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- W2016089329 abstract "5-Hydroxy-2-methylnaphtho[1,2-b]furan (I; R = H) was obtained by decarboxylation of its 3-carboxylic acid. Treated with a number of one-electron oxidants, it underwent attack ortho to the hydroxy-group, generally giving rise to the corresponding ortho-quinone (II) but in the case of lead tetra-acetate yielding the related gem-diacetate (III). Treated with sodium in ethanol, it was reduced in the unsubstituted benzenoid ring, forming the 6,9-dihydro-derivative (IV). Oxidation or reduction of the furan ring was not observed." @default.
- W2016089329 created "2016-06-24" @default.
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- W2016089329 date "1967-01-01" @default.
- W2016089329 modified "2023-09-26" @default.
- W2016089329 title "Oxidation and reduction of 5-hydroxy-2-methylnaphtho[1,2-b]furan" @default.
- W2016089329 doi "https://doi.org/10.1039/j39670002126" @default.
- W2016089329 hasPublicationYear "1967" @default.
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