83464-20-4

Upstream product

• 108-24-7 acetic anhydride 
• 71906-66-6 benzyl-2-acetamido-4,6-O-benzyliden-3-O-(4,6-O-benzyliden-3-O-chloroacetyl-β-D-galactopyranosyl)-2-desoxy-α-D-glucopyranoside 
• 13343-63-0 benzyl 4,6-O-benzylidene-2-acetylamino-2-deoxy-α-D-glucopyranoside 
• 83464-21-5 1,2-di-O-acetyl-3,4,6-tri-O-chloroacetyl-α-D-galactopyranose 
• 67673-35-2 N-[(4aR,6S,7R,8R,8aS)-6-Benzyloxy-8-((4aR,6R,7R,8R,8aR)-7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl]-acetamide 

Downstream Products

• 79781-74-1 benzyl O-(2-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-galactopyranosyl)-(1-3)-O-(4,6-O-benzylidene-β-D-galactopyranosyl)-(1-3)-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 

Relevant academic research and scientific papers

STEREOSELECTIVITY OF GLYCOSYLATION WITH DERIVATIVES OF 2-AZIDO-2-DEOXY-D-GALACTOPYRANOSE. THE SYNTHESIS OF A DETERMINANT OLIGOSACCHARIDE RELATED TO BLOOD-GROUP A (TYPE 1)

The stereoselective glycosylation of a model alcohol (cyclohexanol) by derivatives of 2-azido-2-deoxy-D-galactopyranose was studied under various conditions. 2-Azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-galactopyranosyl chloride (9) was found to be the most eff