{"title":"FeCl3/K2S2O8/Et3SiH体系介导的β-酮砜与DMF的α-甲基化反应","authors":"Meng-Yang Chang, Chi-Ru Yang","doi":"10.1002/adsc.202400476","DOIUrl":null,"url":null,"abstract":"FeCl3/K2S2O8/Et3SiH system-mediated α-methylation of β-ketosulfones with N,N-dimethylformamide (DMF) was developed. In the overall process, DMF takes up the role of one methyl group in the generation of α-methyl β-ketosulfones via single carbon-carbon (C-C) bond formation under the reflux condition. Herein, a plausible reaction mechanism is proposed.","PeriodicalId":118,"journal":{"name":"Advanced Synthesis & Catalysis","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"FeCl3/K2S2O8/Et3SiH System-Mediated α-Methylation of β-Ketosulfones with DMF\",\"authors\":\"Meng-Yang Chang, Chi-Ru Yang\",\"doi\":\"10.1002/adsc.202400476\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"FeCl3/K2S2O8/Et3SiH system-mediated α-methylation of β-ketosulfones with N,N-dimethylformamide (DMF) was developed. In the overall process, DMF takes up the role of one methyl group in the generation of α-methyl β-ketosulfones via single carbon-carbon (C-C) bond formation under the reflux condition. Herein, a plausible reaction mechanism is proposed.\",\"PeriodicalId\":118,\"journal\":{\"name\":\"Advanced Synthesis & Catalysis\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-07-30\",\"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.202400476\",\"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.202400476","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
FeCl3/K2S2O8/Et3SiH System-Mediated α-Methylation of β-Ketosulfones with DMF
FeCl3/K2S2O8/Et3SiH system-mediated α-methylation of β-ketosulfones with N,N-dimethylformamide (DMF) was developed. In the overall process, DMF takes up the role of one methyl group in the generation of α-methyl β-ketosulfones via single carbon-carbon (C-C) bond formation under the reflux condition. Herein, a plausible reaction mechanism is proposed.
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.