Catalytic asymmetric Michael addition with curcumin derivative

被引：38

作者：

Li, Wenjun ^{[1
]}

Wu, Wenbin ^{[1
]}

Yu, Feng ^{[1
]}

Huang, Huicai ^{[1
]}

Liang, Xinmiao ^{[1
]}

Ye, Jinxing ^{[1
]}

机构：

[1] E China Univ Sci & Technol, Engn Res Ctr Pharmaceut Proc Chem, Minist Educ, Sch Pharm, Shanghai 200237, Peoples R China

来源：

ORGANIC & BIOMOLECULAR CHEMISTRY | 2011年 / 9卷 / 07期

基金：

中国国家自然科学基金;

关键词：

ENANTIOSELECTIVE CONJUGATE ADDITION; HYDROGEN-BONDING DONORS; CINCHONA ALKALOID DERIVATIVES; AMINE-THIOUREA CATALYST; BIFUNCTIONAL ORGANOCATALYSTS; EFFICIENT ORGANOCATALYSTS; 1,3-DICARBONYL COMPOUNDS; ORGANIC CATALYST; MANNICH REACTION; BASE CATALYSTS;

D O I：

10.1039/c0ob00757a

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Catalytic asymmetric Michael additions with curcumin derivatives were achieved by a new series of tertiary amine-thiourea organocatalysts to afford the Michael adducts in high yields and excellent enantioselectivities.

引用

页码：2505 / 2511

页数：7

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