Photocatalytic Perfluoroalkenylation of Ketones and Its Application in the Synthesis of Fluorinated Heterocycles

A mild and efficient photocatalytic method for the α-perfluoroalkenylation of ketones via the corresponding enol silanes has been developed. Using a commercial ruthenium photocatalyst and DABCO under visible light irradiation, perfluoroenones were obtained in up to 89% yield and excellent <i>Z</i>-selectivity. The protocol is applicable to a broad range of (hetero)aromatic and aliphatic substrates. The resulting perfluoroenones serve as versatile intermediates for the synthesis of perfluorinated heterocycles such as pyrazoles, pyrimidines, or isoxazoles.

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Publication Details

Journal
Organic Letters
Published
2026-03-11
DOI
https://doi.org/10.1021/acs.orglett.6c00279
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

Photocatalytic Perfluoroalkenylation of Ketones and Its Application in the Synthesis of Fluorinated Heterocycles

Constantin Czekelius, Max M. Schreier
Organic Letters
Fluorine in Organic Chemistry
article

Photocatalytic Perfluoroalkenylation of Ketones and Its Application in the Synthesis of Fluorinated Heterocycles

Constantin Czekelius, Max M. Schreier
article en

Abstract

A mild and efficient photocatalytic method for the α-perfluoroalkenylation of ketones via the corresponding enol silanes has been developed. Using a commercial ruthenium photocatalyst and DABCO under visible light irradiation, perfluoroenones were obtained in up to 89% yield and excellent <i>Z</i>-selectivity. The protocol is applicable to a broad range of (hetero)aromatic and aliphatic substrates. The resulting perfluoroenones serve as versatile intermediates for the synthesis of perfluorinated heterocycles such as pyrazoles, pyrimidines, or isoxazoles.

Organic LettersVol. 28(11)
Heinrich Heine University Düsseldorf (DE)
Clean water and sanitation
Openalex Percentile: Top 25%
Fluorine in Organic Chemistry
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