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dc.contributor.authorYanmaz V.
dc.contributor.authorDisli A.
dc.contributor.authorYavuz S.
dc.contributor.authorOgutcu H.
dc.contributor.authorDilek G.
dc.date.accessioned2019-11-24T20:36:37Z
dc.date.available2019-11-24T20:36:37Z
dc.date.issued2019
dc.identifier.issn1303-9709
dc.identifier.urihttps://hdl.handle.net/20.500.12513/2196
dc.description.abstractA series of novel substituted isoxazolidine derivatives were synthesized by 1,3-dipolar cycloaddition reactions of a-aryl-N-methyl nitrones with diethyl maleate. The structures of the synthesized compounds were characterized using spectroscopic methods. All the synthesized compounds were screened for their antibacterial activities against Gram-positive and Gram-negative bacteria and for their antifungal activities against a yeast strain. The results show that all the synthesized compounds displayed significant activity against S. epidermidis, M. luteus, B. cereus, B. abortus and C. albicans when compared to standard drugs. © 2019, Gazi University Eti Mahallesi. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherGazi University Eti Mahallesien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject1,3-dipolaren_US
dc.subjectAntimicrobial activityen_US
dc.subjectCycloaddition reactionen_US
dc.subjectIsoxazolidineen_US
dc.subjectNitroneen_US
dc.titleSynthesis of some novel isoxazolidine derivatives via 1,3-dipolar cycloaddition and their biological evaluationen_US
dc.typearticleen_US
dc.relation.journalGazi University Journal of Scienceen_US
dc.contributor.departmentKırşehir Ahi Evran Üniversitesi, Fen-Edebiyat Fakültesi, Biyoloji Bölümüen_US
dc.identifier.volume32en_US
dc.identifier.issue1en_US
dc.identifier.startpage78en_US
dc.identifier.endpage89en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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