Selective oxidation of alkanes and ethers mediated by ruthenium(II) complexes

Abstract
Selective hydroxylation (or ketonization) of cyclic alkanes and conversion of ethers to esters and of secondary alcohols to ketones, with significant rates (up to ca. 1 turnover per minute at room temperature), were achieved by using hypochlorite as oxidant and a choice of ruthenium(II) complexes as catalysts, in a biphastic water–dichloromethane system.

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