Abstract
Ammonium salts bearing but-2-ynyl and phenacyl or 2-(naphth-2-yl)-2-oxoethyl moieties at the nitrogen atom underwent Stevens rearrangement to form substituted furan-3-amines. Quaternization of the latter afforded appropriate iodomethylates.
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Original Russian Text © M.O. Manukyan, T.A. Sahakyan, A.Kh. Gyulnazaryan, A.V. Babakhanyan, N.S. Minasyan, K.S. Barseghyan, 2016, published in Zhurnal Obshchei Khimii, 2016, Vol. 86, No. 12, pp. 1956–1960.
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Manukyan, M.O., Sahakyan, T.A., Gyulnazaryan, A.K. et al. Stevens rearrangement of unsaturated ammonium salts. Synthesis of substituted furans. Russ J Gen Chem 86, 2594–2598 (2016). https://doi.org/10.1134/S1070363216120045
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DOI: https://doi.org/10.1134/S1070363216120045