K. Jatczak, Mariusz M. Gruza, Katarzyna Filip, P. Cmoch, G. Grynkiewicz
{"title":"选择性保护原叶香素衍生物的制备,用于合成叶香素类似物和新糖缀合物","authors":"K. Jatczak, Mariusz M. Gruza, Katarzyna Filip, P. Cmoch, G. Grynkiewicz","doi":"10.2478/s11532-014-0572-9","DOIUrl":null,"url":null,"abstract":"Protoescigenin, the main aglycone of horse chestnut saponin mixture known as escin, was selected as substrate for exploratory chemistry towards selective protection, followed by propargyl ether formation and subsequent condensation with azido-monosaccharides, to obtain novel triazole linked conjugates of the triterpene.","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"10 1","pages":"1222-1231"},"PeriodicalIF":0.0000,"publicationDate":"2014-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Preparation of selectively protected protoescigenin derivatives for synthesis of escin analogs and neoglycoconjugates\",\"authors\":\"K. Jatczak, Mariusz M. Gruza, Katarzyna Filip, P. Cmoch, G. Grynkiewicz\",\"doi\":\"10.2478/s11532-014-0572-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Protoescigenin, the main aglycone of horse chestnut saponin mixture known as escin, was selected as substrate for exploratory chemistry towards selective protection, followed by propargyl ether formation and subsequent condensation with azido-monosaccharides, to obtain novel triazole linked conjugates of the triterpene.\",\"PeriodicalId\":9888,\"journal\":{\"name\":\"Central European Journal of Chemistry\",\"volume\":\"10 1\",\"pages\":\"1222-1231\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Central European Journal of Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2478/s11532-014-0572-9\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Central European Journal of Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2478/s11532-014-0572-9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Preparation of selectively protected protoescigenin derivatives for synthesis of escin analogs and neoglycoconjugates
Protoescigenin, the main aglycone of horse chestnut saponin mixture known as escin, was selected as substrate for exploratory chemistry towards selective protection, followed by propargyl ether formation and subsequent condensation with azido-monosaccharides, to obtain novel triazole linked conjugates of the triterpene.