{"title":"光化学同二聚化是天然产物合成的关键步骤","authors":"Ellie F. Plachinski, Tehshik P. Yoon","doi":"10.1016/j.tet.2025.134706","DOIUrl":null,"url":null,"abstract":"<div><div>Photochemical dimerizations constitute a relatively simple but important class of bimolecular reactions. Nature produces several classes of dimeric natural products, some of which appear to be arise from radical or excited-state coupling reactions that could be photochemically initiated. This review focuses on natural products syntheses that exploit these photochemical dimerization reactions; selected total syntheses are discussed as examples, with particular attention given to the photochemical key step and its stereoselectivity.</div></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":"183 ","pages":"Article 134706"},"PeriodicalIF":2.1000,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photochemical homodimerization as a key step in natural product synthesis\",\"authors\":\"Ellie F. Plachinski, Tehshik P. Yoon\",\"doi\":\"10.1016/j.tet.2025.134706\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Photochemical dimerizations constitute a relatively simple but important class of bimolecular reactions. Nature produces several classes of dimeric natural products, some of which appear to be arise from radical or excited-state coupling reactions that could be photochemically initiated. This review focuses on natural products syntheses that exploit these photochemical dimerization reactions; selected total syntheses are discussed as examples, with particular attention given to the photochemical key step and its stereoselectivity.</div></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":\"183 \",\"pages\":\"Article 134706\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-05-08\",\"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/S0040402025002625\",\"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/S0040402025002625","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Photochemical homodimerization as a key step in natural product synthesis
Photochemical dimerizations constitute a relatively simple but important class of bimolecular reactions. Nature produces several classes of dimeric natural products, some of which appear to be arise from radical or excited-state coupling reactions that could be photochemically initiated. This review focuses on natural products syntheses that exploit these photochemical dimerization reactions; selected total syntheses are discussed as examples, with particular attention given to the photochemical key step and its stereoselectivity.
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.