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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