A Chiral Bis-Sulfoxide Ligand in Late-Transition Metal Catalysis; Rhodium-Catalyzed Asymmetric Addition of Arylboronic Acids to Electron-Deficient Olefins
A bis-sulfoxide with a binaphthyl backbone is introduced as a readily available, chiral ligand entity in late-transition metal catalysis. Ligand p-tol-BINASO [where p-tol-BINASO is 1,1‘-binaphthalene-2,2‘-diyl-bis-(p-tolylsulfoxide)] is obtained in pure form in one single synthetic step from relativ...
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Veröffentlicht in: | Journal of the American Chemical Society 2008-02, Vol.130 (7), p.2172-2173 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A bis-sulfoxide with a binaphthyl backbone is introduced as a readily available, chiral ligand entity in late-transition metal catalysis. Ligand p-tol-BINASO [where p-tol-BINASO is 1,1‘-binaphthalene-2,2‘-diyl-bis-(p-tolylsulfoxide)] is obtained in pure form in one single synthetic step from relatively cheap, commercially available starting materials. Precatalyst [{(P,R,R)-p-tol-BINASO}RhCl]2 was synthesized in high yield and structurally characterized by X-ray diffraction, and structural data were compared to the free ligand. The precatalyst shows both excellent reactivity and selectivity in the asymmetric 1,4-addition of arylboronic acids to cyclic α,β-unsaturated ketones and esters. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja710665q |