Advances in Sulfenamide Chemistry: Synthetic Strategies and Reactivity Profiles

Sulfenamides, as S(II) compounds, occupy a critical role in modern synthetic chemistry, driven by their multifaceted applications across pharmaceuticals, agrochemicals, and diverse industrial sectors. Functioning as versatile intermediates, sulfenamides facilitate a broad array of transformations, including oxidation, amination, and sulfuration, underscoring their utility in complex molecular construction. This review presents an in‐depth analysis of sulfenamide synthesis, reactivity patterns, and multifarious applications, with a particular focus on recent mechanistic insights and prospective advances poised to shape the next generation of sulfenamide chemistry.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-04-14
DOI
https://doi.org/10.1002/ejoc.202500026
Citations
14
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
13.10
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article

Advances in Sulfenamide Chemistry: Synthetic Strategies and Reactivity Profiles

Ganesh Chandra Nandi, V. R. Padma Priya
14 citations
European Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
13.10
article

Advances in Sulfenamide Chemistry: Synthetic Strategies and Reactivity Profiles

Ganesh Chandra Nandi, V. R. Padma Priya
article en
14 citations

Abstract

Sulfenamides, as S(II) compounds, occupy a critical role in modern synthetic chemistry, driven by their multifaceted applications across pharmaceuticals, agrochemicals, and diverse industrial sectors. Functioning as versatile intermediates, sulfenamides facilitate a broad array of transformations, including oxidation, amination, and sulfuration, underscoring their utility in complex molecular construction. This review presents an in‐depth analysis of sulfenamide synthesis, reactivity patterns, and multifarious applications, with a particular focus on recent mechanistic insights and prospective advances poised to shape the next generation of sulfenamide chemistry.

European Journal of Organic ChemistryVol. 28(19)
National Institute of Technology Tiruchirappalli (IN)
Openalex Percentile: Top 1%
Sulfur-Based Synthesis Techniques
13.10
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