914955-20-7

Upstream product

• 914955-17-2 methyl (phenyl 4-O-levulinoyl-2,3-di-O-benzyl-1-thio-α-D-mannopyranoside)uronate 
• 914955-19-4 3-azidopropyl (methyl 2,3-di-O-benzyl-β-D-mannopyranoside)uronate 
• 1093383-66-4 C₃₂H₃₄O₈S 
• 449761-78-8 phenyl 2,3-di-O-benzyl-1-thio-α-D-mannopyranoside 
• 40608-06-8 levulinic anhydride 
• 914955-24-1 phenyl 2,3-di-O-benzyl-1-thio-α-D-mannopyranosiduronic acid 
• 914955-27-4 methyl (phenyl 2,3-di-O-benzyl-1-thio-α-D-mannopyranoside)uronate 
• 904745-28-4 methyl (phenyl 4-O-acetyl-2,3-di-O-benzyl-1-thio-α-D-mannopyranoside)uronate 

Relevant academic research and scientific papers

The stereodirecting effect of the glycosyl C5-carboxylate ester: Stereoselective synthesis of β-mannuronic acid alginates

(Chemical Equation Presented) Glycosylations of mannuronate ester donors proceed highly selectively to produce the 1,2-cis-linked products. We here forward a mechanistic rationale for mis counterintuitive selectivity, based on the remote stereodirecting e

Stereocontrolled synthesis of β-D-mannuronic acid esters: Synthesis of an alginate trisaccharide

A facile synthesis route toward β-linked mannuronic acid oligomers using the corresponding 1-thiomannuronic acid esters in combination with the Ph2SO/Tf2O or NIS/TMSOTf reagent combinations is presented. The presence of the remotely