147589-19-3

Upstream product

• 147589-18-2 2-[(2S,3R,4R,5S,6R)-5-((2S,3R,4S,5R,6R)-4-Allyloxy-3,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-4-benzyloxy-6-benzyloxymethyl-2-ethylsulfanyl-tetrahydro-pyran-3-yl]-isoindole-1,3-dione 
• 77-76-9 2,2-dimethoxy-propane 
• 100-39-0 benzyl bromide 
• 129519-28-4 2-((6S,7R,8aS)-6-ethylsulfanyl-8-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione 
• 115533-35-2 ethyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 129519-27-3 2-((6S,7R,8aS)-8-benzyloxy-6-ethylsulfanyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione 
• 147589-17-1 ethyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-4-O-(2,4,6-tri-O-acetyl-3-O-allyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside 
• 147589-20-6 ethyl 4-O-(3-O-allyl-4,6-O-isopropylidene-β-D-arabino-hexopyranosyl-2-ulose)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 

Downstream Products

• 147589-23-9 ethyl 4-O-<3-O-allyl-2-O-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-β-D-mannopyranosyl>-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 147589-22-8 ethyl 4-O-<3-O-allyl-4,6-O-isopropylidene-2-O-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-β-D-mannopyranosyl>-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 147589-21-7 ethyl (3-O-allyl-4,6-O-isopropylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 147589-20-6 ethyl 4-O-(3-O-allyl-4,6-O-isopropylidene-β-D-arabino-hexopyranosyl-2-ulose)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 

Relevant academic research and scientific papers

New factors governing stereoselectivity in borohydride reductions of β-D-glycoside-2-uloses - The peculiar effect of 'activated' DMSO

Comparative evaluation of the manno/gluco ratios obtained in the conventional reductions of β-D-glucoside-2-uloses (1-4, 13 and 14) reveals the influence of the substitution pattern: the presence of a 4,6-O-acetal function results in lower stereoselectivi

Synthesis of a selectively protected trisaccharide building block that is part of xylose-containing carbohydrate chains from N-glycoproteins

The synthesis is reported of ethyl 4-O--3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside (16), a key intermediate in the synthesis of xylose-cont