83075-46-1

Upstream product

• 81825-63-0 methyl 2-O-benzyl-4,6-O-benzylidene-3-O-methyl-α-D-galactopyranoside 
• 76-83-5 trityl chloride 
• 83075-45-0 methyl 2-O-benzyl-3-O-methyl-α-D-galactopyranoside 

Downstream Products

• 35942-19-9 methyl (methyl 2-O-benzyl-3,4-di-O-methyl-α-D-galactopyranosid)uronate 
• 76-84-6 triphenylmethyl alcohol 
• 83075-56-3 methyl 2-O-benzyl-3,4-di-O-methyl-α-D-galactopyranoside 
• 83075-48-3 methyl 2,4-di-O-benzyl-3-O-methyl-α-D-galactopyranoside 
• 83076-36-2 methyl (methyl 2,4-di-O-benzyl-3-O-methyl-α-D-galactopyranosid)uronate 
• 83075-55-2 methyl 2-O-benzyl-3,4-di-O-methyl-6-O-trityl-α-D-galactopyranoside 
• 83075-47-2 methyl 2,4-di-O-benzyl-3-O-methyl-6-O-trityl-α-D-galactopyranoside 

Relevant academic research and scientific papers

SYNTHESIS OF METHYL DERIVATIVES OF URONIC ACIDS. I. SYNTHESIS OF METHYL (METHYL Α-D-GALACTOPYRANOSID)URONATE AND ITS 2-, 3-, AND 4-O-METHYL ETHERS

Alternative unidirectional methods for synthesizing methyl (methyl α-D-galactopyranosid)uronate and its mono-O-methyl ethers by the oxidation (with CrO3-H2SO4-acetone) of the corresponding methyl O-benzyl-O-methyl-α-D-galactopyranosides having unsubstituted 6-OH groups to the corresponding methyl O-benzyl-O-methyl-α-D-galactouronic acids followed by esterification with CH2N2 and the catalytic hydrogenolysis of the benzyl groups are proposed.