Приказ основних података о документу

dc.creatorJovanović, B.Ž.
dc.creatorTadić, Ž.D.
dc.creatorVajs, Vlatka
dc.creatorPešić, Mirjana
dc.date.accessioned2020-12-17T17:33:33Z
dc.date.available2020-12-17T17:33:33Z
dc.date.issued1990
dc.identifier.issn0022-2860
dc.identifier.urihttp://aspace.agrif.bg.ac.rs/handle/123456789/67
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.en
dc.rightsrestrictedAccess
dc.sourceJournal of Molecular Structure
dc.title13C N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracilsen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage322
dc.citation.issueC
dc.citation.other219(C): 317-322
dc.citation.spage317
dc.citation.volume219
dc.identifier.doi10.1016/0022-2860(90)80075-U
dc.identifier.scopus2-s2.0-45149137557
dc.type.versionpublishedVersion


Документи

Thumbnail

Овај документ се појављује у следећим колекцијама

Приказ основних података о документу