Abstract
The reaction of benzothiazolin- and benzooxazolin-2-thiones with acrylonitrile, acrylamide, and methylacrylate under conditions of acid catalysis takes place at the sulfur atom. The formation of minor amounts of N-derivatives is attributed to isomerization of the principal reaction products.
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Deceased.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 554–557, April, 1986.
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Anan'eva, K.V., Rozhkov, N.K. Benzazolin-2-thiones in the michael reaction. 1. Reaction of benzothiazolin- and benzoxazolin-2-thiones with acrylonitrile, acrylamide, and methylacrylate in the presence of acid catalysts. Chem Heterocycl Compd 22, 456–459 (1986). https://doi.org/10.1007/BF00542791
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DOI: https://doi.org/10.1007/BF00542791