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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
ZUSAMMENFASSUNG

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%).

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

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