PREPARATION AND NMR-SPECTROSCOPY OF HOSPHINO)ETHANE)(ETA(3)-1,3-DIARYLALLYL)-PALLADIUM TETRAFLUOROBORATES - CORRELATION OF CHEMICAL-SHIFTS WITH HAMMETT SUBSTITUENT CONSTANTS AND WITH THE REGIOSELECTIVITY OF NUCLEOPHILIC-ATTACK
M. Morenomanas et al., PREPARATION AND NMR-SPECTROSCOPY OF HOSPHINO)ETHANE)(ETA(3)-1,3-DIARYLALLYL)-PALLADIUM TETRAFLUOROBORATES - CORRELATION OF CHEMICAL-SHIFTS WITH HAMMETT SUBSTITUENT CONSTANTS AND WITH THE REGIOSELECTIVITY OF NUCLEOPHILIC-ATTACK, Organometallics, 16(2), 1997, pp. 205-209
C-13 NMR chemical shifts of the terminal allyl carbon atoms C-1 and C-
3 of (1, 2-bis(diphenylphosphino)ethane)(eta(3)-1, 3-diarylallyl)palla
dium tetrafluoroborates correlate with sigma Hammett substituent const
ants. For each complex the chemical shift at lower field indicates the
site of preferred attack by soft nucleophiles in the Tsuji-Trost reac
tion.