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Synthesis of 5-azaandrostane-3β,17β-diol protected at the 17β-hydroxyl group

dc.creatorPavlović, Vladimir D.
dc.creatorDabović, Milan
dc.creatorMartinović, Saša B.
dc.creatorLorenc, Ljubinka
dc.creatorKalvoda, J
dc.date.accessioned2019-04-26T14:31:39Z
dc.date.available2019-04-26T14:31:39Z
dc.date.issued2004
dc.identifier.issn0352-5139
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/2705
dc.description.abstractIn the present paper, the preparation of 3β-hydroxy-17β-dimethyl- tert-butylsilyloxy-5-azaandrostane (15) in fourteen steps is described. B-nor-17-oxoandrost-5-en-3β-yl acetate (1) 1,2 was used as the starting material, which was transformed to the key intermediate of the synthesis, B-nor-17β-dimethyl-tert-butylsilyloxyandrost-4-en-3β-yl acetate (7).en
dc.publisherSerbian Chemical Society
dc.relationMinistry of Science and Enviroment of Serbia (Part of the project “Synthesis and chemical transformations of steroidal and modified steroid molecules” – Project No. 1702)
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceJournal of the Serbian Chemical Society
dc.subject5-azasteroids
dc.subjectB-nor-17-oxoandrost-5-en-3-yl acetate
dc.subject3β-hydroxy-17β-dimethyl-tert-butylsilyloxy-5-azaandrostane
dc.titleSynthesis of 5-azaandrostane-3β,17β-diol protected at the 17β-hydroxyl groupen
dc.typearticleen
dc.rights.licenseBY-NC-ND
dcterms.abstractДабовић, М.; Калвода, Ј; Павловић, В Д; Мартиновић, С; Лоренц, Љубинка;
dc.citation.volume69
dc.citation.issue11
dc.citation.spage861
dc.citation.epage869
dc.citation.rankM23
dc.identifier.doi10.2298/JSC0411861P
dc.identifier.fulltexthttps://cer.ihtm.bg.ac.rs//bitstream/id/6434/0352-51390411861P.pdf
dc.identifier.scopus2-s2.0-31544483352
dc.identifier.wos000226120300004
dc.type.versionpublishedVersion


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