119824-72-5

Upstream product

• 10257-28-0 D-Galactose 
• 129172-95-8 methyl 6-deoxy-α/β-D-galactopyranoside 
• 129171-96-6 methyl 3,4-O-benzylidene-6-deoxy-D-galactopyranoside 
• 4064-06-6 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 4026-27-1 1,2:3,4-di-O-isopropylidene-α-D-fucopyranose 
• 4478-43-7 (1,2:3,4-di-O-isopropylidene-6-O-(p-toluensulfonate))-D-galactopiranose 
• 53437-41-5 methyl 2,3-anhydro-6-deoxy-β-D-gulo-pyranoside 
• 73-34-7 D-Fucose 
• 111476-68-7 methyl (3S)-<3-(2)H>-3,6-dideoxy-β-D-xylo-hexapyranoside 
• 98-88-4 benzoyl chloride 
• 111476-68-7 methyl (3S)-<3-(2)H>-3,6-dideoxy-α-L-arabino-hexopyranoside 
• 64880-45-1 (1R,2R,4S,5S,6R)-2-Methoxy-4-methyl-3,7-dioxa-bicyclo[4.1.0]heptan-5-ol 
• 64880-43-9 methyl 2-O-benzoyl-3-bromo-3,6-dideoxy-α-L-altropyranoside 
• 61199-73-3 methyl 2,3-O-benzylidene-6-deoxy-α-L-mannopyranoside 

Relevant academic research and scientific papers

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.

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

The general problem of the synthesis of 3,6-dideoxy sugars containing stereospecifically labeled hydrogen isotope at C-3 is adressed for the specific case of ascarylose (3,6-dideoxy-L-arabino-hexose).