Issue 10, 1987

The first acid and ester enols: 2,2-bis(pentamethylphenyl)ethene-1,1-diol and 1-t-butoxy-2,2-bis(pentamethylphenyl)ethenol, and their oxidation to stable free radicals

Abstract

Desilylation of the ketene acetals (5) and (9) provides the ene-1,1-diols (6) and (10) which undergo relatively slow ketonisation and are oxidized to stable free radicals in basic solution.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 744-745

The first acid and ester enols: 2,2-bis(pentamethylphenyl)ethene-1,1-diol and 1-t-butoxy-2,2-bis(pentamethylphenyl)ethenol, and their oxidation to stable free radicals

P. O'Neill and A. F. Hegarty, J. Chem. Soc., Chem. Commun., 1987, 744 DOI: 10.1039/C39870000744

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