220734-68-9

Upstream product

• 220734-60-1 Chloro-acetic acid (2R,3R,4S,5S,6R)-5-acetoxy-4-benzyloxy-3-[(2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-(2,2,2-trichloro-acetylamino)-tetrahydro-pyran-2-yloxy]-6-(4-methoxy-phenoxy)-tetrahydro-pyran-2-ylmethyl ester 
• 28541-75-5 p-methoxyphenyl α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 220734-56-5 Acetic acid (2R,3S,4S,5R,6R)-4-benzyloxy-5-hydroxy-6-hydroxymethyl-2-(4-methoxy-phenoxy)-tetrahydro-pyran-3-yl ester 
• 220734-57-6 Chloro-acetic acid (2R,3R,4S,5S,6R)-5-acetoxy-4-benzyloxy-3-hydroxy-6-(4-methoxy-phenoxy)-tetrahydro-pyran-2-ylmethyl ester 
• 220734-55-4 3,4,6-tri-O-benzyl-2-deoxy-2-trichloroacetamido-α-D-galactopyranosyl trichloroacetimidate 
• 220734-67-8 thexyldimethylsilyl 3,4,6-tri-O-benzyl-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside 
• 220734-53-2 thexyldimethylsilyl 2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-galactopyranoside 

Relevant academic research and scientific papers

Synthesis of the glycosyl phosphatidyl inositol anchor of rat brain thy- 1

Disintegration of the target molecule 1 into building blocks A-E was performed. For D, an efficient synthesis of mannose derivative 5, representing mannose residue c in the target molecule, could be performed; 5 permits the required regioselective access