857466-18-3

Upstream product

• 50-00-0 formaldehyd 
• 100-46-9 benzylamine 
• 705951-25-3 (2R,3R,4S,5S,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-(2-isocyano-ethoxy)-tetrahydro-pyran 
• 705951-27-5 ((2S,3S,4S,5R,6R)-2,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-acetic acid 
• 61134-30-3 benzyl 3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 617691-71-1 2'-hydroxyethyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 140428-83-7 2-azidoethyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 705951-26-4 ((2S,3S,4S,5R,6R)-2,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-acetic acid tert-butyl ester 
• 705951-42-4 N-[2-((2S,3S,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-ethyl]-formamide 
• 705951-23-1 (2S,3S,4S,5R,6R)-2-(2-Azido-ethoxy)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran 
• 705951-24-2 2-[1-O-α-d-(2,3,4,6-tetra-O-benzyl)mannopyranosyl]ethylamine 

Relevant academic research and scientific papers

GLYCOSAMINOGLYCAN (GAG) MIMETICS

The invention relates to compounds that are designed to mimic the structure of GAGs; methods for the preparation of the compounds; compositions comprising the compounds; and use of the compounds and compositions thereof for the anti-angiogenic, anti-metas

Application of the four-component Ugi condensation for the preparation of sulfated glycoconjugate libraries

A focused library of novel, sulfated glycoconjugates was synthesized by utilizing carbohydrate-derived blocks in the four-component Ugi condensation. Library members comprise a sulfated monosaccharide linked by various spacers to either an aromatic or mon