354986-52-0

Upstream product

• 354986-48-4 methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-(2-picolinyl)-α-D-glucopyranoside 
• 6619-02-9 methyl N-acetyl-2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 6959-47-3 2-chloromethylpyridine hydrochloride 
• 314740-77-7 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranosyl triflate 
• 354986-50-8 methyl 2-acetamido-2-deoxy-4-O-benzyl-3-O-(2-picolinyl)-α-D-glucopyranoside 

Relevant academic research and scientific papers

Why are the hydroxy groups of partially protected N-acetylglucosamine derivatives such poor glycosyl acceptors, and what can be done about it? A comparative study of the reactivity of N-acetyl-, N-phthalimido-, and 2-azido-2-deoxy-glucosamine derivatives

Competition experiments were used to determine that the 4-OH of a 2-deoxy-2-azidoglucose derivative is more reactive than that of the corresponding N-phthalimido glucose derivative which, in turn, is more easily glycosylated than the N-acetyl derivative.