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 azo
methine
m>Nm>-oxide (
) have afforded novel isoxazolidine (
) in excellent yield. The
ir structures have been char
acterized fro
m the
ir IR,
1H-NMR,
13C-NMR,
1H,
1H-COSY, MS(ESI), and ele
mental analysis techniques.
m>In vitrom>
m6">antibacterial activity of the synthesized co
mpounds were investigated against a representative panel of pathogenic strains specifically two Gra
m-positive b
acteria (
m>Staphylococcus aureusm> and
m>Streptococcus pyogenesm>) and two Gra
m-negative b
acteria (
m>Pseudomonas aeruginosam> and
m>Escherichia colim>) using agar-well diffusion assay. So
me of the co
mpounds (
,
,
, and
) exhibited pro
mising antib
acterial
activities. All the synthesized co
mpounds have also been screened for the
ir antioxidant
activities and were found to be significantly
active.