Discovery and development of ferrocene-based tetradentate ligands for Ir-catalysed asymmetric hydrogenation of ketone
Chemical technology
Iridium-catalysed
Tetradentate ligands
Ferrocene-based ligands
TP1-1185
QD415-436
Asymmetric hydrogenation of ketones
Biochemistry
01 natural sciences
0104 chemical sciences
DOI:
10.1016/j.gresc.2022.03.004
Publication Date:
2022-03-11T12:08:27Z
AUTHORS (8)
ABSTRACT
The development of highly active and enantioselective ligands and catalysts for the asymmetric hydrogenation of ketone has been the goal of synthetic chemists for more than fifty years. Herein, a series of ferrocene-based tetradentate ligands were developed and applied in Ir-catalysed asymmetric hydrogenation of ketone. The hydrolytic ring-opening of the oxazoline moiety of ligand f-amphox leads to the accidental discovery of a highly efficient and enantioselective tetradentate ligand f-phamidol which showed extraordinarily high reactivity and enantioselectivity (up to 99% yield, up to >99% ee and up to 1,000,000 TON). In addition, two types of other tetradentate ligands f-phamida and f-phamide were also synthesized and evaluated.
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CITATIONS (29)
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