Electrochemical Radical Fluorosufonylation of Allyl Bromides

A radical fluorosulfonylation of allyl bromides was achieved under electroreductive conditions. This catalyst-free protocol employs mild conditions and enables straightforward access to a new and structurally diverse variety of previously inaccessible allyl sulfonyl fluorides. We have also illustrated the synthetic value of this method by performing scaled-up reactions and product derivatization.

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Publication Details

Journal
Organic Letters
Published
2025-02-20
DOI
https://doi.org/10.1021/acs.orglett.5c00256
Citations
3
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
2.37

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article

Electrochemical Radical Fluorosufonylation of Allyl Bromides

Shenlin Huang, Yanju Lu, Bingcong Liu, Hui Liang
3 citations
Organic Letters
Fluorine in Organic Chemistry
2.37
article

Electrochemical Radical Fluorosufonylation of Allyl Bromides

Shenlin Huang, Yanju Lu, Bingcong Liu, Hui Liang
article en
3 citations

Abstract

A radical fluorosulfonylation of allyl bromides was achieved under electroreductive conditions. This catalyst-free protocol employs mild conditions and enables straightforward access to a new and structurally diverse variety of previously inaccessible allyl sulfonyl fluorides. We have also illustrated the synthetic value of this method by performing scaled-up reactions and product derivatization.

Organic LettersVol. 27(9)
Nanjing Forestry University (CN)
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 13%
Fluorine in Organic Chemistry
2.37
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