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dc.creatorJovanović, Bratislav Ž.
dc.creatorPerić-Grujić, Aleksandra
dc.creatorMarinković, Aleksandar
dc.creatorVajs, Vlatka
dc.date.accessioned2021-03-10T10:00:47Z
dc.date.available2021-03-10T10:00:47Z
dc.date.issued2002
dc.identifier.issn0951-4198
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/436
dc.description.abstractMass spectrometry has been applied in order to study the main fragmentation routes of some 4-pyrimidene carboxylic acids. Differences in fragmentation were caused by the nature of the substituent in position 2 of the pyrimidine ring, while the methyl group in position 1, 3 or 6 did not influence the fragmentation route.en
dc.publisherWiley, Hoboken
dc.rightsrestrictedAccess
dc.sourceRapid Communications in Mass Spectrometry
dc.titleMass spectrometric study of some 4-pyrimidine carboxylic acidsen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage2047
dc.citation.issue21
dc.citation.other16(21): 2044-2047
dc.citation.rankM21
dc.citation.spage2044
dc.citation.volume16
dc.identifier.doi10.1002/rcm.825
dc.identifier.pmid12391578
dc.identifier.scopus2-s2.0-0036410488
dc.identifier.wos000178955900006
dc.type.versionpublishedVersion


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