The Chemistry of 5-Oxodihydroisoxazoles. II. Photolysis and Pyrolysis of 2-(Isoquinolin-1-yl)-3-methyl-5-oxo-2, 5-dihydroisoxazole-4-carboxylate

Yogendra Singh, Rolf H. Prager

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    31 Citations (Scopus)

    Abstract

    Photolysis of ethyl 2-(isoquinolin-l-yl)-3-methyl-5-oxo-2, 5-dihydroisoxazol4carbolaotcecurs by two pathways. The major pathway involves the loss of COz to form an imino carbene which may cyclize to form the expected (6) or rearranged (8) imidazo[2, 1-a]isoquinolineso r react with nucleophiles and recyclize to form the 4-oxopyrimido[2, 1-alisoquinolinesT. he minor pathway involves electrocyclic ring opening of the isoxazolone and ring closure with or without loss of CO. Pyrolysis leads predominantly to an imino carbene which reacts intramolecularly to give (6) or undergoes insertion into CH bonds.

    Original languageEnglish
    Pages (from-to)1811-1823
    Number of pages13
    JournalAustralian Journal of Chemistry
    Volume45
    Issue number11
    DOIs
    Publication statusPublished - 1992

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