Combined Photoredox and Carbene Catalysis for the Synthesis of γ-Aryloxy Ketones
Overview
Affiliations
-heterocyclic carbenes (NHCs) have emerged as catalysts for the construction of C-C bonds in the synthesis of substituted ketones under single-electron processes. Despite these recent reports, there still remains a need to increase the utility and practicality of these reactions by exploring new radical coupling partners. Herein, we report the synthesis of γ-aryloxyketones via combined NHC/photoredox catalysis. In this reaction, an α-aryloxymethyl radical is generated via oxidation of an aryloxymethyl potassium trifluoroborate salt, which is then added into styrene derivatives to provide a stabilized benzylic radical. Subsequent radical-radical coupling reaction with an azolium radical affords the γ-aryloxy ketone products.
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PMID: 38948905 PMC: 11210951. DOI: 10.1055/s-0041-1738448.
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PMID: 38464363 PMC: 10923595. DOI: 10.1002/adsc.202300253.
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Cao J, Zhu J, Scheidt K Chem Sci. 2023; 15(1):154-159.
PMID: 38131082 PMC: 10732008. DOI: 10.1039/d3sc05162e.
Recent advances in combining photo- and N-heterocyclic carbene catalysis.
Wang X, Wu S, Yang R, Song H, Liu Y, Wang Q Chem Sci. 2023; 14(46):13367-13383.
PMID: 38033906 PMC: 10685334. DOI: 10.1039/d3sc03274d.
Acyl Azolium-Photoredox-Enabled Synthesis of -Keto Sulfides.
Rourke M, Wang C, Schull C, Scheidt K ACS Catal. 2023; 13(12):7987-7994.
PMID: 37969469 PMC: 10651059. DOI: 10.1021/acscatal.3c01558.