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The reaction of exo-glycals with azidotrimethylsilane in the presence of a Brønsted acid leads to the generation of the corresponding C,N-glycosyl azides. The majority of these glycosylation reactions proceed at room temperature with short reaction times. In addition, the targeted products were obtained in high yields with exclusive diastereoselectivity to the α-anomer in pyranose-based derivatives.
The first supramolecular cage formed by three benzo-15-crown-5 macrocycles encapsulating a [Dy(OH2)¬8]3+ guest cation is reported, with the Dy(III) centre exhibiting local square antiprismatic D4d symmetry.
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