Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2191
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dc.contributor.authorVijaya Laxmi, S.-
dc.contributor.authorSuresh Kuarm, B.-
dc.contributor.authorRajitha, B.-
dc.date.accessioned2024-12-30T05:06:53Z-
dc.date.available2024-12-30T05:06:53Z-
dc.date.issued2012-05-
dc.identifier.citation10.1007/s00044-012-0078-yen_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2191-
dc.descriptionNITWen_US
dc.description.abstractA series of 5-((3-(2-oxo-2H-chromen-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-trione (4a–f) and dihydro-5-((3-(2-oxo-2H-chromen-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene)-2-thioxopyrimidine-4,6(1H,5H)-dione (5a–f) derivatives were synthesized by the condensation of 3-(2-oxo2H-chromen-3-yl)-1-phenyl-1H-pyrazole-4-carbaldehyde (3a–f) with barbituric acid and thiobarbituric acid in acetic acid under microwave irradiation method. The newly synthesized compounds were evaluated for their antibacterial activity against Bcillus subtilis, Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Pseudomonas aeoginosa, and Klebsiella pneumoniae. All the compounds were found to be moderately active against used microorganisms, whereas compounds (4d) and (4e) exhibited good antifungal activity against Aspergillus niger.en_US
dc.language.isoenen_US
dc.publisherMedicinal Chemistry Researchen_US
dc.subjectAntimicrobial activityen_US
dc.subjectBarbituric aciden_US
dc.subjectCoumarinen_US
dc.subjectMicrowave irradiationen_US
dc.titleSynthesis and antimicrobial activity of coumarin pyrazole pyrimidine 2,4,6(1H,3H,5H)triones and thioxopyrimidine4,6(1H,5H)dionesen_US
dc.typeArticleen_US
Appears in Collections:Chemistry

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