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Chemoenzymic Approaches to the Preparation of 5-C-(Hydroxymethyl)hexoses
Adam W. Mazur1, George D. Hiler GD 2nd
1Procter & Gamble Pharmaceuticals, Health Care Research Center, P.O. Box 8006, Mason, Ohio 45040-8006.
Abstract:
Synthesis of 5-C-(hydroxymethyl)hexoses, carbohydrates resistant to metabolism, is described. These compounds are obtained in the reaction of hexose 6-aldehydes with formaldehyde. 5-C-(Hydroxymethyl)-L-arabino-hexopyranoses can be efficiently obtained from D-galactosides by a two-step chemoenzymic synthesis using galactose oxidase for the preparation of required hexose 6-aldehydes. This method is an example of carbohydrate synthesis without use of protecting groups. Other 5-C-(hydroxymethyl)hexoses are prepared by a typical chemical methodology requiring specific protection of the hexose hydroxyl groups.