115152-51-7

Upstream product

• 115152-50-6 ethyl 4,6-O-benzylidene-2-deoxy-3-O-(p-methoxybenzyl)-2-phthalimido-1-thio-β-D-glucopyranoside 
• 824-94-2 p-methoxybenzyl chloride 
• 99409-33-3 ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalamido-1-thio-β-Dglucopyranoside 

Downstream Products

• 495391-16-7 2-[(2R,3R,4R,5S,6R)-2-(3-Azido-propoxy)-6-benzyloxymethyl-5-hydroxy-4-(4-methoxy-benzyloxy)-tetrahydro-pyran-3-yl]-isoindole-1,3-dione 
• 115152-53-9 p-nitrophenylethyl O-<2-O-acetyl-4,6-O-benzylidene-3-O-(chloroacetyl)-β-D-galactopyranosyl>-(1->4)-6-O-benzyl-2-deoxy-3-O-(p-methoxybenzyl)-2-phthalimido-β-D-glucopyranoside 
• 120336-43-8 p-nitrophenylethyl O-(2-O-acetyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-6-O-benzyl-2-deoxy-3-O-(p-methoxybenzyl)-2-phthalimido-β-D-glucopyranoside 
• 495391-18-9 C₅₉H₆₅N₅O₁₄Si 
• 495391-19-0 N-[6-[5-acetylamino-6-(3-azido-propoxy)-2-benzyloxymethyl-4-(4-methoxy-benzyloxy)-tetrahydro-pyran-3-yloxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl]-acetamide 
• 495391-21-4 N-[(2R,3R,4R,5S,6R)-5-((2R,4aR,6S,7R,8R,8aS)-7-Acetylamino-8-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-(3-azido-propoxy)-6-benzyloxymethyl-4-(4-methoxy-benzyloxy)-tetrahydro-pyran-3-yl]-acetamide 
• 495391-23-6 N-[(2R,4aR,6S,7R,8R,8aR)-6-[(2R,3S,4R,5R,6R)-5-Acetylamino-6-(3-azido-propoxy)-2-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yloxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl]-acetamide 
• 115152-52-8 ethyl 4-O-<2-O-acetyl-4,6-O-benzylidene-3-O-(chloroacetyl)-β-D-galactopyranosyl>-6-O-benzyl-2-deoxy-3-O-(p-methoxybenzyl)-2-phthalimido-1-thio-β-D-glucopyranoside 

Relevant academic research and scientific papers

A highly convergent approach for the synthesis of disaccharide repeating units of peptidoglycan

A highly convergent strategy has been developed for the synthesis of the two possible saccharide-repeating units of peptidoglycan using TBDMS and PMB ethers as orthogonal protecting groups and a two-directional glycosylation strategy for the efficient ass

SYNTHESIS OF A DIMERIC LEWIS X HEXASACCHARIDE DERIVATIVE CORRESPONDING TO A TUMOR-ASSOCIATED GLYCOLIPID

The dimeric Lewis X hexasaccharide p-trifluoroacetamidophenylethyl O-β-D-galactopyranosyl-(1->4)-O-3)>-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->3)-O-β-D-galactopyranosyl-(1->4)-O-3)>-2-acetamido-2-deoxy-