102475-61-6

Upstream product

• 29388-46-3 methyl 2,3-di-O-benzyl-α-D-galactopyranoside 
• 29600-81-5 methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranoside 
• 83075-49-4 methyl 2,3-di-O-benzyl-4-O-methyl-6-O-trityl-α-D-galactopyranoside 
• 51433-17-1 Methyl 2,3-di-O-benzyl-4-O-methyl-β-D-glucopyranoside 
• 6988-40-5 methyl 2,3-di-O-benzyl-β-D-glucopyranoside 
• 876659-94-8 methyl-(O²,O³-dibenzyl-O⁴-methyl-O⁶-trityl-β-D-glucopyranoside) 
• 71756-38-2 methyl 2,3-di-O-benzyl-6-O-trityl-α-D-galactopyranoside 
• 83075-50-7 methyl 2,3-di-O-benzyl-4-O-methyl-α-D-galactopyranoside 

Downstream Products

• 83075-51-8 methyl (methyl 2,3-di-O-benzyl-4-O-methyl-α-D-galactopyranosid)uronate 

Relevant academic research and scientific papers

SYNTHESIS OF A PRECURSOR OF 3-O-(2-ACETAMIDO-2-DEOXY-3-O-METHYL-α-D-GALACTOPYRANOSYL)-4-O-(4-O-METHYL-β-D-GLUCOPYRANOSYLURONIC ACID)-L-FUCOSE

The glycosphingolipids isolated from spermatozoa of a fresh-water bivalve, Hyriopsis schlegelii, have a unique structure containing one or two mannosyl residues, novel linkages including an internal fucopyranosyl residue, as well as terminal xylosyl and 4

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.