172291-43-9

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 24424-99-5 di-tert-butyl dicarbonate 
• 14193-51-2 methyl 3-amino-3-deoxy-α-D-mannopyranoside 

Downstream Products

• 172342-17-5 methyl 3,6-dideoxy-3,6-bis(3,4,6-tri-O-benzyl-5a-carba-α-D-mannopyranosylamino)-α-D-mannopyranoside 
• 172291-50-8 methyl 6-azido-3,6-dideoxy-3-(3,4,6-tri-O-benzyl-5a-carba-α-D-mannopyranosylamino)-α-D-mannopyranoside 
• 172291-51-9 (2R,3S,4S,5S,6S)-2-Aminomethyl-4-((1S,2R,3R,4R,5R)-3,4-bis-benzyloxy-5-benzyloxymethyl-2-hydroxy-cyclohexylamino)-6-methoxy-tetrahydro-pyran-3,5-diol 
• 172291-44-0 methyl 3-amino-6-azido-3,6-dideoxy-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of carboxylic analogues of the mannosyl trisaccharide: ether- and imino-linked methyl 3,6-bis(5a-carba-α-D-mannopyranosyl)-3,6-dideoxy-α-D-mannopyranosides

Carboxylic analogues 2 and 3 of the "trimannosyl structure 1", methyl 3,6-bis(5a-carba-α-D-mannopyranosyl)-3,6-dideoxy-α-D-mannopyranosides bonded by way of respective ether and imino linkages, were synthesized.The ether 2 had no inhibitory activity again