Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/6228
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dc.contributor.authorJhala, Yajuvendra S-
dc.contributor.authorDulawat, Shiv S-
dc.contributor.authorVerma, B L-
dc.date.accessioned2009-10-21T04:42:40Z-
dc.date.available2009-10-21T04:42:40Z-
dc.date.issued2006-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6228-
dc.description466-469en_US
dc.description.abstractMicrowave induced solvent-free solid phase syntheses of substituted 1,3-diarylpropenones (chalcones) 3a-f using basic alumina and their subsequent rapid transformation to 3,5-diaryl-6-carbethoxycyclohexenones 4a-f with ethyl acetoacetate in the presence of basic alumina and piperidine under solvent free condition using domestic microwave oven has been described. This process has advantages over conventional methods such as shorter reaction time, higher yields and environmental acceptability. All the synthesized compounds have been screened for their antibacterial activity.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Cen_US
dc.sourceIJC-B Vol.45B(02) [February 2006]en_US
dc.subjectMicrowaveen_US
dc.subjectSolvent-free synthesesen_US
dc.subject3, 5-diaryl-6-carbethoxycyclohexenonesen_US
dc.subjectantibacterial activityen_US
dc.titleSolvent-free improved syntheses of some substituted 1, 3-diaryl-propenones and 3,5-diaryl-6-carbethoxycyclohexenones under microwave irradiation and their antibacterial activityen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(02) [February 2006]

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