79494-69-2

Upstream product

• 100-39-0 benzyl bromide 
• 13343-62-9 benzyl 2-acetamido-2-deoxy-α-D-glucopyranoside 
• 13343-63-0 benzyl 4,6-O-benzylidene-2-acetylamino-2-deoxy-α-D-glucopyranoside 
• 60920-82-3 benzyl 2-acetamido-3-O-allyl-6-O-benzyl-2-deoxy-α-D-glucopyranoside 

Downstream Products

• 161686-87-9 (S)-3-((2S,3R,4R,5S,6R)-3-Acetylamino-2-benzyloxy-6-benzyloxymethyl-5-hydroxy-tetrahydro-pyran-4-yloxy)-butyric acid 
• 856409-94-4 benzyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-[3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->4)]-2-acetamido-6-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 856409-95-5 benzyl 2-amino-2-deoxy-β-D-glucopyranosyl-(1->3)-[2-amino-2-deoxy-β-D-glucopyranosyl-(1->4)]-2-acetamido-6-O-benzyl-2-deoxy-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of linear and branched regioisomeric chitooligosaccharides as potential mimetics of natural oligosaccharide ligands of natural killer cells NKR-P1 and CD69 lectin receptors

Regioisomer of chitobiose 13 with β(1→3) glycosidic bond and branched analog of chitotriose 25 having β(1→4) and β(1→3) glycosidic bonds, were prepared and tested as potential mimetics of natural oligosaccharide ligands for activating lectin receptors NKR

Carbohydrates as Nucleophiles in Conjugate Addition for Preparation of Muramic Acid Analogues

Benzyl 2-acetamido-6-O-benzyl-3-O--α-D-glucopyranoside (15) was synthesized stereoselectively by conjugate addition reaction, starting from benzyl 2-acetamido-6-O-benzyl-2-deoxy-α-D-glucopyranoside (9) and crotonic acid ethyl este