Abstract
The synthesis of some new regioselectively silylated β-cyclodextrin derivatives is described. It is shown that by means of 29Si NMR spectroscopy it is possible to reliably determine the regioselectivity position of the silyl protective groups on the cyclodextrin frame and to control silylation of the cyclodextrin by utilizing chlorosilanes that have different sized substituents.
GRAPHICAL ABSTRACT
Acknowledgments
The authors are grateful to Russian Fund for Basic Research (Grant #12-03-00147) for the financial support of this work.