19342-75-7

Upstream product

• 6931-68-6 methyl (5-acetamido-2,4,7,8,9-penta-O-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate 
• 100-51-6 benzyl alcohol 
• 6931-68-6 methyl 5-acetamido-2,4,7,8,9-penta-O-acetyl-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate 
• 108740-39-2 (1S,2R)-1-((2R,3R,4S,6R)-3-acetamido-4,6-diacetoxy-6-(methoxycarbonyl)tetrahydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate 
• 144240-36-8 methyl (methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycero-D-galacto-2-nonulopyranosid)onate 
• 83107-51-1 Methyl-(5-acetamido-4,7,8,9-tetra-O-acetyl-2,3,5-tridesoxy-D-glycero-β-D-galacto-2-nonulopyranosylbromid)onat 
• 67670-69-3 N-acetyl-4,7,8,9-tetra-O-acetyl-2-chloro-2-deoxyneuraminic acid methyl ester 

Downstream Products

• 162018-18-0 methyl (benzyl 5-acetoxyacetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate 
• 284037-41-8 (2R,4S,5R,6R)-4-Acetoxy-2-benzyloxy-5-[1-ethoxy-eth-(Z)-ylideneamino]-6-((1S,2R)-1,2,3-triacetoxy-propyl)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 352437-48-0 methyl (benzyl 4,7,8,9-tetra-O-acetyl-3,5-dideoxy-5-(N-nitrosoacetamido)-D-glycero-α-D-galacto-non-2-ulopyranosid)onate 
• 57777-97-6 methyl (benzyl 5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate 
• 765302-19-0 N-iso-butanoyl-D-neuraminic acid benzyl glycoside 
• 15964-51-9 N-propionyl-D-neuraminic acid benzyl glycoside 
• 765302-20-3 (2R,4S,5R,6R)-2-Benzyloxy-5-(2,2-dimethyl-propionylamino)-4-hydroxy-6-((1R,2R)-1,2,3-trihydroxy-propyl)-tetrahydro-pyran-2-carboxylic acid 
• 15964-52-0 N-butanoyl-D-neuraminic acid benzyl glycoside 
• 15964-53-1 N-benzoyl-D-neuraminic acid benzyl glycoside 
• 765302-21-4 N-phenylacetyl-D-neuraminic acid benzyl glycoside 
• 284036-93-7 methyl (benzyl 4,7,8,9-tetra-O-acetyl-3,5-dideoxy-5-ethoxycarbonylamino-D-glycero-α-D-galacto-2-nonulopyranosid)onate 
• 284036-91-5 methyl (benzyl 4,7,8,9-tetra-O-acetyl-3,5-dideoxy-5-valeroylamino-D-glycero-α-D-galacto-2-nonulopyranosid)onate 
• 284036-92-6 methyl (benzyl 4,7,8,9-tetra-O-acetyl-3,5-dideoxy-5-(N-trifluoroacetylglycylamido)-D-glycero-α-D-galacto-2-nonulopyranosid)onate 
• 174312-83-5 (2R,4S,5R,6R)-4-Acetoxy-6-((1R,2R)-1-acetoxy-3-benzoyloxy-2-hydroxy-propyl)-2-benzyloxy-5-(2-benzyloxy-acetylamino)-tetrahydro-pyran-2-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

Synthesis of sialic acid derivatives as ligands for the myelin-associated glycoprotein (MAG)

The trisaccharide substructure 13 of the ganglioside GQ1bα shows a remarkable affinity for the myelin-associated glycoprotein (MAG). In the search for structurally simplified and pharmacokinetically improved mimics of 13, sialosides with modifications at

Enhanced sialylating activity of O-chloroacetylated 2-thioethyl sialosides

It has been shown that O-chloroacetyl protecting groups enhance significantly sialylating activity of 2-thioethyl sialosides in model reactions of α(2-8)-sialylation. Ethyl 4,7,8,9-tetra-O-chloroacetyl-3,5-dideoxy-2- thio-5-trifluoroacetamido-D-glycero-α-

A simple procedure for the synthesis of the methyl and benzyl glycosides of Neu5Ac and 4-epi-Neu5Ac. Conversion of the benzyl and methyl glycosides of Neu5Ac into N-trifluoroacetylneuraminic acid benzyl glycosides

From the reaction products of the Kuhn-Bashang synthesis of Neu5Ac, 5-acetamido-3,5-dideoxy-α- and -β-D-glycero-D-talo-2-nonulopyranosonic acid (4-epi-Neu5Ac) were isolated as the acetylated methyl esters (1 and 2).Treatment of methyl (5-acetamido-4,7,8,9

Lipid A and related compounds. XXVI. Syntheses of biologically active penta-O-acetyl-N-glycoloylneuraminyl- and penta-O-acetyl-3-deoxy-D-glycero-D-galacto-2-nonulopyranosonic acid-(α 2 → 6)-D-glucosamine-4-phosphate analogs of lipid A

The syntheses of novel penta-O-acetyl-N-glycoloylneuraminyl- and penta-O-acetyl-3-deoxy-n-glycero-D-galacto-2-nonulopyranosonic acid-(α 2 → 6)-D-glucosamine-4-phosphate analogues of lipid A containing sialic acid in place of 3-deoxy-D-manno-2-octulosonic acid are described. Preliminary examination of the biological activity revealed that two synthetic disaccharides showed mitogenic activities and weak antitumor activities.