Regio- and enantio-selective allylic alkylation catalysed by a chiral monophosphine-palladium complex

被引:118
作者
Hayashi, T
Kawatsura, M
Uozumi, Y
机构
[1] Department of Chemistry, Faculty of Science, Kyoto University, Sakyo
关键词
D O I
10.1039/a700045f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Allylic alkylation of racemic 1-arylprop-2-enyl acetates [ArCH(OAc)CH=CH2] with the sodium enolate of dimethyl methylmalonate in the presence of a palladium catalyst coordinated with (R)-2-diphenylphosphino-2'-methoxyl-1,1'-binaphthyl [(R)-MeO-MOP] proceeds with high branch selectivity (90%) to give chiral products [ArC*H-(Nu)CH=CH2] of up to 87% ee.
引用
收藏
页码:561 / 562
页数:2
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