Visible-Light-Induced Radical Hydroaroylation of VinylBoronic Ester with Aroyl Chlorides to Access β‑BorylKetones

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.

Publication Details

Journal: Figshare
Published: 2025-03-27
DOI: https://doi.org/10.1021/acs.orglett.5c00996.s001
Primary Topic: Mycorrhizal Fungi and Plant Interactions
Type: article
Field-Weighted Citation Impact: 0.00

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article

Visible-Light-Induced Radical Hydroaroylation of VinylBoronic Ester with Aroyl Chlorides to Access β‑BorylKetones

Mar 27, 2025

Figshare

Mycorrhizal Fungi and Plant Interactions

article

Visible-Light-Induced Radical Hydroaroylation of VinylBoronic Ester with Aroyl Chlorides to Access β‑BorylKetones

March 27, 2025article en

Abstract

Figshare

Openalex Percentile: Top 53%

Mycorrhizal Fungi and Plant Interactions

DOI Source OpenAlex

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Visible-Light-Induced Radical Hydroaroylation of VinylBoronic Ester with Aroyl Chlorides to Access β‑BorylKetones · Figshare (2025) | TGRS Research Map | TGRS