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dc.contributor.advisorYüksek, Haydar
dc.contributor.authorSadi, Sibel
dc.date.accessioned2020-12-06T10:12:19Z
dc.date.available2020-12-06T10:12:19Z
dc.date.submitted2003
dc.date.issued2018-08-06
dc.identifier.urihttps://acikbilim.yok.gov.tr/handle/20.500.12812/97257
dc.description.abstractÖZET Bu çalışmada, bazı 3-alkil(aril)-4-amino-4,5-dihidro-lH-l,2,4-triazol-5-on bileşiklerinin, 5-metilfuran-2-karboksialdeh.it ile reaksiyonu incelenmiş ve 4 adet yeni 3-alkil(aril)-4-(5-metil-2-ftırilmetilenamino)-4,5-dihidro-lH-l,2,4-triazol-5-on bileşikle ri elde edilmiştir. Çalışmada elde edilen 4 yeni bileşiğin yapı aydınlatmaları için mikroanaliz, İR, *H NMR, 13C NMR ve UV spektroskop! yöntemleri kullanılmıştır. Anahtar Kelimeler: 3-Alkil(aril)-4-amino-4,5-dihidro-lH-l,2,4-triazol-5-on, 5- metil-2-furan karbaldehit VI
dc.description.abstractSUMMARY SYNTHESIS OF SOME NEW 4,5-DHYDRO-lH-l,2,4-TRIAZOL-5-ONE COMPOUNDS In this study, the reactions of some 3-alkyl(aryl)-4-amino-4,5-dihydro-lH-l,2,4- triazol-5-ones with 5-methylfuran-2-carboxyaldehyde were investigated and 4 new 3- alkyl(aryl)-4-(5-methyl-2-fury lmethy lenamino)-4, 5-dihydro- 1 H- 1,2,4-triazol-5-ones were synthesized. In order to identify the new compounds synthesized in the study, microanalysis and spectroscopic methods including IR, *H-NMR, 13C-NMR and UV were used. Key Words: 3-Alkyl(aryl)-4-amino-4,5-dihydro-lH-l,2,4-triazol-5-ones, 5- methylfuran-2-carboxy aldehyde VIIen_US
dc.languageTurkish
dc.language.isotr
dc.rightsinfo:eu-repo/semantics/embargoedAccess
dc.rightsAttribution 4.0 United Statestr_TR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectKimyatr_TR
dc.subjectChemistryen_US
dc.titleBazı yeni 4,5-dihidro-1H-1,2,4 triazol-5-on bileşiklerinin sentezi
dc.title.alternativeSynthesis of some new 4,5-dihydro-1H-1,2,4 triazole-5-one compounds
dc.typemasterThesis
dc.date.updated2018-08-06
dc.contributor.departmentDiğer
dc.identifier.yokid143816
dc.publisher.instituteFen Bilimleri Enstitüsü
dc.publisher.universityKAFKAS ÜNİVERSİTESİ
dc.identifier.thesisid136262
dc.description.pages46
dc.publisher.disciplineDiğer


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