20187-72-8

Upstream product

• 100-39-0 benzyl bromide 
• 4860-82-6 2,3-anhydro-α-D-ribofuranoside de methyle 

Downstream Products

• 143604-37-9 5-O-Benzyl-2-desoxy-2-dimethylamino-α-D-arabinofuranoside de methyle 
• 143604-35-7 5-O-Benzyl-3-desoxy-3-dimethylamino-α-D-xylofuranoside de methyle 
• 60019-09-2 3-Amino-5-O-benzyl-3-desoxy-α-D-xylofuranoside de methyle 
• 143604-31-3 2-Amino-5-O-benzyl-2-desoxy-α-D-arabinofuranoside de methyle 
• 171071-44-6 Methyl 5-O-benzyl-2-cyano-2-deoxy-α-D-arabinofuranoside 
• 171071-43-5 Methyl 5-O-benzyl-3-cyano-3-deoxy-α-D-xylofuranoside 
• 20535-09-5 2,3-Anhydro-5-O-benzyl-β-D-ribofuranoside de methyle 
• 143604-42-6 5-O-Benzyl-3-desoxy-3-dimethylamino-2-O-methanesulfonyl-α-D-xylofuranoside de methyle 
• 143604-44-8 5-O-Benzyl-2-desoxy-2-dimethylamino-3-O-methanesulfonyl-α-D-arabinofuranoside de methyle 
• 1137931-41-9 5-methoxy-2-(benzyloxymethyl)-4-[(4-methylphenyl)sulfanyl]tetrahydrofuran-3-ol 

Relevant academic research and scientific papers

Methyl-α-D-2-selenonyl Pent-2-enofuranoside: A Reactive Selenosugar for the Diversity Oriented Synthesis of Enantiomerically Pure Heterocycles, Carbocycles, and Isonucleosides

The construction of vinyl selenone on a furanoside led to a highly reactive synthetic intermediate methyl-α-d-2-selenonyl pent-2-enofuranoside composed of a masked aldehyde, an electron-deficient double bond along with an excellent leaving group. This new

The synthesis and thermodynamic equilibrium of eight 5-O-benzyl-2 (or 3)-dimethylamino-3 (or 2)-o-mesyl-α (or β)-d-xylo (or arabino) methylfuranosides

Regioselectivity of the opening of 2,3-anhydrofuranosides 1 (α and β) and 2 (α and β) by dimethylamine (and by ammonia for 1) has been determined. Thermic stability of the eight corresponding vic-dimethylaminomesylates 11-14 (α and β) in CD3CN