MOLECULAR-STRUCTURE OF 1,3-DISUBSTITUTED PI-ALLYL PALLADIUM(II) COMPLEXES WITH A CHIRAL DIPHOSPHINE - THE INTERMEDIATE OF PALLADIUM-CATALYZED ASYMMETRIC ALLYLIC ALKYLATION

Citation
M. Yamaguchi et al., MOLECULAR-STRUCTURE OF 1,3-DISUBSTITUTED PI-ALLYL PALLADIUM(II) COMPLEXES WITH A CHIRAL DIPHOSPHINE - THE INTERMEDIATE OF PALLADIUM-CATALYZED ASYMMETRIC ALLYLIC ALKYLATION, Chemistry Letters, (3), 1996, pp. 241-242
Citations number
15
Categorie Soggetti
Chemistry
Journal title
ISSN journal
03667022
Issue
3
Year of publication
1996
Pages
241 - 242
Database
ISI
SICI code
0366-7022(1996):3<241:MO1PPC>2.0.ZU;2-W
Abstract
Structural studies by X-ray analysis and NMR spectroscopy of the pi-al lyl complex, [Pd(eta(3)-1,3-diphenylallyl)((S)-BINAP)]-PF6 . AcOEt, ha ve been carried out, and revealed the stereochemical feature for the i ntermediate of palladium-catalyzed asymmetric allylic alkylation. The dissimilarity of the two phenyl groups attached to the pi-allyl moiety is assumed to be one of the origin of the selectivity. In solution tw o configurational isomers, (syn, syn) and (syn, anti), exist.