Nickel-Catalyzed Atroposelective Cross-Electrophile Coupling of Aryl Halides: A General and Practical Route to Diverse MOP-Type Ligands

We report a highly cross- and atroposelective coupling between ortho-(chloro)­arylphosphine oxides and ortho-(bromo)­aryl ethers. This previously unknown asymmetric nickel-catalyzed reaction offers a direct route to highly enantioenriched axially chiral biaryl monophosphine oxides that are difficult...

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Veröffentlicht in:Journal of the American Chemical Society 2024-07, Vol.146 (26), p.17606-17612
Hauptverfasser: Kim, Raphael S., Kgoadi, Lebogang O., Hayes, Jacob C., Rainboth, Derek P., Mudd, Catherine M., Yap, Glenn P. A., Watson, Donald A.
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Sprache:eng
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Zusammenfassung:We report a highly cross- and atroposelective coupling between ortho-(chloro)­arylphosphine oxides and ortho-(bromo)­aryl ethers. This previously unknown asymmetric nickel-catalyzed reaction offers a direct route to highly enantioenriched axially chiral biaryl monophosphine oxides that are difficult to access by other means. These products can be readily reduced to generate chiral MOP-type ligands bearing complex skeletal backbones. The utility of these chiral ligands in asymmetric catalysis is also demonstrated.
ISSN:0002-7863
1520-5126
1520-5126
DOI:10.1021/jacs.4c04608