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Asymmetric hydrogenation of α,β-unsaturated carboxylic esters with chiral iridium N,P ligand complexes

机译:α,β-不饱和羧酸酯与手性铱N,P配体配合物的不对称氢化

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摘要

Enantioselective conjugate reduction of a wide range of α,β-unsaturated carboxylic esters was achieved using chiral Ir N,P complexes as hydrogenation catalysts. Depending on the substitution pattern of the substrate, different ligands perform best. α,β-Unsaturated carboxylic esters substituted at the α position are less problematic substrates than originally anticipated and in some cases α-substituted substrates actually reacted with higher enantioselectivity than their β-substituted analogues. The resulting saturated esters with a stereogenic center in the α or β position were obtained in high enantiomeric purity.
机译:使用手性Ir N,P配合物作为氢化催化剂,可以实现多种α,β-不饱和羧酸酯的对映选择性共轭还原。根据底物的取代方式,不同的配体表现最佳。在α位取代的α,β-不饱和羧酸酯是比最初预期的问题少的底物,在某些情况下,α-取代的底物实际上以比其β-取代的类似物更高的对映选择性反应。以高对映体纯度获得了在α或β位置具有立体异构中心的所得饱和酯。

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