Abstract
2-Piperidinomethylene-2H pyrrolo[l,2-a]indole-3,9-dione can readily react with substances having an. active methylene unit to form piperidinium salts which are converted to 2-vinyl pyrrolojl,2-a]indoles. They can also undergo O-methylation using dimethyl sulfate in polar and non polar solvents to form the 9-alkoxy derivatives.
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Additional information
Center for Medicinal Chemistry, All-Russian Science Research Chemico-Pharmaceutical Institute, Moscow 119021. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 781–792, June, 1994. Original article submitted June 22, 1994.
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Tugusheva, N.Z., Ryabova, S.Y., Solov'eva, N.P. et al. Synthesis, alkylation, and structural studies of 2-vinylpyrrolo[1,2-a]indoles. Chem Heterocycl Compd 30, 683–691 (1994). https://doi.org/10.1007/BF01166309
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DOI: https://doi.org/10.1007/BF01166309