194997-08-5

Upstream product

• 552849-02-2 4-O-acetyl-3-(N-acetyl-N-allylamino)-1,6-anhydro-2-O-benzyl-3-deoxy-β-D-mannopyranose 
• 552849-01-1 3-N-allylamino-1,6-anhydro-2-O-benzyl-3-deoxy-β-D-mannopyranose 
• 3868-04-0 1,6:3,4-dianhydro-β-D-altropyranose 
• 213594-43-5 1,6:3,4-dianhydro-2-O-benzyl-β-D-altropyranose 
• 100-39-0 benzyl bromide 
• 552849-03-3 3-(N-acetyl-N-allylamino)-1,6-anhydro-2-O-benzyl-3-deoxy-β-D-mannopyranose 

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