{"title":"钴催化非活化烯烃的分子内氟烷基羰基化。","authors":"Donghao Jiang,Zhudi He,Wei Li,Li-Jie Cheng","doi":"10.1021/acs.orglett.5c03691","DOIUrl":null,"url":null,"abstract":"A cobalt-catalyzed intramolecular fluoroalkylative carbonylation of unactivated alkenes has been developed, enabling the highly regioselective synthesis of fluoroalkylated γ-lactones in good yields. The mild reaction conditions exhibit good functional group tolerance, and the reaction can be performed on a large scale. Preliminary mechanistic investigations support a radical pathway in which a cationic acylcobalt(IV) complex is proposed as the key intermediate.","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"53 1","pages":""},"PeriodicalIF":5.0000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cobalt-Catalyzed Intramolecular Fluoroalkylative Carbonylation of Unactivated Alkenes.\",\"authors\":\"Donghao Jiang,Zhudi He,Wei Li,Li-Jie Cheng\",\"doi\":\"10.1021/acs.orglett.5c03691\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A cobalt-catalyzed intramolecular fluoroalkylative carbonylation of unactivated alkenes has been developed, enabling the highly regioselective synthesis of fluoroalkylated γ-lactones in good yields. The mild reaction conditions exhibit good functional group tolerance, and the reaction can be performed on a large scale. Preliminary mechanistic investigations support a radical pathway in which a cationic acylcobalt(IV) complex is proposed as the key intermediate.\",\"PeriodicalId\":54,\"journal\":{\"name\":\"Organic Letters\",\"volume\":\"53 1\",\"pages\":\"\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-09-30\",\"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.5c03691\",\"RegionNum\":1,\"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 Letters","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.orglett.5c03691","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Cobalt-Catalyzed Intramolecular Fluoroalkylative Carbonylation of Unactivated Alkenes.
A cobalt-catalyzed intramolecular fluoroalkylative carbonylation of unactivated alkenes has been developed, enabling the highly regioselective synthesis of fluoroalkylated γ-lactones in good yields. The mild reaction conditions exhibit good functional group tolerance, and the reaction can be performed on a large scale. Preliminary mechanistic investigations support a radical pathway in which a cationic acylcobalt(IV) complex is proposed as the key intermediate.
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.