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Regioselective opening of proximally sulfato-capped cyclodextrins†
Matthieu Jouffroy,Rafael Gramage-Doria,Dominique Armspach,Dominique Matt,Loïc Toupet
Chemical Communications Pub Date : 04/26/2012 00:00:00 , DOI:10.1039/C2CC31302B
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.

Graphical abstract: Regioselective opening of proximally sulfato-capped cyclodextrins
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