50605-62-4

Upstream product

• 191916-39-9 methyl (-)-quinate 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 77-95-2 D-(-)-quinic acid 

Downstream Products

• 17515-18-3 (3R,4S,5R)-methyl 3,4,5-triacetoxy-1-cyclohexene-1-carboxylate (methyl (-)-shikimate triacetate) 
• 1053628-62-8 (1R,2S,3S,4R,6R)-3-Benzyloxy-4-methyl-6-(naphthalen-1-ylmethoxy)-cyclohexane-1,2-diol 
• 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 
• 352533-37-0 methyl (3R,4S,5R)-4-acetamido-5-acetoxy-3-azidocyclohex-1-ene-1-carboxylate 
• 352533-39-2 methyl (3R,4S,5R)-4-acetamido-5-acetoxy-3-aminocyclohex-1-ene-1-carboxylate 
• 352533-29-0 methyl (3S,4R,5R)-5-acetoxy-3-azido-4-hydroxycyclohex-1-ene-1-carboxylate 
• 40983-58-2 methyl shikimate 

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

An efficient transformation of (-)-quinic acid into carba-L-rhamnose

A novel stereoselective synthesis of carba-L-rhamnose from (-)-quinic acid is described. The title compound is obtained with an appropriate pattern of protecting groups to be used for the preparation of Streptococcus pneumoniae type 19F capsular polysacch