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The application of planar and central chiral [2,2]paracyclophane-based N,O-
ligands in asymmetric alkenylzinc additions to various aldehydes is describ
ed, which gives rise to very high ee's especially for difficult substrates.
A fine-tuning of the alkenylzinc species by employing different transmetal
ation reagents is reported, allowing control of the steric bulk of the alke
nylzinc species and thus the selectivity of the catalysis.