Abstract
AbstractFor the first time, we report the application of [RuCl2(η6‐p‐cymene)]2 in the arylation of N‐activated aldimines with boronic acids and its derivatives to afford chiral amines, which are important intermediates in the syntheses of key bioactive compounds. The behavior of the chiral ligands, the imine substrates, and the organoboron reagents were studied. Very good enantioselectivities were obtained.
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