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Wiley, Journal of Physical Organic Chemistry, 9(17), p. 787-792, 2004

DOI: 10.1002/poc.795

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Stereochemical studies by molecular palpation

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

The conformational equilibrium of cyclohexanol was investigated by 129X NMR spectroscopy. While the classical NMR approach focuses on a carbon or proton atom belonging to the molecule under investigation, in our 129Xe NMR methodology we use the xenon atom as an external spy. Xenon is able to monitor the interconversion between the: axial and the equatorial isomers of cyclohexanol. The conformational equilibrium constant was estimated and is in excellent agreement with the values obtained by 1H and 13C NMR. ©2004 John Wiley & Sons, Ltd. ; SCOPUS: cp.j ; info:eu-repo/semantics/published