N-Iodosuccinimide -: An effective reagent for regioselective heterocyclization of o-cyclohex-2'-enylanilines for the synthesis of hexahydrocarbazoles

被引：9

作者：

Majumdar, KC ^{[1
]}

Kundu, UK ^{[1
]}

Das, U ^{[1
]}

Jana, NK ^{[1
]}

Roy, B ^{[1
]}

机构：

[1] Kalyani Univ, Dept Chem, Kalyani 741235, W Bengal, India

来源：

CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE | 2005年 / 83卷 / 01期

关键词：

N-iodosuccinimide; hexahydrocarbazole; heterocyclization; carbazole; Claisen rearrangement;

D O I：

10.1139/V04-162

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A number of carbazoles are synthesized in good yields by the N-iodosuccinimide mediated heterocyclization of o-cyclohex-2'-enylanilines in acetonitrile at -10 degreesC for 45 min followed by heating with palladium-charcoal (10%) in benzene (80 degreesC) for 18-20 h.

引用

页码：63 / 67

页数：5

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