Photocatalytic α-nucleophilic fluorination of α,β-unsaturated carbonyl compounds

A redox-neutral photocatalytic α-nucleophilic fluorination of α,β-unsaturated carbonyls under mild conditions enables access to α-fluorinated carbonyls via an α-carbonyl cation, with potential for late-stage fluorination of bioactive molecules.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00877h
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

Photocatalytic α-nucleophilic fluorination of α,β-unsaturated carbonyl compounds

Jian‐Ping Qu, Fang Wang, Jie Gong
Organic Chemistry Frontiers
Fluorine in Organic Chemistry
article

Photocatalytic α-nucleophilic fluorination of α,β-unsaturated carbonyl compounds

Jian‐Ping Qu, Fang Wang, Jie Gong
article en

Abstract

A redox-neutral photocatalytic α-nucleophilic fluorination of α,β-unsaturated carbonyls under mild conditions enables access to α-fluorinated carbonyls via an α-carbonyl cation, with potential for late-stage fluorination of bioactive molecules.

Organic Chemistry FrontiersVol. 12(22)
University of Science and Technology of China (CN), Nanjing Tech University (CN)
Openalex Percentile: Top 85%
Fluorine in Organic Chemistry
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Photocatalytic α-nucleophilic fluorination of α,β-unsaturated carbonyl compounds — Jian‐Ping Qu, Fang Wang, et al. · Organic Chemistry Frontiers (2025) | TGRS Research Map | TGRS