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Issue 1, 1970
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The mechanism of the thermal rearrangement of 1-substituted 1H-azepines to 6-aminofulvenes

Abstract

Thermal rearrangement of the fully-substituted azepine (VII) yields a 1,1-disubstituted cyclopentadiene (VIII): such compounds are considered to be intermediates in the thermal rearrangement of 1-substituted 1H-azepines to fulvanes where a subsequent [1,5]-sigmatropic rearrangement of the ketone-imine group is also involved.

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Article type: Paper
DOI: 10.1039/C29700000010
Citation: J. Chem. Soc. D, 1970,0, 10-10
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    The mechanism of the thermal rearrangement of 1-substituted 1H-azepines to 6-aminofulvenes

    M. Mahendran and A. W. Johnson, J. Chem. Soc. D, 1970, 0, 10
    DOI: 10.1039/C29700000010

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