Abstract
A number of 2-formyl-3-hydroxybenzo[b]selenophene anils and their derivatives, which model the individual tautometic forms, were synthesized. A ketone—amine structure was assigned to the anils as a result of physicochemical investigation.
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Communication XIX from the series “Benzoid—Quinoid Tautomerism of Azomethines and Their Structural Analogs.” See [1] for communication XVIII.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 781–783, June, 1975.
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Minkin, Z.I., Bren', V.A. & Palui, G.D. Synthesis and structure of 2-formyl-3-hydroxybenzo[b]-selenophene anils. Chem Heterocycl Compd 11, 679–681 (1975). https://doi.org/10.1007/BF00959960
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DOI: https://doi.org/10.1007/BF00959960