A novel route to arylacetones via a masked α-acylcarbonium intermediate

S Shatzmiller, R Lidor, E Shalon…

Index: Shatzmiller, Shimon; Lidor, Ramy; Shalom, Eytan; Bahar, Eliezer Journal of the Chemical Society, Chemical Communications, 1984 , # 12 p. 795 - 796

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Abstract

Oxime ethers can be efficiently metallated at the a-carbon communication we describe a method for the conversion of atoms and the derived enolate equivalents (1) can then oxime ethers into functionalized ketones using reactive participate in a variety of useful carbon- carbon bond-forming intermediates of type (1) or (2), employing acetone O-methylreactions. 1 The &-carbon atom might also support a positive oxime as a model compound. charge [ ...

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