Synthesis of batzelladine E and its E isomer

被引：52

作者：

Snider, BB ^{[1
]}

Chen, JS ^{[1
]}

机构：

[1] Brandeis Univ, Dept Chem, Waltham, MA 02254 USA

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 32期

基金：

美国国家卫生研究院;

关键词：

guanidines; Biginelli reaction;

D O I：

10.1016/S0040-4039(98)01196-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The synthesis of 4E established that batzelladine E (4Z) has the Z- rather than the E-stereochemistry previously depicted. Batzelladine E (4Z) has been synthesized by an efficient 9-step route in 3% overall yield. (C) 1998 Elsevier Science Ltd. All rights reserved.

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页码：5697 / 5700

页数：4

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