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Selective Enzymatic C−H‐Oxyfunctionalization for the Efficient Synthesis of Grevillic Acid

  • In this study, a selective C−H‐oxyfunctionalization using an unspecific peroxygenase (UPO) enabled an efficient biosynthetic route for the synthesis of grevillic acid (GA), a natural antioxidant. The route commenced with the release of o‐coumaric acid (oCA) from trans‐2‐coumaric acid glucoside (trans‐CAG) using commercially available β‐glucosidase from almonds. In addition, a cis‐to‐trans photoisomerization of cis‐CAG was implemented to increase the synthetic access of oCA. The key step, the para‐hydroxylation relative to the existing hydroxyl group of oCA, was accomplished by an UPO with full conversion and 93% isolated yield. Despite its name, the UPO turned out to exhibit excellent regioselectivity in this C−H functionalization, requiring only H2O2 as a cosubstrate.

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Metadaten
Author: Clemens CzieglerORCiD, Benjamin BaumertORCiD, Christoffel P. S. BadenhorstORCiD, Karsten Siems, Uwe T. BornscheuerORCiD
URN:urn:nbn:de:gbv:9-opus-132200
DOI:https://doi.org/10.1002/adsc.202401421
ISSN:1615-4150
ISSN:1615-4169
Parent Title (English):Advanced Synthesis & Catalysis
Publisher:Wiley
Place of publication:Hoboken, NJ
Document Type:Article
Language:English
Date of Publication (online):2024/11/28
Date of first Publication:2025/02/04
Release Date:2025/10/22
Tag:Antioxidants; Biocatalysis; Hydroxylation; Photoisomerization; Unspecific peroxygenase
Volume:367
Issue:3
Article Number:e202401421
Page Number:7
Faculties:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie
Collections:weitere DFG-förderfähige Artikel
Licence (German):License LogoCreative Commons - Namensnennung-Nicht kommerziell-Keine Bearbeitung 4.0 International