Cyclodextrins selectively modified on both rims using an O-3-debenzylative post-functionalisation, a consequence of the Sorrento meeting-Reference-Cited by-同舟云学术

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Cyclodextrins selectively modified on both rims using an O-3-debenzylative post-functionalisation, a consequence of the Sorrento meeting

Published:2012-07 Issue: Volume:356 Page:278-281
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Guitet Maxime,Beaumais Ségolène Adam de,Blériot Yves,Vauzeilles Boris,Zhang Yongmin,Ménand Mickaël,Sollogoub Matthieu

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference39 articles.

1. Protecting groups

2. Regioselective Manipulation of Carbohydrate-Hydroxyl Groups. Selective Activation of a Hydroxyl Group by Tin Compounds.

3. Protecting groups

4. Protective Group Strategies;Oscarson,2006

5. Regioselective one-pot protection of carbohydrates

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1. Molecular complexes of triterpenes and their glycosides with cyclodextrins: Recent advances and application prospects;Studies in Natural Products Chemistry;2024

2. Cyclodextrin Inclusion Complexes for Improved Drug Bioavailability and Activity: Synthetic and Analytical Aspects;Pharmaceutics;2023-09-19

3. Cyclodextrin-based nanostructures;Progress in Materials Science;2022-02

4. Functionalized Cyclodextrins and Their Applications in Biodelivery;Handbook of Macrocyclic Supramolecular Assembly;2020

5. Direct and Regioselective Di‐α‐fucosylation on the Secondary Rim of β‐Cyclodextrin;Chemistry – A European Journal;2019-03-21

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