110336-60-2

Upstream product

• 114924-71-9 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(3-phenylureido)-β-D-glucopyranose 
• 67-56-1 methanol 
• 124-41-4 sodium methylate 
• 114924-70-8 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-(3-phenylureido)-α-D-glucopyranose 
• 14131-62-5 D-glucosamine hydrochloride 
• 103637-78-1 1,3,4,6-tetra-O-acetyl-2-amino-2-deoxy-α-D-glucopyranose hydrobromide 
• 3006-60-8 2-acetamido-3,4,6-tri-O-acetyl-D-glucopyranosyl acetate 
• 103-71-9 phenyl isocyanate 
• 10034-19-2 1,3,4,6-tetra-O-acetyl-2-amino-2-deoxy-α-D-glucopyranose hydrochloride 
• 134122-77-3 2-deoxy-2-(3-phenylureido)-D-glucopyranose 

Relevant academic research and scientific papers

THE REACTION OF 2-AMINO-2-DEOXYHEXOPYRANOSES WITH ISOCYANATES. SYNTHESIS OF UREAS AND THEIR TRANSFORMATION INTO HETEROCYCLIC DERIVATIVES.

The reactions of 2-amino-2-deoxyglycopyranoses with aryl isocyanates have been investigated in detail and ureas and heterocyclic derivatives are obtained.The mechanism of formation of glycofuranoimidazolidin-2-ones 62 has now become visible, while

A NOVEL REGIO- AND HIGHLY STEREOSELECTIVE ANOMERIC DEACETYLATION OF 2-AMINOSUGAR DERIVATIVES.

Silica gel-mediated anomeric deacetylation of per-acetylated 2-amino-2-deoxy-glycopyranose derivatives in methanol constitutes a mild and inexpensive protocol for the selective deprotection of these relevant carbohydrate templates.The reaction proceeds wi