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).

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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

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article

Visible-light–enabled reduction of arylsulfonyl and benzoyl azides to access primary arylsulfonamides and benzoyl amides

Yanlan Bi, Xianwei Sui, Qing Li, Ping Zhang et al.
Chemical Communications
Sulfur-Based Synthesis Techniques
article

Visible-light–enabled reduction of arylsulfonyl and benzoyl azides to access primary arylsulfonamides and benzoyl amides

Yanlan Bi, Xianwei Sui, Qing Li, Ping Zhang, Ming‐Chun Ma, Xiaoxu Ma
article en

Abstract

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).

Chemical CommunicationsVol. 61(66)
Huaibei Normal University (CN)
University Natural Science Research Project of Anhui Province
Openalex Percentile: Top 87%
Sulfur-Based Synthesis Techniques
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