Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/8756
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dc.contributor.authorPardasani, R T-
dc.contributor.authorPardasani, Pushpa-
dc.contributor.authorAbraham, Ignatious-
dc.date.accessioned2010-05-04T10:44:37Z-
dc.date.available2010-05-04T10:44:37Z-
dc.date.issued2010-05-
dc.identifier.urihttp://hdl.handle.net/123456789/8756-
dc.description561-564en_US
dc.description.abstractReaction of cyclohexan-1,4-dione with different active methylene heterocycles affords tetrahydroquinodimethane derivatives, in moderate to good yield. Semiempirical calculations indicate that introduction of double bonds in tetrahydroquinodimethane stabilizes the system due to the extended conjugation. All the synthesized products have been characterized by spectral techniques and their conformations ascertained by MO calculations.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJC-B Vol.49B(05) [May 2010]en_US
dc.subjectIndigoen_US
dc.subjectquinodimethaneen_US
dc.subjectcyclohexan-1,4-dioneen_US
dc.subjectdyeen_US
dc.subjectchromophoreen_US
dc.titleSynthesis and semiempirical studies of quinodimethane derivatives as precursors for indigoid dyesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.49B(05) [May 2010]

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