TANDEM MICHAEL REACTIONS FOR THE CONSTRUCTION OF PYRROLIDINE AND PIPERIDINE RING-SYSTEMS

被引：26

作者：

BARCO, A ^{[1
]}

BENETTI, S ^{[1
]}

CASOLARI, A ^{[1
]}

POLLINI, GP ^{[1
]}

SPALLUTO, G ^{[1
]}

机构：

[1] DIPARTIMENTO SCI FARMACEUT,I-44100 FERRARA,ITALY

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 21期

关键词：

D O I：

10.1016/S0040-4039(00)89020-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A convergent one-pot construction of disubstituted pyrrolidine and piperidine frameworks has been accomplished through a simple protocol involving intermolecular conjugate addition of a nitrogen nucleophile to an electrophilic olefin followed by intramolecular trapping of the generated enolate by a built-in α,β,-unsaturated acceptor. © 1990.

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页码：3039 / 3042

页数：4

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