Modification of chiral monodentate phosphine (MOP) ligands for palladium-catalyzed asymmetric hydrosilylation of styrenes

被引：26
|
作者：
Hayashi, T [1 ]
Hirate, S [1 ]
Kitayama, K [1 ]
Tsuji, H [1 ]
Torii, A [1 ]
Uozumi, Y [1 ]
机构：
[1] Kyoto Univ, Grad Sch Sci, Dept Chem, Sakyo Ku, Kyoto 6068502, Japan
来源：
CHEMISTRY LETTERS | 2000年 / 11期
关键词：
D O I：
10.1246/cl.2000.1272
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
In the palladium-catalyzed asymmetric hydrosilylation of styrene with trichlorosilane, several chiral monophosphine ligands, (R)-2-diarylphosphino-1,1'-binaphthyls (2), were examined for their enantioselectivity. The highest enantioselectivity was observed in the reaction with (R)-2-bis[3,5-bis(trifluoromethyl)phenyl]phosphino- 1,1'-binaphthyl (2g), which gave (S)-1-phenylethanol of 98% ee after oxidation of the hydrosilylation product.
引用
收藏
页码：1272 / 1273
页数：2
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