1. University of Kragujevac Digital Archive
  2. University of Kragujevac
  3. Faculty of Science, Kragujevac
Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/12205
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dc.rights.licenserestrictedAccess-
dc.contributor.authorMinić, Aleksandra-
dc.contributor.authorStevanović, Dragana-
dc.contributor.authorDamljanović, Ivan-
dc.contributor.authorPejović, Anka-
dc.contributor.authorVukićević, Miomir-
dc.contributor.authorBogdanovic, Goran A.-
dc.contributor.authorRadulovic, Niko-
dc.contributor.authorVukicevic R.-
dc.date.accessioned2021-04-20T20:16:07Z-
dc.date.available2021-04-20T20:16:07Z-
dc.date.issued2015-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/12205-
dc.description.abstract© The Royal Society of Chemistry. A series of ferrocene-containing six-membered cyclic ureas (1-aryl-4-ferrocenyl-3-phenyltetrahydropyrimidin-2(1H)-ones) was synthesized (in high-to-excellent yields) by reacting the corresponding aminopropanols with phenyl isocyanate and the subsequent intramolecular cyclization of the thus obtained β-hydroxy ureas (prompted by acetic acid), via an α-ferrocenyl carbocation. This journal is-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourceRSC Advances-
dc.titleSynthesis of ferrocene-containing six-membered cyclic ureas via α-ferrocenyl carbocations-
dc.typearticle-
dc.identifier.doi10.1039/c5ra01383f-
dc.identifier.scopus2-s2.0-84924871534-
Appears in Collections:Faculty of Science, Kragujevac

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