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Issue 77, 2012
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Synthesis of fused N-heterocycles via tandem C–H activation

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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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Supplementary files

Article information


Submitted
10 Jun 2012
Accepted
23 Jul 2012
First published
24 Jul 2012

Chem. Commun., 2012,48, 9601-9603
Article type
Communication

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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