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Conclusion

  1. 1.

    In the series of chlorides of zinc, aluminum, iron(III), nickel(II), and cobalt(II), zinc chloride is the most active and selective reagent for stoichiometric indolization of phenylhydrazones in the liquid phase.

  2. 2.

    In the presence of laminar graphite compounds, indolization of phenylhydrazones with zinc chloride has a catalytic character.

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1585–1589, July, 1984.

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Zamyshlyaeva, L.I., Fomin, O.A., Kvacheva, L.D. et al. Fischer liquid-phase cyclization of arylhydrazones. Russ Chem Bull 33, 1455–1458 (1984). https://doi.org/10.1007/BF00956525

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  • DOI: https://doi.org/10.1007/BF00956525

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