Issue 23, 1984

Interception of photochemical intermediate of thiazole derivatives. Formation and isomeristion of iminoazetine and azetinone intermediates

Abstract

Irradiation of 4-aminothiazolium salts (7) in the presence of tributylphosphine gave enaminonitriles 9) and benzoylacetonotrile (8) by isomerisation and hydration of the iminoazetine intermediates (11), while a similar irradiation of the mesoionic triphenylthiazolium-4-oate (1) gave the quinolinol (5) by isomerisation of the azetione intermediate (3).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1558-1559

Interception of photochemical intermediate of thiazole derivatives. Formation and isomeristion of iminoazetine and azetinone intermediates

H. Kato, K. Wakao, A. Yamada and M. Kojima, J. Chem. Soc., Chem. Commun., 1984, 1558 DOI: 10.1039/C39840001558

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