Efficient entry to polysubstituted pyrrolizidines, indolizidines and quinolizidines via a sequential reaction process

被引：5

作者：

Ma, Dawei ^{[1
]}

Zhu, Wei ^{[1
]}

机构：

[1] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R China

来源：

SYNLETT | 2006年 / 08期

关键词：

cascade reactions; pyrrolizidines; indolizidines; quinolizidines;

D O I：

10.1055/s-2006-932488

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A sequential S(N)2-Michael addition-Michael addition reaction process between omega-iodo-alpha,beta-alkynoates and delta- or gamma-amino alpha,beta-unsaturated esters is developed, which affords polysubstituted pyrrolizidines, indolizidines or quinolizidines in good yields.

引用

页码：1181 / 1184

页数：4

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