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Azaheterocycles based on 1,5-diketones, cyclic β-ketols, and ethanolamine

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The peculiarities of the hydroxyethylamination of 1,5-diketones and three-ring β-ketols under heterogeneous-catalysis conditions as a function of the type of carbonyl compound were ascertained. Catalytic hydroxyethylamination is a convenient preparative method for the production of N-β-hydroxyethyl derivatives of 2,3,5,6-dicycloalkanopiperidines and 9-substituted perhydroacridines.

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Literature cited

  1. V. G. Kharchenko, A. P. Kriven'ko, O. V. Fedotova, and T. G. Nikolaeva, Khim. Geterotsikl. Soedin., No. 7, 944 (1982).

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Authors and Affiliations

  1. N. G. Chernyshevskii Saratov State University, 410601, Saratov

    T. G. Nikolaeva, P. V. Reshetov, A. P. Kriven'ko & V. G. Kharchenko

Authors
  1. T. G. Nikolaeva
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  2. P. V. Reshetov
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  3. A. P. Kriven'ko
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  4. V. G. Kharchenko
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1370–1372, October, 1983.

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Nikolaeva, T.G., Reshetov, P.V., Kriven'ko, A.P. et al. Azaheterocycles based on 1,5-diketones, cyclic β-ketols, and ethanolamine. Chem Heterocycl Compd 19, 1090–1093 (1983). https://doi.org/10.1007/BF00505762

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  • DOI: https://doi.org/10.1007/BF00505762

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