Asymmetric Hydrogenation of Unsaturated Ureas with the BIPI Ligands

Asymmetric hydrogenation of unsaturated urea esters with the BIPI Ligands has been examined. Optimization of the P−N ligand structure has led to the development of chiral rhodium catalysts capable of producing the targets with >99% ee. The critical phosphine borane SNAr reaction needed for ligand...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Organic letters 2008-01, Vol.10 (2), p.341-344
Hauptverfasser: Busacca, Carl A, Lorenz, Jon C, Grinberg, Nelu, Haddad, Nizar, Lee, Heewon, Li, Zhibin, Liang, Mary, Reeves, Diana, Saha, Anjan, Varsolona, Rich, Senanayake, Chris H
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Asymmetric hydrogenation of unsaturated urea esters with the BIPI Ligands has been examined. Optimization of the P−N ligand structure has led to the development of chiral rhodium catalysts capable of producing the targets with >99% ee. The critical phosphine borane SNAr reaction needed for ligand synthesis has been optimized to give the adducts in high yield at ambient temperature with no racemization. An extremely concise, economical, and scalable sequence to these important new ligands for catalysis of asymmetric hydrogenation has been developed.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol7028542