Abstract
Heptakis (2,6-di-O-pentyl)-β-CD 1b and heptakis (2,3,6-tri-O-pentyl)-β-CD 2b were synthesized by etherification of β-CD, Acetylation of 1b yielded heptakis (2,6-di-O-pentyl,3-O-acetyl)-β-CD. The corresponding α-CD derivatives were obtained in the same way. All of these compounds are well soluble in most aprotic organic solvents and they are able to complex polar guest molecules. The stability constants of these complexes were measured by an improved Benesi-Hildebrand procedure using NMR data.
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© 1988 Kluwer Academic Publishers
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Wenz, G., von der Bey, E. (1988). Inclusion Properties of Hydrophobic Derivatives of Cyclodextrins (CDs). In: Huber, O., Szejtli, J. (eds) Proceedings of the Fourth International Symposium on Cyclodextrins. Advances in Inclusion Science, vol 5. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-2637-0_21
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DOI: https://doi.org/10.1007/978-94-009-2637-0_21
Publisher Name: Springer, Dordrecht
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