Microwave-induced, Montmorillonite K10-catalyzed Ferrier rearrangement of tri-O-acetyl-d-galactal: mild, eco-friendly, rapid glycosidation with allylic rearrangement

Montmorillonite K10 was found to catalyze, under microwave irradiation, rapid O-glycosidation of 3,4,6-tri-O-acetyl-d-galactal to afford exclusively the alkyl and aryl 2,3-dideoxy-d-threo-hex-2-enopyranosides with very high α-selectivity and without the formation of the 2-deoxy-d-lyxo-hexopyranosides. Under these conditions, 3,4,6-tri-O-acetyl-d-glucal as usual also underwent the Ferrier rearrangement.