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dc.creatorJovanović, Bratislav Ž.
dc.creatorPerić, Aleksandra
dc.creatorVajs, Vlatka
dc.date.accessioned2021-03-10T09:36:46Z
dc.date.available2021-03-10T09:36:46Z
dc.date.issued1995
dc.identifier.issn0951-4198
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/64
dc.description.abstractMass spectrometry was used to study the main fragmentation routes of some 3‐alkyl‐5‐substituted‐6‐methyl uracils. Differences in fragmentation were caused by changes in the structure of the alkyl group in position 3 of the uracil ring, with the same substituent in position 5, and by differences in the substituent in position 5.en
dc.publisherWiley, Hoboken
dc.rightsrestrictedAccess
dc.sourceRapid Communications in Mass Spectrometry
dc.titleElectron‐impact induced decomposition of some 3‐alkyl‐5‐substituted‐6‐methyl uracilsen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage855
dc.citation.issue9
dc.citation.other9(9): 854-855
dc.citation.spage854
dc.citation.volume9
dc.identifier.doi10.1002/rcm.1290090927
dc.identifier.pmid
dc.identifier.rcubconv_7382
dc.identifier.scopus2-s2.0-85024821993
dc.type.versionpublishedVersion


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