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dc.contributor.authorÖğretir, Cemil
dc.contributor.authorYarlıgan, S
dc.contributor.authorDemirayak, Şeref
dc.contributor.authorArslan, T
dc.date.accessioned2019-10-19T14:02:34Z
dc.date.available2019-10-19T14:02:34Z
dc.date.issued2003
dc.identifier.issn0166-1280
dc.identifier.urihttps://dx.doi.org/10.1016/j.theochem.2003.08.085
dc.identifier.urihttps://hdl.handle.net/11421/12281
dc.descriptionSymposium on Role of Chemistry in the Evolution of Molecular Medicine -- JUN 27-29, 2003 -- UNIV SZEGED, SZEGED, HUNGARYen_US
dc.descriptionWOS: 000188928800067en_US
dc.description.abstractThe acid dissociation constants, pK(a) values, of 12 biologically active 6-[p- or p- and m-substituted] phenyl-4,5-dihydro-3(2H)-pyridazinone derivatives were computed using semi-empirical methods. Correlations between the experimental and computed acid dissociations constants were found to be satisfactory.en_US
dc.language.isoengen_US
dc.publisherElsevier Science BVen_US
dc.relation.isversionof10.1016/j.theochem.2003.08.085en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSemi-Empirical Calculationsen_US
dc.subjectAcidity-Basicity Behaviouren_US
dc.subjectPyridazinonesen_US
dc.subjectTautomerismen_US
dc.subjectTheoretical Calculationsen_US
dc.subjectComputed And Dissociation Constantsen_US
dc.titleA theoretical approach to acidity-basicity behaviour of some biologically active 6-phenyl-4,5-dihydro-3(2H)-pyridazinone derivativesen_US
dc.typeconferenceObjecten_US
dc.relation.journalJournal of Molecular Structure-Theochemen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesien_US
dc.identifier.volume666en_US
dc.identifier.startpage609en_US
dc.identifier.endpage615en_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorDemirayak, Şeref


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