Electrochemical Trifluoromethylthiolation/Cyclization of <i>N</i>-Arylacrylamides with AgSCF<sub>3</sub>: Access to SCF<sub>3</sub>-Containing Oxindoles

An environmentally friendly electrochemical strategy for the synthesis of SCF<sub>3</sub>-containing oxindoles was developed. This electrochemical transformation was accomplished through a cascade trifluoromethylthiolation/cyclization of <i>N</i>-acrylamides with AgSCF<sub>3</sub>, obviating the requirement for external oxidants. A variety of functional groups were well tolerated in this transformation.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-08-19
DOI
https://doi.org/10.1021/acs.joc.4c00433
Citations
3
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.62

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article

Electrochemical Trifluoromethylthiolation/Cyclization of N-Arylacrylamides with AgSCF3: Access to SCF3-Containing Oxindoles

Wenbo Chen, Siqi Wang, Yu Zhou, Yu Wang et al.
3 citations
The Journal of Organic Chemistry
Fluorine in Organic Chemistry
0.62
article

Electrochemical Trifluoromethylthiolation/Cyclization of N-Arylacrylamides with AgSCF3: Access to SCF3-Containing Oxindoles

Wenbo Chen, Siqi Wang, Yu Zhou, Yu Wang, Sheng Wang, Ye Wang
article en
3 citations

Abstract

An environmentally friendly electrochemical strategy for the synthesis of SCF<sub>3</sub>-containing oxindoles was developed. This electrochemical transformation was accomplished through a cascade trifluoromethylthiolation/cyclization of <i>N</i>-acrylamides with AgSCF<sub>3</sub>, obviating the requirement for external oxidants. A variety of functional groups were well tolerated in this transformation.

The Journal of Organic ChemistryVol. 89(17)
Shanghai University of Electric Power (CN)
Natural Science Foundation of Shanghai, Science and Technology Commission of Shanghai Municipality
Clean water and sanitation
Openalex Percentile: Top 37%
Fluorine in Organic Chemistry
0.62
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