60894-74-8

Upstream product

• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 

Downstream Products

• 2771-48-4 methyl 2-acetamido-3,4,6-O-triacetyl-2-deoxy-β-D-glucopyranoside 
• 2595-39-3 methyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranoside 
• 10375-65-2 benzyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 22244-42-4 N-acetylglucosamine 1-phosphate 
• 13088-77-2 N,N',N'',N'''-tetraacetylchitotetraose 
• 13319-33-0 GlcNAcβ(1,4)GlcNAcβ(1,4)GlcNAcβ(1,4)GlcNAcβ(1,4)GlcNAcβ(1,4)GlcNAc 
• 1243575-79-2 C₄₂H₅₇NO₁₄ 
• 1243575-80-5 C₄₂H₅₇NO₁₄ 
• 107715-15-1 2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranosyl fluoride 

Relevant academic research and scientific papers

A facile method for synthesis of 1,2-oxazoline derivative of N-acetylglucosamine promoted by potassium fluoride

A potassium fluoride-promoted intramolecular cyclization reaction of 2-acetamido-2-deoxy-α-D-glucopyranosyl chloride took place smoothly, giving the corresponding 1,2-oxazoline derivative in good yield. Potassium fluoride behaves as a nucleophile for anomerization of the glycosyl chloride as well as an acid captor to scavenge the protonic acid liberated. This is an extremely practical method for preparation of sugar oxazoline derivatives with simple experimental procedures.