A P-O CHELATION WITH PALLADIUM - TOWARD UNDERSTANDING OF THE STEREOCHEMISTRY OF AN OPTICALLY-ACTIVE SULFINYL-SUBSTITUTED PHOSPHINE WITH 5 STEREOGENIC CENTERS
Sy. Siah et al., A P-O CHELATION WITH PALLADIUM - TOWARD UNDERSTANDING OF THE STEREOCHEMISTRY OF AN OPTICALLY-ACTIVE SULFINYL-SUBSTITUTED PHOSPHINE WITH 5 STEREOGENIC CENTERS, Tetrahedron : asymmetry, 7(2), 1996, pp. 357-360
The enantiomerically pure Diels-Alder product (-)-1 was subjected to c
hloride abstraction to give the title complex (-)-2. The absolute ster
eochemistry of the optically active ligand, -5-vinylsulfinyl-7-phospha
bicyclo[2.2.1]hept-2-ene 3, in (-)-2 was confirmed by crystallographic
analysis. 3 formed a six-membered P-O chelate with the ethylamino)eth
yl]-2-naphthalenyl-C,N]palladium(II) unit.