Abstract
The reaction of β-cyclodextrinwith N-2,3-epoxypropylphthalimide yielded a set of newamorphous host compounds with high solubility whichwas transmitted to the corresponding host-guestcomplexes. The structure was determined by comparing the 1H- and 13C-NMR spectra with those of theparent compound, the degree of substitution by integration of the corresponding NMR signals, and C, H,and N elemental analysis.
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DELGADO, R., VIRGILI, A., GARCIA-ANTON, J.M. et al. Reaction of β-Cyclodextrin with N-2,3-Epoxypropylphthalimide. Preparation, Characterisation and Study of a New Substituted Cycloheptaamylose. Effects on the Water Solubility of Drugs. Journal of Inclusion Phenomena 28, 205–212 (1997). https://doi.org/10.1023/A:1007928520661
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DOI: https://doi.org/10.1023/A:1007928520661