144988-66-9

Upstream product

• 67670-69-3 N-acetyl-4,7,8,9-tetra-O-acetyl-2-chloro-2-deoxyneuraminic acid methyl ester 
• 1849-36-1 para-nitrobenzenethiol 
• 124974-13-6 methyl (4-nitrophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-2-nonulopyranosid)onate 
• 108-24-7 acetic anhydride 
• 124925-06-0 methyl (4-aminophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-α-D-glycero-D-galacto-2-nonulopyranosid)onate 

Relevant academic research and scientific papers

Mild stereoselective syntheses of thioglycosides under PTC conditions and their use as active and latent glycosyl donors

Mild and stereoselective arylthio glycoside syntheses were accomplished by inversion of configuration of glycosyl halides under phase transfer catalyzed conditions. Under such conditions, aryl α-thiosialosides having electron donating and withdrawing subs

"Active" and "latent" thioglycosyl donors in oligosaccharide synthesis. Application to the synthesis of α-sialosides

The use of a new "active" and "latent" thioglycosyl donor strategy in glycoside synthesis is described using arylthio α-sialosides of different reactivities.