Abstract
Methods for the synthesis of isomeric thienothiophenes by cyclization of methyl γ-thienylmercaptoacetoacetates in polyphosphoric acid (PPA) were developed. It is shown that the acylation of the acetonyl derivaties of isomeric thienothiophenes in an aliphatic acid anhydride—70% perchloric acid system leads to the corresponding pyrylium salts. Some reactions of the latter with nucleophilic reagents were studied. The structures of the substance obtained were confirmed by the IR and PMR spectra.
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Translated from Khimiya Geterotsiklicheskikh Soedinenoi, No. 1, pp. 37–41, January, 1983.
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Dulenko, V.I., Tolkunov, S.V. & Alekseev, N.N. Synthesis and reactions of thieno[2′,3′:5,4]thieno [2,3-c]- and thieno[2′,3′:4,5]thieno[2,3-c]pyrylium salts. Chem Heterocycl Compd 19, 32–37 (1983). https://doi.org/10.1007/BF00512810
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DOI: https://doi.org/10.1007/BF00512810