dc.creator | Mihailović, Milhailo Lj. | |
dc.creator | Pavlović, Vladimir D. | |
dc.creator | Bondarenko-Gheorghiu, Lidija | |
dc.creator | Krstić, Natalija | |
dc.creator | Dabović, Milan | |
dc.creator | Lorenc, Ljubinka | |
dc.date.accessioned | 2019-04-26T15:14:23Z | |
dc.date.available | 2019-04-26T15:14:23Z | |
dc.date.issued | 1996 | |
dc.identifier.issn | 0352-5139 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/2708 | |
dc.description.abstract | In 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.publisher | Serbian Chemical Society | |
dc.rights | openAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.source | Journal of the Serbian Chemical Society | |
dc.subject | Lactones | |
dc.subject | Acetates | |
dc.subject | secosteroidal macrocycles | |
dc.title | Synthesis of modified 5,10:8,14-bisfragmentation cholestane derivatives | en |
dc.type | article | en |
dc.rights.license | BY-NC-ND | |
dcterms.abstract | Крстић, Н М; Михаиловић, М. Љ.; Лоренц, Љубинка; Павловић, В. Д.; Бондаренко-Гхеоргхиу, Л Г; Дабовић, М. М.; | |
dc.citation.volume | 61 | |
dc.citation.issue | 11 | |
dc.citation.spage | 941 | |
dc.citation.epage | 946 | |
dc.identifier.rcub | https://hdl.handle.net/21.15107/rcub_cer_2708 | |
dc.identifier.scopus | 2-s2.0-21444459541 | |
dc.type.version | publishedVersion | |