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dc.date.accessioned2024-03-07T05:30:10Z
dc.date.available2024-03-07T05:30:10Z
dc.date.issued2023tr
dc.identifier.urihttps://hdl.handle.net/20.500.12418/14819
dc.description.abstractHerein, we report the preparation of methyl 6-methyl-4-(4-nitrophenyl)-2-oxo-1,2- dihydropyrimidine-5-carboxylate 2, obtained by the regioselective oxidative dehydrogenation of the dihydropyrimidine derivative 1 in the presence of cerium ammonium nitrate. The structure of compound 2 was investigated by single-crystal X-ray diffraction (SC-XRD), which allowed the determination of its tautomeric form. Moreover, the presence of non-covalent interactions and their impact on the crystal structure were analyzed. To better characterize the intermolecular contacts, the Hirshfeld surface and enrichment ratio analyses were performed. Furthermore, the antimycotic activity of compounds 1 and 2 was investigated against Candida albicans, Aspergillus flavus, and Aspergillus niger, and their efficacy was compared to that of fluconazole. Computational investigations on the putative target of the compounds provided insights to explain the better activity of 2 with respect to its synthetic precursor.tr
dc.rightsinfo:eu-repo/semantics/openAccesstr
dc.titleCrystal Structure, Hirshfeld Surface Analysis, In-Silico and Antimycotic Investigations of Methyl 6-methyl-4-(4- nitrophenyl)-2-oxo-1,2-dihydropyrimidine-5-carboxylatetr
dc.typearticletr
dc.contributor.departmentEğitim Bilimleri Enstitüsütr
dc.relation.publicationcategoryRaportr


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