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Issue 16, 2019
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Intermolecular, redox-neutral azidoarylation of alkenes via photoredox catalysis

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Abstract

An intermolecular, redox-neutral azidoarylation of alkenes with pyridines and TMSN3 has been reported via visible light-induced photoredox catalysis. This protocol utilized a radical addition/radical coupling sequence, allowing for facile and regioselective installation of versatile β-azido pyridines under redox-neutral and mild conditions.

Graphical abstract: Intermolecular, redox-neutral azidoarylation of alkenes via photoredox catalysis

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Publication details

The article was received on 10 Jan 2019, accepted on 01 Feb 2019 and first published on 01 Feb 2019


Article type: Communication
DOI: 10.1039/C9CC00241C
Citation: Chem. Commun., 2019,55, 2336-2339

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    Intermolecular, redox-neutral azidoarylation of alkenes via photoredox catalysis

    J. Chen, S. Zhu, J. Qin and L. Chu, Chem. Commun., 2019, 55, 2336
    DOI: 10.1039/C9CC00241C

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