259751-65-0

Upstream product

• 259751-64-9 methyl 2,6-di-O-benzyl-3,4-O-isopropylidene-5-C-methoxy-β-D-talopyranoside 
• 100-39-0 benzyl bromide 
• 259751-55-8 methyl 2,6-di-O-benzyl-3,4-O-isopropylidene-5-C-methoxy-β-D-galactopyranoside 
• 259751-61-6 methyl 3,4-O-isopropylidene-5-C-methoxy-β-D-talopyranoside 
• 218913-73-6 methyl 3,4-O-isopropylidene-5-C-methoxy-6-O-(1-methoxy-1-methylethyl)-β-D-galactopyranoside 
• 218913-76-9 methyl 3,4-O-isopropylidene-5-C-methoxy-β-D-galactopyranoside 
• 134039-09-1 methyl 2,6-di-O-benzyl-5-C-methoxy-β-D-galactopyranoside 
• 259751-60-5 methyl 3,4-O-isopropylidene-5-C-methoxy-6-O-(1-methoxy-1-methylethyl)-β-D-talopyranoside 
• 259751-58-1 methyl 3,4-O-isopropylidene-5-C-methoxy-6-O-(1-methoxy-1-methylethyl)-β-D-lyxo-hexopyranosid-2-ulose 
• 259751-59-2 methyl 6-O-acetyl-3,4-O-isopropylidene-5-C-methoxy-β-D-lyxo-hexopyranosid-2-ulose 
• 259751-57-0 methyl 6-O-acetyl-3,4-O-isopropylidene-5-C-methoxy-β-D-galactopyranoside 

Relevant academic research and scientific papers

The first synthesis of a ribo-hexos-5-ulose: The l-enantiomer

The title compound, previously unreported in either enantioform, and its 2,6-di-O-benzyl derivative have been synthesized through a stereocontrolled epimerization at C-2 of 6-O-protected methyl 3,4-O-isopropylidene-5-C-methoxy-ss-D-galactopyranosides. The