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Issue 8, 1999
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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.

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Article information


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

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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