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N-Substituted 3-methoxycarbonyl-4-phenyl-2-pyrrolidones in reactions with nitroethenes

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Abstract

N-Substituted 3-methoxycarbonyl-4-phenyl-2-pyrrolidones react with 2-aryl(heteryl)-1-nitroethenes as typical CH-acids to give nucleophilic addition products. The structure of compounds obtained was studied by IR, 1H and 13C NMR spectroscopy using HOESY experiment.

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References

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Authors and Affiliations

  1. Hertzen Russian State Pedagogical University, nab. r. Moiki 48, St. Petersburg, 191186, Russia

    O. V. Artemova, O. S. Vasil’eva, E. S. Ostroglyadov, M. M. Zobacheva & V. M. Berestovitskaya

Authors
  1. O. V. Artemova
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  2. O. S. Vasil’eva
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  3. E. S. Ostroglyadov
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  4. M. M. Zobacheva
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  5. V. M. Berestovitskaya
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Correspondence to O. V. Artemova.

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Original Russian Text © O.V. Artemova, O.S. Vasil’eva, E.S. Ostroglyadov, M.M. Zobacheva, V.M. Berestovitskaya, 2009, published in Zhurnal Obshchei Khimii, 2009, Vol. 79, No. 10, pp. 1707–1712.

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Artemova, O.V., Vasil’eva, O.S., Ostroglyadov, E.S. et al. N-Substituted 3-methoxycarbonyl-4-phenyl-2-pyrrolidones in reactions with nitroethenes. Russ J Gen Chem 79, 2201–2206 (2009). https://doi.org/10.1134/S107036320910020X

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  • DOI: https://doi.org/10.1134/S107036320910020X

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