Abstract
A convenient procedure for modification of β-enaminones by α-C-acylation and subsequent
acidic cleavage is described. The unsymmetrical β-enamino ketones obtained in this
way could be hydrolyzed to provide an entry towards various unsymmetrical 1,3-diketones.
Key words
enaminones - C-acylation - cleavage - 1,3-diketones - unsymmetrical
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