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.
Authors
- Xiaoyun Feng
- Qun Liu (ORCID: https://orcid.org/0000-0002-8308-7636)
- Fang Xie (ORCID: https://orcid.org/0000-0003-0801-4696)
- Hua Jiang (ORCID: https://orcid.org/0000-0002-7948-484X)
- Jin Wang (ORCID: https://orcid.org/0000-0001-5511-1910)
- Y.‐S. LAI
- Yuyang Jiao
Institutions
- Shandong Normal University (CN)
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
Funders
- National Natural Science Foundation of China