55942-01-3

Upstream product

• 66492-24-8 3,4,6-tri-O-benzyl-1,2-O-(1-ethoxyethylidene)-α-D-galactopyranose 
• 107-18-6 allyl alcohol 
• 112344-80-6 2-propenyl 2,3,4,6-tetra-O-benzyl-α-D-glactopyranoside 
• 3254-15-7 3,4,6-tri-O-acetyl-1,2-O-(1-ethoxyethylidene)-α-D-galactopyranose 
• 75801-94-4 tetra-O-acetyl-α-iodogalactopyranose 
• 4163-60-4 β-D-galactose peracetate 

Downstream Products

• 959925-61-2 carboxymethyl-3,4,6-tri-O-benzyl-α-D-galactopyranoside-2-O-lactone 

Relevant academic research and scientific papers

Carboxymethylglycoside lactones (CMGLs): structural variations on the carbohydrate moiety

New glucose and galactose based bicyclic lactones, with variations in the anomeric configuration, the protecting groups (acetyl or benzyl) and the furanosyl or pyranosyl rings were synthesized from allyl glycosides and used for the preparation of a series

Versatile use of ytterbium(III) triflate and acid washed molecular sieves in the activation of glycosyl trifluoroacetimidate donors. Assemblage of a biologically relevant tetrasaccharide sequence of Globo H

The nonreducing tetrasaccharide terminus of Globo H has been assembled in good yield and excellent stereocontrol exclusively by using mild and moisture stable agents such as Yb(OTf)3 and acid washed molecular sieves for the activation of glycos