Issue 2, 1985

Conformational dependence of the β-deuterium equilibrium isotope effect in acyclic carbocations. Suppression of hyperconjugation by restricted rotation in the 2,4,4,6-tetramethylheptyl cation

Abstract

Steric inhibition of hyperconjunction leads to suppression of the equilibrium isotope effect which in turn is used to assign conformations of acyclic carbocations in solution.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 76-78

Conformational dependence of the β-deuterium equilibrium isotope effect in acyclic carbocations. Suppression of hyperconjugation by restricted rotation in the 2,4,4,6-tetramethylheptyl cation

H. Siehl and H. Walter, J. Chem. Soc., Chem. Commun., 1985, 76 DOI: 10.1039/C39850000076

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