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- W2006252196 abstract "Kinetic criteria show that the nitration of 3,5-dimethoxypyridine proceeds on the conjugate acid species in the 2-position, and that the 6-nitration of 3,5-dimethoxy-2-nitropyridine occurs on the free base. Relative reactivities are compared with the corresponding benzenoid compounds. A set of rules is proposed for the nitration of substituted pyridines and their synthetic applications discussed." @default.
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- W2006252196 date "1967-01-01" @default.
- W2006252196 modified "2023-09-26" @default.
- W2006252196 title "The mechanism of the electrophilic substitution of heteroaromatic compounds. Part VII. The nitration of pyridines in the α-position and rules for the nitration of substituted pyridines" @default.
- W2006252196 doi "https://doi.org/10.1039/j29670001211" @default.
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