Substituent‐Controlled Reactivity of DMSO‐Derived Methyl and Methanesulfonyl Radicals in the N─H Functionalization of Arylamines

) affords the corresponding trideuteromethylated and trideuteromethanesulfonylated products with controllable selectivity, underscoring the method's versatility. It is worth noting that this represents the first DMSO-assisted method for N─H mesylation and methylation, both in general and specifically for arylamines.

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Publication Details

Journal
Chemistry - A European Journal
Published
2026-04-17
DOI
https://doi.org/10.1002/chem.71007
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Substituent‐Controlled Reactivity of DMSO‐Derived Methyl and Methanesulfonyl Radicals in the N─H Functionalization of Arylamines

Palani Natarajan, Önder Metin, Burkhard Koenig
Chemistry - A European Journal
Catalytic C–H Functionalization Methods
article

Substituent‐Controlled Reactivity of DMSO‐Derived Methyl and Methanesulfonyl Radicals in the N─H Functionalization of Arylamines

Palani Natarajan, Önder Metin, Burkhard Koenig
article en

Abstract

) affords the corresponding trideuteromethylated and trideuteromethanesulfonylated products with controllable selectivity, underscoring the method's versatility. It is worth noting that this represents the first DMSO-assisted method for N─H mesylation and methylation, both in general and specifically for arylamines.

Chemistry - A European Journal
Koç University (TR), Panjab University (IN), University of Regensburg (DE)
Türkiye Bilimsel ve Teknolojik Araştırma Kurumu
Openalex Percentile: Top 15%
Catalytic C–H Functionalization Methods
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