A Metal-Free Oxidative Azidation Method for Selective Azidation of C(sp3)-H Bonds and Diazidation of Alkenes.

IF 4.9 1区 化学 Q1 CHEMISTRY, ORGANIC
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
{"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.
C(sp3)-H键选择性叠氮化和烯烃重氮化的无金属氧化叠氮化方法。
目前合成烷基(1,2-二)叠氮化物的无金属方法主要依靠高活性的高价碘试剂和电化学方法,这需要专门的电化学装置。在此,我们展示了一种强大的选择性氟促进氧化叠氮化方法,该方法可以在不涉及任何金属催化剂和添加剂的情况下,有效地实现烷烃/甲基芳烃中C(sp3)-H键的选择性叠氮化和烯烃的重氮化。这种方法的实用性突出体现在广泛的底物范围、后期功能化和克级合成。机理研究表明,该反应是通过自由基过程进行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Organic Letters
Organic Letters 化学-有机化学
CiteScore
9.30
自引率
11.50%
发文量
1607
审稿时长
1.5 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信