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- W2013071811 abstract "4,6-Dibromoresorcinol dimethyl ether has been converted into 4,6-dihydroxyisophthalaldehyde (11) by lithium–bromine interchange, formylation, and demethylation. Similarly the 5-methyl and 5-methoxy-derivatives were prepared, all in good overall yields. Three dioxa-anthracenediones have been prepared from the isophthalaldehydes. Low-temperature lithium–bromine interchange, formylation, and selective demethylation provided a route to 5-bromo-3,4-dimethoxysalicylaldehyde (14), which has potential as an intermediate for the synthesis of oxygen heterocycles." @default.
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- W2013071811 date "1970-01-01" @default.
- W2013071811 modified "2023-09-23" @default.
- W2013071811 title "Synthesis of 4,6-dihydroxyisophthalaldehyde and the 5-methyl and 5-methoxy-derivatives" @default.
- W2013071811 doi "https://doi.org/10.1039/j39700000227" @default.
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