808741-02-8

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 173935-67-6 ethyl 3-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 503830-08-8 ethyl 4,6-O-benzylidene-2-O-(4-methoxybenzyl)-1-thio-α-D-mannopyranoside 
• 7473-36-1 ethyl 1-thio-α-D-mannopyranoside 
• 100-52-7 benzaldehyde 
• 142924-31-0 S-ethyl 4,6-O-benzylidene-1-thio-α-D-mannopyranoside 

Downstream Products

• 351060-35-0 cyclohexyl 3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl-(1->2)-3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranoside 
• 351060-34-9 cyclohexyl 3-O-benzyl-4,6-O-benzylidene-2-O-(4-methoxybenzyl)-β-D-mannopyranosyl-(1->2)-3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranoside 
• 351060-37-2 cyclohexyl 3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl-(1->2)-3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl-(1->2)-3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranoside 
• 351060-36-1 cyclohexyl 3-O-benzyl-4,6-O-benzylidene-2-O-(4-methoxybenzyl)-β-D-mannopyranosyl-(1->2)-3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl-(1->2)-3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranoside 

Relevant academic research and scientific papers

Blockwise synthesis of a pentasaccharide structurally related to the mannan fragment from the Candida albicans cell wall corresponding to the antigenic factor 6

A spacer-armed pentasaccharide structurally related to a fragment of the mannan from the cell wall of the fungus Candida albicans and corresponding to the antigenic factor 6 has been synthesized. This compound, comprising two α-(1→2)- and three β-(1→2)-li

H2SO4-silica: An efficient promoter for selective removal of benzylidene and isopropylidene groups in the presence of p-methoxybenzyl group

Selective removal of the benzylidene and isopropylidene protections in the presence of acid-labile p-methoxybenzyl group using H2SO4-silica in methanol is reported. The deprotection reactions were found to be clean and result in the

Direct chemical synthesis of the β-D-mannans: The β-(1→2) and β-(1→4) series

The direct syntheses of β-(1→2)-mannooctaose and of β-(1→4)-mannohexaose are reported by means of 4,6-O-benzylidene- protected β-mannosyl donors. The synthesis of the (1→2)-mannan was achieved by means of the sulfoxide coupling protocol, whereas the (1→4)