A Class of Benzene Backbone-Based Olefin–Sulfoxide Ligands for Rh-Catalyzed Enantioselective Addition of Arylboronic Acids to Enones
A class of readily available and easily tunable benzene backbone-based olefin–sulfoxide ligands was developed for the rhodium-catalyzed asymmetric conjugate addition reaction of arylboronic acids to enones with up to 97% yield and 97% ee.
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Veröffentlicht in: | Journal of organic chemistry 2011-09, Vol.76 (17), p.7256-7262 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A class of readily available and easily tunable benzene backbone-based olefin–sulfoxide ligands was developed for the rhodium-catalyzed asymmetric conjugate addition reaction of arylboronic acids to enones with up to 97% yield and 97% ee. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/jo2011472 |