The optimization of rhodium(II) carbene mediated quaternarization of the anomeric
position of carbohydrates is reported. Preparation of ketopyranosides in good and
reliable yields requires reverse addition of the substrate to a highly diluted suspension
of the catalyst in refluxing 1,2-dichloroethane, as well as addition of a carefully
controlled amount of molecular sieves, and vigorous stirring. Following these optimized
reaction conditions, functionalization of the anomeric position of carbohydrates can
finally be performed on a preparative scale.
Key words
rhodium - carbenes - molecular sieves - insertion - carbohydrates