Decarboxylative Fluorination Catalyzed by Pyridine-Containing Charge-Transfer Complex

Herein, we present a novel organic photoredox decarboxylation system that employs a charge-transfer complex formed between pyridine derivatives and Selectfluor as the catalytic species. Under basic conditions, this system facilitates the decarboxylative fluorination of alkyl carboxylic acids upon visible light irradiation. The methodology applies to primary, secondary, and tertiary carboxylic acids, demonstrating good substrate scope.

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Publication Details

Journal
Organic Letters
Published
2025-08-20
DOI
https://doi.org/10.1021/acs.orglett.5c03110
Citations
2
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
1.58

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article

Decarboxylative Fluorination Catalyzed by Pyridine-Containing Charge-Transfer Complex

Yahao Huang, Jinglan Wen, Zhiyang Ma, Peng Hu et al.
2 citations
Organic Letters
Fluorine in Organic Chemistry
1.58
article

Decarboxylative Fluorination Catalyzed by Pyridine-Containing Charge-Transfer Complex

Yahao Huang, Jinglan Wen, Zhiyang Ma, Peng Hu, Liang Zhang
article en
2 citations

Abstract

Herein, we present a novel organic photoredox decarboxylation system that employs a charge-transfer complex formed between pyridine derivatives and Selectfluor as the catalytic species. Under basic conditions, this system facilitates the decarboxylative fluorination of alkyl carboxylic acids upon visible light irradiation. The methodology applies to primary, secondary, and tertiary carboxylic acids, demonstrating good substrate scope.

Organic LettersVol. 27(34)
Institute of Molecular Functional Materials (CN)
National Natural Science Foundation of China, Guangdong Science and Technology Department, Guangzhou Municipal Science and Technology Bureau
Openalex Percentile: Top 15%
Fluorine in Organic Chemistry
1.58
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Decarboxylative Fluorination Catalyzed by Pyridine-Containing Charge-Transfer Complex — Yahao Huang, Jinglan Wen, et al. · Organic Letters (2025) | TGRS Research Map | TGRS