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α-Nitrocinnamic Acid Esters in the Transalkenylation Reaction with Cyano-Containing CH-Acids

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Abstract

The base-mediated reaction of representatives of α-nitrocinnamic esters with malononitrile (cyanoacetates) leads to transalkenylation products—benzylidenemalononitriles (benzylidenecyanoacetates).

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ACKNOWLEDGMENTS

Physical and chemical studies were performed using the equipment of the Center for Collective Use “Physical and chemical methods for studying nitro compounds, coordination, biologically active substances and nanostructured materials” of the Interdisciplinary Resource Center for Collective Use “Modern physical and chemical methods for the formation and study of materials for the needs of industry, science and education” of the Herzen State Pedagogical University of Russia.

Funding

This work was supported by the Russian Ministry of Education (project no. FSZN-2020-0026).

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Authors and Affiliations

  1. Kirov Military Medical Academy, 194044, St. Petersburg, Russia

    L. V. Baichurina, A. V. Fel’gendler & O. B. Vuks

  2. Herzen State Pedagogical University of Russia, 191186, St. Petersburg, Russia

    R. I. Baichurin

Authors
  1. L. V. Baichurina
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  2. R. I. Baichurin
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  3. A. V. Fel’gendler
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  4. O. B. Vuks
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Correspondence to R. I. Baichurin.

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Baichurina, L.V., Baichurin, R.I., Fel’gendler, A.V. et al. α-Nitrocinnamic Acid Esters in the Transalkenylation Reaction with Cyano-Containing CH-Acids. Russ J Gen Chem 92, 944–948 (2022). https://doi.org/10.1134/S1070363222060044

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