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dc.contributor.authorALI, Aen_US
dc.contributor.authorRAO, CPen_US
dc.date.accessioned2011-08-19T04:54:05Zen_US
dc.date.accessioned2011-12-26T12:56:04Zen_US
dc.date.accessioned2011-12-27T05:44:12Z
dc.date.available2011-08-19T04:54:05Zen_US
dc.date.available2011-12-26T12:56:04Zen_US
dc.date.available2011-12-27T05:44:12Z
dc.date.issued2005en_US
dc.identifier.citationINDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 44(3), 549-552en_US
dc.identifier.issn0376-4699en_US
dc.identifier.urihttp://dspace.library.iitb.ac.in/xmlui/handle/10054/10233en_US
dc.identifier.urihttp://hdl.handle.net/10054/10233
dc.description.abstractThe formation of mono- and di (1,2 and 1,3)-amide derivatives of p-tert-butylcalix[4]arene in the presence of sodium hydride has been demonstrated. All the compounds have been purified and characterized by various spectral methods. Both H-1 and C-13 NMR spectra exhibit clear-cut differences between the 1,2-di- and 1,3-di-amide derivatives.en_US
dc.language.isoenen_US
dc.publisherNATL INST SCIENCE COMMUNICATIONen_US
dc.titleFormation of mono- and di-amide-calix[4]arene derivatives from the reaction of p-tert-butyl-calix[4]arene and alpha-chloro-N,N-diethylacetamide in the presence of sodium hydrideen_US
dc.typeArticleen_US


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