详细信息

Highly enantioselective Michael addition of acetone to nitroolefins catalyzed by chiral bifunctional primary amine-thiourea catalysts with acetic acid  ( SCI-EXPANDED收录)  

文献类型:期刊文献

英文题名:Highly enantioselective Michael addition of acetone to nitroolefins catalyzed by chiral bifunctional primary amine-thiourea catalysts with acetic acid

作者:Gu, Qing;Guo, Xing-Tao;Wu, Xin-Yan[1]

机构:[1]E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China; E China Univ Sci & Technol, Inst Fine Chem, Shanghai 200237, Peoples R China

年份:2009

卷号:65

期号:27

起止页码:5265

外文期刊名:TETRAHEDRON

收录:;WOS:【SCI-EXPANDED(收录号:WOS:000267587600017),CCR-EXPANDED(收录号:WOS:000267587600017)】;

基金:We thank the National Natural Science Foundation of China (20402004, 20772029) and New Century Excellent Talents in University (NCET-07-0286) for financial support.

语种:英文

摘要:Highly enantioselective Michael reaction of acetone with a variety of nitroolefins catalyzed by N-[(1R,2R)-2-aminocyclohexyl]-N'-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)-)-thiourea (1b) together with acetic acid is described. The Michael addition products were obtained in high yields (76-94%) and Lip to 96% ee. (C) 2009 Elsevier Ltd. All rights reserved.

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