{"title":"二甲基(甲基硫)磺酸盐引发烯烃与CS2和胺的二硫代氨基化反应。","authors":"Sha Peng , Cheng-Mei Qi , Li-Mei Duan , Ding Luo , Lu-Can Cheng , Si-Si Tian , Li-Hua Yang , Long-Yong Xie","doi":"10.1039/d5ob01043h","DOIUrl":null,"url":null,"abstract":"<div><div>In this work, a straightforward and practical four-component reaction involving alkenes, CS<sub>2</sub>, amines, and dimethyl(methylthio)sulfonium trifluoromethanesulfonate (DMTSM) is reported. This reaction enables the convenient synthesis of various <em>S</em>-alkyl dithiocarbamates in good to excellent yields. The mild reaction conditions, readily available starting materials and operational simplicity, along with numerous examples of late-stage functionalization, render this method highly attractive for organic synthesis.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 33","pages":"Pages 7638-7642"},"PeriodicalIF":2.7000,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dimethyl(methylthio)sulfonium salt triggered dithiocarbamation of alkenes with CS2 and amines\",\"authors\":\"Sha Peng , Cheng-Mei Qi , Li-Mei Duan , Ding Luo , Lu-Can Cheng , Si-Si Tian , Li-Hua Yang , Long-Yong Xie\",\"doi\":\"10.1039/d5ob01043h\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In this work, a straightforward and practical four-component reaction involving alkenes, CS<sub>2</sub>, amines, and dimethyl(methylthio)sulfonium trifluoromethanesulfonate (DMTSM) is reported. This reaction enables the convenient synthesis of various <em>S</em>-alkyl dithiocarbamates in good to excellent yields. The mild reaction conditions, readily available starting materials and operational simplicity, along with numerous examples of late-stage functionalization, render this method highly attractive for organic synthesis.</div></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"23 33\",\"pages\":\"Pages 7638-7642\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-08-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1477052025006184\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1477052025006184","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Dimethyl(methylthio)sulfonium salt triggered dithiocarbamation of alkenes with CS2 and amines
In this work, a straightforward and practical four-component reaction involving alkenes, CS2, amines, and dimethyl(methylthio)sulfonium trifluoromethanesulfonate (DMTSM) is reported. This reaction enables the convenient synthesis of various S-alkyl dithiocarbamates in good to excellent yields. The mild reaction conditions, readily available starting materials and operational simplicity, along with numerous examples of late-stage functionalization, render this method highly attractive for organic synthesis.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.