Cyclopropanation reactions by a class I unspecific peroxygenase

Non-natural biotransformations, such as alkene cyclopropanation through carbene insertion, have been demonstrated for the hemoproteins cytochrome P450 and myoglobin, but have not been investigated for unspecific peroxygenases (UPOs). Here we demonstrate that the diastereo- and enantioselective cyclopropanation of styrenes with ethyldiazoacetate can be performed by the class I enzyme artUPO.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00426h
Citations
8
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
7.49

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article

Cyclopropanation reactions by a class I unspecific peroxygenase

Jared Cartwright, Gideon Grogan, Benjamin Melling, William P. Unsworth et al.
8 citations
Organic & Biomolecular Chemistry
Cyclopropane Reaction Mechanisms
7.49
article

Cyclopropanation reactions by a class I unspecific peroxygenase

Jared Cartwright, Gideon Grogan, Benjamin Melling, William P. Unsworth, Jiacheng Li, Balázs Pogrányi, Katy A S Cornish
article en
8 citations

Abstract

Non-natural biotransformations, such as alkene cyclopropanation through carbene insertion, have been demonstrated for the hemoproteins cytochrome P450 and myoglobin, but have not been investigated for unspecific peroxygenases (UPOs). Here we demonstrate that the diastereo- and enantioselective cyclopropanation of styrenes with ethyldiazoacetate can be performed by the class I enzyme artUPO.

Organic & Biomolecular ChemistryVol. 23(20)
University of York (GB)
Engineering and Physical Sciences Research Council
Openalex Percentile: Top 3%
Cyclopropane Reaction Mechanisms
7.49
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Cyclopropanation reactions by a class I unspecific peroxygenase — Jared Cartwright, Gideon Grogan, et al. · Organic & Biomolecular Chemistry (2025) | TGRS Research Map | TGRS