Visible-light–enabled reduction of arylsulfonyl and benzoyl azides to access primary arylsulfonamides and benzoyl amides
Photocatalyzed reduction of arylsulfonyl and benzoyl azides, which could serve as temporary masking groups for amides, was achieved to access primary sulfonamides and benzoyl amides in mild conditions using organic reductant. A wide range of structurally diverse arylsulfonamides and benzoyl amides were accessed in good yields using this protocol. The mechanistic pathway of this reaction might generate the key amidyl radical through single-electron transfer (SET).
Authors
- Yanlan Bi (ORCID: https://orcid.org/0000-0001-8429-7806)
- Xianwei Sui (ORCID: https://orcid.org/0009-0003-8080-7444)
- Qing Li (ORCID: https://orcid.org/0000-0003-4807-030X)
- Ping Zhang (ORCID: https://orcid.org/0000-0002-5351-0421)
- Ming‐Chun Ma
- Xiaoxu Ma
Institutions
- Huaibei Normal University (CN)
Publication Details
- Journal
- Chemical Communications
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5cc02400e
- Primary Topic
- Sulfur-Based Synthesis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- University Natural Science Research Project of Anhui Province