186532-70-7

Upstream product

• 4163-65-9 per-O-acetyl-α-D-mannopyranose 
• 122920-03-0 2,6-Anhydro-7,8,9-trideoxy-D-glycero-D-manno-non-8-enitol 
• 120520-79-8 2-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)ethyl aldehyde 
• 82659-59-4 3-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)propene 
• 98920-46-8 (2R,3R,4R,5R,6R)-2-(acetoxymethyl)-6-allyltetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 100-39-0 benzyl bromide 

Downstream Products

• 207387-04-0 (2S,3R)-2,3-Dihydroxy-4-((2R,3R,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-butyric acid 
• 207387-05-1 [(2S,3R)-2,3-Dihydroxy-4-((2R,3R,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-butyrylamino]-acetic acid benzyl ester 

Relevant academic research and scientific papers

C-mannose derivatives as potent mimics of sialyl Lewis X

The synthesis of five sialyl Lewis X mimetics was described. Mimetics 2-6 were easily synthesized from readily available starting materials. Mimics 4 and 6 showed activities five-fold better than sialyl Lewis X. Copyright (C) 1996 Elsevier Science Ltd.