Abstract
Mono(6-deoxy-dimethylpyridinium)-β-cyclodextrins have been synthesized in reaction of mono (p-toluenesulfonyl) derivative of β - cyclodextrin with the appropriate lutidine under microwave irradiation and conventional conditions. The results indicate that the mechanism consists of inclusion complex formation. © Central European Science Journals. All rights reserved.
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Musiol, R., & Girek, T. (2005). Inclusion-dependent mechanism of modification of cyclodextrins with heterocycles. Central European Journal of Chemistry, 3(4), 742–746. https://doi.org/10.2478/BF02475201
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