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Issue 18, 1974
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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.

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Article type: Paper
DOI: 10.1039/C39740000738
Citation: J. Chem. Soc., Chem. Commun., 1974,0, 738-739
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    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, 0, 738
    DOI: 10.1039/C39740000738

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