{"title":"N - tosylhydra腙与苯酚/噻吩偶联的光诱导C - O/S键形成","authors":"Er‐Jun Hao, Miaomiao Zhuo, Tong Li, Jinxin Wang, Chi Zhang, Tongtong Li, Ruiyang Tang, Hai‐Ming Guo, Qiannan Li, Yu Zhang","doi":"10.1002/adsc.70159","DOIUrl":null,"url":null,"abstract":"The formation of the CO/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 <jats:italic>N</jats:italic>‐tosylhydrazones and (thio)phenols under photoinduced conditions is presented. This strategy exhibits a broad scope of substrates including various <jats:italic>N</jats:italic>‐tosylhydrazones and (thio)phenols, thus demonstrating the feasibility of this concept for CO/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.","PeriodicalId":118,"journal":{"name":"Advanced Synthesis & Catalysis","volume":"7 1","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photoinduced CO/S Bond Formation via Coupling of N‐Tosylhydrazones with Phenols/Thiophenols\",\"authors\":\"Er‐Jun Hao, Miaomiao Zhuo, Tong Li, Jinxin Wang, Chi Zhang, Tongtong Li, Ruiyang Tang, Hai‐Ming Guo, Qiannan Li, Yu Zhang\",\"doi\":\"10.1002/adsc.70159\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The formation of the CO/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 <jats:italic>N</jats:italic>‐tosylhydrazones and (thio)phenols under photoinduced conditions is presented. This strategy exhibits a broad scope of substrates including various <jats:italic>N</jats:italic>‐tosylhydrazones and (thio)phenols, thus demonstrating the feasibility of this concept for CO/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.\",\"PeriodicalId\":118,\"journal\":{\"name\":\"Advanced Synthesis & Catalysis\",\"volume\":\"7 1\",\"pages\":\"\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-10-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Synthesis & Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/adsc.70159\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Synthesis & Catalysis","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/adsc.70159","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
摘要
C - O/S键的形成在生物活性分子和功能材料的合成中具有重要意义。本文提出了一种无催化剂和过渡金属的方法,可以在光诱导条件下实现N -甲酰基腙和(硫)酚之间的偶联。该策略展示了广泛的底物范围,包括各种N -甲酰基腙和(硫)酚,从而证明了该概念在C - O/S键形成中的可行性。与传统的金属催化不同,目前的反应具有反应速度快的优点,允许在室温下仅一小时内制备产品。此外,硫醚的克级合成和医药中间体的生成突出了它的实用性。
Photoinduced CO/S Bond Formation via Coupling of N‐Tosylhydrazones with Phenols/Thiophenols
The formation of the CO/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 CO/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.
期刊介绍:
Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry.
The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.