Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/9702
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dc.rights.licenseBY-NC-ND-
dc.contributor.authorĐekić, Vera-
dc.contributor.authorRadulovic, Niko-
dc.contributor.authorVukicevic, Rastko-
dc.contributor.authorDekić B.-
dc.contributor.authorStojanovic-Radic Z.-
dc.contributor.authorPalić R.-
dc.date.accessioned2020-09-19T18:55:17Z-
dc.date.available2020-09-19T18:55:17Z-
dc.date.issued2011-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/9702-
dc.description.abstractTwo new and six previously known coumarin derivatives with promising biological properties were synthesized in moderate to good yields by reaction of 4-chloro-3-nitro-coumarin and the appropriate arylamine in ethyl acetate in the presence of triethylamine. The synthesized compounds were evaluated for their in vitro antibacterial and antifungal activities against pathogenic strains. A correlation between the aryl substituent identity and antimicrobial activity was discussed. © 2011 Academic Journals.-
dc.rightsopenAccess-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.sourceAfrican Journal of Pharmacy and Pharmacology-
dc.titleInfluence of the aryl substituent identity in 4-arylamino- 3-nitrocoumarins on their antimicrobial activity-
dc.typearticle-
dc.identifier.doi10.5897/AJPP10.408-
dc.identifier.scopus2-s2.0-79957949391-
Appears in Collections:Faculty of Science, Kragujevac

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