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Catechol-Based Phosphoramidites: A New Class of Chiral Ligands for Rhodium-Catalyzed Asymmetric Hydrogenations

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1521-3773(19980504)37:8<1100::aid-anie1100>3.0.co;2-3openalex-snapshot
Highly Enantioselective Hydrogenation of Simple Ketones Catalyzed by a Rh-PennPhos Complex
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Highly Enantioselective or Not?—Chiral Monodentate Monophosphorus Ligands in the Asymmetric Hydrogenation
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Monodentate Chiral Spiro Phosphoramidites: Efficient Ligands for Rhodium-Catalyzed Enantioselective Hydrogenation of Enamides
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Rhodium/MonoPhos-Catalysed Asymmetric Hydrogenation of Enamides
inferredcites →https://doi.org/10.1002/adsc.200390026openalex-snapshot
Monodentate Phosphoramidites: A Breakthrough in Rhodium‐Catalysed Asymmetric Hydrogenation of Olefins
inferredcites →https://doi.org/10.1002/anie.200390209openalex-snapshot
A New Principle in Combinatorial Asymmetric Transition‐Metal Catalysis: Mixtures of Chiral Monodentate P Ligands
inferredcites →https://doi.org/10.1002/ejoc.200300222openalex-snapshot
Highly Enantioselective Rhodium‐Catalyzed Hydrogenation of 2‐(2‐Methoxy‐2‐oxoethyl)acrylic Acid − A Convenient Access of Enantiomerically Pure Isoprenoid Building Blocks
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Highly enantioselective hydrogenation of enamides catalyzed by rhodium-monodentate phosphoramidite complex derived from H8-BINOL
inferredcites →https://doi.org/10.1016/s0022-328x(03)00223-7openalex-snapshot
Synthesis of new chiral monodentate aminophosphinites and their use in catalytic asymmetric hydrogenations
inferredcites →https://doi.org/10.1016/s0040-4039(01)00319-7openalex-snapshot
Enantioselective hydrogenation with inexpensive, easily available monodentate phosphite ligands
inferredcites →https://doi.org/10.1016/s0040-4039(01)01895-0openalex-snapshot
Asymmetric activation of conformationally flexible monodentate phosphites for enantioselective hydrogenation
inferredcites →https://doi.org/10.1016/s0040-4039(02)00943-7openalex-snapshot
Synthesis of new chiral monodentate phosphines and their use in asymmetric hydrogenation
inferredcites →https://doi.org/10.1016/s0040-4039(02)01142-5openalex-snapshot
Highly enantioselective hydrogenation of enamides catalyzed by rhodium–monodentate phosphoramidite complex
inferredcites →https://doi.org/10.1016/s0040-4039(02)01838-5openalex-snapshot
Enantioselective hydrogenation of enamides catalyzed by chiral rhodium–monodentate phosphite complexes
inferredcites →https://doi.org/10.1016/s0040-4039(03)00976-6openalex-snapshot
Mixtures of chiral and achiral monodentate ligands in asymmetric Rh-catalyzed olefin hydrogenation: reversal of enantioselectivity
inferredcites →https://doi.org/10.1016/s0957-4166(00)00208-1openalex-snapshot
A simple enantioselective preparation of (2S,5S)-2,5-diphenylpyrrolidine and related diaryl amines
inferredcites →https://doi.org/10.1016/s0957-4166(03)00253-2openalex-snapshot
Polymer-supported phosphoramidites: highly efficient and recyclable catalysts for asymmetric hydrogenation of dimethylitaconate and dehydroamino acids and esters
inferredcites →https://doi.org/10.1021/cr020049iopenalex-snapshot
New Chiral Phosphorus Ligands for Enantioselective Hydrogenation
inferredcites →https://doi.org/10.1021/ja00088a047openalex-snapshot
A Novel Easily Accessible Chiral Ferrocenyldiphosphine for Highly Enantioselective Hydrogenation, Allylic Alkylation, and Hydroboration Reactions
inferredcites →https://doi.org/10.1021/ja00460a018openalex-snapshot
Asymmetric hydrogenation. Rhodium chiral bisphosphine catalyst
inferredcites →https://doi.org/10.1021/ja00547a020openalex-snapshot
Synthesis of 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (BINAP), an atropisomeric chiral bis(triaryl)phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of .alpha.-(acylamino)acrylic acids
inferredcites →https://doi.org/10.1021/ja00773a028openalex-snapshot
Asymmetric catalytic reduction with transition metal complexes. I. Catalytic system of rhodium(I) with (-)-2,3-0-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, a new chiral diphosphine
inferredcites →https://doi.org/10.1021/ja010161iopenalex-snapshot
Asymmetric Hydrogenation of Enamides with Rh-BisP* and Rh-MiniPHOS Catalysts. Scope, Limitations, and Mechanism
inferredcites →https://doi.org/10.1021/ja028235topenalex-snapshot
Highly Enantioselective Rhodium-Catalyzed Hydrogenation of β-Dehydroamino Acid Derivatives Using Monodentate Phosphoramidites
inferredcites →https://doi.org/10.1021/jo026869copenalex-snapshot
Highly Efficient Rhodium/Monodentate Phosphoramidite Catalyst and Its Application in the Enantioselective Hydrogenation of Enamides and α-Dehydroamino Acid Derivatives
inferredcites →https://doi.org/10.1021/jo9809332openalex-snapshot
A Three-Step Procedure for Asymmetric Catalytic Reductive Amidation of Ketones
inferredcites →https://doi.org/10.1021/jo9824605openalex-snapshot
Highly Enantioselective Hydrogenation of Cyclic Enamides Catalyzed by a Rh-PennPhos Catalyst
inferredcites →https://doi.org/10.1021/ol0261884openalex-snapshot
Rh(I)-Catalyzed Enantioselective Hydrogenation of (E)- and (Z)-β-(Acylamino)acrylates Using 1,4-Bisphosphine Ligands under Mild Conditions
inferredcites →https://doi.org/10.1021/ol027457topenalex-snapshot
Mono- versus Bidentate Ligands in Rhodium-Catalyzed Asymmetric Hydrogenation. A Comparative Rate Study
inferredcites →https://doi.org/10.1021/ol035076popenalex-snapshot
Enantioselective Rh-Catalyzed Hydrogenation of Vinyl Carboxylates with Monodentate Phosphite Ligands
inferredcites →https://doi.org/10.1021/ol035343ropenalex-snapshot
Synthesis of New Chiral Monodentate Phosphite Ligands and Their Use in Catalytic Asymmetric Hydrogenation
inferredcites →https://doi.org/10.1039/b109827fopenalex-snapshot
Novel monodentate spiro phosphorus ligands for rhodium-catalyzed hydrogenation reactions
inferredcites →https://doi.org/10.1039/b302097eopenalex-snapshot
Improving conversion and enantioselectivity in hydrogenation by combining different monodentate phosphoramidites; a new combinatorial approach in asymmetric catalysisElectronic supplementary information (ESI) available: Experimental details. See http://www.rsc.org/suppdata/ob/b3/b302097e/
inferredcites →https://doi.org/10.1039/b306793aopenalex-snapshot
New monodentate chiral phosphite ligands for asymmetric hydrogenation
inferredcites →https://doi.org/10.1039/c29710000481openalex-snapshot
The asymmetric synthesis of hydratropic acid and amino-acids by homogeneous catalytic hydrogenation
inferredcites →https://doi.org/10.1039/c39720000010openalex-snapshot
Catalytic asymmetric hydrogenation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Ir-Catalyzed enantioselective allylic enolization of 6,6-dimethyl-3-((trimethylsilyl)oxy)cyclohex-2-en-1-one involving keto-enol isomerization
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(S)-α-Methylbenzylamine
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Chiral auxiliaries and catalysts
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Chiral auxiliaries and catalysts
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Chiral Auxiliaries and Catalysts
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Chiral Auxiliaries and Catalysts
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Chiral Auxiliaries and Catalysts
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Chiral Auxiliaries and Catalysts
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Phosphoramidite Ligands
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Formation of Alkanes and Arenes by Reduction
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Enantioselective Alkene Hydrogenation: Monodentate Ligands
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Mechanism of Enantioselective Hydrogenation
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Reduction of Functionalized Alkenes
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Enantioselective Hydrogenation of Enamines with Monodentate Phosphorus Ligands
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Asymmetric Hydrogenation of a 2‐Isopropylcinnamic Acid Derivativeen Routeto the Blood Pressure‐Lowering Agent Aliskiren
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Catalytic Asymmetric Synthesis
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MOP‐Type Binaphthyl Phosphite and Diamidophosphite Ligands and Their Application in Catalytic Asymmetric Transformations
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Practical by Ligand Design: A New Class of Monodentate Phosphoramidite Ligands for Rhodium‐Catalyzed Enantioselective Hydrogenations
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Asymmetric Hydrogenation of Quinolines Catalyzed by Iridium Complexes of Monodentate BINOL‐Derived Phosphoramidites
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Chiral Amine Synthesis – Recent Developments and Trends for Enamide Reduction, Reductive Amination, and Imine Reduction
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Ruthenium‐Catalysed Hydrogenation of Aromatic Ketones using Monodentate Phosphoramidite Ligands
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Practical Enantioselective Hydrogenation of α‐Aryl‐ and α‐Carboxyamidoethylenes by Rhodium(I)‐{1,2‐Bis[(o‐tert‐butoxyphenyl)(phenyl)phosphino]ethane}
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Rhodium‐Catalyzed Asymmetric Hydrogenation of Tetrasubstituted Cyclic Enamides: Efficient Access to Chiral Cycloalkylamine Derivatives
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Alternatives to Phosphinooxazoline (t‐BuPHOX) Ligands in the Metal‐Catalyzed Hydrogenation of Minimally Functionalized Olefins and Cyclic β‐Enamides
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Indene Derived Phosphorus‐Thioether Ligands for the Ir‐Catalyzed Asymmetric Hydrogenation of Olefins with Diverse Substitution Patterns and Different Functional Groups
inferred← citeshttps://doi.org/10.1002/ange.200503663openalex-snapshot
Screening of a Supramolecular Catalyst Library in the Search for Selective Catalysts for the Asymmetric Hydrogenation of a Difficult Enamide Substrate
inferred← citeshttps://doi.org/10.1002/ange.200704327openalex-snapshot
Kombinatorische Übergangsmetallkatalyse: Mischungen einzähniger Liganden zur Kontrolle der Enantio‐, Diastereo‐ und Regioselektivität
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Weak Attractive Noncovalent Interactions in Metal‐Catalyzed Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/anie.200503663openalex-snapshot
Screening of a Supramolecular Catalyst Library in the Search for Selective Catalysts for the Asymmetric Hydrogenation of a Difficult Enamide Substrate
inferred← citeshttps://doi.org/10.1002/anie.200704327openalex-snapshot
Combinatorial Transition‐Metal Catalysis: Mixing Monodentate Ligands to Control Enantio‐, Diastereo‐, and Regioselectivity
inferred← citeshttps://doi.org/10.1002/anie.202425589openalex-snapshot
Weak Attractive Noncovalent Interactions in Metal‐Catalyzed Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/asia.200900441openalex-snapshot
Diastereo‐ and Enantioselective Hydrogenation of a Challenging Enamide Derived from 4‐Phenyl‐2‐tetralone: An Appealing Shortcut Towards Enantiopure cis‐2‐Aminotetraline Derivatives
inferred← citeshttps://doi.org/10.1002/chem.200500464openalex-snapshot
Rh‐Catalyzed Asymmetric Hydrogenation of Prochiral Olefins with a Dynamic Library of Chiral TROPOS Phosphorus Ligands
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The Combinatorial Approach to Asymmetric Hydrogenation: Phosphoramidite Libraries, Ruthenacycles, and Artificial Enzymes
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Self‐Supported Chiral Catalysts for Heterogeneous Enantioselective Reactions
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Enantioselective Transformation of Allyl Carbonates into Branched Allyl Carbamates by Using Amines and Recycling CO 2 under Iridium Catalysis
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Phosphite‐Thiother Ligands Derived from Carbohydrates allow the Enantioswitchable Hydrogenation of Cyclic β‐Enamides by using either Rh or Ir Catalysts
inferred← citeshttps://doi.org/10.1002/chin.200436023openalex-snapshot
Catechol‐Based Phosphoramidites: A New Class of Chiral Ligands for Rhodium‐Catalyzed Asymmetric Hydrogenations.
inferred← citeshttps://doi.org/10.1002/ejic.201001176openalex-snapshot
Synthesis and Structural Characterization of a Series of New Chiral‐at‐Metal Ruthenium Allenylidene Complexes
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Synthesis and Desymmetrization of meso‐2,3‐Diphenylpiperazine for Application in Asymmetric Transformations
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Features and Application in Asymmetric Catalysis of Chiral Phosphine–Phosphite Ligands
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Transition‐Metal‐Catalyzed Asymmetric Hydrogenation and Transfer Hydrogenation: Sustainable Chemistry to Access Bioactive Molecules
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Transition Metal-Catalyzed Enantioselective Hydrogenation of Enamides and Enamines
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Iridium-Catalyzed Asymmetric Hydrogenation
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New ionic phosphite ligands: synthesis and application in asymmetric Rh-catalyzed hydrogenation
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High throughput screening of Monophos instant ligand library leads to a ton-scale asymmetric hydrogenation process
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8.17 Homogeneous Catalytic Hydrogenation of CåC and CåC
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Chiral Phosphorous Ligands in Asymmetric Catalysis
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Homogeneous Catalytic Hydrogenation of C=C and C≡C
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Synthetic access to syn-functionalised chiral hydroxy pyrrolidines and pyrrolidones: Evaluation of α-glucosidase inhibition activity, docking studies and pharmacokinetics prediction
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Ruthenium-catalyzed asymmetric hydrogenation of N-(3,4-dihydro-2-naphthalenyl)-acetamide
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Evolution in heterodonor P-N, P-S and P-O chiral ligands for preparing efficient catalysts for asymmetric catalysis. From design to applications
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A highly active palladium-phosphoramidite catalyst for the Suzuki cross-coupling of aryl bromides
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Synthesis of highly functionalized 2,5-disubstituted pyrrolidines via an aza-Morita–Baylis–Hillman-type reaction
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Iridium-catalyzed enantioselective allylation of sodium 2-aminobenzenethiolate: an access to chiral benzo-fused N,S-heterocycles
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α-Alkylation versus retro-O-Michael/γ-alkylation of bicyclic N,O-acetals: an entry to α-methylthreonine
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Chiral amine–imine ligands based on trans-2,5-disubstituted pyrrolidines and their application in the palladium-catalyzed allylic alkylation
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Asymmetric hydrogenation of trisubstituted N-acetyl enamides derived from 2-tetralones using ruthenium-SYNPHOS catalysts: a practical synthetic approach to the preparation of β3-adrenergic agonist SR58611A
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Asymmetric hydrogenation reactions with Rh and Ru complexes bearing phosphine–phosphites with an oxymethylene backbone
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Rh-catalysed asymmetric hydrogenations with a dynamic library of chiral tropos phosphorus-ligands
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Me-AnilaPhos: a new chiral phosphine–phosphoramidite ligand for a highly efficient Rh-catalyzed asymmetric olefin hydrogenation
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A new easily accessible chiral phosphite–phosphoramidite ligand based on 2-anilinoethanol and R-BINOL moieties for Rh-catalyzed asymmetric olefin hydrogenation
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Enantioselective iridium-catalyzed allylation of sodium benzotriazolide: an efficient way to chiral allylbenzotriazoles
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New synthetic strategy for chiral 2-oxazolidinones derivatives via rhodium-catalyzed asymmetric hydrogenation
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New catalytic route for the synthesis of an optically active tetralone-derived amine for rotigotine
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Asymmetric Hydrogenation of Nonaromatic Cyclic Substrates
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Density Functional Theory-Inspired Design of Ir/P,S-Catalysts for Asymmetric Hydrogenation of Olefins
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Ir/Thioether–Carbene, −Phosphinite, and −Phosphite Complexes for Asymmetric Hydrogenation. A Case for Comparison
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Iridium-Catalyzed Asymmetric Hydrogenation of Tetrasubstituted α-Fluoro-β-enamino Esters: Efficient Access to Chiral α-Fluoro-β-amino Esters with Two Adjacent Tertiary Stereocenters
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Chemoselective, Regioselective, and Enantioselective Allylations of NH2OH under Iridium Catalysis
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PHOX-Based Phosphite-Oxazoline Ligands for the Enantioselective Ir-Catalyzed Hydrogenation of Cyclic β-Enamides
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Asymmetric Hydrogenation Using Monodentate Phosphoramidite Ligands
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Catalytic Asymmetric Synthesis of α-Amino Acids
inferred← citeshttps://doi.org/10.1021/cr100031fopenalex-snapshot
Use of Nonfunctionalized Enamides and Enecarbamates in Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1021/cr100218mopenalex-snapshot
Transition Metal-Catalyzed Enantioselective Hydrogenation of Enamines and Imines
inferred← citeshttps://doi.org/10.1021/ja509005eopenalex-snapshot
Rhodium-Catalyzed Enantioselective Hydrogenation of Tetrasubstituted α-Acetoxy β-Enamido Esters: A New Approach to Chiral α-Hydroxyl-β-amino Acid Derivatives
inferred← citeshttps://doi.org/10.1021/jo048212sopenalex-snapshot
Synthesis and Highly Enantioselective Hydrogenation of Exocyclic Enamides: (Z)-3-Arylidene-4-acetyl-3,4-dihydro-2H- 1,4-benzoxazines
inferred← citeshttps://doi.org/10.1021/jo048374oopenalex-snapshot
PipPhos and MorfPhos: Privileged Monodentate Phosphoramidite Ligands for Rhodium-Catalyzed Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1021/jo052451dopenalex-snapshot
Enantioselective Rh-Catalyzed Hydrogenation of N-Formyl Dehydroamino Esters with Monodentate Phosphoramidite Ligands
inferred← citeshttps://doi.org/10.1021/jo400345vopenalex-snapshot
Rhodium Phosphine–Phosphite Catalysts in the Hydrogenation of ChallengingN-(3,4-dihydronaphthalen-2-yl) Amide Derivatives
inferred← citeshttps://doi.org/10.1021/jo502885vopenalex-snapshot
Synthesis of Enantiopure trans-2,5-Disubstituted Trifluoromethylpyrrolidines and (2S,5R)-5-Trifluoromethylproline
inferred← citeshttps://doi.org/10.1021/jo701385yopenalex-snapshot
Stereochemical Features Making Deoxycholic Acid Derived tropos Biphenylphosphites Efficient Chiral Ligands for Rhodium: The Asymmetric Hydrogenation of Dimethylitaconate as a Case Study
inferred← citeshttps://doi.org/10.1021/ol048519dopenalex-snapshot
Unsymmetrical Hybrid Ferrocene-Based Phosphine-Phosphoramidites: A New Class of Practical Ligands for Rh-Catalyzed Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1021/ol048528mopenalex-snapshot
Synthesis of New Monodentate Spiro Phosphoramidite Ligand and Its Application in Rh-Catalyzed Asymmetric Hydrogenation Reactions
inferred← citeshttps://doi.org/10.1021/ol200197vopenalex-snapshot
Carbon−Sulfur Bond Formation via Iridium-Catalyzed Asymmetric Allylation of Aliphatic Thiols
inferred← citeshttps://doi.org/10.1021/ol301676zopenalex-snapshot
“Customizable” Units in Di- and Tripeptides: Selective Conversion into Substituted Dehydroamino Acids
inferred← citeshttps://doi.org/10.1039/b212010kopenalex-snapshot
2 Synthetic methods : Part (ii) Oxidation and reduction methods
inferred← citeshttps://doi.org/10.1039/b418910hopenalex-snapshot
2 Synthetic methods : Part (ii) Oxidation and reduction methods
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Asymmetric allylation of aryl aldehydes: studies on the scope and mechanism of the palladium catalysed diethylzinc mediated umpolung using phosphoramidite ligands
inferred← citeshttps://doi.org/10.1039/b606045popenalex-snapshot
Bidentate ligands by supramolecular chemistry—the future for catalysis?
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Highly enantioselective synthesis of non-natural aliphatic α-amino acids via asymmetric hydrogenation
inferred← citeshttps://doi.org/10.1039/c7cc03902fopenalex-snapshot
Rhodium-catalyzed asymmetric hydrogenation of tetrasubstituted β-acetoxy-α-enamido esters and efficient synthesis of droxidopa
inferred← citeshttps://doi.org/10.1039/c9cy02501dopenalex-snapshot
Ir–Biaryl phosphite–oxazoline catalyst libraries: a breakthrough in the asymmetric hydrogenation of challenging olefins
inferred← citeshttps://doi.org/10.1039/d0cc04145aopenalex-snapshot
Evolution of phosphorus–thioether ligands for asymmetric catalysis
inferred← citeshttps://doi.org/10.1055/sos-sd-226-00002openalex-snapshot
1.1.1 Homogeneous Reduction of Alkenes
inferred← citeshttps://doi.org/10.1134/s1070428015060123openalex-snapshot
Oxidative cycloaddition of electron-deficient arenesulfonamides to hexa-1,5-diene
inferred← citeshttps://doi.org/10.3390/molecules27206981openalex-snapshot
Ir-Catalyzed Chemo-, Regio-, and Enantioselective Allylic Enolization of 6,6-Dimethyl-3-((trimethylsilyl)oxy)cyclohex-2-en-1-one Involving Keto-Enol Isomerization
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