Prop-1-en-2-ylbenzene (alpha-Methylstyrene)

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Reaxys ID 969405 View in Reaxys

1/1 CAS Registry Number: 98-83-9 Chemical Name: isopropenylbenzene; α-methyl-styrene; 1methyl-1-phenyl-ethylene; 1-methyl-1-phenylethene; 2-methyl-2-phenylethene; α-methyl styrene; α-methyl styrene Linear Structure Formula: CH3C(CH2)C6H5 Molecular Formula: C9H10 Molecular Weight: 118.178 Type of Substance: isocyclic; Isotope or isotope containing compound InChI Key: XYLMUPLGERFSHI-UHFFFAOYSA-N Note:

Substance Label (309) Label References 2

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1t

Wang, Fei; Qi, Xiaoxu; Liang, Zhaoli; Chen, Pinhong; Liu, Guosheng; Angewandte Chemie - International Edition; vol. 53; nb. 7; (2014); p. 1881 - 1886; Angew. Chem.; vol. 126; nb. 07; (2014); p. 1912 - 1917,6, View in Reaxys

21a

Wu, Shuke; Chen, Yongzheng; Xu, Yi; Li, Aitao; Xu, Qisong; Glieder, Anton; Li, Zhi; ACS Catalysis; vol.

4; nb. 2; (2014); p. 409 - 420, View in Reaxys

9cb

Hartog, Tim Den; Toro, Juan Manuel Sarria; Chen, Peter; Organic Letters; vol. 16; nb. 4; (2014); p. 1100 1103, View in Reaxys

II-11a

Quan, Mimi L.; Wong, Pancras C.; Wang, Cailan; Woerner, Francis; Smallheer, Joanne M.; Barbera, Frank A.; Bozarth, Jeffrey M.; Brown, Randi L.; Harpel, Mark R.; Luettgen, Joseph M.; Morin, Paul E.; Peterson, Tara; Ramamurthy, Vidhyashankar; Rendina, Alan R.; Rossi, Karen A.; Watson, Carol A.; Wei, Anzhi; Zhang, Ge; Seiffert, Dietmar; Wexler, Ruth R.; Journal of Medicinal Chemistry; vol. 57; nb. 3; (2014); p. 955 - 969, View in Reaxys

2r

Li, Bin; Lee, Seungeon; Shin, Kwangmin; Chang, Sukbok; Organic Letters; vol. 16; nb. 7; (2014); p. 2010 - 2013, View in Reaxys

9j

Malkov, Andrei V.; Derrien, Nolwenn; Barlog, Maciej; Kocovsky, Pavel; Chemistry - A European Journal; vol. 20; nb. 16; (2014); p. 4542 - 4547, View in Reaxys

8h

Holthausen, Michael H.; Mehta, Meera; Stephan, Douglas W.; Angewandte Chemie - International Edition; vol. 53; nb. 25; (2014); p. 6538 - 6541; Angew. Chem.; vol. 126; nb. 25; (2014); p. 6656 - 6659,4, View in Reaxys

α-Me-styrene

Di Giovanni, Carlo; Poater, Albert; Benet-Buchholz, Jordi; Cavallo, Luigi; Sola, Miquel; Llobet, Antoni; Chemistry - A European Journal; vol. 20; nb. 14; (2014); p. 3898 - 3902, View in Reaxys

1r

Wang, Guang-Zu; Li, Xing-Long; Dai, Jian-Jun; Xu, Hua-Jian; Journal of Organic Chemistry; vol. 79; nb.

15; (2014); p. 7220 - 7225, View in Reaxys

4i

Han, Feng; Yang, Lei; Li, Zhen; Zhao, Yingwei; Xia, Chungu; Advanced Synthesis and Catalysis; vol. 356; nb. 11-12; (2014); p. 2506 - 2516, View in Reaxys

2s

Zhang, Zhenming; Ouyang, Lu; Wu, Wanqing; Li, Jianxiao; Zhang, Zhicai; Jiang, Huanfeng; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 10734 - 10742, View in Reaxys

8b

Rathore, Kuldeep Singh; Katukojvala, Sreenivas; Tetrahedron Letters; vol. 55; nb. 46; (2014); p. 6370 6372, View in Reaxys

2w

Tomita, Ren; Yasu, Yusuke; Koike, Takashi; Akita, Munetaka; Angewandte Chemie - International Edition; vol. 53; nb. 28; (2014); p. 7144 - 7148; Angew. Chem.; vol. 126; nb. 28; (2014); p. 7272 - 7276,5, View in Reaxys

28a

Edwards, Andrew; Ryabchuk, Pavel; Barkov, Alexey; Rubina, Marina; Rubin, Michael; Tetrahedron Asymmetry; vol. 25; nb. 23; (2014); p. 1537 - 1549, View in Reaxys

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30

Hong, Xin; Küük, Hatice Bapinar; Maji, Modhu Sudan; Yang, Yun-Fang; Rueping, Magnus; Houk; Journal of the American Chemical Society; vol. 136; nb. 39; (2014); p. 13769 - 13780, View in Reaxys

8q

Shenje, Raynold; Martin, M. Cynthia; France, Stefan; Angewandte Chemie - International Edition; vol. 53; nb. 50; (2014); p. 13907 - 13911; Angew. Chem.; vol. 126; nb. 50; (2014); p. 14127 - 14131,5, View in Reaxys

8a

Srimani, Dipankar; Leitus, Gregory; Ben-David, Yehoshoa; Milstein, David; Angewandte Chemie - International Edition; vol. 53; nb. 41; (2014); p. 11092 - 11095; Angew. Chem.; vol. 126; nb. 41; (2014); p. 11272 11275,4, View in Reaxys

11

Kubo, Yasuo; Yoshioka, Masahiro; Nakajima, Satoshi; Inamura, Isamu; Tetrahedron Letters; vol. 40; nb.

12; (1999); p. 2335 - 2338, View in Reaxys; Tokuyasu, Takahiro; Kunikawa, Shigeki; McCullough, Kevin J.; Masuyama, Araki; Nojima, Masatomo; Journal of Organic Chemistry; vol. 70; nb. 1; (2005); p. 251 260, View in Reaxys; Stavber, Gaj; Zupan, Marko; Stavber, Stojan; Tetrahedron Letters; vol. 47; nb. 48; (2006); p. 8463 - 8466, View in Reaxys; Wu, Ji-Cheng; Gong, Lu-Bing; Xia, Yuanzhi; Song, Ren-Jie; Xie, Ye-Xiang; Li, Jin-Heng; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9909 - 9913, View in Reaxys; Toda, Hiroshi; Imae, Ryouta; Itoh, Nobuya; Tetrahedron Asymmetry; vol. 23; nb. 22-23; (2012); p. 1542 - 1549, View in Reaxys; Greb, Lutz; Tussing, Sebastian; Schirmer, Birgitta; Ona-Burgos, Pascual; Kaupmees, Karl; Lokov, Maert; Leito, Ivo; Grimme, Stefan; Paradies, Jan; Chemical Science; vol. 4; nb. 7; (2013); p. 2788 - 2796, View in Reaxys

5b

Schmidt, Axel M.; Eilbracht, Peter; Organic and Biomolecular Chemistry; vol. 3; nb. 12; (2005); p. 2333 2343, View in Reaxys; Purohit, Vikram C.; Allwein, Shawn P.; Bakale, Roger P.; Organic Letters; vol. 15; nb. 7; (2013); p. 1650 - 1653, View in Reaxys; Kirai, Naohiro; Iguchi, Shoichiro; Ito, Tatsuyoshi; Takaya, Jun; Iwasawa, Nobuharu; Bulletin of the Chemical Society of Japan; vol. 86; nb. 7; (2013); p. 784 - 799, View in Reaxys

2f

Kobayashi, Kazuhiro; Uneda, Tomokazu; Tanaka, Koujirou; Mori, Masako; Tanaka, Hideo; Morikawa, Osamu; Konishi, Hisatoshi; Bulletin of the Chemical Society of Japan; vol. 71; nb. 7; (1998); p. 1691 1697, View in Reaxys; Nishio, Takchiko; Iida, Ikuo; Sugiyama, Kunjo; Journal of the Chemical Society, Perkin Transactions 1; nb. 18; (2000); p. 3039 - 3046, View in Reaxys; Pan, Jia-Fu; Venkatesham, Uppala; Chen, Kwunmin; Tetrahedron Letters; vol. 45; nb. 51; (2004); p. 9345 - 9347, View in Reaxys; Yoshino, Hideaki; Matsumoto, Kazuhiko; Hagiwara, Rika; Ito, Yasuhiko; Oshima, Koichiro; Matsubara, Seijiro; Journal of Fluorine Chemistry; vol. 127; nb. 1; (2006); p. 29 - 35, View in Reaxys; Hu, Yinjun; Kamitanaka, Tohru; Mishima, Yusuke; Dohi, Toshifumi; Kita, Yasuyuki; Journal of Organic Chemistry; vol. 78; nb. 11; (2013); p. 5530 - 5543, View in Reaxys

6h

Li; Huang; Zhou; Che; Journal of the American Chemical Society; vol. 123; nb. 20; (2001); p. 4843 - 4844, View in Reaxys; Liu, Zicheng; Xu, Junjie; Ruan, Wenqing; Fu, Chen; Zhang, Hui-Jun; Wen, Ting-Bin; Dalton Transactions; vol. 42; nb. 33; (2013); p. 11976 - 11980, View in Reaxys

23

Nishiwaki, Yoshiki; Sakaguchi, Satoshi; Ishii, Yasutaka; Journal of Organic Chemistry; vol. 67; nb. 16; (2002); p. 5663 - 5668, View in Reaxys; Kozuch, Sebastian; Leifels, Tycho; Meyer, Dominik; Sbaragli, Laura; Shaik, Sason; Woggon, Wolf-D.; Synlett; nb. 4; (2005); p. 675 - 684; Art.No: Y04604ST, View in Reaxys; Li, Aitao; Liu, Ji; Pham, Son Q.; Li, Zhi; Chemical Communications; vol. 49; nb. 98; (2013); p. 11572 - 11574, View in Reaxys

3b

Endres, Andreas; Maas, Gerhard; Tetrahedron Letters; vol. 40; nb. 35; (1999); p. 6365 - 6368, View in Reaxys; Loeffler, Frank; Hagen, Martin; Luening, Ulrich; Synlett; nb. 11; (1999); p. 1826 - 1828, View in Reaxys; Margarita, Roberto; Mercanti, Chiara; Parlanti, Luca; Piancatelli, Giovanni; European Journal of Organic Chemistry; nb. 10; (2000); p. 1865 - 1870, View in Reaxys; Baciocchi, Enrico; Del Giacco, Tiziana; Giombolini, Paolo; Lanzalunga, Osvaldo; Tetrahedron; vol. 62; nb. 27; (2006); p. 6566 - 6573, View in Reaxys; Zhang, Wei; Huang, Limin; Wang, Junpu; Synthesis; nb. 12; (2006); p. 2053 - 2063, View in Reaxys; Greb, Lutz; Paradies, Jan; Ona-Burgos, Pascual; Schirmer, Birgitta; Grimme, Stefan; Stephan, Douglas W.; Angewandte Chemie, International Edition; vol. 51; nb. 40; (2012); p. 10164 10168,5; Angewandte Chemie; vol. 124; nb. 40; (2012); p. 10311 - 10315,5, View in Reaxys; Kanagaraj, Kuppusamy; Pitchumani, Kasi; Chemistry - A European Journal; vol. 19; nb. 43; (2013); p. 14425 - 14431, View in Reaxys

8

Eames, Jason; Mitchell, Helen J.; Nelson, Adam; O'Brien, Peter; Warren, Stuart; Wyatt, Paul; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); nb. 8; (1999); p. 1095 - 1104, View in Reaxys; Lantano, Beatriz; Aguirre, Jose M.; Finkieisztein, Liliana; Aiesso, Elba N.; Brunet, Ernesto; Moltrasio, Graciela Y.; Synthetic Communications; vol. 34; nb. 4; (2004); p. 625 - 641, View in Reaxys; Hartung, Jens; Schneiders, Nina; Gottwald, Thomas; Tetrahedron Letters; vol. 48; nb.

34; (2007); p. 6027 - 6030, View in Reaxys; Cao, Zhong-Yan; Wang, Xiaoming; Tan, Chen; Zhao, Xiao-Li; Zhou, Jian; Ding, Kuiling; Journal of the American Chemical Society; vol. 135; nb. 22; (2013); p. 8197 8200, View in Reaxys

3l

Nebra, Noel; Lescot, Camille; Dauban, Philippe; Mallet-Ladeira, Sonia; Martin-Vaca, Blanca; Bourissou, Didier; European Journal of Organic Chemistry; nb. 5; (2013); p. 984 - 990, View in Reaxys

54

Doni, Eswararao; O'Sullivan, Steven; Murphy, John A.; Angewandte Chemie - International Edition; vol.

52; nb. 8; (2013); p. 2239 - 2242; Angew. Chem.; vol. 125; nb. 8; (2013); p. 2295 - 2298,4, View in Reaxys

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8; 6

Zhuang, Minyang; Du, Haifeng; Organic and Biomolecular Chemistry; vol. 11; nb. 9; (2013); p. 1460 - 1462, View in Reaxys

10d

Gore, Rohitkumar G.; Truong, Thi-Kim-Thu; Pour, Milan; Myles, Lauren; Connon, Stephen J.; Gathergood, Nicholas; Green Chemistry; vol. 15; nb. 10; (2013); p. 2727 - 2739, View in Reaxys

S7

Cusso, Olaf; Garcia-Bosch, Isaac; Ribas, Xavi; Lloret-Fillol, Julio; Costas, Miquel; Journal of the American Chemical Society; vol. 135; nb. 39; (2013); p. 14871 - 14878, View in Reaxys

4; Me-Sty

Rocha, Mariana; Rebelo, Susana L.H.; Freire, Cristina; Applied Catalysis A: General; vol. 460-461; (2013); p. 116 - 123, View in Reaxys

22

Ikeno, Taketo; Sato, Mitsuo; Sekino, Hiroyuki; Nishizuka, Asae; Yamada, Tohru; Bulletin of the Chemical Society of Japan; vol. 74; nb. 11; (2001); p. 2139 - 2150, View in Reaxys; Bloom, Steven; Pitts, Cody Ross; Miller, David Curtin; Haselton, Nathan; Holl, Maxwell Gargiulo; Urheim, Ellen; Lectka, Thomas; Angewandte Chemie, International Edition; vol. 51; nb. 42; (2012); p. 10580 - 10583,4; Angewandte Chemie; vol. 124; nb. 42; (2012); p. 10732 - 10735,4, View in Reaxys

1e

Tong, Kit-Ho; Wong, Kwok-Yin; Chan, Tak Hang; Tetrahedron; vol. 61; nb. 25; (2005); p. 6009 - 6014, View in Reaxys; Boyd, Derek R.; Sharma, Narain D.; Bowers, Nigel I.; Brannigan, Ian N.; Groocock, Melanie R.; Malone, John F.; McConville, Gareth; Allen, Christopher C. R.; Advanced Synthesis and Catalysis; vol. 347; nb. 7-8; (2005); p. 1081 - 1089, View in Reaxys; Kaspar, Ludwig T.; Fingerhut, Benjamin; Ackermann, Lutz; Angewandte Chemie - International Edition; vol. 44; nb. 37; (2005); p. 5972 - 5974, View in Reaxys; Santi, Claudio; Di Lorenzo, Rosalia; Tidei, Caterina; Bagnoli, Luana; Wirth, Thomas; Tetrahedron; vol. 68; nb. 51; (2012); p. 10530 - 10535,6, View in Reaxys

13

Yang; Zhang; Journal of Organic Chemistry; vol. 66; nb. 14; (2001); p. 4814 - 4818, View in Reaxys; Itoh, Akichika; Kodama, Tomohiro; Masaki, Yukio; Inagaki, Shinji; Synlett; nb. 3; (2002); p. 522 - 524, View in Reaxys; Geng, Xue-Li; Wang, Zhi; Li, Xiao-Qiang; Zhang, Chi; Journal of Organic Chemistry; vol.

70; nb. 23; (2005); p. 9610 - 9613, View in Reaxys; Masruri; Willis, Anthony C.; McLeod, Malcolm D.; Journal of Organic Chemistry; vol. 77; nb. 19; (2012); p. 8480 - 8491, View in Reaxys

2c

Bogdanowicz-Szwed, Krystyna; Palasz, Aleksandra; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 56; nb. 4-5; (2001); p. 416 - 422, View in Reaxys; Kerverdo; Loiseau; Lizzani-Cuvelier; Dunach; Chemical Communications; nb. 21; (2001); p. 2284 - 2285, View in Reaxys; Fristrup, Peter; Dideriksen, Brian B.; Tanner, David; Norrby, Per-Ola; Journal of the American Chemical Society; vol. 127; nb. 39; (2005); p. 13672 - 13679, View in Reaxys; Yang, Jie; Tan, Jia-Neng; Gu, Yanlong; Green Chemistry; vol. 14; nb. 12; (2012); p. 3304 - 3317, View in Reaxys

47; 30a

Geoghegan, Kimberly; Evans, Paul; Rozas, Isabel; Alkorta, Ibon; Chemistry - A European Journal; vol.

18; nb. 42; (2012); p. 13379 - 13387, View in Reaxys

2v

Hartmann, Marcel; Li, Yi; Studer, Armido; Journal of the American Chemical Society; vol. 134; nb. 40; (2012); p. 16516 - 16519,4, View in Reaxys

olefin, Tab. 2, entry 6

Balagam, Bharathi; Mitra, Ranjan; Richardson, David E.; Tetrahedron Letters; vol. 49; nb. 6; (2008); p.

1071 - 1075, View in Reaxys

substrate, tab 2/2

Dhakshinamoorthy, Amarajothi; Pitchumani, Kasi; Tetrahedron Letters; vol. 49; nb. 11; (2008); p. 1818 1823, View in Reaxys

27a

Hsu, Yu-Chia; Datta, Swarup; Ting, Chun-Ming; Liu, Rai-Shung; Organic Letters; vol. 10; nb. 3; (2008); p.

521 - 524, View in Reaxys

Table 2, subs. 11

Ranu, Brindaban C.; Bhadra, Sukalyan; Adak, Laksmikanta; Tetrahedron Letters; vol. 49; nb. 16; (2008); p. 2588 - 2591, View in Reaxys

1c

Tong, Kit-Ho; Wong, Kwok-Yin; Chan, Tak Hang; Organic Letters; vol. 5; nb. 19; (2003); p. 3423 - 3425, View in Reaxys; Castillo, Maria R.; Fousse, Leslie; Fraile, Jose M.; Garcia, Jose I.; Mayoral, Jose A.; Chemistry - A European Journal; vol. 13; nb. 1; (2007); p. 287 - 291, View in Reaxys; Yadav; Reddy, B.V. Subba; Hara Gopal; Narayana Kumar; Madavi; Kunwar; Tetrahedron Letters; vol. 49; nb. 28; (2008); p.

4420 - 4423, View in Reaxys

29

Lebel, Helene; Davi, Michael; Diez-Gonzalez, Silvia; Nolan, Steven P.; Journal of Organic Chemistry; vol.

72; nb. 1; (2007); p. 144 - 149, View in Reaxys

Substrate, Tab.1, run 4

Moriuchi, Toshiyuki; Yamaguchi, Mitsuaki; Kikushima, Kotaro; Hirao, Toshikazu; Tetrahedron Letters; vol. 48; nb. 15; (2007); p. 2667 - 2670, View in Reaxys

styrene to 14

Michaux, Julien; Terrasson, Vincent; Marque, Sylvain; Wehbe, Johny; Prim, Damien; Campagne, JeanMarc; European Journal of Organic Chemistry; nb. 16; (2007); p. 2601 - 2603, View in Reaxys

35f

Shitama, Hiroaki; Katsuki, Tsutomu; Chemistry - A European Journal; vol. 13; nb. 17; (2007); p. 4849 4858, View in Reaxys

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Tab 6/2 Substrate

Venkateswaran, Ramalingam; Balakrishna, Maravanji S.; Mobin, Shaikh M.; European Journal of Inorganic Chemistry; nb. 13; (2007); p. 1930 - 1938, View in Reaxys

4g

Ishihara, Kazuaki; Nakano, Kazuhiko; Journal of the American Chemical Society; vol. 129; nb. 29; (2007); p. 8930 - 8931, View in Reaxys

1b; 1a

Karwowska; Jonczyk; Polish Journal of Chemistry; vol. 81; nb. 1; (2007); p. 45 - 49, View in Reaxys

d

Luo, He-Kuan; Khim, Lim Bee; Schumann, Herbert; Lim, Christina; Jie, Tan Xiang; Yang, Hai-Yan; Advanced Synthesis and Catalysis; vol. 349; nb. 10; (2007); p. 1781 - 1795, View in Reaxys

C6H5(CH3)C=CH Nishiyama, Yutaka; Tanimizu, Hana; Tomita, Tsuyoshi; Tetrahedron Letters; vol. 48; nb. 36; (2007); p.

2 6405 - 6407, View in Reaxys 4d

Pandey, Sushil K.; Greene, Andrew E.; Poisson, Jean-Francois; Journal of Organic Chemistry; vol. 72; nb. 20; (2007); p. 7769 - 7770, View in Reaxys

14a

Sarma, Kuladip; Borthakur, Naleen; Goswami, Amrit; Tetrahedron Letters; vol. 48; nb. 38; (2007); p. 6776 - 6778, View in Reaxys

educt to 3ba

Chu, Cheng-Ming; Huang, Wan-Ju; Liu, Ju-Tsung; Yao, Ching-Fa; Tetrahedron Letters; vol. 48; nb. 39; (2007); p. 6881 - 6885, View in Reaxys

styrene educt T2/14

Seshu Babu; Mohan Reddy; Sai Prasad; Suryanarayana; Lingaiah; Tetrahedron Letters; vol. 48; nb. 43; (2007); p. 7642 - 7645, View in Reaxys

tab3, olefin, entry5,6

Hoang, Vo D.M.; Reddy, Pattubala A.N.; Kim, Tae-Jeong; Tetrahedron Letters; vol. 48; nb. 45; (2007); p.

8014 - 8017, View in Reaxys

table 2, entry 6

Yeung, Chi-Tung; Yeung, Ho-Lun; Tsang, Chui-Shan; Wong, Wai-Yeung; Kwong, Hoi-Lun; Chemical Communications; nb. 48; (2007); p. 5203 - 5205, View in Reaxys

X = p-H

Pytela, Oldrich; Trlida, Bronislav; Collection of Czechoslovak Chemical Communications; vol. 72; nb. 8; (2007); p. 1025 - 1036, View in Reaxys

12d

Ikeda, Hiroshi; Hoshi, Yosuke; Namai, Hayato; Tanaka, Futoshi; Goodman, Joshua L.; Mizuno, Kazuhiko; Chemistry - A European Journal; vol. 13; nb. 33; (2007); p. 9207 - 9215, View in Reaxys

Tab.1, alkene, en- Yeung, Chi-Tung; Teng, Pang-Fei; Yeung, Ho-Lun; Wong, Wing-Tak; Kwong, Hoi-Lun; Organic and Biotry 9 molecular Chemistry; vol. 5; nb. 23; (2007); p. 3859 - 3864, View in Reaxys 7f

Kobayashi, Kazuhiro; Nagase, Katsunori; Morikawa, Osamu; Konishi, Hisatoshi; Heterocycles; vol. 60; nb. 4; (2003); p. 939 - 946, View in Reaxys; Wang, Peng-Fei; Gao, Peng; Xu, Peng-Fei; Synlett; nb. 7; (2006); p. 1095 - 1099, View in Reaxys

Subst.,Tab. 1,run1-2/7-8

Pandey, Manoj K.; Bisai, Alakesh; Singh, Vinod K.; Tetrahedron Letters; vol. 47; nb. 6; (2006); p. 897 900, View in Reaxys

olefin, tab 2/2

Handy, Scott T.; Ivanow, Anatole; Czopp, Mark; Tetrahedron Letters; vol. 47; nb. 11; (2006); p. 1821 1823, View in Reaxys

Tab. 1, entry 4

Lee, Daewon; Lee, Jinwoo; Lee, Honggeun; Jin, Sunmi; Hyeon, Taeghwan; Kim, B. Moon; Advanced Synthesis and Catalysis; vol. 348; nb. 1-2; (2006); p. 41 - 46, View in Reaxys

25, Tab. 3, entry 3 Werner, Heiko; Herrerias, Clara I.; Glos, Michael; Gissibl, Anja; Fraile, Jose M.; Perez, Ignacio; Mayoral, Jose A.; Reiser, Oliver; Advanced Synthesis and Catalysis; vol. 348; nb. 1-2; (2006); p. 125 - 132, View in Reaxys MST

Veerman, Marcel; Resendiz, Marino J. E.; Garcia-Garibay, Miguel A.; Organic Letters; vol. 8; nb. 12; (2006); p. 2615 - 2617, View in Reaxys

tab1, substrate/5,6

Lou, Lan-Lan; Yu, Kai; Ding, Fei; Zhou, Wei; Peng, Xiaojie; Liu, Shuangxi; Tetrahedron Letters; vol. 47; nb. 37; (2006); p. 6513 - 6516, View in Reaxys

Byproduct,Tab.3, run 13

Pluempanupat, Wanchai; Chavasiri, Warinthorn; Tetrahedron Letters; vol. 47; nb. 38; (2006); p. 6821 6823, View in Reaxys

Substrate, Tab.1, run 2

Ranu, Brindaban C.; Mandal, Tanmay; Tetrahedron Letters; vol. 47; nb. 38; (2006); p. 6911 - 6914, View in Reaxys

Tab.5.entry2

Scianowski, Jacek; Rafinski, Zbigniew; Wojtczak, Andrzej; European Journal of Organic Chemistry; nb.

14; (2006); p. 3216 - 3225, View in Reaxys

145

Waser, Jerome; Gaspar, Boris; Nambu, Hisanori; Carreira, Erick M.; Journal of the American Chemical Society; vol. 128; nb. 35; (2006); p. 11693 - 11712, View in Reaxys

Tab. 1, entry 14

Le Rouzo, Guillaume; Morel-Grepet, Marielle; Simonato, Jean-Pierre; Journal of Chemical Research; nb.

8; (2006); p. 521 - 522, View in Reaxys

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2016-05-12 11:27:45

T.1. Entry 4. Substrate

Whitehead, Daniel C.; Travis, Benjamin R.; Borhan, Babak; Tetrahedron Letters; vol. 47; nb. 22; (2006); p. 3797 - 3800, View in Reaxys

Tab.1.col.2.r.2.

Mohajer, Daryoush; Solati, Zahra; Tetrahedron Letters; vol. 47; nb. 39; (2006); p. 7007 - 7010, View in Reaxys

Tab.5., Ent.10., olefin

Tse, Man Kin; Jiao, Haijun; Anilkumar, Gopinathan; Bitterlich, Bianca; Gelalcha, Feyissa Gadissa; Beller, Matthias; Journal of Organometallic Chemistry; vol. 691; nb. 21; (2006); p. 4419 - 4433, View in Reaxys

Tab. 1, Ent. 8, subs.

Lai, Tat-Shing; Chan, Fung-Yi; So, Pui-Kin; Ma, Dik-Lung; Wong, Kwok-Yin; Che, Chi-Ming; Dalton Transactions; nb. 40; (2006); p. 4845 - 4851, View in Reaxys

Tab. 8, entry 2

Choudary, Boyapati M.; Roy, Moumita; Roy, Sarabindu; Kantam, M. Lakshmi; Sreedhar, Bojja; Kumar, Karasala Vijay; Advanced Synthesis and Catalysis; vol. 348; nb. 12-13; (2006); p. 1734 - 1742, View in Reaxys

Tab. 2

Muniz, Kilian; Almodovar, Iriux; Streuff, Jan; Nieger, Martin; Advanced Synthesis and Catalysis; vol. 348; nb. 14; (2006); p. 1831 - 1835, View in Reaxys

Ph(Me)C=CH2

Buch, Frank; Brettar, Julie; Harder, Sjoerd; Angewandte Chemie - International Edition; vol. 45; nb. 17; (2006); p. 2741 - 2745, View in Reaxys

Mesty

Cinellu, Maria A.; Minghetti, Giovanni; Cocco, Fabio; Stoccoro, Sergio; Zucca, Antonio; Manassero, Mario; Arca, Massimiliano; Dalton Transactions; nb. 48; (2006); p. 5703 - 5716, View in Reaxys

tab1, start

Hao, Xiuhua; Hoshi, Nobuto; Chemistry Letters; vol. 35; nb. 10; (2006); p. 1102 - 1103, View in Reaxys

substrate, T1/E2

Sato, Takashi; Watanabe, Shoji; Kiuchi, Hiroyoshi; Oi, Shuichi; Inoue, Yoshio; Tetrahedron Letters; vol.

47; nb. 44; (2006); p. 7703 - 7705, View in Reaxys

Table 2 entry 2

Masuyama, Yoshiro; Ohtsuka, Masaru; Harima, Masaru; Kurusu, Yasuhiko; Heterocycles; vol. 67; nb. 2; (2006); p. 503 - 506, View in Reaxys

subs., entry 1, Tab. 10

De Almeida, Leonardo S.; Esteves, Pierre M.; De Mattos, Marcio C. S.; Synlett; nb. 10; (2006); p. 1515 1518, View in Reaxys

olefin, tab. 2, entry 2

Minakata, Satoshi; Morino, Yoshinobu; Oderaotoshi, Yoji; Komatsu, Mitsuo; Chemical Communications; nb. 31; (2006); p. 3337 - 3339, View in Reaxys

PhC(=CH2)CH3

Berkessel, Albrecht; Kaiser, Patrick; Lex, Johann; Chemistry - A European Journal; vol. 9; nb. 19; (2003); p. 4746 - 4756, View in Reaxys; Alajarin, Mateo; Pastor, Aurelia; Cabrera, Jose; Synlett; nb. 6; (2004); p.

995 - 998, View in Reaxys; Kanth, S. Ravi; Reddy, G. Venkat; Maitraie; Narsaiah; Rao, P. Shanthan; Kumar, K. Ravi; Sridhar; Journal of Fluorine Chemistry; vol. 127; nb. 9; (2006); p. 1211 - 1221, View in Reaxys

14

Charette, Andre B.; Francoeur, Sebastien; Martel, Jonathan; Wilb, Nicole; Angewandte Chemie - International Edition; vol. 39; nb. 24; (2000); p. 4539 - 4542, View in Reaxys; Tang, Wenjun; Hu, Xinquan; Zhang, Xumu; Tetrahedron Letters; vol. 43; nb. 16; (2002); p. 3075 - 3078, View in Reaxys; Yu, Su; Rabalakos, Constantinos; Mitchell, William D.; Wulff, William D.; Organic Letters; vol. 7; nb. 3; (2005); p. 367 369, View in Reaxys

CH2=C(Me)Ph

Knuehl, Bernhard; Marque, Sylvain; Fischer, Hanns; Helvetica Chimica Acta; vol. 84; nb. 8; (2001); p.

2290 - 2300, View in Reaxys; Ageno, Takafumi; Okauchi, Tatsuo; Minami, Toru; Ishida, Masaru; Organic and Biomolecular Chemistry; vol. 3; nb. 5; (2005); p. 924 - 931, View in Reaxys

10

Harada, Hironori; Kazami, Jun-Ichi; Watanuki, Susumu; Tsuzuki, Ryuji; Sudoh, Katsumi; Fujimori, Akira; Tokunaga, Tatsuhiro; Tanaka, Akihiro; Tsukamoto, Shin-Ichi; Yanagisawa, Isao; Chemical and Pharmaceutical Bulletin; vol. 49; nb. 12; (2001); p. 1593 - 1603, View in Reaxys; Bohe, Luis; Kammoun, Majed; Tetrahedron Letters; vol. 43; nb. 5; (2002); p. 803 - 805, View in Reaxys; Yamada, Yoichi M.A.; Ichinohe, Masato; Takahashi, Hideyo; Ikegami, Shiro; Tetrahedron Letters; vol. 43; nb. 18; (2002); p. 3431 3434, View in Reaxys; Sekiguti, Tetuya; Iizuka, Yoshimasa; Takizawa, Shinobu; Jayaprakash, Doss; Arai, Takayoshi; Sasai, Hiroaki; Organic Letters; vol. 5; nb. 15; (2003); p. 2647 - 2650, View in Reaxys; Langner, Martin; Remy, Pauline; Bolm, Carsten; Synlett; nb. 5; (2005); p. 781 - 784; Art.No: G00205ST, View in Reaxys

PhC(Me)=CH2

Yadav, Jhillu S; Reddy, B.V.Subba; Parisse, Celine; Carvalho, Peter; Rao, T.Prabhakar; Tetrahedron Letters; vol. 43; nb. 16; (2002); p. 2999 - 3002, View in Reaxys; Murakami, Satoru; Ishii, Hideki; Fuchigami, Toshio; Journal of Fluorine Chemistry; vol. 125; nb. 4; (2004); p. 609 - 614, View in Reaxys; Arai, Takayoshi; Mizukami, Tomoe; Yokoyama, Naota; Nakazato, Daisuke; Yanagisawa, Akira; Synlett; nb. 17; (2005); p. 2670 - 2672; Art.No: U26105ST, View in Reaxys

substrate, tab 2/4-5

Caselli, Alessandro; Gallo, Emma; Ragaini, Fabio; Oppezzo, Alessandro; Cenini, Sergio; Journal of Organometallic Chemistry; vol. 690; nb. 8 SPEC. ISS.; (2005); p. 2142 - 2148, View in Reaxys

Tab. 1, case xiii

Yu, Kunquan; Sommer, William; Richardson, John M.; Weck, Marcus; Jones, Christopher W.; Advanced Synthesis and Catalysis; vol. 347; nb. 1; (2005); p. 161 - 171, View in Reaxys

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2016-05-12 11:27:45

8, 10

Van Alem, Kaj; Belder, Geerte; Lodder, Gerrit; Zuilhof, Han; Journal of Organic Chemistry; vol. 70; nb. 1; (2005); p. 179 - 190, View in Reaxys

T. 1. Entry 2.

Product

Firouzabadi, Habib; Iranpoor, Nasser; Jafarpour, Maasoumeh; Tetrahedron Letters; vol. 46; nb. 23; (2005); p. 4107 - 4110, View in Reaxys

Tab.2. col.2. run 1 Kiyooka, Syun-Ichi; Takeshita, Yushi; Tetrahedron Letters; vol. 46; nb. 25; (2005); p. 4279 - 4282, View in Reaxys alkene; Tab.1, en- Yoshino, Hideaki; Matsubara, Seijiro; Oshima, Koichiro; Matsumoto, Kazuhiko; Hagiwara, Rika; Ito, try 7 Yasuhiko; Journal of Fluorine Chemistry; vol. 126; nb. 1; (2005); p. 121 - 123, View in Reaxys 2b (R1=H,R2=Ph,R3 =Me)

Zhang, Wei; Zheng, Airong; Liu, Zhengang; Yang, Li; Liu, Zhongli; Tetrahedron Letters; vol. 46; nb. 34; (2005); p. 5691 - 5694, View in Reaxys

Tab 1/3

Johansson, Mikael; Linden, Auri A.; Baeckvall, Jan-E.; Journal of Organometallic Chemistry; vol. 690; nb.

15; (2005); p. 3614 - 3619, View in Reaxys

1 R1=Ph R2=Me

Asahi, Kentaro; Nishino, Hiroshi; Heterocyclic Communications; vol. 11; nb. 5; (2005); p. 379 - 384, View in Reaxys

table 2, entry 7

Ishida, Tasuku; Akiyama, Ryo; Kobayashi, Shu; Advanced Synthesis and Catalysis; vol. 347; nb. 9; (2005); p. 1189 - 1192, View in Reaxys

18d

Clay, Julia M.; Vedejs, Edwin; Journal of the American Chemical Society; vol. 127; nb. 16; (2005); p. 5766 5767, View in Reaxys

educt for 4

Finn, Kevin J.; Rochon, Lena; Hudlicky, Tomas; Tetrahedron Asymmetry; vol. 16; nb. 21; (2005); p. 3606 3613, View in Reaxys

11i

Li, Jiayin; Chan, Philip Wai Hong; Che, Chi-Ming; Organic Letters; vol. 7; nb. 26; (2005); p. 5801 - 5804, View in Reaxys

alkene, Tab. 1, entry 2

Hilt, Gerhard; Bolze, Patrick; Kieltsech, Iris; Chemical Communications; nb. 15; (2005); p. 1996 - 1998, View in Reaxys

substrate, Tab2, entry8

Sun, Wei; Herdtweck, Eberhardt; Kuehn, Fritz E.; New Journal of Chemistry; vol. 29; nb. 12; (2005); p.

1577 - 1580, View in Reaxys

Educt to entry 6

Werle, Thorsten; Schaeffler, Lutz; Maas, Gerhard; Journal of Organometallic Chemistry; vol. 690; nb.

24-25; (2005); p. 5562 - 5569, View in Reaxys

3h

Okamoto, Kazuki; Nishibayashi, Yoshiaki; Uemura, Sakae; Toshimitsu, Akio; Angewandte Chemie - International Edition; vol. 44; nb. 23; (2005); p. 3588 - 3591, View in Reaxys

Tab3, olefin, entry Grill, Joseph M.; Reibenspies, Joseph H.; Miller, Stephen A.; Journal of Organometallic Chemistry; vol.

3 690; nb. 12; (2005); p. 3009 - 3017, View in Reaxys 4c

Che; Huang; Lee; Li; Lai; Kwong; Teng; Lo; Peng; Zhou; Journal of the American Chemical Society; vol.

123; nb. 18; (2001); p. 4119 - 4129, View in Reaxys; Georgakopoulou; Kalogiros; Hadjiarapoglou; Synlett; nb. 12; (2001); p. 1843 - 1846, View in Reaxys; Gaonkar; Rai, K. M. Lokanatha; Journal of Heterocyclic Chemistry; vol. 42; nb. 5; (2005); p. 877 - 881, View in Reaxys; Gaonkar; Lokanatha Rai; Tetrahedron Letters; vol. 46; nb. 35; (2005); p. 5969 - 5970, View in Reaxys

3c

Fraile, Jose M.; Garcia, Jose I.; Herrerias, Clara I.; Mayoral, Jose A.; Reiser, Oliver; Vaultier, Michel; Tetrahedron Letters; vol. 45; nb. 36; (2004); p. 6765 - 6768, View in Reaxys; Hoevelmann, Claas H.; Muniz, Kilian; Chemistry - A European Journal; vol. 11; nb. 13; (2005); p. 3951 - 3958, View in Reaxys; Creary, Xavier; Willis, Elizabeth D.; Gagnon, Madeleine; Journal of the American Chemical Society; vol. 127; nb.

51; (2005); p. 18114 - 18120, View in Reaxys

α-MS

Murachev; Nesmelov; Ezhova; Byrikhin; Russian Chemical Bulletin; vol. 48; nb. 10; (1999); p. 1920 1924, View in Reaxys; Kalninsh; Podolskii; Journal of Structural Chemistry; vol. 41; nb. 4; (2000); p. 572 578, View in Reaxys; Verevkin; Heintz; Journal of Chemical and Engineering Data; vol. 46; nb. 1; (2001); p.

41 - 46, View in Reaxys; Gagarin; Mamedov; Kharlampidi; Petroleum Chemistry; vol. 42; nb. 3; (2002); p.

187 - 191, View in Reaxys; Williams, Federico J.; Cropley, Rachael L.; Vaughan, Owain P. H.; Urquhart, Andrew J.; Tikhov, Mintcho S.; Kolczewski, Christine; Hermann, Klaus; Lambert, Richard M.; Journal of the American Chemical Society; vol. 127; nb. 48; (2005); p. 17007 - 17011, View in Reaxys; Prikhod'ko; Komarova; Gorelova; Gorlova; Bondaletov; Russian Journal of Applied Chemistry; vol. 78; nb. 3; (2005); p.

399 - 403, View in Reaxys

3e

Hendricks, Ian S.; Lewis, Adolphus; Journal of Organic Chemistry; vol. 64; nb. 20; (1999); p. 7342 - 7346, View in Reaxys; Horino, Yoshikazu; Livinghouse, Tom; Stan, Magdalena; Synlett; nb. 14; (2004); p. 2639 - 2641, View in Reaxys

title comp/2

Cao, Yujuan; Xiao, Xiaohua; Ji, Shengfu; Lu, Runhua; Guo, Qingxiang; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 60; nb. 4; (2004); p. 815 - 820, View in Reaxys

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2016-05-12 11:27:45

entry e. tab 1.

Snider, Barry B.; Che, Qinglin; Heterocycles; vol. 62; (2004); p. 325 - 332, View in Reaxys

educt

Khalilov, Leonard M.; Parfenova, Ludmila V.; Pechatkina, Svetlana V.; Ibragimov, Askhat G.; Genet, Jean P.; Dzhemilev, Usein M.; Beletskaya, Irina P.; Journal of Organometallic Chemistry; vol. 689; nb. 2; (2004); p. 444 - 453, View in Reaxys

Table 2, entry 9

Vyas, Renu; Gao, Guang-Yao; Harden, Jeremiah D.; Zhang, X. Peter; Organic Letters; vol. 6; nb. 12; (2004); p. 1907 - 1910, View in Reaxys

T.1 col.1 run 1

Justik, Michael W.; Koser, Gerald F.; Tetrahedron Letters; vol. 45; nb. 32; (2004); p. 6159 - 6163, View in Reaxys

PhCMe=CH2

Myint, Yi Yi; Pasha; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 43; nb. 3; (2004); p. 590 - 592, View in Reaxys

alkene,Tab. 1,entry 7

Yoshino, Hideaki; Matsubara, Seijiro; Oshima, Koichiro; Matsumoto, Kazuhiko; Hagiwara, Rika; Ito, Yasuhiko; Journal of Fluorine Chemistry; vol. 125; nb. 3; (2004); p. 455 - 458, View in Reaxys

tab. 1, entry 3

Kantam, Lakshmi M.; Neeraja, V.; Kavita, B.; Haritha, Y.; Synlett; nb. 3; (2004); p. 524 - 527, View in Reaxys

Tab. 2, entry 3

Choudary, Boyapati M.; Jyothi, Karangula; Roy, Moumita; Kantam, Mannepalli L.; Sreedhar, Bojja; Advanced Synthesis and Catalysis; vol. 346; nb. 12; (2004); p. 1471 - 1480, View in Reaxys

28

Terao, Jun; Watabe, Hiroyasu; Watanabe, Hiroyuki; Kambe, Nobuaki; Advanced Synthesis and Catalysis; vol. 346; nb. 13-15; (2004); p. 1674 - 1678, View in Reaxys

subs., Tab. 1, entry 2

Closson, Adam; Johansson, Mikael; Baeckvall, Jan-E.; Chemical Communications; nb. 13; (2004); p.

1494 - 1495, View in Reaxys

(Me)(Ph)C=CH2

Xi, Chanjuan; Lai, Chunbo; Chen, Chao; Wang, Ruji; Synlett; nb. 9; (2004); p. 1595 - 1597, View in Reaxys

substr., Tab.1, en- Kumar, G. D. Kishore; Baskaran, Sundarababu; Chemical Communications; nb. 8; (2004); p. 1026 - 1027, try 2 View in Reaxys tab2, entry 5

Liang, Jun; Tang, Qinghu; Meng, Guanyu; Wu, Hongli; Zhang, Qinghong; Wang, Ye; Chemistry Letters; vol. 33; nb. 9; (2004); p. 1140 - 1141, View in Reaxys

13a

Mandoli, Alessandro; Orlandi, Simonetta; Pini, Dario; Salvadori, Piero; Tetrahedron Asymmetry; vol. 15; nb. 20; (2004); p. 3233 - 3244, View in Reaxys

Table 3, entry 5

Ho, Chi-Ming; Yu, Wing-Yiu; Che, Chi-Ming; Angewandte Chemie - International Edition; vol. 43; nb. 25; (2004); p. 3303 - 3307, View in Reaxys

23b

Bei, Xiaohong; Hagemeyer, Alfred; Volpe, Anthony; Saxton, Robert; Turner, Howard; Guram, Anil S.; Journal of Organic Chemistry; vol. 69; nb. 25; (2004); p. 8626 - 8633, View in Reaxys

8c

Stavber, Gaj; Zupan, Marko; Jereb, Marjan; Stavber, Stojan; Organic Letters; vol. 6; nb. 26; (2004); p.

4973 - 4976, View in Reaxys

PhC(=CH2)Me

DeClue, Michael S.; Siegel, Jay S.; Organic and Biomolecular Chemistry; vol. 2; nb. 16; (2004); p. 2287 2298, View in Reaxys

5d

Yusubov, Mehman S.; Drygunova, Larisa A.; Zhdankin, Viktor V.; Synthesis; nb. 14; (2004); p. 2289 2292, View in Reaxys

t.3, olefin, entry 1

Fujita, Ken-Ichi; Muraki, Takahito; Hashimoto, Shigeru; Oishi, Akihiro; Taguchi, Yoichi; Bulletin of the Chemical Society of Japan; vol. 77; nb. 11; (2004); p. 2097 - 2098, View in Reaxys

PhC(CH3)=CH2

Dussault, Patrick H.; Lee, Hyung-Jae; Liu, Xuejun; Journal of the Chemical Society, Perkin Transactions 1; nb. 17; (2000); p. 3006 - 3013, View in Reaxys; Talybov; Nurieva; Karaev; Russian Journal of Organic Chemistry; vol. 39; nb. 8; (2003); p. 1206 - 1208, View in Reaxys; Sato; Omote; Ando; Kumadaki; Journal of Fluorine Chemistry; vol. 125; nb. 4; (2004); p. 509 - 515, View in Reaxys

1, T.1, e.5,8

Nguyen, Van-Ha; Nishino, Hiroshi; Tetrahedron Letters; vol. 45; nb. 17; (2004); p. 3373 - 3377, View in Reaxys

olefin Tab. 2, ent.

2

Huang, Yangen; Meng, Wei-Dong; Qing, Feng-Ling; Tetrahedron Letters; vol. 45; nb. 9; (2004); p. 1965 1968, View in Reaxys

tab. 2, entries 5,6

Leonel, Eric; Lejaye, Michael; Oudeyer, Sylvain; Paugam, Jean Paul; Nedelec, Jean-Yves; Tetrahedron Letters; vol. 45; nb. 12; (2004); p. 2635 - 2638, View in Reaxys

Table 1, Alkene,Entry 2

Kan, Jovi Tze Wai; Toy, Patrick; Tetrahedron Letters; vol. 45; nb. 33; (2004); p. 6357 - 6359, View in Reaxys

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2016-05-12 11:27:45

tab1, alkene, run3 McNamara, Catherine Anne; King, Frank; Bradley, Mark; Tetrahedron Letters; vol. 45; nb. 46; (2004); p.

8527 - 8529, View in Reaxys CH2=C(CH3)C6H Heberger; Fischer; International Journal of Chemical Kinetics; vol. 25; nb. 4; (1993); p. 249 - 263, 5 View in Reaxys; Heberger; Fischer; International Journal of Chemical Kinetics; vol. 25; nb. 11; (1993); p.

913 - 920, View in Reaxys; Tyrkov; Russian Journal of Organic Chemistry; vol. 39; nb. 6; (2003); p. 890 892, View in Reaxys 1 (tab1 run4)

Jain, Suman L.; Sain, Bir; Tetrahedron Letters; vol. 44; nb. 3; (2003); p. 575 - 577, View in Reaxys

substrate, tab2, entry1

Omura, Kazufumi; Murakami, Masakazu; Uchida, Tatsuya; Irie, Ryo; Katsuki, Tsutomu; Chemistry Letters; vol. 32; nb. 4; (2003); p. 354 - 355, View in Reaxys

6 to 1 u-x

Ferguson, Ron D.; Su, Ning; Smith, Roger A.; Tetrahedron Letters; vol. 44; nb. 14; (2003); p. 2939 - 2942, View in Reaxys

tab1, note c

Srivastava, Rajendra; Venkatathri; Srinivas; Ratnasamy, Paul; Tetrahedron Letters; vol. 44; nb. 18; (2003); p. 3649 - 3651, View in Reaxys

Tab1 col2 run4,9

Srivastava, Radhey S.; Tetrahedron Letters; vol. 44; nb. 16; (2003); p. 3271 - 3274, View in Reaxys

educt to 5,6

Penoni, Andrea; Wanke, Riccardo; Tollari, Stefano; Gallo, Emma; Musella, Danilo; Ragaini, Fabio; Demartin, Francesco; Cenini, Sergio; European Journal of Inorganic Chemistry; nb. 7; (2003); p. 1452 - 1460, View in Reaxys

Tab1 col3 run4-6

Maspero, Angelo; Brenna, Stefano; Galli, Simona; Penoni, Andrea; Journal of Organometallic Chemistry; vol. 672; nb. 1-2; (2003); p. 123 - 129, View in Reaxys

tab2, entry1, alkene

Yamanaka, Hiroyuki; Matsuo, Jun-Ichi; Kawana, Asahi; Mukaiyama, Teruaki; Chemistry Letters; vol. 32; nb. 7; (2003); p. 626 - 627, View in Reaxys

2 (R3=Me,R4=Ph)

Rahman, Md. Taifur; Nishino, Hiroshi; Qian, Chang-Yi; Tetrahedron Letters; vol. 44; nb. 28; (2003); p.

5225 - 5228, View in Reaxys

2g

Rahman, Md. Taifur; Nishino, Hiroshi; Tetrahedron; vol. 59; nb. 42; (2003); p. 8383 - 8392, View in Reaxys

alkene, T.2, e.1,2

Zhang, Jun-Long; Hong Chan, Philip Wai; Che, Chi-Ming; Tetrahedron Letters; vol. 44; nb. 48; (2003); p.

8733 - 8737, View in Reaxys

Tab.1.col.1.run 12-13

Bez, Ghanashyam; Zhao, Cong-Gui; Tetrahedron Letters; vol. 44; nb. 40; (2003); p. 7403 - 7406, View in Reaxys

tab. 2,entry 4, alkene

Lakshmi Kantam; Kavita; Neeraja; Haritha; Chaudhuri; Dehury; Tetrahedron Letters; vol. 44; nb. 50; (2003); p. 9029 - 9032, View in Reaxys

alkene, PhCH(CH3)CH2

O'Neill, Paul M.; Hindley, Stephen; Pugh, Matthew D.; Davies, Jill; Bray, Patrick G.; Park, B. Kevin; Kapu, Dauda S.; Ward, Stephen A.; Stocks, Paul A.; Tetrahedron Letters; vol. 44; nb. 44; (2003); p. 8135 8138, View in Reaxys

substrate Tab. 1, e. 7

Moreno-Dorado, F. Javier; Guerra, Francisco M.; Manzano, Francisco L.; Aladro, F. Javier; Jorge, Zacarias D.; Massanet, Guillermo M.; Tetrahedron Letters; vol. 44; nb. 35; (2003); p. 6691 - 6693, View in Reaxys

T. 2-9, substrate

Huang, Lingyu; Chen, Ying; Gao, Guang-Yao; Zhang, X. Peter; Journal of Organic Chemistry; vol. 68; nb.

21; (2003); p. 8179 - 8184, View in Reaxys

substrate Scheme Karame, Iyad; Tommasino, M. Lorraine; Lemaire, Marc; Tetrahedron Letters; vol. 44; nb. 41; (2003); p.

2 7687 - 7689, View in Reaxys t.2, alkene, entry 6

Ahmed, Moballigh; Seayad, Abdul Majeed; Jackstell, Ralf; Beller, Matthias; Angewandte Chemie - International Edition; vol. 42; nb. 45; (2003); p. 5615 - 5619, View in Reaxys

C9H10

Erben; Maguire; Lajtner; Barcot; Pisi; Bulletin of Environmental Contamination and Toxicology; vol. 70; nb.

1; (2003); p. 124 - 130, View in Reaxys

Table 1, entry 3

Kobayashi, Shu; Ishida, Tasuku; Akiyama, Ryo; Organic Letters; vol. 3; nb. 17; (2001); p. 2649 - 2651, View in Reaxys; Ley, Steven V.; Ramarao, Chandrashekar; Lee, Ai-Lan; stergaard, Niels; Smith, Stephen C.; Shirley, Ian M.; Organic Letters; vol. 5; nb. 2; (2003); p. 185 - 187, View in Reaxys

olefin, Tab.1, entry 2

Chandrasekhar; Narsihmulu; Sultana, S. Shameem; Reddy, N. Ramakrishna; Chemical Communications; nb. 14; (2003); p. 1716 - 1717, View in Reaxys

tab. 1, entry 5, olefin

Jonsson, Sandra Y.; Adolfsson, Hans; Baeckvall, Jan-E.; Chemistry - A European Journal; vol. 9; nb. 12; (2003); p. 2783 - 2788, View in Reaxys

Tab. 4

Roucoux, Alain; Schulz, Juergen; Patin, Henri; Advanced Synthesis and Catalysis; vol. 345; nb. 1-2; (2003); p. 222 - 229, View in Reaxys

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2016-05-12 11:27:45

Tab. 1; 2, entry 4

Klawonn, Markus; Bhor, Santosh; Mehltretter, Gerald; Doebler, Christian; Fischer, Christine; Beller, Matthias; Advanced Synthesis and Catalysis; vol. 345; nb. 3; (2003); p. 389 - 392, View in Reaxys

Tab. 4, entry 3

Ishida, Tasuku; Akiyama, Ryo; Kobayashi, Shu; Advanced Synthesis and Catalysis; vol. 345; nb. 5; (2003); p. 576 - 579, View in Reaxys

tab. 1, entries 1,5-7

Srivastava, Radhey S.; Kolel-Veetil, Manoj; Nicholas, Kenneth M.; Tetrahedron Letters; vol. 43; nb. 6; (2002); p. 931 - 934, View in Reaxys

t.1, alkene, entry 4

Tangestaninejad; Habibi; Mirkhani; Moghadam; Molecules; vol. 7; nb. 2; (2002); p. 264 - 270, View in Reaxys

R=Me

Endres, Andreas; Maas, Gerhard; Tetrahedron; vol. 58; nb. 20; (2002); p. 3999 - 4005, View in Reaxys

t.2, pr., line 13

Al-Aziz Quntar, Abed; Srebnik, Morris; Synthetic Communications; vol. 32; nb. 16; (2002); p. 2575 - 2579, View in Reaxys

52

Kusakabe, Hirokazu; Yamakage, Kohji; Wakuri, Shinobu; Sasaki, Kiyoshi; Nakagawa, Yuzuki; Watanabe, Mika; Hayashi, Makoto; Sofuni, Toshio; Ono, Hiroshi; Tanaka, Noriho; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 517; nb. 1-2; (2002); p. 187 - 198, View in Reaxys

Tab.1, prod., entry Hilt, Gerhard; Smolko, Konstantin I.; Lotsch, Bettina V.; Synlett; nb. 7; (2002); p. 1081 - 1084, 3 View in Reaxys tab1, alkene, run1 Hayashi, Yujiro; Takeda, Mitsuhiro; Miyamoto, Yuji; Shoji, Mitsuru; Chemistry Letters; nb. 3; (2002); p.

414 - 415, View in Reaxys Ia

Soldatenkov; Polyanskii; Zh. A. Mamyrbekova; Russian Journal of Organic Chemistry; vol. 38; nb. 3; (2002); p. 460 - 461, View in Reaxys

5c

Batsila, Christina; Kostakis, George; Hadjiarapoglou, Lazaros P; Tetrahedron Letters; vol. 43; nb. 34; (2002); p. 5997 - 6000, View in Reaxys

alkene, entry 3

Brule, Emilie; De Miguel, Yolanda R; Tetrahedron Letters; vol. 43; nb. 47; (2002); p. 8555 - 8558, View in Reaxys

olefin Table 3, Run 4

Yanada, Reiko; Takemoto, Yoshiji; Tetrahedron Letters; vol. 43; nb. 38; (2002); p. 6849 - 6851, View in Reaxys

educt to 4c

Shavrin, Konstantin N.; Gvozdev, Valentin D.; Nefedov, Oleg M.; Mendeleev Communications; vol. 12; nb. 6; (2002); p. 224 - 225, View in Reaxys

Tab1, col1, run4,8,10

Hogan, Gregg A.; Gallo, August A.; Nicholas, Kenneth M.; Srivastava, Radhey S.; Tetrahedron Letters; vol. 43; nb. 52; (2002); p. 9505 - 9508, View in Reaxys

VIII

Yusubov; Yusubova; Filimonov; Ki-Whan, Chi; Russian Journal of Organic Chemistry; vol. 38; nb. 6; (2002); p. 902 - 904, View in Reaxys

1, Z = H

Garner, Charles M.; Chiang, Shirley; Nething, Matthew; Monestel, Robert; Tetrahedron Letters; vol. 43; nb. 46; (2002); p. 8339 - 8342, View in Reaxys

7c

Tiecco, Marcello; Testaferri, Lorenzo; Santi, Claudio; Tomassini, Cristina; Marini, Francesca; Bagnoli, Luana; Temperini, Andrea; Chemistry - A European Journal; vol. 8; nb. 5; (2002); p. 1118 - 1124, View in Reaxys

α-methyl styrene

Pezet, Frederic; Ait-Haddou, Hassan; Daran, Jean-Claude; Sasaki, Isabelle; Balavoine, Gilbert G. A.; Chemical Communications; nb. 5; (2002); p. 510 - 511, View in Reaxys

c

Wurz, Ryan P.; Charette, Andre B.; Organic Letters; vol. 4; nb. 25; (2002); p. 4531 - 4533, View in Reaxys

educt to 13

Suau, Rafael; Sanchez-Sanchez, Cristobal; Garcia-Segura, Rafael; Perez-Inestrosa, Ezequiel; European Journal of Organic Chemistry; nb. 12; (2002); p. 1903 - 1911, View in Reaxys

alkene Tab. 4, en- Zhang, Rui; Yu, Wing-Yiu; Sun, Hong-Zhe; Liu, Wei-Sheng; Che, Chi-Ming; Chemistry - A European try 14 Journal; vol. 8; nb. 11; (2002); p. 2495 - 2507, View in Reaxys Tab. 1, entry 5

Choudary, Boyapati M.; Chowdari, Naidu S.; Jyothi, Karangula; Madhi, Sateesh; Kantam, Mannepalli L.; Advanced Synthesis and Catalysis; vol. 344; nb. 5; (2002); p. 503 - 506, View in Reaxys

2, T.1, e.10

Kumabe, Ryoukou; Nishino, Hiroshi; Yasutake, Mikio; Nguyen, Van-Ha; Kurosawa, Kazu; Tetrahedron Letters; vol. 42; nb. 1; (2001); p. 69 - 72, View in Reaxys

educt to 5a

Wang, Qinwei; Hossain, M. Mahmun; Journal of Organometallic Chemistry; vol. 617; (2001); p. 751 - 754, View in Reaxys

Tab.1, substr., en- Krief; Castillo-Colaux; Synlett; nb. 4; (2001); p. 501 - 504, View in Reaxys try a

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15b

Auricchio, Sergio; Grassi, Simona; Malpezzi, Luciana; Sartori, Attilio Sarzi; Truscello, Ada M.; European Journal of Organic Chemistry; nb. 6; (2001); p. 1183 - 1187, View in Reaxys

correspond. styrene

Nenajdenko, Valentine G.; Smolko, Konstantin I.; Balenkova, Elizabeth S.; Tetrahedron Asymmetry; vol.

12; nb. 9; (2001); p. 1259 - 1266, View in Reaxys

1; R1=R2=R4=H, R3=Me

Seijas; Vazquez-Tato; Martinez; Synlett; nb. 6; (2001); p. 875 - 877, View in Reaxys

olefin, entry 3

Kuang, Yong-Qing; Zhang, Sheng-Yong; Wei, Ling-Ling; Tetrahedron Letters; vol. 42; nb. 34; (2001); p.

5925 - 5927, View in Reaxys

α-mst

Kalninsh; Physical Chemistry Chemical Physics; vol. 3; nb. 20; (2001); p. 4542 - 4546, View in Reaxys

alkene 10

Pezet, Frederic; Sasaki, Isabelle; Daran, Jean-Claude; Hydrio, Jerome; Ait-Haddou, Hassan; Balavoine, Gilbert; European Journal of Inorganic Chemistry; nb. 10; (2001); p. 2669 - 2674, View in Reaxys

tab. 2, entry 2a

Takaki, Ken; Takeda, Mitsuhiro; Koshoji, Go; Shishido, Tetsuya; Takehira, Katsuomi; Tetrahedron Letters; vol. 42; nb. 36; (2001); p. 6357 - 6360, View in Reaxys

X

Maksyuta; Suprun; Opeida; Turovskii; Russian Journal of Organic Chemistry; vol. 37; nb. 6; (2001); p. 814 - 818, View in Reaxys

1 (table 2)

Song, Qishi; Yang, Darong; Zhang, Guangming; Yang, Chongren; Journal of Chemical Ecology; vol. 27; nb. 10; (2001); p. 1929 - 1942, View in Reaxys

AMS, A

De; Sathyanarayana; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 40; nb. 12; (2001); p. 1282 - 1287, View in Reaxys

AMeSt

Karalin; Busygin; Batyrshin; Cherkasova; Kharlampidi; Petroleum Chemistry; vol. 41; nb. 6; (2001); p.

419 - 421, View in Reaxys

Tab. 1, entry 3, subs.

Grenz; Ceccarelli; Bolm; Chemical Communications; nb. 18; (2001); p. 1726 - 1727, View in Reaxys

3r

Barrett, Anthony G. M.; Braddock, D. Christopher; Lenoir, Isabelle; Tone, Hitoshi; Journal of Organic Chemistry; vol. 66; nb. 24; (2001); p. 8260 - 8263, View in Reaxys

alkene,t.1,R=H

Kezuka, Satoko; Ikeno, Taketo; Yamada, Tohru; Organic Letters; vol. 3; nb. 12; (2001); p. 1937 - 1939, View in Reaxys

t.3,substrate,entry Sakaguchi; Yamaga; Ishii; Journal of Organic Chemistry; vol. 66; nb. 13; (2001); p. 4710 - 4712, 7 View in Reaxys table 3, entry 3

Sheeller, Brad; Ingold, Keith U.; Journal of the Chemical Society. Perkin Transactions 2; nb. 4; (2001); p.

480 - 486, View in Reaxys

Table 1, run 1, col Javier Aladro; Guerra, Francisco M.; Javier Moreno-Dorado; Bustamante, Jesus M.; Jorge, Zacarias 1 D.; Massanet, Guillermo M.; Tetrahedron Letters; vol. 41; nb. 17; (2000); p. 3209 - 3213, View in Reaxys CH2=CXY, X=Me Y=Ph

Zytowski, Torsten; Knuehl, Bernhard; Fischer, Hanns; Helvetica Chimica Acta; vol. 83; nb. 3; (2000); p.

658 - 675, View in Reaxys

Table 2 Entry 4 Subst.

Niimi, Tatsuo; Uchida, Tatsuya; Irie, Ryo; Katsuki, Tsutomu; Tetrahedron Letters; vol. 41; nb. 19; (2000); p. 3647 - 3651, View in Reaxys

Table 2, olefin

Marchetti; Mangano; Paganelli; Botteghi; Tetrahedron Letters; vol. 41; nb. 19; (2000); p. 3717 - 3720, View in Reaxys

substrate, entry 8

Campos, Pedro J.; Garcia, Barbara; Rodriguez, Miguel A.; Tetrahedron Letters; vol. 41; nb. 6; (2000); p.

979 - 982, View in Reaxys

5 Table 1, entry 10

Bauta, William; Dodd, John; Bullington, James; Gauthier, Diane; Leo, Gregory; McDonnell, Patricia; Tetrahedron Letters; vol. 41; nb. 10; (2000); p. 1491 - 1494, View in Reaxys

13c

Takemoto, Toshiyasu; Iio, Yukiko; Nishi, Takahide; Tetrahedron Letters; vol. 41; nb. 11; (2000); p. 1785 1788, View in Reaxys

Tab 1, starting en- Bernasconi, Silvana; Orsini, Fulvia; Sello, Guido; Colmegna, Andrea; Galli, Enrica; Bestetti, Giuseppitry 3 na; Tetrahedron Letters; vol. 41; nb. 47; (2000); p. 9157 - 9161, View in Reaxys 8d

Gogonas; Hadjiarapoglou; Tetrahedron Letters; vol. 41; nb. 48; (2000); p. 9299 - 9303, View in Reaxys

olefin, table/entry 9

Bertilsson, Sophie K.; Andersson, Pher G.; Journal of Organometallic Chemistry; vol. 603; nb. 1; (2000); p. 13 - 17, View in Reaxys

V

Tyrkov; Kosova; Russian Journal of Organic Chemistry; vol. 36; nb. 12; (2000); p. 1826 - 1827, View in Reaxys

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8, X=Me

Xu, Yuelian; Dolbier Jr., William R.; Journal of Organic Chemistry; vol. 65; nb. 7; (2000); p. 2134 - 2137, View in Reaxys

table 1, entry 4

Vaino; Journal of Organic Chemistry; vol. 65; nb. 13; (2000); p. 4210 - 4212, View in Reaxys

4f

Adam, Waldemar; Saha-Moeller, Chantu R.; Weichold, Oliver; Journal of Organic Chemistry; vol. 65; nb.

10; (2000); p. 2897 - 2899, View in Reaxys

Table 2, entry 13

Shu; Shi; Journal of Organic Chemistry; vol. 65; nb. 25; (2000); p. 8807 - 8810, View in Reaxys

tab. 2, entry 6, olefin

Quadrelli; Mella; Caramella; Tetrahedron Letters; vol. 40; nb. 4; (1999); p. 797 - 800, View in Reaxys

H2C=CMePh

Bianchini, Claudio; Peruzzini, Maurizio; Zanobini, Fabrizio; Lopez, Carlos; De Los Rios, Isaac; Romerosa, Antonio; Chemical Communications; nb. 5; (1999); p. 443 - 444, View in Reaxys

Table 2, col 1, run Simal, Francois; Jan, Dominique; Demonceau, Albert; Noels, Alfred F.; Tetrahedron Letters; vol. 40; nb.

6 9; (1999); p. 1653 - 1656, View in Reaxys 1, T.1, e.6

Chowdhury, Firoz Alam; Kajikawa, Shougo; Nishino, Hiroshi; Kurosawa, Kazu; Tetrahedron Letters; vol.

40; nb. 19; (1999); p. 3765 - 3768, View in Reaxys

2 (R3=Me,R2=R4= H)

Beller, Matthias; Breindl, Claudia; Riermeier, Thomas H.; Eichberger, Martin; Trauthwein, Harald; Angewandte Chemie - International Edition; vol. 37; nb. 24; (1999); p. 3389 - 3391, View in Reaxys

Olefin, Tab. 1, run Adolfsson, Hans; Converso, Antonella; Sharpless, K. Barry; Tetrahedron Letters; vol. 40; nb. 21; (1999); 2 p. 3991 - 3994, View in Reaxys Table entry 4 sub- Chavan, Subhash P.; Subbarao, Y. Tripura; Tetrahedron Letters; vol. 40; nb. 27; (1999); p. 5073 - 5074, strate View in Reaxys Tab.1, substr., en- Keck, Gary E.; Grier, Mark C.; Synlett; nb. 10; (1999); p. 1657 - 1659, View in Reaxys try 2 precursor to 1i

Dussault, Patrick H.; Liu, Xuejun; Tetrahedron Letters; vol. 40; nb. 36; (1999); p. 6553 - 6556, View in Reaxys

t.1, entry 2

Liu, Chun-Jin; Yu, Wing-Yiu; Che, Chi-Ming; Yeung, Chi-Hung; Journal of Organic Chemistry; vol. 64; nb.

20; (1999); p. 7365 - 7374, View in Reaxys

3f

Kobayashi, Kazuhiro; Sakashita, Kouji; Akamatsu, Hideki; Tanaka, Koujirou; Uchida, Masaharu; Uneda, Tomokazu; Kitamura, Taichi; Morikawa, Osamu; Konishi, Hisatoshi; Heterocycles; vol. 51; nb. 12; (1999); p. 2881 - 2892, View in Reaxys

Table 2. Olefin 5

Ikeno, Taketo; Sato, Mitsuo; Yamada, Tohru; Chemistry Letters; nb. 12; (1999); p. 1345 - 1346, View in Reaxys

5g

Asensio, Gregorio; Andreu, Cecilia; Boix-Bernardini, Carmen; Mello, Rossella; Gonzalez-Nunez, Maria Elena; Organic Letters; vol. 1; nb. 13; (1999); p. 2125 - 2128, View in Reaxys

4h

Miura, Masanori; Arai, Noriyoshi; Narasaka, Koichi; Bulletin of the Chemical Society of Japan; vol. 71; nb.

6; (1998); p. 1437 - 1441, View in Reaxys

II

Zorin; Maslennikov; Shavshukova; Shakhova; Rakhmankulov; Russian Journal of Organic Chemistry; vol. 34; nb. 5; (1998); p. 725 - 726, View in Reaxys

α-MSt

Alam; Fujitsuka; Watanabe; Ito; Journal of Physical Chemistry A; vol. 102; nb. 8; (1998); p. 1338 - 1344, View in Reaxys

Patent-Specific Data (16) Prophetic ComLocation in Patent References pound Page/Page column

Patent; Idemitsu Kosan Co., Ltd.; Sekiguchi, Hiroki; Tsubouchi, Toshiyuki; Oda, Sumihiro; Koga, Hidetoshi; US2013/123553; (2013); (A1) English, View in Reaxys; Patent; Honshu Chemical Industry Co., Ltd.; ASHIDA, Kazuhito; HASHIMOTO, Yuki; YAMAMOTO, Tomoya; LU, Xuwang; EP2851359; (2015); (A1) English, View in Reaxys

Page/Page column

Patent; Technische Universität Berlin; Oestreich, Martin, Prof. Dr.; Simonneau, Antoine, Dr.; EP2845857; (2015); (A1) English, View in Reaxys Patent; PRESIDENT AND FELLOWS OF HARVARD COLLEGE; BETLEY, Theodore, Alexander; HENNESSY, Elisabeth, Therese; WO2014/134141; (2014); (A1) English, View in Reaxys

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Patent; NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY; ARAKAWA CHEMICAL INDUSTRIES, LTD.; US2012/108830; (2012); (A1) English, View in Reaxys Patent; BASF SE; US2010/191000; (2010); (A1) English, View in Reaxys Patent; UNIVERSITY OF SOUTH FLORIDA; ZHANG, X. Peter; WO2010/99206; (2010); (A2) English, View in Reaxys Patent; Kaneka Corporation; EP1914217; (2008); (A1) English, View in Reaxys Patent; Magerlein, Wolfgang; Beller, Matthias; Tse, Man-Kin; Bhor, Santosh; Klawonn, Markus; Anilkumar, Gopinathan; US2006/161011; (2006); (A1) English, View in Reaxys Patent; Che, Chi-Ming; Yu, Wing-Yiu; Ho, Chi-Ming; US2005/234260; (2005); (A1) English, View in Reaxys Patent; IHARA CHEMICAL INDUSTRY CO., LTD.; JP2005/350427; (2005); (A) Japanese, View in Reaxys Patent; NOK Corporation; JP2005/200424; (2005); (A) Japanese, View in Reaxys Patent; RohMax Additives GmbH; US2004/186302; (2004); (A1) English, View in Reaxys Patent; Sanofi-Synthelabo; US6639083; (2003); (B1) English, View in Reaxys Patent; Colorado State University Research Foundation; US6369245; (2002); (B1) English, View in Reaxys prophetic product

Patent; The Goodyear Tire and Rubber Company; US4143076; (1979); (A1) English, View in Reaxys; Patent; Basell Polypropylen GmbH; US6492539; (2002); (B1) English, View in Reaxys Patent; Laboratorios del Dr. Esteve, S.A.; US6353117; (2002); (B1) English, View in Reaxys

Related Structure (2) Related Structure References Kornblum,N. et al.; Journal of the American Chemical Society; vol. 101; (1979); p. 647 - 657, View in Reaxys Neuere zusammenfassende Darstellungen.

Derivative (7) Comment (Derivative)

Ohlinger,H.; Polystyrol, Tl. 1 <Berlin 1955> S. 36, 78, 90, 118, 132, View in Reaxys; Schildknecht,C.E.; Vinyl and Related Polymers <New York 1952> S. 132-239, View in Reaxys

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Komplex m. Tetracyanoethylen

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Na-Verb.

Comyn; Irin; European Polymer Journal; vol. 5; (1969); p. 587,588,589,593, View in Reaxys

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54.5 - 55

14

Auwers; Eisenlohr; Journal fuer Praktische Chemie (Leipzig); vol. <2>82; (1910); p. 116; Journal fuer Praktische Chemie (Leipzig); vol. <2>84; (1911); p. 13, View in Reaxys; Auwers; Roth; Eisenlohr; Justus Liebigs Annalen der Chemie; vol. 373; (1910); p. 282, View in Reaxys; Lewina et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1185,1096; Chem.Abstr.; nb. 25809; (1961), View in Reaxys; Lewina et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 33; (1963); p. 2825,2751, View in Reaxys

59

20

Mamedaliew et al.; Doklady - Akademiya Nauk Azerbaidzhanskoi SSR; vol. 19; nb. 1; (1963); p. 13,16; Chem.Abstr.; vol. 59; nb.

6279g; (1963), View in Reaxys

60 - 61

17

Tiffeneau; Annales de Chimie (Cachan, France); vol. <8>10; (1907); p. 190; Annales de Chimie (Cachan, France); vol. <8>11; (1907); p.

144, View in Reaxys; Jui Bao-Schan' et al.; Zhurnal Fizicheskoi Khimii; vol. 36; (1962); p. 681,686; ; p. 356, View in Reaxys

161

Terent'ew et al.; Neftekhimiya; vol. 1; (1962); p. 567,462, View in Reaxys

85 - 87

42

Traynelis,V.J. et al.; Journal of Organic Chemistry; vol. 27; (1962); p. 2377 - 2383, View in Reaxys

53

12

Hawkins,E.G.E.; Thompson,R.D.; Journal of the Chemical Society; (1961); p. 370 - 377, View in Reaxys

160 - 161

Lapkin; Rybakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 1227,1248; Chem.Abstr.; nb. 442; (1961), View in Reaxys

163.7

758

Schtscherbak et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 29; (1956); p. 353,391, View in Reaxys

163.5

763.1

Woronkow; Broun; Karpenko; Zhurnal Obshchei Khimii; vol. 19; (1949); p. 1927,1939; Chem.Abstr.; (1950); p. 1955, View in Reaxys

165.38

760

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Rossini; Selected Values 1953 S. 75, View in Reaxys

60

17

Woronkow; Broun; Karpenko; Zhurnal Obshchei Khimii; vol. 19; (1949); p. 1927,1939; Chem.Abstr.; (1950); p. 1955, View in Reaxys

69 - 69.2

27

Walling; Seymour; Wolfstirn; Journal of the American Chemical Society; vol. 70; (1948); p. 1544,1546, View in Reaxys

56

13

Danilow; Venus-Danilowa; Chemische Berichte; vol. 60; (1927); p.

1062; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol.

59; (1927); p. 204, View in Reaxys

60.5 - 61.5

18

Danilow; Venus-Danilowa; Chemische Berichte; vol. 60; (1927); p.

1062; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol.

59; (1927); p. 204, View in Reaxys

163 - 164

752

v. Braun; Heider; Neumann; Chemische Berichte; vol. 49; (1916); p. 2616, View in Reaxys

164

749

Thorpe; Wood; Journal of the Chemical Society; vol. 103; (1913); p.

1575; Journal of the Chemical Society; vol. 123; (1923); p. 63, View in Reaxys

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68 - 69

27

Tiffeneau; Annales de Chimie (Cachan, France); vol. <8>10; (1907); p. 190; Annales de Chimie (Cachan, France); vol. <8>11; (1907); p.

144, View in Reaxys

165

764

61 - 62

18

Klages; Chemische Berichte; vol. 35; (1902); p. 3507, View in Reaxys

106

126

Grignard; Chem. Zentralbl.; vol. 72; nb. II; (1901); p. 624, View in Reaxys

158 - 160

748

Grignard; Chem. Zentralbl.; vol. 72; nb. II; (1901); p. 624, View in Reaxys

Fluessigkeit.

163.38

Matsubara; Perkin; Journal of the Chemical Society; vol. 87; (1905); p. 671, View in Reaxys

Dow Chem. Co. bei C.E. Schildknecht; Vinyl and Related Polymers <New York 1952> S. 133, View in Reaxys

Refractive Index (46) Refractive Index Wavelength (Refractive Index) [nm]

Temperature (Refractive Index) [°C]

References

1.5342

589

20

Prusek, Ondrej; Bures, Filip; Pytela, Oldrich; Collection of Czechoslovak Chemical Communications; vol. 74; nb. 1; (2009); p. 85 99, View in Reaxys

1.5381

589

20

Klimova; Berestneva, T. Klimova; Mendoza, J. M. Martinez; Stivalet, J. M. Mendez; Toscano; Garcia, M. Martinez; Synthetic Communications; vol. 38; nb. 14; (2008); p. 2299 - 2315, View in Reaxys

1.5382

589

20

Klimova; Berestneva, T. Klimova; Mendoza, J. M. Martinez; Stivalet, J. M. Mendez; Toscano; Garcia, M. Martinez; Synthetic Communications; vol. 38; nb. 14; (2008); p. 2299 - 2315, View in Reaxys

1.538

589

20

Pytela, Oldrich; Trlida, Bronislav; Collection of Czechoslovak Chemical Communications; vol. 72; nb. 8; (2007); p. 1025 - 1036, View in Reaxys

1.5368

589

17

Bolesov, I. G.; Ignatchenko, A. V.; Bovin, N. V.; Prudchenko, I. A.; Surmina, L. S.; et al.; Journal of Organic Chemistry USSR (English Translation); vol. 26; nb. 1.2; (1990); p. 87 - 100; Zhurnal Organicheskoi Khimii; vol. 26; nb. 1; (1990); p. 102 - 119, View in Reaxys

1.5359

589

25

Dow Chem. Co. bei C.E. Schildknecht; Vinyl and Related Polymers <New York 1952> S. 133, View in Reaxys; Lebedeva, V. I.; Gryaznov, V. M.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 37; nb. 5; (1988); p. 1018 - 1020; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 5; (1988); p. 1158 - 1160, View in Reaxys

1.5376

589

20

Traynelis,V.J. et al.; Journal of Organic Chemistry; vol. 27; (1962); p. 2377 - 2383, View in Reaxys; Amelichev, V. A.; Nosovskii, M. V.; Saidov, G. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 8; (1981); p. 1879 - 1885,1613 - 1619, View in Reaxys

1.5571

589

20

Sychkova, L. D.; Shabarov, Yu. S.; Journal of Organic Chemistry USSR (English Translation); vol. 16; nb. 10; (1980); p. 1775 - 1779; Zhurnal Organicheskoi Khimii; vol. 16; nb. 10; (1980); p. 2086 2091, View in Reaxys

1.5329

589

20

Neumann,H.; Seebach,D.; Chemische Berichte; vol. 111; (1978); p.

2785 - 2812, View in Reaxys

1.54

589

22

Uijttewaal,A.P. et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3306 - 3311, View in Reaxys

1.536

589

20

Westmijze,H. et al.; Recueil des Travaux Chimiques des Pays-Bas; vol. 95; (1976); p. 304 - 307, View in Reaxys; Lewina et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1185,1096; Chem.Abstr.; nb. 25809; (1961), View in Reaxys; Lewina et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 33; (1963); p. 2825,2751, View in Reaxys

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2016-05-12 11:27:45

1.5368

589

20

Stepovik; Khamylova; J. Gen. Chem. USSR (Engl. Transl.); vol. 45; (1975); p. 61,54, View in Reaxys

1.5362

589

21

Humphris; Scott; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 831,834, View in Reaxys

1.538

589

20

Hawkins,E.G.E.; Thompson,R.D.; Journal of the Chemical Society; (1961); p. 370 - 377, View in Reaxys; Odyakov; Matveev; Kinetics and Catalysis; vol. 14; (1973); p. 1276,1277, View in Reaxys

1.537

589

21

Reisdorf,D.; Normant,H.; Organometallics in Chemical Synthesis; vol. 1; (1972); p. 375 - 391, View in Reaxys Zhuravlev et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 45; (1972); p. 462,471, View in Reaxys

1.5418

589

20

Isagulyants; Safarov; J. Appl. Chem. USSR (Engl. Transl.); vol. 39; (1966); p. 1148,1076,1078,1081, View in Reaxys; Isagulyants et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p.

2703,2742,2745, View in Reaxys

1.5372

589

18.5

Mastagli,P.; de Nanteuil,M.; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 268; (1969); p. 1970 - 1972, View in Reaxys

1.5372

589

21.5

Mastagli,P.; de Nanteuil,M.; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 268; (1969); p. 1970 - 1972, View in Reaxys

1.5778

589

20

Tashchuk,K.G. et al.; Sov. Prog. Chem. (Engl. Transl.); vol. 34; nb.

11; (1968); p. 1148 - 1150,50 - 51, View in Reaxys

1.5384

589

20

Kokoschko et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 37; (1967); p. 58,51, View in Reaxys

1.5372

589

20

Mihailovic et al.; Tetrahedron; vol. 23; (1967); p. 3095, View in Reaxys

1.5375

589

20

Bahachanow et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 6; (1966); p. 54; Chem.Abstr.; vol. 67; nb. 73262; (1967), View in Reaxys

1.5341

589

20

Kirillov; Zhurnal Organicheskoi Khimii; vol. 1; (1965); p. 1226,1237, View in Reaxys

1.5382

589

20

Nerdel,F. et al.; Chemische Berichte; vol. 98; (1965); p. 728 - 734, View in Reaxys

1.5373

589

20

Beier et al.; Journal fuer Praktische Chemie (Leipzig); vol. 26; (1964); p. 304, View in Reaxys

1.5349

589

20

Mamedaliew et al.; Doklady - Akademiya Nauk Azerbaidzhanskoi SSR; vol. 19; nb. 1; (1963); p. 13,16; Chem.Abstr.; vol. 59; nb.

6279g; (1963), View in Reaxys

1.533

589

21

Tiffeneau; Annales de Chimie (Cachan, France); vol. <8>10; (1907); p. 190; Annales de Chimie (Cachan, France); vol. <8>11; (1907); p.

144, View in Reaxys; Jui Bao-Schan' et al.; Zhurnal Fizicheskoi Khimii; vol. 36; (1962); p. 681,686; ; p. 356, View in Reaxys

1.537

589

20

Terent'ew et al.; Neftekhimiya; vol. 1; (1962); p. 567,462, View in Reaxys

1.5384

589

17.5

Lewina et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1185,1096; Chem.Abstr.; nb. 25809; (1961), View in Reaxys

1.5325

589

20

Lapkin; Rybakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 1227,1248; Chem.Abstr.; nb. 442; (1961), View in Reaxys

1.535

589

20

Schtscherbak et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 29; (1956); p. 353,391, View in Reaxys

1.5386

589

20

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Rossini; Selected Values 1953 S. 75, View in Reaxys

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2016-05-12 11:27:45

1.5358

589

25

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Rossini; Selected Values 1953 S. 75, View in Reaxys

1.5278

656.3

20

Woronkow; Broun; Karpenko; Zhurnal Obshchei Khimii; vol. 19; (1949); p. 1927,1939; Chem.Abstr.; (1950); p. 1955, View in Reaxys

1.5334

589

20

Woronkow; Broun; Karpenko; Zhurnal Obshchei Khimii; vol. 19; (1949); p. 1927,1939; Chem.Abstr.; (1950); p. 1955, View in Reaxys

1.5481

486.1

20

Woronkow; Broun; Karpenko; Zhurnal Obshchei Khimii; vol. 19; (1949); p. 1927,1939; Chem.Abstr.; (1950); p. 1955, View in Reaxys

1.5383

589

20

Walling; Seymour; Wolfstirn; Journal of the American Chemical Society; vol. 70; (1948); p. 1544,1546, View in Reaxys

1.5381

589

20

Scafe; Herman; Analytical Chemistry; vol. 19; (1947); p. 971,972, View in Reaxys

1.5418

589

12

Nesmejanow; Freidlina; Zhurnal Obshchei Khimii; vol. 7; (1937); p.

2748,2751; Chem. Zentralbl.; vol. 110; nb. I; (1939); p. 103, View in Reaxys

1.5326

656.3

17.4

Auwers; Eisenlohr; Journal fuer Praktische Chemie (Leipzig); vol. <2>82; (1910); p. 116; Journal fuer Praktische Chemie (Leipzig); vol. <2>84; (1911); p. 13, View in Reaxys

1.5384

589

17.4

Auwers; Eisenlohr; Journal fuer Praktische Chemie (Leipzig); vol. <2>82; (1910); p. 116; Journal fuer Praktische Chemie (Leipzig); vol. <2>84; (1911); p. 13, View in Reaxys

1.5535

486.1

17.4

Auwers; Eisenlohr; Journal fuer Praktische Chemie (Leipzig); vol. <2>82; (1910); p. 116; Journal fuer Praktische Chemie (Leipzig); vol. <2>84; (1911); p. 13, View in Reaxys

1.5664

434

17.4

Auwers; Eisenlohr; Journal fuer Praktische Chemie (Leipzig); vol. <2>82; (1910); p. 116; Journal fuer Praktische Chemie (Leipzig); vol. <2>84; (1911); p. 13, View in Reaxys

1.5311

589

24

Klages; Chemische Berichte; vol. 35; (1902); p. 3507, View in Reaxys

1.54207

589

9.6

Grignard; Chem. Zentralbl.; vol. 72; nb. II; (1901); p. 624, View in Reaxys

Density (24) 1 of 24

Density [g·cm-3]

0.7934 - 0.8866

Measurement Temperature [°C]

50 - 150

Steele; Chirico; Knipmeyer; Nguyen; Journal of Chemical and Engineering Data; vol. 42; nb. 6; (1997); p. 1008 1020, View in Reaxys 2 of 24

Density [g·cm-3]

0.911

Measurement Temperature [°C]

20

Nurok, David; Kleyle, Robert M.; Lipkowitz, Kenneth B.; Myers, Steven S.; Kearns, Michelle L.; Analytical Chemistry; vol. 65; nb. 24; (1993); p. 3701 - 3707, View in Reaxys 3 of 24

Makitra; Tsikanchuk; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 2582,2564,2565, View in Reaxys

4 of 24

Density [g·cm-3]

0.9108

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Isagulyants; Safarov; J. Appl. Chem. USSR (Engl. Transl.); vol. 39; (1966); p. 1148,1076,1078,1081, View in Reaxys; Isagulyants et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 2703,2742,2745, View in Reaxys 5 of 24

Density [g·cm-3]

0.9134

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Hala; Chemicky Prumysl; vol. 18; (1968); p. 412; Chem.Abstr.; vol. 69; nb. 83193; (1968), View in Reaxys 6 of 24

Density [g·cm-3]

0.89

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Kokoschko et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 37; (1967); p. 58,51, View in Reaxys 7 of 24

Density [g·cm-3]

0.9128

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Bahachanow et al.; Azerbaidzhanskii Khimicheskii Zhurnal; vol. 6; (1966); p. 54; Chem.Abstr.; vol. 67; nb. 73262; (1967), View in Reaxys 8 of 24

Density [g·cm-3]

0.914

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Beier et al.; Journal fuer Praktische Chemie (Leipzig); vol. 26; (1964); p. 304, View in Reaxys 9 of 24

Density [g·cm-3]

0.908

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Mamedaliew et al.; Doklady - Akademiya Nauk Azerbaidzhanskoi SSR; vol. 19; nb. 1; (1963); p. 13,16; Chem.Abstr.; vol. 59; nb. 6279g; (1963), View in Reaxys; Schtscherbak et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 29; (1956); p. 353,391, View in Reaxys 10 of 24

Density [g·cm-3]

0.9085

Measurement Temperature [°C]

21

Tiffeneau; Annales de Chimie (Cachan, France); vol. <8>10; (1907); p. 190; Annales de Chimie (Cachan, France); vol. <8>11; (1907); p. 144, View in Reaxys; Jui Bao-Schan' et al.; Zhurnal Fizicheskoi Khimii; vol. 36; (1962); p.

681,686; ; p. 356, View in Reaxys 11 of 24

Density [g·cm-3]

0.9134

Reference Temperature [°C]

4

Measurement Temperature [°C]

17.5

Lewina et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1185,1096; Chem.Abstr.; nb. 25809; (1961), View in Reaxys 12 of 24

Density [g·cm-3]

0.9055

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Lapkin; Rybakowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 1227,1248; Chem.Abstr.; nb. 442; (1961), View in Reaxys 13 of 24

Density [g·cm-3]

0.9082

Reference Temperature [°C]

4

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Measurement Temperature [°C]

20

Woronkow; Broun; Karpenko; Zhurnal Obshchei Khimii; vol. 19; (1949); p. 1927,1939; Chem.Abstr.; (1950); p.

1955, View in Reaxys 14 of 24

Density [g·cm-3]

0.9106

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Rossini; Selected Values 1953 S. 75, View in Reaxys 15 of 24

Density [g·cm-3]

0.9062

Reference Temperature [°C]

4

Measurement Temperature [°C]

25

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Rossini; Selected Values 1953 S. 75, View in Reaxys 16 of 24

Density [g·cm-3]

0.9182

Reference Temperature [°C]

4

Measurement Temperature [°C]

12

Nesmejanow; Freidlina; Zhurnal Obshchei Khimii; vol. 7; (1937); p. 2748,2751; Chem. Zentralbl.; vol. 110; nb. I; (1939); p. 103, View in Reaxys 17 of 24

Density [g·cm-3]

0.9142

Reference Temperature [°C]

20

Measurement Temperature [°C]

20

Danilow; Venus-Danilowa; Chemische Berichte; vol. 60; (1927); p. 1062; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 59; (1927); p. 204, View in Reaxys 18 of 24

Density [g·cm-3]

0.9154

Reference Temperature [°C]

20

Measurement Temperature [°C]

20

Danilow; Venus-Danilowa; Chemische Berichte; vol. 60; (1927); p. 1062; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 59; (1927); p. 204, View in Reaxys 19 of 24

Density [g·cm-3]

0.9272

Reference Temperature [°C]

0

Measurement Temperature [°C]

0

Danilow; Venus-Danilowa; Chemische Berichte; vol. 60; (1927); p. 1062; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 59; (1927); p. 204, View in Reaxys 20 of 24

Density [g·cm-3]

0.9273

Reference Temperature [°C]

0

Measurement Temperature [°C]

0

Copyright © 2016 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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Danilow; Venus-Danilowa; Chemische Berichte; vol. 60; (1927); p. 1062; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 59; (1927); p. 204, View in Reaxys 21 of 24

Density [g·cm-3]

0.9134

Reference Temperature [°C]

4

Measurement Temperature [°C]

17.4

Auwers; Eisenlohr; Journal fuer Praktische Chemie (Leipzig); vol. <2>82; (1910); p. 116; Journal fuer Praktische Chemie (Leipzig); vol. <2>84; (1911); p. 13, View in Reaxys 22 of 24

Density [g·cm-3]

0.9278

Measurement Temperature [°C]

0

Tiffeneau; Annales de Chimie (Cachan, France); vol. <8>10; (1907); p. 190; Annales de Chimie (Cachan, France); vol. <8>11; (1907); p. 144, View in Reaxys 23 of 24

Density [g·cm-3]

0.9044

Reference Temperature [°C]

4

Measurement Temperature [°C]

24

Klages; Chemische Berichte; vol. 35; (1902); p. 3507, View in Reaxys 24 of 24

Density [g·cm-3]

0.9165

Reference Temperature [°C]

4

Measurement Temperature [°C]

9.6

Grignard; Chem. Zentralbl.; vol. 72; nb. II; (1901); p. 624, View in Reaxys Adsorption (MCS) (1) 1 of 1

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

-98.15

Partner (Adsorption (MCS))

Cu(111)

Williams, Federico J.; Cropley, Rachael L.; Vaughan, Owain P. H.; Urquhart, Andrew J.; Tikhov, Mintcho S.; Kolczewski, Christine; Hermann, Klaus; Lambert, Richard M.; Journal of the American Chemical Society; vol.

127; nb. 48; (2005); p. 17007 - 17011, View in Reaxys Association (MCS) (30) 1 of 30

Description (Association Association with compound (MCS)) Partner (Association (MCS))

C32H28N4O4

Geer, Michael F.; Walla, Michael D.; Solntsev, Kyril M.; Strassert, Cristian A.; Shimizu, Linda S.; Journal of Organic Chemistry; vol. 78; nb. 11; (2013); p. 5568 - 5578, View in Reaxys 2 of 30

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

(MCS)) Partner (Association (MCS))

cycloheptaamylose

Cao, Yujuan; Xiao, Xiaohua; Ji, Shengfu; Lu, Runhua; Guo, Qingxiang; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 60; nb. 4; (2004); p. 815 - 820, View in Reaxys 3 of 30

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

(MCS))

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Partner (Association (MCS))

alpha cyclodextrin

Cao, Yujuan; Xiao, Xiaohua; Lu, Runhua; Guo, Qingxiang; Journal of Molecular Structure; vol. 660; nb. 1-3; (2003); p. 73 - 80, View in Reaxys 4 of 30

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

(MCS)) Partner (Association (MCS))

cyclomaltooctaose

Cao, Yujuan; Xiao, Xiaohua; Lu, Runhua; Guo, Qingxiang; Journal of Molecular Structure; vol. 660; nb. 1-3; (2003); p. 73 - 80, View in Reaxys 5 of 30

Description (Association Association with compound (MCS)) Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

sodium dodecyl-sulfate

Buchviser, Silmara F.; Gehlen, Marcelo H.; Journal of the Chemical Society - Faraday Transactions; vol. 93; nb. 6; (1997); p. 1133 - 1139, View in Reaxys 6 of 30

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

(MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

4-Fluorophenol

Besseau, Francois; Laurence, Christian; Berthelot, Michel; Bulletin de la Societe Chimique de France; vol. 133; nb. 4; (1996); p. 381 - 387, View in Reaxys 7 of 30

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

CCl4

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

4-Fluorophenol

Besseau, Francois; Laurence, Christian; Berthelot, Michel; Bulletin de la Societe Chimique de France; vol. 133; nb. 4; (1996); p. 381 - 387, View in Reaxys 8 of 30

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

hexane

Partner (Association (MCS))

triethylamine

Lewis; Reddy; Bassani; Schneider; Gahr; Journal of the American Chemical Society; vol. 116; nb. 2; (1994); p.

597 - 605, View in Reaxys 9 of 30

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

dibutyl ether

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Partner (Association (MCS))

triethylamine

Lewis; Reddy; Bassani; Schneider; Gahr; Journal of the American Chemical Society; vol. 116; nb. 2; (1994); p.

597 - 605, View in Reaxys 10 of 30

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

diethyl ether

Partner (Association (MCS))

triethylamine

Lewis; Reddy; Bassani; Schneider; Gahr; Journal of the American Chemical Society; vol. 116; nb. 2; (1994); p.

597 - 605, View in Reaxys 11 of 30

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

tetrahydrofuran

Partner (Association (MCS))

triethylamine

Lewis; Reddy; Bassani; Schneider; Gahr; Journal of the American Chemical Society; vol. 116; nb. 2; (1994); p.

597 - 605, View in Reaxys 12 of 30

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

acetonitrile

Partner (Association (MCS))

triethylamine

Lewis; Reddy; Bassani; Schneider; Gahr; Journal of the American Chemical Society; vol. 116; nb. 2; (1994); p.

597 - 605, View in Reaxys 13 of 30

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

1,16-dimethyldodecahedrane

Santos, Ivan; Balogh, Douglas W.; Doecke, Christopher W.; Marshall, Alan G.; Paquette, Leo A.; Journal of the American Chemical Society; vol. 108; (1986); p. 8183 - 8185, View in Reaxys 14 of 30

Description (Association UV/VIS spectrum of the complex (MCS)) Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Nakahara, Masaru; Uosaki, Yasuhiro; Sasaki, Muneo; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol.

53; nb. 12; (1980); p. 3395 - 3399, View in Reaxys; Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 15 of 30

Description (Association UV/VIS spectrum of the complex (MCS)) Solvent (Association (MCS))

CHCl3

Pressure (Association (MCS)) [Torr]

750.06

Partner (Association (MCS))

ethenetetracarbonitrile

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Tsuzuki, Hideaki; Uosaki, Yasuhiro; Nakahara, Masaru; Sasaki, Muneo; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 5; (1982); p. 1348 - 1351, View in Reaxys 16 of 30

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

(MCS)) Solvent (Association (MCS))

CHCl3

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 17 of 30

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

(MCS)) Solvent (Association (MCS))

CH2Cl2

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 18 of 30

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

(MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 19 of 30

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

(MCS)) Solvent (Association (MCS))

1,2-dichloro-ethane

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 20 of 30

Description (Association UV/VIS spectrum of the complex (MCS)) Solvent (Association (MCS))

CHCl3

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys

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21 of 30

Description (Association UV/VIS spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 22 of 30

Description (Association UV/VIS spectrum of the complex (MCS)) Solvent (Association (MCS))

1,2-dichloro-ethane

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 23 of 30

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

CHCl3

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 24 of 30

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

CH2Cl2

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 25 of 30

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

CCl4

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 26 of 30

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

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Solvent (Association (MCS))

1,2-dichloro-ethane

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 41 - 44, View in Reaxys 27 of 30

Description (Association UV/VIS spectrum of the complex (MCS)) Solvent (Association (MCS))

CHCl3

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Sasaki, Muneo; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol.

54; nb. 10; (1981); p. 2893 - 2897, View in Reaxys 28 of 30

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

(MCS)) Solvent (Association (MCS))

CHCl3

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Sasaki, Muneo; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol.

54; nb. 10; (1981); p. 2893 - 2897, View in Reaxys 29 of 30

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

(MCS)) Solvent (Association (MCS))

1,2-dichloro-ethane

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ethenetetracarbonitrile

Uosaki, Yasuhiro; Nakahara, Masaru; Sasaki, Muneo; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol.

54; nb. 10; (1981); p. 2893 - 2897, View in Reaxys 30 of 30

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

(MCS)) Bogomolova et al.; Polymer Science U.S.S.R; vol. 14; (1972); p. 2587; ; p. 2210, View in Reaxys

Chromatographic Data (5) Chromatographic Location data

References

GC (Gas chroma- supporting infortography) mation

Geer, Michael F.; Walla, Michael D.; Solntsev, Kyril M.; Strassert, Cristian A.; Shimizu, Linda S.; Journal of Organic Chemistry; vol. 78; nb. 11; (2013); p. 5568 - 5578, View in Reaxys; Hartog, Tim Den; Toro, Juan Manuel Sarria; Chen, Peter; Organic Letters; vol. 16; nb. 4; (2014); p. 1100 - 1103, View in Reaxys; Hajnal, Ivan; Faber, Kurt; Schwab, Helmut; Hall, Mlanie; Steiner, Kerstin; Advanced Synthesis and Catalysis; vol. 357; nb. 14-15; (2015); p. 3309 - 3316, View in Reaxys

TLC (Thin layer chromatography)

Friedfeld, Max R.; Margulieux, Grant W.; Schaefer, Brian A.; Chirik, Paul J.; Journal of the American Chemical Society; vol. 136; nb. 38; (2014); p. 13178 - 13181, View in Reaxys

supporting information

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TLC (Thin layer chromatography) HPLC (High performance liquid chromatography)

Li, Xiaoyong; Shen, Qinchao; Zhang, Guangbin; Zhang, Donghua; Zheng, Aqun; Guan, Fang; Sun, Yang; Catalysis Communications; vol. 41; (2013); p. 126 - 131, View in Reaxys supporting information

GC (Gas chromatography)

Li, Aitao; Liu, Ji; Pham, Son Q.; Li, Zhi; Chemical Communications; vol. 49; nb. 98; (2013); p. 11572 - 11574, View in Reaxys Filip, Miuta R.; Pop, Aurelia; Perhaita, Ioana; Moldovan, Marioara; Trusca, Roxana; Central European Journal of Chemistry; vol. 11; nb. 5; (2013); p. 725 - 735, View in Reaxys

Compressibility (1) Description (Com- References pressibility) Isothermal compressibility

Sasuga, Tsuneo; Kawanishi, Shunichi; Takehisa, Masaaki; Journal of Physical Chemistry; vol. 84; nb. 20; (1980); p. 2595 - 2598, View in Reaxys

Conformation (1) Object of Investi- References gation Conformation

Fateley et al.; Applied Spectroscopy; vol. 22; (1968); p. 650,656, View in Reaxys; Grassian, V. H.; Bernstein, E. R.; Secor, Henry V.; Seeman, Jeffrey I.; Journal of Physical Chemistry; vol. 94; nb. 17; (1990); p.

6691 - 6695, View in Reaxys; Schaefer, Ted; Sebastian, Rudy; Penner, Glenn H.; Canadian Journal of Chemistry; vol. 66; (1988); p. 584 - 590, View in Reaxys; Seeman, Jeffrey I.; Grassian, V. H.; Bernstein, E. R.; Journal of the American Chemical Society; vol. 110; nb. 25; (1988); p. 8542 - 8543, View in Reaxys

Critical Density (1) Critical Density References [g·cm-3] 0.288

Steele; Chirico; Knipmeyer; Nguyen; Journal of Chemical and Engineering Data; vol. 42; nb. 6; (1997); p.

1008 - 1020, View in Reaxys

Critical Pressure (1) Critical Pressure References [Torr] 26627.1

Steele; Chirico; Knipmeyer; Nguyen; Journal of Chemical and Engineering Data; vol. 42; nb. 6; (1997); p.

1008 - 1020, View in Reaxys

Critical Temperature (1) Critical Tempera- References ture [°C] 371.85

Steele; Chirico; Knipmeyer; Nguyen; Journal of Chemical and Engineering Data; vol. 42; nb. 6; (1997); p.

1008 - 1020, View in Reaxys

Crystal Property Description (2) Colour & Other Location Properties

References

colourless

supporting information

Wu, Ji-Cheng; Gong, Lu-Bing; Xia, Yuanzhi; Song, Ren-Jie; Xie, Ye-Xiang; Li, JinHeng; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9909 9913, View in Reaxys; Tripathi, Chandra Bhushan; Mukherjee, Santanu; Angewandte Chemie - International Edition; vol. 52; nb. 32; (2013); p. 8450 - 8453; Angew. Chem.; vol. 125; nb. 32; (2013); p. 8608 - 8611,4, View in Reaxys

colourless

supporting information

Wang, Bin; Wong, O. Andrea; Zhao, Mei-Xin; Shi, Yian; Journal of Organic Chemistry; vol. 73; nb. 24; (2008); p. 9539 - 9543, View in Reaxys; Davi, Michael; Lebel, Helene; Organic Letters; vol. 11; nb. 1; (2009); p. 41 - 44, View in Reaxys; Kesharwani, Tanay; Verma, Akhilesh K.; Emrich, Daniel; Ward, Jeffrey A.; Larock, Richard C.; Organic Letters; vol. 11; nb. 12; (2009); p. 2591 - 2593, View in Reaxys; Flores-Gaspar, Areli; Martin, Ruben; Advanced Synthesis and Catalysis; vol. 353; nb. 8; (2011); p. 1223 1228, View in Reaxys

Dielectric Constant (2) Dielectric ConReferences stant Dreisbach; Advances in Chemistry Series; vol. 15; (1955); p. 160, View in Reaxys 2.46

Briner; Ryffel; Perrottet; Helvetica Chimica Acta; vol. 22; (1939); p. 927,928, 933, View in Reaxys; Dow Chem. Co. bei C.E. Schildknecht; Vinyl and Related Polymers <New York 1952> S. 133, View in Reaxys

Dynamic Viscosity (1)

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Dynamic Viscosity [P]

Temperature (Dynamic Viscosity) [°C]

References

0.0094

20 - 160

Dow Chem. Co. bei C.E. Schildknecht; Vinyl and Related Polymers <New York 1952> S. 133, View in Reaxys

Electrical Data (1) 1 of 1

Description (Electrical Data)

Electrical conductivity

Hayashi et al.; Transactions of the Faraday Society; vol. 63; (1967); p. 1489,1495, View in Reaxys Electrical Moment (5) 1 of 5

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

0.2

Nurok, David; Kleyle, Robert M.; Hajdu, Paul; Ellsworth, Brenda; Myers, Steven S.; Brogan, Terrance M.; Lipkowitz, Kenneth B.; Glen, Robert C.; Analytical Chemistry; vol. 67; nb. 23; (1995); p. 4423 - 4430, View in Reaxys 2 of 5

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ

Arbuzov et al.; Doklady Chemistry; vol. 205; (1972); p. 648; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 205; (1972); p. 1096, View in Reaxys 3 of 5

Description (Electrical Moment)

Dipole moment

Gey; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 823, View in Reaxys; Hala; Chemicky Prumysl; vol. 18; (1968); p. 412; Chem.Abstr.; vol. 69; nb. 83193; (1968), View in Reaxys 4 of 5

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

0.77 D

Kokoschko et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 37; (1967); p. 58,51, View in Reaxys 5 of 5

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

0.75

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

benzene

Briner; Ryffel; Perrottet; Helvetica Chimica Acta; vol. 22; (1939); p. 927,928, 933, View in Reaxys Electrical Polarizability (1) Description (Elec- References trical Polarizability) Molar polarization Kawabata,N. et al.; Bulletin of the Chemical Society of Japan; vol. 36; (1963); p. 1168 - 1172, View in Reaxys Electrochemical Behaviour (2) Description (Elec- References trochemical Behaviour) Electrochemical properties

Schaefer,H.; Al Azrak,A.; Chemische Berichte; vol. 105; (1972); p. 2398 - 2418, View in Reaxys; Engels,R. et al.; Justus Liebigs Annalen der Chemie; (1977); p. 204 - 224, View in Reaxys; Hanazaki; Nagakura; Tetrahedron; vol. 21; (1965); p. 2441,2442, View in Reaxys

Polarography

Bezuglyi; Ponomarev; J. Anal. Chem. USSR (Engl. Transl.); vol. 22; (1967); p. 422,369, View in Reaxys

Electrochemical Characteristics (9)

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1 of 9

Description (Electrochemical Characteristics)

voltammetry

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

24.84

Location

supporting information

Comment (Electrochem- transmitted electrons 1; 1.41 V; Saturated silver chloride electrode; potential diagram; 0.10 ical Characteristics) M tetrabutylammonium hexafluorophosphine Park, Jiyun; Lee, Yong-Min; Ohkubo, Kei; Nam, Wonwoo; Fukuzumi, Shunichi; Inorganic Chemistry; vol. 54; nb. 12; (2015); p. 5806 - 5812, View in Reaxys 2 of 9

Description (Electrochemical Characteristics)

Electrochemical characteristics given

Lu, Zhi-Feng; Shen, Yong-Miao; Yue, Jia-Jun; Hu, Hong-Wen; Xu, Jian-Hua; Journal of Organic Chemistry; vol.

73; nb. 20; (2008); p. 8010 - 8015, View in Reaxys 3 of 9

Description (Electrochemical Characteristics)

oxidation potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

24.85

Zhang, Min; Lu, Zhi-Feng; Liu, Yun; Grampp, Guenter; Hu, Hong-Wen; Xu, Jian-Hua; Tetrahedron; vol. 62; nb.

24; (2006); p. 5663 - 5674, View in Reaxys 4 of 9

Description (Electrochemical Characteristics)

oxidation potential

Solvent (Electrochemical Characteristics)

acetonitrile

Jia, Xiaodong; Lin, Hechun; Huo, Congde; Zhang, Wei; Lue, Jianming; Yang, Li; Zhao, Guangyu; Liu, ZhongLi; Synlett; nb. 11; (2003); p. 1707 - 1709, View in Reaxys; Huo, Congde; Jia, Xiaodong; Zhang, Wei; Yang, Li; Lue, Jianming; Liu, Zhong-Li; Synlett; nb. 2; (2004); p. 251 - 254, View in Reaxys; Suga, Kyou; Ohkubo, Kei; Fukuzumi, Shunichi; Journal of Physical Chemistry A; vol. 107; nb. 22; (2003); p. 4339 - 4346, View in Reaxys; Shiraishi, Yasuhiro; Saito, Naoya; Hirai, Takayuki; Chemical Communications; nb. 7; (2006); p. 773 - 775, View in Reaxys 5 of 9

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Yamamoto, Yoshimasa; Maekawa, Hirofumi; Goda, Satoshi; Nishiguchi, Ikuzo; Organic Letters; vol. 5; nb. 15; (2003); p. 2755 - 2758, View in Reaxys 6 of 9

Description (Electrochemical Characteristics)

reduction potential

Senboku; Komatsu; Fujimura; Tokuda; Synlett; nb. 3; (2001); p. 418 - 420, View in Reaxys 7 of 9

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochem- 1.85 V; Type: Irreversible half-wave potential. Product: /BRN= 3537431/. No. of transm. ical Characteristics) electrons: 1. Method: potentiometry. Description: SCE

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Product

α-methyl-styrene radical cation

Schepp, Norman P.; Johnston, Linda J.; Journal of the American Chemical Society; vol. 118; nb. 12; (1996); p.

2872 - 2881, View in Reaxys 8 of 9

Description (Electrochemical Characteristics)

oxidation potential

Lewis, Frederick D.; Bassani, Dario M.; Reddy, G. Dasharatha; Journal of Organic Chemistry; vol. 58; nb. 23; (1993); p. 6390 - 6393, View in Reaxys; Lopez, Luigi; Calo, Vincenzo; Journal of the Chemical Society, Chemical Communications; nb. 19; (1984); p. 1266 - 1268, View in Reaxys 9 of 9

Description (Electrochemical Characteristics)

polarographic half-wave potential

Mushina et al.; European Polymer Journal; vol. 15; (1979); p. 99, View in Reaxys; Korunova et al.; J. Gen. Chem.

USSR (Engl. Transl.); vol. 40; (1970); p. 1452,1439, View in Reaxys; Mizuno et al.; Journal of the Chemical Society, Chemical Communications; (1978); p. 594, View in Reaxys; Yamazaki et al.; Kogyo Kagaku Zasshi; vol. 70; (1967); p. 1978,1979, 1981, View in Reaxys Electron Binding (1) Description (Elec- References tron Binding) Electron affinity

Gey; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 823, View in Reaxys

Energy Barriers (2) Energy Barriers Barrier Type [Jmol-1] 17579.1

Ph-C

Solvent (Energy Barriers)

References

methylcyclohexane

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 8; (2003); p. 2046 - 2047, View in Reaxys Polowoi et al.; Voprosy Stereokhimii; vol. 3; (1973); p. 51; Chem.Abstr.; vol. 81; nb. 143566; (1974), View in Reaxys

Energy Data (MCS) (8) 1 of 8

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25 - 40

Partner (Energy Data (MCS))

methanol

Malijevska; Oswald; Heintz; Journal of Chemical Thermodynamics; vol. 28; nb. 11; (1996); p. 1247 - 1253, View in Reaxys 2 of 8

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

ethanol

Malijevska; Oswald; Heintz; Journal of Chemical Thermodynamics; vol. 28; nb. 11; (1996); p. 1247 - 1253, View in Reaxys 3 of 8

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

propan-1-ol

Malijevska; Oswald; Heintz; Journal of Chemical Thermodynamics; vol. 28; nb. 11; (1996); p. 1247 - 1253, View in Reaxys 4 of 8

Description (Energy Data (MCS))

Enthalpy of mixing

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Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

AsCl3

Tsvetkov, V. G.; Krylov, V. A.; Nikolaev, A. E.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 3; (1984); p. 574 577,506 - 508, View in Reaxys 5 of 8

Description (Energy Data (MCS))

Enthalpy of solution

Fuchs; Rodewald; Journal of the American Chemical Society; vol. 95; (1973); p. 5897,5898, View in Reaxys; Mel'nikova; Korol'; Theoretical and Experimental Chemistry; vol. 6; (1970); p. 62; ; p. 72, View in Reaxys 6 of 8

Description (Energy Data (MCS))

Thermodynamic properties of system with

Yoshida; Ishibe; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p.

893,896, View in Reaxys; Schtscherbak et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 29; (1956); p. 353,391, View in Reaxys 7 of 8

Description (Energy Data (MCS))

Enthalpy of mixing

Canagaratna et al.; Transactions of the Faraday Society; vol. 62; (1966); p. 3058,3059,3061, View in Reaxys 8 of 8

Description (Energy Data (MCS))

Heat capacity of mixtures

Partner (Energy Data (MCS))

1-methyl-4-isopropenylbenzene

Walling; Seymour; Wolfstirn; Journal of the American Chemical Society; vol. 70; (1948); p. 1544,1546, View in Reaxys Enthalpy of Combustion (3) Enthalpy of Com- Temperature (Enbustion [Jmol-1] thalpy of Combustion) [°C]

Comment (Enthalpy of Combustion)

References

Krall; Roberts; Preprints - American Chemical Society, Division of Petroleum Chemistry; vol. 3; nb. 4; (1958); p. B63,B64; Chem.Abstr.; nb. 23511; (1960), View in Reaxys -5.0445E+06 -5.08712E+06

25

Enthalpy of Formation (2) Enthalpy of ForTemperature (Enmation [Jmol-1] thalpy of Formation) [°C] 115300

24.9

Standard.

Roberts; Jessup; Journal of Research of the National Bureau of Standards (United States); vol. 46; (1951); p. 11,14, View in Reaxys

unter konstantem Druck.

Rossini; Selected Values 1953 S. 463, View in Reaxys

References

Abboud, Jose-Luis M.; Jimenez, Pilar; Roux, M. Victoria; Turrion, Concepcion; Lopez-Mardomingo, Carmen; et al.; Journal of Physical Organic Chemistry; vol. 8; (1995); p. 15 - 25, View in Reaxys Guthrie; Canadian Journal of Chemistry; vol. 56; (1978); p. 962,965, View in Reaxys; Polowoi et al.; Voprosy Stereokhimii; vol. 3; (1973); p. 51; Chem.Abstr.; vol. 81; nb.

143566; (1974), View in Reaxys

Enthalpy of Hydrogenation (1) Enthalpy of HyTemperature (Endrogenation thalpy of Hydro[Jmol-1] genation) [°C]

Product Name

References

-111300

cumol

Abboud, Jose-Luis M.; Jimenez, Pilar; Roux, M. Victoria; Turrion, Concepcion; Lopez-Mardomingo, Carmen; et al.; Journal of Physical Organic Chemistry; vol. 8; (1995); p. 15 - 25, View in Reaxys

24.9

Further Information (34) Description (Fur- References ther Information)

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Further information

Baltes,H. et al.; Liebigs Annalen der Chemie; (1979); p. 318 - 327, View in Reaxys

Further information

Van der Greef; Nibbering; Organic Mass Spectrometry; vol. 14; (1979); p. 537,540, 541, View in Reaxys

Further information

Mushina et al.; European Polymer Journal; vol. 15; (1979); p. 99, View in Reaxys

Further information

Perrier-Datin; Lebas; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 76; (1979); p. 935, View in Reaxys

Further information

Mizuno et al.; Journal of the Chemical Society, Chemical Communications; (1978); p. 594, View in Reaxys

Further information

Bertucci et al.; Journal of Chemical Physics; vol. 66; (1977); p. 605,612, View in Reaxys

Further information

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

Further information

Hayashi et al.; Journal of Physical Chemistry; vol. 80; (1976); p. 2807, View in Reaxys

Further information

Jones; McDonnell; Tetrahedron Letters; (1975); p. 4633, View in Reaxys

Further information

Tancheva et al.; Bulletin de la Societe Chimique de France; (1974); p. 1033, View in Reaxys

Further information

Khvostenko et al.; Theoretical and Experimental Chemistry; vol. 9; (1973); p. 406,410, View in Reaxys

Further information

Bulkin et al.; Analytical Chemistry; vol. 43; (1971); p. 974,975, View in Reaxys

Further information

Korunova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 40; (1970); p. 1452,1439, View in Reaxys

Further information

Rasuwaew et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 39; (1969); p. 123,110, View in Reaxys

Further information

Brown; Butcher; Australian Journal of Chemistry; vol. 22; (1969); p. 1457,1468, View in Reaxys

Further information

Comyn; Irin; European Polymer Journal; vol. 5; (1969); p. 587,588,589,593, View in Reaxys

Further information

Schoellkopf; Gerhart; Angewandte Chemie; vol. 80; (1968); p. 842, View in Reaxys

Further information

Moreno Manas; Pascual Vila; Anales de Quimica (1968-1979); vol. 64; (1968); p. 993, View in Reaxys

Further information

Ullman; Henderson; Journal of the American Chemical Society; vol. 89; (1967); p. 4390,4391, View in Reaxys

Further information

Zaitsev; Organic Reactivity (New York, English Translation); vol. 4; (1967); p. 145,146, View in Reaxys

Further information

Mollard et al.; Bulletin de la Societe Chimique de France; (1966); p. 83,87, View in Reaxys

Further information

Minisci; Galli; Chimica e l'Industria (Milan, Italy); vol. 47; (1965); p. 178, View in Reaxys

Further information

Iino; Tokura; Bulletin of the Chemical Society of Japan; vol. 38; (1965); p. 1094, View in Reaxys

Further information

Goldstein; Amundson; Chemical Engineering Science; vol. 20; (1965); p. 195,207, View in Reaxys

Further information

Vigdergauz; Chabrova; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 1549,1514,1515, View in Reaxys

Further information

Safranskii et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 37; (1964); p. 230,241, View in Reaxys

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Further information

Besuglyi et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 19; (1964); p. 881,817, View in Reaxys

Further information

Poljanskii et al.; Neftekhimiya; vol. 3; (1963); p. 144; Neftekhimiya; vol. 3; (1963); p. 348, View in Reaxys

Further information

Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys

Further information

Belomestrich et al.; Neftekhimiya; vol. 2; (1962); p. 467; ; p. 341, View in Reaxys

Further information

Polyanskii et al.; Neftekhimiya; vol. 2; (1962); p. 348, View in Reaxys

Further information

Lewina et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1185,1096; Chem.Abstr.; nb. 25809; (1961), View in Reaxys

Further information

Wiberley et al.; Analytical Chemistry; vol. 32; (1960); p. 217,219, View in Reaxys

Further information

Morigaki et al.; Bulletin of the Chemical Society of Japan; vol. 33; (1960); p. 958,960, View in Reaxys

Heat Capacity Cp0 (1) Heat Capacity Temperature Cp0 [Jmol-1K-1] (Heat Capacity Cp0) [°C] 145.28 - 383.51

25 - 1227

References

Beckett; Pitzer; Journal of the American Chemical Society; vol. 68; (1946); p. 2213, View in Reaxys; Dow Chem. Co. bei C.E. Schildknecht; Vinyl and Related Polymers <New York 1952> S. 133, View in Reaxys; Rossini; Selected Values 1953 S. 534, 556, 578, 651, View in Reaxys; Kilpatrick et al.; Journal of Research of the National Bureau of Standards (United States); vol. 42; (1949); p. 225,229, View in Reaxys

Interatomic Distances and Angles (2) Description References Electron distribution

Engels,R. et al.; Justus Liebigs Annalen der Chemie; (1977); p. 204 - 224, View in Reaxys; Gey; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 823, View in Reaxys; Polowoi et al.; Voprosy Stereokhimii; vol. 3; (1973); p. 51; Chem.Abstr.; vol. 81; nb. 143566; (1974), View in Reaxys

Interatomic distances and angles

Maier; Turner; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 69; (1973); p. 196, View in Reaxys

Ionization Potential (6) Ionization Poten- Method (Ionizatial [eV] tion Potential)

Comment (Ioniza- References tion Potential)

8.5

Photoionization

Type: not given.

Higher potentials: IP2 = 9.24 eV; IP3 = 10.14 eV

Opeida, Iosyp O.; Suprun, Wolodymyr Ya.; Journal of the Chemical Society. Perkin Transactions 2; nb. 6; (2000); p. 1273 - 1279, View in Reaxys

8.5

PE

Type: vertical

Suprun; Journal fuer Praktische Chemie - Practical Applications and Applied Chemistry (Germany); vol. 341; nb. 1; (1999); p. 52 - 58, View in Reaxys

8.5

PE

Higher potentials: Opeida; Suprun; Dmitruk; Russian Journal of Physical Chemistry A; 9.24, 10.14, 11.24 vol. 72; nb. 9; (1998); p. 1481 - 1486, View in Reaxys eV

8.4

Electron impact

Type: vertical

8.27

spectrographical

Stavber, Stojan; Sotler, Tjasa; Zupan, Marko; Popovic, Arkadij; Journal of Organic Chemistry; vol. 59; nb. 20; (1994); p. 5891 - 5894, View in Reaxys Samuilov, Ya. D.; Gainullin, V. I.; Solov'eva, S. E.; Konovalov, A. I.; Journal of Organic Chemistry USSR (English Translation); vol. 24; (1988); p. 717 - 724; Zhurnal Organicheskoi Khimii; vol. 24; nb. 4; (1988); p. 795 - 803, View in Reaxys Ishigami,T. et al.; Journal of the Chemical Society, Chemical Communications; (1978); p. 786 - 788, View in Reaxys; Jones; McDonnell; Tetrahedron Letters; (1975); p. 4633, View in Reaxys; Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys; Gey; Journal

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fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 823, View in Reaxys; Koeppel et al.; Organic Mass Spectrometry; vol. 8; (1974); p. 25,26, View in Reaxys; Strasak; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 33; (1978); p. 224, View in Reaxys; Maier; Turner; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 69; (1973); p. 196, View in Reaxys Liquid/Liquid Systems (MCS) (2) 1 of 2

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

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

50 - 60

Partner (Liquid/Liquid Systems (MCS))

acetone

Mafra, Marcos R.; Kraehenbuehl, Maria A.; Journal of Chemical and Engineering Data; vol. 51; nb. 2; (2006); p.

753 - 756, View in Reaxys 2 of 2

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O

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

24.9

Partner (Liquid/Liquid Systems (MCS))

octanol

Buchviser, Silmara F.; Gehlen, Marcelo H.; Journal of the Chemical Society - Faraday Transactions; vol. 93; nb. 6; (1997); p. 1133 - 1139, View in Reaxys Liquid/Solid Systems (MCS) (1) 1 of 1

Description (Liquid/Solid Melting diagram Systems (MCS)) Makitra; Tsikanchuk; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 2582,2564,2565, View in Reaxys

Liquid/Vapour Systems (MCS) (20) 1 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

1-indene; styrene

Prikhod'ko; Komarova; Gorelova; Gorlova; Bondaletov; Russian Journal of Applied Chemistry; vol. 78; nb. 3; (2005); p. 399 - 403, View in Reaxys 2 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

styrene

Prikhod'ko; Komarova; Gorelova; Gorlova; Bondaletov; Russian Journal of Applied Chemistry; vol. 78; nb. 3; (2005); p. 399 - 403, View in Reaxys 3 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

bi(cyclopentadiene)

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Prikhod'ko; Komarova; Gorelova; Gorlova; Bondaletov; Russian Journal of Applied Chemistry; vol. 78; nb. 3; (2005); p. 399 - 403, View in Reaxys 4 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

1-indene

Prikhod'ko; Komarova; Gorelova; Gorlova; Bondaletov; Russian Journal of Applied Chemistry; vol. 78; nb. 3; (2005); p. 399 - 403, View in Reaxys 5 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

o-xylene

Prikhod'ko; Komarova; Gorelova; Gorlova; Bondaletov; Russian Journal of Applied Chemistry; vol. 78; nb. 3; (2005); p. 399 - 403, View in Reaxys 6 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 756.06 - 762.061 Systems (MCS)) [Torr] Comment (Liquid/ concentration dependence Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

phenol

Aristovich; Sokolov; Fulmer; Russian Journal of Applied Chemistry; vol. 76; nb. 2; (2003); p. 195 - 197, View in Reaxys 7 of 20

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 49.95 - 80.95 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide

Heintz, Andreas; Kulikov, Dmitry D.; Verevkin, Sergey P.; Journal of Chemical and Engineering Data; vol. 47; nb.

4; (2002); p. 894 - 899, View in Reaxys 8 of 20

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 60.15 - 91.25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-Ethyl-2-methyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)amide

Heintz, Andreas; Kulikov, Dmitry D.; Verevkin, Sergey P.; Journal of Chemical and Engineering Data; vol. 47; nb.

4; (2002); p. 894 - 899, View in Reaxys 9 of 20

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 60.18 - 90.21 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

4-methyl-N-butylpyridinium tetrafluoroborate

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Heintz, Andreas; Kulikov, Dmitry V.; Verevkin, Sergey P.; Journal of Chemical and Engineering Data; vol. 46; nb.

6; (2001); p. 1526 - 1529, View in Reaxys 10 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 62.6 - 66.6 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 20.03 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

1,2-epoxy-7-octene

Emel'yanov, A. O.; Mel'nik, L. V.; Bobylev, B. N.; Danilova, A. S.; J. Appl. Chem. USSR (Engl. Transl.); vol. 63; nb. 9.2; (1990); p. 2090 - 2093,1932 - 1934, View in Reaxys 11 of 20

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 62.6 - 66.6 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 20.03 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

1,2-epoxy-7-octene

Emel'yanov, A. O.; Mel'nik, L. V.; Bobylev, B. N.; Danilova, A. S.; J. Appl. Chem. USSR (Engl. Transl.); vol. 63; nb. 9.2; (1990); p. 2090 - 2093,1932 - 1934, View in Reaxys 12 of 20

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 - 40 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tetrahydrofuran

Bui, Van Tam; Leonard, Jacques; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 81; (1985); p. 1745 - 1754, View in Reaxys 13 of 20

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 22.5 - 99 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

acetone

Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 2; (1983); p. 192 - 196, View in Reaxys 14 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 22.5 - 99 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

acetone

Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 2; (1983); p. 192 - 196, View in Reaxys 15 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS))

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Laevskaya et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 52; (1979); p. 687,649, View in Reaxys; Mozgovaya et al.; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 276; ; p. 485, View in Reaxys; Beregovykh et al.; Russian Journal of Physical Chemistry; vol. 51; (1977); p. 272; ; p. 470, View in Reaxys 16 of 20

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Canagaratna et al.; Transactions of the Faraday Society; vol. 62; (1966); p. 3058,3059,3061, View in Reaxys

17 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Comment (Liquid/ bzw. 50 Torr; im ternaeren System.

Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

water; phenol

Schtscherback et al.; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol. 29; (1956); p. 353,359; engl. Ausg. S. 391, 396, View in Reaxys 18 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 50 Systems (MCS)) [Torr] Comment (Liquid/ im ternaeren System.

Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

water; phenol

Byk et al.; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol. 29; (1956); p. 1380; engl. Ausg. S. 2023, View in Reaxys; Schtscherback et al.; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol.

29; (1956); p. 353,359; engl. Ausg. S. 391, 396, View in Reaxys 19 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

cumol; phenol

Byk; Stroitelewa; Zhurnal Fizicheskoi Khimii; vol. 30; (1956); p. 2451,2454; Chem.Abstr.; (1957); p. 9246, View in Reaxys 20 of 20

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 760 Systems (MCS)) [Torr] Comment (Liquid/ im binaeren System.

Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

phenol

Schtscherbak et al.; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol. 28; (1955); p.

1120,1122; engl. Ausg. S. 1075, 1077, View in Reaxys Mechanical & Physical Properties (MCS) (4) 1 of 4

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25

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Partner (Mechanical & Physical Properties (MCS))

1,2-dichloro-ethane

Uosaki, Yasuhiro; Nakahara, Masaru; Sasaki, Muneo; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol.

54; nb. 10; (1981); p. 2893 - 2897, View in Reaxys 2 of 4

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25

Partner (Mechanical & Physical Properties (MCS))

dichloromethane

Uosaki, Yasuhiro; Nakahara, Masaru; Sasaki, Muneo; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol.

54; nb. 10; (1981); p. 2893 - 2897, View in Reaxys 3 of 4

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25

Partner (Mechanical & Physical Properties (MCS))

chloroform

Uosaki, Yasuhiro; Nakahara, Masaru; Sasaki, Muneo; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol.

54; nb. 10; (1981); p. 2893 - 2897, View in Reaxys 4 of 4

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25

Partner (Mechanical & Physical Properties (MCS))

tetrachloromethane

Uosaki, Yasuhiro; Nakahara, Masaru; Sasaki, Muneo; Osugi, Jiro; Bulletin of the Chemical Society of Japan; vol.

54; nb. 10; (1981); p. 2893 - 2897, View in Reaxys Mechanical Properties (2) Description (MeReferences chanical Properties) Molar volume

Makitra; Tsikanchuk; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 2582,2564,2565, View in Reaxys; Nurok, David; Kleyle, Robert M.; Lipkowitz, Kenneth B.; Myers, Steven S.; Kearns, Michelle L.; Analytical Chemistry; vol. 65; nb. 24; (1993); p. 3701 - 3707, View in Reaxys

Viscosity

Makitra; Tsikanchuk; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 2582,2564,2565, View in Reaxys

Optics (3) Description (Optics)

Comment (Optics)

References

Magnetorotation

Castan et al.; Tetrahedron; vol. 35; (1979); p. 1093,1095, View in Reaxys

Electric birefringence (Kerr effect)

Britton et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p.

2100, View in Reaxys; Arbuzov et al.; Doklady Chemistry; vol. 205; (1972); p. 648; Dokl.

Akad. Nauk SSSR Ser. Khim.; vol. 205; (1972); p. 1096, View in Reaxys

Crystal refractive indices

im Temperaturbereich von

Dow Chem. Co. bei C.E. Schildknecht; Vinyl and Related Polymers <New York 1952> S. 133, View in Reaxys

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20grad bis 35grad.

Other Thermochemical Data (4) Description (Oth- Comment (Other er Thermochemi- Thermochemical cal Data) Data)

References

Thermodynamic properties

Laevskaya et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 52; (1979); p. 687,649, View in Reaxys; Crosby et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1977); p. 182,183-184, View in Reaxys; Cordoba et al.; Journal of Magnetic Resonance (1969-1992); vol. 6; (1972); p. 570, View in Reaxys

Enthalpy

Worsfold; Bywater; Journal of Polymer Science; vol. 26; (1957); p. 299, View in Reaxys; Makitra; Tsikanchuk; J. Gen. Chem. USSR (Engl. Transl.); vol. 43; (1973); p. 2582,2564,2565, View in Reaxys; Holroyd; Berichte der Bunsen-Gesellschaft; vol. 81; (1977); p. 298,300, View in Reaxys

Entropy

Holroyd; Berichte der Bunsen-Gesellschaft; vol. 81; (1977); p. 298,300, View in Reaxys

Heat of combustion at constant volume

1203,1 kcal/Mol.

Lemoult; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 152; (1911); p. 1402, View in Reaxys; Auwers; Roth; Eisenlohr; Justus Liebigs Annalen der Chemie; vol. 385; (1911); p. 107; Justus Liebigs Annalen der Chemie; vol.

373; (1910); p. 273, View in Reaxys

Solubility (MCS) (1) 1 of 1

Comment (Solubility (MCS))

poor solubility in H2O

Shimakoshi, Hisashi; Hisaeda, Yoshio; ChemPlusChem; vol. 79; nb. 9; (2014); p. 1250 - 1253, View in Reaxys Solution Behaviour (MCS) (3) 1 of 3

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Behaviour (MCS)) [°C]

34.85 - 49.85

Pressure (Solution Behaviour (MCS)) [Torr]

7500.6 - 97507.8

Partner (Solution Behaviour (MCS))

H2

Phiong, Hon-Sang; Lucien, Frank P.; Journal of Chemical and Engineering Data; vol. 47; nb. 3; (2002); p. 474 477, View in Reaxys 2 of 3

Description (Solution Behaviour (MCS))

Dissolving capacity

Herskowitz et al.; Journal of Chemical and Engineering Data; vol. 23; (1978); p. 227,228, View in Reaxys; Muchnik et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 48; (1975); p. 1322,1373, View in Reaxys 3 of 3

Description (Solution Behaviour (MCS))

Mutual solubility

Solvent (Solution Behaviour (MCS))

H2O

Dow Chem. Co. bei C.E. Schildknecht; Vinyl and Related Polymers <New York 1952> S. 133, View in Reaxys Surface Tension (1) Surface Tension Temperature [g·s-2] (Surface Tension) [°C] 31.99

20

Vapour Pressure (4) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C] 15.0162 1074.31

57.8 - 179.3

References

Woronkow; Broun; Karpenko; Zhurnal Obshchei Khimii; vol. 19; (1949); p. 1927,1939; Chem.Abstr.; (1950); p. 1955, View in Reaxys Comment (Vapour Pressure)

References

Table exists

Steele; Chirico; Knipmeyer; Nguyen; Journal of Chemical and Engineering Data; vol. 42; nb. 6; (1997); p. 1008 - 1020, View in Reaxys

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2.513 - 95.505

22.5 - 99

Muthu, Ol; Munjal, Sarat; Smith, Buford D.; Journal of Chemical & Engineering Data; vol. 28; nb. 2; (1983); p. 192 - 196, View in Reaxys Mozgovaya et al.; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 276; ; p. 485, View in Reaxys; Canagaratna et al.; Transactions of the Faraday Society; vol. 62; (1966); p. 3058,3059,3061, View in Reaxys

1.9

20

Dow Chem. Co. bei C.E. Schildknecht; Vinyl and Related Polymers <New York 1952> S. 133, View in Reaxys

NMR Spectroscopy (68) 1 of 68

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

1H

Solvents (NMR Spectro- [D3]acetonitrile scopy) Temperature (NMR Spectroscopy) [°C]

24.84

Location

supporting information

Park, Jiyun; Lee, Yong-Min; Ohkubo, Kei; Nam, Wonwoo; Fukuzumi, Shunichi; Inorganic Chemistry; vol. 54; nb. 12; (2015); p. 5806 - 5812, View in Reaxys 2 of 68

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

1H

Temperature (NMR Spectroscopy) [°C]

25

Frequency (NMR Spectroscopy) [MHz]

400

Ouardad, Samira; Wirotius, Anne-Laure; Kostjuk, Sergei; Ganachaud, Franois; Peruch, Frdric; RSC Advances; vol. 5; nb. 73; (2015); p. 59218 - 59225, View in Reaxys 3 of 68

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

1H

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

400

Location

supporting information

Davi, Michael; Lebel, Helene; Organic Letters; vol. 11; nb. 1; (2009); p. 41 - 44, View in Reaxys; Dong, Jia Jia; Harvey, Emma C.; Faans-Mastral, Martn; Browne, Wesley R.; Feringa, Ben L.; Journal of the American Chemical Society; vol. 136; nb. 49; (2014); p. 17302 - 17307, View in Reaxys 4 of 68

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

Kuschel, Andreas; Polarz, Sebastian; Journal of the American Chemical Society; vol. 132; nb. 18; (2010); p. 6558 - 6565, View in Reaxys; Intrieri, Daniela; Le Gac, Stephane; Caselli, Alessandro; Rose, Eric; Boitrel, Bernard; Gallo, Emma; Chemical Communications; vol. 50; nb. 15; (2014); p. 1811 - 1813, View in Reaxys

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5 of 68

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

1H

Solvents (NMR Spectro- [(2)H6]acetone scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Dong, Jia Jia; Harvey, Emma C.; Faans-Mastral, Martn; Browne, Wesley R.; Feringa, Ben L.; Journal of the American Chemical Society; vol. 136; nb. 49; (2014); p. 17302 - 17307, View in Reaxys 6 of 68

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

1H

Coupling Nuclei

1H

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

21.84

Frequency (NMR Spectroscopy) [MHz]

500

Location

supporting information

Friedfeld, Max R.; Margulieux, Grant W.; Schaefer, Brian A.; Chirik, Paul J.; Journal of the American Chemical Society; vol. 136; nb. 38; (2014); p. 13178 - 13181, View in Reaxys 7 of 68

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

13C

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

21.84

Frequency (NMR Spectroscopy) [MHz]

126

Location

supporting information

Friedfeld, Max R.; Margulieux, Grant W.; Schaefer, Brian A.; Chirik, Paul J.; Journal of the American Chemical Society; vol. 136; nb. 38; (2014); p. 13178 - 13181, View in Reaxys 8 of 68

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

1H

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

26.84

Frequency (NMR Spectroscopy) [MHz]

400.1

Location

supporting information

Doni, Eswararao; O'Sullivan, Steven; Murphy, John A.; Angewandte Chemie - International Edition; vol. 52; nb.

8; (2013); p. 2239 - 2242; Angew. Chem.; vol. 125; nb. 8; (2013); p. 2295 - 2298,4, View in Reaxys

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9 of 68

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

13C

Coupling Nuclei

19F

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

26.84

Frequency (NMR Spectroscopy) [MHz]

100.6

Location

supporting information

Doni, Eswararao; O'Sullivan, Steven; Murphy, John A.; Angewandte Chemie - International Edition; vol. 52; nb.

8; (2013); p. 2239 - 2242; Angew. Chem.; vol. 125; nb. 8; (2013); p. 2295 - 2298,4, View in Reaxys 10 of 68

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

Tripathi, Chandra Bhushan; Mukherjee, Santanu; Angewandte Chemie - International Edition; vol. 52; nb. 32; (2013); p. 8450 - 8453; Angew. Chem.; vol. 125; nb. 32; (2013); p. 8608 - 8611,4, View in Reaxys 11 of 68

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

Tripathi, Chandra Bhushan; Mukherjee, Santanu; Angewandte Chemie - International Edition; vol. 52; nb. 32; (2013); p. 8450 - 8453; Angew. Chem.; vol. 125; nb. 32; (2013); p. 8608 - 8611,4, View in Reaxys 12 of 68

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

Flores-Gaspar, Areli; Martin, Ruben; Advanced Synthesis and Catalysis; vol. 353; nb. 8; (2011); p. 1223 - 1228, View in Reaxys; Wu, Ji-Cheng; Gong, Lu-Bing; Xia, Yuanzhi; Song, Ren-Jie; Xie, Ye-Xiang; Li, Jin-Heng; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9909 - 9913, View in Reaxys 13 of 68

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

13C

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

125

Location

supporting information

Wu, Ji-Cheng; Gong, Lu-Bing; Xia, Yuanzhi; Song, Ren-Jie; Xie, Ye-Xiang; Li, Jin-Heng; Angewandte Chemie International Edition; vol. 51; nb. 39; (2012); p. 9909 - 9913, View in Reaxys 14 of 68

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

Flores-Gaspar, Areli; Martin, Ruben; Advanced Synthesis and Catalysis; vol. 353; nb. 8; (2011); p. 1223 - 1228, View in Reaxys 15 of 68

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

1H

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

-50

Frequency (NMR Spectroscopy) [MHz]

300

Howard, Fredrick; Sawadjoon, Supaporn; Samec, Joseph S.M.; Tetrahedron Letters; vol. 51; nb. 32; (2010); p.

4208 - 4210, View in Reaxys 16 of 68

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

1H

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

25

Frequency (NMR Spectroscopy) [MHz]

400

Tse, Sunny Kai San; Xue, Peng; Lin, Zhenyang; Jia, Guochen; Advanced Synthesis and Catalysis; vol. 352; nb.

9; (2010); p. 1512 - 1522, View in Reaxys 17 of 68

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

1H

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

25

Frequency (NMR Spectroscopy) [MHz]

360

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Prusek, Ondrej; Bures, Filip; Pytela, Oldrich; Collection of Czechoslovak Chemical Communications; vol. 74; nb.

1; (2009); p. 85 - 99, View in Reaxys 18 of 68

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

Davi, Michael; Lebel, Helene; Organic Letters; vol. 11; nb. 1; (2009); p. 41 - 44, View in Reaxys 19 of 68

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

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

300

Location

supporting information

Davi, Michael; Lebel, Helene; Organic Letters; vol. 11; nb. 1; (2009); p. 41 - 44, View in Reaxys 20 of 68

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

1H

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

300

Location

supporting information

Kesharwani, Tanay; Verma, Akhilesh K.; Emrich, Daniel; Ward, Jeffrey A.; Larock, Richard C.; Organic Letters; vol. 11; nb. 12; (2009); p. 2591 - 2593, View in Reaxys 21 of 68

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

1H

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

17.14

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Wang, Xiao; Chen, Yong-Fei; Niu, Liang-Feng; Xu, Peng-Fei; Organic Letters; vol. 11; nb. 15; (2009); p. 3310 3313, View in Reaxys 22 of 68

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

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Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

299.95

Balagam, Bharathi; Mitra, Ranjan; Richardson, David E.; Tetrahedron Letters; vol. 49; nb. 6; (2008); p. 1071 1075, View in Reaxys 23 of 68

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

1H

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

200

Barbero, Margherita; Cadamuro, Silvano; Dughera, Stefano; Venturello, Paolo; Synthesis; nb. 22; (2008); p.

3625 - 3632, View in Reaxys 24 of 68

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

1H

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

Whitehouse, Christopher J.C.; Bell, Stephen G.; Wong, Luet-Lok; Chemistry - A European Journal; vol. 14; nb.

35; (2008); p. 10905 - 10908, View in Reaxys 25 of 68

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) Fraenkel, Gideon; Geckle, Michael J.; Kaylo, Allan; Estes, Don W.; Journal of Organometallic Chemistry; vol.

197; nb. 3; (1980); p. 249 - 260, View in Reaxys; Lebel, Helene; Davi, Michael; Diez-Gonzalez, Silvia; Nolan, Steven P.; Journal of Organic Chemistry; vol. 72; nb. 1; (2007); p. 144 - 149, View in Reaxys 26 of 68

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

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Haefelinger, Guenter; Knapp, Wolfgang; Zuschneid, Thomas; Dietrich, Frank Peter; Journal of Physical Organic Chemistry; vol. 18; nb. 8; (2005); p. 800 - 817, View in Reaxys; Lebel, Helene; Davi, Michael; Diez-Gonzalez, Silvia; Nolan, Steven P.; Journal of Organic Chemistry; vol. 72; nb. 1; (2007); p. 144 - 149, View in Reaxys 27 of 68

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

400

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Haefelinger, Guenter; Knapp, Wolfgang; Zuschneid, Thomas; Dietrich, Frank Peter; Journal of Physical Organic Chemistry; vol. 18; nb. 8; (2005); p. 800 - 817, View in Reaxys; Lebel, Helene; Davi, Michael; Diez-Gonzalez, Silvia; Nolan, Steven P.; Journal of Organic Chemistry; vol. 72; nb. 1; (2007); p. 144 - 149, View in Reaxys 28 of 68

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Lebel, Helene; Davi, Michael; Diez-Gonzalez, Silvia; Nolan, Steven P.; Journal of Organic Chemistry; vol. 72; nb.

1; (2007); p. 144 - 149, View in Reaxys 29 of 68

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

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Pandey, Sushil K.; Greene, Andrew E.; Poisson, Jean-Francois; Journal of Organic Chemistry; vol. 72; nb. 20; (2007); p. 7769 - 7770, View in Reaxys 30 of 68

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Pandey, Sushil K.; Greene, Andrew E.; Poisson, Jean-Francois; Journal of Organic Chemistry; vol. 72; nb. 20; (2007); p. 7769 - 7770, View in Reaxys 31 of 68

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

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

75

Lebel, Helene; Davi, Michael; Diez-Gonzalez, Silvia; Nolan, Steven P.; Journal of Organic Chemistry; vol. 72; nb.

1; (2007); p. 144 - 149, View in Reaxys; Pandey, Sushil K.; Greene, Andrew E.; Poisson, Jean-Francois; Journal of Organic Chemistry; vol. 72; nb. 20; (2007); p. 7769 - 7770, View in Reaxys 32 of 68

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

75

Pandey, Sushil K.; Greene, Andrew E.; Poisson, Jean-Francois; Journal of Organic Chemistry; vol. 72; nb. 20; (2007); p. 7769 - 7770, View in Reaxys

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33 of 68

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

1H

Solvents (NMR Spectro- CD2Cl2 scopy) Temperature (NMR Spectroscopy) [°C]

19.85

Frequency (NMR Spectroscopy) [MHz]

300

Cinellu, Maria A.; Minghetti, Giovanni; Cocco, Fabio; Stoccoro, Sergio; Zucca, Antonio; Manassero, Mario; Arca, Massimiliano; Dalton Transactions; nb. 48; (2006); p. 5703 - 5716, View in Reaxys 34 of 68

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

1H

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

19.85

Frequency (NMR Spectroscopy) [MHz]

300

Cinellu, Maria A.; Minghetti, Giovanni; Cocco, Fabio; Stoccoro, Sergio; Zucca, Antonio; Manassero, Mario; Arca, Massimiliano; Dalton Transactions; nb. 48; (2006); p. 5703 - 5716, View in Reaxys 35 of 68

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

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

19.85

Frequency (NMR Spectroscopy) [MHz]

300

Cinellu, Maria A.; Minghetti, Giovanni; Cocco, Fabio; Stoccoro, Sergio; Zucca, Antonio; Manassero, Mario; Arca, Massimiliano; Dalton Transactions; nb. 48; (2006); p. 5703 - 5716, View in Reaxys 36 of 68

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectro- CD2Cl2 scopy) Temperature (NMR Spectroscopy) [°C]

19.85

Frequency (NMR Spectroscopy) [MHz]

300

Cinellu, Maria A.; Minghetti, Giovanni; Cocco, Fabio; Stoccoro, Sergio; Zucca, Antonio; Manassero, Mario; Arca, Massimiliano; Dalton Transactions; nb. 48; (2006); p. 5703 - 5716, View in Reaxys 37 of 68

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

13C

Solvents (NMR Spectro- CD2Cl2 scopy)

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Temperature (NMR Spectroscopy) [°C]

19.85

Frequency (NMR Spectroscopy) [MHz]

75.4

Cinellu, Maria A.; Minghetti, Giovanni; Cocco, Fabio; Stoccoro, Sergio; Zucca, Antonio; Manassero, Mario; Arca, Massimiliano; Dalton Transactions; nb. 48; (2006); p. 5703 - 5716, View in Reaxys 38 of 68

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

13C

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

19.85

Frequency (NMR Spectroscopy) [MHz]

75.4

Cinellu, Maria A.; Minghetti, Giovanni; Cocco, Fabio; Stoccoro, Sergio; Zucca, Antonio; Manassero, Mario; Arca, Massimiliano; Dalton Transactions; nb. 48; (2006); p. 5703 - 5716, View in Reaxys 39 of 68

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- various solvent(s) scopy) Temperature (NMR Spectroscopy) [°C]

25

Comment (NMR Spectroscopy)

in the presence of organic compounds

Creary, Xavier; Willis, Elizabeth D.; Gagnon, Madeleine; Journal of the American Chemical Society; vol. 127; nb.

51; (2005); p. 18114 - 18120, View in Reaxys 40 of 68

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Liu, Yang; He, Junpo; Xu, Jiangtao; Fan, Deqin; Tang, Wei; Yang, Yuliang; Macromolecules; vol. 38; nb. 24; (2005); p. 10332 - 10335, View in Reaxys 41 of 68

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

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Liu, Yang; He, Junpo; Xu, Jiangtao; Fan, Deqin; Tang, Wei; Yang, Yuliang; Macromolecules; vol. 38; nb. 24; (2005); p. 10332 - 10335, View in Reaxys 42 of 68

Description (NMR Spec- Chemical shifts troscopy)

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Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

250

Firouzabadi, Habib; Iranpoor, Naser; Hazarkhani, Hassan; Karimi, Babak; Synthetic Communications; vol. 33; nb. 21; (2003); p. 3653 - 3660, View in Reaxys 43 of 68

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

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

62.89

Firouzabadi, Habib; Iranpoor, Naser; Hazarkhani, Hassan; Karimi, Babak; Synthetic Communications; vol. 33; nb. 21; (2003); p. 3653 - 3660, View in Reaxys 44 of 68

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Koptyug, Igor V.; Kulikov, Alexander V.; Lysova, Anna A.; Kirillov, Valery A.; Parmon, Valentin N.; Sagdeev, Renad Z.; Journal of the American Chemical Society; vol. 124; nb. 33; (2002); p. 9684 - 9685, View in Reaxys 45 of 68

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

1H

Grossman, G.; Komber, G.; Kroshvitts, G.; Kirpichnikov, P. A.; Mukmeneva, N. A.; Pobedimskii, D. G.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 38; nb. 1.1; (1989); p. 26 - 32; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 1; (1989); p. 34 - 41, View in Reaxys; Ravindranath, B.; Srinivas, P.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 22; nb. 6; (1983); p. 592 - 594, View in Reaxys; Koptyug, Igor V.; Kulikov, Alexander V.; Lysova, Anna A.; Kirillov, Valery A.; Parmon, Valentin N.; Sagdeev, Renad Z.; Journal of the American Chemical Society; vol. 124; nb. 33; (2002); p. 9684 - 9685, View in Reaxys 46 of 68

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

1H

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

19.85

Frequency (NMR Spectroscopy) [MHz]

200.13

Bianchini, Claudio; De los Rios, Isaac; Lopez, Carlos; Peruzzini, Maurizio; Romerosa, Antonio; Journal of Organometallic Chemistry; vol. 593-594; (2000); p. 485 - 488, View in Reaxys 47 of 68

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

19.85

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Frequency (NMR Spectroscopy) [MHz]

200.13

Bianchini, Claudio; De los Rios, Isaac; Lopez, Carlos; Peruzzini, Maurizio; Romerosa, Antonio; Journal of Organometallic Chemistry; vol. 593-594; (2000); p. 485 - 488, View in Reaxys 48 of 68

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

1H

Solvents (NMR Spectro- CDCl3 scopy) Schonk, Ruud M.; Bakker, Bert H.; Cerfontain, Hans; Recueil des Travaux Chimiques des Pays-Bas; vol. 111; nb.

1; (1992); p. 49 - 55, View in Reaxys; Vaccher; Berthelot; Flouquet; Debaert; Synthetic Communications; vol. 23; nb. 5; (1993); p. 671 - 679, View in Reaxys; Galli, Carlo; Magnetic Resonance in Chemistry; vol. 27; nb. 3; (1989); p. 214 - 215, View in Reaxys 49 of 68

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

1H

Solvents (NMR Spectro- CCl4 scopy) Pine; Shen; Hoang; Synthesis; nb. 2; (1991); p. 165 - 167, View in Reaxys; Pine, Stanley H.; Pettit, Robert J.; Geib, Gregory D.; Cruz, Susana G.; Gallego, Claudio H.; et al.; Journal of Organic Chemistry; vol. 50; nb. 8; (1985); p. 1212 - 1216, View in Reaxys 50 of 68

Description (NMR Spec- Spin-lattice relaxation time (T1) troscopy) Kelly, David P.; Leslie, D. Ralph; Journal of the American Chemical Society; vol. 112; nb. 25; (1990); p. 9078 9084, View in Reaxys

51 of 68

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

13C

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

30

Grossman, G.; Komber, G.; Kroshvitts, G.; Kirpichnikov, P. A.; Mukmeneva, N. A.; Pobedimskii, D. G.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 38; nb. 1.1; (1989); p. 26 - 32; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 1; (1989); p. 34 - 41, View in Reaxys 52 of 68

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

13C

Solvents (NMR Spectro- CDCl3 scopy) Galli, Carlo; Magnetic Resonance in Chemistry; vol. 27; nb. 3; (1989); p. 214 - 215, View in Reaxys 53 of 68

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CDCl3 scopy) Comment (NMR Spectroscopy)

1H-13C.

Galli, Carlo; Magnetic Resonance in Chemistry; vol. 27; nb. 3; (1989); p. 214 - 215, View in Reaxys

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

1H

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

26.9

Schaefer, Ted; Sebastian, Rudy; Penner, Glenn H.; Canadian Journal of Chemistry; vol. 66; (1988); p. 584 - 590, View in Reaxys 55 of 68

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- acetone-d6 scopy) Temperature (NMR Spectroscopy) [°C]

26.9

Comment (NMR Spectroscopy)

1H-1H.

Schaefer, Ted; Sebastian, Rudy; Penner, Glenn H.; Canadian Journal of Chemistry; vol. 66; (1988); p. 584 - 590, View in Reaxys 56 of 68

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

13C

Solvents (NMR Spectro- CCl4; cyclohexane-d12 scopy) Temperature (NMR Spectroscopy) [°C]

32

Reynolds, William F.; Gomes, Anabela; Maron, Antonina; MacIntyre, Douglas W.; Maunder, Robert G.; et al.; Canadian Journal of Chemistry; vol. 61; (1983); p. 2367 - 2375, View in Reaxys 57 of 68

Description (NMR Spec- Spin-spin coupling constants troscopy) Comment (NMR Spectroscopy)

1H-1H

Ravindranath, B.; Srinivas, P.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 22; nb. 6; (1983); p. 592 - 594, View in Reaxys 58 of 68

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

1H

Solvents (NMR Spectro- dioxane-d8 scopy) Griendt, Freek van de; Cerfontain, Hans; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 23 - 27, View in Reaxys 59 of 68

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

13C

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

33

Fraenkel,G.; Geckle,J.M.; Journal of the American Chemical Society; vol. 102; (1980); p. 2869, View in Reaxys

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60 of 68

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

13C

Fraenkel, Gideon; Geckle, Michael J.; Kaylo, Allan; Estes, Don W.; Journal of Organometallic Chemistry; vol.

197; nb. 3; (1980); p. 249 - 260, View in Reaxys 61 of 68

Description (NMR Spec- NMR troscopy) Hamer,G.K. et al.; Canadian Journal of Chemistry; vol. 51; (1973); p. 915 - 926, View in Reaxys; Tobey,S.W.; Journal of Organic Chemistry; vol. 34; (1969); p. 1281 - 1298, View in Reaxys; Uijttewaal,A.P. et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3306 - 3311, View in Reaxys; Uijttewaal,A.P. et al.; Journal of Organic Chemistry; vol.

44; (1979); p. 3157 - 3168, View in Reaxys; Voronkov,M.G. et al.; Zhurnal Organicheskoi Khimii; vol. 8; (1972); p.

2347 - 2352,2394 - 2399, View in Reaxys; Petragnani,N. et al.; Journal of Organometallic Chemistry; vol. 124; (1977); p. 1 - 12, View in Reaxys; Douglas,A.W.; Organic Magnetic Resonance; vol. 9; (1977); p. 69, View in Reaxys; Sandberg; Ragnarsson; International Journal of Peptide and Protein Research; vol. 6; (1974); p.

111,115, View in Reaxys; Yamamoto et al.; Analytical Chemistry; vol. 44; (1972); p. 2180,2183, View in Reaxys; Porter et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 3664, View in Reaxys; Jackman; Wiley; Journal of the Chemical Society; (1960); p. 2886,2887, View in Reaxys; Voegeli; Philipsborn; Organic Magnetic Resonance; vol. 7; (1975); p. 617, View in Reaxys; Reetz; Eibach; Justus Liebigs Annalen der Chemie; (1977); p.

242,249,252,253, View in Reaxys; Gey; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 823, View in Reaxys; Firl et al.; Chemistry Letters; (1975); p. 51, View in Reaxys; Benito; Seidl; Anales de Quimica (1968-1979); vol. 68; (1972); p. 1389,1393, View in Reaxys; Inamoto et al.; Chemistry Letters; (1977); p. 759,760, View in Reaxys; Bertelli et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 5286,5291, View in Reaxys; Neumann; Seebach; Chemische Berichte; vol. 111; (1978); p. 2785,2811, 2812, View in Reaxys; Aeyaes; Organic Magnetic Resonance; vol. 9; (1977); p. 663, View in Reaxys; Alberola; Borque; Anales de Quimica (1968-1979); vol. 70; (1974); p. 882, View in Reaxys; Dedina; Schraml; Collection of Czechoslovak Chemical Communications; vol. 42; (1977); p. 3239,3251, View in Reaxys; Senda et al.; Bulletin of the Chemical Society of Japan; vol. 50; (1977); p. 1608,1610, View in Reaxys; Lynch; Canadian Journal of Chemistry; vol. 55; (1977); p.

541,543, View in Reaxys; Bywater et al.; Journal of Organometallic Chemistry; vol. 135; (1977); p. 145,148, View in Reaxys; Kingsbury et al.; Journal of Organic Chemistry; vol. 41; (1976); p. 3863,3864, 3866, View in Reaxys; Pines; Schappell; Journal of Organic Chemistry; vol. 29; (1964); p. 1503,1507, View in Reaxys; Forsyth et al.; Journal of the American Chemical Society; vol. 98; (1976); p. 2512,2513, View in Reaxys

62 of 68

Description (NMR Spec- CIDNP troscopy) Porter et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 3664, View in Reaxys; Sweang; Halpern; Journal of the American Chemical Society; vol. 99; (1977); p. 8335, View in Reaxys

63 of 68

Description (NMR Spec- Chemical shifts troscopy) Cordoba et al.; Journal of Magnetic Resonance (1969-1992); vol. 6; (1972); p. 570, View in Reaxys

64 of 68

Description (NMR Spec- Spin-spin coupling constants troscopy) Kowalewski; Journal of Magnetic Resonance (1969-1992); vol. 4; (1971); p. 249, View in Reaxys; Bartuska; Maciel; Journal of Magnetic Resonance (1969-1992); vol. 7; (1972); p. 36, View in Reaxys

65 of 68

Description (NMR Spec- Spectrum troscopy) Kowalewski; Journal of Magnetic Resonance (1969-1992); vol. 4; (1971); p. 249, View in Reaxys

66 of 68

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

(CCl4): τ 9.2(m), 4.87 (m), 4.59 (m), 2.70 (m)

Okada; Hashimoto; Kogyo Kagaku Zasshi; vol. 70; (1967); p. 2152,2153, 2155, View in Reaxys 67 of 68

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

im 13C-NMR

Dhami,K.S.; Stothers,J.B.; Canadian Journal of Chemistry; vol. 43; (1965); p. 510, View in Reaxys

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Description (NMR Spec- Spectrum troscopy) Comment (NMR Spectroscopy)

bei 60 Mc

Davis; Roberts; Journal of the American Chemical Society; vol. 84; (1962); p. 2252,2256, View in Reaxys IR Spectroscopy (9) 1 of 9

Description (IR Spectroscopy)

Intensity of IR bands; Bands; Spectrum

Karthikeyan, N.; Joseph Prince, J.; Ramalingam, S.; Periandy, S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 143; (2015); p. 107 - 119, View in Reaxys 2 of 9

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

sodium chloride

Location

supporting information

Comment (IR Spectroscopy)

film

Doni, Eswararao; O'Sullivan, Steven; Murphy, John A.; Angewandte Chemie - International Edition; vol. 52; nb.

8; (2013); p. 2239 - 2242; Angew. Chem.; vol. 125; nb. 8; (2013); p. 2295 - 2298,4, View in Reaxys 3 of 9

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

film

Firouzabadi, Habib; Iranpoor, Naser; Hazarkhani, Hassan; Karimi, Babak; Synthetic Communications; vol. 33; nb. 21; (2003); p. 3653 - 3660, View in Reaxys; Pandey, Sushil K.; Greene, Andrew E.; Poisson, Jean-Francois; Journal of Organic Chemistry; vol. 72; nb. 20; (2007); p. 7769 - 7770, View in Reaxys 4 of 9

Description (IR Spectroscopy)

Bands

Zatsepina et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 2354,2075,2078, View in Reaxys; Jui Bao-Schan' et al.; Zhurnal Fizicheskoi Khimii; vol. 36; (1962); p. 681,686; ; p. 356, View in Reaxys; Badger; Novotny; Australian Journal of Chemistry; vol. 16; (1963); p. 613,614, 621, View in Reaxys 5 of 9

Description (IR Spectroscopy)

Spectrum

Wiberley et al.; Analytical Chemistry; vol. 32; (1960); p. 217,219, View in Reaxys; Perrier-Datin; Lebas; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 76; (1979); p. 935, View in Reaxys 6 of 9

Description (IR Spectroscopy)

Intensity of IR bands

Zatsepina et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 2354,2075,2078, View in Reaxys 7 of 9

Description (IR Spectroscopy)

IR

Vig et al.; Journal of the Indian Chemical Society; vol. 45; (1968); p. 1026,1031, View in Reaxys; Sekiguchi et al.; Kogyo Kagaku Zasshi; vol. 73; (1970); p. 2325,2326, 2327; Chem.Abstr.; vol. 74; nb. 124439; (1971), View in Reaxys; Baker et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 34; (1978); p. 683,686, View in Reaxys; Ellis et al.; Tetrahedron; vol. 35; (1979); p. 843,844-846, View in Reaxys; Fliszar; Renard; Canadian Journal of Chemistry; vol. 48; (1970); p. 3002,3016, View in Reaxys; Terent'ew et al.; Neftekhimiya; vol. 1; (1962); p. 567,462, View in Reaxys; Okada; Hashimoto; Kogyo Kagaku Zasshi; vol. 70; (1967); p.

2152,2153, 2155, View in Reaxys 8 of 9

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1111 - 667 cm**(-1)

Patterson; Analytical Chemistry; vol. 26; (1954); p. 823,826,832; Chem.Abstr.; vol. 48; nb. 11928h, View in Reaxys

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9 of 9

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

3333 - 667 cm**(-1); Fluessigkeit.

A.P.I. Res. Project; 44 Nr. 329 <1945>, View in Reaxys Mass Spectrometry (10) Description (Mass Location Spectrometry)

Comment (Mass Spectrometry)

References

gas chromatogra- supporting inforphy mass specmation trometry (GCMS); spectrum

Geer, Michael F.; Walla, Michael D.; Solntsev, Kyril M.; Strassert, Cristian A.; Shimizu, Linda S.; Journal of Organic Chemistry; vol.

78; nb. 11; (2013); p. 5568 - 5578, View in Reaxys; Chen, Hong-Jie; Tseng, Mei-Chun; Hsu, I.-Jui; Chen, Wei-Ting; Han, ChienChung; Shyu, Shin-Guang; Dalton Transactions; vol. 44; nb. 27; (2015); p. 12086 - 12090, View in Reaxys

electron impact (EI); spectrum

Wu, Ji-Cheng; Gong, Lu-Bing; Xia, Yuanzhi; Song, Ren-Jie; Xie, Ye-Xiang; Li, Jin-Heng; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9909 - 9913, View in Reaxys

supporting information mol peak

Barbero, Margherita; Cadamuro, Silvano; Dughera, Stefano; Venturello, Paolo; Synthesis; nb. 22; (2008); p. 3625 - 3632, View in Reaxys

spectrum

Seeman, Jeffrey I.; Grassian, V. H.; Bernstein, E. R.; Journal of the American Chemical Society; vol. 110; nb. 25; (1988); p. 8542 - 8543, View in Reaxys; Fowley, Lissa A.; Lee, Jesse C.; Crabtree, Robert H.; Siegbahn, Per E. M.; Journal of Organometallic Chemistry; vol.

504; nb. 1-2; (1995); p. 57 - 68, View in Reaxys; Helmig, Detlev; Klinger, Lee F.; Guenther, Alex; Vierling, Lee; Geron, Chris; Zimmerman, Patrick; Chemosphere; vol. 38; nb. 9; (1999); p. 2163 2187, View in Reaxys; Bianchini, Claudio; De los Rios, Isaac; Lopez, Carlos; Peruzzini, Maurizio; Romerosa, Antonio; Journal of Organometallic Chemistry; vol. 593-594; (2000); p. 485 - 488, View in Reaxys; Liu, Yang; He, Junpo; Xu, Jiangtao; Fan, Deqin; Tang, Wei; Yang, Yuliang; Macromolecules; vol. 38; nb. 24; (2005); p. 10332 - 10335, View in Reaxys

spectrum; electron impact (EI)

Aitken, R. Alan; Boeters, Christine; Morrison, John J.; Journal of the Chemical Society - Perkin Transactions 1; nb. 17; (1997); p. 2625 - 2631, View in Reaxys

electron impact (EI)

Bartmess, John E.; Burnham, Robert D.; Journal of Organic Chemistry; vol. 49; (1984); p. 1382 - 1387, View in Reaxys

spectrum

field ionization; collisional activation

Lay, J. O.; Gross, M. L.; Zwinselman, J. J.; Nibbering, N. M. M.; Organic Mass Spectrometry; vol. 18; nb. 1; (1983); p. 16 - 21, View in Reaxys

chemical ionization (CI); spectrum

collisional activation

Lay, J. O.; Gross, M. L.; Journal of the American Chemical Society; vol. 105; nb. 11; (1983); p. 3445 - 3451, View in Reaxys Taylor et al.; Analytical Chemistry; vol. 20; (1948); p. 397, View in Reaxys; Roberts; Johnsen; Analytical Chemistry; vol. 20; (1948); p. 1225,1229; A.P.I. Res. Project; vol. 44; nb. 263; (1948); p.

317 <1949>, View in Reaxys; Van der Greef; Nibbering; Organic Mass Spectrometry; vol. 14; (1979); p. 537,540, 541, View in Reaxys; Koeppel et al.; Organic Mass Spectrometry; vol. 8; (1974); p. 25,26, View in Reaxys; Khvostenko et al.; Theoretical and Experimental Chemistry; vol. 9; (1973); p. 406,410, View in Reaxys; Szabo et al.; Justus Liebigs Annalen der Chemie; (1977); p.

747,758, View in Reaxys

appearance potentials

Koeppel et al.; Organic Mass Spectrometry; vol. 8; (1974); p. 25,26, View in Reaxys

UV/VIS Spectroscopy (14) 1 of 14

Description (UV/VIS Spectroscopy)

Spectrum

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Absorption Maxima (UV/ 257; 260; 264; 289 VIS) [nm] Lei; Lu; Zhang; Wei; Zhou; Xia; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 52; nb. 6; (2013); p. 709 - 716, View in Reaxys 2 of 14

Solvent (UV/VIS Spectroscopy)

neat liquid

Absorption Maxima (UV/ 246 VIS) [nm] Pytela, Oldrich; Trlida, Bronislav; Collection of Czechoslovak Chemical Communications; vol. 72; nb. 8; (2007); p.

1025 - 1036, View in Reaxys 3 of 14

Solvent (UV/VIS Spectroscopy)

methylcyclohexane

Comment (UV/VIS Spectroscopy)

Remark: T=298 K

Absorption Maxima (UV/ 244 VIS) [nm] Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8806 8813, View in Reaxys 4 of 14

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

methylcyclohexane

Comment (UV/VIS Spectroscopy)

Remark: T=298 K

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8806 8813, View in Reaxys 5 of 14

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

concentration dependence

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 8; (2003); p. 2046 2047, View in Reaxys 6 of 14

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

aq. ethanol

Absorption Maxima (UV/ 242.5 VIS) [nm] Ext./Abs. Coefficient [l·mol-1cm-1]

10400

Jiang, Xi-Kui; Ji, Guo-Zhen; Wang, Daniel Ze-Rong; Journal of Physical Organic Chemistry; vol. 8; (1995); p. 143 - 148, View in Reaxys 7 of 14

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

neat (no solvent)

Comment (UV/VIS Spectroscopy)

320 - 380 nm

Kudryavtseva, T. V.; Khaikin, S. Ya.; Moldavskaya, V. M.; Domareva, N. M.; Rupyshev, V. G.; et al.; J. Appl.

Chem. USSR (Engl. Transl.); vol. 63; nb. 7.2; (1990); p. 1571 - 1575,1445 - 1449, View in Reaxys 8 of 14

Description (UV/VIS Spectroscopy)

Spectrum

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Solvent (UV/VIS Spectroscopy)

cyclohexene

Comment (UV/VIS Spectroscopy)

300 - 800 nm

Yamamoto, Yukio; Chikai, Yukio; Hayashi, Koichiro; Bulletin of the Chemical Society of Japan; vol. 58; nb. 11; (1985); p. 3369 - 3370, View in Reaxys 9 of 14

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

300 - 750 nm

Andrews, Lester; Harvey, James A.; Kelsall, Benuel J.; Duffey, Donald C.; Journal of the American Chemical Society; vol. 103; nb. 21; (1981); p. 6415 - 6422, View in Reaxys 10 of 14

Description (UV/VIS Spectroscopy)

Absorption maxima

Brede et al.; Radiochemical and Radioanalytical Letters; vol. 39; (1979); p. 169, View in Reaxys; Inaki et al.; Bulletin of the Chemical Society of Japan; vol. 42; (1969); p. 2605,2606, View in Reaxys; Lettin; Hall; Journal of Physical Chemistry; vol. 66; (1962); p. 1457,1458, View in Reaxys 11 of 14

Description (UV/VIS Spectroscopy)

UV/VIS

Bertoli,V.; Plesch,P.H.; Journal of the Chemical Society [Section] B: Physical Organic; (1968); p. 1500 - 1516, View in Reaxys; Gey; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 823, View in Reaxys; Ellis et al.; Tetrahedron; vol. 35; (1979); p. 843,844-846, View in Reaxys 12 of 14

Description (UV/VIS Spectroscopy)

Spectrum

Suzuki,H.; Bulletin of the Chemical Society of Japan; vol. 33; (1960); p. 619 - 628, View in Reaxys; Ramart-Lucas; Amagat; Bulletin de la Societe Chimique de France; vol. <4> 51; (1932); p. 108,117, View in Reaxys; Walsh; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 191; (1931); p. 32, View in Reaxys; Lin et al.; Transactions of the Faraday Society; vol. 64; (1968); p. 2896,2903, View in Reaxys; Chambers et al.; Transactions of the Faraday Society; vol. 63; (1967); p. 1699,1706, View in Reaxys; Crosby et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1977); p. 182,183-184, View in Reaxys; Lavrushin; Tarakhno; Zhurnal Organicheskoi Khimii; vol. 1; (1965); p. 1642,1664, View in Reaxys; Comyn; Irin; European Polymer Journal; vol. 5; (1969); p. 587,588,589,593, View in Reaxys; Irie et al.; Journal of Physical Chemistry; vol. 76; (1972); p. 1419, View in Reaxys; Mason; Vane; Tetrahedron Letters; (1965); p. 1593,1595, View in Reaxys; Jui Bao-Schan' et al.; Zhurnal Fizicheskoi Khimii; vol.

36; (1962); p. 681,686; ; p. 356, View in Reaxys; Bywater; Worsfold; Canadian Journal of Chemistry; vol. 44; (1966); p. 1671,1673, View in Reaxys; Katayama et al.; Bulletin of the Chemical Society of Japan; vol. 38; (1965); p. 851, View in Reaxys 13 of 14

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

petroleum ether

Comment (UV/VIS Spectroscopy)

210 - 300 nm

Beaven; Johnson; Journal of the Chemical Society; (1957); p. 651,653, View in Reaxys 14 of 14

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Ley; Z. wiss. Phot.; vol. 18; p. 177; Chem. Zentralbl.; vol. 90; nb. I; (1919); p. 946, View in Reaxys ESR Spectroscopy (2) 1 of 2

Description (ESR Spectroscopy)

ESR

Jonkman et al.; Journal of Physical Chemistry; vol. 74; (1970); p. 1650, View in Reaxys 2 of 2

Description (ESR Spectroscopy)

Spectrum

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Lin et al.; Transactions of the Faraday Society; vol. 64; (1968); p. 2896,2903, View in Reaxys Rotational Spectroscopy (1) Description (Rota- References tional Spectroscopy) Rotational spectrum

Schaefer, Ted; Sebastian, Rudy; Penner, Glenn H.; Canadian Journal of Chemistry; vol. 66; (1988); p. 584 - 590, View in Reaxys

Raman Spectroscopy (3) Description (Ram- References an Spectroscopy) Bands; Spectrum

Karthikeyan, N.; Joseph Prince, J.; Ramalingam, S.; Periandy, S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 143; (2015); p. 107 - 119, View in Reaxys

Spectrum

Lespieau; Bourguel; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 190; (1930); p. 1504; Bulletin de la Societe Chimique de France; vol. <4> 47; (1930); p. 1365,1375, View in Reaxys; Briner; Ryffel; Perrottet; Helvetica Chimica Acta; vol. 22; (1939); p. 927,928, 933, View in Reaxys; Donzelot bei Richard; Mirjolet; Gschwind; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 223; (1946); p. 1007, View in Reaxys; Krabbe; Schmidt; Eisenlohr; Chemische Berichte; vol. 74; (1941); p. 1905,1910, View in Reaxys; Lewina et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 1185,1096; Chem.Abstr.; nb. 25809; (1961), View in Reaxys; Perrier-Datin; Lebas; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 76; (1979); p. 935, View in Reaxys; Bulkin et al.; Analytical Chemistry; vol. 43; (1971); p. 974,975, View in Reaxys

Bands

Lippincott; et al.; Spectrochimica Acta; vol. 22; (1966); p. 1493,1495, View in Reaxys; Jui Bao-Schan' et al.; Zhurnal Fizicheskoi Khimii; vol. 36; (1962); p. 681,686; ; p. 356, View in Reaxys

Luminescence Spectroscopy (5) Description (LuComment (Lumiminescence nescence SpecSpectroscopy) troscopy) Luminescence quantum yield

Luminescence lifetime

References

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Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol.

125; nb. 8; (2003); p. 2046 - 2047, View in Reaxys

Luminescence lifetime

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Thermoluminescence

Backes, Clare A.; Brocklehurst, Brian; Plimley, Simon; Stevenson, Jean; Tawn, D. Nicholas; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol.

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Radioluminescence

Backes, Clare A.; Brocklehurst, Brian; Plimley, Simon; Stevenson, Jean; Tawn, D. Nicholas; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol.

39; nb. 10; (1983); p. 917 - 920, View in Reaxys

Fluorescence Spectroscopy (11) Description (Fluo- Solvent (Fluoresrescence Speccence Spectrotroscopy) scopy)

Temperature (Flu- Comment (Fluoorescence Spec- rescence Spectroscopy) [°C] troscopy)

References

Fluorescence decay kinetics

298

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8806 - 8813, View in Reaxys

Fluorescence lifetime

-193.15 - 24.85

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8806 - 8813, View in Reaxys

Fluorescence excitation spectrum

24.85

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8806 - 8813, View in Reaxys

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Intersystem crossing [singlet>triplet]

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8806 - 8813, View in Reaxys

Fluorescence quantum yield

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8806 - 8813, View in Reaxys

Spectrum

methylcyclohexane

24.85

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8806 - 8813, View in Reaxys

Maxima

methylcyclohexane

24.85

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8806 - 8813, View in Reaxys

Spectrum

Lewis, Frederick D.; Zuo, Xiaobing; Journal of the American Chemical Society; vol. 125; nb. 8; (2003); p. 2046 - 2047, View in Reaxys

Maxima

methylcyclohexane; 2-methyl-butane

279 nm; 320 nm

Backes, Clare A.; Brocklehurst, Brian; Plimley, Simon; Stevenson, Jean; Tawn, D. Nicholas; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 39; nb. 10; (1983); p. 917 - 920, View in Reaxys

Maxima

methylcyclohexane; 2-methyl-butane

467.5 nm; 504.5 nm

Backes, Clare A.; Brocklehurst, Brian; Plimley, Simon; Stevenson, Jean; Tawn, D. Nicholas; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 39; nb. 10; (1983); p. 917 - 920, View in Reaxys

Fluorescence

Crowell et al.; Analytical Chemistry; vol. 35; (1963); p. 184, View in Reaxys; Crosby et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1977); p. 182,183-184, View in Reaxys; Brede et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 259; (1978); p. 705,709-714, View in Reaxys; Crosby; Salisbury; Journal of the Chemical Society, Chemical Communications; (1975); p. 477, View in Reaxys

Other Spectroscopic Methods (1) Description (Oth- References er Spectroscopic Methods) Photoelectron spectrum

Maier; Turner; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 69; (1973); p. 196, View in Reaxys; Opeida; Suprun; Dmitruk; Russian Journal of Physical Chemistry A; vol. 72; nb. 9; (1998); p. 1481 - 1486, View in Reaxys

Pharmacological Data (3) 1 of 3

Comment (Pharmacological Data)

Bioactivities present

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76; (1957); p. 297,310, View in Reaxys; Malinowskii; Jaworowskii; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 21; (1955); p. 240,243; Chem.Abstr.; (1956); p. 9313, View in Reaxys; Ziegler; Dislich; Chemische Berichte; vol. 90; (1957); p. 1107,1113, View in Reaxys; Hock; Kropf; Chemische Berichte; vol. 91; (1958); p.

1681,1682, 1686, View in Reaxys; Sokolow; Schuschunow; Trudy Chim. chim. Technol.; vol. 2; (1959); p. 29,33; Chem.Abstr.; (1960); p. 6275, View in Reaxys; Jurshenko; Doklady 7. Konf. vysokomol. Soedin. Moskau; (1952); p.

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317 <1949>, View in Reaxys; Walling et al.; Journal of the American Chemical Society; vol. 70; (1948); p. 1537, View in Reaxys; Beckett; Pitzer; Journal of the American Chemical Society; vol. 68; (1946); p. 2213, View in Reaxys; Briner; Ryffel; Perrottet; Helvetica Chimica Acta; vol. 22; (1939); p. 927,928, 933, View in Reaxys; Lora; Tomayo; Viguera; Anales de la Real Sociedad Espanola de Fisica y Quimica; vol. 38; (1942); p. 184,190, View in Reaxys; Broockmann,K.; Diss. <Koeln 1948> S. 31, View in Reaxys; Alder; Broockmann bei Alder in K. Ziegler; Praeparative Organische Chemie Tl. II (= Naturf. Med. Dtschld. 1939 bis 1946, Bd. 37) <Weinheim 1953> S. 141, View in Reaxys; Schmitz-Dumont; Diebold; Thoemke; Chemische Berichte; vol. 70; (1937); p. 2189,2198, View in Reaxys; Seymour; Harris; Branum; Industrial and Engineering Chemistry; vol. 41; (1949); p. 1509, View in Reaxys; Hersberger; Reid; Heiligmann; Industrial and Engineering Chemistry; vol. 37; (1945); p.

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2489, View in Reaxys; Patent; I.G. Farbenind.; DE532456; (1929); Fortschr. Teerfarbenfabr. Verw. Industriezweige; vol. 18; p. 2148, View in Reaxys; Patent; Atlantic Refining Co.; US2448976; (1945), View in Reaxys; Pepper; Transactions of the Faraday Society; vol. 45; (1949); p. 397,398, View in Reaxys; Patent; Atlantic Refining Co.; US2472589; (1946), View in Reaxys; Patent; Distillers Co.; US2249987; (1938), View in Reaxys; Patent; Atlantic Refining Co.; US2429719; (1946), View in Reaxys; Evans; Higginson; Wooding; Recueil des Travaux Chimiques des Pays-Bas; vol. 68; (1949); p. 1069,1071, View in Reaxys; Dow Chem. Co. bei C.E. Schildknecht; Vinyl and Related Polymers <New York 1952> S. 133, View in Reaxys; Walsh; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 191; (1931); p. 32, View in Reaxys; Donzelot bei Richard; Mirjolet; Gschwind; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol.

223; (1946); p. 1007, View in Reaxys; A.P.I. Res. Project; 44 Nr. 329 <1945>, View in Reaxys; Rossini; Selected Values 1953 S. 75, View in Reaxys; Scafe; Herman; Analytical Chemistry; vol. 19; (1947); p. 971,972, View in Reaxys; Rossini; Selected Values 1953 S. 463, View in Reaxys; Rossini; Selected Values 1953 S. 534, 556, 578, 651, View in Reaxys; Patent; E. Lilly and Co.; US2404235; (1945), View in Reaxys; Patent; Dow Chem.

Co.; US2443217; (1945), View in Reaxys; Nickels et al.; Industrial and Engineering Chemistry; vol. 41; (1949); p.

563,565, View in Reaxys; Patent; Distiller Co.; US2342980; (1942), View in Reaxys; Patent; I.G. Farbenind.; DE550055; (1931); Fortschr. Teerfarbenfabr. Verw. Industriezweige; vol. 19; p. 611,613, View in Reaxys; Ohlinger,H.; Polystyrol, Tl. 1 <Berlin 1955> S. 36, 78, 90, 118, 132, View in Reaxys; Schildknecht,C.E.; Vinyl and Related Polymers <New York 1952> S. 132-239, View in Reaxys; Kilpatrick et al.; Journal of Research of the National Bureau of Standards (United States); vol. 42; (1949); p. 225,229, View in Reaxys; Alder; Pascher; Vagt; Chemische Berichte; vol. 75; (1942); p. 1501,1510, View in Reaxys; Sapiro; Linstead; Newitt; Journal of the Chemical Society; (1937); p. 1784,1790, View in Reaxys; Bergmann; Bondi; Chemische Berichte; vol. 63; (1930); p.

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nal Organicheskoi Khimii; vol. 24; nb. 4; (1988); p. 795 - 803, View in Reaxys; Kostikov, R. R.; Molchanov, A. P.; Nagi, Sh. M.; Journal of Organic Chemistry USSR (English Translation); vol. 19; (1983); p. 1291 - 1297; Zhurnal Organicheskoi Khimii; vol. 19; nb. 7; (1983); p. 1437 - 1444, View in Reaxys; Barashenkov, G. G.; Derkach, N. Ya.; Journal of Organic Chemistry USSR (English Translation); (1986); p. 1069 - 1074; Zhurnal Organicheskoi Khimii; vol. 22; nb. 6; (1986); p. 1189 - 1195, View in Reaxys; Ohta, Hiromichi; Kobayashi, Naoki; Ozaki, Kazuhiko; Journal of Organic Chemistry; vol. 54; nb. 8; (1989); p. 1802 - 1804, View in Reaxys; Brown, John M.; Parker, David; Journal of Organic Chemistry; vol. 47; nb. 14; (1982); p. 2722 - 2730, View in Reaxys; Ogle, Craig A.; Riley, Patrick A.; Dorchak, Joseph J.; Hubbard, John L.; Journal of Organic Chemistry; vol. 53; nb. 18; (1988); p. 4409 4412, View in Reaxys; Johnson, Carl R.; Tait, Bradley D.; Journal of Organic Chemistry; vol. 52; nb. 2; (1987); p.

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26, View in Reaxys; Sheeller, Brad; Ingold, Keith U.; Journal of the Chemical Society. Perkin Transactions 2; nb. 4; (2001); p. 480 - 486, View in Reaxys; Katritzky; Ghiviriga; Chen; Tymoshenko; Abdel-Fattah; Journal of the Chemical Society, Perkin Transactions 2; nb. 4; (2001); p. 530 - 537, View in Reaxys; Handy, Scott T.; Czopp, Mark; Organic Letters; vol. 3; nb. 10; (2001); p. 1423 - 1425, View in Reaxys; Evans, David A.; Tregay, Steven W.; Burgey, Christopher S.; Paras, Nick A.; Vojkovsky, Tomas; Journal of the American Chemical Society; vol. 122; nb. 33; (2000); p. 7936 - 7943, View in Reaxys; Krief; Castillo-Colaux; Synlett; nb. 4; (2001); p. 501 - 504, View in Reaxys; Charette, Andre B.; Francoeur, Sebastien; Martel, Jonathan; Wilb, Nicole; Angewandte Chemie - International Edition; vol. 39; nb. 24; (2000); p. 4539 - 4542, View in Reaxys; Ikeno; Nishizuka; Sato; Yamada; Synlett; nb. 3; (2001); p. 406 - 408, View in Reaxys; Senboku; Komatsu; Fujimura; Tokuda; Synlett; nb. 3; (2001); p. 418 - 420, View in Reaxys; Barberis; Lahuerta; Perez-Prieto; Sanau; Chemical Communications; nb. 5; (2001); p. 439 - 440, View in Reaxys; Jeon; Nguyen; Chemical Communications; nb. 3; (2001); p. 235 - 236, View in Reaxys; Tsukada; Sato; Inoue; Chemical Communications; nb. 3; (2001); p. 237 - 238, View in Reaxys; Xue, Jie; Zhang, Yan; Wu, Tao; Fun, Hoong-Kun; Xu, Jian-Hua; Journal of the Chemical Society. Perkin Transactions 1; nb. 2; (2001); p. 183 - 191, View in Reaxys; Bertilsson, Sophie K.; Andersson, Pher G.; Journal of Organometallic Chemistry; vol. 603; nb. 1; (2000); p. 13 - 17, View in Reaxys; Kanagasabapathy, Subbareddy; Sudalai, Arumugam; Benicewicz, Brian C.; Tetrahedron Letters; vol. 42; nb. 23; (2001); p. 3791 - 3794, View in Reaxys; Auricchio, Sergio; Grassi, Simona; Malpezzi, Luciana; Sartori, Attilio Sarzi; Truscello, Ada M.; European Journal of Organic Chemistry; nb. 6; (2001); p. 1183 - 1187, View in Reaxys; Tyrkov; Kosova; Russian Journal of Organic Chemistry; vol. 36; nb. 12; (2000); p. 1826 - 1827, View in Reaxys; Niimi, Tatsuo; Uchida, Tatsuya; Irie, Ryo; Katsuki, Tsutomu; Advanced Synthesis and Catalysis; vol. 343; nb. 1; (2001); p. 79 - 88, View in Reaxys; Nenajdenko, Valentine G.; Smolko, Konstantin I.; Balenkova, Elizabeth S.; Tetrahedron Asymmetry; vol. 12; nb. 9; (2001); p. 1259 - 1266, View in Reaxys; Sakaguchi; Yamaga; Ishii; Journal of Organic Chemistry; vol. 66; nb. 13; (2001); p. 4710 - 4712, View in Reaxys; Sanders, Christopher J.; Gillespie, Kevin M.; Scott, Peter; Tetrahedron Asymmetry; vol. 12; nb. 7; (2001); p. 1055 - 1061, View in Reaxys; Bar, Gregory; Parsons, Andrew F; Thomas, C.Barry; Tetrahedron; vol. 57; nb. 22; (2001); p. 4719 - 4728, View in Reaxys; Barsy, Magda A.; Latif, Fawi M. Abd el; Ahmed, S. M.; El-Magharaby, M. A.; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 165; nb. 1; (2000); p. 1 - 6, View in Reaxys; Jonsson; Faernegardh; Baeckvall; Journal of the American Chemical Society; vol. 123; nb. 7; (2001); p. 1365 - 1371, View in Reaxys; Lane; Burgess; Journal of the American Chemical Society; vol. 123; nb. 12; (2001); p. 2933 - 2934, View in Reaxys; Pandiaraju; Chen; Lough; Yudin; Journal of the American Chemical Society; vol. 123; nb. 16; (2001); p. 3850 - 3851, View in Reaxys; Doebler, Christian; Mehltretter, Gerald M.; Sundermeier, Uta; Beller, Matthias; Journal of the American Chemical Society; vol.

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3; nb. 17; (2001); p. 2649 - 2651, View in Reaxys; Tsuritani, Takayuki; Shinokubo, Hiroshi; Oshima, Koichiro; Organic Letters; vol. 3; nb. 17; (2001); p. 2709 - 2711, View in Reaxys; Aggarwal, Varinder K.; De Vicente, Javier; Bonnert, Roger V.; Organic Letters; vol. 3; nb. 17; (2001); p. 2785 - 2788, View in Reaxys; Nenajdenko, Valentine G; Lebedev, Mikhail V; Balenkova, Elisabeth S; Tetrahedron; vol. 57; nb. 43; (2001); p. 9017 - 9024, View in Reaxys; Lee, Hong Myung; Kim, Sang-Wook; Hyeon, Taeghwan; Kim, B. Moon; Tetrahedron Asymmetry; vol. 12; nb. 11; (2001); p. 1537 - 1541, View in Reaxys; Yang; Zhang; Journal of Organic Chemistry; vol. 66; nb.

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6; (2001); p. 1526 - 1529, View in Reaxys; Ferraris; Young; Cox; Dudding; Drury III; Ryzhkov; Taggi; Lectka; Journal of the American Chemical Society; vol. 124; nb. 1; (2002); p. 67 - 77, View in Reaxys; Aitken, R. Alan; Hodgson, Philip K.G.; Morrison, John J.; Oyewale, Adebayo O.; Journal of the Chemical Society. Perkin Transactions 1; nb. 3; (2002); p. 402 - 415, View in Reaxys; Pezet, Frederic; Ait-Haddou, Hassan; Daran, Jean-Claude; Sasaki, Isabelle; Balavoine, Gilbert G. A.; Chemical Communications; nb. 5; (2002); p. 510 - 511, View in Reaxys; Tiecco, Marcello; Testaferri, Lorenzo; Santi, Claudio; Tomassini, Cristina; Marini, Francesca; Bagnoli, Luana; Temperini, Andrea; Chemistry - A European Journal; vol. 8; nb. 5; (2002); p. 1118 - 1124, View in Reaxys; Itoh, Akichika; Kodama, Tomohiro; Masaki, Yukio; Inagaki, Shinji; Synlett; nb. 3; (2002); p. 522 - 524, View in Reaxys; Song, Qishi; Yang, Darong; Zhang, Guangming; Yang, Chongren; Journal of Chemical Ecology; vol. 27; nb. 10; (2001); p. 1929 - 1942, View in Reaxys; Annunziata, Alfonso; Galli, Carlo; Gentili, Patrizia; Guarnieri, Alessandra; Beit-Yannai, Michal; Rappoport, Zvi; European Journal of Organic Chemistry; nb. 13; (2002); p. 2136 - 2143, View in Reaxys; Yadav, Jhillu S; Reddy, B.V.Subba; Parisse, Celine; Carvalho, Peter; Rao, T.Prabhakar; Tetrahedron Letters; vol. 43; nb. 16; (2002); p. 2999 - 3002, View in Reaxys; Kuang, Yong-Qing; Zhang, Sheng-Yong; Jiang, Ru; Wei, Ling-Ling; Tetrahedron Letters; vol. 43; nb. 20; (2002); p. 3669 - 3671, View in Reaxys; Simonneaux, Gerard; De Montigny, Frederic; Paul-Roth, Christine; Gulea, Mihaela; Masson, Serge; Tetrahedron Letters; vol. 43; nb. 20; (2002); p. 3685 - 3687, View in Reaxys; Nishino, Toshiki; Nishiyama, Yutaka; Sonoda, Noboru; Tetrahedron Letters; vol. 43; nb. 20; (2002); p. 3689 - 3691, View in Reaxys; Yamada, Yoichi M.A.; Ichinohe, Masato; Takahashi, Hideyo; Ikegami, Shiro; Tetrahedron Letters; vol. 43; nb. 18; (2002); p. 3431 - 3434, View in Reaxys; Choudary, Boyapati M.; Chowdari, Naidu S.; Jyothi, Karangula; Madhi, Sateesh; Kantam, Mannepalli L.; Advanced Synthesis and Catalysis; vol. 344; nb. 5; (2002); p. 503 - 506, View in Reaxys; Yao, Qingwei; Organic letters; vol. 4; nb. 13; (2002); p. 2197 - 2199, View in Reaxys; Endres, Andreas; Maas, Gerhard; Tetrahedron; vol. 58; nb. 20; (2002); p. 3999 - 4005, View in Reaxys; Al-Aziz Quntar, Abed; Srebnik, Morris; Synthetic Communications; vol. 32; nb. 16; (2002); p. 2575 - 2579, View in Reaxys; Kusakabe, Hirokazu; Yamakage, Kohji; Wakuri, Shinobu; Sasaki, Kiyoshi; Nakagawa, Yuzuki; Watanabe, Mika; Hayashi, Makoto; Sofuni, Tosh-

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517; nb. 1-2; (2002); p. 187 - 198, View in Reaxys; Nishiwaki, Yoshiki; Sakaguchi, Satoshi; Ishii, Yasutaka; Journal of Organic Chemistry; vol. 67; nb. 16; (2002); p. 5663 - 5668, View in Reaxys; De; Sathyanarayana; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 40; nb. 12; (2001); p.

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1189 - 1192, View in Reaxys; Boyd, Derek R.; Sharma, Narain D.; Bowers, Nigel I.; Brannigan, Ian N.; Groocock, Melanie R.; Malone, John F.; McConville, Gareth; Allen, Christopher C. R.; Advanced Synthesis and Catalysis; vol. 347; nb. 7-8; (2005); p. 1081 - 1089, View in Reaxys; Davies, Huw M. L.; Dai, Xing; Journal of Organic Chemistry; vol. 70; nb. 17; (2005); p. 6680 - 6684, View in Reaxys; Gao, Guang-Yao; Harden, Jeremiah D.; Zhang, X. Peter; Organic Letters; vol. 7; nb. 15; (2005); p. 3191 - 3193, View in Reaxys; Hodgson, David M.; Fleming, Matthew J.; Stanway, Steven J.; Organic Letters; vol. 7; nb. 15; (2005); p. 3295 - 3298, View in Reaxys; Wu, Hugjiltu; Xu, Li-Wen; Xia, Chun-Gu; Ge, Jin; Yang, Lei; Synthetic Communications; vol. 35; nb. 10; (2005); p. 1413 - 1417, View in Reaxys; Zhang, Huidong; Zhang, Yanmei; Li, Can; Tetrahedron Asymmetry; vol. 16; nb.

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1580 - 1586, View in Reaxys; Hatefi Ardakani; Moghadam; Saeednia; Pakdin-Parizi; Journal of the Iranian Chemical Society; vol. 13; nb. 4; (2016); p. 631 - 636, View in Reaxys; Bertolotti, Mattia; Brenna, Elisabetta; Crotti, Michele; Gatti, Francesco G.; Monti, Daniela; Parmeggiani, Fabio; Santangelo, Sara; ChemCatChem; vol. 8; nb. 3; (2016); p. 577 - 583, View in Reaxys; Yue, Hui-Lan; Zhao, Xiao-Hui; Jiang, Lei; Shao, Yun; Mei, Li-Juan; Synthetic Communications; vol. 46; nb. 2; (2016); p. 179 - 186, View in Reaxys; Huang; Qi; Cai; Chen; RSC Advances; vol. 6; nb. 23; (2016); p. 19507 - 19514, View in Reaxys; Fardjahromi, Mahsa Asadniaye; Moghadam, Majid; Tangestaninejad, Shahram; Mirkhani, Valiollah; Mohammadpoor-Baltork, Iraj; RSC Advances; vol. 6; nb. 24; (2016); p. 20128 - 20134, View in Reaxys; Wang, Bin; Lee, Yong-Min; Clmancey, Martin; Seo, Mi Sook; Sarangi, Ritimukta; Latour, Jean-Marc; Nam, Wonwoo; Journal of the American Chemical Society; vol. 138; nb.

7; (2016); p. 2426 - 2436, View in Reaxys; Li, Yanjie; Koike, Takashi; Akita, Munetaka; Synlett; vol. 27; nb. 5; (2016); p. 736 - 740, View in Reaxys; Noda, Daisuke; Tahara, Atsushi; Sunada, Yusuke; Nagashima, Hideo; Journal of the American Chemical Society; vol. 138; nb. 8; (2016); p. 2480 - 2483, View in Reaxys; Kannaboina, Prakash; Kumar, K. Anil; Das, Parthasarathi; Organic Letters; vol. 18; nb. 5; (2016); p. 900 - 903, View in Reaxys; Zarnegaryan, Ali; Moghadam, Majid; Tangestaninejad, Shahram; Mirkhani, Valiollah; Mohammdpoor-Baltork, Iraj; New Journal of Chemistry; vol. 40; nb. 3; (2016); p. 2280 - 2286, View in Reaxys; Lazar, Anish; Vinod, Chathakudath P.; Singh, Anand Pal; New Journal of Chemistry; vol. 40; nb. 3; (2016); p. 2423 - 2432, View in Reaxys; Zhang, Teng; Manna, Kuntal; Lin, Wenbin; Journal of the American Chemical Society; vol. 138; nb. 9; (2016); p.

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Effect (Pharmacological Data)

genotoxic

Species or Test-System (Pharmacological Data)

Chinese hamster lung cells

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Method (Pharmacological Data)

cells were cultured with Eagle's medium; 2E4 cells were plated on 60 mm plate and cultured for 72 h at 37 deg C; treated with title comp. with or without metabolic activation for 6 h and without metabolic activation for 24 h and 48 h

Further Details (Pharmacological Data)

chromosome aberrations (CA) were scored

Results

CA-negative at doses manifesting 50 percent or less than 50 percent cytotoxicity

Kusakabe, Hirokazu; Yamakage, Kohji; Wakuri, Shinobu; Sasaki, Kiyoshi; Nakagawa, Yuzuki; Watanabe, Mika; Hayashi, Makoto; Sofuni, Toshio; Ono, Hiroshi; Tanaka, Noriho; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 517; nb. 1-2; (2002); p. 187 - 198, View in Reaxys 3 of 3

Effect (Pharmacological Data)

growth inhibition

Species or Test-System (Pharmacological Data)

E. coli JM101

Concentration (Pharmacological Data)

1 - 5 percent v/v

Method (Pharmacological Data)

bacteria incubated in M9 medium, bis(2-ethylhexyl) phthalate (50percent v/v) and title comp. up to 24 h

Results

no significant influence on growth rate up to 5percent (v/v); graphical representation

Schmid, Andreas; Hofstetter, Karin; Feiten, Hans-Juergen; Hollmann, Frank; Witholt, Bernard; Advanced Synthesis and Catalysis; vol. 343; nb. 6-7; (2001); p. 732 - 737, View in Reaxys Ecotoxicology (4) 1 of 4

Effect (Ecotoxicology)

toxicity to invertebrates

Species or Test-System (Ecotoxicology)

Viviparus viviparus L., freshwater snail

Exposure Period (Ecotoxicology)

24 - 96 h

Method (Ecotoxicology)

mean values; animals collected from the streams and rivers on the outskirts of Zagreb; in dechlorinated tap water; solution conditions: 18 deg C, pH 7.0-7.8, hardness 324.8-359.0 mg/L as CaCO3; LC50 determined by Probit method

Further Details (Ecotoxi- 10 animals/dish; experiment repeated 3 times cology) Type (Ecotoxicology)

LC50

Value of Type (Ecotoxicology)

2.398 - 5.646 percent v/v

Erben; Maguire; Lajtner; Barcot; Pisi; Bulletin of Environmental Contamination and Toxicology; vol. 70; nb. 1; (2003); p. 124 - 130, View in Reaxys 2 of 4

Effect (Ecotoxicology)

toxicity to invertebrates

Species or Test-System (Ecotoxicology)

Amphimelania holandi Fer., freshwater snail

Exposure Period (Ecotoxicology)

24 - 96 h

Method (Ecotoxicology)

mean values; animals collected from the streams and rivers on the outskirts of Zagreb; in dechlorinated tap water; solution conditions: 18 deg C, pH 7.0-7.8, hardness 324.8-359.0 mg/L as CaCO3; LC50 determined by Probit method

Further Details (Ecotoxi- 10 animals/dish; experiment repeated 3 times cology) Type (Ecotoxicology)

LC50

Value of Type (Ecotoxicology)

0.117 - 0.621 percent v/v

Erben; Maguire; Lajtner; Barcot; Pisi; Bulletin of Environmental Contamination and Toxicology; vol. 70; nb. 1; (2003); p. 124 - 130, View in Reaxys 3 of 4

Effect (Ecotoxicology)

toxicity to invertebrates

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Species or Test-System (Ecotoxicology)

Asellus aquaticus L., freshwater crustacean

Exposure Period (Ecotoxicology)

24 - 96 h

Method (Ecotoxicology)

mean values; animals collected from the streams and rivers on the outskirts of Zagreb; in dechlorinated tap water; solution conditions: 18 deg C, pH 7.0-7.8, hardness 324.8-359.0 mg/L as CaCO3; LC50 determined by Probit method

Further Details (Ecotoxi- 10 animals/dish; experiment repeated 3 times cology) Type (Ecotoxicology)

LC50

Value of Type (Ecotoxicology)

0.096 - 0.294 percent v/v

Erben; Maguire; Lajtner; Barcot; Pisi; Bulletin of Environmental Contamination and Toxicology; vol. 70; nb. 1; (2003); p. 124 - 130, View in Reaxys 4 of 4

Effect (Ecotoxicology)

toxicity to invertebrates

Species or Test-System (Ecotoxicology)

Gammarus fossarum Koch., freshwater crustacean

Exposure Period (Ecotoxicology)

24 - 96 h

Method (Ecotoxicology)

mean values; animals collected from the streams and rivers on the outskirts of Zagreb; in dechlorinated tap water; solution conditions: 18 deg C, pH 7.0-7.8, hardness 324.8-359.0 mg/L as CaCO3; LC50 determined by Probit method

Further Details (Ecotoxi- 10 animals/dish; experiment repeated 3 times cology) Type (Ecotoxicology)

LC50

Value of Type (Ecotoxicology)

0.037 - 0.055 percent v/v

Erben; Maguire; Lajtner; Barcot; Pisi; Bulletin of Environmental Contamination and Toxicology; vol. 70; nb. 1; (2003); p. 124 - 130, View in Reaxys Exposure Assessment (4) Exposure Sources presence in emis- heating of nitrosions gen-containing plastics such as acetonitrile-butadiene-styrene at low temp. (<=300 deg C); table

References Watanabe, Mafumi; Nakata, Chisto; Wu, Wei; Kawamoto, Katsuya; Noma, Yukio; Chemosphere; vol. 68; nb. 11; (2007); p. 2063 - 2072, View in Reaxys

presence in carbonaceous aerosol particles

diesel soot and Matuschek, Georg; Karg, Erwin; Schroeppel, Andreas; Schulz, Holger; Schmid, Otparticles from tire mar; Environmental Science and Technology; vol. 41; nb. 24; (2007); p. 8406 - 8411, and break wear View in Reaxys and laboratory generated aerosol (diffusion flame soot)

presence in air

biogenic volatile Helmig, Detlev; Klinger, Lee F.; Guenther, Alex; Vierling, Lee; Geron, Chris; Zimcompounds merman, Patrick; Chemosphere; vol. 38; nb. 9; (1999); p. 2163 - 2187, View in Reaxys (BVOCs) emissions from vegetation species; fluxes were measured in three ecosystems: Fernbank Forest, Atlanta GA; Willow Springs, Chequamegon National Forest, northern Wiscon-

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sin; Temple Ridge, western Colorado presence in air

biogenic volatile Helmig, Detlev; Klinger, Lee F.; Guenther, Alex; Vierling, Lee; Geron, Chris; Zimorganic commerman, Patrick; Chemosphere; vol. 38; nb. 9; (1999); p. 2189 - 2204, View in Reaxys pounds (BVOCs) emissions from vegetation species; fluxes were measured in three ecosystems: Fernbank Forest, Atlanta GA; Willow Creek, Rhinelander, WI; Temple Ridge, CO

Concentration in the Environment (2) 1 of 2

Media (Concentration in the Environment)

sludge

Contamination Concentration

1600 ppm

Method, Remarks (Concentration in the Environment)

the sludge was a mixture of styrene manufacturing wastes and petroleum products; extracted with acetone; GC/MS

Washington, Michael D.; Larsen, David W.; Manahan, Stanley E.; Environmental Science and Technology; vol.

33; nb. 8; (1999); p. 1263 - 1268, View in Reaxys 2 of 2

Media (Concentration in the Environment)

emission of TOL/CCl4 incineration

Location

U.S. EPA

Contamination Concentration

75 ng/l

Method, Remarks (Concentration in the Environment)

73 kW rotary kiln incinerator simulator; charges consisted of a mixture of 50 percent toluene and 50 percent CCl4; total mass, 200 g; adsorbed into 180 g of ground corncob; steady-state gas flow conditions; 870 deg C; collected in Tedlar bags; GC/MS analysis

Lemieux; Linak; DeBenedictis; Ryan; Wendt; Dunn; Hazardous Waste and Hazardous Materials; vol. 11; nb. 1; (1994); p. 111 - 128, View in Reaxys Use (6) Use Pattern Stabilization of 3carbon chloroolefins and/or chloroalkanes during storage in ferrous containers

Location

References

Page/Page column 8

Patent; ARKEMA INC.; ELSHEIKH, Maher Y.; BONNET, Philippe; WO2011/60211; (2011); (A1) English, View in Reaxys

Monomer unit for macroinitiator

Patent; THE PROCTER and GAMBLE COMPANY; EP983039; (2005); (B1) English, View in Reaxys

styrene monomer

Patent; Liechty, Anne; Thibout, Camille; US2005/287092; (2005); (A1) English, View in Reaxys; Patent; Liechty, Anne; Thibout, Camille; US2005/287099; (2005); (A1) English, View in Reaxys

Monomer for hydrophobic polymeric core of adhesin-specific nanoparticles

Patent; CLEMSON UNIVERSITY; WO2005/30126; (2005); (A2) English, View in Reaxys

rective phlegmatiser

Patent; Akzo Nobel N.V.; EP1216991; (2002); (A1) English, View in Reaxys

useful as rective phlegmatiser in polymer industry

Patent; Akzo Nobel N.V.; EP1216991; (2002); (A1) English, View in Reaxys

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Quantum Chemical Calculations (2) Calculated Prop- Method (Quantum References erties Chemical Calculations) Atom distances, HF - Hartree-Fock Karthikeyan, N.; Joseph Prince, J.; Ramalingam, S.; Periandy, S.; Spectrochimica angles; IR bands, (calcns.)

Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 143; (2015); p. 107 - 119, intensities, transiView in Reaxys tion moments; Raman bands, intensities, transition moments Atom distances, DFT - density angles; IR bands, functional methintensities, transi- ods tion moments; Raman bands, intensities, transition moments; NMR shifts, signals, intensities, transition moments; Molecular orbitals; Electronic energy levels; Band structure; UV/VIS wave lengths; Oscillator strength, transition probability; Electronegativity; Dipole moment, dipole moment derivative; Polarizability, polarizability derivatives; Contour map

Karthikeyan, N.; Joseph Prince, J.; Ramalingam, S.; Periandy, S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 143; (2015); p. 107 - 119, View in Reaxys

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