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Dimerization of 2-hydroxybenzindolequinones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It is shown that the decarboxylation of 2-hydroxybenz[f]indolequinone-3-carboxylic acids and the demethylation of 2-methoxybenz[f]indolequinone are accompanied by oxidative dimerization and lead to the 3,3′-dimers of 2-hydroxybenz[f]indolequinones.

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Literature cited

  1. Z. Kitasato and C. Sone, Bull. Chem. Soc. Jpn., 5, 348 (1930).

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  2. B. V. Salov and A. I. Shakhnovich, Khim. Geterotsikl. Soedin., No. 7, 911 (1976).

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  3. J. Bourdais, A. Deberly, and C. Mahieu, French Patent No. 1529901 (1968); Chem. Abstr., 71, 70492 (1969).

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Authors and Affiliations

  1. Scientific-Research Institute of Organic Intermediates and Dyes, 103787, Moscow

    A. I. Shakhnovich, B. V. Salov & M. V. Gorelik

Authors
  1. A. I. Shakhnovich
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  2. B. V. Salov
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  3. M. V. Gorelik
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1636–1641, December, 1978.

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Shakhnovich, A.I., Salov, B.V. & Gorelik, M.V. Dimerization of 2-hydroxybenzindolequinones. Chem Heterocycl Compd 14, 1329–1333 (1978). https://doi.org/10.1007/BF00487400

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  • DOI: https://doi.org/10.1007/BF00487400

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