Synthesis and Evaluation of Novel 5-cyclohexyl-2-(4″-substitutedphenyl)-3-(2″-substitutedphenyl)4m>Hm>-2,3,3a,5,6,6a-hexahydropyrrolo[3,4-m>dm>]isoxazole-4,6-dione Derivatives for Their m>In Vitrom> Antioxidant and Antibacterial Activities
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m4">1,3-Dipolar cycloaddition reactions of mlns:w="http://www.wiley.com/namespaces/wiley" xmlns:cr="urn://wiley-online-library/content/render" xmlns:mml="http://www.w3.org/1998/Math/MathML" id="jhet2543-eo-0001">m3">m>Nm>-cyclohexyl maleimide () with azomethine m>Nm>-oxide () have afforded novel isoxazolidine () in excellent yield. Their structures have been characterized from their IR, 1H-NMR, 13C-NMR, 1H,1H-COSY, MS(ESI), and elemental analysis techniques. m>In vitrom> m6">antibacterial activity of the synthesized compounds were investigated against a representative panel of pathogenic strains specifically two Gram-positive bacteria (m>Staphylococcus aureusm> and m>Streptococcus pyogenesm>) and two Gram-negative bacteria (m>Pseudomonas aeruginosam> and m>Escherichia colim>) using agar-well diffusion assay. Some of the compounds (, , , and ) exhibited promising antibacterial activities. All the synthesized compounds have also been screened for their antioxidant activities and were found to be significantly active.

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