Issue 5, 1977

Experiments on the synthesis of tetracycline. Part 15. Oxidation of phenols and ring A model phenols to o-hydroxy-dienones with benzeneseleninic anhydride

Abstract

Benzeneseleninic anhydride has been used to oxidise simple alkylphenols and tetracycline ring A model phenols to hydroxy-dienones. The corresponding phenolate salts with benzeneseleninic anhydride give increased yields of o-hydroxylated products

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1977, 567-572

Experiments on the synthesis of tetracycline. Part 15. Oxidation of phenols and ring A model phenols to o-hydroxy-dienones with benzeneseleninic anhydride

D. H. R. Barton, S. V. Ley, P. D. Magnus and M. N. Rosenfeld, J. Chem. Soc., Perkin Trans. 1, 1977, 567 DOI: 10.1039/P19770000567

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