Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/12020
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dc.contributor.authorPejović, Anka-
dc.contributor.authorDanneels B.-
dc.contributor.authorDesmet T.-
dc.contributor.authorCham B.-
dc.contributor.authorNguyen V.-
dc.contributor.authorRadulovic, Niko-
dc.contributor.authorVukicevic R.-
dc.contributor.authorD'hooghe, Matthias-
dc.date.accessioned2021-04-20T19:48:44Z-
dc.date.available2021-04-20T19:48:44Z-
dc.date.issued2015-
dc.identifier.issn0936-5214-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/12020-
dc.description.abstract© Georg Thieme Verlag. Abstract 3-Arylamino-1-ferrocenylpropan-1-ones, prepared through aza-Michael addition of aromatic amines to 1-ferrocenylpropenone, were transformed into the corresponding 1,3-amino alcohols upon NaBH4-mediated carbonyl reduction. The latter amino alcohols were deployed as eligible substrates for the synthesis of a variety of ferrocene-containing heterocycles including 1,3-oxazinanes, 1,3-oxazinan-2-ones, and tetrahydropyrimidin-2-ones, which were subsequently evaluated for their antimicrobial and cytotoxic activities.-
dc.rightsrestrictedAccess-
dc.sourceSynlett-
dc.titleSynthesis and antimicrobial/cytotoxic assessment of ferrocenyl oxazinanes, oxazinan-2-ones, and tetrahydropyrimidin-2-ones-
dc.typearticle-
dc.identifier.doi10.1055/s-0034-1380348-
dc.identifier.scopus2-s2.0-84929836855-
Appears in Collections:Faculty of Science, Kragujevac

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