Synthesis and Evaluation of Novel 5-cyclohexyl-2-(4″-substitutedphenyl)-3-(2″-substitutedphenyl)4H-2,3,3a,5,6,6a-hexahydropyrrolo[3,4-d]isoxazole-4,6-dione Derivatives for Their In Vitro Antioxidant and Antibacterial Activities
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4">1,3-Dipolar cycloaddition reactions of 43-eo-0001">N-cyclohexyl maleimide (43-eo-0001" rel="references:#jhet2543-eo-0001">) with azomethine N-oxide (43-eo-0002" rel="references:#jhet2543-eo-0002">) have afforded novel isoxazolidine (43-eo-0003" rel="references:#jhet2543-eo-0003">) in excellent yield. Their structures have been characterized from their IR, 1H-NMR, 13C-NMR, 1H,1H-COSY, MS(ESI), and elemental analysis techniques. In vitro antibacterial activity of the synthesized compounds were investigated against a representative panel of pathogenic strains specifically two Gram-positive bacteria (Staphylococcus aureus and Streptococcus pyogenes) and two Gram-negative bacteria (Pseudomonas aeruginosa and Escherichia coli) using agar-well diffusion assay. Some of the compounds (43-eo-0004" rel="references:#jhet2543-eo-0004">, 43-eo-0014" rel="references:#jhet2543-eo-0014">, 43-eo-0017" rel="references:#jhet2543-eo-0017">, and 43-eo-0018" rel="references:#jhet2543-eo-0018">) 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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