Abstract
A number of thienylmercaptoethynyl alcohols, which were oxidized to the corresponding ketones, were synthesized via the Iotsich reaction of thiophene-2-aldehyde with mercaptoethynyl ethers. On reaction with hydrazine the ketones undergo intramolecular cyclization to form substituted pyrazoles. The IR spectra of the compounds obtained are discussed.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 33–36, January, 1971.
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Nakhmanovich, A.S., Deryagina, é.N. Synthesis and some transformations of secondary mercaptoethynyl alcohols and ketones of the thiophene series. Chem Heterocycl Compd 7, 30–32 (1971). https://doi.org/10.1007/BF00477941
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DOI: https://doi.org/10.1007/BF00477941