New homochiral xantphos-type diphosphonite ligands with binaphthoxy substituents have been prepared and characterized by NMR spectroscopy. These ligands have been applied in the nickel-catalyzed hydrocyanation of styrene and other vinylarenes. Enantioselectivities up to 63% ee have been obtained by using 4-isobutylstyrene as a substrate. Addition of an excess of ligand strongly inhibits the hydrocyanation reaction since the bis-chelate nickel complexes formed are highly stable and catalytically inactive.
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Using computer navigation, it is possible to determine pelvic inclination and lateral tilt during an operation by calculating the angular difference between the anatomic frontal plane and the "real world" frontal plane (i.e., the OR table). This method may be helpful in increasing the accuracy of positioning of acetabular cups.
Using computer navigation, it is possible to determine pelvic inclination and lateral tilt during an operation by calculating the angular difference between the anatomic frontal plane and the "real world" frontal plane (i.e., the OR table). This method may be helpful in increasing the accuracy of positioning of acetabular cups.
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