{"title":"醋酸铜介导的2-吡啶取代丙烯腈与DMSO的硫甲基化反应","authors":"Min Ye, Jie Yang, Cheng Huang and Zhengwang Chen","doi":"10.1039/D5RA07270K","DOIUrl":null,"url":null,"abstract":"<p >An efficient synthesis of a variety of alkenyl methyl thioethers from acrylonitriles and dimethyl sulfoxide is described. This copper acetate mediated thiomethylation reaction provides the corresponding products with broad substrate scope in moderate to excellent yields. This transformation is achieved through direct functionalization of vinylic C–H bonds, resulting in stereospecific formation of the formal cyanothiolation product of internal alkynes.</p>","PeriodicalId":102,"journal":{"name":"RSC Advances","volume":" 46","pages":" 38832-38835"},"PeriodicalIF":4.6000,"publicationDate":"2025-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/ra/d5ra07270k?page=search","citationCount":"0","resultStr":"{\"title\":\"Copper acetate mediated thiomethylation of 2-pyridine-substituted acrylonitriles with DMSO\",\"authors\":\"Min Ye, Jie Yang, Cheng Huang and Zhengwang Chen\",\"doi\":\"10.1039/D5RA07270K\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >An efficient synthesis of a variety of alkenyl methyl thioethers from acrylonitriles and dimethyl sulfoxide is described. This copper acetate mediated thiomethylation reaction provides the corresponding products with broad substrate scope in moderate to excellent yields. This transformation is achieved through direct functionalization of vinylic C–H bonds, resulting in stereospecific formation of the formal cyanothiolation product of internal alkynes.</p>\",\"PeriodicalId\":102,\"journal\":{\"name\":\"RSC Advances\",\"volume\":\" 46\",\"pages\":\" 38832-38835\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-10-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2025/ra/d5ra07270k?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RSC Advances\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/ra/d5ra07270k\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Advances","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ra/d5ra07270k","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Copper acetate mediated thiomethylation of 2-pyridine-substituted acrylonitriles with DMSO
An efficient synthesis of a variety of alkenyl methyl thioethers from acrylonitriles and dimethyl sulfoxide is described. This copper acetate mediated thiomethylation reaction provides the corresponding products with broad substrate scope in moderate to excellent yields. This transformation is achieved through direct functionalization of vinylic C–H bonds, resulting in stereospecific formation of the formal cyanothiolation product of internal alkynes.
期刊介绍:
An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.