{"title":"D-lyxo-和d -xylo-植物旋光素和全酰化旋光素B的合成","authors":"Gangarajulu Kesavulu, Kavirayani R. Prasad","doi":"10.1016/j.tet.2025.134657","DOIUrl":null,"url":null,"abstract":"<div><div>A short synthetic sequence for the synthesis of D-<em>lyxo</em> and D-<em>xylo</em>-phytosphingosine and fully acylated sphingofungin B methyl ester is presented. The key reaction in the synthesis is the addition of lithio tris(methylthio)methane to sulfinimine to install the required chiral amino acid/amino alcohol component.</div></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":"180 ","pages":"Article 134657"},"PeriodicalIF":2.1000,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Total synthesis of D-lyxo- and D-xylo-phytospingosines and fully acylated sphingofungin B\",\"authors\":\"Gangarajulu Kesavulu, Kavirayani R. Prasad\",\"doi\":\"10.1016/j.tet.2025.134657\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A short synthetic sequence for the synthesis of D-<em>lyxo</em> and D-<em>xylo</em>-phytosphingosine and fully acylated sphingofungin B methyl ester is presented. The key reaction in the synthesis is the addition of lithio tris(methylthio)methane to sulfinimine to install the required chiral amino acid/amino alcohol component.</div></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":\"180 \",\"pages\":\"Article 134657\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-04-12\",\"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/S0040402025002133\",\"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/S0040402025002133","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Total synthesis of D-lyxo- and D-xylo-phytospingosines and fully acylated sphingofungin B
A short synthetic sequence for the synthesis of D-lyxo and D-xylo-phytosphingosine and fully acylated sphingofungin B methyl ester is presented. The key reaction in the synthesis is the addition of lithio tris(methylthio)methane to sulfinimine to install the required chiral amino acid/amino alcohol component.
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.