1384985-99-2

Upstream product

• 162920-12-9 C₁₆H₂₁NO₅ 
• 1730-25-2 allylmagnesium bromide 

Downstream Products

• 1384986-06-4 (S,E)-N-benzylidene-1-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)but-3-en-1-amine oxide 
• 1384986-43-9 (2S,4R,6R)-2-((3aS,4R,6S,6aS)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-6-phenylpiperidin-4-ol 
• 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

Intramolecular 1,3-dipolar cycloaddition of N-alkenyl nitrones en route to glycosyl piperidines

Stereoselective intramolecular 1,3-dipolar cycloaddition of homochiral N-(alkenylglycosyl)nitrones, prepared by allylation of C-(glycosyl)nitrones and subsequent oxidation, is described. The previously described 2-aza-Cope rearrangement was not observed f