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 CX (H, Cl, OTf, B(OH) 2 ) trifluoromethylthiolation reaction from 2014 to 2024. The discussion is organized into three major sections: 1) transition metal‐catalyzed CH 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.

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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
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article

Recent Advances in Transition Metal‐Catalyzed/Mediated CSCF3 Bond Formation Reaction

X.‐Z. QIN, Peng Xu
4 citations
European Journal of Organic Chemistry
Fluorine in Organic Chemistry
3.16
article

Recent Advances in Transition Metal‐Catalyzed/Mediated CSCF3 Bond Formation Reaction

X.‐Z. QIN, Peng Xu
article en
4 citations

Abstract

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 CX (H, Cl, OTf, B(OH) 2 ) trifluoromethylthiolation reaction from 2014 to 2024. The discussion is organized into three major sections: 1) transition metal‐catalyzed CH 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.

European Journal of Organic ChemistryVol. 28(22)
Changzhou Institute of Technology (CN), Jining Medical University (CN)
Openalex Percentile: Top 9%
Fluorine in Organic Chemistry
3.16
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Recent Advances in Transition Metal‐Catalyzed/Mediated CSCF<sub>3</sub> Bond Formation Reaction — X.‐Z. QIN, Peng Xu · European Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS