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Updated: May 22, 2026

Constructing Cyclic Peptides Using an On-Tether Sulfonium Center
Published on: September 28, 2022
Regioselective opening of proximally sulfato-capped cyclodextrins
Matthieu Jouffroy1, Rafael Gramage-Doria, Dominique Armspach
1Laboratoire de Chimie Inorganique Moléculaire et Catalyse, Institut de Chimie UMR 7177 CNRS, Université de Strasbourg, 67008 Strasbourg Cedex, France.
Abstract:
Sulfato groups capping one or two pairs of adjacent glucose units in methylated cyclodextrin (CD) derivatives have been found to undergo regioselective opening with various nucleophiles; the reported methodology opens the way to the efficient synthesis of tridifferentiated α- and β-cyclodextrins that constitute key starting materials for the preparation of heteropolydentate cavitands.
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