Please use this identifier to cite or link to this item:
https://scidar.kg.ac.rs/handle/123456789/11720
Full metadata record
DC Field | Value | Language |
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dc.rights.license | restrictedAccess | - |
dc.contributor.author | Muškinja, Jovana | - |
dc.contributor.author | Janković, Nenad | - |
dc.contributor.author | Ratković, Zoran | - |
dc.contributor.author | Bogdanovic, Goran A. | - |
dc.contributor.author | Bugarčić Z. | - |
dc.date.accessioned | 2021-04-20T19:03:45Z | - |
dc.date.available | 2021-04-20T19:03:45Z | - |
dc.date.issued | 2016 | - |
dc.identifier.issn | 1381-1991 | - |
dc.identifier.uri | https://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.rights | info:eu-repo/semantics/restrictedAccess | - |
dc.rights | info:eu-repo/semantics/restrictedAccess | - |
dc.source | Molecular Diversity | - |
dc.title | Vanillic aldehydes for the one-pot synthesis of novel 2-oxo-1,2,3,4-tetrahydropyrimidines | - |
dc.type | article | - |
dc.identifier.doi | 10.1007/s11030-016-9658-y | - |
dc.identifier.scopus | 2-s2.0-84977450850 | - |
Appears in Collections: | Faculty of Science, Kragujevac Institute for Information Technologies, Kragujevac |
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PaperMissing.pdf Restricted Access | 29.86 kB | Adobe PDF | View/Open |
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