129171-96-6

Upstream product

• 4478-43-7 (1,2:3,4-di-O-isopropylidene-6-O-(p-toluensulfonate))-D-galactopiranose 
• 4026-27-1 1,2:3,4-di-O-isopropylidene-α-D-fucopyranose 
• 4064-06-6 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 73-34-7 D-Fucose 
• 10257-28-0 D-Galactose 
• 618-31-5 benzylidene dibromide 
• 129172-95-8 methyl 6-deoxy-α/β-D-galactopyranoside 

Downstream Products

• 129090-79-5 methyl (3S)-<3-(2)H>-2,4-di-O-(p-bromobenzoyl)-3,6-dideoxy-β-D-xylo-hexopyranoside 
• 119824-71-4 methyl (3S)-<3-(2)H>-4-O-benzoyl-3,6-dideoxy-β-D-xylo-hexopyranoside 
• 56879-72-2 Methyl-4-O-benzoyl-3,6-dideoxy-β-D-xylo-hexapyranosid 
• 119824-72-5 C₂₁H₂₁⁽²⁾HO₆ 
• 56879-71-1 methyl 4-O-benzoyl-3-bromo-3,6-dideoxy-β-D-gulopyranoside 
• 92983-86-3 methyl 4-O-benzoyl-3-bromo-3,6-dideoxy-α-D-gulopyranoside 

Relevant academic research and scientific papers

Synthesis of stereospecifically labeled 3,6-dideoxyhexoses.

Preparations of ascarylose (3,6-dideoxy-L-arabino-hexose), abequose (3,6-dideoxy-D-xylo-hexose), and paratose (3,6-dideoxy-D-ribo-hexose) with stereospecific deuterium labeling at C-3 are discussed. The methods used to synthesize these sugars, such as the

SYNTHESIS OF STEREOSPECIFICALLY LABELED CARBOHYDRATES II: PREPARATION OF (3S)- AND (3R)-ABEQUOSE

Preparation of methyl 3,6-dideoxy-D-xylo-hexapyranoside (methyl abequoside) having deuterium stereospecifically labeled at the 3S (1) and 3R (2) position, respectively, via three different routes is described.