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Abstract

All solvents were purified by distillation before use following standard procedures. Absolute solvents were obtained by distillation over appropriate drying agent (vide infra) and then kept under an atmosphere of argon: diethyl ether, tetrahydrofuran, toluene, and n-hexane (sodium, benzophenone as indicator), chloroform, dichloromethane, triethylamine (calcium hydride), ethanol (magnesium). Absolute 1,4-dioxane, TBME, di(n-butyl)ether, DME, NMP, acetonitrile, and DMSO were purchased from Sigma-Aldrich and used as received. Other commercial reagents were obtained from various sources and used without further purification.

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Notes

  1. 1.

    Relative configuration was assigned on the basis of NOE correlations in collaboration with the NMR department of the Max-Planck-Institut für Kohlenforschung.

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Correspondence to Corinna Reisinger .

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Reisinger, C. (2012). Experimental Part. In: Epoxidations and Hydroperoxidations of α,β-Unsaturated Ketones. Springer Theses. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-28118-1_7

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