COPPER-CATALYZED DOMINO REACTION OF HETEROALLENES TOWARDS BENZO-HETEROCYCLE COMPOUNDS

被引：8

作者：

Wang, Fei ^{[1
]}

Zhao, Peng ^{[1
]}

Xi, Chanjuan ^{[1
]}

机构：

[1] Tsinghua Univ, Dept Chem, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Minist Educ, Beijing 100084, Peoples R China

来源：

HETEROCYCLES | 2012年 / 84卷 / 01期

基金：

中国国家自然科学基金;

关键词：

Carbodiimide; Isothiocyanate; Carbon Disulfide; Domino Reaction; Benzo-Heterocycle; ONE-POT SYNTHESIS; BENZIMIDAZOLE DERIVATIVES; O-HALOANILINES; TANDEM REACTION; SMALL-MOLECULE; INHIBITORS; EFFICIENT; 2(3H)-BENZOTHIAZOLETHIONES; 2-AMINOBENZIMIDAZOLES; ISOTHIOCYANATES;

D O I：

10.3987/REV-11-SR(P)6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The present review summarizes information on the copper-catalyzed reaction of heteroallenes, including carbodiimides, isothiocyanates, and carbon disulfide, with o-halobenzenamines or o-halophenols or o-halobenzamides for constructing benzo-heterocycle compounds via domino nucleophilic addition/cyclization reactions.

引用

页码：209 / 221

页数：13

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