Abstract
New 2,5-disubstituted 4-formylthiazoles have been obtained by the reaction of acetal-containing α-chloroxiranes or their rearrangement products, chloroketones, with thioamides and N-allylurea.
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References
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Additional information
Kazan' State Technological University, Kazan' 420015, Russia. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 124–129, January, 1998.
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Guseinov, F.I., Yudina, N.A. New routes for the synthesis of 2,5-disubstituted 4-formylthiazoles. Chem Heterocycl Compd 34, 115–120 (1998). https://doi.org/10.1007/BF02290623
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DOI: https://doi.org/10.1007/BF02290623