Journal of the Serbian Chemical Society (Jan 2001)
Preparation of some D-glucofuranosides from unprotected D-glucose
Abstract
O-Glycosidation of 3-(4-methoxyphenyl) propyl alcohol, benzyl alcohol and vanillin with totally unprotected D-glucose, performed in a heterogeneous media and promoted by anhydrous ferric chloride, afforded competent D-glucofuranosides as the major and D-glucopyranosides as the minor products of the reaction.
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