Issue 18, 1992

N-(2-phenylprop-1-enyl)proline methyl ester: equilibrium between the enamine and the aza methine ylide form

Abstract

The title compound reacted with nitroolefins to give either cyclobutanes or pyrrolizidine derivatives, depending on whether it acted as an enamine or as a 1,3-dipole.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1992, 2331-2335

N-(2-phenylprop-1-enyl)proline methyl ester: equilibrium between the enamine and the aza methine ylide form

F. Felluga, P. Nitti, G. Pitacco and E. Valentin, J. Chem. Soc., Perkin Trans. 1, 1992, 2331 DOI: 10.1039/P19920002331

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