Enamines of several ketones having phenyl groups at the α or β positions have been deprotonated to give allylic anions which are reactive nucleophiles; treatment of these intermediates with methyl iodide has led to high yields of methylated ketones.
H. W. Thompson and B. S. Huegi, J. Chem. Soc., Chem. Commun., 1973, 636 DOI: 10.1039/C39730000636
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