Abstract
The cyclization of N-alkylated (arylated) α-ureidocarboxylic acids gives a series of 3-mono- and 3,5-disubstituted hydantoins, and nitrosation of the latter yields their nitroso derivatives. The rotational isomerism of 3-(α-naphthyl)hydantoins has been studied by PMR spectroscopy.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1404–1406, October,
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1404–1406, October,
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Klimavichyus, K.A.V., Lutsenko, V.V., Paulauskaite, G.V. et al. Synthesis and nitrosation of 3- and 3,5-substituted hydantoins. Chem Heterocycl Compd 20, 1160–1162 (1984). https://doi.org/10.1007/BF00503612
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DOI: https://doi.org/10.1007/BF00503612