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.
Authors
- Liang Shen (ORCID: https://orcid.org/0000-0002-9533-9140)
- Lili Zeng (ORCID: https://orcid.org/0000-0002-1959-510X)
- Ronghui Huang (ORCID: https://orcid.org/0000-0003-1080-3029)
- Fen‐Er Chen (ORCID: https://orcid.org/0000-0002-6734-3388)
- Xiao-Qing Feng
- Xian Feng (ORCID: https://orcid.org/0009-0006-1878-3412)
- Jian Han (ORCID: https://orcid.org/0009-0001-2025-8370)
- Shi-Han Xu
Institutions
- 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)
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