Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/3875
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dc.contributor.authorBaskar, G-
dc.contributor.authorGopalakrishnan, M-
dc.contributor.authorJabaraj, J Winfred-
dc.date.accessioned2009-04-17T04:26:55Z-
dc.date.available2009-04-17T04:26:55Z-
dc.date.issued2009-04-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/3875-
dc.description580-584en_US
dc.description.abstractAnalysis of the spectral data (1H NMR and13C NMR) indicates that out of ten N-hydroxypiperidin-4-one oximes 3a-j, the compounds 3b and 3c exist predominantly in chair conformation with the aryl and alkyl substituents in the equatorial positions, whereas the compounds 3d-j exist in boat conformation. The introduction of an oxime group at C-4 causes a flattening of the ring about C(5)-C(6) bond. The NOESY spectrum (Nuclear Overhauser effect) recorded for the compound 3d further supports the assigned boat conformation.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJC-B Vol.48B(04) [April 2009]en_US
dc.subject1H NMRen_US
dc.subject 13C NMRen_US
dc.subjectNOESYen_US
dc.subjectconformation and N-hydroxypiperidone oximesen_US
dc.titleConformational analysis of some N-hydroxypiperidin-4-one oximesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.48B(04) [April 2009]

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