80127-62-4

Upstream product

• 60656-87-3 benzyloxyacetoaldehyde 
• 80127-39-5 2-benzyloxymethyl-2,3-dihydropyran-4-one 
• 100-44-7 benzyl chloride 
• 22870-42-4 methyl 2,3,4-trideoxy-α-DL-glycero-hex-2-enopyranoside 
• 67-56-1 methanol 
• 80127-54-4 (2S*,4S*)-2-benzyloxymethyl-3,4-dihydro-2H-pyran-4-ol 

Downstream Products

• 124485-17-2 3-O-(6-O-benzyl-2,3,4-trideoxy-α-D-glycero-hex-2-enopyranosyl)-α-D-glucofuranoside 
• 124485-17-2 3-O-(6-O-benzyl-2,3,4-trideoxy-α-L-glycero-hex-2-enopyranosyl)-α-D-glucofuranoside 
• 124485-18-3 2-O-(6-O-benzyl-2,3,4-trideoxy-α-D-glycero-hex-2-enopyranosyl)-1,3,4,6-tetra-O-acetyl-β-D-mannopyranose 
• 124485-18-3 2-O-(6-O-benzyl-2,3,4-trideoxy-α-L-glycero-hex-2-enopyranosyl)-1,3,4,6-tetra-O-acetyl-β-D-mannopyranose 

Relevant academic research and scientific papers

Displacement of the Anomeric Alkyl Group in Racemic Methyl 2,3,4-Trideoxy-glycero-hex-2-enopyranosides by Sugar Units: Syntheses of Enantiomeric Pair of α-D-D-, α-L-D-, and α-L-L-Disaccharides

SnCl4-catalysed coupling of the title compounds with substituted D- and L-monosaccharides possessing single OH group free at position 2,3,4 or 6 is presented.The reaction leads to 1:1 mixture of two enantiomeric diasaccharides with D- and L-configuration