A series of alkenyl beta -D-C-glucopyranosides has been glycosylated with a
lpha -D-glucopyranosyl fluoride in a 'Glycosynthase' reaction to yield a ra
nge of alkenyl beta -C-cellobiosides and -triosides and in one case a beta
-C-cellotetraoside. Conversion of some of the alkenyl beta -D-C-oligosaccha
ride products into their corresponding epoxides and subsequent deprotection
under standard conditions have afforded a panel of epoxyalkyl beta -C-olig
osaccharides for evaluation as inhibitors of retaining beta -glycan hydrola
ses.