352533-39-2

Upstream product

• 143308-74-1 (3aR,7R,7aS)-methyl 7-acetoxy-2,2-dimethyl-3a,6,7,7atetrahydrobenzo[d][1,3]dioxole-5-carboxylate 
• 352533-33-6 methyl (3S,4R,5R)-3-acetamido-5-acetoxy-4-(methanesulfonyloxy)cyclohex-1-ene-1-carboxylate 
• 352533-31-4 methyl (3S,4R,5R)-5-acetoxy-3-azido-4-(methanesulfonyloxy)cyclohex-1-ene-1-carboxylate 
• 352533-29-0 methyl (3S,4R,5R)-5-acetoxy-3-azido-4-hydroxycyclohex-1-ene-1-carboxylate 
• 352533-27-8 methyl 5-O-acetylshikimate 3,4-cyclic sulfite 
• 352533-35-8 methyl (3S,4S,5R)-5-acetoxy-3,4-(acetylepimino)cyclohex-1-ene-1-carboxylate 
• 352533-24-5 (3R,4S,5R)-methyl 3,4-O-thionylshikimate 
• 191916-39-9 methyl (-)-quinate 
• 17515-18-3 (3R,4S,5R)-methyl 3,4,5-triacetoxy-1-cyclohexene-1-carboxylate (methyl (-)-shikimate triacetate) 
• 40983-58-2 methyl shikimate 
• 50605-62-4 3,4,5-tri-O-acetyl quinate de methyle 
• 77-95-2 D-(-)-quinic acid 
• 88165-26-8 methyl 3,4-O-isopropylideneshikimate 
• 352533-37-0 methyl (3R,4S,5R)-4-acetamido-5-acetoxy-3-azidocyclohex-1-ene-1-carboxylate 

Relevant academic research and scientific papers

Synthesis of a carbocyclic sialic acid analogue for the inhibition of influenza virus neuraminidase

The influenza virus neuraminidase (NA) is essential for viral infection and offers a potential target for antiviral drug development. We prepared a carbocyclic sialic acid analogue, potentially able to inhibit NA. Its structure is an analogue of the trans