{"title":"异芳酮三环骨架的合成。","authors":"Guoqing Sui, Xiaoqing Song, Huihui Guo, Xiaolan Xie, Li Ren, Wenming Zhou, Hong-Dong Hao","doi":"10.1039/d5ob00644a","DOIUrl":null,"url":null,"abstract":"<p><p>A synthesis of the 6-5-5 tricyclic skeleton of the diterpenoid aberrarone is reported. The synthesis strategically features an intermolecular Diels-Alder reaction to construct the <i>cis</i>-hydrindane moiety and a cross-coupling-isomerization-intramolecular Alder-ene cyclization cascade to efficiently assemble the 6-5-5 tricyclic skeleton of aberrarone.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of the tricyclic skeleton of aberrarone.\",\"authors\":\"Guoqing Sui, Xiaoqing Song, Huihui Guo, Xiaolan Xie, Li Ren, Wenming Zhou, Hong-Dong Hao\",\"doi\":\"10.1039/d5ob00644a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A synthesis of the 6-5-5 tricyclic skeleton of the diterpenoid aberrarone is reported. The synthesis strategically features an intermolecular Diels-Alder reaction to construct the <i>cis</i>-hydrindane moiety and a cross-coupling-isomerization-intramolecular Alder-ene cyclization cascade to efficiently assemble the 6-5-5 tricyclic skeleton of aberrarone.</p>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-05-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5ob00644a\",\"RegionNum\":3,\"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 & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5ob00644a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Synthesis of the tricyclic skeleton of aberrarone.
A synthesis of the 6-5-5 tricyclic skeleton of the diterpenoid aberrarone is reported. The synthesis strategically features an intermolecular Diels-Alder reaction to construct the cis-hydrindane moiety and a cross-coupling-isomerization-intramolecular Alder-ene cyclization cascade to efficiently assemble the 6-5-5 tricyclic skeleton of aberrarone.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.