Abstract
We have studied the reaction of 1-vinyl-2-(2-furyl)- and -(2-thienyl)pyrroles with trifluoroacetic anhydride, with hydrogen in the presence of catalysts (Raney nickel, palladium black, palladous chloride), with propargyl alcohol in electrophilic conditions [catalysis by perfluorobutyric acid in the system azoisobutyrodinitrile (AIBN)-CCl4), and with alkane thiols with AIBN initiation. The products are novel substituted hetarylpyrroles.
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See [1] for Communication 40.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 337–342, March, 1991.
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Korostova, S.E., Nesterenko, R.N., Mikhaleva, A.I. et al. Pyrroles from ketoximes and acetylene. 41. Some reactions of 1-vinyl-2-(2-furyl)- and-(2-thienyl)pyrroles. Chem Heterocycl Compd 27, 273–278 (1991). https://doi.org/10.1007/BF00474228
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DOI: https://doi.org/10.1007/BF00474228