Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C.

被引：19

作者：

Dubovitskii, SV

机构：

[1] Chemistry Department, Far Eastern State University, 690600, Vladivostok

来源：

TETRAHEDRON LETTERS | 1996年 / 37卷 / 29期

关键词：

D O I：

10.1016/0040-4039(96)01052-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

An efficient synthesis of a 12H-pyrido[1,2-a:3,4-b']diindole system is proposed. 3-Methylindole has been converted into homofascaplysin C by a four reaction sequence in which the last step is dehydrogenation and oxidation of the methyl- to formyl group at the same time. Copyright (C) 1996 Elsevier Science Ltd

引用

页码：5207 / 5208

页数：2

共 7 条

[1] TOTAL SYNTHESES OF THE MARINE SPONGE PIGMENTS FASCAPLYSIN AND HOMOFASCAPLYSIN-B AND HOMOFASCAPLYSIN-C [J].