Photocatalyst‐Free Visible‐Light Induced Radical Difluoromethylation/Cyclization Cascade Reaction for the Synthesis of Difluoromethylated Oxindoles with Difluoromethyl Phenoxathiinium Salt

Abstract A photocatalyst‐free photoinduced radical difluoromethylation approach for the convenient synthesis of difluoromethylated oxindoles from N ‐arylacrylamides with difluoromethyl phenoxathiinium salt (PT‐CF 2 H + BF 4 − ) was developed, this transformation involves radical difluoromethylation/cyclization cascade process and features photocatalyst‐free, mild reaction conditions, broad substrate scope and good functional groups tolerance. With this method, a wide variety of N ‐arylacrylamides were successfully converted to desired difluoromethylated oxindoles in good to excellent yields.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-09-23
DOI
https://doi.org/10.1002/ejoc.202400948
Citations
2
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.42

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article

Photocatalyst‐Free Visible‐Light Induced Radical Difluoromethylation/Cyclization Cascade Reaction for the Synthesis of Difluoromethylated Oxindoles with Difluoromethyl Phenoxathiinium Salt

Guo‐Kai Liu, Hong‐Xin Long
2 citations
European Journal of Organic Chemistry
Fluorine in Organic Chemistry
0.42
article

Photocatalyst‐Free Visible‐Light Induced Radical Difluoromethylation/Cyclization Cascade Reaction for the Synthesis of Difluoromethylated Oxindoles with Difluoromethyl Phenoxathiinium Salt

Guo‐Kai Liu, Hong‐Xin Long
article en
2 citations

Abstract

Abstract A photocatalyst‐free photoinduced radical difluoromethylation approach for the convenient synthesis of difluoromethylated oxindoles from N ‐arylacrylamides with difluoromethyl phenoxathiinium salt (PT‐CF 2 H + BF 4 − ) was developed, this transformation involves radical difluoromethylation/cyclization cascade process and features photocatalyst‐free, mild reaction conditions, broad substrate scope and good functional groups tolerance. With this method, a wide variety of N ‐arylacrylamides were successfully converted to desired difluoromethylated oxindoles in good to excellent yields.

European Journal of Organic ChemistryVol. 27(48)
Shenzhen University (CN)
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 43%
Fluorine in Organic Chemistry
0.42
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