1387509-35-4

Upstream product

• 19488-48-3 methyl O-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 394212-35-2 methyl 2,3,6-tri-O-benzyl-4-S-acetyl-4-thio-α-D-galactopyranoside 

Downstream Products

• 1387509-56-9 methyl (2-S-(methyl 2,3,6-tri-O-benzyl-4-thio-α-D-galactopyranoside)-5-N-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranoside)onate 
• 1387509-48-9 methyl (2-S-(methyl 2,3,6-tri-O-benzyl-4-thio-α-D-galactopyranoside)-5-N-acetyl-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranoside)onate 
• 1448617-46-6 methyl (3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1→4)-2,3,6-tri-O-benzyl-4-deoxy-4-thio-α-D-galactopyranoside 

Relevant academic research and scientific papers

Highly stereoselective synthesis of primary, secondary, and tertiary α-S-sialosides under lewis acidic conditions

N-Acetyl 4-O,5-N-oxazolidinone protected sialyl phosphates of either anomeric configuration are excellent donors for the formation of α-S-sialosides at -78 °C in dichloromethane with primary, secondary, and tertiary thiols including galactose 3-, 4-, and