α—Selective cross-coupling reaction of allyltrifluorosilanes: Remarkable ligand effect on the regiochemistry
Y Hatanaka, K Goda, T Hiyama
Index: Hatanaka, Yasuo; Goda, Ken-Ichi; Hiyama, Tamejiro Tetrahedron Letters, 1994 , vol. 35, # 35 p. 6511 - 6514
Full Text: HTML
Citation Number: 38
Abstract
Abstract The cross-coupling reaction of allyltrifluorosilanes with aryl halides or aryl triflates promoted by a fluoride salt takes place at the α-carbon of the allyltrifluorosilanes in the presence of a catalytic amount of PdCl 2 [Ph 2 P (CH 2) n PPh 2](n= 2, 3), giving allylic arenes with high regioselectivity.
Related Articles:
[Lee, Kooyeon; Kim, Hyunseok; Mo, Juntae; Lee, Phil Ho Chemistry - An Asian Journal, 2011 , vol. 6, # 8 p. 2147 - 2157]
[Zimmerman, Howard E.; Swafford, Richard L. Journal of Organic Chemistry, 1984 , vol. 49, # 17 p. 3069 - 3083]
[Zimmerman, Howard E.; Swafford, Richard L. Journal of Organic Chemistry, 1984 , vol. 49, # 17 p. 3069 - 3083]
[Mizuno, Kazuhiko; Nakanishi, Kazuhisa; Otsuji, Yoshio Chemistry Letters, 1988 , p. 1833 - 1836]
[Mizuno, Kazuhiko; Ikeda, Munehiro; Otsuji, Yoshio Tetrahedron Letters, 1985 , vol. 26, # 4 p. 461 - 464]