134645-97-9

Upstream product

• 95120-18-6 methyl 6-deoxy-6-iodo-3,4-O-isopropylidene-β-D-galactopyranoside 
• 4137-35-3 methyl 2,3-bis-O-benzoyl-α-D-galactopyranoside 
• 74135-23-2 methyl 3,4-O-isopropylidene-2-O-methyl-α-D-fucopyranoside 
• 98-88-4 benzoyl chloride 
• 59981-27-0 methyl 2-O-methyl-α-D-fucopyranoside 
• 73-34-7 D-Fucose 
• 123076-85-7 methyl 2-O-benzoyl-6-deoxy-3,4-O-isopropylidene-β-D-galactopyranoside 
• 1128-40-1 methyl 6-deoxy-β-D-galactopyranoside 
• 73-34-7 6-deoxy-L-galactose 
• 1128-40-1 methyl β-L-fucopyranoside 

Downstream Products

• 134645-98-0 C₂₁H₂₁N₃O₆ 
• 134645-99-1 C₂₀H₁₉NO₆ 
• 134646-00-7 (2R,3S,4S)-2-((R)-1-Hydroxy-ethyl)-1-oxy-3,4-dihydro-2H-pyrrole-3,4-diol 
• 125569-51-9 C₂₁H₂₃NO₇ 
• 125569-50-8 C₂₁H₂₃NO₆ 
• 134659-74-8 methyl 2,3-di-O-benzoyl-6-deoxy-4-O-trifluoromethanesulfonyl-β-D-galactopyranoside 
• 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

Some approaches to glycosylated versions of methyl β-acarviosin

In a first approach to a glycosylated version of 'methyl β-acarviosin', a putative inhibitor of cellulases, cellobiose was converted into a carbocyclic enone that could not be transformed into the required amine for a subsequent alkylation. Alternatively,

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.