Photoinduced CO/S Bond Formation via Coupling of <i>N</i> ‐Tosylhydrazones with Phenols/Thiophenols

The formation of the CO/S bonds is of great importance in the synthesis of biologically active molecules and functional materials. Herein, a catalyst‐ and transition metal‐free approach enabling the coupling between N ‐tosylhydrazones and (thio)phenols under photoinduced conditions is presented. This strategy exhibits a broad scope of substrates including various N ‐tosylhydrazones and (thio)phenols, thus demonstrating the feasibility of this concept for CO/S bond formation. Unlike the traditional metal‐catalyzed version, the present reaction offers the advantages of high reaction speed, permitting the preparation of products within just one hour at room temperature. Moreover, the gram‐scale synthesis of thioethers and the generation of pharmaceutical intermediates highlight its practical applicability.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-10-14
DOI
https://doi.org/10.1002/adsc.70159
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

Photoinduced CO/S Bond Formation via Coupling of N ‐Tosylhydrazones with Phenols/Thiophenols

Er‐Jun Hao, Tongtong Li, Hai‐Ming Guo, Jinxin Wang et al.
Advanced Synthesis & Catalysis
Fluorine in Organic Chemistry
article

Photoinduced CO/S Bond Formation via Coupling of N ‐Tosylhydrazones with Phenols/Thiophenols

Er‐Jun Hao, Tongtong Li, Hai‐Ming Guo, Jinxin Wang, Yu Zhang, Chi Zhang, Qiannan Li, Ruiyang Tang, Miaomiao Zhuo, Tong Li
article en

Abstract

The formation of the CO/S bonds is of great importance in the synthesis of biologically active molecules and functional materials. Herein, a catalyst‐ and transition metal‐free approach enabling the coupling between N ‐tosylhydrazones and (thio)phenols under photoinduced conditions is presented. This strategy exhibits a broad scope of substrates including various N ‐tosylhydrazones and (thio)phenols, thus demonstrating the feasibility of this concept for CO/S bond formation. Unlike the traditional metal‐catalyzed version, the present reaction offers the advantages of high reaction speed, permitting the preparation of products within just one hour at room temperature. Moreover, the gram‐scale synthesis of thioethers and the generation of pharmaceutical intermediates highlight its practical applicability.

Advanced Synthesis & CatalysisVol. 367(24)
Second Military Medical University (CN), Shanghai University of Traditional Chinese Medicine (CN), Henan Normal University (CN)
Openalex Percentile: Top 78%
Fluorine in Organic Chemistry
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