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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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Publication details

The article was received on 10 Jun 2012, accepted on 23 Jul 2012 and first published on 24 Jul 2012


Article type: Communication
DOI: 10.1039/C2CC34158A
Citation: 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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