); p.

7756 - 7766, View in Reaxys

Fluorescence

Kovi et al.; Spectroscopy Letters; vol. 6; (1973); p. 7,11, 13, View in Reaxys

Phosphorescence Spectroscopy (3) Description Solvent (PhosComment (Phos(Phosphoresphorescence phorescence cence SpectroSpectroscopy) Spectroscopy) scopy) Maxima

propan-2-ol; H2O

480 nm

Phosphorescence

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References

Gorner, Helmut; Kuhn, Hans Jochen; Journal of Physical Chemistry; vol. 90; nb. 22; (1986); p. 5946 - 5955, View in Reaxys Smaller et al.; Journal of Chemical Physics; vol. 46; (1967); p.

3976,3979, View in Reaxys; Herkstroeter et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 4537,4539, View in Reaxys; Heller; Wasserman; Journal of Chemical Physics; vol. 42; (1965); p. 949,952, View in Reaxys; Shimada; Goodman; Journal of Chemical Physics; vol. 43; (1965); p. 2027,2030, 2033, View in Reaxys; Kovi et al.; Spectroscopy Letters; vol. 6; (1973); p.

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7,11, 13, View in Reaxys; Akagi et al.; Nippon Kagaku Zasshi; vol.

87; (1966); p. 689,693, View in Reaxys; Nurmukhametov; Optics and Spectroscopy; vol. 23; (1967); p. 209; ; p. 389, View in Reaxys; Zander; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 28; (1973); p. 1869, View in Reaxys Maxima

ethanol; diethyl ether

506.33 nm; bei -196grad.

Exposure Assessment (3) Exposure Sources

Ermolaew; Switaschew; Optika i Spektroskopiya; vol. 7; (1959); p.

664; engl. Ausg. S. 399, View in Reaxys

References

presence in river natural and anElbe surface sedi- thropogenic sourment samples ces collected at Prelouc Czech Republic

Skoczynska, Ewa; Korytar, Peter; De Boer, Jacob; Environmental Science and Technology; vol. 42; nb. 17; (2008); p. 6611 - 6618, View in Reaxys

presence in carbonaceous aerosol particles

diesel exhaust particles generated by a car at idle motor condition

Matuschek, Georg; Karg, Erwin; Schroeppel, Andreas; Schulz, Holger; Schmid, Otmar; Environmental Science and Technology; vol. 41; nb. 24; (2007); p. 8406 - 8411, View in Reaxys

presence in fly ash

municipal solid Akimoto, Yoshio; Aoki, Tadamitu; Nito, Shin'ichi; Inouye, Yoshio; Chemosphere; vol. waste incinerators 34; nb. 2; (1997); p. 263 - 273, View in Reaxys (MSWI)

Concentration in the Environment (6) 1 of 6

Media (Concentration in the Environment)

light-duty gasoline emission, gas-phase

Location

El Monte, California

Contamination Concentration

9.3 - 45 μg/l

Method, Remarks (Concentration in the Environment)

gas-phase emissions collec. from low-emission and three catalyst-equipped vehicles at Haagen-Smit Laboratory during Aug.-Sep. 2002; ultrasonic extrac. in 1:1 hexane/DCM (v/v) and methanol; derivatization by PFBHA for 24 h; HPLC-APCI-ITMS; GC-ITMS; tab.

Jakober, Chris A.; Robert, Michael A.; Riddle, Sarah G.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.; Environmental Science and Technology; vol. 42; nb. 13; (2008); p. 4697 - 4703, View in Reaxys 2 of 6

Media (Concentration in the Environment)

heavy-duty diesel emission, gas-phase

Location

California

Contamination Concentration

230 - 1300 μg/l

Method, Remarks (Concentration in the Environment)

emissions from 1999 Freightliner Tractor operated under idle-creep, heavy heavy-duty diesel truck driving cycle condition; June 2003; ultrasonic extrac. in 1:1 hexane/DCM (v/v), methanol; derivatization by PFBHA for 24 h; HPLC-APCI-ITMS; GC-ITMS; tab.

Jakober, Chris A.; Robert, Michael A.; Riddle, Sarah G.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.; Environmental Science and Technology; vol. 42; nb. 13; (2008); p. 4697 - 4703, View in Reaxys 3 of 6

Media (Concentration in the Environment)

exhaust air

Location

Roseville, California, USA

Contamination Concentration

560 pg/l

Method, Remarks (Concentration in the Environment)

average conc.; emission samples collected from 1986 Ford Mustang jeep during 10 min at California Air Resources Board on North Sunrise Blvd; derivatization with pentafluorohydroxylamine; extraction with hexane; GC/MS-NCI

Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys

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4 of 6

Media (Concentration in the Environment)

wood smoke

Location

Roseville, California, USA

Contamination Concentration

29000 pg/l

Method, Remarks (Concentration in the Environment)

average conc.; samples collected from Douglas fir fire during 3 min at California Air Resources Board on North Sunrise Blvd; derivatization with pentafluorohydroxylamine; extraction with hexane; GC/MS-NCI

Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys 5 of 6

Media (Concentration in the Environment)

wood smoke

Location

Roseville, California, USA

Contamination Concentration

11000 pg/l

Method, Remarks (Concentration in the Environment)

average conc.; samples collected from Blue Oak fire during 3 min at California Air Resources Board on North Sunrise Blvd; derivatization with pentafluorohydroxylamine; extraction with hexane; GC/MS-NCI

Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys 6 of 6

Media (Concentration in the Environment)

exhaust air

Location

Roseville, California, USA

Contamination Concentration

2300 pg/l

Method, Remarks (Concentration in the Environment)

average conc.; emission samples collected from 1997 Toyota Corolla car during 10 min at California Air Resources Board on North Sunrise Blvd; derivatization with pentafluorohydroxylamine; extraction with hexane; GC/MS-NCI

Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys Medchem (16) 1 of 16

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

386082View in Reaxys

Substance Name

173943

Qualitative Results

Showed antifeedant activity toward larvae of Pieris rapae crucivora, antifeedant index: 76.7+/-6.4.

Measurement Parameter

Qualitative

Yano, Katsumi; Tanaka, Noriyuki; Bioscience, Biotechnology, and Biochemistry; vol. 59; nb. 6; (1995); p. 1130 1132, View in Reaxys 2 of 16

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : mononuclear leucocytes (MNL); toxicity toBioassay : ToxicologyThe in vitro assay used human mononuclear leucocytes (MNL, white blood cells) which were incubated with the test compound for 18 hours and cell death determined by tryptan blue exclusion (tryptan blue is a dye, which stains dead cells, whilst living cells extrude it). The main results of interest

Biological Species/NCBI human ID Substance RN

386082View in Reaxys

Substance Name

173943

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Qualitative Results

leucocytes death was 9.2 % (see Table 6)

Measurement Parameter

Qualitative

Patent; ASTON UNIVERSITY; WO2006/75159; (2006); (A1) English, View in Reaxys 3 of 16

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Genotoxicity was measured using SOS Chromotest in presence of S9 rat liver; IMAX = maximal SOS induction factor

Biological Species/NCBI Escherichia coli ID Substance RN

386082View in Reaxys

Measurement Parameter

Activity

Measurement Object

Genotoxicity

Quantitative value

1.32

He, Linnan; Jurs, Peter C.; Custer, Laura L.; Durham, Stephen K.; Pearl, Greg M.; Chemical Research in Toxicology; vol. 16; nb. 12; (2003); p. 1567 - 1580, View in Reaxys 4 of 16

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Genotoxicity was measured using SOS Chromotest in absence of S9 rat liver; IMAX = maximal SOS induction factor

Biological Species/NCBI Escherichia coli ID Substance RN

386082View in Reaxys

Measurement Parameter

Activity

Measurement Object

Genotoxicity

Quantitative value

1.69

He, Linnan; Jurs, Peter C.; Custer, Laura L.; Durham, Stephen K.; Pearl, Greg M.; Chemical Research in Toxicology; vol. 16; nb. 12; (2003); p. 1567 - 1580, View in Reaxys 5 of 16

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

50% inhibitory growth concentration for Tetrahymena pyriformis;Acute toxicity

Biological Species/NCBI Tetrahymena pyriformis ID Substance RN

386082View in Reaxys

Measurement Parameter

Qualitative

Qualitative value

Not Published

Dimitrov, Sabcho; Koleva, Yana; Schultz, T. Wayne; Walker, John D.; Mekenyan, Ovanes; Environmental Toxicology and Chemistry; vol. 23; nb. 2; (2004); p. 463 - 470, View in Reaxys 6 of 16

Target Name

Sulfotransferase 1C2 [Rattus norvegicus]

Target Synonyms

rsult1c2; st1c2; sulfotransferase 1c2; sulfotransferase k1; sult1c2; sultk1

Target Uniprot ID

q9wuw8

Target, Subunit, Species Sulfotransferase 1C2 [Rattus norvegicus] Target Mutant/Chimera Details

Sulfotransferase 1C2 [Rattus norvegicus]:Wild

Target Species (Bioactivity)

Rattus norvegicus

Substance Action on Target

Inhibitor

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Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Inhibitory constant of the compound against rat liver SULT1C1

Biological Species/NCBI Rattus norvegicus ID

7 of 16

Organs/Tissues

liver

Substance RN

386082View in Reaxys

Measurement Parameter

Ki

Unit

µM

Qualitative value

=

Quantitative value

29

Measurement pX

4.54

Target Name

Serine/threonine-protein kinase/endoribonuclease IRE1 [human]

Target Synonyms

endoplasmic reticulum-to-nucleus signaling 1; ern1; hire1p; inositol-requiring protein 1; ire1; ire1-alpha; ire1a; serine/threonine-protein kinase/endoribonuclease ire1

Target Uniprot ID

o75460

Target PDB ID

2hz6; 3p23; 4u6r; 4z7g; 4z7h

Target, Subunit, Species Serine/threonine-protein kinase/endoribonuclease IRE1 [human] Target Mutant/Chimera Details

Serine/threonine-protein kinase/endoribonuclease IRE1 [human]:Wild

Target Species (Bioactivity)

human

Substance Effect

inhibitory activity

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

In vitro inhibitory concentration of the compound against recombinant human INOSITOL REQUIRING ENZYME-1 RNase activity expressed in Baculovirus using SF21 cells upon incubation in 20 mM Hepes, pH 7.5 at RT for 30 mins was determined by FRET assay

Substance RN

386082View in Reaxys

Measurement Parameter

IC50

Unit

nM

Qualitative value

>

Quantitative value

20000

Measurement pX

1

Ranatunga, Sujeewa; Tang, Chih-Hang Anthony; Kang, Chang Won; Kriss, Crystina L.; Kloppenburg, Bernhard J.; Hu, Chih-Chi Andrew; Del Valle, Juan R.; Journal of Medicinal Chemistry; vol. 57; nb. 10; (2014); p. 4289 - 4301, View in Reaxys 8 of 16

Target Name

hydroxynitrilase [Baliospermum montanum]

Target Synonyms

hydroxynitrilase

Target, Subunit, Species hydroxynitrilase [Baliospermum montanum] Target Mutant/Chimera Details

hydroxynitrilase [Baliospermum montanum]:Wild

Target Species (Bioactivity)

Baliospermum montanum

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

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Biological Species/NCBI Escherichia coli BL21 (DE3) ID

9 of 16

Substance RN

386082View in Reaxys

Substance Name

1-naphthalenecarboxaldehyde

Measurement Parameter

Vmax

Unit

μmol/min/mg

Quantitative value

12

Target Name

hydroxynitrilase [Baliospermum montanum]

Target Synonyms

hydroxynitrilase

Target, Subunit, Species hydroxynitrilase [Baliospermum montanum] Target Mutant/Chimera Details

hydroxynitrilase [Baliospermum montanum]:Wild

Target Species (Bioactivity)

Baliospermum montanum

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI Escherichia coli BL21 (DE3) ID

10 of 16

Substance RN

386082View in Reaxys

Substance Name

1-naphthalenecarboxaldehyde

Measurement Parameter

kcat

Unit

s-1

Quantitative value

6

Target Name

hydroxynitrilase [Baliospermum montanum]

Target Synonyms

hydroxynitrilase

Target, Subunit, Species hydroxynitrilase [Baliospermum montanum] Target Mutant/Chimera Details

hydroxynitrilase [Baliospermum montanum]:Wild

Target Species (Bioactivity)

Baliospermum montanum

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI Escherichia coli BL21 (DE3) ID Substance RN

386082View in Reaxys

Substance Name

1-naphthalenecarboxaldehyde

Measurement Parameter

Km

Unit

mM

Quantitative value

0.2

Measurement pX

3.7

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11 of 16

Target Name

hydroxynitrilase [cassava]

Target Synonyms

hydroxynitrilase

Target, Subunit, Species hydroxynitrilase [cassava] Target Mutant/Chimera Details

hydroxynitrilase [cassava]:Wild

Target Species (Bioactivity)

cassava

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI Escherichia coli BL21 (DE3) ID

12 of 16

Substance RN

386082View in Reaxys

Substance Name

1-naphthalenecarboxaldehyde

Measurement Parameter

Vmax

Unit

μmol/min/mg

Quantitative value

47.7

Target Name

hydroxynitrilase [cassava]

Target Synonyms

hydroxynitrilase

Target, Subunit, Species hydroxynitrilase [cassava] Target Mutant/Chimera Details

hydroxynitrilase [cassava]:Wild

Target Species (Bioactivity)

cassava

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI Escherichia coli BL21 (DE3) ID

13 of 16

Substance RN

386082View in Reaxys

Substance Name

1-naphthalenecarboxaldehyde

Measurement Parameter

kcat

Unit

s-1

Quantitative value

23.5

Target Name

hydroxynitrilase [cassava]

Target Synonyms

hydroxynitrilase

Target, Subunit, Species hydroxynitrilase [cassava] Target Mutant/Chimera Details

hydroxynitrilase [cassava]:Wild

Target Species (Bioactivity)

cassava

Target Transfection

Transfected

Substance Action on Target

Substrate

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Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI Escherichia coli BL21 (DE3) ID

14 of 16

Substance RN

386082View in Reaxys

Substance Name

1-naphthalenecarboxaldehyde

Measurement Parameter

Km

Unit

mM

Quantitative value

1.4

Measurement pX

2.85

Target Name

α-Chymotrypsin

Target Synonyms

945;-chymotrypsin

Target, Subunit, Species α-Chymotrypsin Target Mutant/Chimera Details

α-Chymotrypsin:Wild

Substance Action on Target

Inhibitor

Bioassay Category

In Vitro (Efficacy)

Substance RN

386082View in Reaxys

Measurement Parameter

Ki

Unit

μM

Quantitative value

25.31

Measurement pX

4.6

Siddiqui, Hina; Farooq, Rabia; Marasini, Bishnu P.; Malik, Rizwana; Syed, Naima; Moin, Syed Tarique; Attaur-Rahman; Choudhary, M. Iqbal; Bioorganic and Medicinal Chemistry; vol. 24; nb. 16; (2016); p. 3387 - 3395, View in Reaxys 15 of 16

Target Name

α-Chymotrypsin

Target Synonyms

945;-chymotrypsin

Target, Subunit, Species α-Chymotrypsin Target Mutant/Chimera Details

α-Chymotrypsin:Wild

Substance Action on Target

Inhibitor

Bioassay Category

In Vitro (Efficacy)

Substance RN

386082View in Reaxys

Measurement Parameter

IC50

Unit

μM

Quantitative value

20.9

Measurement pX

4.68

Siddiqui, Hina; Farooq, Rabia; Marasini, Bishnu P.; Malik, Rizwana; Syed, Naima; Moin, Syed Tarique; Attaur-Rahman; Choudhary, M. Iqbal; Bioorganic and Medicinal Chemistry; vol. 24; nb. 16; (2016); p. 3387 - 3395, View in Reaxys 16 of 16

Substance Effect

Cytotoxic

Bioassay Category

Toxicity/Safety Pharmacology

Cells/Cell Lines

3T3 cell line

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Substance RN

386082View in Reaxys

Measurement Parameter

IC50

Unit

μM

Quantitative value

11.577

Measurement pX

4.94

Siddiqui, Hina; Farooq, Rabia; Marasini, Bishnu P.; Malik, Rizwana; Syed, Naima; Moin, Syed Tarique; Attaur-Rahman; Choudhary, M. Iqbal; Bioorganic and Medicinal Chemistry; vol. 24; nb. 16; (2016); p. 3387 - 3395, View in Reaxys

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