{"title":"咪唑[2,1-b]噻唑与DMSO的电化学区域选择性甲基硫化","authors":"Meng Xiao , Liyu Yi , Wenjie Liu , Gao Cao","doi":"10.1080/00397911.2025.2453872","DOIUrl":null,"url":null,"abstract":"<div><div>With DMSO both as the source of -SMe unit and solvent, an efficient and green electrochemical methylthiolation reaction of imidazo[2,1-<em>b</em>]thiazoles was developed. The transformation was performed at room temperature in 8 h under external transition metal- and oxidant-free condition. Moreover, the 2,3-dihydroimidazo[2,1-<em>b</em>]thiazoles and 2-phenylbenzo[d]imidazo[2,1-<em>b</em>]thiazole also proceeded smoothly. This strategy provides C-5 methylthiolation products with broad scope in 73–91% yields.</div></div>","PeriodicalId":22119,"journal":{"name":"Synthetic Communications","volume":"55 4","pages":"Pages 338-349"},"PeriodicalIF":1.8000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrochemical regioselective methylthiolation of imidazo[2,1-b]thiazoles with DMSO\",\"authors\":\"Meng Xiao , Liyu Yi , Wenjie Liu , Gao Cao\",\"doi\":\"10.1080/00397911.2025.2453872\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>With DMSO both as the source of -SMe unit and solvent, an efficient and green electrochemical methylthiolation reaction of imidazo[2,1-<em>b</em>]thiazoles was developed. The transformation was performed at room temperature in 8 h under external transition metal- and oxidant-free condition. Moreover, the 2,3-dihydroimidazo[2,1-<em>b</em>]thiazoles and 2-phenylbenzo[d]imidazo[2,1-<em>b</em>]thiazole also proceeded smoothly. This strategy provides C-5 methylthiolation products with broad scope in 73–91% yields.</div></div>\",\"PeriodicalId\":22119,\"journal\":{\"name\":\"Synthetic Communications\",\"volume\":\"55 4\",\"pages\":\"Pages 338-349\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-01-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synthetic Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S0039791125000086\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthetic Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S0039791125000086","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Electrochemical regioselective methylthiolation of imidazo[2,1-b]thiazoles with DMSO
With DMSO both as the source of -SMe unit and solvent, an efficient and green electrochemical methylthiolation reaction of imidazo[2,1-b]thiazoles was developed. The transformation was performed at room temperature in 8 h under external transition metal- and oxidant-free condition. Moreover, the 2,3-dihydroimidazo[2,1-b]thiazoles and 2-phenylbenzo[d]imidazo[2,1-b]thiazole also proceeded smoothly. This strategy provides C-5 methylthiolation products with broad scope in 73–91% yields.
期刊介绍:
Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.