Solvent-induced anomeric diastereoselectivity switching using a single glycosyl donor.

ABSTRACT

Highly diastereoselective glycosylation reactions have been developed; however, not all glycosylation reactions are diastereoselective and these reactions have probably not been reported. For some fucosylation reactions, unusually low or abnormally opposite selectivities have been demonstrated. In the present study, the fucosylation reaction of long-chain hydrocarbon alcohols, ethyl 9-hydroxynonanoate and decanol using a series of the 2-O-benzyl-protected fucopyranosyl donors were investigated. The resulting products demonstrated the solvent-induced diastereoselectivity switching using diethyl ether (Et(2)O) or dichloromethane (CH(2)Cl(2)). Practical α-selectivities were observed using ether solvents. In contrast, practical ß-selectivities were observed using CH(2)Cl(2). The anomeric diastereoselectivity switching was similarly observed in the alcohol galactosylation reaction. The larger spin-lattice relaxation time constant (T(1)) actually indicated that molecular motion of ethyl 9-hydroxynonanoate was more vigorous in Et(2)O than in CH(2)Cl(2), suggesting its dissociation in Et(2)O and association in CH(2)Cl(2). The bulkiness of the associated alcohols is most likely responsible for the observed diastereoselectivity.