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dc.contributor.authorÇetin, Ahmet
dc.date.accessioned2016-06-03T06:43:52Z
dc.date.available2016-06-03T06:43:52Z
dc.date.issued2016-05-23
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/815
dc.description.abstractAromatic heterocycles are very important motifs in medicinal chemistry field. 1,3,4-oxadiazole exhibits a wide range of biological especially antifungal, activities [1]. 1,3,4-oxadiazole and their fused heterocyclic derivatives has gained notable attention due to their effective bio-synthetic importance[2-5]. In this work, various new compounds including ring 1,3,4-Oxadiazole were synthesized from the reactions of hydrazide compounds with carbon sulphur in basic medium. Acid derivatives were prepared by thiol tautomer form of 1,3,4-Oxadiazole (Scheme 1). Furthermore, structure-activity relationship was evaluated in respect to effect of different substitutions in newly synthesized 1,3,4-oxadiazole series. Then these compounds were characterized by performing of melting point, FT-IR, 1H-NMR (400 MHz), and 13C-NMR(100 MHz).tr_TR
dc.publisher2 nd International Conference on Organic Electronic Material Technologies (OEMT2016)tr_TR
dc.subject1,3,4-oxadiazole, Mannich Bases, Thiol-thione tautomerism.tr_TR
dc.titleThe Synthesis of Acid Derived Compounds Bearing 1,3,4-oxadiazole-2-thion Ring as Potential Antimicrobial Agentstr_TR
dc.typePresentationtr_TR


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