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Issue 0, 1968
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Azabenzocycloheptenones. Part VII. The chemistry of some bromobenz[b]azepines and the syntheis of an azatropone dimer

Abstract

Transformations, particularly debromination and hydrolysis of 4,4,7,9-tetrabromo-2,3,4,5-tetrahydrobenz[b]-azepin-5-one are described. While various new compounds are reported, attempts at dehydrogenation have been generally unsuccessful except that 2,3-dihydro-1-N-toluene-p-sulphonylbenz[b]azepin-3-one gave an azatropone dimer on treatment with sodium hydride in tetrahydrofuran.

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Article type: Paper
DOI: 10.1039/J39680001280
Citation: J. Chem. Soc. C, 1968,0, 1280-1284
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    Azabenzocycloheptenones. Part VII. The chemistry of some bromobenz[b]azepines and the syntheis of an azatropone dimer

    E. D. Hannah, W. C. Peaston and G. R. Proctor, J. Chem. Soc. C, 1968, 0, 1280
    DOI: 10.1039/J39680001280

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