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.
Authors
- Constantin Czekelius (ORCID: https://orcid.org/0000-0002-2814-8686)
- Max M. Schreier
Institutions
- Heinrich Heine University Düsseldorf (DE)
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
- Field-Weighted Citation Impact
- 0.00