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Formation of derivatives of 5,6-dihydro-1,3-thiazines in the reaction of acetothioacetic acid ethyl ester under the conditions of the Hantzsch synthesis

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Derivatives of 2H-5,6-dihydro-1,3-thiazine are formed by the reaction of acetothioacetic acid ethyl ester with aromatic aldehydes on heating in ethanol in the presence of aqueous ammonia.

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Latvian Institute of Organic Chemistry, Riga LV-1006, Latvia; e-amil: arcady@osi.lv. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 978–985, July, 2000.

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Vigante, B., Ozols, J., Mishnev, A. et al. Formation of derivatives of 5,6-dihydro-1,3-thiazines in the reaction of acetothioacetic acid ethyl ester under the conditions of the Hantzsch synthesis. Chem Heterocycl Compd 36, 862–869 (2000). https://doi.org/10.1007/BF02256924

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  • DOI: https://doi.org/10.1007/BF02256924

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