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N1-(2-furoylmethyl) and N1-(5-nitro-2- furoylmethyl) derivatives of uracil and its 5-substituted derivatives

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The corresponding N1-(2-furoylmethyl) and N1-(5-nitro-2-furoylmethyl) derivatives of uracil and its 5-substituted derivatives were obtained by the reaction of 2-bromo- and 5-nitro-2-bromoacetylfurans with uracil, 5-fluorouracil, and thymine. The structures of these compounds as N1-substituted uracils were proved by a study of the UV spectra at various pH values. The computational method of expanding the UV spectra into individual bands was used.

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Authors and Affiliations

  1. Institute of Organic Synthesis, Academy of Sciences of the Latvian SSR, Riga

    S. A. Giller, A. Ya. Perkone, I. N. Getsova, A. B. Rozenblit & V. E. Golender

Authors
  1. S. A. Giller
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  2. A. Ya. Perkone
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  3. I. N. Getsova
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  4. A. B. Rozenblit
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  5. V. E. Golender
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1268–1270, September, 1971.

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Giller, S.A., Perkone, A.Y., Getsova, I.N. et al. N1-(2-furoylmethyl) and N1-(5-nitro-2- furoylmethyl) derivatives of uracil and its 5-substituted derivatives. Chem Heterocycl Compd 7, 1191–1193 (1971). https://doi.org/10.1007/BF00510035

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  • DOI: https://doi.org/10.1007/BF00510035

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