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dc.contributor.author | Tsepaeva O.V. | |
dc.contributor.author | Nemtarev A.V. | |
dc.contributor.author | Kundina A.V. | |
dc.contributor.author | Grigor'eva L.R. | |
dc.contributor.author | Mironov V.F. | |
dc.date.accessioned | 2022-02-09T20:34:47Z | |
dc.date.available | 2022-02-09T20:34:47Z | |
dc.date.issued | 2021 | |
dc.identifier.issn | 0959-9436 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/169160 | |
dc.description.abstract | A general approach to lupane monodesmosides containing a C-28 phosphonioalkyl group is based on the initial glycosylation of triterpene acid ω-haloalkyl esters at the C-3 position. The subsequent phosphorylation with triphenylphosphine and deprotection in the carbohydrate moiety finalize the synthesis. | |
dc.relation.ispartofseries | Mendeleev Communications | |
dc.subject | betulinic acid | |
dc.subject | glycoside | |
dc.subject | glycosylation | |
dc.subject | lupane | |
dc.subject | mannopyranose | |
dc.subject | phosphonium salts | |
dc.subject | saponins | |
dc.subject | triterpenes | |
dc.title | Synthesis of novel mannopyranosyl betulinic acid phosphoniohexyl ester | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 1 | |
dc.relation.ispartofseries-volume | 31 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 110 | |
dc.source.id | SCOPUS09599436-2021-31-1-SID85100691268 |