A convenient route to spiropyrrolidinyl-oxindole alkaloids via C-3 substituted ene-pyrrolidine carbamate radical cyclization

被引：25

作者：

Cossy, J ^{[1
]}

Cases, M ^{[1
]}

Pardo, DG ^{[1
]}

机构：

[1] ESPCI, Chim Organ Lab, CNRS, F-75231 Paris 05, France

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 16期

关键词：

D O I：

10.1016/S0040-4039(98)00193-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A short access to spiropyrrolidinyl-oxindole alkaloids via a substituted ene-pyrrolidine carbamate, synthesized from the commercially available tert-butyl 1-pyrrolidine carboxylate, is described. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：2331 / 2332

页数：2

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