SEARCH Articles Figures Tables 2-Deoxy-a-glycosides A Molecular Basis for the Cluster Glycoside Effect A- and -Glycosides A- and B-Glycosides A-1,4-Glycosidic bonds A-Allyl glycosides A-Allyl glycosides from D-glucal triacetate A-Benzyl glycosides A-C-Glycosides by reaction of acyl ester A-C-Glycosides stereoselectivity A-C-glycoside synthesis by Sml2mediated reduction A-C-glycosides A-Glycosidation A-Glycoside synthesis A-Glycosides benzyl-type protecting groups A-Glycosides stereoselective construction A-Selective thermal glycosidation A-d- -glycoside bonds A-glycosidic linkage A-l,4 glycosidic linkage A-l,4-Glycosidic link A-l,6-Glycosidic bonds Allylic a-C-glycoside As components of cardiac glycosides C-Glycosides as Stable Pharmacophores Carbocations as intermediates in glycoside formation Carbohydrates as components of cardiac glycosides Enzymatic Synthesis of Alkyl Glycosides with Ionic Liquid as a Modulator Flavonoids as glycosides Formation of a Glycoside Glycosidation a-selective Glycosidations on a Solid Phase Glycosides (s. a. Carbohydrates Glycosides (s. a. Carbohydrates Ethers, Thioglycosides Glycosides (s. a. Carbohydrates acylglycosides Glycosides a glycoside Glycosides as glycosyl donors Hydrolysis of a Glycoside Isopropenyl glycosides as glycosyl donors Methyl a-glycoside Pentenyl Glycosides as Glycosyl Donors Regio- and a-Stereoselective Sialyl Glycoside Syntheses Using Thioglycosides of Sialic Acids in Acetonitrile Use of vinyl glycosides as glycosyl donors