Organocatalytic Asymmetric Synthesis of β??Aryl?螃漫?isocyano Esters
F Morana, A Basso, M Bella, R Riva…
Index: Morana, Fabio; Basso, Andrea; Bella, Marco; Riva, Renata; Banfi, Luca Advanced Synthesis and Catalysis, 2012 , vol. 354, # 11-12 p. 2199 - 2210
Full Text: HTML
Citation Number: 7
Abstract
Abstract The asymmetric addition of malonates to in situ generated N-formylimines of aromatic aldehydes was achieved under phase-transfer catalysis using Cinchona alkaloids- derived quaternary ammonium salts. The resulting β-formamidomalonates have been efficiently converted into β-aryl-β-isocyano esters. Their utility in the multicomponent Ugi reaction with chiral cyclic imines has been demonstrated.
Related Articles:
[Sisko, Joseph; Mellinger, Mark; Sheldrake, Peter W.; Baine, Neil H. Tetrahedron Letters, 1996 , vol. 37, # 45 p. 8113 - 8116]
[van Leusen,A.M. et al. Journal of Organic Chemistry, 1977 , vol. 42, # 7 p. 1153 - 1159]