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Oxidative reactions of azines. 2.* Synthesis and molecular structure of 3,4-dihydroxy-1-methyl-2-oxo-4-(γ-pyridyl)piperidine

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The oxidative ketodihydroxylation of a 1,2,3,6-tetrahydropyridine is reported. Using PMR and x-ray structured analysis, the product was shown to be 3,4-dihydroxy-1-methyl-2-oxo-4-(γ-pyridyl)piperidine.

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References

  1. A. T. Soldatenkov, I. A. Bekro, Zh. A. Mamyrbekova, S. A. Soldatova, A. Temesgen, N. D. Sergeeva, L. N. Kuleshova, and V. N. Khrustalev, Khim. Geterotsikl. Soedin., No. 2, 222 (1996).

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Authors
  1. I. A. Bekro
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  2. A. T. Soldatenkov
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  3. A. I. Stash
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  4. N. Yu. Chernikova
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  5. A. I. Chernyshev
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Additional information

For communications 1, see [1].

Russian University of National Friendship, Moscow 117198. L. Ya. Karpov Physicochemical Science Research Institute, Moscow 103603. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1372–1375, October, 1996. Original article submitted June 20, 1996.

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Bekro, I.A., Soldatenkov, A.T., Stash, A.I. et al. Oxidative reactions of azines. 2.* Synthesis and molecular structure of 3,4-dihydroxy-1-methyl-2-oxo-4-(γ-pyridyl)piperidine. Chem Heterocycl Compd 32, 1178–1181 (1996). https://doi.org/10.1007/BF01169230

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  • DOI: https://doi.org/10.1007/BF01169230

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