Intramolecular Oxidative Coupling of Aromatic Compounds. I. Oxidation of Diphenolic Substrates
Autor: | AS Krauss, WC Taylor |
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Rok vydání: | 1991 |
Předmět: | |
Zdroj: | Australian Journal of Chemistry. 44:1307 |
ISSN: | 0004-9425 |
DOI: | 10.1071/ch9911307 |
Popis: | The synthesis of (2RS,3SR)-1-(3,5-dihydroxy-4-methoxyphenyl)-(4-hydroxy-3,5-dimethoxy-phenyl)-2,3-dimethylbutan-1-one (26) is described. Diphenolic oxidative coupling of (26) did not produce a eupodienone -type product. An aryltetralin derivative was formed instead by aryl-benzyl coupling and was further oxidized to the novel oxa spiro dienone (63). The acetoxy compound (71) derived by reduction of the carbonyl group in (26) gave a similar product (72). |
Databáze: | OpenAIRE |
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