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dc.creatorSaičić, Radomir
dc.creatorMatović, Radomir
dc.creatorČeković, Živorad
dc.date.accessioned2018-11-22T00:02:46Z
dc.date.available2018-11-22T00:02:46Z
dc.date.issued1999
dc.identifier.issn0352-5139
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/419
dc.description.abstractFrom the needles of domestic yew, (Taxus baccata), 10-deacetylbaccatin III (10-DAB) call be isolated in quantities of up to 297 mg per kg of fresh needles. Additional quantities of 10-DAB call be obtained from the extract by NaBH4 mediated reductive hydrolysis of baccatin esters. A four-step procedure converts 10-DAB into taxol in 58% overall yield.en
dc.publisherSerbian Chemical Soc, Belgrade
dc.rightsrestrictedAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceJournal of the Serbian Chemical Society
dc.subjectanti-tumor agentsen
dc.subjecttaxolen
dc.subjectnatural productsen
dc.subjectsemisynthesisen
dc.titleSemisynthesis of Taxol (R): an improved procedure far the isolation of 10-deacetylbaccatin IIIen
dc.typearticle
dc.rights.licenseBY-NC-ND
dcterms.abstractМатовиц, Р; Саичић, Радомир; Цековиц, З;
dc.citation.volume64
dc.citation.issue9
dc.citation.spage497
dc.citation.epage503
dc.identifier.wos000082557600001
dc.citation.other64(9): 497-503
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-0038929346
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_cherry_419


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