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Imidazole derivatives bearing potentially labile groups on the n-atom

III. N-(β-Aminoethyl)- and N-(β-Hydroxyethyl)benzimidazoles, and their behavior toward sodamide. The mechanism of the Chichibabin reaction

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A number of N-aminoethyl-, N-hydroxyethyl-, and N-mercapto-ethylbenzimidazoles have been synthesized, and their behavior toward sodamide investigated. The influence of the basicity of the benzimidazoles on the course of the Chichibabin reaction is discussed.

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Authors and Affiliations

  1. Rostov on Don State University, USSR

    A. F. Pozharskii, A. M. Simonov, É. A. Zvezdina & V. A. Anisimova

Authors
  1. A. F. Pozharskii
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  2. A. M. Simonov
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  3. É. A. Zvezdina
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  4. V. A. Anisimova
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Additional information

For part II, see [20].

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Pozharskii, A.F., Simonov, A.M., Zvezdina, É.A. et al. Imidazole derivatives bearing potentially labile groups on the n-atom. Chem Heterocycl Compd 5, 645–648 (1969). https://doi.org/10.1007/BF00957380

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  • DOI: https://doi.org/10.1007/BF00957380

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