132867-66-4

Upstream product

• 73-34-7 6-deoxy-L-galactose 
• 1128-40-1 methyl β-L-fucopyranoside 
• 358-23-6 trifluoromethylsulfonic anhydride 
• 14686-83-0 C₂₁H₂₂O₇ 
• 14687-15-1 methyl L-fucopyranoside 
• 98-88-4 benzoyl chloride 
• 71071-83-5 methyl 2,3-O-dibenzoyl-α-L-fucopyranoside 

Downstream Products

• 132867-67-5 methyl 2,3-di-O-benzoyl-4,6-dideoxy-4-iodo-α-L-glucopyranoside 
• 125569-51-9 C₂₁H₂₃NO₇ 
• 125569-50-8 C₂₁H₂₃NO₆ 
• 134645-99-1 C₂₀H₁₉NO₆ 
• 134646-01-8 (2S,3R,4R)-2-((S)-1-Hydroxy-ethyl)-1-oxy-3,4-dihydro-2H-pyrrole-3,4-diol 
• 132867-69-7 methyl 2,3-di-O-benzoyl-4,6-dideoxy-α-L-xylo-hexopyranoside 

Relevant academic research and scientific papers

Stereochemical studies on Esperamicins: Determination of the absolute configuration of hydroxyamino sugar fragment

The β-D-gluco-hexopyranose configuration has been assigned for the hydroxyamino sugar fragment or esperamicin A. This determination concluded our study on the absolute configuration of the carbohydrate portion of esperamicins.

Synthesis of 4-deoxy and 4-deoxy-4-halogeno derivatives of L-fucose as potential enzyme inhibitors

Methyl-2,3-di-O-benzoyl-6-deoxy-α-L-galactopyranoside (2) was converted into the 4-deoxy-4-iodo-α-L-gluco derivative 4 by triflate-mediated inversion.Catalytic reduction of 4 gave methyl 2,3-di-O-benzoyl-4,6-dideoxy-α-L-xylo-hexopyranoside (6) and subsequ