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Structural study of methyl 2,6-diphenyl-N-methyl-4-oxopiperidine-3,5-dicarboxylate enolic forms
Authors:M. J. Fern  ndez,J. M. Casares,E. G  lvez,J. Bellanato
Affiliation:M. J. Fernàndez,J. M. Casares,E. Gálvez,J. Bellanato
Abstract:The methyl 2,6-diphenyl-1-methyl-4-oxopiperidine-3,5-dicarboxylates 1 were synthesized by the Mannich procedure from methyl 3-oxoglutarate, benzaldehyde and methylamine. Keto-enol tautomerism as well as configurational isomerism at C-2 were observed. The stereochemistry of the Ib and Ic enolic forms were determined by 1H and 13C nmr data.
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