89177-18-4

Upstream product

• 89177-17-3 methyl 2,4-di-O-benzyl-3-O-methyl-6-O-trityl-α-D-mannopyranoside 
• 71439-35-5 Methyl 2-O-benzyl-4,6-O-benzylidene-3-O-methyl-α-D-mannopyranoside 
• 27552-06-3 methyl 3-O-methyl-α-D-mannopyranoside 
• 52260-48-7 Methyl 4,6-O-benzylidene-3-O-methyl-α-D-mannopyranoside 
• 774-48-1 (diethoxymethyl)benzene 
• 100-39-0 benzyl bromide 
• 84856-56-4 methyl 3-O-methyl-6-O-trityl-α-D-mannopyranoside 

Downstream Products

• 89177-19-5 methyl (methyl 2,4-di-O-benzyl-3-O-methyl-α-D-mannopyranosid)uronate 

Relevant academic research and scientific papers

Synthesis of a hexasaccharide acceptor corresponding to the reducing terminus of mycobacterial 3-O-methylmannose polysaccharide (MMP)

The title compound methyl O-(2,6-di-O-benzyl-3-O-methyl-α-D-mannopyranosyl)-[( 1 → 4)-O-(2,6-di-O-benzyl-3-O-methyl-α-D-mannopyranosyl)]4-(1 → 4)-2,6-di-O-benzyl-3-O-methyl-α-D mannopyranoside (2) was synthesized in a blockwise manner, employin

SYNTHESES OF METHYL ESTERS OF URONIC ACIDS. IV. SYNTHESIS OF THE 3-O-, 2,3-, 2,4-, AND 3,4-DI-O-, AND 2,3,4-TRI-O-METHYL ETHERS OF METHYL (METHYL α-D-MANNOPYRANOSID)URONATE

The synthesis is described of methyl O-benzyl-O-methyl-α-D-mannopyranosides and their oxidation by chromium trioxide, leading, after catalytic hydrogenolysis, to the 3-O, 2,3-, 2,4-, and 3,4-di-O-, and 2,3,4-tri-O-methyl ethers of methyl (methyl α-D-manno