Radical reactivity of aryl thianthrenium salts

Aryl thianthrenium salts, accessed through highly selective arene thianthrenation, offer a versatile platform for generating aryl radicals under mild conditions, enabling streamlined C–D, C–C, and C–heteroatom bond formation among diverse substrates.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-12-18
DOI
https://doi.org/10.1039/d5qo01417d
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Radical reactivity of aryl thianthrenium salts

Organic Chemistry Frontiers
Radical Photochemical Reactions
article

Radical reactivity of aryl thianthrenium salts

article en

Abstract

Aryl thianthrenium salts, accessed through highly selective arene thianthrenation, offer a versatile platform for generating aryl radicals under mild conditions, enabling streamlined C–D, C–C, and C–heteroatom bond formation among diverse substrates.

Organic Chemistry FrontiersVol. 13(4)
Texas College (US), Texas A&M University (US)
Openalex Percentile: Top 34%
Radical Photochemical Reactions
DOIOpen Access PDFOpenAlex
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Radical reactivity of aryl thianthrenium salts · Organic Chemistry Frontiers (2025) | TGRS Research Map | TGRS