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Visible Light-Mediated Direct C–H Aroylation and Alkylation of Heteroarenes

[Image: see text] Herein, we describe the photocatalytic generation of nucleophilic aroyl radicals from simple aroyl chlorides as a universal and efficient cross-coupling strategy for the direct aroylation of heteroarenes. Furthermore, visible light-mediated direct alkylation of heteroarenes has als...

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Detalles Bibliográficos
Autores principales: Chang, Rui, Fang, Jie, Chen, Jian-Qiang, Liu, Dan, Xu, Guo-Qiang, Xu, Peng-Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714600/
https://www.ncbi.nlm.nih.gov/pubmed/31497720
http://dx.doi.org/10.1021/acsomega.9b01674
Descripción
Sumario:[Image: see text] Herein, we describe the photocatalytic generation of nucleophilic aroyl radicals from simple aroyl chlorides as a universal and efficient cross-coupling strategy for the direct aroylation of heteroarenes. Furthermore, visible light-mediated direct alkylation of heteroarenes has also been achieved using unactivated bromoalkanes as radical precursors. These two strategies feature high functional group tolerance, exclusive regioselectivity for reaction at the more electrophilic position of heteroarenes, easily accessible substrates, and mild reaction conditions. Moreover, mechanism studies of two reactions are carried out to support our hypotheses.