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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4997
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dc.contributor.authorBasawaraj R
dc.contributor.authorAli A
dc.contributor.authorKhandre O
dc.contributor.authorSangapure S.S.
dc.date.accessioned2020-06-12T15:05:56Z-
dc.date.available2020-06-12T15:05:56Z-
dc.date.issued2007
dc.identifier.citationIndian Journal of Heterocyclic Chemistry , Vol. 17 , 1 , p. 11 - 14en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4997-
dc.description.abstractThe Claisen-Schmidt reaction of 5-chloro-2-hydroxyacetophenone 1 with aromatic aldehydes gave 1-(5?-chloro-2?-hydroxy-phenyl)-3-phenyl-2- propen-1-ones 2a-c which upon cyclization with hydrazine hydrate, hydroxylamine hydrochloride, urea and thiourea furnished the corresponding 1H/acetyl-3,5-diaryl-2-pyrazolines 3a-c and 4a-c, 3-(5?-chloro-2?- ;hydroxy-phenyl)-5-aryl isoxazolines 5a-c and 4-(5?-chloro-2?- hydroxy-phenyl)-6-aryl-2-oxo/thio-1,2,5,6-tetrahydropyrimidines 6a-c and 7a-c respectively. The newly synthesized compounds were characterized by spectral data and elemental analysis. Compounds were screened for antibacterial and antifungal activity.en_US
dc.titleSynthesis of some new pyrazolines, isoxazoles and pyrimidines as potential antimicrobial agentsen_US
dc.typeArticle
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