Enantioselective hydrogenation of α-dehydroamino acid esters catalyzed by rhodium complexes with chiral bisaminophosphine ligands

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Abstract

A highly efficient strategy for the synthesis of a series of chiral bisaminophosphine ligands was well established with several remarkable features. The synthetic utility of these ligands was explored for rhodium-catalyzed asymmetric hydrogenations of α-dehydroamino acid esters. Up to 98% ee values were achieved for the enantioselective synthesis of aminocarboxylic acids and their derivatives, which are very important chiral building blocks for the synthesis of a variety of natural products and biologically active molecules. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA.

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Sun, X., Li, W., Zhou, L., & Zhang, X. (2010). Enantioselective hydrogenation of α-dehydroamino acid esters catalyzed by rhodium complexes with chiral bisaminophosphine ligands. Advanced Synthesis and Catalysis, 352(7), 1150–1154. https://doi.org/10.1002/adsc.201000038

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