Issue 18, 1974

Adamantanone: stereochemistry of its homoenolization as shown by 2H nuclear magnetic resonance

Abstract

With 2H n.m.r. spectroscopy, it is established that adamantanone undergoes homoenolization with predominant exo β-proton exchange under conditions comparable to those required for a v ariety of polycyclic ketones.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 738-739

Adamantanone: stereochemistry of its homoenolization as shown by 2H nuclear magnetic resonance

J. B. Stothers and C. T. Tan, J. Chem. Soc., Chem. Commun., 1974, 738 DOI: 10.1039/C39740000738

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