Rearrangement of α-Aminoketones during Clemmensen Reduction. V. Influence of Alkyl Substitution on the α-Carbon1, 2, 3

NJ Leonard, E Barthel Jr

Index: Leonard; Barthel Journal of the American Chemical Society, 1950 , vol. 72, p. 3632,3635

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Citation Number: 14

Abstract

I 11 kylene gr0up.~ 1~ In order to determine the influence, if any, of a-alkyl substitution on the course of the Clemmensen reduction of a-aminoketones, a series of 1-methyl-3- piperidones has been studied in which the a-carbon was unsubstituted, monoalkyl- substituted, and dialkyl-substituted. The Clemmensen reduction of all of these six-membered ring compounds was found to be accompanied by rearrangement, with the formation of ...

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