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Issue 3, 1991
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Application of electrophile-mediated cyclisations to the synthesis of the hexahydroazepine ring system

Abstract

Allenic oxime 6 undergoes efficient AgI-catalysed cyclisation to give the hexahydroazepine-based nitrone 7; this reactive 1,3-dipole was subsequently trapped by styrene and N-methylmalemide to give the adducts 8 and 9 respectively.

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Article type: Paper
DOI: 10.1039/P19910000659
Citation: J. Chem. Soc., Perkin Trans. 1, 1991,0, 659-660
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    Application of electrophile-mediated cyclisations to the synthesis of the hexahydroazepine ring system

    R. Shaw, D. Lathbury, M. Anderson and T. Gallagher, J. Chem. Soc., Perkin Trans. 1, 1991, 0, 659
    DOI: 10.1039/P19910000659

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