Photoredox-Catalyzed Hydrofluoromethylthiolation of Unactivated Alkenes to Access Alkyl Di- and Trifluoromethyl Sulfides

Herein, a visible-light-induced photocatalytic hydrofluoromethylthiolation of unactivated alkenes for the efficient construction of aliphatic di- and trifluoromethyl sulfides (47 examples, up to 93% yield) is described. In contrast to previous methods, this protocol eliminates the need for transition metals and oxidants, employing mild and environmentally benign organic photocatalysis instead. This transformation features operational simplicity, excellent chemo- and regioselectivity, and high compatibility with unactivated alkenes while demonstrating effectiveness for late-stage functionalization of commercially available drug derivatives. Preliminary mechanistic studies suggest that a radical pathway is involved in the catalytic cycle.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-10-08
DOI
https://doi.org/10.1021/acs.joc.5c01829
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79
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article

Photoredox-Catalyzed Hydrofluoromethylthiolation of Unactivated Alkenes to Access Alkyl Di- and Trifluoromethyl Sulfides

Liang Shen, Lili Zeng, Ronghui Huang, Fen‐Er Chen et al.
1 citations
The Journal of Organic Chemistry
Fluorine in Organic Chemistry
0.79
article

Photoredox-Catalyzed Hydrofluoromethylthiolation of Unactivated Alkenes to Access Alkyl Di- and Trifluoromethyl Sulfides

Liang Shen, Lili Zeng, Ronghui Huang, Fen‐Er Chen, Xiao-Qing Feng, Xian Feng, Jian Han, Shi-Han Xu
article en
1 citations

Abstract

Herein, a visible-light-induced photocatalytic hydrofluoromethylthiolation of unactivated alkenes for the efficient construction of aliphatic di- and trifluoromethyl sulfides (47 examples, up to 93% yield) is described. In contrast to previous methods, this protocol eliminates the need for transition metals and oxidants, employing mild and environmentally benign organic photocatalysis instead. This transformation features operational simplicity, excellent chemo- and regioselectivity, and high compatibility with unactivated alkenes while demonstrating effectiveness for late-stage functionalization of commercially available drug derivatives. Preliminary mechanistic studies suggest that a radical pathway is involved in the catalytic cycle.

The Journal of Organic ChemistryVol. 90(41)
Fudan University (CN), Soochow University (CN), Russian Research Center for Molecular Diagnostics and Therapy (RU), Shijiazhuang Yiling Pharmaceutical (China) (CN), Suzhou Vocational Health College (CN), Changzhou University (CN), Chemical Synthesis Lab (SG)
Openalex Percentile: Top 23%
Fluorine in Organic Chemistry
0.79
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Photoredox-Catalyzed Hydrofluoromethylthiolation of Unactivated Alkenes to Access Alkyl Di- and Trifluoromethyl Sulfides — Liang Shen, Lili Zeng, et al. · The Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS