Chlorosilane-accelerated conjugate addition of catalytic and stoichiometric organocopper reagents
S Matsuzawa, Y Horiguchi, E Nakamura, I Kuwajima
Index: Matsuzawa, Satoshi; Horiguchi, Yoshiaki; Nakamura, Eiichi; Kuwajima, Isao Tetrahedron, 1989 , vol. 45, # 2 p. 349 - 362
Full Text: HTML
Citation Number: 151
Abstract
Trialkylsilyl chlorides, particularly in combination with hexamethylphosphoramide or 4- dimethylaminopyridine, dramatically accelerates the conjugate addition of catalytic and stoichiometric organocopper reagents onto enones, enals, and enoates, in which very high degrees of stereo-and chemoselectivities were observed.
Related Articles:
[Nakao, Yoshiaki; Chen, Jinshui; Imanaka, Hidekazu; Hiyama, Tamejiro; Ichikawa, Yoshitaka; Duan, Wei-Liang; Shintani, Ryo; Hayashi, Tamio Journal of the American Chemical Society, 2007 , vol. 129, # 29 p. 9137 - 9143]
[Varadharaj, Govindarajulu; Hazell, Keith; Reeve, Christopher D. Tetrahedron Asymmetry, 1998 , vol. 9, # 7 p. 1191 - 1195]
[Yang, Jingyue; Dudley, Gregory B. Tetrahedron Letters, 2007 , vol. 48, # 44 p. 7887 - 7889]
[Yamamoto, Keiji; Ikeda, Kiyoshi; Yin, Leong Kwai Journal of Organometallic Chemistry, 1989 , vol. 370, p. 319 - 332]
[Gini, Francesca; Hessen, Bart; Minnaard, Adriaan J. Organic Letters, 2005 , vol. 7, # 23 p. 5309 - 5312]