Design of rigid chiral bipyridine-2NO tetradentate ligands: application in asymmetric catalysis
Expanding the chemical space of chiral N -oxides and chiral 2,2′-bipyridine ligands is in great demand in asymmetric catalysis. Herein, a new class of C 2 -symmetric bipyridine-tertiary amine-derived chiral N , N ′-dioxide (bipyridine-2NO) ligands, featuring structural fine-tunability, chemical stab...
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Veröffentlicht in: | Organic Chemistry Frontiers 2024-02, Vol.11 (5), p.1314-1321 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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Zusammenfassung: | Expanding the chemical space of chiral
N
-oxides and chiral 2,2′-bipyridine ligands is in great demand in asymmetric catalysis. Herein, a new class of
C
2
-symmetric bipyridine-tertiary amine-derived chiral
N
,
N
′-dioxide (bipyridine-2NO) ligands, featuring structural fine-tunability, chemical stability, and ready accessibility, was rationally designed and developed, and the effectiveness was demonstrated in a Ni(
ii
)-catalyzed asymmetric Michael-type Friedel–Crafts alkylation reaction of indoles and β,γ-unsaturated α-keto esters. Excellent yields (up to 92%) and high enantioselectivities (up to 99% ee) were obtained for a wide range of substrates under mild conditions. These results demonstrated the promising potential of the chiral bipyridine-2NO scaffold as an efficient type of tetradentate ligand. |
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ISSN: | 2052-4129 2052-4110 2052-4129 2052-4110 |
DOI: | 10.1039/D3QO01748F |