Organocatalytic asymmetric epoxidation of olefins by chiral ketones

被引：410
作者：
Shi, Y [1 ]
机构：
[1] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
来源：
ACCOUNTS OF CHEMICAL RESEARCH | 2004年 / 37卷 / 08期
关键词：
D O I：
10.1021/ar030063x
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Chiral ketones have been shown to be effective organocatalysts for asymmetric epoxidation of olefins with broad substrate scope. High enantioselectivity has been obtained for a wide variety of trans and trisubstituted olefins, as well as a number of cis olefins, with encouragingly high ee's for some terminal olefins. The stereochemical outcome of the reaction can be rationalized by a spiro transition state model.
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收藏
页码：488 / 496
页数：9
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