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HERO ID
3491307
Reference Type
Journal Article
Title
Towards preparative peroxygenase-catalyzed oxyfunctionalization reactions in organic media
Author(s)
Fernandez-Fueyo, E; Ni, Yan; Baraibar, AG; Alcalde, M; van Langen, LM; Hollmann, F
Year
2016
Is Peer Reviewed?
Yes
Journal
Journal of Molecular Catalysis B: Enzymatic
ISSN:
1381-1177
Publisher
Elsevier
Volume
134
Issue
Elsevier
Page Numbers
347-352
DOI
10.1016/j.molcatb.2016.09.013
Web of Science Id
WOS:000391074700012
URL
https://linkinghub.elsevier.com/retrieve/pii/S1381117716301771
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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 (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.
Keywords
Biocatalysis; Oxyfunctionalization; Hydroxylation; Non-aqueous reaction media; Peroxygenase
Tags
IRIS
•
Ethylbenzene
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