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• W2799339902 abstract "A second generation of phosphine–phosphite (P–OP) ligands, incorporating a more sterically bulky phosphite group than previous P–OP ligand designs, gave very efficient catalysts for the Rh‐catalysed asymmetric hydrogenation of a diverse array of substrates (11 examples, 93–99 % ee ) containing structurally diverse substituents and chelating groups at the C=C double bond. The presence of the sterically bulky ( S a )‐3,3′‐diphenyl‐5,5′,6,6′,7,7′,8,8′‐octahydro‐[1,1′‐binaphthalene]‐2,2′‐diol‐derived phosphite fragment caused significant increases in enantioselectivity (up to Δ ee = 58 %), and provided improved results compared to those obtained with the first generation of P–OP‐derived rhodium catalysts {i.e., rhodium complexes incorporating phosphine–phosphite ligands with ( R a )‐ and ( S a )‐BINOL‐derived phosphite groups; BINOL = [1,1′‐binaphthalene]‐2,2′‐diol}. Overall, the optimal ligand L8 provided very high enantioselectivities for a range of structurally diverse olefins (up to 99 % ee )." @default.
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• W2799339902 date "2018-04-09" @default.
• W2799339902 modified "2023-10-07" @default.
• W2799339902 title "Structural Investigations on Enantiopure P-OP Ligands: A High-Performing P-OP Ligand for Rhodium-Catalysed Hydrogenations" @default.
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• W2799339902 doi "https://doi.org/10.1002/ejoc.201701760" @default.
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