Complete assignment of the <sup>1</sup>H and <sup>13</sup>C NMR spectra of antimicrobial 4-arylamino- 3-nitrocoumarin derivatives

dc.contributor.authorĐekić, Vera
dc.contributor.authorRadulovic, Niko
dc.contributor.authorVukicevic R.
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.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.identifier.doi10.1002/mrc.2681
dc.identifier.issn0749-1581
dc.identifier.scopus2-s2.0-78649680583
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/10134
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

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