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Manganese catalyzed chemoselective transfer hydrogenation of unsaturated esters switched by solvent

https://doi.org/10.2139/ssrn.6226887
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Modern Reduction Methods
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Inexpensive Ruthenium NNS‐Complexes as Efficient Ester Hydrogenation Catalysts with High C=O vs. C=C Selectivities
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Generalized Chemoselective Transfer Hydrogenation/Hydrodeuteration
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Hydrogenation of Esters by Manganese Catalysts
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Hydrogenation of Esters to Alcohols Catalyzed by Defined Manganese Pincer Complexes
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Non‐Pincer‐Type Manganese Complexes as Efficient Catalysts for the Hydrogenation of Esters
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Lutidine‐Based Chiral Pincer Manganese Catalysts for Enantioselective Hydrogenation of Ketones
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Manganese‐Catalyzed anti ‐Selective Asymmetric Hydrogenation of α‐Substituted β‐Ketoamides
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Earth‐abundant Metal‐catalyzed Reductive Amination: Recent Advances and Prospect for Future Catalysis
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Ruthenium‐Catalyzed Chemoselective Olefin Transfer Hydrogenation of alpha, beta‐Unsaturated Carbonyl Systems By Using EtOH as Hydrogen Source
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Selective Transfer Hydrogenation of C=O and Conjugated C=C Bonds Using An NHC‐Based Pincer (CNC)MnI Complex in Methanol**
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Manganese-catalyzed homogeneous hydrogenation of ketones and conjugate reduction of α,β-unsaturated carboxylic acid derivatives: A chemoselective, robust, and phosphine-free in situ-protocol
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Homogeneous manganese-catalyzed hydrogenation and dehydrogenation reactions
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Manganese-catalyzed asymmetric transfer hydrogenation of hydrazones
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A triphos-modified tungsten piano-stool complex for the homogeneous (conjugate) hydrogenation of ketones and esters
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Selective hydrogenation of carbonyl compounds and olefins using an efficient combination of homogeneous RuCl3/1,10-Phenanthroline
inferredcites →https://doi.org/10.1016/j.jcat.2024.115680openalex-snapshot
Manganese catalyzed asymmetric transfer hydrogenation of hindered ketones bearing a 2,6-disubstituted phenyl group
inferredcites →https://doi.org/10.1016/j.tet.2020.131439openalex-snapshot
Benzimidazole fragment containing Mn-complex catalyzed hydrosilylation of ketones and nitriles
inferredcites →https://doi.org/10.1021/acs.accounts.5b00043openalex-snapshot
Iron-, Cobalt-, and Nickel-Catalyzed Asymmetric Transfer Hydrogenation and Asymmetric Hydrogenation of Ketones
inferredcites →https://doi.org/10.1021/acs.chemrev.9b00846openalex-snapshot
Continuous Flow Upgrading of Selected C2–C6 Platform Chemicals Derived from Biomass
inferredcites →https://doi.org/10.1021/acs.joc.5c00151openalex-snapshot
Solvent-Controlled and Highly Chemoselective Reduction of α,β-Unsaturated Ketones and Aldehydes
inferredcites →https://doi.org/10.1021/acs.orglett.3c03664openalex-snapshot
Mild and Selective Hydrogenation of Unsaturated Compounds Using Mn/Water as a Hydrogen Gas Source
inferredcites →https://doi.org/10.1021/acs.orglett.4c00277openalex-snapshot
Chemoselective Hydrogenation of α,β-Unsaturated Ketones Catalyzed by a Manganese(I) Hydride Complex
inferredcites →https://doi.org/10.1021/acs.orglett.6b01812openalex-snapshot
Rhodium-Catalyzed Asymmetric Hydrogenation of α,β-Unsaturated Carbonyl Compounds via Thiourea Hydrogen Bonding
inferredcites →https://doi.org/10.1021/acs.orglett.7b01657openalex-snapshot
Transfer Hydrogenation of Carbonyl Derivatives Catalyzed by an Inexpensive Phosphine-Free Manganese Precatalyst
inferredcites →https://doi.org/10.1021/acscatal.1c00616openalex-snapshot
Amino Acid Derived Chiral Aminobenzimidazole Manganese Catalysts for Asymmetric Transfer Hydrogenation of Ketones
inferredcites →https://doi.org/10.1021/acscatal.2c05458openalex-snapshot
Combining Electro-, Photo-, and Biocatalysis for One-Pot Selective Conversion of Furfural into Value-Added C4 Chemicals
inferredcites →https://doi.org/10.1021/acscatal.3c01654openalex-snapshot
Acridine PNP-Pincer Ligands Enabling Transition Metal-Catalyzed Photoreactions
inferredcites →https://doi.org/10.1021/acscatal.4c00019openalex-snapshot
Hydrogenation of Esters Catalyzed by Bis(N-Heterocyclic Carbene) Molybdenum Complexes
inferredcites →https://doi.org/10.1021/acscatal.7b00623openalex-snapshot
Additive-Free Cobalt-Catalyzed Hydrogenation of Esters to Alcohols
inferredcites →https://doi.org/10.1021/acscatal.7b01338openalex-snapshot
Metal-Free Catalytic Reduction of α,β-Unsaturated Esters by 1,3,2-Diazaphospholene and Subsequent C–C Coupling with Nitriles
inferredcites →https://doi.org/10.1021/acssuschemeng.0c04891openalex-snapshot
Bimetallic PtFe-Catalyzed Selective Hydrogenation of Furfural to Furfuryl Alcohol: Solvent Effect of Isopropanol and Hydrogen Activation
inferredcites →https://doi.org/10.1021/acssuschemeng.8b03101openalex-snapshot
Effect of the Solvent in Enhancing the Selectivity to Furan Derivatives in the Catalytic Hydrogenation of Furfural
inferredcites →https://doi.org/10.1021/ie000349vopenalex-snapshot
Solvent Effect in Liquid-Phase Hydrogenation of Toluene
inferredcites →https://doi.org/10.1021/ja311087copenalex-snapshot
The Isolation of [Pd{OC(O)H}(H)(NHC)(PR3)] (NHC = N-Heterocyclic Carbene) and Its Role in Alkene and Alkyne Reductions Using Formic Acid
inferredcites →https://doi.org/10.1021/ja504034qopenalex-snapshot
Iron-Based Catalysts for the Hydrogenation of Esters to Alcohols
inferredcites →https://doi.org/10.1021/jacs.0c11110openalex-snapshot
Temperature and Solvent Effects on H 2 Splitting and Hydricity: Ramifications on CO 2 Hydrogenation by a Rhenium Pincer Catalyst
inferredcites →https://doi.org/10.1021/jacs.1c09626openalex-snapshot
A Bifunctional Copper Catalyst Enables Ester Reduction with H 2 : Expanding the Reactivity Space of Nucleophilic Copper Hydrides
inferredcites →https://doi.org/10.1021/jacs.2c00548openalex-snapshot
Basic Promotors Impact Thermodynamics and Catalyst Speciation in Homogeneous Carbonyl Hydrogenation
inferredcites →https://doi.org/10.1021/jacs.4c02096openalex-snapshot
Enhancing Hydride Transfer in Catalytic Hydrogenation via σ-Electron-Induced Polarization of Imines
inferredcites →https://doi.org/10.1021/jacs.4c05365openalex-snapshot
Ruthenium-Catalyzed Carbocycle-Selective Hydrogenation of Fused Heteroarenes
inferredcites →https://doi.org/10.1021/jacs.5c00362openalex-snapshot
Amplifying the Reactivity of Anionic Mn(I)–H Catalysts via the Cation Effect: Mechanistic Investigation and Application to the Hydrogenation of α-Trisubstituted Carboxylic Esters
inferredcites →https://doi.org/10.1021/jacs.5c08335openalex-snapshot
Manganese-Catalyzed Asymmetric Transfer Hydrogenation of Heteroatom-Containing Imines and Diarylimines
inferredcites →https://doi.org/10.1021/jacs.6b00519openalex-snapshot
Nickel-Catalyzed Asymmetric Alkene Hydrogenation of α,β-Unsaturated Esters: High-Throughput Experimentation-Enabled Reaction Discovery, Optimization, and Mechanistic Elucidation
inferredcites →https://doi.org/10.1021/jo0622429openalex-snapshot
Highly Enantioselective Hydrogenation of α-Dehydroamino Esters and Itaconates with Triphosphorous Bidentate Ligands and the Unprecedented Solvent Effect Thereof
inferredcites →https://doi.org/10.1038/s41557-025-01945-2openalex-snapshot
Tunable cobalt-catalysed hydrogenation of allenes enabled by multiple metal–ligand cooperative functionalities
inferredcites →https://doi.org/10.1038/s41570-018-0001-2openalex-snapshot
Earth-abundant transition metal catalysts for alkene hydrosilylation and hydroboration
inferredcites →https://doi.org/10.1038/s41586-024-07581-zopenalex-snapshot
Asymmetric hydrogenation of ketimines with minimally different alkyl groups
inferredcites →https://doi.org/10.1039/c2cc38145aopenalex-snapshot
Tandem ammonia borane dehydrogenation/alkene hydrogenation mediated by [Pd(NHC)(PR 3 )] (NHC = N-heterocyclic carbene) catalysts
inferredcites →https://doi.org/10.1039/c2gc00006gopenalex-snapshot
Selective reduction of aldehydes and ketones to alcohols with ammonia borane in neat water
inferredcites →https://doi.org/10.1039/c3gc41935eopenalex-snapshot
Green and sustainable manufacture of chemicals from biomass: state of the art
inferredcites →https://doi.org/10.1039/c6cc09067bopenalex-snapshot
Copper( i )-catalysed transfer hydrogenations with ammonia borane
inferredcites →https://doi.org/10.1039/c8ob02661kopenalex-snapshot
Iron catalysed selective reduction of esters to alcohols
inferredcites →https://doi.org/10.1039/d0cc02598dopenalex-snapshot
Manganese-catalysed transfer hydrogenation of esters
inferredcites →https://doi.org/10.1039/d1gc00638jopenalex-snapshot
A critical review on the progress and challenges to a more sustainable, cost competitive synthesis of adipic acid
inferredcites →https://doi.org/10.1039/d2sc05274aopenalex-snapshot
Room temperature chemoselective hydrogenation of CC, CO and CN bonds by using a well-defined mixed donor Mn( i ) pincer catalyst
inferredcites →https://doi.org/10.1039/d4gc00506fopenalex-snapshot
Manganese-catalyzed asymmetric transfer hydrogenation of quinolines in water using ammonia borane as a hydrogen source
inferredcites →https://doi.org/10.1039/d4qo02326aopenalex-snapshot
Ligand-modulated phosphine-free Ni( ii ) complexes for Z -selective semi-transfer hydrogenation of alkynes and dual transfer hydrogenation of α,β-unsaturated ketones using ammonia borane
inferredcites →https://doi.org/10.1126/sciadv.aav3680openalex-snapshot
General and selective deoxygenation by hydrogen using a reusable earth-abundant metal catalyst
inferredcites →https://doi.org/10.3390/molecules29245912openalex-snapshot
Iridium-Catalyzed Highly Selective 1,4-Reduction of α,β-Unsaturated Carbonyl Compounds
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