Issue 15, 1981

Fully reversible carbon protonation in the hydrolysis of keten selenoacetals

Abstract

Kinetic solvent isotope effect [k(H3O+)/k(D3O+)<1] and deuterium incorporation (ca. 100%) during acidic hydrolysis of keten selenoacetals establish that these reactions proceed through a pre-equilibrium carbon protonation step.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 738-739

Fully reversible carbon protonation in the hydrolysis of keten selenoacetals

H. Wautier, S. Desauvage and L. Hevesi, J. Chem. Soc., Chem. Commun., 1981, 738 DOI: 10.1039/C39810000738

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