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Volumn 8, Issue 20, 2010, Pages 4767-4774

A highly efficient asymmetric Michael addition of α,α- disubstituted aldehydes to maleimides catalyzed by primary amine thiourea salt

(6) Yu, Feng a Jin, Zhichao a Huang, Huicai a Ye, Tingting a Liang, Xinmiao a Ye, Jinxing a

a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACID SYSTEMS; BIFUNCTIONAL; HIGH YIELD; MALEIMIDES; MICHAEL ADDITIONS; PRIMARY AMINES; QUATERNARY CARBON;

ACIDS; ADDITION REACTIONS; ALDEHYDES; CATALYSIS; ENANTIOSELECTIVITY; THIOUREAS;

UREA;

ALDEHYDE; AMINE; BENZOIC ACID; MALEIMIDE DERIVATIVE; THIOUREA;

ARTICLE; CATALYSIS; CHEMISTRY; STEREOISOMERISM;

ALDEHYDES; AMINES; BENZOIC ACID; CATALYSIS; MALEIMIDES; STEREOISOMERISM; THIOUREA;

EID: 77957671263 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c0ob00154f Document Type: Article

Times cited : (76)

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