{"title":"(−)-塑胶酸的合成研究:镍催化还原环化策略构建芳基四氢萘骨架","authors":"Xiao-Wei Cong , Yu Peng","doi":"10.1016/j.tet.2025.134724","DOIUrl":null,"url":null,"abstract":"<div><div>Plicatic acid is an aryltetralin lignan that can cause inflammatory and allergic reactions. A new construction of its carbon framework has been achieved herein. This synthetic strategy features the following key steps: asymmetric conjugate addition for installation of one aryl fragment, and an intramolecular Ni-catalyzed reductive cyclization to build the desired aryltetralin core structure.</div></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":"183 ","pages":"Article 134724"},"PeriodicalIF":2.1000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthetic studies towards (−)-plicatic acid: A Ni-catalyzed reductive cyclization strategy for the construction of its aryltetralin framework\",\"authors\":\"Xiao-Wei Cong , Yu Peng\",\"doi\":\"10.1016/j.tet.2025.134724\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Plicatic acid is an aryltetralin lignan that can cause inflammatory and allergic reactions. A new construction of its carbon framework has been achieved herein. This synthetic strategy features the following key steps: asymmetric conjugate addition for installation of one aryl fragment, and an intramolecular Ni-catalyzed reductive cyclization to build the desired aryltetralin core structure.</div></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":\"183 \",\"pages\":\"Article 134724\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-05-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0040402025002807\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040402025002807","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Synthetic studies towards (−)-plicatic acid: A Ni-catalyzed reductive cyclization strategy for the construction of its aryltetralin framework
Plicatic acid is an aryltetralin lignan that can cause inflammatory and allergic reactions. A new construction of its carbon framework has been achieved herein. This synthetic strategy features the following key steps: asymmetric conjugate addition for installation of one aryl fragment, and an intramolecular Ni-catalyzed reductive cyclization to build the desired aryltetralin core structure.
期刊介绍:
Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry.
Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters.
Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.