{"title":"实现紫苏萜 A 和 B 的立体化学分配:天然产物可能结构的全合成。","authors":"Kenichi Kobayashi , Yusuke Honma , Kosaku Tanaka , Momoko Suzuki , Kazuhiko Takatori , Hiroshi Kogen","doi":"10.1039/d4ob01118j","DOIUrl":null,"url":null,"abstract":"<div><div>The possible structures of euvesperins A and B were synthesized. The results of our synthesis suggest that euvesperin A may be a mixture of the (2<em>R</em>,3<em>R</em>,4<em>S</em>,7<em>S</em>) and (2<em>S</em>,3<em>S</em>,4<em>R</em>,7<em>S</em>) isomers and euvesperin B may be a mixture of the (2<em>R</em>,3<em>S</em>,4<em>S</em>,7<em>S</em>) and (2<em>S</em>,3<em>R</em>,4<em>R</em>,7<em>S</em>) isomers in consideration of their putative biosynthetic pathways.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"22 36","pages":"Pages 7307-7310"},"PeriodicalIF":2.7000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ob/d4ob01118j?page=search","citationCount":"0","resultStr":"{\"title\":\"Toward the stereochemical assignment of euvesperins A and B: total synthesis of the possible structures of the natural products†\",\"authors\":\"Kenichi Kobayashi , Yusuke Honma , Kosaku Tanaka , Momoko Suzuki , Kazuhiko Takatori , Hiroshi Kogen\",\"doi\":\"10.1039/d4ob01118j\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The possible structures of euvesperins A and B were synthesized. The results of our synthesis suggest that euvesperin A may be a mixture of the (2<em>R</em>,3<em>R</em>,4<em>S</em>,7<em>S</em>) and (2<em>S</em>,3<em>S</em>,4<em>R</em>,7<em>S</em>) isomers and euvesperin B may be a mixture of the (2<em>R</em>,3<em>S</em>,4<em>S</em>,7<em>S</em>) and (2<em>S</em>,3<em>R</em>,4<em>R</em>,7<em>S</em>) isomers in consideration of their putative biosynthetic pathways.</div></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"22 36\",\"pages\":\"Pages 7307-7310\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/ob/d4ob01118j?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1477052024007377\",\"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://www.sciencedirect.com/org/science/article/pii/S1477052024007377","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
摘要
合成了紫罗兰茄素 A 和 B 的可能结构。我们的合成结果表明,考虑到它们的推定生物合成途径,紫罗兰香精 A 可能是(2R,3R,4S,7S)和(2S,3S,4R,7S)异构体的混合物,而紫罗兰香精 B 可能是(2R,3S,4S,7S)和(2S,3R,4R,7S)异构体的混合物。
Toward the stereochemical assignment of euvesperins A and B: total synthesis of the possible structures of the natural products†
The possible structures of euvesperins A and B were synthesized. The results of our synthesis suggest that euvesperin A may be a mixture of the (2R,3R,4S,7S) and (2S,3S,4R,7S) isomers and euvesperin B may be a mixture of the (2R,3S,4S,7S) and (2S,3R,4R,7S) isomers in consideration of their putative biosynthetic pathways.
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.