Issue 77, 2012
From the journal:

Chemical Communications

Synthesis of fused N-heterocycles via tandem C–H activation†

Ge Meng,a   Hong-Ying Niu,b   Gui-Rong Qu,a   John S. Fossey,ac   Jian-Ping Li*a  and  Hai-Ming Guo*a  

* Corresponding authors

a College of Chemistry and Environmental Science, Key Laboratory of Green Chemical Media and Reactions of Ministry of Education, Henan Normal University, Xinxiang 453007, Henan, China
E-mail: jplig@163.com, guohm518@hotmail.com
Fax: +86 373 3329276
Tel: +86 373 3329255

b School of Chemistry and Chemical Engineering, Henan Institute of Science and Technology, Xinxiang 453003, China

c School of Chemistry, University of Birmingham, Edgbaston, Birmingham, West Midlands, UK
E-mail: j.s.fossey@bham.ac.uk

Abstract

The synthesis of fused N-heterocycles has been developed using an intramolecular cyclisation of purines or benzimidazoles. A range of medium and large rings were prepared.

Graphical abstract: Synthesis of fused N-heterocycles via tandem C–H activation

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Article information

DOI
https://doi.org/10.1039/C2CC34158A
Article type
Communication
Submitted
10 Jun 2012
Accepted
23 Jul 2012
First published
24 Jul 2012

Chem. Commun., 2012,48, 9601-9603

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Synthesis of fused N-heterocycles via tandem C–H activation

G. Meng, H. Niu, G. Qu, J. S. Fossey, J. Li and H. Guo, Chem. Commun., 2012, 48, 9601 DOI: 10.1039/C2CC34158A

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