Visible-Light-Induced Radical Hydroaroylation of Vinyl Boronic Ester with Aroyl Chlorides to Access β-Boryl Ketones

A visible-light-induced radical hydroaroylation of vinyl boronic ester with aroyl chlorides has been developed, yielding a variety of β-boryl ketones in moderate to good yields with broad functional group tolerance. This metal-free transformation offers a convenient and practical route to access valuable β-boryl ketones from readily available aroyl chlorides and vinyl boronic ester.

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Publication Details

Journal
Organic Letters
Published
2025-03-26
DOI
https://doi.org/10.1021/acs.orglett.5c00996
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Visible-Light-Induced Radical Hydroaroylation of Vinyl Boronic Ester with Aroyl Chlorides to Access β-Boryl Ketones

Shuai Tang, Hua Zhang, Shuting Wang
Organic Letters
Radical Photochemical Reactions
article

Visible-Light-Induced Radical Hydroaroylation of Vinyl Boronic Ester with Aroyl Chlorides to Access β-Boryl Ketones

Shuai Tang, Hua Zhang, Shuting Wang
article en

Abstract

A visible-light-induced radical hydroaroylation of vinyl boronic ester with aroyl chlorides has been developed, yielding a variety of β-boryl ketones in moderate to good yields with broad functional group tolerance. This metal-free transformation offers a convenient and practical route to access valuable β-boryl ketones from readily available aroyl chlorides and vinyl boronic ester.

Organic LettersVol. 27(13)
Minzu University of China (CN)
Clean water and sanitation
Openalex Percentile: Top 96%
Radical Photochemical Reactions
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