51236-57-8

Upstream product

• 98-88-4 benzoyl chloride 
• 1128-40-1 methyl-6-desoxy-β-D-glucopyranoside 
• 1128-40-1 methyl β-L-fucopyranoside 
• 73-34-7 6-deoxy-L-galactose 
• 4137-35-3 methyl 2,3-bis-O-benzoyl-α-D-galactopyranoside 
• 59981-27-0 methyl 2-O-methyl-α-D-fucopyranoside 
• 74135-23-2 methyl 3,4-O-isopropylidene-2-O-methyl-α-D-fucopyranoside 

Downstream Products

• 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 
• 132867-66-4 C₂₂H₂₁F₃O₉S 

Relevant academic research and scientific papers

Synthesis and Structural Characteristics of all Mono- And Difluorinated 4,6-Dideoxy- d - Xylo-hexopyranoses

Protein-carbohydrate interactions are implicated in many biochemical/biological processes that are fundamental to life and to human health. Fluorinated carbohydrate analogues play an important role in the study of these interactions and find application a

The synthesis of methyl-3-O-(β-D-fucopyranosyl)-β-D-quinovopyranoside and its 3′-O-, 2,3′-di-O-, and 2′,3′-di-O-methyl derivatives

Methyl-3-O-(β-D-fucopyranosyl)-β-D-quinovopyranoside and its 3′-O-, 2,3′-di-O-, and 2′,3′-di-O-methyl derivatives were obtained by the regioselective Helferich glycosylation of methyl-2-O-benzyl-β-D-quinovopyranoside with the 2,3,4-tri-O-benzoyl-α-D-fucopyranosyl bromide followed by the methylation with diazomethane or methyl iodide.

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.