Issue 6, 1994

Highly stereoselective synthesis of αβ-unsaturated ketones by CeCl3 mediated addition of grignard reagents to β-enamino ketones

Abstract

A stereoselective synthesis of αβ-unsaturated ketones by direct addition of Grignard reagents to β-enamino ketones, mediated by dry cerium(III) chloride, is described and a trans relationship between the introduced framework and the carbonyl group is predominantly observed.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 715-716

Highly stereoselective synthesis of αβ-unsaturated ketones by CeCl3 mediated addition of grignard reagents to β-enamino ketones

G. Bartoli, C. Cimarelli, E. Marcantoni, G. Palmieri and M. Petrini, J. Chem. Soc., Chem. Commun., 1994, 715 DOI: 10.1039/C39940000715

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