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13C N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracils
dc.creator | Jovanović, Bratislav Ž. | |
dc.creator | Tadić, Ž. D. | |
dc.creator | Vajs, Vlatka | |
dc.creator | Pešić, Mirjana B. | |
dc.date.accessioned | 2019-04-30T21:53:56Z | |
dc.date.available | 2019-04-30T21:53:56Z | |
dc.date.issued | 1990 | |
dc.identifier.issn | 0022-2860 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/2791 | |
dc.description.abstract | 13C 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.publisher | Elsevier Science Publishers B.V., Amsterdam | |
dc.rights | restrictedAccess | |
dc.source | Journal of Molecular Structure | |
dc.title | 13C N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracils | en |
dc.type | article | en |
dc.rights.license | ARR | |
dcterms.abstract | Јовановић, Б Ж; Тадић, Ж Д; Вајс, В Е; Пешић, М Б; | |
dc.rights.holder | Elsevier | |
dc.citation.volume | 219 | |
dc.citation.issue | C | |
dc.citation.spage | 317 | |
dc.citation.epage | 322 | |
dc.identifier.doi | 10.1016/0022-2860(90)80075-U | |
dc.identifier.scopus | 2-s2.0-45149137557 | |
dc.type.version | publishedVersion |