Novel N,N,P ligand stabilized rhodium complexes exhibiting high activities and enantioselectivities in the asymmetric hydrogenation of N ‐aryl imines are introduced. The ligands were synthesized from inexpensive starting materials and their modular design allows for the introduction of a broad variety of substitution patterns. Additionally, a rather low catalyst loading could be employed.
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Kutlescha et al. (2010) studied this question.
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