Catalysis Letters, Vol.141, No.7, 925-930, 2011
Environmentally Benign Synthesis of 2,3-Unsaturated Glycopyranosides in Task-Specific Ionic Liquid
A green reaction condition has been developed for the synthesis of 2,3-unsaturated glycopyranosides by the Ferrier rearrangement of glycals using alcohols and thiols in 1-butyl-3-methylimidazolium trifluoromethanesulfonate ([BMIM]center dot OTf) in excellent yield. [BMIM]center dot OTf has been applied as a task specific ionic liquid organo-catalyst. Operational simplicity, environmentally benign reaction condition, use of task specific ionic liquid, short reaction time, high yields are the notable features of this methodology.
Keywords:Ferrier rearrangement;Ionic liquid;Environmentally benign;2,3-unsaturated glycosides;Glycal