Photocatalytic Vicinal Trifluoromethylation and Disulfuration of Alkenes Using Langlois' Reagent and Tetrasulfides
Comprehensive Summary In this study, we outline a versatile method for the preparation of trifluoromethyl‐containing unsymmetrical disulfides via catalytic photoredox difunctionalization of alkenes using symmetrical tetrasulfide (RSSSSR) and Langlois' reagent (CF₃SO₂Na). Notably, this method is also suitable for the late‐stage modification of pharmaceutical molecule derivatives. Furthermore, a set of experimental investigations, such as radical trapping experiment, scrambling experiment, cyclic voltammetry (CV) measurement, Stern‐Volmer analysis, on/off light‐control experiments and a radical cascade experiment have been performed to support the photocatalytic reductive quenching cycle and radical‐radical coupling reaction pathway.
Authors
- Yingming Song (ORCID: https://orcid.org/0000-0001-7502-1285)
- Liu Ju-bin
- Yue Su (ORCID: https://orcid.org/0000-0002-6987-3737)
- Hua Cao (ORCID: https://orcid.org/0000-0001-8825-0175)
- Yuhao Jiang (ORCID: https://orcid.org/0009-0004-9436-7109)
- Jianmin Huang
- Yue Yu (ORCID: https://orcid.org/0000-0002-0807-8713)
Institutions
- Guangdong Pharmaceutical University (CN)
- First Affiliated Hospital of Guangdong Pharmaceutical University (CN)
Publication Details
- Journal
- Chinese Journal of Chemistry
- Published
- 2025-08-20
- DOI
- https://doi.org/10.1002/cjoc.70247
- Citations
- 1
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.79