Unspecific Peroxygenases (UPOs) are increasingly significant enzymes for selective oxygenations as they are stable, highly active and catalyze their reactions at the expense of only hydrogen peroxide as the oxidant. Their structural similarity to chloroperoxidase (CPO) means that UPOs can also catalyze halogenation reactions based upon the generation of hypohalous acids from halide and HO. Here we show that the halogenation and oxygenation modes of a UPO can be stimulated at different pH values. Using simple aromatic compounds such as thymol, we show that, at a pH of 3.0 and 6.0, either brominated or oxygenated products respectively are produced. Preparative 100 mg scale transformations of substrates were performed with 60-72 % isolated yields of brominated products obtained. A one-pot bromination-oxygenation cascade reaction on 4-ethylanisole, in which the pH was adjusted from 3.0 to 6.0 at the halfway stage, yielded sequentially brominated and oxygenated products 1-(3-bromo-4-methoxyphenyl)ethyl alcohol and 3-bromo-4-methoxy acetophenone with 82 % combined conversion. These results identify UPOs as an unusual example of a biocatalyst that is tunable for entirely different chemical reactions, dependent upon the reaction conditions.
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http://dx.doi.org/10.1002/chem.202401706 | DOI Listing |
ACS Appl Mater Interfaces
December 2024
Department of Chemistry, NIS Interdepartmental and INSTM Reference Centre, University of Torino, Via G. Quarello 15/A, 10135 and Via P. Giuria 7, 10125 Turin, Italy.
In this study, we present for the first time the incorporation of two distinct nonsymmetrical squaraines (SQ) into hierarchically porous Hafnium-based UiO-66 Metal-Organic Frameworks (MOFs), each functionalized with various moieties, for application as photosensitizers in photodynamic therapy. SQs are meticulously designed to feature COOH moieties for interaction with the MOF's metallic cluster and bromine atoms to enhance intersystem crossing and reactive oxygen species (ROS) production. The distinct central functionalizations, one with squaric acid and the other with a dicyanovinyl-substituted squaric acid derivative, result in unique geometric conformations.
View Article and Find Full Text PDFACS ES T Water
December 2024
Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625, United States.
Seasonal algal blooms in surface waters can adversely impact drinking water quality. Oxidative treatment has been demonstrated as an effective measure for the removal of algal cells. However, this, in turn, leads to the release of algal organic matter (AOM).
View Article and Find Full Text PDFJ Org Chem
December 2024
Hunan Provincial Key Laboratory of Cytochemistry, School of Chemistry and Chemical Engineering, Changsha University of Science and Technology, Changsha 410114, China.
Here we report a strategy that eliminates the need for photocatalysts and external additives, which provides an operable and mild method for halogen radical-enabled dearomatization of -arylpropiolamides under an oxygen atmosphere at room temperature. The method is applicable to a wide range of substrates, extending beyond the limited scope of -methoxyl -phenylpropynamides. Furthermore, several functional synthetic intermediates and anticancer bioactive molecules were successfully derived from 3-halogenated azaspiro[4.
View Article and Find Full Text PDFChem Sci
December 2024
State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University Tianjin 300071 China
1,2--Aryl furanosides are prevalent in nature and exhibit significant biological activities. The 1,2- configuration is less favorable in terms of stereoelectronic and steric effects, making the synthesis of this type of skeleton highly challenging. Traditional methods for the synthesis of 1,2--aryl furanosides usually require complicated protection manipulations, resulting in lengthy synthetic routes and low overall efficiency.
View Article and Find Full Text PDFBeilstein J Org Chem
November 2024
University of Bristol, School of Chemistry, Bristol, BS8 1TS, UK.
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