Issue 8, 1999

Rhodium promoted isomerisation of allylic alkoxides: a new method for enolate anion formation

Abstract

Transition metal mediated isomerisation of allylic alkoxides is presented as a new method for enolate anion generation. The scope and limitations of enolate formation with the catalysts [Rh(dppe)(THF)2]+ClO4 and (Ph3P)3RhCl are explored and the synthetic potential of the methodology demonstrated in the stereoselective formation and reactions of certain ketone and aldehyde enolates.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1999, 979-994

Rhodium promoted isomerisation of allylic alkoxides: a new method for enolate anion formation

L. J. Gazzard, W. B. Motherwell and D. A. Sandham, J. Chem. Soc., Perkin Trans. 1, 1999, 979 DOI: 10.1039/A901370I

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