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dc.contributor.authorMathada, BSD
dc.contributor.authorMathada, MBH
dc.date.accessioned2020-06-12T15:05:55Z-
dc.date.available2020-06-12T15:05:55Z-
dc.date.issued2009
dc.identifier.citationCHEMICAL & PHARMACEUTICAL BULLETIN , Vol. 57 , 6 , p. 557 - 560en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4993-
dc.description.abstractEthyl 3-oxo-3-{2-[(5-substituted-3-phenyl-1H-indol-2-yl)carbonyl]hydrazinyl}propanoates 5a-b were synthesized according to the literature method. These on further reaction with substituted-2-hydroxy-3-formylquinolines 3a-e yielded 5-substituted-N-beta-(2-oxo-2H-pyrano[2,3-b]quinoline-3-carbonyl)-3-phenyl-1H-indole-2-carbohydrazides 6a-j. Structures of the all the newly synthesized compounds were confirmed by spectral data. All these compounds have been screened for their antibacterial activity, against Staphylococcus aureus, Escherichia coli and Bacillus sublilus, antifungal activity against Aspergillus niger and Candida albicans and antituberculosis activity against Mycobacterium tuberculosis (H37R(v)).en_US
dc.publisherPHARMACEUTICAL SOC JAPAN
dc.subjectindole
dc.subjectquinoline
dc.subjectpyrano-quinoline-2-one
dc.subjectantimicrobial activity
dc.titleSynthesis and Antimicrobial Activity of Some 5-Substituted-3-phenyl-N-beta-(Substituted-2-oxo-2H-pyrano[2,3-b]quinoline-3-carbonyl)-1H-indole-2-carboxyhydrazideen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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