Chiral bisphosphine ligands based on quinoline oligoamide foldamers: application in asymmetric hydrogenation

A series of chiral bisphosphine ligands were designed and synthesized based on single-handed quinoline oligoamide foldamers. The bisphosphine ligands can coordinate with Rh(cod) 2 BF 4 in a 1 : 1 stoichiometry and the resulted chiral Rh( i ) catalysts were applied in the asymmetric hydrogenation of...

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Veröffentlicht in:Organic & biomolecular chemistry 2019-11, Vol.17 (44), p.9573-9577
Hauptverfasser: Zheng, Lu, Zheng, Dan, Wang, Yanru, Yu, Chengyuan, Zhang, Kun, Jiang, Hua
Format: Artikel
Sprache:eng
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Zusammenfassung:A series of chiral bisphosphine ligands were designed and synthesized based on single-handed quinoline oligoamide foldamers. The bisphosphine ligands can coordinate with Rh(cod) 2 BF 4 in a 1 : 1 stoichiometry and the resulted chiral Rh( i ) catalysts were applied in the asymmetric hydrogenation of α-dehydroamino acid esters, in which excellent conversions and promising levels of enantioselectivity were achieved. Single-handed quinoline oligoamide foldamer-based bisphosphine ligands that can coordinate with Rh(cod) 2 BF 4 were used as a platform in asymmetric hydrogenation.
ISSN:1477-0520
1477-0539
DOI:10.1039/c9ob01649j