Organocatalytic and enantioselective Michael reaction of malonates to 3-Nitro-2H-chromenes

被引：12

作者：

Chen, Wei-Yi ^{[1
]}

Li, Ping ^{[2
]}

Xie, Jian-wu ^{[2
]}

Li, Xin-Sheng ^{[2
]}

机构：

[1] Suzhou Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China

[2] Zhejiang Normal Univ, Zhejiang Key Lab React Chem Solid Surfaces, Inst Phys Chem, Jinhua 321004, Peoples R China

来源：

CATALYSIS COMMUNICATIONS | 2011年 / 12卷 / 06期

关键词：

Enantioselective Michael addition; 3-nitro-2H-chromene; Malonates; Organocatalytic; Cinchona alkaloid; BIFUNCTIONAL ORGANOCATALYSTS; THIOUREA; NITROOLEFINS; NITROALKENES; DERIVATIVES; KETONES;

D O I：

10.1016/j.catcom.2010.11.014

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

An organocatalytic enantioselective Michael reaction of malonates to 3-nitro-2H-chromenes has been developed; the products could be obtained in high yields and good enantioselectivities. (C) 2010 Published by Elsevier B.V.

引用

页码：502 / 504

页数：3

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