Defluorinative Alkylation of Trifluoromethylbenzimidazoles Enabled by Spin-Center Shift: A Synergistic Photocatalysis/Thiol Catalysis Process with CO 2
We describe a catalytic strategy for direct single C(sp )-F bond alkylation of trifluoromethylbenzimidazoles under a photoinduced thiol catalysis process. The CO radical anion (CO ) proved to be the most efficient single-electron reductant to realize such a transformation. The spin-center shift of t...
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Veröffentlicht in: | Organic letters 2022-06, Vol.24 (22), p.4075-4080 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | We describe a catalytic strategy for direct single C(sp
)-F bond alkylation of trifluoromethylbenzimidazoles under a photoinduced thiol catalysis process. The CO
radical anion (CO
) proved to be the most efficient single-electron reductant to realize such a transformation. The spin-center shift of the generated radical anion intermediate is the key step in realizing C-F bond activation under mild conditions with high efficiency. |
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ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/acs.orglett.2c01533 |