Lipase-catalyzed dynamic kinetic resolution of chiral amines: Use of palladium as the racemization catalyst

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Abstract

The simultaneous use of a biocatalyst (lipase Candida antarctica) and a transition-metal catalyst (palladium) makes the dynamic kinetic resolution of racemic phenylethylamine possible, conversion to the enantiomerically pure N-acylated form being 75-77% (ee = 99%).

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Reetz, M. T., & Schimossek, K. (1996). Lipase-catalyzed dynamic kinetic resolution of chiral amines: Use of palladium as the racemization catalyst. Chimia, 50(12), 668–669. https://doi.org/10.2533/chimia.1996.668

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