Visible Light‐Mediated C─H Monofluoromethylation of (Hetero)Arenes

Abstract We report the design and application of a monofluoromethylation reagent: 1‐((bromofluoromethyl)sulfonyl)‐4‐chlorobenzene. By taking advantage of the electron‐withdrawing property of the sulfonyl group, the polarity of the monofluoride radical can be regulated; moreover, the sulfonyl group's facile removability is exploited. These combined features enable direct monofluoromethylation of (hetero)arenes under mild visible‐light conditions.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-04-14
DOI
https://doi.org/10.1002/ajoc.202500297
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79

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article

Visible Light‐Mediated C─H Monofluoromethylation of (Hetero)Arenes

Liu Hon, Xin Liu, Yingsheng Zhao, Huiming Dai et al.
1 citations
Asian Journal of Organic Chemistry
Fluorine in Organic Chemistry
0.79
article

Visible Light‐Mediated C─H Monofluoromethylation of (Hetero)Arenes

Liu Hon, Xin Liu, Yingsheng Zhao, Huiming Dai, Xuefeng Gu, Yilian Song, Chuangchuang Liu, Zhibin Huang
article en
1 citations

Abstract

Abstract We report the design and application of a monofluoromethylation reagent: 1‐((bromofluoromethyl)sulfonyl)‐4‐chlorobenzene. By taking advantage of the electron‐withdrawing property of the sulfonyl group, the polarity of the monofluoride radical can be regulated; moreover, the sulfonyl group's facile removability is exploited. These combined features enable direct monofluoromethylation of (hetero)arenes under mild visible‐light conditions.

Asian Journal of Organic ChemistryVol. 14(7)
Soochow University (TW), Soochow University (CN), Institute of New Materials (CN)
National Natural Science Foundation of China, Priority Academic Program Development of Jiangsu Higher Education Institutions
Openalex Percentile: Top 29%
Fluorine in Organic Chemistry
0.79
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