Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/1744
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dc.contributor.authorTandel, R C-
dc.contributor.authorMammen, Denni-
dc.date.accessioned2008-07-25T09:50:06Z-
dc.date.available2008-07-25T09:50:06Z-
dc.date.issued2008-06-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/1744-
dc.description932-937en_US
dc.description.abstractSynthesis of the oxazolone ring has been performed by the condensation of 4-substituted alkoxy benzoyl glycine with appropriate 4-substituted alkoxy benzaldehyde, in the presence of acetic anhydride and anhydrous sodium acetate. The antibacterial activity has been checked against Micrococcus luteus and Escherichia coli and antifungal activity against Alternaria alternate and Phoma multirostata for all the compounds. The cytotoxicity has been checked against the monocots barley seeds; Hordeum vulgare L and dicots moong seeds; Phaseolus aureus. The compounds having electron releasing group exhibit antibacterial activity. Compounds with nitro group cause total inhibition of seed germination, exhibiting cytotoxic behaviour. The structures of the synthesized compounds have been characterized by elemental analysis and spectral data and the purity of the compounds has been checked by TLC method.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.47B(6) [June 2008]en_US
dc.subjectPhenyloxazol-5-oneen_US
dc.subjectBenzoyl glycineen_US
dc.subjectAntibacterial activityen_US
dc.subjectAntifungal activityen_US
dc.subjectSeed germinationen_US
dc.subjectLiquid crystalline propertyen_US
dc.titleSynthesis and study of some compounds containing oxazolone ring, showing biological activityen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.47B(06) [June 2008]

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