Synthetic studies on the erythrina alkaloids.: Preparation of (±)-2-epi-erythrinitol

被引：38

作者：

Rigby, JH ^{[1
]}

Deur, C ^{[1
]}

Heeg, MJ ^{[1
]}

机构：

[1] Wayne State Univ, Dept Chem, Detroit, MI 48202 USA

来源：

TETRAHEDRON LETTERS | 1999年 / 40卷 / 38期

关键词：

alkaloids; Heck reaction; isocyanates;

D O I：

10.1016/S0040-4039(99)01389-1

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The erythrina alkaloid, 1,3,4,6-tetrahydro-3,15,1 6-trimethoxyerythrinan-2-ol (2-epi-erythrinitol), has been synthesized by a sequence featuring a [1+4] vinyl isocyanate-isocyanide cycloaddition followed by an intramolecular Heck reaction for assembly of the erythrinan ring system. (C) 1999 Elsevier Science Ltd. All rights reserved.

引用

页码：6887 / 6890

页数：4

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