Iron-Catalyzed Photochemical Defluorinative Functionalization of Polyfluorinated Aromatics

Iron photocatalysis has emerged as a sustainable platform for C-H functionalization. This study describes a photocatalytic strategy for the selective defluorinative functionalization of polyfluorinated aromatics. The developed methodology enables selective defluorosulfonylation with sulfur dioxide and defluorinative alkylation with alkanes under visible light irradiation. Additionally, direct defluorinative functionalization with carboxylic acids has been achieved. These protocols demonstrate excellent site-selectivity and broad substrate scope, tolerating diverse functional groups, including cyano, acetyl, ester, and trifluoromethyl substituents. Notably, the methodology is compatible with drug-like molecules containing complex structures, thereby expanding the synthetic utility of iron photocatalysis in the construction of complex polyfluorinated molecules.

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Publication Details

Journal
Organic Letters
Published
2025-09-01
DOI
https://doi.org/10.1021/acs.orglett.5c03114
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79

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article

Iron-Catalyzed Photochemical Defluorinative Functionalization of Polyfluorinated Aromatics

Wujiong Xia, Lin Guo, Li Mei, Chao Yang et al.
1 citations
Organic Letters
Fluorine in Organic Chemistry
0.79
article

Iron-Catalyzed Photochemical Defluorinative Functionalization of Polyfluorinated Aromatics

Wujiong Xia, Lin Guo, Li Mei, Chao Yang, Ao-Men Hu, Ke Wang, Jia‐Lin Tu
article en
1 citations

Abstract

Iron photocatalysis has emerged as a sustainable platform for C-H functionalization. This study describes a photocatalytic strategy for the selective defluorinative functionalization of polyfluorinated aromatics. The developed methodology enables selective defluorosulfonylation with sulfur dioxide and defluorinative alkylation with alkanes under visible light irradiation. Additionally, direct defluorinative functionalization with carboxylic acids has been achieved. These protocols demonstrate excellent site-selectivity and broad substrate scope, tolerating diverse functional groups, including cyano, acetyl, ester, and trifluoromethyl substituents. Notably, the methodology is compatible with drug-like molecules containing complex structures, thereby expanding the synthetic utility of iron photocatalysis in the construction of complex polyfluorinated molecules.

Organic LettersVol. 27(36)
Harbin Institute of Technology (CN), Henan Normal University (CN)
Science and Technology Foundation of Shenzhen City, National Natural Science Foundation of China, State Key Laboratory of Urban Water Resource and Environment
Openalex Percentile: Top 24%
Fluorine in Organic Chemistry
0.79
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