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

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

Abstract 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 perben...

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Bibliographic Details
Main Authors: Matthieu Pélingre, Dr. Meriem Smadhi, Abed Bil, Dr. Véronique Bonnet, Prof. José Kovensky
Format: Article
Language:English
Published: Wiley-VCH 2021-04-01
Series:ChemistryOpen
Subjects:
Allylation
Azidation
Cyclodextrin ring-opening
Functionalization
Oligomaltosides synthesis
Propargylation
Online Access:https://doi.org/10.1002/open.202100079

Internet

https://doi.org/10.1002/open.202100079

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