Visible-Light-InducedNHC-Catalyzed CarboacylationReaction of Alkenes from Aryl Thianthrenium Salts and Aldehydes

A metal-free, visible-light-induced NHC-catalyzed multiple-component reaction involving aldehydes and aryl thianthrenium salts for the carboacylation reaction of alkenes is reported. In this reaction, NHC-activated aldehydes afforded Breslow intermediates, which reduced thianthrenium salts and generated aryl radicals. The resulting aryl radicals underwent radical addition reactions to yield arylacylation products, in the presence of iodoalkane, and participated in the halogen atom transfer process to generate alkyl radicals and facilitate olefin alkylacylation.

Publication Details

Journal
Figshare
Published
2025-02-21
DOI
https://doi.org/10.1021/acs.orglett.5c00394.s001
Primary Topic
Wheat and Barley Genetics and Pathology
Type
article
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0.00
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article

Visible-Light-InducedNHC-Catalyzed CarboacylationReaction of Alkenes from Aryl Thianthrenium Salts and Aldehydes

Figshare
Wheat and Barley Genetics and Pathology
article

Visible-Light-InducedNHC-Catalyzed CarboacylationReaction of Alkenes from Aryl Thianthrenium Salts and Aldehydes

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Abstract

A metal-free, visible-light-induced NHC-catalyzed multiple-component reaction involving aldehydes and aryl thianthrenium salts for the carboacylation reaction of alkenes is reported. In this reaction, NHC-activated aldehydes afforded Breslow intermediates, which reduced thianthrenium salts and generated aryl radicals. The resulting aryl radicals underwent radical addition reactions to yield arylacylation products, in the presence of iodoalkane, and participated in the halogen atom transfer process to generate alkyl radicals and facilitate olefin alkylacylation.

Figshare
Clean water and sanitation
Openalex Percentile: Top 41%
Wheat and Barley Genetics and Pathology
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Visible-Light-InducedNHC-Catalyzed CarboacylationReaction of Alkenes from Aryl Thianthrenium Salts and Aldehydes · Figshare (2025) | TGRS Research Map | TGRS