Abstract
It is demonstrated that, depending on the position of the acetyl substituent in the furan ring of benzofuran, the Schmidt rearrangement leads to benzofuran-2-carboxylic acid methylamide or to 3-acetamidobenzofuran derivatives.
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See [1] for communication II.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1040–1042, August, 1977.
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Trofimov, F.A., Shevchenko, L.I., Mukhanova, T.I. et al. Research on 2-acyl-3-aminobenzofurans. Chem Heterocycl Compd 13, 835–837 (1977). https://doi.org/10.1007/BF00488902
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DOI: https://doi.org/10.1007/BF00488902