{"title":"A Metal-Free Oxidative Azidation Method for Selective Azidation of C(sp3)-H Bonds and Diazidation of Alkenes.","authors":"Yihang Bai,Yuedi Li,Xuehan Yu,Jing He,Xiaobo Sun,Luchuan Ou,Shuang Li,Xinghua Wang,Shihan Liu,Shi-Jun Li,Linbin Niu,Yu Lan","doi":"10.1021/acs.orglett.5c01241","DOIUrl":null,"url":null,"abstract":"Current metal-free methods for the synthesis of alkyl (1,2-di)azides mainly rely on highly reactive hypervalent iodine reagents and electrochemical methods, which require specialized electrochemical devices. Herein, we show a robust Selectfluor-promoted oxidative azidation method, which can effectively achieve the selective azidation of C(sp3)-H bonds in alkanes/methylarenes and the diazidation of alkenes, without involving any metal catalyst and additive. The utility of this method is highlighted by the broad substrate scope, late-stage functionalization, and gram-scale synthesis. Mechanistic studies indicate that the reaction proceeds via a radical process.","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"131 1","pages":""},"PeriodicalIF":4.9000,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Letters","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.orglett.5c01241","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
Current metal-free methods for the synthesis of alkyl (1,2-di)azides mainly rely on highly reactive hypervalent iodine reagents and electrochemical methods, which require specialized electrochemical devices. Herein, we show a robust Selectfluor-promoted oxidative azidation method, which can effectively achieve the selective azidation of C(sp3)-H bonds in alkanes/methylarenes and the diazidation of alkenes, without involving any metal catalyst and additive. The utility of this method is highlighted by the broad substrate scope, late-stage functionalization, and gram-scale synthesis. Mechanistic studies indicate that the reaction proceeds via a radical process.
期刊介绍:
Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.