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dc.creatorSimić, Milena
dc.creatorPetković, Miloš
dc.creatorJovanović, Predrag
dc.creatorTasić, Gordana
dc.creatorSavić, Vladimir
dc.date.accessioned2019-09-02T11:58:27Z
dc.date.available2019-09-02T11:58:27Z
dc.date.issued2017
dc.identifier.issn0352-5139
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/2842
dc.description.abstractPd-catalysed arylation-acetoxylation cascade, a previously reported methodology, was applied in the functionalisation of unsymmetrical dienes. Both explored classes of compounds, isoquinoline and ss-carboline-derived dienes, afforded single regioisomers. Although further improvements of the process are necessary, primarily due to lower yields, the described functionalisation of the studied compounds might be useful in the synthesis of emetine and related naturally occurring compounds.en
dc.publisherSrpsko hemijsko društvo, Beograd
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172009/RS//
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceJournal of the Serbian Chemical Society
dc.titleSynthesis of substituted allyl acetates from heterocyclic dienes by a Pd-promoted arylation-acetoxylation cascadeen
dc.typearticle
dc.rights.licenseBY-NC-ND
dcterms.abstractСавић, Владимир; Симић, Милена; Петковић, Милош; Тасић, Гордана; Јовановић, Предраг;
dc.citation.volume82
dc.citation.issue12
dc.citation.spage1335
dc.citation.epage1341
dc.citation.other82(12): 1335-1341
dc.citation.rankM23
dc.identifier.wos000419391700001
dc.identifier.doi10.2298/JSC170317046S
dc.identifier.scopus2-s2.0-85040055713
dc.identifier.fulltexthttps://farfar.pharmacy.bg.ac.rs//bitstream/id/1473/2840.pdf
dc.identifier.rcubconv_4029
dc.type.versionpublishedVersion


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