Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water

被引：25
|
作者：
Lin, Jin-Hong [1 ]
Zhang, Cheng-Pan [1 ]
Xiao, Ji-Chang [1 ]
机构：
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Organofluorine Chem, Shanghai 200032, Peoples R China
来源：
GREEN CHEMISTRY | 2009年 / 11卷 / 11期
关键词：
MICHAEL ADDITION; ORGANOCATALYST; ACID; PROLINAMIDES; DESIGN;
D O I：
10.1039/b916583e
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Water was found to be a suitable reaction medium for the direct asymmetric aldol reaction of various cyclic ketones with aryl aldehydes catalyzed by a primary-tertiary diamine-Bronsted acid.
引用
收藏
页码：1750 / 1753
页数：4
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