73646-11-4

Upstream product

• 60920-84-5 benzyl 2-acetamido-3-O-allyl-4,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 143416-39-1 N-[(2R,4aR,6S,7R,8R,8aS)-6-Benzyloxy-8-(4-methoxy-benzyloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl]-acetamide 
• 78246-81-8 benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 143416-40-4 N-[(2S,3R,4R,5S,6R)-2,5-Bis-benzyloxy-6-benzyloxymethyl-4-(4-methoxy-benzyloxy)-tetrahydro-pyran-3-yl]-acetamide 

Downstream Products

• 856409-78-4 benzyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2-acetamido-4,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 143416-61-9 Acetic acid (2R,3R,4S,5R,6R)-2-((2S,3R,4R,5S,6R)-3-acetylamino-2,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-4-yloxy)-5-benzyloxy-6-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl ester 
• 856409-82-0 benzyl 2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1->3)-2-acetamido-4,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 856409-79-5 benzyl 2-amino-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1->3)-2-acetamido-4,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 856409-83-1 benzyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->3)-2-acetamido-4,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 856409-85-3 benzyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-2-acetamido-4,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 856409-81-9 benzyl 2-amino-2-deoxy-β-D-glucopyranosyl-(1->3)-2-acetamido-4,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 856409-76-2 benzyl 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2-acetamido-4,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 143416-60-8 benzyl 2-acetamido-3-O-(2-acetyl-4,6-di-O-benzyl-3-O-chloroacetyl-β-D-galactopyranosyl)-4,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of linear and branched regioisomeric chitooligosaccharides as potential mimetics of natural oligosaccharide ligands of natural killer cells NKR-P1 and CD69 lectin receptors

Regioisomer of chitobiose 13 with β(1→3) glycosidic bond and branched analog of chitotriose 25 having β(1→4) and β(1→3) glycosidic bonds, were prepared and tested as potential mimetics of natural oligosaccharide ligands for activating lectin receptors NKR

n-Pentenyl glycosides in the efficient assembly of the blood group substance B tetrasaccharide

The fact that n-pentenyl glycosides (nPGs) are stable to a wide variety of reaction conditions but yet can be chemospecifically activated is advantageous for the efficient, convergent assembly of oligosaccharides. The nPGs are prepared directly from the a