Visible Light-Promoted Phosphine-Catalyzed Difluoroalkylation of Arenes and Heterocycles
A visible light-promoted difluoroalkylation reaction of arenes or heterocycles, using triaryl phosphine as the catalyst and difluoroalkyl iodide as the alkylating agent, is presented. The strategy is highlighted by photocatalyst-free, mild reaction conditions and a broad substrate scope. Mechanistic...
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Veröffentlicht in: | Journal of organic chemistry 2020-01, Vol.85 (2), p.942-951 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A visible light-promoted difluoroalkylation reaction of arenes or heterocycles, using triaryl phosphine as the catalyst and difluoroalkyl iodide as the alkylating agent, is presented. The strategy is highlighted by photocatalyst-free, mild reaction conditions and a broad substrate scope. Mechanistic experiments indicate that this reaction involves a radical-chain process that is initiated by an electron donor–acceptor complex formed from difluoroalkyl iodide and phosphine. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/acs.joc.9b02882 |