Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/6629
Full metadata record
DC FieldValueLanguage
dc.contributor.authorBishnoi, Abha-
dc.contributor.authorSrivastava, Krishna-
dc.contributor.authorJoshi, M N-
dc.date.accessioned2009-11-18T07:42:56Z-
dc.date.available2009-11-18T07:42:56Z-
dc.date.issued2006-08-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6629-
dc.description1961-1964en_US
dc.description.abstractThe synthesis of N-[p-{3'-(2'-aryl-4'-oxo-1',3'-thiazolyl)}diphenyl]-7-hydroxy-4-methyl-2-oxoquinolines 4 have been achieved starting from resorcinol. 7-hydroxy-4-methylcoumarin(4-methylumbelliferone) 1 is obtained by the reaction of resorcinol with ethylacetoacetate. 1 on treatment with benzidine gives N-(p-aminodiphenyl)-7-hydroxy-4-methyl-2-oxoquinoline 2. 2 on treatment with different aryl aldehydes in presence of glacial acetic acid furnishes_N-(p-arylidinoamino-diphenyl-7-hydroxy-4-methyl-2-oxoquinolines 3a-e. The latter on treatment with thioglycollic acid in presence of anhydrous ZnCl2 yields 4a-e. The in vitro anti-JEV activity of these compounds has also been evaluated.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt. Cl.8 C07Den_US
dc.sourceIJC-B Vol.45B(08) [August 2006]en_US
dc.subjectN-(p-aminodiphenyl)-7-hydroxy-4-methyl-2-oxoqui-no­lineen_US
dc.subject7-hydroxy-4-methyl-coumarinen_US
dc.subjectthioglycollic aciden_US
dc.subjectbenzidineen_US
dc.subjectethylacetotateen_US
dc.subjectarylaldehydeen_US
dc.titleSynthesis, characterization and in vitro anti-JEV activity of N-[p-{3'-(2'-aryl-4'-oxo-1',3'-thiazolyl)} diphenyl]-7-hydroxy-4-methyl-2-oxoquinolinesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(08) [August 2006]

Files in This Item:
File Description SizeFormat 
IJCB 45B(8) 1961-1964.pdf42.85 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.