Intramolecular nitrone cycloaddition: Stereoselective synthesis of piperidine systems

被引：7
作者：
Chiacchio, U
Rescifina, A
Casuscelli, F
Piperno, A
Pisani, V
Romeo, R
机构：
[1] UNIV MESSINA,DIPARTIMENTO FARMACOCHIM,I-98168 MESSINA,ITALY
[2] UNIV ARCAVACATA DI RENDE,DIPARTIMENTO CHIM,I-87036 RENDE,ITALY
来源：
TETRAHEDRON | 1996年 / 52卷 / 45期
关键词：
D O I：
10.1016/0040-4020(96)00883-6
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A synthetic approach to isomerically functionalized piperidine systems has been designed by intramolecular nitrone cycloaddition, starting from beta-enamidoaldehydes, and by subsequent reductive ring-opening of the obtained fused delta-lactams. Copyright (C) 1996 Published by Elsevier Science Ltd
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页码：14311 / 14322
页数：12
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