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 |
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Hauptverfasser: | , , , , , |
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. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/c9ob01649j |