Trifluoromethylative\nand Pentafluoroethylative Heterofunctionalization\n(C–O, C–S, and C–N) of Alkenes Using Visible\nLight Photocatalysis

A mild and general method for photoredox-catalyzed trifluoromethylative\nand pentafluoroethylative heterofunctionalization of alkenes is proposed.\nIn this reaction, the Togni reagent serves as a CF<sub>3</sub>- or\nCF<sub>2</sub>CF<sub>3</sub>-radical source for the regioselective\nformation of the C–CF<sub>3</sub> and C–CF<sub>2</sub>CF<sub>3</sub> bonds from alkenes, and additional nucleophiles (O,\nS, N) provide C–O, C–S, and C–N bonds, respectively.\nThese reactions provide a common gateway to access the fluoroalkylative\nheterofunctionalization of alkenes.

Publication Details

Journal
Figshare
Published
2024-11-19
DOI
https://doi.org/10.1021/acsomega.4c06017.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
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article

Trifluoromethylative\nand Pentafluoroethylative Heterofunctionalization\n(C–O, C–S, and C–N) of Alkenes Using Visible\nLight Photocatalysis

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Mycorrhizal Fungi and Plant Interactions
article

Trifluoromethylative\nand Pentafluoroethylative Heterofunctionalization\n(C–O, C–S, and C–N) of Alkenes Using Visible\nLight Photocatalysis

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Abstract

A mild and general method for photoredox-catalyzed trifluoromethylative\nand pentafluoroethylative heterofunctionalization of alkenes is proposed.\nIn this reaction, the Togni reagent serves as a CF<sub>3</sub>- or\nCF<sub>2</sub>CF<sub>3</sub>-radical source for the regioselective\nformation of the C–CF<sub>3</sub> and C–CF<sub>2</sub>CF<sub>3</sub> bonds from alkenes, and additional nucleophiles (O,\nS, N) provide C–O, C–S, and C–N bonds, respectively.\nThese reactions provide a common gateway to access the fluoroalkylative\nheterofunctionalization of alkenes.

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Mycorrhizal Fungi and Plant Interactions
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Trifluoromethylative\nand Pentafluoroethylative Heterofunctionalization\n(C–O, C–S, and C–N) of Alkenes Using Visible\nLight Photocatalysis · Figshare (2024) | TGRS Research Map | TGRS