<i>gem</i> ‐Difluorinated Phosphonium Salts as Sources of Difluoroalkyl Radicals

The advent of photoredox catalysis established difluorinated phosphonium salts as the valuable type of difluoroalkyl radical sources that stand out from the row of fluoroalkylative reagents. The synthetic application of this class of compounds varies from simple, yet robust and universal photoinduced difluoromethylation to assembling rather complex difluorinated frameworks. This review summarizes the radical difluoroalkylation reactions, which utilize difluorinated phosphonium salts employed as reagents or intermediate compounds from the first report in 2015.

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Publication Details

Journal
The Chemical Record
Published
2026-04-17
DOI
https://doi.org/10.1002/tcr.70150
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

gem ‐Difluorinated Phosphonium Salts as Sources of Difluoroalkyl Radicals

Alexander D. Dilman, Alexey L. Trifonov
The Chemical Record
Fluorine in Organic Chemistry
article

gem ‐Difluorinated Phosphonium Salts as Sources of Difluoroalkyl Radicals

Alexander D. Dilman, Alexey L. Trifonov
article en

Abstract

The advent of photoredox catalysis established difluorinated phosphonium salts as the valuable type of difluoroalkyl radical sources that stand out from the row of fluoroalkylative reagents. The synthetic application of this class of compounds varies from simple, yet robust and universal photoinduced difluoromethylation to assembling rather complex difluorinated frameworks. This review summarizes the radical difluoroalkylation reactions, which utilize difluorinated phosphonium salts employed as reagents or intermediate compounds from the first report in 2015.

The Chemical Record
N.D. Zelinsky Institute of Organic Chemistry (RU)
Clean water and sanitation
Openalex Percentile: Top 10%
Fluorine in Organic Chemistry
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