Aza-Baylis-Hillman reaction of N-tosylated imines with β-substituted α,β-unsaturated esters

被引：39

作者：

Shi, YL ^{[1
]}

Shi, M ^{[1
]}

机构：

[1] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organomet Chem, Shanghai 200032, Peoples R China

来源：

TETRAHEDRON | 2006年 / 62卷 / 2-3期

基金：

中国国家自然科学基金;

关键词：

N-tosylated imine; Aza-Baylis-Hillman reaction; beta-substituted activated olefins; Lewis base;

D O I：

10.1016/j.tet.2005.09.058

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Aza-Baylis-Hillman reaction of N-tosylated imines with beta-substituted alpha,beta-unsaturated esters can take place under mild reaction conditions to give the corresponding Baylis-Hillman adducts in moderate to excellent Yields. (c) 2005 Elsevier Ltd. All rights reserved.

引用

页码：461 / 475

页数：15

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