322479-15-2

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 322479-14-1 2-[(2S,3R,4R,5S,6R)-4-Benzyloxy-5-((2S,3R,4S,5R,6R)-4-benzyloxy-3,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-6-benzyloxymethyl-2-ethylsulfanyl-tetrahydro-pyran-3-yl]-isoindole-1,3-dione 
• 322479-13-0 ethyl (2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 115533-35-2 ethyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 34339-69-0 2,4,6-tri-O-acetyl-3-O-benzyl-α-D-glucopyranosyl bromide 
• 322479-10-7 ethyl (3-O-benzyl-4,6-O-isopropylidene-β-D-arabino-hexopyranosyl-2-ulose)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 

Downstream Products

• 322479-10-7 ethyl (3-O-benzyl-4,6-O-isopropylidene-β-D-arabino-hexopyranosyl-2-ulose)-(1->4)-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