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The aminomethylation of 2-nitro-3-hydroxpyridine

Conclusions

  1. 1.

    The aminomethylation of 2-nitro-3-hydroxypyridine has been studied.

  2. 2.

    On aminomethylation 2-nitro-3-hydroxypyridine forms 6-monosubstituted Mannich bases.

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Literature cited

  1. 1.

    H. Hellmann and G. Opitz,α-Aminoalkylierung, Verlag Chemie (1960).

  2. 2.

    L. D. Smirnov, V. P. Lezina, V. F. Bystrov, and K. M. Dyumaev, Izv. AN SSSR, Ser. Khim.,1965, 198.

  3. 3.

    K. M. Dyumaev, L. D. Smirnov, and V. F. Bystrov, Izv. AN SSSR, Otd. khim. n.,1962, 883; L. D. Smirnov, S. L. Or lova, V. P. Lezina, and K. M. Dyumaev, Izv. AN SSSR, Ser. Khim.1967, 1816. 2611

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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2742–2744, December, 1967.

The authors are grateful to N. M. Émanuel for his continuous interest in the work.

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Smirnov, L.D., Kartasheva, T.P., Lezina, V.P. et al. The aminomethylation of 2-nitro-3-hydroxpyridine. Russ Chem Bull 16, 2609–2611 (1967). https://doi.org/10.1007/BF00908508

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Keywords

  • Mannich Base