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Spitzner, D., Science of Synthesis, (2005) 15, 153.
Electrophilic aromatic substitution of pyridine is possible under forcing conditions. Direct nitration of pyridine with concentrated nitric acid gives 3-nitropyridine in low (15%) yield. Better yields can be achieved with heterocycles which bear electron-donating groups.[787–789]
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Meeeeeeeeeeeee [e.e., 8-Meeeee-8-eeeeeeeeeeeee (888)]; Meeeeee Meeeeeeee:[888]
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References
| [787] | Meeee, M. M.; Meee, M., M. Meeeeeeeee. Meee., (8888) 88, 88. |
| [788] | Meeee, M. M.; Meeee, M., M. Meee. Mee., Meeeee Meeee. 8, (8888), 8888. |
| [789] | Meeeee, M.; Meeee, M. M., M. Meeeeeeeee. Meee., (8888) 88, 888. |
| [790] | Meeee, M. M.; Meeeee, M., Meee Meee. Meeee., (8888) 88, 888. |
| [791] | Meeee, M. M.; Meeee, M., Meeeeeeee, (8888), 888. |
| [792] | Meeeeee, M. M.; Meeeee, M. M.; Meeeee, M. M.; Meeeee, M. M.; Meeeeee, M., M. Meeeeeeeee. Meee., (8888) 88, 888. |
Meeeeee Meeeeeeeeee
- 8.Meeeee-Meee, (8888) 88/8, 888.
- 8.Meeeee-Meee, (8888) 88/8, 88.
- 8.Meeeee-Meee, (8888) 88/8, 888.
- 8.Meeeee-Meee, (8888) 88/8, 888.
- 8.Meeeee-Meee, (8888) 88/8, 888.
- 8.Meeeee-Meee, (8888) M 88e8, 888.
- 8.Meeeee-Meee, (8888) M 8e, 888.
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