N-(trans-1-Propenyl)carbazole:: an excellent dienophile for cation radical Diels-Alder cycloadditions

被引：10

作者：

Gao, DX ^{[1
]}

Bauld, NL ^{[1
]}

机构：

[1] Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA

来源：

TETRAHEDRON LETTERS | 2000年 / 41卷 / 32期

基金：

美国国家科学基金会;

关键词：

cycloaddition; Diels-Alder; propenylcarbazole; aminium salt;

D O I：

10.1016/S0040-4039(00)01046-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The efficient, regiospecific, and periselective Diels-Alder cycloadditions of N-(trans-1-propenyl)carbazole, a highly electron rich dienophile, to both acyclic and cyclic conjugated dienes is found to be induced by tris(4-bromophenyl)aminium hexachloroantimonate. (C) 2000 Elsevier Science Ltd. All rights reserved.

引用

页码：5997 / 6000

页数：4

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