The rearranged alcohol from the deamination of cyclohex-1-enylmethylamine is 2-methylenecyclohexanol, the product of an allylic rearrangement, and not the ring-expanded alcohol previously reported. An analogous reaction has been shown to take place with cyclohexa-1,4-dienylmethylamine.
K. S. J. Stapleford, J. Chem. Soc. C, 1971, 2580 DOI: 10.1039/J39710002580
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