13320-00-8

Upstream product

• 127-09-3 sodium acetate 
• 100-51-6 benzyl alcohol 
• 3055-51-4 benzyl 2-acetamido-2-deoxy-β-D-glucopyranoside 
• 3006-60-8 Acetic acid (2R,3R,4R,5S,6R)-2,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-4-yl ester 
• 13343-61-8 benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 108-24-7 acetic anhydride 
• 19374-64-2 N-((4aR,6R,7R,8S,8aS)-6-Benzyloxy-8-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide 
• 176167-78-5 benzyl 2-acetamido-3,6-di-O-benzoyl-β-D-allopyranoside 
• 10375-65-2 benzyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 

Relevant academic research and scientific papers

Direct formation of β-glycosides of N-acetyl glycosamines mediated by rare earth metal triflates

A direct, mild and efficient protocol for the preparation of β-glycosides of N-acetyl glucosamine (GlcNAc) and N-acetyl galactosamine (GalNAc) has been developed using peracetylated β-GlcNAc and β-GalNAc as donors. All rare Earth metal triflate promoters

Use of cyclic sulfamidates derived from D-allosamine in nucleophilic displacements: Scope and limitations

A cyclic 2,3-sulfamidate derived from N-acetyl-D-allosamine has been treated with a variety of S-. N-, O-. and C-nucleophiles, leading to nucleophilic displacement at C-3, elimination, or deacetylation reactions depending on the type of nucleophile used. Nucleophilic displacement is achieved with thio-nucleophiles and NaN3. allowing the preparation of 3-thio- or 3-azido glucosamine derivatives difficult to obtain by use of sulfonates.