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dc.contributor.authorKidwai, Mazaahir-
dc.contributor.authorPriya-
dc.date.accessioned2009-07-13T12:30:43Z-
dc.date.available2009-07-13T12:30:43Z-
dc.date.issued2009-07-
dc.identifier.issn0975-0983 (Online); 0376-4699 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/5211-
dc.description1045-1048en_US
dc.description.abstractCopper sulphate has been found to be an effective catalyst in water-ethanol solvent system for the synthesis of various tetra-substituted pyridine derivatives via Michael addition of -dicarbonyl compounds to ,-unsaturated oximes and subsequent ring closure. A rapid synthesis of heterocycles by this methodology is ecofriendly in nature in addition to remarkably improved yield and reduced reaction times.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJC-B Vol.48B(07) [July 2009]en_US
dc.subjectMichael additionen_US
dc.subjectcopper-sulphateen_US
dc.subjectunsaturated oxime solvent-systemen_US
dc.subjecttetra-substituted pyridineen_US
dc.titleA copper sulphate catalysed synthesis of derivatives of tetra substituted pyridineen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.48B(07) [July 2009]

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