130450-70-3

Upstream product

• 130450-69-0 Allyl 2,3-di-O-benzyl-4-O-(p-methoxybenzyl)-β-D-xylopyranoside 
• 100-39-0 benzyl bromide 
• 73787-48-1 allyl β-D-xylopyranoside 
• 10323-20-3 D-Arabinose 
• 111192-28-0 allyl 3,4-O-isopropylidene-α-L-arabinopyranoside 
• 130450-67-8 Allyl 2,3-anhydro-4-O-(p-methoxybenzyl)-β-D-ribopyranoside 
• 130450-68-9 Allyl 4-O-(p-methoxybenzyl)-β-D-xylopyranoside 
• 130450-65-6 Allyl 2-O-p-tolylsulfonyl-β-D-arabinopyranoside 
• 130450-64-5 Allyl 3,4-O-isopropylidene-2-O-p-tolylsulfonyl-β-D-arabinopyranoside 
• 130450-63-4 Allyl β-D-arabinopyranoside 
• 130450-66-7 Allyl 2,3-anhydro-β-D-ribopyranoside 

Downstream Products

• 130450-87-2 Allyl 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-xylopyranoside 
• 130450-71-4 Allyl 4-O-acetyl-2,3-di-O-benzyl-β-D-xylopyranoside 
• 130450-83-8 Benzyl 2,3,6-tri-O-benzyl-4-O-<2,3-di-O-benzyl-4-O-(p-methoxybenzyl)-α-D-xylopyranosyl>-β-D-glucopyranoside 
• 130450-86-1 Benzyl 2,3,6-tri-O-benzyl-4-O-<2,3-di-O-benzyl-4-O-(p-methoxybenzyl)-β-D-xylopyranosyl>-β-D-glucopyranoside 
• 130450-82-7 Benzyl 4-O-(4-O-acetyl-2,3-di-O-benzyl-α-D-xylopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 130450-85-0 Benzyl 4-O-(4-O-acetyl-2,3-di-O-benzyl-β-D-xylopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 130450-92-9 2,3-Di-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-α-D-xylopyranosyl chloride 
• 130450-84-9 benzyl O-(2,3-di-O-benzyl-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 127874-48-0 4-O-Acetyl-2,3-di-O-benzyl-D-xylopyranose 
• 130450-74-7 4-O-Acetyl-2,3-di-O-benzyl-α-D-xylopyranosyl chloride 

Relevant academic research and scientific papers

Design, synthesis and preliminary biological evaluation of a focused combinatorial library of stereodiverse carbohydrate-scaffold-based peptidomimetics

A focused combinatorial library of 126 mimetics of the RGD sequence based on sugar scaffolds have been rationally constructed using molecular modeling, with a particular emphasis on the stereodiversity of the library. A liquid phase, mix and divide synthesis was used, active compounds being identified by using orthogonal libraries and recursive deconvolution strategies.

Synthesis of O-alpha-D-glucopyranosyl-(1----4)-O-alpha -D-xylopyranosyl-(1----4)-O-alpha -D-xylopyranosyl-(1----4)-D-glucopyranose as a substrate analogue of alpha amylase.

The tetrasaccharide a-D-Glcp-(1----4)-a-D-Xylp-(1----4)-a-D-Xylp-(1----4)-D- Glcp (1) has been synthesized, as a substrate analogue of alpha amylase, by silver perchlorate-catalyzed glycosylation of benzyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-a-D-xylopyranosyl)-beta-D- glucopyranoside (30) with 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-a-D- glucopyranosyl)-a-D-xylopyranosyl chloride or by methyl triflate-promoted condensation of 30 with methyl 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-a-D-glucopyranosyl)-1-thio- beta-D-xylopyranoside, followed by removal of protecting groups of the resulting tetrasaccharide derivative 40.