Cu(II)/Photoredox-Catalyzed Aminoacylation of Vinyl Bromides

A novel C-C coupling reaction of vinyl bromides with carboxamides has been developed through Cu(OAc)<sub>2</sub>/photocatalysis. This process features regioselective carboxamido carbon-vinylation under mild reaction conditions. Mechanistic studies suggest that the formation of an acyl-Cu(I) intermediate plays a crucial role with regard to enabling this transformation.

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Publication Details

Journal
Organic Letters
Published
2025-03-24
DOI
https://doi.org/10.1021/acs.orglett.5c01104
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.87

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article

Cu(II)/Photoredox-Catalyzed Aminoacylation of Vinyl Bromides

Wei Zeng, Huanfeng Jiang, Qiang Zeng, Guojin Huang
2 citations
Organic Letters
Catalytic C–H Functionalization Methods
1.87
article

Cu(II)/Photoredox-Catalyzed Aminoacylation of Vinyl Bromides

Wei Zeng, Huanfeng Jiang, Qiang Zeng, Guojin Huang
article en
2 citations

Abstract

A novel C-C coupling reaction of vinyl bromides with carboxamides has been developed through Cu(OAc)<sub>2</sub>/photocatalysis. This process features regioselective carboxamido carbon-vinylation under mild reaction conditions. Mechanistic studies suggest that the formation of an acyl-Cu(I) intermediate plays a crucial role with regard to enabling this transformation.

Organic LettersVol. 27(13)
Key Laboratory of Guangdong Province (CN), South China University of Technology (CN)
National Natural Science Foundation of China, Basic and Applied Basic Research Foundation of Guangdong Province
Clean water and sanitation
Openalex Percentile: Top 17%
Catalytic C–H Functionalization Methods
1.87
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