Issue 96, 2012
From the journal:

Chemical Communications

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

Min Yang,a   Jie Tang*a  and  Renhua Fan*b  

* Corresponding authors

a Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, East China Normal University, Shanghai 200062, China
E-mail: jtang@chem.ecnu.edu.cn

b Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433, China
E-mail: rhfan@fudan.edu.cn
Fax: +86-21-6510-2412
Tel: +86-21-6564-2019

Abstract

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 N1-benzylbenzene-1,2-diamine.

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

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Article information

DOI
https://doi.org/10.1039/C2CC36113B
Article type
Communication
Submitted
23 Aug 2012
Accepted
19 Oct 2012
First published
22 Oct 2012

Chem. Commun., 2012,48, 11775-11777

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

M. Yang, J. Tang and R. Fan, Chem. Commun., 2012, 48, 11775 DOI: 10.1039/C2CC36113B

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