Heterogeneous photocatalytic cyanomethylarylation of alkenes with acetonitrile: Synthesis of diverse nitrogenous heterocyclic compounds

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Abstract

A visible light-mediated heterogeneous photocatalytic cyanomethylarylation of alkenes with acetonitrile has been established using K-modified carbon nitride (CN-K) as a recyclable semiconductor photocatalyst. This protocol, employing readily accessible alkyl N-hydroxyphthalimide (NHPI) ester as a radical initiator, allows the efficient construction of a broad array of structural diverse nitrogenous heterocyclic compounds including indolines, oxindoles, isoquinolinones, and isoquinolinediones.

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Pan, G., Yang, Q., Wang, W., Tang, Y., & Cai, Y. (2021). Heterogeneous photocatalytic cyanomethylarylation of alkenes with acetonitrile: Synthesis of diverse nitrogenous heterocyclic compounds. Beilstein Journal of Organic Chemistry, 17, 1171–1180. https://doi.org/10.3762/bjoc.17.89

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