118249-75-5

Upstream product

• 118249-74-4 octyl 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 118249-73-3 n-octyl 4,6-O-benzylidene-β-D-glucopyranoside 
• 29836-26-8 n-octyl β-D-glucopyranoside 

Downstream Products

• 118249-76-6 octyl 6-O-acetyl-2,3-di-O-benzyl-β-D-glucopyranoside 
• 1252592-32-7 C₃₈H₅₂O₈ 
• 118270-90-9 octyl 6-O-<2-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-3,4,6,-tri-O-benzyl-α-D-mannopyranosyl>-2,3-di-O-benzyl-4-O-methyl-β-D-glucopyranoside 
• 118250-13-8 octyl 6-O-<2-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-3,4,6,-tri-O-benzyl-α-D-mannopyranosyl>-2,3-di-O-benzyl-4-deoxy-β-D-xylo-hexopyranoside 
• 118249-96-0 octyl 6-O-(2-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-2,3-di-O-benzyl-4-O-methyl-β-D-glucopyranoside 
• 118249-95-9 octyl 6-O-(2-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-2,3-di-O-benzyl-4-deoxy-β-D-xylo-hexopyranoside 
• 118250-01-4 (2S,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((2S,4S,5R,6R)-4,5-bis-benzyloxy-6-octyloxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3-ol 
• 118250-02-5 (2S,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-3-methoxy-6-octyloxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3-ol 
• 118249-81-3 octyl 2,3-di-O-benzyl-6-O-(4-methoxyphenyldiphenylmethyl)-4-O-methyl-β-D-glucopyranoside 
• 118249-77-7 octyl 6-O-acetyl-2,3-di-O-benzyl-4-O-phenoxythiocarbonyl-β-D-glucopyranoside 
• 118249-78-8 octyl 6-O-acetyl-2,3-di-O-benzyl-4-deoxy-β-D-xylohexopyranoside 
• 118249-82-4 octyl 2,3-di-O-benzyl-4-O-methyl-β-D-glucopyranoside 
• 118249-79-9 octyl 2,3-di-O-benzyl-4-deoxy-β-D-xylo-hexopyranoside 
• 118250-08-1 octyl 2,3-di-O-benzyl-4-O-methyl-6-O-<3,4,6-tri-O-benzyl-2-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-mannopyranosyl>-β-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis and evaluation of antimigratory and antiproliferative activities of lipid-linked [13]-macro-dilactones

The biological activities of a family of novel, lipid-linked 13-membered-ring macro-dilactones are reported. These [13]-macro-dilactones were synthesized by diacylation of functionalized diols, followed by ring-closing metathesis under conditions we had p

Recognition of oligosaccharide substrates by N-acetyl-glucosaminyltransferase-V.

Six analogs of the trisaccharide 8-methoxycarbonyloctyl 6-O-[2-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-alpha-D-mannopyrano syl] -beta-D-mannopyranoside (3), a previously reported acceptor for N-acetylglucosaminyltransferase-V (GnT-V) have been chemi