Synthesis of Sulfenamides via Photoredox N–S Coupling of Dialkyl Azodicarboxylates and Thiols

We herein report a photoredox N-S coupling reaction between dialkyl azodicarboxylates and thiols to access sulfenamide scaffolds. This reaction proceeds under mild, green, and operationally simple conditions, offering a broad scope of sulfenamides with high yields and excellent atom efficiency. Mechanistic investigations revealed this reaction followed a photoinitiated radical pathway in which iodide plays a crucial role as both a radical initiator and a single-electron reductant.

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Publication Details

Journal
Organic Letters
Published
2024-12-27
DOI
https://doi.org/10.1021/acs.orglett.4c04454
Citations
7
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
1.75

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article

Synthesis of Sulfenamides via Photoredox N–S Coupling of Dialkyl Azodicarboxylates and Thiols

Xiaoyun Feng, Qun Liu, Fang Xie, Hua Jiang et al.
7 citations
Organic Letters
Sulfur-Based Synthesis Techniques
1.75
article

Synthesis of Sulfenamides via Photoredox N–S Coupling of Dialkyl Azodicarboxylates and Thiols

Xiaoyun Feng, Qun Liu, Fang Xie, Hua Jiang, Jin Wang, Y.‐S. LAI, Yuyang Jiao
article en
7 citations

Abstract

We herein report a photoredox N-S coupling reaction between dialkyl azodicarboxylates and thiols to access sulfenamide scaffolds. This reaction proceeds under mild, green, and operationally simple conditions, offering a broad scope of sulfenamides with high yields and excellent atom efficiency. Mechanistic investigations revealed this reaction followed a photoinitiated radical pathway in which iodide plays a crucial role as both a radical initiator and a single-electron reductant.

Organic LettersVol. 27(1)
Shandong Normal University (CN)
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 16%
Sulfur-Based Synthesis Techniques
1.75
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