Synthesis of indolocarbazoles via sequential palladium catalyzed cross-coupling and benzannulation reactions

被引：34

作者：

Merlic, CA

McInnes, DM

机构：

[1] Dept. of Chemistry and Biochemistry, University of California, Los Angeles

来源：

TETRAHEDRON LETTERS | 1997年 / 38卷 / 44期

基金：

美国国家卫生研究院; 美国国家科学基金会;

关键词：

D O I：

10.1016/S0040-4039(97)10088-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Differentially substituted indolocarbazoles are readily prepared via a synthetic route employing two palladium catalyzed reactions. First, biindoles are prepared from a palladium catalyzed cross coupling reaction. Second, a new palladium catalyzed benzannulation reaction employing biindolyl iodides and alkynes provides indolocarbazoles. (C) 1997 Elsevier Science Ltd.

引用

页码：7661 / 7664

页数：4

共 23 条

[1]

[Anonymous], 1993, STUDIES NATURAL PROD

[2] EFFICIENT SYNTHESIS OF 2-CHLOROINDOLE, 2-BROMOINDOLE, AND 2-IODOINDOLE [J].