{"title":"Daphniphyllum 生物碱的全合成:(+)-Daphlongamine E、(+)-Calyciphylline R 和 (-)-10-Deoxydaphnipaxianine A","authors":"Yan Zhang, Yuye Chen, Jing Xu","doi":"10.1055/a-2244-1600","DOIUrl":null,"url":null,"abstract":"Here, we wish to describe our detailed efforts of the total synthesis of three calyciphylline A-type alkaloids, namely (+)-daphlongamine E, (+)-calyciphylline R, and (−)-10-deoxydaphnipaxianine A. Important steps in our approach include a Pt-catalyzed nitrile hydration, a Babler–Dauben rearrangement, a novel selective amide reduction tactic and, an oxidative Nazarov cyclization via an unfunctionalized tertiary divinyl carbinol (TDC).","PeriodicalId":510101,"journal":{"name":"Synthesis","volume":"45 19","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Total Synthesis of Daphniphyllum Alkaloids: (+)-Daphlongamine E, (+)-Calyciphylline R, and (−)-10-Deoxydaphnipaxianine A\",\"authors\":\"Yan Zhang, Yuye Chen, Jing Xu\",\"doi\":\"10.1055/a-2244-1600\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Here, we wish to describe our detailed efforts of the total synthesis of three calyciphylline A-type alkaloids, namely (+)-daphlongamine E, (+)-calyciphylline R, and (−)-10-deoxydaphnipaxianine A. Important steps in our approach include a Pt-catalyzed nitrile hydration, a Babler–Dauben rearrangement, a novel selective amide reduction tactic and, an oxidative Nazarov cyclization via an unfunctionalized tertiary divinyl carbinol (TDC).\",\"PeriodicalId\":510101,\"journal\":{\"name\":\"Synthesis\",\"volume\":\"45 19\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synthesis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1055/a-2244-1600\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthesis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/a-2244-1600","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
在此,我们希望详细描述一下我们对三种萼片紫碱 A 型生物碱(即 (+)-daphlongamine E、(+)-萼片紫碱 R 和 (-)-10-deoxydaphnipaxianine A)进行全合成的过程。我们研究方法的重要步骤包括铂催化的腈水合反应、巴伯勒-道本重排反应、新型选择性酰胺还原反应以及通过未官能化的叔二乙烯基卡宾醇(TDC)进行氧化纳扎罗夫环化反应。
Total Synthesis of Daphniphyllum Alkaloids: (+)-Daphlongamine E, (+)-Calyciphylline R, and (−)-10-Deoxydaphnipaxianine A
Here, we wish to describe our detailed efforts of the total synthesis of three calyciphylline A-type alkaloids, namely (+)-daphlongamine E, (+)-calyciphylline R, and (−)-10-deoxydaphnipaxianine A. Important steps in our approach include a Pt-catalyzed nitrile hydration, a Babler–Dauben rearrangement, a novel selective amide reduction tactic and, an oxidative Nazarov cyclization via an unfunctionalized tertiary divinyl carbinol (TDC).