A Photochemoenzymatic Hunsdiecker‐Borodin‐Type Halodecarboxylation of Ferulic Acid

A photochemoenzymatic halodecarboxylation of ferulic acid was achieved using vanadate‐dependent chloroperoxidase as (bio)catalyst and oxygen and organic solvent as sole stoichiometric reagents in a biphasic system. Performance and selectivity were improved through a phase transfer catalyst, reaching...

Descripción completa

Detalles Bibliográficos
Autores principales: Zippilli, Claudio, Bartolome, Miguel Jimenez, Hilberath, Thomas, Botta, Lorenzo, Hollmann, Frank, Saladino, Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804872/
https://www.ncbi.nlm.nih.gov/pubmed/35921215
http://dx.doi.org/10.1002/cbic.202200367
_version_ 1784862212298375168
author Zippilli, Claudio
Bartolome, Miguel Jimenez
Hilberath, Thomas
Botta, Lorenzo
Hollmann, Frank
Saladino, Raffaele
author_facet Zippilli, Claudio
Bartolome, Miguel Jimenez
Hilberath, Thomas
Botta, Lorenzo
Hollmann, Frank
Saladino, Raffaele
author_sort Zippilli, Claudio
collection PubMed
description A photochemoenzymatic halodecarboxylation of ferulic acid was achieved using vanadate‐dependent chloroperoxidase as (bio)catalyst and oxygen and organic solvent as sole stoichiometric reagents in a biphasic system. Performance and selectivity were improved through a phase transfer catalyst, reaching a turnover number of 660.000 for the enzyme.
format Online
Article
Text
id pubmed-9804872
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-98048722023-01-06 A Photochemoenzymatic Hunsdiecker‐Borodin‐Type Halodecarboxylation of Ferulic Acid Zippilli, Claudio Bartolome, Miguel Jimenez Hilberath, Thomas Botta, Lorenzo Hollmann, Frank Saladino, Raffaele Chembiochem Research Articles A photochemoenzymatic halodecarboxylation of ferulic acid was achieved using vanadate‐dependent chloroperoxidase as (bio)catalyst and oxygen and organic solvent as sole stoichiometric reagents in a biphasic system. Performance and selectivity were improved through a phase transfer catalyst, reaching a turnover number of 660.000 for the enzyme. John Wiley and Sons Inc. 2022-08-23 2022-10-06 /pmc/articles/PMC9804872/ /pubmed/35921215 http://dx.doi.org/10.1002/cbic.202200367 Text en © 2022 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zippilli, Claudio
Bartolome, Miguel Jimenez
Hilberath, Thomas
Botta, Lorenzo
Hollmann, Frank
Saladino, Raffaele
A Photochemoenzymatic Hunsdiecker‐Borodin‐Type Halodecarboxylation of Ferulic Acid
title A Photochemoenzymatic Hunsdiecker‐Borodin‐Type Halodecarboxylation of Ferulic Acid
title_full A Photochemoenzymatic Hunsdiecker‐Borodin‐Type Halodecarboxylation of Ferulic Acid
title_fullStr A Photochemoenzymatic Hunsdiecker‐Borodin‐Type Halodecarboxylation of Ferulic Acid
title_full_unstemmed A Photochemoenzymatic Hunsdiecker‐Borodin‐Type Halodecarboxylation of Ferulic Acid
title_short A Photochemoenzymatic Hunsdiecker‐Borodin‐Type Halodecarboxylation of Ferulic Acid
title_sort photochemoenzymatic hunsdiecker‐borodin‐type halodecarboxylation of ferulic acid
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804872/
https://www.ncbi.nlm.nih.gov/pubmed/35921215
http://dx.doi.org/10.1002/cbic.202200367
work_keys_str_mv AT zippilliclaudio aphotochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT bartolomemigueljimenez aphotochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT hilberaththomas aphotochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT bottalorenzo aphotochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT hollmannfrank aphotochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT saladinoraffaele aphotochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT zippilliclaudio photochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT bartolomemigueljimenez photochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT hilberaththomas photochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT bottalorenzo photochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT hollmannfrank photochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid
AT saladinoraffaele photochemoenzymatichunsdieckerborodintypehalodecarboxylationofferulicacid

Ejemplares similares