Experiments on the synthesis of tetracycline. Part 15. Oxidation of phenols and ring A model phenols to o-hydroxy-dienones with benzeneseleninic anhydride
- 1 January 1977
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 5,p. 567-572
- https://doi.org/10.1039/p19770000567
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 productsThis publication has 2 references indexed in Scilit:
- Experiments on the synthesis of tetracycline. Part XIV. Closure of ring B by base-catalysed photocyclisationJournal of the Chemical Society, Perkin Transactions 1, 1976
- New Methods of Preparative Organic Chmistry IV. Syntheses Using Heterocyclic Amides (Azolides)Angewandte Chemie International Edition in English, 1962