552848-99-4

Upstream product

• 100-39-0 benzyl bromide 
• 90405-86-0 4-O-allyl-1,6-anhydro-β-D-mannopyranose 
• 90405-83-7 4-O-allyl-1,6-anhydro-2,3-O-isopropylidene-β-D-mannopyranose 
• 14440-51-8 1,6-anhydro-2,3-O-isopropylidene-β-D-mannopyranose 

Downstream Products

• 194996-99-1 (1R,2S,4R,5R)-2-Allyloxy-4-benzyloxy-6,8-dioxa-bicyclo[3.2.1]octan-3-one 
• 194997-01-8 (1R,2S,4S,5R)-2-Allyloxy-4-benzyloxy-6,8-dioxa-bicyclo[3.2.1]octan-3-one 
• 194996-97-9 4-O-allyl-1,6-anhydro-2-O-benzyl-3-oxo-β-D-arabino-hexopyranose 

Relevant academic research and scientific papers

Intra- and intermolecular 1,3-dipolar cycloaddition of sugar ketonitrones with mono-, di-, and trisubstituted dipolarophiles

The 1,3-dipolar cycloaddition of sugar ketonitrones is a useful synthetic procedure to build up nitrogenated quaternary centers in terms of scope (substrate, dipolarophile, inter- and intramolecular versions), yield, and regio- and stereoselectivity. The