Abstract
Two 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.
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Dekić, V., Radulović, N., Vukićević, R., Dekić, B., Stojanović-Radić, Z., & Palić, R. (2011). Influence of the aryl substituent identity in 4-arylamino- 3-nitrocoumarins on their antimicrobial activity. African Journal of Pharmacy and Pharmacology, 5(3), 371–375. https://doi.org/10.5897/AJPP10.408
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