Issue 4, 1972

Protonation of (cyclohexadiene)(cyclopentadienyl)rhodium(I). Evidence for endo-proton addition

Abstract

The protonation of (cyclohexadiene)(cyclopentadienyl)rhodium(I), has been shown to proceed with metal–hydrogen interaction via a π-allylic cation to yield the endo-substituted product; the stereochemistry of the product has been established by deuteriation, coupled with studies on trityl and hydride ion attack on the diene and dienyl salt, respectively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 235-236

Protonation of (cyclohexadiene)(cyclopentadienyl)rhodium(I). Evidence for endo-proton addition

B. F. G. Johnson, J. Lewis and D. Yarrow, J. Chem. Soc., Chem. Commun., 1972, 235 DOI: 10.1039/C39720000235

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