Recent Advances in Transition Metal‐Catalyzed/Mediated CSCF<sub>3</sub> Bond Formation Reaction
The trifluoromethylthiolated group (SCF 3 ) is characterized by its strong electron‐withdrawing ability, excellent lipophilicity, good stability, and bioavailability, making it highly relevant for applications in drug design and development. This review summarizes recent advances in CX (H, Cl, OTf, B(OH) 2 ) trifluoromethylthiolation reaction from 2014 to 2024. The discussion is organized into three major sections: 1) transition metal‐catalyzed CH trifluoromethylthiolation reactions facilitated by directing groups, 2) transition metal‐catalyzed trifluoromethylthiolation via cross‐coupling reactions, and 3) light‐assisted transition metal‐catalyzed trifluoromethylthiolation reactions. Additionally, this review examines the substrate scope, limitations, and partial mechanisms associated with these transformations.
Authors
- X.‐Z. QIN (ORCID: https://orcid.org/0000-0003-0367-4505)
- Peng Xu (ORCID: https://orcid.org/0000-0003-2952-6439)
Institutions
- Changzhou Institute of Technology (CN)
- Jining Medical University (CN)
Publication Details
- Journal
- European Journal of Organic Chemistry
- Published
- 2025-04-14
- DOI
- https://doi.org/10.1002/ejoc.202500029
- Citations
- 4
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 3.16