Abstract
Electrophilic substitutions of 2,7-dicarbethoy-1H,6H-pyrrolo[2,3-e]indole (Friedel-Crafts acylation, nitration, bromination) take place both at position 3 of the indole ring and at positions 5 and 8 in the benzene ring.
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References
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Additional information
For communication 15 see [1].
Iv. Dzhavakhishvili State University, Tbilisi 380028. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1197–1201, September, 1994. Original article submitted July 5, 1994.
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Lomadze, N.S., Chikvaidze, I.S., Targamadze, N.L. et al. Pyrroloindoles. 16. Some electrophilic substitution reactions of 2,7-dicarbethoxy-1H,6H-pyrrolo[2,3-e]indoles. Chem Heterocycl Compd 30, 1034–1038 (1994). https://doi.org/10.1007/BF01171158
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DOI: https://doi.org/10.1007/BF01171158