Issue 5, 1977
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

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

Derek H. R. Barton,   Steven V. Ley,   Philip D. Magnus  and  Moshe N. Rosenfeld  

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

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Article information

DOI
https://doi.org/10.1039/P19770000567
Article type
Paper

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

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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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