Stereocomplementary Unspecific Peroxygenases for Asymmetric Anti-Markovnikov Wacker-Type Oxidation and Epoxidation of Styrenes

Abstract

High Resolution Image Download MS PowerPoint Slide The Wacker reaction gives access to carbonyls from olefins and is traditionally relying on metals, mostly palladium. Here, unspecific peroxygenases (UPOs) are spotlighted as palladium-free biocatalysts for asymmetric anti-Markovnikov Wacker-type oxidation of styrenes, moving them beyond their traditional role in C–H oxidation and stereoselective epoxidation. Screening 53 wild-type UPOs for the oxidation of styrene and derivatives revealed examples of high reaction selectivity leading mostly to the epoxide with an epoxide selectivity of up to >99%. For selected UPOs and styrene derivatives, aldehyde formation was found with an aldehyde selectivity of up to 86%. Conversions of up to 89% were reached (preferring epoxidation). Stereocomplementary UPOs were identified for the epoxidation, giving access to the ( R )- and ( S )-epoxides with ee values of up to 94%. Also, for the anti-Markovnikov Wacker-type oxidation of α-methylstyrene, stereocomplementary enzymes were identified, leading to an excess of either the ( R )- or ( S )-enantiomer of 2-phenylpropanal. Most interestingly, it was found that the absolute configuration of the aldehyde formed does not necessarily correlate with the absolute configuration of the epoxide; thus, aldehyde and epoxide may have the same or the opposite absolute configurations.