Accessing N-heteroarylated indoles and benzimidazoles from 2-alkynyl cyclohexadienimines and cyclohexadienones through metal-catalyzed tandem reactions

被引：19

作者：

Yang, Min ^{[1
]}

Tang, Jie ^{[1
]}

Fan, Renhua ^{[2
]}

机构：

[1] E China Normal Univ, Shanghai Engn Res Ctr Mol Therapeut & New Drug De, Shanghai 200062, Peoples R China

[2] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China

来源：

CHEMICAL COMMUNICATIONS | 2012年 / 48卷 / 96期

基金：

中国国家自然科学基金;

关键词：

OXIDATIVE DEAROMATIZATION; COUPLING REACTIONS; NATURAL-PRODUCTS; ARYL; ARYLATION; COPPER; ANILINES; METHANESULFONAMIDE; FUNCTIONALIZATION; BIOSYNTHESIS;

D O I：

10.1039/c2cc36113b

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

N-Indolyl or N-benzofuranyl indoles and benzimidazoles were prepared through metal-catalyzed tandem reactions between 2-alkynyl cyclohexadienimines or cyclohexadienones and 2-alkynylanilines or N-1-benzylbenzene-1,2-diamine.

引用

页码：11775 / 11777

页数：3

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