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Issue 6, 1979
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Cyclohexadienone photochemistry: chemical trapping and stereochemistry of the type A zwitterion

Abstract

Irradiation of 4-methyl-4-trichloromethylcyclohexa-2,5-dienone in the presence of cyclopentadiene gives two 1:1 adducts whose structures demonstrate the intermediacy of the type A zwitterion and whose stereochemistry shows that the walk rearrangement to the lumiketone proceeds with inversion of configuration.

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Article type: Paper
DOI: 10.1039/C39790000275
Citation: J. Chem. Soc., Chem. Commun., 1979,0, 275-276
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    Cyclohexadienone photochemistry: chemical trapping and stereochemistry of the type A zwitterion

    C. J. Samuel, J. Chem. Soc., Chem. Commun., 1979, 0, 275
    DOI: 10.1039/C39790000275

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