Electrochemical hydrotrifluoromethylation of alkynes

We report the electrochemical hydrotrifluoromethylation of alkynes using the Langlois reagent as a CF<sub>3</sub> source. The mild conditions enable broad functional group tolerance and allow late-stage functionalization. Mechanistic studies reveal that DMSO serves a dual role as both solvent and hydrogen atom donor.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc02370j
Citations
2
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
1.58
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article

Electrochemical hydrotrifluoromethylation of alkynes

Eun Jin Cho, Jihoon Jang
2 citations
Chemical Communications
Fluorine in Organic Chemistry
1.58
article

Electrochemical hydrotrifluoromethylation of alkynes

Eun Jin Cho, Jihoon Jang
article en
2 citations

Abstract

We report the electrochemical hydrotrifluoromethylation of alkynes using the Langlois reagent as a CF<sub>3</sub> source. The mild conditions enable broad functional group tolerance and allow late-stage functionalization. Mechanistic studies reveal that DMSO serves a dual role as both solvent and hydrogen atom donor.

Chemical CommunicationsVol. 61(63)
Chung-Ang University (KR)
Openalex Percentile: Top 16%
Fluorine in Organic Chemistry
1.58
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Electrochemical hydrotrifluoromethylation of alkynes — Eun Jin Cho, Jihoon Jang · Chemical Communications (2025) | TGRS Research Map | TGRS