The ubiquity and relevance of oxygenated motifs in biologically active compounds calls for the development of effective and selective C-H and C=Coxidation reactions. Inspired by the impressive selectivity and versatility of Nature oxidation catalysts, and especially nonheme Fe oxygenases, chemists have designed small molecule catalysts that can hydroxylate C-H bonds and epoxidize or syn-di-hydroxylate C=C bonds with