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dc.contributor.authorDekić, Vidosav-
dc.contributor.authorRadulovic, Niko-
dc.contributor.authorVukicevic, Rastko-
dc.contributor.authorDekić B.-
dc.contributor.authorSkropeta, Danielle-
dc.contributor.authorPalić R.-
dc.date.accessioned2021-04-20T14:57:35Z-
dc.date.available2021-04-20T14:57:35Z-
dc.date.issued2010-
dc.identifier.issn0749-1581-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/10134-
dc.description.abstractHerein, we describe the synthesis and complete assignment of the 1H and 13C NMR chemical shifts of a series of antimicrobial 4-arylamino-3-nitrocoumarin derivatives based on a combination of 1H and 13C NMR, 1H-1H-COSY, NOESY, HSQC and HMBC experiments. Conformational effects upon the chemical shifts of the coumarin moiety arising from the anisotropy of the aryl side group are briefly discussed. This study provides the first complete and fully assigned NMR data for this important group of antimicrobial compounds and bridges the gap existing in the literature with regard to NMR structural data for 4-arylamino-3-nitrocoumarins. Copyright © 2010 John Wiley & Sons, Ltd.-
dc.rightsrestrictedAccess-
dc.sourceMagnetic Resonance in Chemistry-
dc.titleComplete assignment of the <sup>1</sup>H and <sup>13</sup>C NMR spectra of antimicrobial 4-arylamino- 3-nitrocoumarin derivatives-
dc.typearticle-
dc.identifier.doi10.1002/mrc.2681-
dc.identifier.scopus2-s2.0-78649680583-
Appears in Collections:Faculty of Science, Kragujevac

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