Reaction of 1-tetralones with palladium-carbon

JM Springer, JM Springer, CW Hinman…

Index: Springer,J.M. et al. Journal of Organic Chemistry, 1971 , vol. 36, p. 686 - 689

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Citation Number: 4

Abstract

Dehydrogenation of cyclic ketones may lead to arenes or, with retention of oxygen, to phenolic compounds or neutral oxygen-containing condensation products. The nature of the dehydrogenation product is governed by the structure and stereochemistry, the type of dehydrogenating agent, the reaction temperature, the presence of hydrogen acceptor and/or sulfur compounds, and the solvent (if any).*