Molecular orbital study of the oxidation of steroidal phenols into quinols and epoxyquinols

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Abstract

The MO study showed that the radical oxidation of phenols into quinols occurs readily. Further radical oxidation (in the m-CPBA/ (BzO)2 /Av system) of quinols occurs through appropriate biradical species with an activation energy of 79.5 kJ/mol yielding syn-epoxyquinols. The stereochemical outcome presented in this study is in full agreement with the experimental results.

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Marković, Z., Šolaja, B., Milić, D., Juranić, I., & Gašić, M. J. (2000). Molecular orbital study of the oxidation of steroidal phenols into quinols and epoxyquinols. Journal of the Serbian Chemical Society, 65(7), 491–496. https://doi.org/10.2298/jsc0007491m

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