{"title":"通过aza -角三醌策略的外周衍生构建达芙龙胺B的四环核心框架。","authors":"Huijuanzi Rao, Bin-Bin Deng, Peijie Sun, Qidong Xia, Hanfeng Ding","doi":"10.1021/acs.orglett.4c04548","DOIUrl":null,"url":null,"abstract":"<p><p>A synthetic route to the highly functionalized tetracyclic core framework of daphlongamine B is described. Key features of the strategy involve an oxidative dearomatization-induced [4+2] cycloaddition, a di-π-methane rearrangement, and a ring-closing metathesis reaction. Our approach enables the reliable construction of a fully elaborated tetracyclic precursor, which, in turn, provides valuable functional handles for further elaboration to the target molecule.</p>","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":" ","pages":"1779-1785"},"PeriodicalIF":5.0000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Forging the Tetracyclic Core Framework of Daphlongamine B Enabled by a Peripheral Derivation of the Aza-Angular Triquinane Strategy.\",\"authors\":\"Huijuanzi Rao, Bin-Bin Deng, Peijie Sun, Qidong Xia, Hanfeng Ding\",\"doi\":\"10.1021/acs.orglett.4c04548\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A synthetic route to the highly functionalized tetracyclic core framework of daphlongamine B is described. Key features of the strategy involve an oxidative dearomatization-induced [4+2] cycloaddition, a di-π-methane rearrangement, and a ring-closing metathesis reaction. Our approach enables the reliable construction of a fully elaborated tetracyclic precursor, which, in turn, provides valuable functional handles for further elaboration to the target molecule.</p>\",\"PeriodicalId\":54,\"journal\":{\"name\":\"Organic Letters\",\"volume\":\" \",\"pages\":\"1779-1785\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-02-28\",\"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.4c04548\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/19 0:00:00\",\"PubModel\":\"Epub\",\"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.4c04548","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Forging the Tetracyclic Core Framework of Daphlongamine B Enabled by a Peripheral Derivation of the Aza-Angular Triquinane Strategy.
A synthetic route to the highly functionalized tetracyclic core framework of daphlongamine B is described. Key features of the strategy involve an oxidative dearomatization-induced [4+2] cycloaddition, a di-π-methane rearrangement, and a ring-closing metathesis reaction. Our approach enables the reliable construction of a fully elaborated tetracyclic precursor, which, in turn, provides valuable functional handles for further elaboration to the target molecule.
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.