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Glycolurils in α-ureido- and α-aminoalkylation reactions

2. α-Ureidoalkylation of ureas with N-(hydroxymethyl)glycolurils

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Abstract

α-Ureidoalkylation of 1,3- and 1,1-dimethylureas with 2-(hydroxymethyl)-, 2,6- and 2,8-di(hydroxymethyl)-, and 2,4,6,8-tetra(hydroxymethyl)glycolurils gave novel bi-, tri-, tetra-, and pentacyclic fused systems combining the glycoluril and urea fragments.

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References

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Authors and Affiliations

  1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

    A. N. Kravchenko, G. A. Gazieva, N. G. Kolotyrkina & N. N. Makhova

Authors
  1. A. N. Kravchenko
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  2. G. A. Gazieva
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  3. N. G. Kolotyrkina
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  4. N. N. Makhova
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Corresponding author

Correspondence to A. N. Kravchenko.

Additional information

For Part 1, see Ref. 1.

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1726–1730, May, 2008.

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Kravchenko, A.N., Gazieva, G.A., Kolotyrkina, N.G. et al. Glycolurils in α-ureido- and α-aminoalkylation reactions. Russ Chem Bull 57, 1760–1764 (2008). https://doi.org/10.1007/s11172-008-0233-2

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  • DOI: https://doi.org/10.1007/s11172-008-0233-2

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