Intramolecular nitrile oxide cycloaddition (INOC) of substituted amido-oximes

被引：15

作者：

Chiacchio, U ^{[1
]}

Corsaro, A ^{[1
]}

Librando, V ^{[1
]}

Rescifina, A ^{[1
]}

Romeo, R ^{[1
]}

Romeo, G ^{[1
]}

机构：

[1] UNIV MESSINA,DIPARTIMENTO FARMACOCHIM,I-98168 MESSINA,ITALY

来源：

TETRAHEDRON | 1996年 / 52卷 / 45期

关键词：

D O I：

10.1016/0040-4020(96)00884-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Functionalized enantiomerically pure 3,4-dehydropyrrolidin-2-one and 1,2-dehydropyrrolizidin-3-one systems have been achieved by intramolecular nitrile oxide cycloaddition, starting from enamido-oximes, and by subsequent reduction of the obtained cycloadducts. Copyright (C) 1996 Published by Elsevier Science Ltd

引用

页码：14323 / 14334

页数：12

共 37 条

[1]

ANNUNZIATA R, 1989, GAZZ CHIM ITAL, V119, P253

[2]

[Anonymous], 1991, CHEM HETEROCYCL COM+, DOI DOI 10.1021/jp212588h

[3] THE INTRAMOLECULAR NITRILE OXIDE CYCLOADDITION ROUTE TO FORSKOLIN [J].