Electronic Control of Chiral Quaternary Center Creation in the Intramolecular Asymmetric Heck Reaction

The Boehringer-Ingelheim phosphinoimidazoline (BIPI) ligands were applied to the formation of chiral quaternary centers in the asymmetric Heck reaction. Several different substrates were examined in detail, using more than 70 members of this new ligand class. Hammett relationships were determined th...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of organic chemistry 2004-08, Vol.69 (16), p.5187-5195
Hauptverfasser: Busacca, Carl A, Grossbach, Danja, Campbell, Scot J, Dong, Yong, Eriksson, Magnus C, Harris, Robert E, Jones, Paul-James, Kim, Ji-Young, Lorenz, Jon C, McKellop, Keith B, O'Brien, Erin M, Qiu, Fenghe, Simpson, Robert D, Smith, Lana, So, Regina C, Spinelli, Earl M, Vitous, Jana, Zavattaro, Chiara
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The Boehringer-Ingelheim phosphinoimidazoline (BIPI) ligands were applied to the formation of chiral quaternary centers in the asymmetric Heck reaction. Several different substrates were examined in detail, using more than 70 members of this new ligand class. Hammett relationships were determined through systematic variation of the ligand electronics. All substrates showed essentially the same Hammett behavior, where enantioselectivity increased as the ligands were made more electron-deficient. Ligand optimization has led to catalysts which give the highest enantioselectivities reported to date for these difficult systems.
ISSN:0022-3263
1520-6904
DOI:10.1021/jo049448z