Abstract
The influence of protecting groups on the reactivity of glycosyl acceptors has been investigated through a series of competitive glycosylation experiments using differently substituted C2 symmetric d -chiro -inositol derivatives. It has been shown that, for a given glycosyl donor, the protective group pattern effectively modulates the reactivity of these derivatives in the glycosylation reaction.
Key words
glycosylation - reactivity - stereoselectivity
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[3 ]
).