Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/8971
Title: Formation of mono- and di-amide-calix[4]arene derivatives from the reaction of <i>p-tert</i>-butyl-calix[4]arene and <img src='/image/spc_char/alpha.gif' border=0>-chloro-<i>N</i>,<i>N</i>-diethylacetamide in the presence of sodium hydride
Authors: Ali, Amjad
Rao, Chebrolu P
Issue Date: Mar-2005
Publisher: CSIR
Series/Report no.: <b>Int</b>.<b>Cl</b>.<b><sup>7</sup> C 07 C 15/20</b>
Abstract: The formation of mono- and di (1,2 and 1,3)-amide derivatives of <i>p-tert</i>-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 <sup>1</sup>H and <sup>13</sup>C NMR spectra exhibit clear-cut differences between the 1,2-di- and 1,3-di-amide derivatives. 
Description: 549-552
URI: http://hdl.handle.net/123456789/8971
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.44B(03) [March 2005]

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