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2, 9 -Di (carbohydrazide)-1 H, IOH-benzo[elpyrrolo[3, 2-g]indole and 2, 9-di (carbohydrazide)-3H, 8H-indolo[4, 5-e]indole have been prepared. Nitrosation of the dihydrazides has been effected. The aryl azides do not undergo the curtius rearrangment.
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Sh. A. Samsoniya, N. N. Ovsyannikov, and N. N. Suvorov, Khim. Geterotsikl. Soedin, No. 1, 40 1994.
Sh. A. Samsoniya, M. V. Trapaidze, N. A. Kuprashvili, A. M. Kolesnikov, and N. N. Suvorov, Khim. Geterotsikl. Soedin., No. 9, 1222 (1985).
Sh. A. Samsoniya, M. V. Trapaidze, S. V. Dolidze, N. A. Ésakiya, N. N. Suvorov, A. M. Kolesnikov, and F. A. Mikhailenko, Khim. Geterotsikl. Soedin., No. 3, 352 (1984).
N. N. Suvorov, V. S. Velezheva, A. N. Yarosh, Yu. V. Erofeev, and T. N. Kozik, Khim. Geterotsikl. Soedin., No. 8, 1099 (1975).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1048-1051, August, 1994.
Communication 33, see [1].
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Samsoniya, S.A., Trapaidze, M.V., Kuprashvili, N.A. et al. Bisindoles 34. Preparation and reactions of dehydrazides of the benzo[e]pyrrolo[3,8-g]-indole and indolo[4,5-e]indole series. Chem Heterocycl Compd 30, 901–904 (1994). https://doi.org/10.1007/BF01165027
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DOI: https://doi.org/10.1007/BF01165027