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New method of isolating N-substituted 3-aminomethylenethiol-4-en-2-ones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The methods for the synthesis of the little-studied N-substituted 3-aminomethylenethiol-4-en-2-ones (I) — thiophene analogs of aromatic o-hydroxyazomethines — are based on the application of the not readily accessible and labile hydroxy and methoxy derivatives of thiophene [1, 2].

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Literature cited

  1. P. Demerseman, J. P. Lechartier, A. Cheutin, M. J. Desvoe, and P. Royer, Compt. Rend.,254, 1652 (1962).

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  2. Ya. L. Gol'dfarb and M. A. Kalik, Khim. Geterotsikl. Soedin, No. 2, 178 (1971).

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  3. Ch. Grundmann and P. Grunanger, The Nitrile Oxides, Springer-Verlag, Berlin (1971), p. 122.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 854–855, June, 1986.

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Kalik, M.A., Gol'dfarb, Y.L. & Krayushkin, M.M. New method of isolating N-substituted 3-aminomethylenethiol-4-en-2-ones. Chem Heterocycl Compd 22, 679 (1986). https://doi.org/10.1007/BF00575257

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  • DOI: https://doi.org/10.1007/BF00575257

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