186600-44-2

Upstream product

• 94715-59-0 (2S,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6R)-4-acetoxy-2-(acetoxymethyl)-5-azido-6-(2,2,2-trichloro-1-iminoethoxy)tetrahydro-2H-pyran-3-yl)oxy)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 172939-67-2 Benzoic acid (2S,3R,4R,5R,6R)-3-acetylamino-2-[(S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-(2-oxo-2-phenyl-ethoxycarbonyl)-ethoxy]-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-4-yl ester 

Downstream Products

• 186600-56-6 C₆₃H₇₃N₃O₂₉ 
• 186600-54-4 C₆₁H₇₁N₃O₂₈ 

Relevant academic research and scientific papers

Mucin Type Glycopeptides: Synthesis of Core 2, Core 6 and F1-α Building Blocks and Some Unexpected Reactions

Protected Core 2 and 6 and F1-α analogs were synthesized using the 4,6-diol of Tn-Ser/Thr and TF-Ser/Thr.Acetylation of glucosamine in acetic anhydride/pyridine resulted in an additional and unusual N-acetylation at the Fmoc protected amine of serine and threonine followed by β-elimination of the aglycons.Normal glucosamine acetylation was carried out at -20 deg C for 20 minutes to accomplish in synthesis of Core 2, Core 6 and F1-α as glycopeptide building blocks.