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Vinylation of pyrroles in dimethyl sulfoxide

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A number of 1-vinylpyrroles were obtained in up to 97% yields by base-catalyzed addition of substituted pyrroles to acetylene in dimethyl sulfoxide at 80–100°C.

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Literature cited

  1. P. Waculik, The Chemistry of Monomers [Russian translation], Inostr. Lit., Moscow (1960).

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  2. M. F. Shostakovskii, G. G. Skvortsova, and E. S. Domnina, Usp. Khim., 38, 892 (1969).

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  3. B. A. Trofimov, A. I. Mikhaleva, G. A. Kalabin, and A. S. Atavin, Summaries of Papers Presented at the Fourth All-Union Colloquium on the Chemistry and Pharmacology of Indole Compounds [in Russian], Kishinev (1975), p. 24.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 213–214, February, 1977.

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Trofimov, B.A., Mikhaleva, A.I., Korostova, S.E. et al. Vinylation of pyrroles in dimethyl sulfoxide. Chem Heterocycl Compd 13, 170–171 (1977). https://doi.org/10.1007/BF00497870

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  • DOI: https://doi.org/10.1007/BF00497870

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