4-(acetoacetamido) arsanilic acid (II), which was then condensed with aryl aldehydes.
The resulting product on reaction with hydrazine hydrate and hydroxyl amine
hydrochloride yielded Pyrazolines (IV) and Isoxazolines (V), respectively. The
antimicrobial activity of compounds against a number of microorganisms was
evaluated. Some of these compounds showed significant antimicrobial activity
. (1993). PYRAZOLINES AND ISOXAZOLINES (I).
SYNTHESIS AND ANTIMICROBIAL ACTIVITIES
OF P-(1-ACYL-3-METHYL-5-ARYL-4
PYRAZOLINOYL / P-(3-METHYL-5-ARYL-4ISOXAZOLINOYL)
ARSANILIC ACID. (e31561). Journal of Sciences, Islamic Republic of Iran, 4(3), e31561
MLA
. "PYRAZOLINES AND ISOXAZOLINES (I).
SYNTHESIS AND ANTIMICROBIAL ACTIVITIES
OF P-(1-ACYL-3-METHYL-5-ARYL-4
PYRAZOLINOYL / P-(3-METHYL-5-ARYL-4ISOXAZOLINOYL)
ARSANILIC ACID" .e31561 , Journal of Sciences, Islamic Republic of Iran, 4, 3, 1993, e31561.
HARVARD
. (1993). 'PYRAZOLINES AND ISOXAZOLINES (I).
SYNTHESIS AND ANTIMICROBIAL ACTIVITIES
OF P-(1-ACYL-3-METHYL-5-ARYL-4
PYRAZOLINOYL / P-(3-METHYL-5-ARYL-4ISOXAZOLINOYL)
ARSANILIC ACID', Journal of Sciences, Islamic Republic of Iran, 4(3), e31561.
CHICAGO
, "PYRAZOLINES AND ISOXAZOLINES (I).
SYNTHESIS AND ANTIMICROBIAL ACTIVITIES
OF P-(1-ACYL-3-METHYL-5-ARYL-4
PYRAZOLINOYL / P-(3-METHYL-5-ARYL-4ISOXAZOLINOYL)
ARSANILIC ACID," Journal of Sciences, Islamic Republic of Iran, 4 3 (1993): e31561,
VANCOUVER
. PYRAZOLINES AND ISOXAZOLINES (I).
SYNTHESIS AND ANTIMICROBIAL ACTIVITIES
OF P-(1-ACYL-3-METHYL-5-ARYL-4
PYRAZOLINOYL / P-(3-METHYL-5-ARYL-4ISOXAZOLINOYL)
ARSANILIC ACID. J. Sci. I. R. I.. 1993;4(3):e31561.