Abstract
AbstractA ruthenocenyl phosphino‐oxazoline‐ruthenium complex (RuPHOX‐Ru) was applied successfully to the asymmetric hydrogenation of β‐secondary amino ketones, directly affording the corresponding chiral γ‐secondary amino alcohols in up to 99% yield and with 99% ee. Reaction with β‐(benzylamino)‐1‐phenylpropan‐1‐one could be performed on a gram‐scale with a relatively low catalyst loading (up to 2000 S/C). The resulting hydrogenated product could be used for the synthesis of synthetically useful compounds.magnified image
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