Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/11720
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dc.rights.licenserestrictedAccess-
dc.contributor.authorMuškinja, Jovana-
dc.contributor.authorJanković, Nenad-
dc.contributor.authorRatković, Zoran-
dc.contributor.authorBogdanovic, Goran A.-
dc.contributor.authorBugarčić Z.-
dc.date.accessioned2021-04-20T19:03:45Z-
dc.date.available2021-04-20T19:03:45Z-
dc.date.issued2016-
dc.identifier.issn1381-1991-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/11720-
dc.description.abstract© 2016, Springer International Publishing Switzerland. A small library of novel 2-oxo-1,2,3,4-tetrahydropyrimidines was synthesized via a one-pot multicomponent Biginelli reaction. Copper complex (PhNH3)2CuCl4, which was used for the first time as a homogeneous and heterogeneous catalyst, makes this a facile and efficient reaction at room temperature. All the obtained products fall out of the solution in pure form and are easily isolated via filtration in good-to-excellent yields. The molecular structure of one of the products, ethyl 6-methyl-2-oxo-4-(4′-isopropoxy-3′-methoxyphenyl) - 1,2,3,4 - tetrahydropyrimidine-5- carboxylate, has been determined by X-ray crystallography. All non-hydrogen atoms in the heterocyclic, six-membered ring are determined to be approximately coplanar.-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourceMolecular Diversity-
dc.titleVanillic aldehydes for the one-pot synthesis of novel 2-oxo-1,2,3,4-tetrahydropyrimidines-
dc.typearticle-
dc.identifier.doi10.1007/s11030-016-9658-y-
dc.identifier.scopus2-s2.0-84977450850-
Appears in Collections:Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac

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