Novel routes to pyrroles, indoles and carbazoles -: Applications in natural product synthesis

被引：207

作者：

Agarwal, S ^{[1
]}

Cämmerer, S ^{[1
]}

Filali, S ^{[1
]}

Fröhner, W ^{[1
]}

Knöll, J ^{[1
]}

Krahl, MP ^{[1
]}

Reddy, KR ^{[1
]}

Knölker, HJ ^{[1
]}

机构：

[1] Tech Univ Dresden, Inst Organ Chem, D-01069 Dresden, Germany

来源：

CURRENT ORGANIC CHEMISTRY | 2005年 / 9卷 / 15期

关键词：

D O I：

10.2174/138527205774370496

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Using organometallic chemistry several novel methods for the efficient construction of pyrroles, indoles, and carbazoles have been developed. The key reactions are transition metal-mediated or -catalyzed oxidative cyclizations and cycloadditions. In the present article we summarize some recent applications of these methods to short and convergent total syntheses of naturally occurring biologically active alkaloids including fused indolizidines, yohimbanes, Amaryllidaceae alkaloids, and carbazoles.

引用

页码：1601 / 1614

页数：14

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