Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/26093
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dc.contributor.authorPihlaja, Kalevi-
dc.contributor.authorHeinonen, Sanna-
dc.contributor.authorMartiskainen, Olli-
dc.contributor.authorAğırbaş, Hikmet-
dc.date.accessioned2022-04-26T10:55:26Z-
dc.date.available2022-04-26T10:55:26Z-
dc.date.issued2009-
dc.identifier.citationPihlaja, K. vd. (2009). "Electron ionization (EI) mass spectra of some 3,4-disubstituted-1,2,4- oxadiazin-5-ones and-thiones and 3,5-disubstituted 1,2,4-oxadiazin-6-ones". Arkivoc, 337-345, 14.en_US
dc.identifier.issn1551-7004-
dc.identifier.urihttps://doi.org/10.3998/ark.5550190.0010.e28-
dc.identifier.urihttps://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0010.e28-
dc.identifier.urihttp://hdl.handle.net/11452/26093-
dc.description.abstractThe EI mass spectra of 3,4-disubstituted-1,2,4-oxadiazin-5-ones 1-6 and -thiones 7,8 and 3,5-disubstituted 1,2,4-oxadiazin-6-ones 9,10 were recorded and their fragmentation pathways solved and compared with each other. The fragmentation routes of 5-ones and 5-thiones do not differ very much from each other but compounds 9 and 10 behave differently as could be expected based on their lactone type structures. Only compounds 4-6 exhibit a loss of CO and compound 7 a loss of NO. The loss of a benzyl group dominates the behaviour of compounds 1 and 2 which showed only few additional fragmentations. Some earlier data on some 3,4-disubstituted-1,2,4-diazin-5-ones 11-13 and -thiones 14,15 have been reanalyzed and discussed in further detail.en_US
dc.language.isoenen_US
dc.publisherArkat Usaen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectElectron ionization mass spectrometryen_US
dc.subjectFragmentation pathwaysen_US
dc.subjectHeterocyclic compoundsen_US
dc.subjectReaction mechanismen_US
dc.subjectAntimicrobial activitiesen_US
dc.subjectChemistryen_US
dc.titleElectron ionization (EI) mass spectra of some 3,4-disubstituted-1,2,4- oxadiazin-5-ones and-thiones and 3,5-disubstituted 1,2,4-oxadiazin-6-onesen_US
dc.typeArticleen_US
dc.identifier.wos000277913400028tr_TR
dc.identifier.scopus2-s2.0-77953240458tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Anabilim Dalı.tr_TR
dc.identifier.startpage337tr_TR
dc.identifier.endpage345tr_TR
dc.relation.journalArkivoctr_TR
dc.contributor.buuauthorArıkan, Nevin-
dc.contributor.researcheridAAH-6337-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.subject.wosChemistry, organicen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid57210000996tr_TR
dc.subject.scopusAmmonium Salts; Moieties; Rearrangementen_US
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