862730-71-0

Upstream product

• 40653-15-4 methyl 2,3,4-tri-O-benzyl-α-D-manno-hexodialdo-1,5-pyranoside 
• 34212-64-1 methyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 63598-38-9 1,5-anhydro-4,6-O-benzylidene-2-deoxy-D-ribo-hex-1-enopyranose 
• 81369-73-5 methyl 2,3,4-tri-O-benzyl-α-D-mannosiduronic acid 

Downstream Products

• 862730-77-6 methyl 1,5-anhydro-6-O-(4',6'-O-benzylidene-3'-O-yl-D-allal)-7-deoxy-2,3,4-tri-O-benzyl-α-D-manno-hept-6-enopyranose 

Relevant academic research and scientific papers

An approach to the synthesis of α-(1-6)-C-disaccharides by tandem Tebbe methylenation and Claisen rearrangement

Uronic acids, most efficiently synthesised from the corresponding alcohols by two step Dess-Martin and sodium chlorite mediated oxidation, may be used as coupling partners for esterification with an allo glycal as substrates for the tandem Tebbe/Claisen a