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Title: Iridium-catalyzed asymmetric hydrogenation of unfunctionalized enamines. Author: Baeza A, Pfaltz A. Journal: Chemistry; 2009; 15(10):2266-9. PubMed ID: 19177480. Abstract: Optically active tertiary amines are readily prepared by iridium-catalyzed asymmetric hydrogenation of unfunctionalized enamines (see scheme). The best enantioselectivities with >90% ee were obtained with N-aryl- and N-benzyl-substituted enamines with a terminal double bond. The hydrogenation of enamines derived from cyclic ketones, which has not been reported yet with other catalysts, gave enantiomeric excesses of up to 87%.[Abstract] [Full Text] [Related] [New Search]