172291-50-8

Upstream product

• 152203-03-7 (1R,2R,3S,4R,5R)-1,2-anhydro-3,4-di-O-benzyl-5-benzyloxymethylcyclohexan-1,2,3,4-tetraol 
• 172291-44-0 methyl 3-amino-6-azido-3,6-dideoxy-α-D-mannopyranoside 
• 14193-51-2 methyl 3-amino-3-deoxy-α-D-mannopyranoside 
• 141257-85-4 (1R)-(1,2,3,5/4)-1,2-Anhydro-5-hydroxymethylcyclohexane-1,2,3,4-tetrol 
• 172291-43-9 methyl 3-tert-butoxycarbonylamino-3-deoxy-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 

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 
• 172291-51-9 (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 

Relevant academic research and scientific papers

Synthesis of carbasugar-containing non-glycosidically linked pseudodisaccharides and higher pseudooligosaccharides

This minireview covers synthetic methods towards carbasugar-containing non-glycosidically linked pseudodisaccharides or higher pseudooligosaccharides. Carbocyclic pyranose mimetics (saturated or unsaturated between C-5 and C-5a) are linked by ether, thioe

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