Reaction between 5-methyl-3-aminoisoxazole and ?-acetamidophenylsulpho-nylchloride yielded compound 1. Hydrolysis of compound 1 gave a starting compound 4-methoxybenzal-?-5-methyl isoxazol-3-yl-sulphonamido aniline 2. The compound 2 on condensation with different aldehydes and potassium cyanide yielded the nitriles 3a-l. Cyclocondensation between oxazolinone and compound 2 yielded imidazolines 4a-l. All compounds have been characterised using IR, 1H NMR and Mass spectral data and have been evaluated for their antimicrobial activity against different strains of bacteria and fungi.
. (2004). Preparation, Characterisation and Antimicrobial Activities of Some Novel Nitriles and Imidazolines. (e31592). Journal of Sciences, Islamic Republic of Iran, 15(2), e31592
MLA
. "Preparation, Characterisation and Antimicrobial Activities of Some Novel Nitriles and Imidazolines" .e31592 , Journal of Sciences, Islamic Republic of Iran, 15, 2, 2004, e31592.
HARVARD
. (2004). 'Preparation, Characterisation and Antimicrobial Activities of Some Novel Nitriles and Imidazolines', Journal of Sciences, Islamic Republic of Iran, 15(2), e31592.
CHICAGO
, "Preparation, Characterisation and Antimicrobial Activities of Some Novel Nitriles and Imidazolines," Journal of Sciences, Islamic Republic of Iran, 15 2 (2004): e31592,
VANCOUVER
. Preparation, Characterisation and Antimicrobial Activities of Some Novel Nitriles and Imidazolines. J. Sci. I. R. I.. 2004;15(2):e31592.