S‐Trideuteromethylation of Sulfenamides: Synthesis of Trideuteromethyl Sulfilimines

ABSTRACT In this study, we present a base‐mediated, metal‐free method for synthesizing trideuteromethyl sulfilimines, which are significant in organic and medicinal chemistry. Our approach involves the modification of sulfenamides and the use of an electrophilic trideuteromethylating reagent under anionic conditions. This method has been successfully applied to a wide range of sulfenamides, generally providing the desired products in good yields and effective deuteration rates. Through detailed mechanistic studies, we have determined that the reaction proceeds without a free radical pathway. Our findings contribute to advancing the methodology for sulfilimine synthesis, underlining its relevance in modern chemical research.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2026-04-01
DOI
https://doi.org/10.1002/ajoc.202500616
Citations
1
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
12.70

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article

S‐Trideuteromethylation of Sulfenamides: Synthesis of Trideuteromethyl Sulfilimines

Xunbo Lu, Z. Huang, Guoling Huang, Shanyan Zhou et al.
1 citations
Asian Journal of Organic Chemistry
Synthesis and Catalytic Reactions
12.70
article

S‐Trideuteromethylation of Sulfenamides: Synthesis of Trideuteromethyl Sulfilimines

Xunbo Lu, Z. Huang, Guoling Huang, Shanyan Zhou, Jiaqi Sun, Juntao Ye
article en
1 citations

Abstract

ABSTRACT In this study, we present a base‐mediated, metal‐free method for synthesizing trideuteromethyl sulfilimines, which are significant in organic and medicinal chemistry. Our approach involves the modification of sulfenamides and the use of an electrophilic trideuteromethylating reagent under anionic conditions. This method has been successfully applied to a wide range of sulfenamides, generally providing the desired products in good yields and effective deuteration rates. Through detailed mechanistic studies, we have determined that the reaction proceeds without a free radical pathway. Our findings contribute to advancing the methodology for sulfilimine synthesis, underlining its relevance in modern chemical research.

Asian Journal of Organic ChemistryVol. 15(4)
Lingnan Normal University (CN), Southern University of Science and Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 1%
Synthesis and Catalytic Reactions
12.70
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S‐Trideuteromethylation of Sulfenamides: Synthesis of Trideuteromethyl Sulfilimines — Xunbo Lu, Z. Huang, et al. · Asian Journal of Organic Chemistry (2026) | TGRS Research Map | TGRS