Chemistry and spectroscopy in strongly acidic solutions. Part XXVI: Reduction of the norbornyl cation with molecular hydrogen. Ring opening of norbornane with protons
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/recl.19690880612/fullpdf
Reference8 articles.
1. A.F. Bickel C.J. Gaasbeek H. Hogeveen J.M. Oelderik J.C. Platteeuw Chem. Commun 1967 634
2. Chemistry and spectroscopy in strongly acidic solutions. Part XXIII: Reversible reaction between carbonium ions and hydrogen
3. Stable Carbonium Ions. X.1 Direct Nuclear Magnetic Resonance Observation of the 2-Norbornyl Cation
4. Adamantane: Consequences of the Diamondoid Structure
5. The Synthesis of Three Monodeuterionorbornanes, and the Stereochemistry of Acid-Catalyzed Cleavage of Nortricyclene
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1. The importance of orbital orientation as a rate-controlling factor in intramolecular reactions of carbonium ions;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. Rates of reduction of tertiary and secondary carbonium ions with molecular hydrogen;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
3. Chemistry and spectroscopy in strongly acidic solutions. Part XXXI: Rates of carbonylation of stabilized carbonium ions;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
4. Electrophilic Substitutions at Alkanes and in Alkylcarbonium Ions;Progress in Physical Organic Chemistry;2007-04-04
5. Nonclassical Carbocations;Topics in Current Chemistry;1984
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