A facile synthesis of novel cyclodextrin derivatives incorporating one β-(1,4)-glucosidic bond and their unique inclusion ability
Literature Information
Toshiyuki Kida, Akira Kikuzawa, Yohji Nakatsuji, Mitsuru Akashi
Novel cyclodextrin derivatives incorporating one β-(1,4)-glucosidic bond are easily synthesized in three steps from permethylated α- and β-cyclodextrins, and such host molecules show inclusion selectivity for sodium m-nitrobenzoate over the corresponding p-isomer, in contrast to the cases of the parent permethylated α- and β-cyclodextrins.
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![(R)-N-[(S)-1-[2-(Diphenylphosphino)phenyl]ethyl]-2-methylpropane-2-sulfinamide structure (R)-N-[(S)-1-[2-(Diphenylphosphino)phenyl]ethyl]-2-methylpropane-2-sulfinamide structure](https://static.chemtradehub.com/structs/159/1595319-98-4-33e7.webp)

