Abstract
A comparative analysis of 1H and 13C NMR spectra of 1-(2-ethoxyethyl)-4-(pentyn-1-yl)-4-hydroxypiperidine, 1-(2-ethoxyethyl)-4-(pentyn-1-yl)-4-benzoyloxypiperidine oxalate and their inclusion complexes with β-cyclodextrin was performed. The differences in values of chemical shifts of 1H and 13C nuclei of the substrates and the receptor in the inclusion complexes were determined. It was found that the formation of complexes of 1-(2-ethoxyethyl)-4-(pentyn-1-yl)-4-hydroxypiperidine and 1-(2-ethoxyethyl)-4-(pentyn-1-yl)-4-benzoyloxypiperidine oxalate with β-cyclodextrin was accompanied by insertion of one N-ethoxyethyl fragment of the substrate molecule into the inner sphere of one molecule of the receptor.
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Original Russian Text © T.M. Seilkhanov, L.A. Nazarenko, N.N. Poplavskii, O.T. Seilkhanov, T.K. Iskakova, K.D. Praliev, A.A. Abzhapparov, T.N. Zharkinbekov, 2016, published in Zhurnal Obshchei Khimii, 2016, Vol. 86, No. 1, pp. 118–123.
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Seilkhanov, T.M., Nazarenko, L.A., Poplavskii, N.N. et al. Investigation of supramolecular inclusion complexes with β-cyclodextrin of 1-(2-ethoxyethyl)-4-(pentyn-1-yl)-4-hydroxypiperidine and 1-(2-ethoxyethyl)-4-(pentyn-1-yl)-4-benzoyloxypiperidine oxalate by NMR spectroscopy. Russ J Gen Chem 86, 110–115 (2016). https://doi.org/10.1134/S1070363216010199
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DOI: https://doi.org/10.1134/S1070363216010199