A new diastereoselective route to 5-substituted-8-methylindolizidines.: Synthesis of indolizidine (-)-209B

被引：24

作者：

Bardou, A ^{[1
]}

Célérier, JP ^{[1
]}

Lhommet, G ^{[1
]}

机构：

[1] Univ Paris 06, CNRS, Lab Chim Heterocycles, F-75252 Paris 05, France

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 29期

关键词：

D O I：

10.1016/S0040-4039(98)01040-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The highly diastereoselective synthesis of the indolizidine alkaloid (-) 209B is described via the diastereoselective alkylation of a chiral cyclic beta-amino ester prepared from (R)-methylbenzylamine. (C) 1998 Published by Elsevier Science Ltd. All rights reserved.

引用

页码：5189 / 5192

页数：4

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