213386-01-7

Upstream product

• 100-39-0 benzyl bromide 
• 213386-00-6 p-nitrophenyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside 
• 80264-82-0 p-nitrophenyl 2,3-O-isopropylidene-α-D-mannopyranoside 
• 213385-99-0 p-nitrophenyl 6-deoxy-6-iodo-2,3-O-isopropylidene-α-D-mannopyranoside 
• 213385-98-9 p-nitrophenyl 2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 

Downstream Products

• 213386-04-0 N-Benzyl-N-{(2S,3S,4R,5R,6S)-4-benzyloxy-6-[(2R,3R,4S,5S,6R)-3-benzyloxy-5-methoxy-2-methyl-6-(4-nitro-phenoxy)-tetrahydro-pyran-4-yloxy]-5-methoxy-2,4-dimethyl-tetrahydro-pyran-3-yl}-formamide 
• 213386-03-9 p-nitrophenyl 4-O-benzyl-6-deoxy-2-O-methyl-α-D-mannopyranoside 
• 213386-02-8 p-nitrophenyl 4-O-benzyl-6-deoxy-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of p-trifluoroacetamidophenyl (4,6-dideoxy-4-formamido-3-C-methyl-2-O-methyl-α-L-mannopyran osyl)-(1→3)-(2-O - methyl-α-D-rhamnopyranosyl)-(1→3)-(2-O-methyl-α-L-fucopyran osyl)-(1 →3)-(α-L-rhamnopyranosyl)-(1 →2)-6-deoxy-α-L-talopyranoside: A sp

Syntheses of p-trifluoroacetamidophenyl glycosides of the haptenic pentasaccharide and the non-reducing disaccharide unit of the title pentasaccharide are reported. The synthesis of the terminal N-formylkansosamine unit started from methyl 6-deoxy-2,3-O-i