Print Email Facebook Twitter Towards preparative peroxygenase-catalyzed oxyfunctionalization reactions in organic media Title Towards preparative peroxygenase-catalyzed oxyfunctionalization reactions in organic media Author Fernandez Fueyo, E. (TU Delft BT/Biocatalysis) Ni, Y. (TU Delft BT/Biocatalysis) Gomez Baraibar, A. (TU Delft BT/Biocatalysis) Alcalde, Miguel (University of the Balearic Islands) van Langen, L.M. (ViaZym) Hollmann, F. (TU Delft BT/Biocatalysis) Date 2016 Abstract The peroxygenase from Agrocybe aegerita (AaeUPO) has been evaluated for stereoselective oxyfunctionalization chemistry under non-aqueous reaction conditions. The stereoselective hydroxylation of ethylbenzene to (R)-1-phenylethanol was performed in neat substrate as reaction medium together with the immobilized biocatalyst and tertBuOOH as oxidant. Stability and activity issues still have to be addressed. Nevertheless, gram-scale production of enantiopure (R)-1-phenylethanol was achieved with respectable 90,000 turnovers of the biocatalyst. Subject BiocatalysisHydroxylationNon-aqueous reaction mediaOxyfunctionalizationPeroxygenase To reference this document use: http://resolver.tudelft.nl/uuid:b79f43a7-febf-4982-b68f-decc63acc5d2 DOI https://doi.org/10.1016/j.molcatb.2016.09.013 ISSN 1381-1177 Source Journal of Molecular Catalysis B: Enzymatic, 134, 347-352 Part of collection Institutional Repository Document type journal article Rights © 2016 E. Fernandez Fueyo, Y. Ni, A. Gomez Baraibar, Miguel Alcalde, L.M. van Langen, F. Hollmann Files PDF 1_s2.0_S1381117716301771_main.pdf 938.6 KB Close viewer /islandora/object/uuid:b79f43a7-febf-4982-b68f-decc63acc5d2/datastream/OBJ/view