Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/9218
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dc.contributor.authorMukherjee, A-
dc.contributor.authorMishra, M-
dc.contributor.authorChatterjee, A-
dc.contributor.authorSarkar, M-
dc.contributor.authorChowdhury, S K Dutta-
dc.contributor.authorMahalanabis, Kumar K-
dc.date.accessioned2010-06-01T04:47:13Z-
dc.date.available2010-06-01T04:47:13Z-
dc.date.issued2005-11-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9218-
dc.description2333-2337en_US
dc.description.abstractRegiospecificity of 3,5-disubstituted pyrazoles derived from reaction of phenylhydrazine with -acyl-β-amino­crotononitriles and esters is primarily deduced on the basis of spectral analyses. The present work provides direct and unambiguous evidences in support of the regiospecificity of these pyrazoles. In addition, this work also shows that -acyl-β-enaminones derived from enaminonitriles and enaminoesters both afford 5-substituted pyrazoles in contrast to earlier observation by Benary.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Den_US
dc.sourceIJC-B Vol.44B(11) [November 2005]en_US
dc.subjectRegiospecificityen_US
dc.subject3,5-disubstituted pyrazolesen_US
dc.subjectenaminonitrilesen_US
dc.subjectphenylhydrazineen_US
dc.subjectaminocrotononitrilesen_US
dc.subjectenaminoestersen_US
dc.subject5-substituted pyrazolesen_US
dc.titleOn the regiospecificity of 3,5-disubstituted pyrazoles derived from C-acylated--enaminonitriles and estersen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(11) [November 2005]

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