Abstract
The reaction of N-[aryl(phenoxy, benzylidene)acetyl]-1,4-benzoquinone imines with sodium 4-methylbenzenesulfinates takes different addition patterns, depending on the LUMO energy and charge distribution over the quinoid ring of the initial quinone imine.
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Original Russian Text © S.A. Konovalova, A.P. Avdeenko, V.M. Vasil’eva, A.L. Yusina, 2014, published in Zhurnal Organicheskoi Khimii, 2014, Vol. 50, No. 10, pp. 1440–1447.
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Konovalova, S.A., Avdeenko, A.P., Vasil’eva, V.M. et al. Reaction of N-[aryl(benzylidene, phenoxy)acetyl]-1,4-benzoquinone imines with sodium 4-methylbenzenesulfinate. Russ J Org Chem 50, 1422–1429 (2014). https://doi.org/10.1134/S1070428014100054
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DOI: https://doi.org/10.1134/S1070428014100054