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
Hauptverfasser: Wang, Yu-Heng, Hu, Pan, Wang, Xi-Rui, Xu, Ke-Lan, Wang, Qi-Lin, Wang, Hui-Juan, Liu, Xiong-Li
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Sprache:eng
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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.
ISSN:2052-4129
2052-4110
2052-4129
2052-4110
DOI:10.1039/D3QO01748F