Abstract
The synthesis of branched beta-cyclodextrins substituted with mannosyl mimetic derivatives at one primary hydroxy group is described. It was shown that the self-inclusion phenomenon observed for the target compounds in water did not preclude the inclusion properties of the cyclodextrin moiety.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Biomimetic Materials / chemical synthesis
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Biomimetic Materials / chemistry
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Carbohydrate Conformation
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Carbohydrate Sequence
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Cyclodextrins / chemical synthesis
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Cyclodextrins / chemistry*
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Glycosylation
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Magnetic Resonance Spectroscopy
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Mannose / chemical synthesis
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Mannose / chemistry*
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Solubility
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Spectrometry, Mass, Electrospray Ionization
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beta-Cyclodextrins*
Substances
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Cyclodextrins
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beta-Cyclodextrins
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betadex
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Mannose