50991-93-0

Upstream product

• 2873-29-2 D-glucal triacetate 
• 223545-38-8 methyl 2-azido-2-deoxy-α-D-mannopyranoside 
• 1110650-02-6 methyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-β-D-glucopyranoside 
• 100-52-7 benzaldehyde 
• 67-56-1 methanol 
• 3006-60-8 1,3,4,6-tetra-O-acetyl-2-acetamido-2-deoxy-α,β-D-mannopyranose 

Relevant academic research and scientific papers

Quantifying the electronic effects of carbohydrate hydroxy groups by using aminosugar models

Methyl amino-deoxy-glycosides with α- and β-gluco, α-galacto, or α-manno stereochemistry with the amino functionality in each of the four possible non-anomeric positions have been synthesized and their pKa values determined by titration. These

Tandem reduction-reductive alkylation of azido sugars

Catalytic hydrogenation of azido sugars has been conducted in the presence of different aldehydes to bring about a tandem reduction-reductive alkylation sequence. The reaction sequence proceeds in generally high yields, and tolerates some benzyl and benzylidene protecting groups that are sensitive to hydrogenolysis.