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Synthesis of modified 5,10:8,14-bisfragmentation cholestane derivatives

dc.creatorMihailović, Milhailo Lj.
dc.creatorPavlović, Vladimir D.
dc.creatorBondarenko-Gheorghiu, Lidija
dc.creatorKrstić, Natalija
dc.creatorDabović, Milan
dc.creatorLorenc, Ljubinka
dc.date.accessioned2019-04-26T15:14:23Z
dc.date.available2019-04-26T15:14:23Z
dc.date.issued1996
dc.identifier.issn0352-5139
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/2708
dc.description.abstractIn this paper is described a synthetic pathway to the modified 5, 10:8, 14-bisfragmentation cholestene derivatives 10, 11 and 12, which involves introduction of the Δ8(14)-double bond and 5α-hydroxyl group in the cholestane molecule and subsequent cleavage of the olefinic C(8)-C(14) bond (with ruthenium tetroxide) and C(5)-C(10) bond (with mercuric oxide/iodine or lead tetracetate/iodine).en
dc.publisherSerbian Chemical Society
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceJournal of the Serbian Chemical Society
dc.subjectLactones
dc.subjectAcetates
dc.subjectsecosteroidal macrocycles
dc.titleSynthesis of modified 5,10:8,14-bisfragmentation cholestane derivativesen
dc.typearticleen
dc.rights.licenseBY-NC-ND
dcterms.abstractКрстић, Н М; Михаиловић, М. Љ.; Лоренц, Љубинка; Павловић, В. Д.; Бондаренко-Гхеоргхиу, Л Г; Дабовић, М. М.;
dc.citation.volume61
dc.citation.issue11
dc.citation.spage941
dc.citation.epage946
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_cer_2708
dc.identifier.scopus2-s2.0-21444459541
dc.type.versionpublishedVersion


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