Issue 18, 2017

Copper-catalysed enantioselective Michael addition of malonic esters to β-trifluoromethyl-α,β-unsaturated imines

Abstract

Copper triflate-BOX complexes catalyse the enantioselective conjugate addition of methyl malonate to β-trifluoromethyl-α,β-unsaturated imines to give the corresponding enamines bearing a trifluoromethylated stereogenic centre with good yields, and diastereo- and enantioselectivities. The usefulness of the method has been shown with the synthesis of optically active β-trifluoromethyl δ-amino esters and optically active trifluoromethyl piperidones.

Graphical abstract: Copper-catalysed enantioselective Michael addition of malonic esters to β-trifluoromethyl-α,β-unsaturated imines

Supplementary files

Article information

Article type
Communication
Submitted
09 Mar 2017
Accepted
06 Apr 2017
First published
06 Apr 2017

Org. Biomol. Chem., 2017,15, 3849-3853

Copper-catalysed enantioselective Michael addition of malonic esters to β-trifluoromethyl-α,β-unsaturated imines

M. Espinosa, J. Herrera, G. Blay, L. Cardona, M. C. Muñoz and J. R. Pedro, Org. Biomol. Chem., 2017, 15, 3849 DOI: 10.1039/C7OB00595D

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