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A series of chiral phosphite ligands based on chiral binaphthol have been designed and synthesized. Their Rhodium(I) complexes were found to be efficient catalysts for the asymmetric hydroformylation of styrene and vinyl acetate and showed excellent catalytic activities and chemos- electivities as well as good regioselectivities (branched aldehyde/linear aldehyde). The enantioselectivities up to 37.0% ee and 38.1% ee were achieved in the hydroformylation of styrene and vinyl acetate respectively. The chiral bidentate phosphite ligands provided better enantioselectivities, however lower regioselectivities than the chiral mono-dentate phosphite ligand.
A series of chiral phosphite ligands based on chiral binaphthol have been designed and synthesized. Their Rhodium (I) complexes were found to be efficient catalysts for the asymmetric hydroformylation of styrene and vinyl acetate and showed excellent catalytic activities and chemos-electivities as well as good The enantioselectivities up to 37.0% ee and 38.1% ee were achieved in the hydroformylation of styrene and vinyl acetate respectively. The chiral bidentate phosphite ligands provided better enantioselectivities, however lower regioselectivities than the chiral mono-dentate phosphite ligand.