Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/17331
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dc.contributor.authorSukdolak, Slobodan-
dc.contributor.authorVukovic, Nenad-
dc.contributor.authorSolujić-Sukdolak, Slavica-
dc.contributor.authorMilosev, M.-
dc.contributor.authorManojlovic, Nedeljko-
dc.contributor.authorKrstic, Lj.-
dc.date.accessioned2023-03-16T10:33:30Z-
dc.date.available2023-03-16T10:33:30Z-
dc.date.issued2006-
dc.identifier.issn0352-5139en_US
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/17331-
dc.description.abstractAminothiazole derivatives of 4-hydroxy-2H-chromen-2-one were prepared by the Hantzsch reaction 1 using 3-(2-bromoacetyl)-4-hydroxy-2H-chromen-2-one and thiourea derivatives. Starting compound for this synthesis 3-(2-bromoacetyl)-4-hydro- xy-2H-chromen-2-one (1) was prepared previously. 2 Also, for this synthesis we used thiourea derivatives (2a-j) as compounds which possess groups with biological activity. Reactions are carried out in refluxing ethanol for a period of 30 - 45 min. Final products (3a-j) are obtained in a high yield. Chemical structure of the obtained compounds was confirmed by elemental and structural analysis (IR and 1 H NMR spectroscopy).en_US
dc.language.isoenen_US
dc.publisherSrpsko hemijsko društvoen_US
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.sourceJournal of the Serbian Chemical Society-
dc.subjectHantzsch reactionen_US
dc.subject3-(2-aminothiazol-4-yl)-4-hydroxy-2H-chromen-2-one derivativesen_US
dc.titleSynthesis of new 3-(2-aminothiazol-4-yl)-4-hydroxy-2H-chromen-2-one derivativesen_US
dc.typearticleen_US
dc.description.versionPublisheden_US
dc.identifier.doi10.2298/JSC0606581Sen_US
dc.type.versionPublishedVersionen_US
Appears in Collections:Faculty of Science, Kragujevac

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