Activation of Stable and Recyclable Phenylpropiolate Glycoside (PPG) Donors via Iron Catalysis

Abstract

Glycosylation reaction is one of the important aspects of carbohydrate chemistry, where two different units are frequently linked through the C-O bonds. In the pursuit of advancing this field, the design and development of sustainable catalytic methods for O-glycosylation, which can provide an alternate and effective tool to traditional protocols involving stoichiometric promoters and classical donors are considered as highly challenging yet important facets of glycochemistry. Herein, we report a simple and efficient Fe(III)-catalyzed method for O-glycosylation through the activation of bifunctional phenylpropiolate glycoside (PPG) donors. This mild and effective method involves the use of inexpensive, and less-toxic FeCl3 as a catalyst and easily synthesizable, benchtop stable glycosyl ester-based PPG donors, which react with various sugar as well as non-sugar-based acceptors to deliver the corresponding O-glycosides in good yields with moderate anomeric selectivity along with regeneration of easily separable phenylpropiolic acid. Importantly, D-mannose and L-rhamnose-based PPG donors afforded the corresponding O-glycosides in high α-anomeric-selectivity. The reaction conditions were further explored for the synthesis of trisaccharide.