1384986-06-4

Upstream product

• 1384985-99-2 C₁₉H₂₇NO₅ 

Downstream Products

• 1384986-25-7 (2S,4R,6R)-2-((3aS,4R,6S,6aS)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-6-phenyl-7-oxa-1-azabicyclo[2.2.1]heptane 
• 1384986-26-8 (2S,4R,6S)-2-((3aS,4R,6S,6aS)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-6-phenyl-7-oxa-1-azabicyclo[2.2.1]heptane 

Relevant academic research and scientific papers

Highly stereoselective synthesis of imino-C-di- and trisaccharides as hydrolytically stable glycomimetics

A new straightforward route to glycomimetics containing a piperidine unit is reported. The key step of the methodology is the intramolecular 1,3-dipolar cycloaddition of easily accessible glycosyl alkenyl nitrones. The reaction takes place in most cases with a complete selectivity in favor of the exo-exo adduct, which facilitates the synthesis of all-cis piperidines bearing the glycosyl units. The direct transformation of adducts into the final imino-C-di and trisaccharide analogues is achieved in one step using simple reagents. Inhibition properties against two glycosidases have been tested but no positive results have been found.