Hypervalent‐Iodine‐Mediated Synthesis of Sulfinamides from Sulfenamides

A concise approach to access sulfinamides from sulfenamides is developed by using PhI(OAc) 2 /H 2 O. This protocol features mild and metal‐free conditions, high to excellent yields, and good functional group compatibility and provides an efficient and green route to sulfinamide derivatives. Importantly, the products obtained can be readily converted into potentially bioactive sulfonamides, sulfilimines, sulfonimidoyl halides, and sulfinimidate compounds for medicinal research, thus exh i biting diversified synthetic potential.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-10-27
DOI
https://doi.org/10.1002/ejoc.202500844
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

Hypervalent‐Iodine‐Mediated Synthesis of Sulfinamides from Sulfenamides

Bin Fu, Yaqing Xie, Zhaohai Qin, Jiawei Chen et al.
European Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
article

Hypervalent‐Iodine‐Mediated Synthesis of Sulfinamides from Sulfenamides

Bin Fu, Yaqing Xie, Zhaohai Qin, Jiawei Chen, Xiaoxu Gao, Liting Xu
article en

Abstract

A concise approach to access sulfinamides from sulfenamides is developed by using PhI(OAc) 2 /H 2 O. This protocol features mild and metal‐free conditions, high to excellent yields, and good functional group compatibility and provides an efficient and green route to sulfinamide derivatives. Importantly, the products obtained can be readily converted into potentially bioactive sulfonamides, sulfilimines, sulfonimidoyl halides, and sulfinimidate compounds for medicinal research, thus exh i biting diversified synthetic potential.

European Journal of Organic ChemistryVol. 29(1)
China Agricultural University (CN)
Openalex Percentile: Top 76%
Sulfur-Based Synthesis Techniques
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