Issue 4, 1974

Unusual alkyl group directing effects during cyclopropane ring hydrogenolysis

Abstract

2-endo-Alkylnorbornanes are the kinetically preferred products of vapour phase hydrogenolysis of 2-methyl- and 2-cyclohexyl-nortricyclenes (1; R = Me and C6H11) over supported Pt and Pd catalysts, whereas 7-alkylnorbornanes predominate for reactions in acetic acid solutions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 155-156

Unusual alkyl group directing effects during cyclopropane ring hydrogenolysis

M. N. Akhtar, W. R. Jackson, J. J. Rooney and N. G. Samman, J. Chem. Soc., Chem. Commun., 1974, 155 DOI: 10.1039/C39740000155

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