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Low-Valent Ene–Amido Iron Complexes for the Asymmetric Transfer Hydrogenation of Acetophenone without Base
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1021/cs5009656openalex-snapshot
Well-Defined Iron Catalysts for the Acceptorless Reversible Dehydrogenation-Hydrogenation of Alcohols and Ketones
inferred← citeshttps://doi.org/10.1021/ic2020176openalex-snapshot
Unexpected Direct Reduction Mechanism for Hydrogenation of Ketones Catalyzed by Iron PNP Pincer Complexes
inferred← citeshttps://doi.org/10.1021/ic402762vopenalex-snapshot
Synthesis and Structure of Six-Coordinate Iron Borohydride Complexes Supported by PNP Ligands
inferred← citeshttps://doi.org/10.1021/ja2061038openalex-snapshot
General and Selective Iron-Catalyzed Transfer Hydrogenation of Nitroarenes without Base
inferred← citeshttps://doi.org/10.1021/ja211658topenalex-snapshot
Iron Nanoparticles Catalyzing the Asymmetric Transfer Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1021/ja300503kopenalex-snapshot
Enantiopure C 1 -Symmetric Bis(imino)pyridine Cobalt Complexes for Asymmetric Alkene Hydrogenation
inferred← citeshttps://doi.org/10.1021/ja3045053openalex-snapshot
Iron-Catalyzed, Highly Regioselective Synthesis of α-Aryl Carboxylic Acids from Styrene Derivatives and CO2
inferred← citeshttps://doi.org/10.1021/ja304814sopenalex-snapshot
The Mechanism of Efficient Asymmetric Transfer Hydrogenation of Acetophenone Using an Iron(II) Complex Containing an (S,S)-Ph2PCH2CH═NCHPhCHPhN═CHCH2PPh2 Ligand: Partial Ligand Reduction Is the Key
inferred← citeshttps://doi.org/10.1021/ja307995fopenalex-snapshot
Activation of Hydrogen and Hydrogenation Catalysis by a Borenium Cation
inferred← citeshttps://doi.org/10.1021/ja4082233openalex-snapshot
Iron(II) Complexes Containing Unsymmetrical P–N–P′ Pincer Ligands for the Catalytic Asymmetric Hydrogenation of Ketones and Imines
inferred← citeshttps://doi.org/10.1021/jacs.8b12506openalex-snapshot
Asymmetric Transfer Hydrogenation with a Bifunctional Iron(II) Hydride: Experiment Meets Computation
inferred← citeshttps://doi.org/10.1021/ol302354zopenalex-snapshot
Application of Ruthenium Complexes of Triazole-Containing Tridentate Ligands to Asymmetric Transfer Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1021/ol503295copenalex-snapshot
Isonitrile Iron(II) Complexes with Chiral N2P2 Macrocycles in the Enantioselective Transfer Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1021/om2005172openalex-snapshot
Stereoelectronic Factors in Iron Catalysis: Synthesis and Characterization of Aryl-Substituted Iron(II) Carbonyl P–N–N–P Complexes and Their Use in the Asymmetric Transfer Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1021/om201170fopenalex-snapshot
Spectroscopic and DFT Study of Ferraaziridine Complexes Formed in the Transfer Hydrogenation of Acetophenone Catalyzed Using trans-[Fe(CO)(NCMe)(PPh2C6H4CH═NCH2−)2-κ4P,N,N,P](BF4)2
inferred← citeshttps://doi.org/10.1021/om300106uopenalex-snapshot
Complexes of Iron(II) and Iron(III) Containing Aryl-Substituted N-Heterocyclic Carbene Ligands
inferred← citeshttps://doi.org/10.1021/om300547fopenalex-snapshot
Variations on an NHC Theme: Which Features Enhance Catalytic Transfer Hydrogenation with Ruthenium Complexes?
inferred← citeshttps://doi.org/10.1021/om300572vopenalex-snapshot
Inner-Sphere Activation, Outer-Sphere Catalysis: Theoretical Study on the Mechanism of Transfer Hydrogenation of Ketones Using Iron(II) PNNP Eneamido Complexes
inferred← citeshttps://doi.org/10.1021/om301260jopenalex-snapshot
Ruthenium Complexes of Triazole-Based Scorpionate Ligands Transfer Hydrogen to Substrates under Base-Free Conditions
inferred← citeshttps://doi.org/10.1021/om400298copenalex-snapshot
Ruthenium(II) Complex Catalysts Bearing a Pyridyl-Based Benzimidazolyl–Benzotriazolyl Ligand for Transfer Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1021/om401150sopenalex-snapshot
(η5-Cp*)Rh(III)/Ir(III) Complexes with Bis(chalcogenoethers) (E, E′ Ligands: E = S/Se; E′ = S/Se): Synthesis, Structure, and Applications in Catalytic Oppenauer-Type Oxidation and Transfer Hydrogenation
inferred← citeshttps://doi.org/10.1021/om500266popenalex-snapshot
Catalyst Activation with Cp*RhIII/IrIII–1,2,3-Triazole-Based Organochalcogen Ligand Complexes: Transfer Hydrogenation via Loss of Cp* andN-MethylmorpholineN-Oxide Based vs Oppenauer-Type Oxidation
inferred← citeshttps://doi.org/10.1021/om500479qopenalex-snapshot
Iron Catalysts Containing Amine(imine)diphosphine P-NH-N-P Ligands Catalyze both the Asymmetric Hydrogenation and Asymmetric Transfer Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1021/om5005989openalex-snapshot
Chiral Macrocyclic N2P2 Ligands and Iron(II): A Marriage of Interest
inferred← citeshttps://doi.org/10.1021/om5008083openalex-snapshot
Synthesis of Iron P-N-P′ and P-NH-P′ Asymmetric Hydrogenation Catalysts
inferred← citeshttps://doi.org/10.1039/9781782626701-00299openalex-snapshot
Enantioselective Nickel-Catalysed Hydrogenation Reactions
inferred← citeshttps://doi.org/10.1039/c1cc14622jopenalex-snapshot
Iron-catalysed, hydride-mediated reductive cross-coupling of vinyl halides and Grignard reagents
inferred← citeshttps://doi.org/10.1039/c1cy00390aopenalex-snapshot
Asymmetric catalysis using iron complexes – ‘Ruthenium Lite’?
inferred← citeshttps://doi.org/10.1039/c1ra00476jopenalex-snapshot
Iron-catalysed reduction of carbonyls and olefins
inferred← citeshttps://doi.org/10.1039/c2cc31091kopenalex-snapshot
Selective iron-catalyzed transfer hydrogenation of terminal alkynes
inferred← citeshttps://doi.org/10.1039/c2ee03300copenalex-snapshot
Using combinations of oxidants and bases as PCET reactants: thermochemical and practical considerations
inferred← citeshttps://doi.org/10.1039/c2nj40175dopenalex-snapshot
Homogeneous asymmetric transfer hydrogenation of ketones using a ruthenium catalyst anchored on chitosan: natural chirality at work
inferred← citeshttps://doi.org/10.1039/c3cc45900dopenalex-snapshot
Cobalt-catalyzed transfer hydrogenation of CO and CN bonds
inferred← citeshttps://doi.org/10.1039/c3dt32876gopenalex-snapshot
Synthesis and characterization of SiO2-supported ruthenium complexes containing aromatic sulfonamides: as catalysts for transfer hydrogenation of acetophenone
inferred← citeshttps://doi.org/10.1039/c4cc08946dopenalex-snapshot
Transfer hydrogenation of unsaturated bonds in the absence of base additives catalyzed by a cobalt-based heterogeneous catalyst
inferred← citeshttps://doi.org/10.1039/c4cy00468jopenalex-snapshot
Distinguishing homogeneous from nanoparticle asymmetric iron catalysis
inferred← citeshttps://doi.org/10.1039/c4dt00475bopenalex-snapshot
Synthesis and structure of a ferric complex of 2,6-di(1H-pyrazol-3-yl)pyridine and its excellent performance in the redox-controlled living ring-opening polymerization of ε-caprolactone
inferred← citeshttps://doi.org/10.1039/c4dt00612gopenalex-snapshot
Rational development of iron catalysts for asymmetric transfer hydrogenation
inferred← citeshttps://doi.org/10.1039/c4dt02799jopenalex-snapshot
Exploring the decomposition pathways of iron asymmetric transfer hydrogenation catalysts
inferred← citeshttps://doi.org/10.1039/c4gc01866dopenalex-snapshot
When iron met phosphines: a happy marriage for reduction catalysis
inferred← citeshttps://doi.org/10.1039/c4ra04136dopenalex-snapshot
Highly efficient homogeneous and heterogenized ruthenium catalysts for transfer hydrogenation of carbonyl compounds
inferred← citeshttps://doi.org/10.1039/c4ra10545aopenalex-snapshot
Polyvinylpyrrolidone-stabilized magnetic nickel nanochains for cancer hyperthermia and catalysis applications
inferred← citeshttps://doi.org/10.1039/c5cy00996kopenalex-snapshot
Activity studies of vanadium, iron, carbon and mixed oxides based catalysts for the oxidative dehydrogenation of ethylbenzene to styrene: a review
inferred← citeshttps://doi.org/10.1039/c5dt02163dopenalex-snapshot
Unusual non-bifunctional mechanism for Co-PNP complex catalyzed transfer hydrogenation governed by the electronic configuration of metal center
inferred← citeshttps://doi.org/10.1039/c6ra02021fopenalex-snapshot
Cobalt( ii )-catalysed transfer hydrogenation of olefins
inferred← citeshttps://doi.org/10.1039/c7ob01123gopenalex-snapshot
Iron catalyzed diastereoselective hydrogenation of chiral imines
inferred← citeshttps://doi.org/10.1039/c7sc02558kopenalex-snapshot
From imine to amine: an unexpected left turn. Cis-β iron( ii ) PNNP′ precatalysts for the asymmetric transfer hydrogenation of acetophenone
inferred← citeshttps://doi.org/10.1039/c9cc09793gopenalex-snapshot
Rh( iii )-Catalyzed diastereoselective transfer hydrogenation: an efficient entry to key intermediates of HIV protease inhibitors
inferred← citeshttps://doi.org/10.1039/d0cs00082eopenalex-snapshot
Asymmetric hydrogenation catalyzed by first-row transition metal complexes
inferred← citeshttps://doi.org/10.1039/d0cs00688bopenalex-snapshot
Organic synthesis with the most abundant transition metal–iron: from rust to multitasking catalysts
inferred← citeshttps://doi.org/10.1039/d0dt03257copenalex-snapshot
Aza-crown compounds synthesised by the self-condensation of 2-amino-benzyl alcohol over a pincer ruthenium catalyst and applied in the transfer hydrogenation of ketones
inferred← citeshttps://doi.org/10.1039/d2dt01177hopenalex-snapshot
Efficient transfer hydrogenation of ketones using molybdenum complexes by comprehensively verifying the auxiliary ligands
inferred← citeshttps://doi.org/10.1039/d2qi01719aopenalex-snapshot
Hydrogen production via the aqueous-phase reforming of methanol catalyzed by Ru( ii ) complexes of PNNP ligands
inferred← citeshttps://doi.org/10.1039/d3dt02022copenalex-snapshot
Robust and efficient transfer hydrogenation of carbonyl compounds catalyzed by NN -Mn( i ) complexes
inferred← citeshttps://doi.org/10.1039/d6qo00178eopenalex-snapshot
DFT and machine learning insights into Ru( ii ) complex-catalyzed transfer hydrogenation
inferred← citeshttps://doi.org/10.1080/02603594.2011.618855openalex-snapshot
SYNTHESIS AND CATALYTIC APPLICATIONS OF IRON PINCER COMPLEXES
inferred← citeshttps://doi.org/10.1126/science.1244466openalex-snapshot
Amine(imine)diphosphine Iron Catalysts for Asymmetric Transfer Hydrogenation of Ketones and Imines
inferred← citeshttps://doi.org/10.3390/catal10020162openalex-snapshot
Transfer Hydrogenation from 2-propanol to Acetophenone Catalyzed by [RuCl2(η6-arene)P] (P = monophosphine) and [Rh(PP)2]X (PP = diphosphine, X = Cl−, BF4−) Complexes
inferred← citeshttps://doi.org/10.3390/molecules28227541openalex-snapshot
Exploring Hydrogen Sources in Catalytic Transfer Hydrogenation: A Review of Unsaturated Compound Reduction
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