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Redox-mediator free, electrochemical S-trifluoromethylation of thiols and disulfides

delete2026-04-17
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OA
AI
M
Marc Lingner
C
Chenghao Lv
J
Jinxuan Liu
A
Andreas Terfort *
DOI:10.1016/j.elecom.2026.108171delete
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Abstract

Abstract

En 中文
• Efficient and sustainable S-trifluoromethylation of thiols and disulfides. • The use of electrical current together with a cheap precursor allows for a cheap, efficient process. • Detailed insight into mechanism. • The direct approach (without redox mediator) changes the mechanism and also the scope of substrates.
Keywords:
electrochemical S-trifluoromethylation
thiols
disulfides
redox-mediator free
mechanism
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Journal

Electrochemistry Communications cover
Electrochemistry Communications
IF:
4.2
Papers:
1.6K
Citations:
1.6W

Organization

G
goethe university frankfurt
Scholars:
2.1K
Papers: 860
Citations: 0
D
Dalian University of Technology
Scholars:
5.7W
Papers: 4.3W
Citations: 5.5W
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