Synthesis and absolute configuration of (-)-normalindine

被引：30
|
作者：
Ohba, M
Kubo, H
Fujii, T
Ishibashi, H
Sargent, MV
Arbain, D
机构：
[1] UNIV WESTERN AUSTRALIA,DEPT CHEM,PERTH,WA 6907,AUSTRALIA
[2] UNIV ANDALAS,FMIPA,DEPT PHARM,PADANG,W SUMATRA,INDONESIA
来源：
TETRAHEDRON LETTERS | 1997年 / 38卷 / 38期
关键词：
D O I：
10.1016/S0040-4039(97)01568-2
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The first chiral synthesis of the Strychnos and Ophiorrhiza alkaloid (-)-normalindine has been accomplished through a route starting from L-alanine methyl ester and exploiting intramolecular oxazole-olefin Diels-Alder reaction. As a result, the absolute stereochemistry of normalindine has been defined as represented by formula(-)-1. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码：6697 / 6700
页数：4
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