Abstract
An assumption regarding the existence of a homoconjugation effect involving enaminoketo and phenyl groups as a result of the drawing together in space of their π orbitals was made on the basis of circular dichroism (CD) data and an examination of the preferred conformations of two-ring enamino ketones with α-phenylethyl and α-benzylethyl substituents. A study of enamino ketones with a chiral alkyl substituent attached to the nitrogen atom made it possible to confirm this assumption.
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