Electrochemical\nTrifluoromethylthiolation/Cyclization\nof <i>N</i>‑Arylacrylamides with AgSCF<sub>3</sub>: Access to SCF<sub>3</sub>‑Containing Oxindoles

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

Publication Details

Journal
Figshare
Published
2024-08-19
DOI
https://doi.org/10.1021/acs.joc.4c00433.s001
Primary Topic
Biological Control of Invasive Species
Type
article
Field-Weighted Citation Impact
0.00
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article

Electrochemical\nTrifluoromethylthiolation/Cyclization\nof N‑Arylacrylamides with AgSCF3: Access to SCF3‑Containing Oxindoles

Figshare
Biological Control of Invasive Species
article

Electrochemical\nTrifluoromethylthiolation/Cyclization\nof N‑Arylacrylamides with AgSCF3: Access to SCF3‑Containing Oxindoles

article en

Abstract

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

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Openalex Percentile: Top 61%
Biological Control of Invasive Species
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Electrochemical\nTrifluoromethylthiolation/Cyclization\nof <i>N</i>‑Arylacrylamides with AgSCF<sub>3</sub>: Access to SCF<sub>3</sub>‑Containing Oxindoles · Figshare (2024) | TGRS Research Map | TGRS