{"title":"通过钌催化和 K2S2O8 介导的 β-酮砜与 DMF 的多米诺环化反应，一步法合成磺酰化 5-丙酰基-2-芳基吡啶","authors":"Meng-Yang Chang, Chi-Ru Yang, Yeh-Long Chen","doi":"10.1002/adsc.202401116","DOIUrl":null,"url":null,"abstract":"Ruthenium-catalyzed and K2S2O8-mediated synthesis of diverse sulfonylated 5-aroyl-2-arylpyridines was developed through one-pot stepwise annulation of two molecules of β-ketosulfones and N,N-dimethylformamide (DMF) under the sealed tube conditions. In the overall process, DMF acts as the synthon of one carbon and one imino moiety in the construction of pyridine skeleton via cascade formation of single (C-C/C-N) and double (C=C/C=N) bonds under refluxing DMF conditions. Plausible reaction mechanism is proposed and discussed.","PeriodicalId":118,"journal":{"name":"Advanced Synthesis & Catalysis","volume":"13 1","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2024-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"One-pot Synthesis of Sulfonylated 5-Aroyl-2-arylpyridines via Ruthenium-Catalyzed and K2S2O8-Mediated Domino Annulation of β-Ketosulfones with DMF\",\"authors\":\"Meng-Yang Chang, Chi-Ru Yang, Yeh-Long Chen\",\"doi\":\"10.1002/adsc.202401116\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ruthenium-catalyzed and K2S2O8-mediated synthesis of diverse sulfonylated 5-aroyl-2-arylpyridines was developed through one-pot stepwise annulation of two molecules of β-ketosulfones and N,N-dimethylformamide (DMF) under the sealed tube conditions. In the overall process, DMF acts as the synthon of one carbon and one imino moiety in the construction of pyridine skeleton via cascade formation of single (C-C/C-N) and double (C=C/C=N) bonds under refluxing DMF conditions. Plausible reaction mechanism is proposed and discussed.\",\"PeriodicalId\":118,\"journal\":{\"name\":\"Advanced Synthesis & Catalysis\",\"volume\":\"13 1\",\"pages\":\"\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-10-04\",\"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.202401116\",\"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.202401116","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
One-pot Synthesis of Sulfonylated 5-Aroyl-2-arylpyridines via Ruthenium-Catalyzed and K2S2O8-Mediated Domino Annulation of β-Ketosulfones with DMF
Ruthenium-catalyzed and K2S2O8-mediated synthesis of diverse sulfonylated 5-aroyl-2-arylpyridines was developed through one-pot stepwise annulation of two molecules of β-ketosulfones and N,N-dimethylformamide (DMF) under the sealed tube conditions. In the overall process, DMF acts as the synthon of one carbon and one imino moiety in the construction of pyridine skeleton via cascade formation of single (C-C/C-N) and double (C=C/C=N) bonds under refluxing DMF conditions. Plausible reaction mechanism is proposed and discussed.
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.
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