848651-19-4Relevant academic research and scientific papers
Highly diastereoselective synthesis of densely functionalized cyclopentanoids by intramolecular azomethine imine cycloadditions in sugar templates
Gallos, John K.,Koumbis, Alexandros E.,Apostolakis, Nicolaos E.
, p. 2457 - 2459 (2007/10/03)
Conversion of a sugar to a σ,ε-unsaturated aldehyde, and subsequent condensation of the aldehyde moiety with BnNHNHCO2Et, yields the respective azomethine imine intermediate dipole which adds intramolecularly to the existing double bond, thus generating a bicyclic adduct with high diastereoselectivity.
