Abstract
The nucleophilic addition-cleavage reactions of 3,8-diformyl-1H,6H-pyrrolo[2,3-e] indole were studied. It is shown that monosubstitution products are primarily formed in the condensation with CH acids (nitroethane, acetone, and malonic and barbituric acids) and aniline.
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See [1] for Communication 6.
Translated from Khimiya Geterotsiklicheskikh Soedineni, No. 5, pp. 608–612, May, 1983.
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Dolidze, S.V., Samsoniya, S.A. & Suvorov, N.N. Pyrroloindoles. 7. Condensation on the basis of 3,8-diformyl-1H,6H-pyrrolo[2,3-e]indole. Chem Heterocycl Compd 19, 488–492 (1983). https://doi.org/10.1007/BF00514455
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DOI: https://doi.org/10.1007/BF00514455