Rhodium-Catalyzed Asymmetric Hydrogenation of Enamides and Dehydroamino Acids
Rhodium-catalyzed asymmetric hydrogenation is the most mature and industrially deployed of all enantioselective metal-catalyzed transformations. The cationic …
12 articles
Rhodium-catalyzed asymmetric hydrogenation is the most mature and industrially deployed of all enantioselective metal-catalyzed transformations. The cationic …
While first-generation (BINAP)RuCl₂ catalysts excel at β-keto esters, they give poor enantioselectivity on unfunctionalized aryl ketones. Noyori’s breakthrough was the …
While most palladium cross-coupling uses achiral phosphines, a growing family of enantioselective Pd-catalyzed reactions uses chiral diphosphines to construct stereocenters and …
Copper-catalyzed asymmetric conjugate addition (ACA) is the method of choice for constructing chiral β-substituted carbonyls and all-carbon quaternary stereocenters. Organozinc, …
Titanium is the dominant Lewis acid metal for asymmetric catalysis, owing to its well-defined octahedral coordination geometry, tunable ligand sphere, and compatibility with a wide …
Manganese occupies a unique position in asymmetric catalysis: it is both the metal of the classic Jacobsen epoxidation catalyst (since 1990) and a leading base-metal candidate in …
Rhodium and ruthenium catalysts dominate asymmetric hydrogenation of functionalized olefins (enamides, enol esters), but they frequently fail on unfunctionalized, tri-substituted, …
Nickel catalysis has emerged as one of the most active frontiers in asymmetric cross-coupling. Nickel’s ability to access both Ni(0)/Ni(II) and Ni(I)/Ni(III) redox cycles, …
The drive to replace scarce, expensive precious metals (Ru, Rh, Ir, Pd) with earth-abundant base metals (Fe, Co, Mn, Ni, Cu) is reshaping asymmetric catalysis. Iron and cobalt, the …
Asymmetric C–H activation — the enantioselective functionalization of an unactivated C–H bond — is one of the most active frontiers in organic synthesis. By converting a C–H bond …
Asymmetric hydroboration and hydrosilylation install boron and silicon, respectively, across a C=C or C=O bond with enantiocontrol. The resulting chiral organoboranes and …
Dual photoredox–metal catalysis, developed since 2014 by MacMillan, Doyle, and others, merges visible-light photoredox catalysis with transition-metal catalysis to achieve …