Scalable biocatalytic oxygenation of aliphatic amine derivatives using a class I unspecific peroxygenase

artUPO is revealed as an effective biocatalyst for the regioselective oxygenation of cycloalkylamines to form cyclic amino ketones on preparative scale. Furthermore, amino alcohols can be formed <i>via</i> the selective C-H oxygenation of isopropyl-tethered amine derivatives. Enantiomerically enriched amino alcohols are also accessible using a kinetic resolution approach.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc03882k
Citations
1
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Scalable biocatalytic oxygenation of aliphatic amine derivatives using a class I unspecific peroxygenase

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1 citations
Chemical Communications
Oxidative Organic Chemistry Reactions
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article

Scalable biocatalytic oxygenation of aliphatic amine derivatives using a class I unspecific peroxygenase

Jared Cartwright, Gideon Grogan, William P. Unsworth, Jiacheng Li, Katy A S Cornish
article en
1 citations

Abstract

artUPO is revealed as an effective biocatalyst for the regioselective oxygenation of cycloalkylamines to form cyclic amino ketones on preparative scale. Furthermore, amino alcohols can be formed <i>via</i> the selective C-H oxygenation of isopropyl-tethered amine derivatives. Enantiomerically enriched amino alcohols are also accessible using a kinetic resolution approach.

Chemical CommunicationsVol. 61(72)
University of York (GB)
Engineering and Physical Sciences Research Council
Clean water and sanitation
Openalex Percentile: Top 23%
Oxidative Organic Chemistry Reactions
0.94
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