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dc.contributor.authorGur, Mahmut
dc.contributor.authorSener, Nesrin
dc.contributor.authorKastas, Cigdem A.
dc.contributor.authorOzkan, Osman Emre
dc.contributor.authorMuglu, Halit
dc.contributor.authorElmaswari, Magboule A. M.
dc.date.accessioned2020-06-21T13:17:53Z
dc.date.available2020-06-21T13:17:53Z
dc.date.issued2017
dc.identifier.issn0022-152X
dc.identifier.issn1943-5193
dc.identifier.urihttps://doi.org/10.1002/jhet.2984
dc.identifier.urihttps://hdl.handle.net/20.500.12712/12140
dc.descriptionOzkan, Osman Emre/0000-0003-4011-8815; gur, mahmut/0000-0001-9942-6324en_US
dc.descriptionWOS: 000422654000071en_US
dc.description.abstractThrough a cyclization reaction of 2-phenylbutyric acid with N-phenylthiosemicarbazide and POCl3, novel 1,3,4-thiadiazole derivatives were synthesized. Their structures were confirmed using IR, H-1 NMR, and C-13 NMR spectroscopies and elemental analysis. The antibacterial activities of the obtained 1,3,4-thiadiazole derivatives were tested against Gram-negative bacteria (Salmonella enteritidis, Salmonella typhimurium, Enterobacter aerogenes, Salmonella infantis, Salmonella kentucky, and Escherichia coli) and Grampositive bacteria (Staphylococcus aureus, Bacillus subtilis, and Enterococcus durans) using a disk diffusion method. Moreover, an antifungal activity experiment was performed against Candida albicans using the disk diffusion method. It was observed that the synthesized 1,3,4-thiadiazole derivatives exhibited effective antimicrobial activity against S. aureus, E. coli, and C. albicans. Based on these results, the 1,3,4-thiadiazole derivatives can be considered as a source of bioactive agents for pharmacological and medicinal applications.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1002/jhet.2984en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleSynthesis and Characterization of Some New Heteroaromatic Compounds Having Chirality Adjacent to a 1,3,4-Thiadiazole Moiety and Their Antimicrobial Activitiesen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume54en_US
dc.identifier.issue6en_US
dc.identifier.startpage3578en_US
dc.identifier.endpage3590en_US
dc.relation.journalJournal of Heterocyclic Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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