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Bisindoles 27. Electrophilic substitution reactions of 7,7-dichlorobis(5-indolyl)methanes

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Formylation, aminomethylation and acetylation have been studied as the most characteristic electrophilic substitution reactions of 7,7′-dichlorobis(5-indolyl)-methane and its diethyl ester.

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Literature Cited

  1. Dzh. Zegkhugkh, D. O. Kadzhrishvili, Sh. A. Samsoniya, N. N. Suvorov, and N. Z. Kedelashvili, Khim. Geterotsikl. Soedin., No. 8, 1062 (1988).

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  2. M. G. Cheshmaritashvili, Sh. A. Samsoniya, L. N. Kurkovskaya, and N. N. Suvorov, Khim. Geterotsikl. Soedin., No. 1, 73 (1984).

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  3. G. I. Zhungietu, V. A. Budilin, and A. N. Kost, Preparative Chemistry of Indole [in Russian], Shtiintsa, Kishinev (1975), p. 116.

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Authors and Affiliations

  1. I. Dzhavakhishvili State University, 380028, Tbilisi

    Dzh. Zegkhugkh, Sh. A. Samsoniya, D. O. Kadzhrishvili & L. M. Mamaladze

Authors
  1. Dzh. Zegkhugkh
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  2. Sh. A. Samsoniya
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  3. D. O. Kadzhrishvili
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  4. L. M. Mamaladze
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Additional information

For Communication 26 see [1].

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1363–1366, October, 1989.

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Zegkhugkh, D., Samsoniya, S.A., Kadzhrishvili, D.O. et al. Bisindoles 27. Electrophilic substitution reactions of 7,7-dichlorobis(5-indolyl)methanes. Chem Heterocycl Compd 25, 1140–1143 (1989). https://doi.org/10.1007/BF00470692

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  • DOI: https://doi.org/10.1007/BF00470692

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