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
Hauptverfasser: Xu, Pei, Wang, Xing-Yu, Wang, Zhijuan, Zhao, Jinjin, Cao, Xu-Dong, Xiong, Xiao-Chun, Yuan, Yu-Chao, Zhu, Songlei, Guo, Dong, Zhu, Xu
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Sprache:eng
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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.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.2c01533