Photoredox-Catalysis\nFluorosulfonyldifluoromethylation\nof Unactivated Alkenes and (Hetero)arenes with ICF<sub>2</sub>SO<sub>2</sub>F

The fluorosulfonyldifluoromethylation of unactivated\nalkenes and\n(hetero)arenes with iododifluoromethanesulfonyl fluoride (ICF<sub>2</sub>SO<sub>2</sub>F) under visible light photoredox catalysis\nwas successfully developed. Key to the successful fluorosulfonyldifluoromethylation\nof aromatic compounds was the usage of AgOTf as an additive to promote\nthe formation of the CF<sub>2</sub>SO<sub>2</sub>F radical. The protocol\nprovided a straightforward way to introduce the interesting and useful\nCF<sub>2</sub>SO<sub>2</sub>F group on sp<sup>3</sup> and sp<sup>2</sup> carbons.

Publication Details

Journal
Figshare
Published
2024-08-08
DOI
https://doi.org/10.1021/acs.orglett.4c02538.s001
Primary Topic
Fluorine in Organic Chemistry
Type
article
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Photoredox-Catalysis\nFluorosulfonyldifluoromethylation\nof Unactivated Alkenes and (Hetero)arenes with ICF2SO2F

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Fluorine in Organic Chemistry
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Photoredox-Catalysis\nFluorosulfonyldifluoromethylation\nof Unactivated Alkenes and (Hetero)arenes with ICF2SO2F

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Abstract

The fluorosulfonyldifluoromethylation of unactivated\nalkenes and\n(hetero)arenes with iododifluoromethanesulfonyl fluoride (ICF<sub>2</sub>SO<sub>2</sub>F) under visible light photoredox catalysis\nwas successfully developed. Key to the successful fluorosulfonyldifluoromethylation\nof aromatic compounds was the usage of AgOTf as an additive to promote\nthe formation of the CF<sub>2</sub>SO<sub>2</sub>F radical. The protocol\nprovided a straightforward way to introduce the interesting and useful\nCF<sub>2</sub>SO<sub>2</sub>F group on sp<sup>3</sup> and sp<sup>2</sup> carbons.

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Openalex Percentile: Top 73%
Fluorine in Organic Chemistry
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