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Article Dans Une Revue ChemistryOpen Année : 2021

One-Pot Synthesis of Asymmetrically Difunctionalized Oligomaltosides by Cyclodextrin Ring Opening

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Résumé

The synthesis of pure difunctionalized hexa-, hepta- and octamaltosides was performed by one-pot chemical reaction from perbenzoylated cyclodextrin. Oligomaltosides with azide, propargyl or allyl on reducing end and an unprotected hydroxyl group on non-reducing end were obtained from perbenzoylated alpha-, beta- and gamma-cyclodextrin with 12 to 48 % yields.

Dates et versions

hal-03613737 , version 1 (18-03-2022)

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Citer

Matthieu Pelingre, Meriem Smadhi, Abed Bil, Veronique Bonnet, Jose Kovensky. One-Pot Synthesis of Asymmetrically Difunctionalized Oligomaltosides by Cyclodextrin Ring Opening. ChemistryOpen, 2021, 10 (4), pp.493-496. ⟨10.1002/open.202100079⟩. ⟨hal-03613737⟩
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