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
收藏
页码：5189 / 5192
页数：4
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