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Enantioselective Hydroxylation of Benzylic C(sp<sup>3</sup>)–H Bonds by an Artificial Iron Hydroxylase Based on the Biotin–Streptavidin Technology

Joan Serrano‐Plana, Corentin Rumo, Johannes G. Rebelein, Ryan L. Peterson, Maxime Barnet, Thomas R. Ward

2020Journal of the American Chemical Society66 citationsDOIOpen Access PDF

Abstract

)-tetralol. X-ray analysis of artificial hydroxylases highlights critical details of the second coordination sphere around the Fe(TAML) cofactor.

Topics & Concepts

ChemistryHydroxylationStreptavidinBiotinylationCofactorCombinatorial chemistryKinetic resolutionEnantioselective synthesisLigand (biochemistry)BiocatalysisCatalysisStereochemistryBiotinEnzymeOrganic chemistryBiochemistryReceptorReaction mechanismMetal-Catalyzed Oxygenation MechanismsCO2 Reduction Techniques and CatalystsCyclopropane Reaction Mechanisms
Enantioselective Hydroxylation of Benzylic C(sp<sup>3</sup>)–H Bonds by an Artificial Iron Hydroxylase Based on the Biotin–Streptavidin Technology | Litcius