A mild and efficient procedure for ring-opening reactions of piperidine and pyrrolidine derivatives by single electron transfer photooxidation

被引：35

作者：

Cocquet, G ^{[1
]}

Ferroud, C ^{[1
]}

Guy, A ^{[1
]}

机构：

[1] Conservatoire Natl Arts & Metiers, CNRS, Chim Organ Lab, F-75141 Paris 03, France

来源：

TETRAHEDRON | 2000年 / 56卷 / 19期

关键词：

photochemistry; oxidation; nitrogen heterocycles; azo compounds; cleavage reactions;

D O I：

10.1016/S0040-4020(00)00048-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Various N-arylamino-1-pyrrolidines and N-arylamino-1-piperidines are selectively converted into the corresponding acyclic aminoaldehydes or amino-dialkylacetals under mild photooxidation conditions. (C) 2000 Elsevier Science Ltd. All rights reserved.

引用

页码：2975 / 2984

页数：10

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