Приказ основних података о документу

dc.creatorJovanović, B.Z.
dc.creatorTadić, Z.D.
dc.creatorMuškatirović, M.D.
dc.creatorPešić, Mirjana
dc.creatorBogdanović, S.I.
dc.date.accessioned2020-12-17T17:33:22Z
dc.date.available2020-12-17T17:33:22Z
dc.date.issued1988
dc.identifier.issn0022-2860
dc.identifier.urihttp://aspace.agrif.bg.ac.rs/handle/123456789/65
dc.description.abstractThe 1H n.m.r. spectra of some 5-substituted-3-isopropyl-6-methyl uracils were determined in deuterated dimethyl sulfoxide (d6-DMSO). The substituents are: H, Cl, Br, I, NO2, NH2, N(CH3)2, C6H5, C6H4-NO2-p and C6H4-NH2-p. It has been shown that relative chemical shift (Δδ) of N(1)-H proton of some of the examined compounds correlated linearly with Hammett σm constant for the substituents in position 5 of uracil ring. The correlation with the σm constant was interpreted as providing evidence that the inductive effect of the substituent on chemical shift is dominating one.en
dc.rightsrestrictedAccess
dc.sourceJournal of Molecular Structure
dc.title1H N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracilsen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage284
dc.citation.issueC
dc.citation.other174(C): 281-284
dc.citation.rankM23
dc.citation.spage281
dc.citation.volume174
dc.identifier.doi10.1016/0022-2860(88)80171-6
dc.identifier.scopus2-s2.0-45449122789
dc.type.versionpublishedVersion


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Приказ основних података о документу