194594-71-3

Upstream product

• 194594-69-9 6-allyloxy-7-benzyloxy-8-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 931098-45-2 (6-allyloxy-5-benzyloxy-2-benzyloxymethyl-4-methoxy-tetrahydro-pyran-3-yloxy)-trimethyl-silane 
• 931098-46-3 benzoic acid 6-allyloxy-5-benzyloxy-2-benzyloxymethyl-4-methoxy-tetrahydro-pyran-3-yl ester 
• 530-26-7 D-Mannose 
• 187732-08-7 allyl 2,6-dibenzyl-3-methyl-α-D-mannopyranoside 
• 194594-70-2 1,4-di-O-acetyl-2,6-di-O-benzyl-3-O-methyl-α-D-mannopyranose 
• 1056479-53-8 allyl-4,6-O-benzylidene-2,3-di-O-hydroxy-D-mannopyranoside 
• 182212-07-3 α,β-O-allyl-D-mannopyranoside 
• 931098-49-6 benzoic acid 6-(6-allyloxy-5-benzyloxy-2-benzyloxymethyl-4-methoxy-tetrahydro-pyran-3-yloxy)-5-benzyloxy-2-benzyloxymethyl-4-methoxy-tetrahydro-pyran-3-yl ester 
• 187732-19-0 allyl 4-acetyl-2,6-dibenzyl-3-methyl-α-D-mannopyranosyl-(1->4)-2,6-dibenzyl-3-methyl-α-D-mannopyranoside 

Downstream Products

• 931098-52-1 [6-(6-allyloxy-5-benzyloxy-2-benzyloxymethyl-4-methoxy-tetrahydro-pyran-3-yloxy)-5-benzyloxy-2-benzyloxymethyl-4-methoxy-tetrahydro-pyran-3-yloxy]-trimethyl-silane 
• 195063-62-8 allyl O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-[(1->4)-O-(2,6-di-O-benzyl-3-O-methyl-α-D-mannopyranosyl)]2-(1->4)-2,6-di-O-benzyl-3-O-methyl-α-D-mannopyranoside 
• 192049-37-9 allyl O-(4-O-acetyl-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)]2-(1->4)-2,6-di-O-benzyl-3-O-methyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthetic 3-O-methylmannose-containing polysaccharides (sMMPs): Design and synthesis

With the hope of mimicking the chemical and biological properties of natural 3-O-methylmannose-containing polysaccharides (MMPs), synthetic 3-O-methylmannose-containing polysaccharides (sMMPs) were designed and synthesized in a convergent manner. With lit

Synthesis of a tetra-and a hexasaccharide donor corresponding to the non-reducing termini of mycobacterial 3-O-methylmannose polysaccharide (MMP)

The blockwise synthesis of the title compounds, namely the tetra-and the hexasaccharide trichloroacetimidates (20) and (23), is described. Both acetates and imidates were employed as glycosyl donors in most of the coupling reactions. As nearly all of the