{"title":"聚乙缩醛全合成的进化研究。","authors":"Huilin Li,Meng Liu,Xingang Xie,Xuegong She","doi":"10.1021/acs.joc.5c00974","DOIUrl":null,"url":null,"abstract":"Pepluacetal is a structurally unique pepluanol family Euphorbia diterpenoid bearing an all-carbon [5-4-7-3] tetracyclic backbone. We describe herein the detailed process of the total synthesis of pepluacetal through the evolution of synthetic strategies. In the final successful strategy, a photoinduced Wolff rearrangement/lactonization cascade reaction gives access to the cyclobutane moiety; a ring-closing metathesis/cyclopropanation sequence rapidly builds up the [7-3] bicycle, and a Rh-catalyzed carbenoid insertion of the cyclobutane methylene C(sp3)-H bond, followed by ring-opening manipulations, introduces the three-carbon branched side chain stereoselectively in a remote traceless stereochemical relay fashion. The synthesis demonstrates excellent control of stereo-, regio-, and chemoselectivities. Moreover, the synthetic route could be performed on a large scale and optimized to a shorter version by running successive reactions in one pot, thus providing a general and practical approach to access pepluacetal.","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"658 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evolutionary Efforts in the Total Synthesis of Pepluacetal.\",\"authors\":\"Huilin Li,Meng Liu,Xingang Xie,Xuegong She\",\"doi\":\"10.1021/acs.joc.5c00974\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Pepluacetal is a structurally unique pepluanol family Euphorbia diterpenoid bearing an all-carbon [5-4-7-3] tetracyclic backbone. We describe herein the detailed process of the total synthesis of pepluacetal through the evolution of synthetic strategies. In the final successful strategy, a photoinduced Wolff rearrangement/lactonization cascade reaction gives access to the cyclobutane moiety; a ring-closing metathesis/cyclopropanation sequence rapidly builds up the [7-3] bicycle, and a Rh-catalyzed carbenoid insertion of the cyclobutane methylene C(sp3)-H bond, followed by ring-opening manipulations, introduces the three-carbon branched side chain stereoselectively in a remote traceless stereochemical relay fashion. The synthesis demonstrates excellent control of stereo-, regio-, and chemoselectivities. Moreover, the synthetic route could be performed on a large scale and optimized to a shorter version by running successive reactions in one pot, thus providing a general and practical approach to access pepluacetal.\",\"PeriodicalId\":57,\"journal\":{\"name\":\"Journal of Organic Chemistry\",\"volume\":\"658 1\",\"pages\":\"\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-07-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Organic Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.joc.5c00974\",\"RegionNum\":2,\"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":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.joc.5c00974","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Evolutionary Efforts in the Total Synthesis of Pepluacetal.
Pepluacetal is a structurally unique pepluanol family Euphorbia diterpenoid bearing an all-carbon [5-4-7-3] tetracyclic backbone. We describe herein the detailed process of the total synthesis of pepluacetal through the evolution of synthetic strategies. In the final successful strategy, a photoinduced Wolff rearrangement/lactonization cascade reaction gives access to the cyclobutane moiety; a ring-closing metathesis/cyclopropanation sequence rapidly builds up the [7-3] bicycle, and a Rh-catalyzed carbenoid insertion of the cyclobutane methylene C(sp3)-H bond, followed by ring-opening manipulations, introduces the three-carbon branched side chain stereoselectively in a remote traceless stereochemical relay fashion. The synthesis demonstrates excellent control of stereo-, regio-, and chemoselectivities. Moreover, the synthetic route could be performed on a large scale and optimized to a shorter version by running successive reactions in one pot, thus providing a general and practical approach to access pepluacetal.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.