114102-94-2

Upstream product

• 108-24-7 acetic anhydride 
• 114102-93-1 (4R)-5-acetamido-4,8-anhydro-7,9-O-benzylidene-1,2-O-cyclohexylidene-5-deoxy-4-C-nitro-D-gluco-L-erythro-nonitol 
• 78008-36-3 (R)-2,3-cyclohexylideneglyceraldehyde 
• 105874-62-2 1-deoxy-1-nitro-N-acetyl-4,6-O-benzylidene-β-D-glucosamine 

Downstream Products

• 114102-95-3 5-acetamido-4,7-di-O-acetyl-2,6-anhydro-1,3-O-benzylidene-8,9-O-cyclohexylidene-5-deoxy-D-arabino-L-gulo-nonitol 
• 114102-98-6 5-acetamido-4,7-di-O-acetyl-2,6-anhydro-1,3-O-benzylidene-8,9-O-cyclohexylidene-5-deoxy-<6-2H>-D-arabino-L-gulo-nonitol 

Relevant academic research and scientific papers

A synthesis of N-acetylneuraminic acid and [6-2H]-N-acetylneuraminic acid from N-acetyl-D-glucosamine.

N-Acetylneuraminic acid (Neu5Ac) and [6-2H]-Neu5Ac were prepared from 2-acetamido-2-deoxy-D-glucose (N-acetyl-D-glucosamine). Then Henry reaction of a 1-deoxy-1-nitro derivative of GlcNAc (protected 1-C-nitroanhydro-D-glucitol) with cyclohexylidene-D-glyceraldehyde, followed by successive acetylation and reductive denitration with Bu3SnH, gave an anhydrononitol intermediate (6) diastereo-selectively in high yields. Debenzylidenation of 6 freed its distal primary carbinol group, which was subjected to catalytic oxidation followed by hydrolysis, esterification (diazomethane), and acetylation to give a protected methyl nononate. This ester was transformed into the known methyl N-acetyl-4,7,8,9-tetra-O-acetyl-2,3-dehydroneuraminate (15), which was identical with a sample prepared from Neu5Ac. Neu5Ac was obtained from 15 by bromoetherification (NBS, methanol) followed by reductive debromination with Bu3SnH and hydrolysis. Similarly, the [6-2H]-derivative of 15 was transformed into [6-2H]-Neu5Ac.