Abstract
The electrophilicity of (E)-2-aryl-1-cyano-1-nitroethenes is not sufficient to induce a zwitterionic course of their [4+2] cycloaddition to cyclopentadiene. The one-step mechanism of these reactions is indicated by the activation parameters, and the substituent and solvent effects on the reaction. © The Author(s) 2012.
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APA
Jasiński, R., Kwiatkowska, M., & Barański, A. (2012). Kinetics of the [4+2] cycloaddition of cyclopentadiene with (E)-2-aryl-1-cyano-1-nitroethenes. Monatshefte Fur Chemie, 143(6), 895–899. https://doi.org/10.1007/s00706-012-0735-3
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