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dc.creatorJovanović, Bratislav Ž.
dc.creatorPerić, A A
dc.creatorVajs, Vlatka
dc.date.accessioned2019-05-01T10:40:25Z
dc.date.available2019-05-01T10:40:25Z
dc.date.issued1995
dc.identifier.issn0951-4198
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/2797
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. Copyright © 1995 John Wiley & Sons, Ltd.en
dc.publisherJohn Wiley & Sons
dc.relationMinistry for Science and Technology of the Republic of Serbia
dc.rightsrestrictedAccess
dc.sourceRapid Communications in Mass Spectrometry
dc.titleElectron‐impact induced decomposition of some 3‐alkyl‐5‐substituted‐6‐methyl uracilsen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractЈовановић, Б Ж; Перић, A A; Вајс, Влатка;
dc.rights.holderJohn Wiley & Sons
dc.citation.volume9
dc.citation.issue9
dc.citation.spage854
dc.citation.epage855
dc.identifier.doi10.1002/rcm.1290090927
dc.identifier.scopus2-s2.0-85024821993
dc.type.versionpublishedVersion


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