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Enabling Catalytic Ketone Hydrogenation by Frustrated Lewis Pairs
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20010105)40:1<40::aid-anie40>3.0.co;2-5openalex-snapshot
Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones
inferredcites →https://doi.org/10.1002/1521-3773(20020617)41:12<1998::aid-anie1998>3.0.co;2-8openalex-snapshot
Asymmetric Hydrogenations (Nobel Lecture) Copyright© The Nobel Foundation 2002. We thank the Nobel Foundation, Stockholm, for permission to print this lecture.
inferredcites →https://doi.org/10.1002/1521-3773(20020617)41:12<2008::aid-anie2008>3.0.co;2-4openalex-snapshot
Asymmetric Catalysis: Science and Opportunities (Nobel Lecture) Copyright© The Nobel Foundation 2002. We thank the Nobel Foundation, Stockholm, for permission to print this lecture.
inferredcites →https://doi.org/10.1002/adsc.200390002openalex-snapshot
Asymmetric Catalysis: Science and Opportunities (Nobel Lecture 2001)
inferredcites →https://doi.org/10.1002/adsc.200390028openalex-snapshot
Asymmetric Hydrogenations (Nobel Lecture 2001)
inferredcites →https://doi.org/10.1002/anie.200702908openalex-snapshot
Metal‐Free Catalytic Hydrogenation
inferredcites →https://doi.org/10.1002/anie.200801432openalex-snapshot
Metal‐Free Catalytic Hydrogenation of Enamines, Imines, and Conjugated Phosphinoalkenylboranes
inferredcites →https://doi.org/10.1002/anie.200905466openalex-snapshot
Non‐Metal‐Mediated Homogeneous Hydrogenation of CO2 to CH3OH
inferredcites →https://doi.org/10.1002/anie.201107958openalex-snapshot
Silyl Cation Mediated Conversion of CO2 into Benzoic Acid, Formic Acid, and Methanol
inferredcites →https://doi.org/10.1002/anie.201204007openalex-snapshot
Metal‐free Catalytic Olefin Hydrogenation: Low‐Temperature H2 Activation by Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1002/anie.201210175openalex-snapshot
Functional‐Group Tolerance in Frustrated Lewis Pairs: Hydrogenation of Nitroolefins and Acrylates
inferredcites →https://doi.org/10.1002/anie.201303166openalex-snapshot
Combinations of Ethers and B(C6F5)3 Function as Hydrogenation Catalysts
inferredcites →https://doi.org/10.1002/anie.201303500openalex-snapshot
Metal‐Free HB(C 6 F 5 ) 2 ‐Catalyzed Hydrogenation of Unfunctionalized Olefins and Mechanism Study of Borane‐Mediated σ‐Bond Metathesis
inferredcites →https://doi.org/10.1002/anie.201309253openalex-snapshot
Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen
inferredcites →https://doi.org/10.1002/anie.201405531openalex-snapshot
Metal‐Free Hydrogenation Catalyzed by an Air‐Stable Borane: Use of Solvent as a Frustrated Lewis Base
inferredcites →https://doi.org/10.1002/asia.201100960openalex-snapshot
Reaction of Frustrated Lewis Pairs with Ketones and Esters
inferredcites →https://doi.org/10.1002/chem.201400349openalex-snapshot
Metal‐Free Reduction of CO2 with Hydroboranes: Two Efficient Pathways at Play for the Reduction of CO2 to Methanol
inferredcites →https://doi.org/10.1002/jlac.18621240215openalex-snapshot
Bildung des Oenanthylalkohols
inferredcites →https://doi.org/10.1002/jlac.19254440112openalex-snapshot
Ein neues Verfahren zur Reduktion von Aldehyden und Ketonen
inferredcites →https://doi.org/10.1016/b978-0-08-052349-1.00217-1openalex-snapshot
Reduction of CO to CHOH by Metal Hydrides
inferredcites →https://doi.org/10.1021/ie50202a005openalex-snapshot
How I Have Been Led to the Direct Hydrogenation Method by Metallic Catalysts1
inferredcites →https://doi.org/10.1021/ja00424a020openalex-snapshot
Catalytic hydrogenation using cationic rhodium complexes. I. Evolution of the catalytic system and the hydrogenation of olefins
inferredcites →https://doi.org/10.1021/ja00424a021openalex-snapshot
Catalytic hydrogenation using cationic rhodium complexes. II. The selective hydrogenation of alkynes to cis olefins
inferredcites →https://doi.org/10.1021/ja00431a020openalex-snapshot
Catalytic hydrogenation using cationic rhodium complexes. 3. The selective hydrogenation of dienes to monoenes
inferredcites →https://doi.org/10.1021/ja01197a060openalex-snapshot
Reduction of Organic Compounds by Lithium Aluminum Hydride. I. Aldehydes, Ketones, Esters, Acid Chlorides and Acid Anhydrides
inferredcites →https://doi.org/10.1021/ja01284a002openalex-snapshot
Hydrides of Boron. VII. Evidence of the Transitory Existence of Borine (BH 3 ): Borine Carbonyl and Borine Trimethylammine
inferredcites →https://doi.org/10.1021/ja01363a009openalex-snapshot
HYDRIDES OF BORON. I. AN EFFICIENT NEW METHOD OF PREPARING DIBORANE; NEW REACTIONS FOR PREPARING BROMO-DIBORANE AND THE STABLER PENTABORANE, B5H9
inferredcites →https://doi.org/10.1021/ja01869a038openalex-snapshot
Metallo Borohydrides. II. Beryllium Borohydride
inferredcites →https://doi.org/10.1021/ja01872a041openalex-snapshot
Hydrides of Boron. XI. The Reaction of Diborane with Organic Compounds Containing a Carbonyl Group
inferredcites →https://doi.org/10.1021/ja01877a072openalex-snapshot
Homogeneous Catalytic Hydrogenation
inferredcites →https://doi.org/10.1021/ja067961jopenalex-snapshot
Facile Heterolytic Cleavage of Dihydrogen by Phosphines and Boranes
inferredcites →https://doi.org/10.1021/ja105320copenalex-snapshot
Tandem Frustrated Lewis Pair/Tris(pentafluorophenyl)borane-Catalyzed Deoxygenative Hydrosilylation of Carbon Dioxide
inferredcites →https://doi.org/10.1021/ja300228aopenalex-snapshot
Metal-Free Aromatic Hydrogenation: Aniline to Cyclohexyl-amine Derivatives
inferredcites →https://doi.org/10.1021/ja300503kopenalex-snapshot
Enantiopure C 1 -Symmetric Bis(imino)pyridine Cobalt Complexes for Asymmetric Alkene Hydrogenation
inferredcites →https://doi.org/10.1021/ja401492sopenalex-snapshot
Stoichiometric Metal-Free Reduction of CO in Syn-Gas
inferredcites →https://doi.org/10.1021/ja404585popenalex-snapshot
A Highly Active Phosphine–Borane Organocatalyst for the Reduction of CO2 to Methanol Using Hydroboranes
inferredcites →https://doi.org/10.1021/ja507536nopenalex-snapshot
A Highly Enantioselective Hydrogenation of Silyl Enol Ethers Catalyzed by Chiral Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1021/ja9104792openalex-snapshot
Room Temperature Reduction of CO 2 to Methanol by Al-Based Frustrated Lewis Pairs and Ammonia Borane
inferredcites →https://doi.org/10.1021/ja960364kopenalex-snapshot
Asymmetric Transfer Hydrogenation of Imines
inferredcites →https://doi.org/10.1021/ja961536gopenalex-snapshot
Tris(pentafluorophenyl)boron-Catalyzed Hydrosilation of Aromatic Aldehydes, Ketones, and Esters
inferredcites →https://doi.org/10.1021/om4000727openalex-snapshot
Metal-Free Hydrogenation of N-Based Heterocycles
inferredcites →https://doi.org/10.1021/om990612wopenalex-snapshot
Synthesis, Crystal Structure, and Application of the Oxonium Acid [H(OEt2)2]+[B(C6F5)4]-
inferredcites →https://doi.org/10.1038/2081203b0openalex-snapshot
Homogeneous Hydrogenation and Hydroformylation using Ruthenium Complexes
inferredcites →https://doi.org/10.1038/nchem.1693openalex-snapshot
A frustrated-Lewis-pair approach to catalytic reduction of alkynes to cis-alkenes
inferredcites →https://doi.org/10.1039/b710475hopenalex-snapshot
Rapid intramolecular heterolytic dihydrogen activation by a four-membered heterocyclic phosphane–borane adduct
inferredcites →https://doi.org/10.1039/b718598gopenalex-snapshot
Lewis acid-catalyzed hydrogenation: B(C6F5)3-mediated reduction of imines and nitriles with H2
inferredcites →https://doi.org/10.1039/b813286kopenalex-snapshot
Heterolytic dihydrogen activation with the 1,8-bis(diphenylphosphino)naphthalene/B(C6F5)3 pair and its application for metal-free catalytic hydrogenation of silyl enol ethers
inferredcites →https://doi.org/10.1039/b905137fopenalex-snapshot
On the possibility of catalytic reduction of carbonyl moieties with tris(pentafluorophenyl)borane and H2: a computational study
inferredcites →https://doi.org/10.1039/c001399dopenalex-snapshot
Catalytic metal-free ketone hydrogenation: a computational experiment
inferredcites →https://doi.org/10.1039/c0cc00719fopenalex-snapshot
Metal-free reductions of N-heterocycles via Lewis acid catalyzed hydrogenation
inferredcites →https://doi.org/10.1039/c2cc33301eopenalex-snapshot
Stoichiometric CO2 reductions using a bis-borane-based frustrated Lewis pair
inferredcites →https://doi.org/10.1039/c2cc37190aopenalex-snapshot
Metal-free hydrogenation catalysis of polycyclic aromatic hydrocarbons
inferredcites →https://doi.org/10.1039/c2dt12268eopenalex-snapshot
Heterolytic dihydrogen activation by B(C6F5)3 and carbonyl compounds
inferredcites →https://doi.org/10.1039/c2ob25339aopenalex-snapshot
“Frustrated Lewis pair” hydrogenations
inferredcites →https://doi.org/10.1039/c3dt00098bopenalex-snapshot
CO2 reduction via aluminum complexes of ammonia boranes
inferredcites →https://doi.org/10.1039/c4cc02103gopenalex-snapshot
Phosphine catalyzed reduction of CO 2 with boranes
inferredcites →https://doi.org/10.1039/c4dt02648aopenalex-snapshot
Stoichiometric reductions of alkyl-substituted ketones and aldehydes to borinic esters
inferredcites →https://doi.org/10.1126/science.1134230openalex-snapshot
Reversible, Metal-Free Hydrogen Activation
inferredcites →https://doi.org/10.1126/science.1242005openalex-snapshot
Nanoscale Fe 2 O 3 -Based Catalysts for Selective Hydrogenation of Nitroarenes to Anilines
inferredcites →https://doi.org/10.1126/science.1243550openalex-snapshot
Cobalt Precursors for High-Throughput Discovery of Base Metal Asymmetric Alkene Hydrogenation Catalysts
inferredcites →https://doi.org/10.1126/science.1244466openalex-snapshot
Amine(imine)diphosphine Iron Catalysts for Asymmetric Transfer Hydrogenation of Ketones and Imines
inferredcites →https://doi.org/10.1126/science.1247240openalex-snapshot
Abundant Metals Give Precious Hydrogenation Performance
inferredcites →https://doi.org/10.5860/choice.50-1224openalex-snapshot
Ullmann's Encyclopedia of Industrial Chemistry
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Construction of Heterogeneous Flps Based on Cofs-Stabilized Boron Cations and Investigation of the Cycloaddition Reaction Performance
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0980openalex-snapshot
Boron‐Based Frustrated L ewis Pairs in Hydrogenation Catalysis
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc2520openalex-snapshot
Small Molecule Activation with Frustrated L ewis P airs
inferred← citeshttps://doi.org/10.1002/9783527651733.ch10openalex-snapshot
New Trends in Organometallic Catalysts
inferred← citeshttps://doi.org/10.1002/9783527814237.ch7openalex-snapshot
Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen
inferred← citeshttps://doi.org/10.1002/adsc.201701418openalex-snapshot
Direct Reductive Amination of Carbonyl Compounds Catalyzed by a Moisture Tolerant Tin(IV) Lewis Acid
inferred← citeshttps://doi.org/10.1002/adsc.202000425openalex-snapshot
Hydroalkylation of Aryl Alkenes with Organohalides Catalyzed by Molybdenum Oxido Based Lewis Pairs
inferred← citeshttps://doi.org/10.1002/ajoc.202100188openalex-snapshot
Chemo‐ and Site‐Selective Fischer Esterification Catalyzed by B(C6F5)3
inferred← citeshttps://doi.org/10.1002/ange.201503087openalex-snapshot
Facile Protocol for Catalytic Frustrated Lewis Pair Hydrogenation and Reductive Deoxygenation of Ketones and Aldehydes
inferred← citeshttps://doi.org/10.1002/ange.201503879openalex-snapshot
Boron‐Catalyzed N‐Alkylation of Amines using Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/ange.201504109openalex-snapshot
Electrophilic Fluorophosphonium Cations in Frustrated Lewis Pair Hydrogen Activation and Catalytic Hydrogenation of Olefins
inferred← citeshttps://doi.org/10.1002/ange.201504941openalex-snapshot
B(C6F5)3‐katalysierter Diwasserstofftransfer von einem ungesättigten Kohlenwasserstoff auf einen anderen
inferred← citeshttps://doi.org/10.1002/ange.201506790openalex-snapshot
Formation of Frustrated Lewis Pairs in Ptx‐Loaded Zeolite NaY
inferred← citeshttps://doi.org/10.1002/ange.201605645openalex-snapshot
Spontaneous Reduction of a Hydroborane To Generate a B−B Single Bond by the Use of a Lewis Pair
inferred← citeshttps://doi.org/10.1002/ange.201606426openalex-snapshot
Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis‐Paare
inferred← citeshttps://doi.org/10.1002/ange.201606639openalex-snapshot
Versatile Catalytic Hydrogenation Using A Simple Tin(IV) Lewis Acid
inferred← citeshttps://doi.org/10.1002/ange.201608583openalex-snapshot
Direct Mannich‐Type Reactions Promoted by Frustrated Lewis Acid/Brønsted Base Catalysts
inferred← citeshttps://doi.org/10.1002/ange.201700231openalex-snapshot
Auto‐Tandem Catalysis with Frustrated Lewis Pairs for Reductive Etherification of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1002/ange.201700324openalex-snapshot
B(C 6 F 5 ) 3 ‐Catalyzed Selective Chlorination of Hydrosilanes
inferred← citeshttps://doi.org/10.1002/ange.201703591openalex-snapshot
Expanding the Boundaries of Water‐Tolerant Frustrated Lewis Pair Hydrogenation: Enhanced Back Strain in the Lewis Acid Enables the Reductive Amination of Carbonyls
inferred← citeshttps://doi.org/10.1002/ange.201802385openalex-snapshot
Accessing Frustrated Lewis Pair Chemistry from a Spectroscopically Stable and Classical Lewis Acid‐Base Adduct
inferred← citeshttps://doi.org/10.1002/ange.201809634openalex-snapshot
Hydrogenation of CO 2 to Formate with H 2 : Transition Metal Free Catalyst Based on a Lewis Pair
inferred← citeshttps://doi.org/10.1002/ange.201900861openalex-snapshot
A New Mode of Chemical Reactivity for Metal‐Free Hydrogen Activation by Lewis Acidic Boranes
inferred← citeshttps://doi.org/10.1002/ange.201914568openalex-snapshot
Asymmetric Hydrogenation of Ketones and Enones with Chiral Lewis Base Derived Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/ange.201915547openalex-snapshot
Nitrenium Salts in Lewis Acid Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202107127openalex-snapshot
Synergistic Catalysis by Brønsted Acid/Carbodicarbene Mimicking Frustrated Lewis Pair‐Like Reactivity
inferred← citeshttps://doi.org/10.1002/ange.202200911openalex-snapshot
Metal‐Free Catalytic Hydrogenolysis of Silyl Triflates and Halides into Hydrosilanes**
inferred← citeshttps://doi.org/10.1002/ange.202213399openalex-snapshot
Chiral Frustrated Lewis Pair@Metal‐Organic Framework as a New Platform for Heterogeneous Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/anie.201503087openalex-snapshot
Facile Protocol for Catalytic Frustrated Lewis Pair Hydrogenation and Reductive Deoxygenation of Ketones and Aldehydes
inferred← citeshttps://doi.org/10.1002/anie.201503879openalex-snapshot
Boron‐Catalyzed N‐Alkylation of Amines using Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/anie.201504109openalex-snapshot
Electrophilic Fluorophosphonium Cations in Frustrated Lewis Pair Hydrogen Activation and Catalytic Hydrogenation of Olefins
inferred← citeshttps://doi.org/10.1002/anie.201504941openalex-snapshot
B(C6F5)3‐Catalyzed Transfer of Dihydrogen from One Unsaturated Hydrocarbon to Another
inferred← citeshttps://doi.org/10.1002/anie.201506790openalex-snapshot
Formation of Frustrated Lewis Pairs in Ptx‐Loaded Zeolite NaY
inferred← citeshttps://doi.org/10.1002/anie.201605645openalex-snapshot
Spontaneous Reduction of a Hydroborane To Generate a B−B Single Bond by the Use of a Lewis Pair
inferred← citeshttps://doi.org/10.1002/anie.201606426openalex-snapshot
Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles
inferred← citeshttps://doi.org/10.1002/anie.201606639openalex-snapshot
Versatile Catalytic Hydrogenation Using A Simple Tin(IV) Lewis Acid
inferred← citeshttps://doi.org/10.1002/anie.201608583openalex-snapshot
Direct Mannich‐Type Reactions Promoted by Frustrated Lewis Acid/Brønsted Base Catalysts
inferred← citeshttps://doi.org/10.1002/anie.201700231openalex-snapshot
Auto‐Tandem Catalysis with Frustrated Lewis Pairs for Reductive Etherification of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1002/anie.201700324openalex-snapshot
B(C6F5)3‐Catalyzed Selective Chlorination of Hydrosilanes
inferred← citeshttps://doi.org/10.1002/anie.201703591openalex-snapshot
Expanding the Boundaries of Water‐Tolerant Frustrated Lewis Pair Hydrogenation: Enhanced Back Strain in the Lewis Acid Enables the Reductive Amination of Carbonyls
inferred← citeshttps://doi.org/10.1002/anie.201802385openalex-snapshot
Accessing Frustrated Lewis Pair Chemistry from a Spectroscopically Stable and Classical Lewis Acid‐Base Adduct
inferred← citeshttps://doi.org/10.1002/anie.201809634openalex-snapshot
Hydrogenation of CO2 to Formate with H2: Transition Metal Free Catalyst Based on a Lewis Pair
inferred← citeshttps://doi.org/10.1002/anie.201900861openalex-snapshot
A New Mode of Chemical Reactivity for Metal‐Free Hydrogen Activation by Lewis Acidic Boranes
inferred← citeshttps://doi.org/10.1002/anie.201914568openalex-snapshot
Asymmetric Hydrogenation of Ketones and Enones with Chiral Lewis Base Derived Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/anie.201915547openalex-snapshot
Nitrenium Salts in Lewis Acid Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202107127openalex-snapshot
Synergistic Catalysis by Brønsted Acid/Carbodicarbene Mimicking Frustrated Lewis Pair‐Like Reactivity
inferred← citeshttps://doi.org/10.1002/anie.202200911openalex-snapshot
Metal‐Free Catalytic Hydrogenolysis of Silyl Triflates and Halides into Hydrosilanes**
inferred← citeshttps://doi.org/10.1002/anie.202213399openalex-snapshot
Chiral Frustrated Lewis Pair@Metal‐Organic Framework as a New Platform for Heterogeneous Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/asia.202300714openalex-snapshot
A Lewis Acid‐Base Pair Catalyzed Dearomative Transformation of Unprotected Indoles via B−H Bond Activation
inferred← citeshttps://doi.org/10.1002/cctc.201601229openalex-snapshot
Tris(pentafluorophenyl)borane‐Catalyzed Reaction of Phosphorus/Boron and Nitrogen/Boron Frustrated Lewis Pair Dihydrogen Activation Products with Alkenes and Alkynes
inferred← citeshttps://doi.org/10.1002/cctc.201700289openalex-snapshot
Less Frustration, More Activity—Theoretical Insights into Frustrated Lewis Pairs for Hydrogenation Catalysis
inferred← citeshttps://doi.org/10.1002/cctc.202101123openalex-snapshot
Electrophilic C(sp 2 )−H Silylation by Supported Gold Catalysts
inferred← citeshttps://doi.org/10.1002/cctc.202200294openalex-snapshot
Frustrated Lewis pair‐catalyzed hydrogenation of unactivated alkenes with sterically hindered 9‐phosphatriptycenes
inferred← citeshttps://doi.org/10.1002/cctc.202400605openalex-snapshot
Preparation of Magnetically Recyclable MIL‐101‐immobilized Frustrated Lewis Pairs for the Reduction of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1002/chem.201500805openalex-snapshot
Autoinduced Catalysis and Inverse Equilibrium Isotope Effect in the Frustrated Lewis Pair Catalyzed Hydrogenation of Imines
inferred← citeshttps://doi.org/10.1002/chem.201503509openalex-snapshot
Extending the Scope of the B(C6F5)3‐Catalyzed CN Bond Reduction: Hydrogenation of Oxime Ethers and Hydrazones
inferred← citeshttps://doi.org/10.1002/chem.201602058openalex-snapshot
Rapid Dihydrogen Cleavage by Persistent Nitroxide Radicals under Frustrated Lewis Pair Conditions
inferred← citeshttps://doi.org/10.1002/chem.201602774openalex-snapshot
On the Mechanism of Frustrated Lewis Pair Catalysed Hydrogenation of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/chem.201603954openalex-snapshot
The Chemistry of a Non‐Interacting Vicinal Frustrated Phosphane/Borane Lewis Pair
inferred← citeshttps://doi.org/10.1002/chem.201605443openalex-snapshot
A Prediction of Proton‐Catalyzed Hydrogenation of Ketones in Lewis Basic Solvent through Facile Splitting of Hydrogen Molecules
inferred← citeshttps://doi.org/10.1002/chem.201605466openalex-snapshot
Expanding Water/Base Tolerant Frustrated Lewis Pair Chemistry to Alkylamines Enables Broad Scope Reductive Aminations
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Carbonyl Activation by Borane Lewis Acid Complexation: Transition States of H2 Splitting at the Activated Carbonyl Carbon Atom in a Lewis Basic Solvent and the Proton‐Transfer Dynamics of the Boroalkoxide Intermediate
inferred← citeshttps://doi.org/10.1002/chem.201700937openalex-snapshot
Computational Elucidation of a Role That Brønsted Acidification of the Lewis Acid‐Bound Water Might Play in the Hydrogenation of Carbonyl Compounds with H2 in Lewis Basic Solvents
inferred← citeshttps://doi.org/10.1002/chem.201702149openalex-snapshot
Theory‐Based Extension of the Catalyst Scope in the Base‐Catalyzed Hydrogenation of Ketones: RCOOH‐Catalyzed Hydrogenation of Carbonyl Compounds with H2 Involving a Proton Shuttle
inferred← citeshttps://doi.org/10.1002/chem.201804370openalex-snapshot
“Inverse” Frustrated Lewis Pairs: An Inverse FLP Approach to the Catalytic Metal Free Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1002/chem.201905793openalex-snapshot
Evidence for Genuine Bimetallic Frustrated Lewis Pair Activation of Dihydrogen with Gold(I)/Platinum(0) Systems
inferred← citeshttps://doi.org/10.1002/chem.202000842openalex-snapshot
Evidence for Genuine Bimetallic Frustrated Lewis Pair Activation of Dihydrogen with Gold(I)/Platinum(0) Systems
inferred← citeshttps://doi.org/10.1002/chem.202201867openalex-snapshot
Molybdenum(VI) Bis(imido) Complexes: From Frustrated Lewis Pairs to Weakly Coordinating Cations
inferred← citeshttps://doi.org/10.1002/chem.202203685openalex-snapshot
Reactivity of Oxygen‐Bridged Geminal Al/P and Si/P Frustrated Lewis Pairs towards Heterocumulenes
inferred← citeshttps://doi.org/10.1002/chem.202400241openalex-snapshot
Stereocontrol via Propeller Chirality in FLP‐Catalyzed Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/chem.202502344openalex-snapshot
Frustrated Lewis Pair (FLP) Reactivity from Carbone–BPh 3 Lewis Adduct
inferred← citeshttps://doi.org/10.1002/chin.201523035openalex-snapshot
ChemInform Abstract: Enabling Catalytic Ketone Hydrogenation by Frustrated Lewis Pairs.
inferred← citeshttps://doi.org/10.1002/chir.23671openalex-snapshot
Asymmetric catalysis by chiral FLPs: A computational mini‐review
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Frustrated Lewis Pairs: Discovery and Overviews in Catalysis
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Frustrated Lewis Pair Catalysis: It Takes Two to Make a Thing Go Right
inferred← citeshttps://doi.org/10.1002/cphc.202100003openalex-snapshot
Lewis Acidity of Carbon in Activated Carbonyl Group vs. B(C6F5)3 for Metal‐Free Catalysis of Hydrogenation of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/ejic.201500861openalex-snapshot
Diboranyl Phosphonium Cations: Synthesis and Chemical Properties
inferred← citeshttps://doi.org/10.1002/ejic.201600834openalex-snapshot
A Ferrocene‐Based Phosphane/Borane Frustrated Lewis Pair for Asymmetric Imine Reduction
inferred← citeshttps://doi.org/10.1002/ejic.202500104openalex-snapshot
Activation of Small Molecules by Readily Accessible Alkylborane‐Based Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/ejoc.201601256openalex-snapshot
1‐Hydrosilatrane: A Locomotive for Efficient Ketone Reductions
inferred← citeshttps://doi.org/10.1002/ejoc.201800847openalex-snapshot
Aldehyde Reduction by a Pyridone Borane Complex through Boron‐Ligand‐Cooperation: Concerted or Not?
inferred← citeshttps://doi.org/10.1002/ejoc.202200759openalex-snapshot
NaOH/BEt3 Catalyzed Regioselective Hydroboration of Epoxides to Secondary Alcohols
inferred← citeshttps://doi.org/10.1002/ejoc.202200853openalex-snapshot
Dual Catalysis Involving Organoboron Compounds
inferred← citeshttps://doi.org/10.1002/ejoc.202201249openalex-snapshot
Boron Catalysis in the Transformation of Carboxylic Acids and Carboxylic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202300904openalex-snapshot
Exhaustive Reduction of Esters, Carboxylic Acids and Carbamates to Methyl Groups Catalyzed by Boronic Acids
inferred← citeshttps://doi.org/10.1002/ijch.201400142openalex-snapshot
Kinetic and Thermodynamic Study of the Reduction of 1,1‐Diphenylethylene by a Thermally Frustrated Diethyl Ether‐BCF Lewis Pair
inferred← citeshttps://doi.org/10.1002/ijch.201400159openalex-snapshot
Chemistry of Intermolecular Frustrated Lewis Pairs in Motion: Emerging Perspectives and Prospects
inferred← citeshttps://doi.org/10.1002/jlcr.3774openalex-snapshot
Frustrated Lewis pairs: A real alternative to deuteride/tritide reductions
inferred← citeshttps://doi.org/10.1002/slct.202102189openalex-snapshot
Can Superhalogen Ligand Make More Reactive Frustrated Lewis Pairs?
inferred← citeshttps://doi.org/10.1002/tcr.201700010openalex-snapshot
Frustrated Lewis Pair Chemistry: Searching for New Reactions
inferred← citeshttps://doi.org/10.1007/430_2015_177openalex-snapshot
Non-conventional Lewis Acids and Bases in Frustrated Lewis Pair Chemistry
inferred← citeshttps://doi.org/10.1007/978-3-030-58888-5_1openalex-snapshot
Frustrated Lewis Pair Catalysis: An Introduction
inferred← citeshttps://doi.org/10.1007/978-3-030-58888-5_10openalex-snapshot
Radicals in Frustrated Lewis Pair Chemistry
inferred← citeshttps://doi.org/10.1007/978-3-030-58888-5_2openalex-snapshot
Frustrated Lewis Pair Catalyzed Asymmetric Reactions
inferred← citeshttps://doi.org/10.1007/978-3-030-58888-5_5openalex-snapshot
Mechanistic Insight into the Hydrogen Activation by Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1007/978-3-030-58888-5_6openalex-snapshot
Lewis Acidic Boranes in Frustrated Lewis Pair Chemistry
inferred← citeshttps://doi.org/10.1007/978-3-030-58888-5_7openalex-snapshot
Heterogeneous Catalysis by Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1007/978-981-99-1673-3_8openalex-snapshot
Highly Selective Hydrothermal Production of Cyclohexanol from Biomass-Derived Cyclohexanone Over Cu Powder
inferred← citeshttps://doi.org/10.1007/s00214-020-02698-6openalex-snapshot
Can a decrease in anti-aromaticity increase the dihydrogen activation ability of a frustrated phosphorous/borane Lewis pair?: a DFT study
inferred← citeshttps://doi.org/10.1007/s11224-022-01934-yopenalex-snapshot
Small molecule activation and dehydrogenation of an amine–borane system using frustrated Lewis pairs
inferred← citeshttps://doi.org/10.1007/s11237-025-09848-6openalex-snapshot
Organocatalysts as Enzyme Mimetics: A Review
inferred← citeshttps://doi.org/10.1007/s12039-021-02010-4openalex-snapshot
Possible C-F bond activation by B(C6F5)3/lutidine and Al(C6F5)3/lutidine frustrated Lewis pair: an in silico study
inferred← citeshttps://doi.org/10.1007/s12039-022-02119-0openalex-snapshot
Unveiling novel reactivity of P/Al frustrated Lewis pair: ring size-dependent activation of cyclic ethers/thioethers and CO2 insertion therein
inferred← citeshttps://doi.org/10.1007/s40242-024-4129-yopenalex-snapshot
Supported Recyclable Metal-free Frustrated Lewis Pair Catalyst for Catalytic Hydrogenation of Substituted Pyridines to Piperidines
inferred← citeshttps://doi.org/10.1016/b978-0-12-818429-5.00003-xopenalex-snapshot
Rivaling transition metal reactivity—an exploration of frustrated Lewis pairs chemistry
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00129-3openalex-snapshot
Frustrated Lewis Pair Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-822127-3.00005-3openalex-snapshot
Applications of boron compounds in catalysis
inferred← citeshttps://doi.org/10.1016/b978-0-12-822943-9.00023-1openalex-snapshot
Application of frustrated Lewis pairs in small molecule activation and associated transformations
inferred← citeshttps://doi.org/10.1016/b978-0-12-823144-9.00011-xopenalex-snapshot
Frustrated lewis pairs in catalysis
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00119-8openalex-snapshot
Reduction of C O to CHOH by Metal-Catalyzed Hydrogenation and Transfer Hydrogenation
inferred← citeshttps://doi.org/10.1016/j.apcata.2023.119447openalex-snapshot
Advances and mechanistic insights in the catalytic semi-hydrogenation of acetylene over non-metallic catalysts
inferred← citeshttps://doi.org/10.1016/j.cattod.2015.11.016openalex-snapshot
Highly selective hydrothermal production of cyclohexanol from biomass-derived cyclohexanone over Cu powder
inferred← citeshttps://doi.org/10.1016/j.ccr.2016.05.005openalex-snapshot
Design principles in frustrated Lewis pair catalysis for the functionalization of carbon dioxide and heterocycles
inferred← citeshttps://doi.org/10.1016/j.ccr.2018.09.014openalex-snapshot
From structure to novel reactivity in frustrated Lewis pairs
inferred← citeshttps://doi.org/10.1016/j.chempr.2020.05.007openalex-snapshot
Catalysis, FLPs, and Beyond
inferred← citeshttps://doi.org/10.1016/j.cplett.2021.138623openalex-snapshot
A computational investigation of the activation of allene (H2C = C = CHR; R = H, CH3, CN) by a frustrated phosphorous/boron Lewis pair
inferred← citeshttps://doi.org/10.1016/j.ijhydene.2023.01.304openalex-snapshot
Balancing molecular level influences of intermolecular frustrated Lewis pairs (FLP) for successful design of FLP catalysts for hydrogen storage applications
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106528openalex-snapshot
Synergistic effect of hydrogen bonds and π-π interactions of B(C6F5)3·H2O/amides complex: Application in photoredox catalysis
inferred← citeshttps://doi.org/10.1016/j.jcou.2025.103216openalex-snapshot
Research trends in CO2 utilization: Catalytic strategies for sustainable energy and environmental protection
inferred← citeshttps://doi.org/10.1016/j.jcou.2026.103485openalex-snapshot
Reaction design strategies for organocatalytic CO2 valorization: Control of reactivity and selectivity with implications for asymmetric synthesis
inferred← citeshttps://doi.org/10.1016/j.jece.2024.114137openalex-snapshot
Construction of heterogeneous frustrated lewis pairs based on covalent organic frameworks stabilized boron cations and investigation of cycloaddition reaction performance
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2019.120879openalex-snapshot
Diels-Alder route to norbornane derived vicinal phosphane/borane frustrated Lewis pairs for the metal-free catalytic hydrogenation of α, β-unsaturated ketones
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2015.04.015openalex-snapshot
Organic reactions for the electrochemical and photochemical production of chemical fuels from CO2 – The reduction chemistry of carboxylic acids and derivatives as bent CO2 surrogates
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146258openalex-snapshot
Vibrational spectroscopic insights into steric and electronic frustration in B(C6F5)3–pyridine Lewis pairs
inferred← citeshttps://doi.org/10.1016/j.mtchem.2024.102224openalex-snapshot
Hydrophobic MIL-101@PDMS composite confined Frustrated Lewis pairs: Excellent water-tolerance emerged in the hydrogenation of carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.rser.2018.04.073openalex-snapshot
Synthesis chemistry of metal-organic frameworks for CO 2 capture and conversion for sustainable energy future
inferred← citeshttps://doi.org/10.1016/j.tchem.2023.100059openalex-snapshot
Strategic use of crude H2 for the catalytic reduction of carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.08.060openalex-snapshot
B(C6F5)3-catalyzed oxidative deamination/cyclization cascade reaction of benzylamines and ketones for the synthesis of 2,4,6-triarylpyridines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153387openalex-snapshot
Synthesis of polyfluorinated aromatic ethers and thioethers by synergistic cleavage of C-B bond and C-F bond of B(C6F5)3
inferred← citeshttps://doi.org/10.1021/acs.accounts.7b00530openalex-snapshot
Frustrated Lewis Pairs Catalyzed Asymmetric Metal-Free Hydrogenations and Hydrosilylations
inferred← citeshttps://doi.org/10.1021/acs.chemmater.2c03507openalex-snapshot
Flexible Borane–Nitrogen Frustrated Lewis Pair Organic Microsphere for Selective Alkyne Hydrogenation
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00168openalex-snapshot
Thermodynamic Hydricity of Transition Metal Hydrides
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00561openalex-snapshot
Metallomimetic Chemistry of Boron
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.2c01902openalex-snapshot
Activation of H–H, HO–H, C(sp2)–H, C(sp3)–H, and RO–H Bonds by Transition-Metal Frustrated Lewis Pairs Based on M/N (M = Rh, Ir) Couples
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6c00833openalex-snapshot
Ruthenium Complexes Containing Pyridinyl-Derived Ligands as FLP Catalysts
inferred← citeshttps://doi.org/10.1021/acs.jcim.0c00862openalex-snapshot
Density Functional Study of Methane Activation by Frustrated Lewis Pairs with Group 13 Trihalides and Group 15 Pentahalides and a Machine Learning Analysis of Their Barrier Heights
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00568openalex-snapshot
Chemoselective Hydrosilylation of the α,β-Site Double Bond in α,β- and α,β,γ,δ-Unsaturated Ketones Catalyzed by Macrosteric Borane Promoted by Hexafluoro-2-propanol
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01278openalex-snapshot
Asymmetric Hydrogenation by Relay Catalysis with FLPs and CPAs: Stereodivergent Synthesis of 3-Substituted Flavanones
inferred← citeshttps://doi.org/10.1021/acs.jpca.0c02799openalex-snapshot
Cycloaddition Reactions between H2C = CHR (R = H, CN, CH3) and a Cyclic P/B Frustrated Lewis Pair: A DFT Study
inferred← citeshttps://doi.org/10.1021/acs.jpca.0c03108openalex-snapshot
Optimizing the Energetics of FLP-Type H2 Activation by Modulating the Electronic and Structural Properties of the Lewis Acids: A DFT Study
inferred← citeshttps://doi.org/10.1021/acs.jpca.7b11851openalex-snapshot
Surprisingly Flexible Oxonium/Borohydride Ion Pair Configurations
inferred← citeshttps://doi.org/10.1021/acs.jpca.8b02151openalex-snapshot
Structurally Flexible Oxocarbenium/Borohydride Ion Pair: Dynamics of Hydride Transfer on the Background of Conformational Roaming
inferred← citeshttps://doi.org/10.1021/acs.jpca.8b06830openalex-snapshot
H 2 Cleavage by Frustrated Lewis Pairs Characterized by the Energy Decomposition Analysis of Transition States: An Alternative to the Electron Transfer and Electric Field Models
inferred← citeshttps://doi.org/10.1021/acs.jpcb.8b07506openalex-snapshot
Water and a Borohydride/Hydronium Intermediate in the Borane-Catalyzed Hydrogenation of Carbonyl Compounds with H2 in Wet Ether: A Computational Study
inferred← citeshttps://doi.org/10.1021/acs.jpcc.1c05786openalex-snapshot
Assessing Tetrel-Based Neutral Frustrated Lewis Pairs for Catalytic Hydrogenation
inferred← citeshttps://doi.org/10.1021/acs.organomet.0c00330openalex-snapshot
Tuning Activity and Selectivity during Alkyne Activation by Gold(I)/Platinum(0) Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1021/acs.organomet.5b00546openalex-snapshot
Diverging Pathways in the Activation of Allenes with Lewis Acids and Bases: Addition, 1,2-Carboboration, and Cyclization
inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00072openalex-snapshot
Synthesis and Reactivity of Oxorhenium(V) Complexes Incorporating 2,6-Bis[(diphenyl)methyl]diamidopyridine (DPMDAP) Pincer Ligands as the Basic Component of Transition Metal Frustrated Lewis-Pair Catalysts
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00158openalex-snapshot
Metal-Free Phosphine Oxide Reductions Catalyzed by B(C6F5)3 and Electrophilic Fluorophosphonium Cations
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00867openalex-snapshot
Dehydrodechlorination of Methylene Chloride, Chloroform, and Chlorodiphenylmethane in the Presence of Ga/N Lewis Pairs
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00035openalex-snapshot
Metal-Free Carbonylation Route to a Reactive Borataepoxide System
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00405openalex-snapshot
Mechanism of Boron-Catalyzed N-Alkylation of Primary and Secondary Arylamines with Ketones Using Silanes under “Wet” Conditions
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02600openalex-snapshot
B(C6F5)3-Catalyzed β-Functionalization of Pyrrolidines Using Isatins via Borrowing Hydrogen: Divergent Access to Substituted Pyrrolidines and Pyrroles
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01150openalex-snapshot
TBAT-Catalyzed Deoxygenative Reduction of Tertiary Amides to Amines
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03578openalex-snapshot
Synthesis of Tetrasubstituted Enamines through Borane-Catalyzed Hydrogenations
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00085openalex-snapshot
Facile Development of Chiral Alkenylboranes from Chiral Diynes for Asymmetric Hydrogenation of Silyl Enol Ethers
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01744openalex-snapshot
The B(C6F5)3-Catalyzed Tandem Meinwald Rearrangement–Reductive Amination
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03868openalex-snapshot
Mechanistic Investigations of Reactions of the Frustrated Lewis Pairs (Triarylphosphines/B(C6F5)3) with Michael Acceptors
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00720openalex-snapshot
B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02701openalex-snapshot
B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01988openalex-snapshot
Boron-Catalyzed O–H Bond Insertion of α-Aryl α-Diazoesters in Water
inferred← citeshttps://doi.org/10.1021/acscatal.0c02023openalex-snapshot
Establishing the Role of Triflate Anions in H2 Activation by a Cationic Triorganotin(IV) Lewis Acid
inferred← citeshttps://doi.org/10.1021/acscatal.0c04263openalex-snapshot
Origin of Stereoselectivity in FLP-Catalyzed Asymmetric Hydrogenation of Imines
inferred← citeshttps://doi.org/10.1021/acscatal.1c01940openalex-snapshot
Transition Metal-Free Direct Hydrogenation of Esters via a Frustrated Lewis Pair
inferred← citeshttps://doi.org/10.1021/acscatal.5b01191openalex-snapshot
Screening Lewis Pair Moieties for Catalytic Hydrogenation of CO 2 in Functionalized UiO-66
inferred← citeshttps://doi.org/10.1021/acscatal.5b01299openalex-snapshot
Moisture-Tolerant Frustrated Lewis Pair Catalyst for Hydrogenation of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1021/acscatal.5b01417openalex-snapshot
Facile Protocol for Water-Tolerant “Frustrated Lewis Pair”-Catalyzed Hydrogenation
inferred← citeshttps://doi.org/10.1021/acscatal.5b02896openalex-snapshot
B(C6F5)3-Catalyzed Reductive Amination using Hydrosilanes
inferred← citeshttps://doi.org/10.1021/acscatal.5c08127openalex-snapshot
Diastereoselective Synthesis of cis -α,α′-Disubstituted Cyclic Ethers via Borane-Catalyzed Reductive Cyclization of Diketones
inferred← citeshttps://doi.org/10.1021/acscatal.6b03581openalex-snapshot
A Viewpoint on Chemical Reductions of Carbon–Oxygen Bonds in Renewable Feedstocks Including CO 2 and Biomass
inferred← citeshttps://doi.org/10.1021/acscatal.7b03077openalex-snapshot
Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Aza-Morita–Baylis–Hillman Adducts and Sequential Organo-FLP Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.7b04489openalex-snapshot
B(C6F5)3: Catalyst or Initiator? Insights from Computational Studies into Surrogate Silicon Chemistry
inferred← citeshttps://doi.org/10.1021/acscatal.8b04485openalex-snapshot
Intramolecular Cyclizations of Vinyl-Substituted N,N-Dialkyl Arylamines Enabled by Borane-Assisted Hydride Transfer
inferred← citeshttps://doi.org/10.1021/acscatal.9b01137openalex-snapshot
Mechanism of Heterolytic Hydrogen Splitting by Frustrated Lewis Pairs: Comparison of Static and Dynamic Models
inferred← citeshttps://doi.org/10.1021/acscentsci.3c00637openalex-snapshot
Incorporation of Chiral Frustrated Lewis Pair into Metal–Organic Framework with Tailored Microenvironment for Heterogeneous Enantio- and Chemoselective Hydrogenation
inferred← citeshttps://doi.org/10.1021/acsomega.3c05388openalex-snapshot
Mechanistic Study of B(C 6 F 5 ) 3 -Catalyzed Transfer Hydrogenation of Aldehydes/Ketones with PhSiH 3 and Stoichiometric Water
inferred← citeshttps://doi.org/10.1021/acsomega.9b03328openalex-snapshot
B(C6F5)3-Catalyzed C–C Coupling of 1,4-Naphthoquinones with the C-3 Position of Indole Derivatives in Water
inferred← citeshttps://doi.org/10.1021/acsorginorgau.3c00064openalex-snapshot
Biomimetic Frustrated Lewis Pair Catalysts for Hydrogenation of CO to Methanol at Low Temperatures
inferred← citeshttps://doi.org/10.1021/acssuschemeng.9b00811openalex-snapshot
Carbonyl Reduction and Biomass: A Case Study of Sustainable Catalysis
inferred← citeshttps://doi.org/10.1021/ar500375jopenalex-snapshot
Frustrated Lewis Pairs: From Concept to Catalysis
inferred← citeshttps://doi.org/10.1021/ja512658mopenalex-snapshot
Chiral Molecular Tweezers: Synthesis and Reactivity in Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1021/jacs.0c05500openalex-snapshot
Metal–Ligand Cooperation Facilitates Bond Activation and Catalytic Hydrogenation with Zinc Pincer Complexes
inferred← citeshttps://doi.org/10.1021/jacs.4c02736openalex-snapshot
Use of Microwave Dielectric Spectroscopy for the In Actu Assessment of Frustrated Lewis Pair Encounter Complexes
inferred← citeshttps://doi.org/10.1021/jacs.4c03756openalex-snapshot
Metal–Organic Frameworks-Based Frustrated Lewis Pairs for Selective Reduction of Nitroolefins to Nitroalkanes
inferred← citeshttps://doi.org/10.1021/jacs.5b05868openalex-snapshot
Highly Selective Hydrogenation of Aromatic Ketones and Phenols Enabled by Cyclic (Amino)(alkyl)carbene Rhodium Complexes
inferred← citeshttps://doi.org/10.1021/jacs.5b12823openalex-snapshot
Stable Borocyclic Radicals via Frustrated Lewis Pair Hydrogenations
inferred← citeshttps://doi.org/10.1021/jacs.5b13545openalex-snapshot
“Inverse” Frustrated Lewis Pairs – Activation of Dihydrogen with Organosuperbases and Moderate to Weak Lewis Acids
inferred← citeshttps://doi.org/10.1021/jacs.6b01349openalex-snapshot
Boron-Catalyzed Aromatic C–H Bond Silylation with Hydrosilanes
inferred← citeshttps://doi.org/10.1021/jacs.7b02548openalex-snapshot
CO-Reduction Chemistry: Reaction of a CO-Derived Formylhydridoborate with Carbon Monoxide, with Carbon Dioxide, and with Dihydrogen
inferred← citeshttps://doi.org/10.1021/jacs.7b03534openalex-snapshot
B(C6F5)3-Catalyzed (Convergent) Disproportionation Reaction of Indoles
inferred← citeshttps://doi.org/10.1021/jacs.7b05408openalex-snapshot
Recyclable Trifluoromethylation Reagents from Fluoroform
inferred← citeshttps://doi.org/10.1021/jacs.7b08143openalex-snapshot
Metal-Free Borylation of Heteroarenes Using Ambiphilic Aminoboranes: On the Importance of Sterics in Frustrated Lewis Pair C–H Bond Activation
inferred← citeshttps://doi.org/10.1021/jacs.8b03626openalex-snapshot
Main-Group-Catalyzed Reductive Alkylation of Multiply Substituted Amines with Aldehydes Using H 2
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