225662-87-3

Upstream product

• 488827-77-6 2,3,4-tri-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-6-O-trityl-β-D-galactopyranosylamine 
• 489459-36-1 2,3,4-tri-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-β-D-galactopyranosylamine 
• 22435-65-0 N-(2,2-diethoxycarbonylvinyl)-β-D-galactopyranosylamine 
• 488827-78-7 2,3,4-tri-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-6-O-mesyl-β-D-galactopyranosylamine 

Downstream Products

• 225663-07-0 C₂₇H₂₃NO₇ 

Relevant academic research and scientific papers

An easy route to seven-membered iminocyclitols from aldohexopyranosyl enamines

A new stereocontrolled and high yielding synthesis of biologically active polyhydroxyperhydroazepines is reported starting from easily available glycosylenamines (D-gluco, D-manno, and D-galacto configurations), which are transformed into 1,6-azaanhydropy

Efficient synthesis of seven-membered iminocyclitols from glycosylenamines

Seven membered iminocyclitols are synthesized in four steps from easily available glycosylenamines (D-gluco, D-galacto, and D-manno configurations) through 1,6-aza-anhydrosugar derivatives. These intermediates are transformed into 2-hydroxy- and 2-unsubstituted azepanes depending on the reactants used for the cleavage of the Cl-O bond. The overall yields are high.