Abstract
Main regularities in reactions of arylacetonitriles with nitroarenes were discussed. The reaction mechanism has been suggested proceeding from the experimental data and the quantum chemical modeling of the limiting stage, the formation of the 2,1-benzisoxazole ring.
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Original Russian Text © V.Yu. Orlov, A.D. Kotov, A.V. Tsivov, A.I. Rusakov, 2015, published in Zhurnal Organicheskoi Khimii, 2015, Vol. 51, No. 2, pp. 255–262.
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Orlov, V.Y., Kotov, A.D., Tsivov, A.V. et al. Mechanism of formation of 2,1-benzisoxazoles in reactions of nitroarenes with arylacetonitriles. Russ J Org Chem 51, 245–252 (2015). https://doi.org/10.1134/S1070428015020190
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DOI: https://doi.org/10.1134/S1070428015020190