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3491307 
Journal Article 
Towards preparative peroxygenase-catalyzed oxyfunctionalization reactions in organic media 
Fernandez-Fueyo, E; Ni, Yan; Baraibar, AG; Alcalde, M; van Langen, LM; Hollmann, F 
2016 
Yes 
Journal of Molecular Catalysis B: Enzymatic
ISSN: 1381-1177 
Elsevier 
134 
Elsevier 
347-352 
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 (BuOOH)-Bu-tert as oxidant.



Stability and activity issues still have to be addressed. Nevertheless, gram-scale production of enan-tiopure (R)-1-phenylethanol was achieved with respectable 90,000 turnovers of the biocatalyst. (C) 2016 The Authors. Published by Elsevier B.V. 
Biocatalysis; Oxyfunctionalization; Hydroxylation; Non-aqueous reaction media; Peroxygenase 
IRIS
• Ethylbenzene
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