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- W2334320562 abstract "The preparation, and rearrangement in 92% sulfuric acid, of 4-X-2-nitramino- (1), 2-X-4-nitramino-(2), and 6-X-2-nitramino-pyridines (3) is reported (X = H, Me, MeO, Br, Cl, CO2H). The product isomer ratios can be explained by differential electronic stabilization of the appropriate a complexes for aromatic nitration and steric effects seem relatively unimportant. Deuteration [3-D in series (1), X = Me] had no effect on the product distribution." @default.
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- W2334320562 date "1982-01-01" @default.
- W2334320562 modified "2023-10-18" @default.
- W2334320562 title "Substituent effects on the isomer ratios in the rearrangement of some 2- and 4-nitraminopyridines" @default.
- W2334320562 doi "https://doi.org/10.1071/ch9822025" @default.
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