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  • Enantioselective Michael addition of ketones to maleimides catalyzed by bifunctional monosulfonyl DPEN salt.

Enantioselective Michael addition of ketones to maleimides catalyzed by bifunctional monosulfonyl DPEN salt.

Chemical communications (Cambridge, England) (2010-05-21)
Feng Yu, Xiaomin Sun, Zhichao Jin, Shigang Wen, Xinmiao Liang, Jinxing Ye
초록

An unprecedented enantioselective Michael addition of various ketones to maleimides catalyzed by a simple bifunctional primary amine, monosulfonyl DPEN salt, is reported and provides the desired adducts in good to excellent yields (up to 99%) with excellent enantioselectivities (up to 99%).

MATERIALS
제품 번호
브랜드
제품 설명

Sigma-Aldrich
N,N′-Diphenylethylenediamine, 98%
Sigma-Aldrich
(1R,2R)-(+)-1,2-Diphenylethylenediamine, 97%