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dc.creatorJovanović, Bratislav Ž.
dc.creatorTadić, Ž. D.
dc.creatorVajs, Vlatka
dc.creatorPešić, Mirjana B.
dc.date.accessioned2019-04-30T21:53:56Z
dc.date.available2019-04-30T21:53:56Z
dc.date.issued1990
dc.identifier.issn0022-2860
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/2791
dc.description.abstract13C 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, J, NO2, NH2, N(CH3)2, C6H5, C6H4-NO2-p and C6H4-NH2-p. It has been shown that 13C chemical shifts of C-5 of some of the examined compounds correlated linearly with the 13C chemical shifts of C-5 in the 5-substituted uracils as well as with the 13C chemical shifts of the substituted carbon in an analogues series of monosubstituted benzenes. The 13C chemical shifts of C-6 in some of the above compounds depend on the steric effects of the substituent in position 5 of the uracil ring. © 1990.en
dc.publisherElsevier Science Publishers B.V., Amsterdam
dc.rightsrestrictedAccess
dc.sourceJournal of Molecular Structure
dc.title13C N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracilsen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractЈовановић, Б Ж; Тадић, Ж Д; Вајс, В Е; Пешић, М Б;
dc.rights.holderElsevier
dc.citation.volume219
dc.citation.issueC
dc.citation.spage317
dc.citation.epage322
dc.identifier.doi10.1016/0022-2860(90)80075-U
dc.identifier.scopus2-s2.0-45149137557
dc.type.versionpublishedVersion


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