526199-54-2

Upstream product

• 197853-41-1 ethyl 2,3-di-O-benzyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 526199-44-0 methyl 2-acetamido-6-O-benzyl-2-N,3-O-carbonyl-2-deoxy-α-D-glucopyranoside 
• 99745-44-5 Methyl 2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 526199-43-9 methyl 2-acetamido-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-α-D-glucopyranoside 
• 526199-42-8 methyl 2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-α-D-glucopyranoside 
• 99679-74-0 Methyl-4,6-O-benzyliden-2-desoxy-2-<(methoxycarbonyl)amino>-α-D-glucopyranosid 
• 128657-58-9 methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 847700-95-2 methyl 2-acetamido-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-β-D-glucopyranoside 
• 847700-93-0 methyl 2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-β-D-glucopyranoside 

Relevant academic research and scientific papers

6-O-benzyl- and 6-O-silyl-N-acetyl-2-amino-2-N,3-O-carbonyl-2- deoxyglucosides: Effective glycosyl acceptors in the glucosamine 4-OH series. Effect of anomeric stereochemistry on the removal of the oxazolidinone group

(Chemical Equation Presented) The 4-OH groups of both α- and β-methyl glycosides of N-acetylglucosamine, protected with an oxazolidinone spanning the nitrogen and O-3, and bearing benzyl or silyl protection on O-6, show excellent reactivity as acceptors i

Oxazolidinone protection of N-acetylglucosamine confers high reactivity on the 4-hydroxy group in glycosylation

(Matrix presented) The preparation of a convenient oxazolidinone protected N-acetyl glucosamine 4-OH derivative is reported. This substance exhibits enhanced reactivity as a glycosyl acceptor in a variety of coupling methods, the products of which are con