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- W2004501333 abstract "The rates and products of nitration of the title compounds have been measured. The quinoline derivatives react as their conjugate acids, but with 4-hydroxycinnoline the free base may be involved to some extent. Surprisingly large proportions of 1-methyl-3-nitro-4-quinolone are formed from 1-methyl-4-quinolone. The 4-substituents in the cations from 4-hydroxy- and 4-methoxy-quinoline activate C(6) by factors of 3·3 × 103 and 1·6 × 103, and C(8) by factors of 29·5 and 23, respectively, the large effect at C(6) being noteworthy." @default.
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- W2004501333 date "1971-01-01" @default.
- W2004501333 modified "2023-09-23" @default.
- W2004501333 title "Heteroaromatic reactivity. Part VI. Kinetics and products of the nitration of 4-hydroxyquinoline, 1-methyl-4-quinolone, 4-methoxyquinoline, and 4-hydroxycinnoline in sulphuric acid" @default.
- W2004501333 doi "https://doi.org/10.1039/j29710001493" @default.
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