Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21674
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dc.contributor.authorKhan, M S Y-
dc.contributor.authorHasan, S M-
dc.date.accessioned2013-10-07T11:12:45Z-
dc.date.available2013-10-07T11:12:45Z-
dc.date.issued2003-08-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21674-
dc.description1970-1974en_US
dc.description.abstractSeveral new flavones/flavanones and 5'-substituted-2'-hydroxy chalcones have been synthesised through Claisen Schmidt condensation. 5-Chloromethyl-2-hydroxy acetophe none 1 on condensation with various aromatic aldehydes yields chalcones 2a and 2b, which on cyclisation in presence of SeO2 give corresponding flavones 2c and 2d respectively. Compound 3 is obtained from 1 by reacting with o-toluidine. Further condensation of 3 with different aromatic aldehydes gives the corresponding chalcone/flavone derivatives 3a-e. The synthesised flavonoid derivatives are evaluated for their antiinflammatory activity on carrageenan induced paw edema in rats and in vitro antibacterial activity. The results have been encouraging.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(08) [August 2003]en_US
dc.titleSynthesis, antiinflammatory and antibacterial activity of some new flavonoidal derivativesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(08) [August 2003]

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