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Frustrated Lewis Pair Mediated Hydrogenations
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-3765(19990104)5:1<24::aid-chem24>3.0.co;2-zopenalex-snapshot
Reactions of Difluorovinylidene—A Super-Electrophilic Carbene
inferredcites →https://doi.org/10.1002/1099-0682(200212)2002:12<3328::aid-ejic3328>3.0.co;2-popenalex-snapshot
Formation and Characterization of Zwitterionic Stereoisomers from the Reaction of B(C6F5)3 and NEt2Ph: (E)- and (Z)-[EtPhN+=CHCH2-B(C6F5)3]
inferredcites →https://doi.org/10.1002/1521-3765(20001215)6:24<4567::aid-chem4567>3.0.co;2-aopenalex-snapshot
4-Oxo-2,3,5,6-tetrafluorocyclohexa-2,5-dienylidene—A Highly Electrophilic Triplet Carbene
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/anie.199508091openalex-snapshot
Bis(pentafluorophenyl)borane: Synthesis, Properties, and Hydroboration Chemistry of a Highly Electrophilic Borane Reagent
inferredcites →https://doi.org/10.1002/anie.200502614openalex-snapshot
The First Liquefaction of High‐Rank Bituminous Coals by Preceding Hydrogenation with Homogeneous Borane or Iodine Catalysts
inferredcites →https://doi.org/10.1002/anie.200702908openalex-snapshot
Metal‐Free Catalytic Hydrogenation
inferredcites →https://doi.org/10.1002/anie.200705586openalex-snapshot
Turning Frustration into Bond Activation: A Theoretical Mechanistic Study on Heterolytic Hydrogen Splitting by Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1002/anie.200705936openalex-snapshot
Metal‐Free Conversion of Methane and Cycloalkanes to Amines and Amides by Employing a Borylnitrene
inferredcites →https://doi.org/10.1002/anie.200800935openalex-snapshot
Facile Heterolytic H2 Activation by Amines and B(C6F5)3
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.200801995openalex-snapshot
Enantioselective Hydrogenation with Racemic and Enantiopure Binap in the Presence of a Chiral Ionic Liquid
inferredcites →https://doi.org/10.1002/anie.200890155openalex-snapshot
Cover Picture: Facile Heterolytic H2 Activation by Amines and B(C6F5)3 (Angew. Chem. Int. Ed. 32/2008)
inferredcites →https://doi.org/10.1002/anie.200903708openalex-snapshot
Frustrated Lewis Pairs: Metal‐free Hydrogen Activation and More
inferredcites →https://doi.org/10.1002/anie.200905484openalex-snapshot
The Mechanism of Dihydrogen Activation by Frustrated Lewis Pairs Revisited
inferredcites →https://doi.org/10.1002/anie.201001518openalex-snapshot
Expanding the Scope of Metal‐Free Catalytic Hydrogenation through Frustrated Lewis Pair Design
inferredcites →https://doi.org/10.1002/anie.201101051openalex-snapshot
Reaction of Frustrated Lewis Pairs with Conjugated Ynones‐Selective Hydrogenation of the Carbon–Carbon Triple Bond
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/asia.201000189openalex-snapshot
Exploring the Limits of Frustrated Lewis Pair Chemistry with Alkynes: Detection of a System that Favors 1,1‐Carboboration over Cooperative 1,2‐P/B‐Addition
inferredcites →https://doi.org/10.1002/cber.19891220415openalex-snapshot
Reduction of Polycyclic Arenes by ‐Boranes, II. Borane Catalyzed Hydrogenation of Naphthalenes to Tetralins
inferredcites →https://doi.org/10.1002/cber.19901230412openalex-snapshot
Partial Hydrogenation: From Anthracene to Coronene
inferredcites →https://doi.org/10.1002/chem.201102438openalex-snapshot
Catalytic Hydrogenation with Frustrated Lewis Pairs: Selectivity Achieved by Size‐Exclusion Design of Lewis Acids
inferredcites →https://doi.org/10.1002/chem.201200244openalex-snapshot
Enantioselective Hydrosilylation with Chiral Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1002/chem.201200246openalex-snapshot
Iridium‐Catalyzed Enantioselective Hydrogenation of Alkenylboronic Esters
inferredcites →https://doi.org/10.1002/hc.20222openalex-snapshot
Metallacyclopentadienes and related heterocycles via 1,1‐organoboration of alkyn‐1‐ylmetal compounds
inferredcites →https://doi.org/10.1016/0010-8545(95)09100-9openalex-snapshot
1,1-Organoboration of alkynylsilicon,-germanium, -tin and -lead compounds
inferredcites →https://doi.org/10.1016/j.jorganchem.2009.03.023openalex-snapshot
Experimental and theoretical treatment of hydrogen splitting and storage in boron–nitrogen systems
inferredcites →https://doi.org/10.1021/ic200663vopenalex-snapshot
Metal-Free Catalytic Hydrogenation of Polar Substrates by Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1021/ja00818a044openalex-snapshot
Strong acid chemistry. II. Catalytic hydrogenation of aromatics in hydrogen fluoride-tantalum pentafluoride and related strong acid systems
inferredcites →https://doi.org/10.1021/ja00848a029openalex-snapshot
Strong acid-catalyzed hydrogenation of aromatics
inferredcites →https://doi.org/10.1021/ja01483a049openalex-snapshot
HOMOGENEOUS HYDROGENATION CATALYZED BY BORANES
inferredcites →https://doi.org/10.1021/ja067961jopenalex-snapshot
Facile Heterolytic Cleavage of Dihydrogen by Phosphines and Boranes
inferredcites →https://doi.org/10.1021/ja106365jopenalex-snapshot
Carbon−Carbon Bond Activation by 1,1-Carboboration of Internal Alkynes
inferredcites →https://doi.org/10.1021/ja300228aopenalex-snapshot
Metal-Free Aromatic Hydrogenation: Aniline to Cyclohexyl-amine Derivatives
inferredcites →https://doi.org/10.1021/ja806627sopenalex-snapshot
Molecular Tweezers for Hydrogen: Synthesis, Characterization, and Reactivity
inferredcites →https://doi.org/10.1021/ja809125ropenalex-snapshot
On the Mechanism of B(C6F5)3-Catalyzed Direct Hydrogenation of Imines: Inherent and Thermally Induced Frustration
inferredcites →https://doi.org/10.1021/ja8100006openalex-snapshot
Catalytic Hydrogenation of Sensitive Organometallic Compounds by Antagonistic N/B Lewis Pair Catalyst Systems
inferredcites →https://doi.org/10.1021/ja903511sopenalex-snapshot
Reactions of an Intramolecular Frustrated Lewis Pair with Unsaturated Substrates: Evidence for a Concerted Olefin Addition Reaction
inferredcites →https://doi.org/10.1021/ja903878zopenalex-snapshot
Rationalizing the Reactivity of Frustrated Lewis Pairs: Thermodynamics of H2 Activation and the Role of Acid−Base Properties
inferredcites →https://doi.org/10.1021/ja991003iopenalex-snapshot
Insertion of Difluorovinylidene into Hydrogen and Methane
inferredcites →https://doi.org/10.1021/jo01059a056openalex-snapshot
Homogeneous Hydrogenation Catalyzed by Boranes
inferredcites →https://doi.org/10.1021/ol102544xopenalex-snapshot
1,1-Carboboration of 1-Alkynes: A Conceptual Alternative to the Hydroboration Reaction
inferredcites →https://doi.org/10.1021/om2005832openalex-snapshot
Metal-Free Transfer Hydrogenation Catalysis by B(C6F5)3
inferredcites →https://doi.org/10.1021/om3006068openalex-snapshot
Alkenylborane-Derived Frustrated Lewis Pairs: Metal-Free Catalytic Hydrogenation Reactions of Electron-Deficient Alkenes
inferredcites →https://doi.org/10.1021/om9004093openalex-snapshot
Functional Group Chemistry at the Group 4 Bent Metallocene Frameworks: Formation and “Metal-Free” Catalytic Hydrogenation of Bis(imino-Cp)zirconium Complexes
inferredcites →https://doi.org/10.1021/om900963popenalex-snapshot
Metal-Free Frustrated Lewis Pair Catalyzed 1,4-Hydrogenation of Conjugated Metallocene Dienamines
inferredcites →https://doi.org/10.1021/om9802313openalex-snapshot
Mechanistic Aspects of the Reactions of Bis(pentafluorophenyl)borane with the Dialkyl Zirconocenes Cp2ZrR2(R = CH3, CH2SiMe3, and CH2C6H5)
inferredcites →https://doi.org/10.1021/om980673eopenalex-snapshot
Synthesis, Properties, and Hydroboration Activity of the Highly Electrophilic Borane Bis(pentafluorophenyl)borane, HB(C6F5)21
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/b801806eopenalex-snapshot
Metal-free catalytic hydrogenation of imines with tris(perfluorophenyl)borane
inferredcites →https://doi.org/10.1039/b804662jopenalex-snapshot
Concerted attack of frustrated Lewis acid–base pairs on olefinic double bonds: a theoretical study
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/b814486aopenalex-snapshot
Reactions of phosphines with electron deficient boranes
inferredcites →https://doi.org/10.1039/b817270fopenalex-snapshot
Insertion into dihydrogen employing the nitrogen centre of a borylnitrene
inferredcites →https://doi.org/10.1039/b909620eopenalex-snapshot
Metal-free hydrogen activation and hydrogenation of imines by 1,8-bis(dipentafluorophenylboryl)naphthalene
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/c1sc00124hopenalex-snapshot
Intramolecular frustrated N/B lewis pairs by enamine hydroboration
inferredcites →https://doi.org/10.1039/j19660001711openalex-snapshot
The preparation and properties of tris(triphenylphosphine)halogenorhodium(I) and some reactions thereof including catalytic homogeneous hydrogenation of olefins and acetylenes and their derivatives
inferredcites →https://doi.org/10.1126/science.1134230openalex-snapshot
Reversible, Metal-Free Hydrogen Activation
inferredcites →https://doi.org/10.1126/science.1141474openalex-snapshot
Facile Splitting of Hydrogen and Ammonia by Nucleophilic Activation at a Single Carbon Center
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4749204openalex-extracted
Advancing Co2 Hydrogenation to Formic Acid: Dft Insights into Frustrated Lewis Pair-Functionalized Uio-67 Catalysts
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc2755openalex-snapshot
Push–Pull Activation of N 2 : Coordination of Lewis Acids to Dinitrogen Complexes
inferred← citeshttps://doi.org/10.1002/9783527681020.ch9openalex-snapshot
Cooperative H 2 Activation by Borane‐Derived Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/9783527814237.ch7openalex-snapshot
Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen
inferred← citeshttps://doi.org/10.1002/ange.201303500openalex-snapshot
Metal‐Free HB(C6F5)2‐Catalyzed Hydrogenation of Unfunctionalized Olefins and Mechanism Study of Borane‐Mediated σ‐Bond Metathesis
inferred← citeshttps://doi.org/10.1002/ange.201409800openalex-snapshot
Chemie frustrierter Lewis‐Paare: Entwicklung und Perspektiven
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.201505974openalex-snapshot
A Strategy to Control the Reactivation of Frustrated Lewis Pairs from Shelf‐Stable Carbene Borane Complexes
inferred← citeshttps://doi.org/10.1002/ange.201606728openalex-snapshot
Reversible Silylene Insertion Reactions into Si−H and P−H σ‐Bonds at Room Temperature
inferred← citeshttps://doi.org/10.1002/ange.201608968openalex-snapshot
A Frustrated and Confused Lewis Pair
inferred← citeshttps://doi.org/10.1002/ange.201610455openalex-snapshot
N,P‐Heterocyclic Germylene/B(C6F5)3 Adducts: A Lewis Pair with Multi‐reactive Sites
inferred← citeshttps://doi.org/10.1002/ange.201806849openalex-snapshot
Alkali Metal Species in the Reversible Activation of H2
inferred← citeshttps://doi.org/10.1002/ange.202000612openalex-snapshot
Using the Secondary PH/BH Functional Groups of an Active Geminal Frustrated Lewis Pair for Carbon Monoxide Reduction and Reactions with Nitriles and Isonitriles
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/anie.201409800openalex-snapshot
Frustrated Lewis Pair Chemistry: Development and Perspectives
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.201505974openalex-snapshot
A Strategy to Control the Reactivation of Frustrated Lewis Pairs from Shelf‐Stable Carbene Borane Complexes
inferred← citeshttps://doi.org/10.1002/anie.201606728openalex-snapshot
Reversible Silylene Insertion Reactions into Si−H and P−H σ‐Bonds at Room Temperature
inferred← citeshttps://doi.org/10.1002/anie.201608968openalex-snapshot
A Frustrated and Confused Lewis Pair
inferred← citeshttps://doi.org/10.1002/anie.201610455openalex-snapshot
N,P‐Heterocyclic Germylene/B(C6F5)3 Adducts: A Lewis Pair with Multi‐reactive Sites
inferred← citeshttps://doi.org/10.1002/anie.201611677openalex-snapshot
Using Ylide Functionalization to Stabilize Boron Cations
inferred← citeshttps://doi.org/10.1002/anie.201806849openalex-snapshot
Alkali Metal Species in the Reversible Activation of H2
inferred← citeshttps://doi.org/10.1002/anie.202000612openalex-snapshot
Using the Secondary PH/BH Functional Groups of an Active Geminal Frustrated Lewis Pair for Carbon Monoxide Reduction and Reactions with Nitriles and Isonitriles
inferred← citeshttps://doi.org/10.1002/cctc.201402838openalex-snapshot
Enantioselective Metal‐Free Hydrogenation Catalyzed by Chiral Frustrated Lewis Pairs
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/chem.201402648openalex-snapshot
Chemistry of Guanidinate‐Stabilised Diboranes: Transition‐Metal‐Catalysed Dehydrocoupling and Hydride Abstraction
inferred← citeshttps://doi.org/10.1002/chem.201404139openalex-snapshot
Gallium‐Assisted Transfer Hydrogenation of Alkenes
inferred← citeshttps://doi.org/10.1002/chem.201501402openalex-snapshot
Bifunctional Behavior of Unsaturated Intramolecular Phosphane–Borane Frustrated Lewis Pairs Derived from Uncatalyzed 1,4‐Hydrophosphination of a Dienylborane
inferred← citeshttps://doi.org/10.1002/chem.201502278openalex-snapshot
Functionalization of Intramolecular Frustrated Lewis Pairs by 1,1‐Carboboration with Conjugated Enynes
inferred← citeshttps://doi.org/10.1002/chem.201502493openalex-snapshot
Frustrated Lewis Pair Chemistry Derived from Bulky Allenyl and Propargyl Phosphanes
inferred← citeshttps://doi.org/10.1002/chem.201601583openalex-snapshot
An Ethylene‐Bridged Phosphane/Borane Frustrated Lewis Pair Featuring the ‐B(Fxyl)2 Lewis Acid Component
inferred← citeshttps://doi.org/10.1002/chem.201603050openalex-snapshot
A Frustrated Phosphane–Borane Lewis Pair and Hydrogen: A Kinetics Study
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.202004733openalex-snapshot
Understanding the C−F Bond Activation Mediated by Frustrated Lewis Pairs: Crucial Role of Non‐covalent Interactions
inferred← citeshttps://doi.org/10.1002/chem.202004991openalex-snapshot
Reversible Addition of Carbon Dioxide to Main Group Metal Complexes at Temperatures about 0 °C
inferred← citeshttps://doi.org/10.1002/chem.202100835openalex-snapshot
Frustrated Lewis‐Pair Neighbors at the Xanthene Framework: Epimerization at Phosphorus and Cooperative Formation of Macrocyclic Adduct Structures
inferred← citeshttps://doi.org/10.1002/chem.202104016openalex-snapshot
Directed Synthesis and Chemistry of Unsymmetric Dicationic Diboranes and Their Use in Frustrated Lewis Pair‐like Chemistry
inferred← citeshttps://doi.org/10.1002/chem.202202037openalex-snapshot
Labile Base‐Stabilized Silyliumylidene Ions. Non‐Metallic Species Capable of Activating Multiple Small Molecules
inferred← citeshttps://doi.org/10.1002/chin.201439277openalex-snapshot
ChemInform Abstract: Frustrated Lewis Pair Mediated Hydrogenations
inferred← citeshttps://doi.org/10.1002/cphc.202100093openalex-snapshot
Effects of Ionic Liquids on the Thermodynamics of Hydrogen Activation by Frustrated Lewis Pairs: A Density Functional Theory Study**
inferred← citeshttps://doi.org/10.1002/ejic.201500861openalex-snapshot
Diboranyl Phosphonium Cations: Synthesis and Chemical Properties
inferred← citeshttps://doi.org/10.1002/ejic.201700016openalex-snapshot
Comparison of Intramolecular and Intermolecular Ammonium and Phosphonium Borohydrides in Hydrogen‐, Proton‐, and Hydride‐Transfer Reactions
inferred← citeshttps://doi.org/10.1002/ijch.201400137openalex-snapshot
Establishing the Steric Bulk of Main Group Hydrides in Reduction Reactions
inferred← citeshttps://doi.org/10.1002/ijch.201400149openalex-snapshot
Structural Characterization of Frustrated Lewis Pairs and Their Reaction Products Using Modern Solid‐State NMR Spectroscopy Techniques
inferred← citeshttps://doi.org/10.1002/ijch.201700085openalex-snapshot
Organic Synthesis: Wherefrom and Whither? (Some Very Personal Reflections)
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_6openalex-snapshot
Lewis Acidic Boranes in Frustrated Lewis Pair Chemistry
inferred← citeshttps://doi.org/10.1007/s00894-024-05997-yopenalex-snapshot
Frustrated Lewis pair-mediated hydro-dehalogenation: crucial role of non-covalent interactions
inferred← citeshttps://doi.org/10.1016/j.cattod.2014.10.040openalex-snapshot
Catalytic reduction of polar substrates without metals: A thermodynamic and kinetic study of heterolytic activation of hydrogen by vacancies in frustrated Lewis pairs
inferred← citeshttps://doi.org/10.1016/j.cclet.2018.02.007openalex-snapshot
Rational design of FLP catalysts for reversible H2 activation: A DFT study of the geometric and electronic effects
inferred← citeshttps://doi.org/10.1016/j.ccr.2015.01.006openalex-snapshot
Cooperative 1,1-addition reactions of vicinal phosphane/borane frustrated Lewis pairs
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.ccr.2025.216948openalex-snapshot
Activation of small molecules by polytopic main-group lewis acids
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115571openalex-snapshot
Advancing CO2 hydrogenation to formic Acid: DFT insights into Frustrated Lewis Pair−Functionalized UiO−67 catalysts
inferred← citeshttps://doi.org/10.1016/j.jcat.2025.116275openalex-snapshot
Unlocking efficient CO2–to–methanol conversion on frustrated Lewis pair-functionalized UiO–67: A synergistic approach using DFT and SISSO
inferred← citeshttps://doi.org/10.1016/j.jcat.2026.116799openalex-snapshot
Organic superbases in Lewis pair catalyzed hydrogenations of imines
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2013.06.005openalex-snapshot
Structural features and reactions of a geminal frustrated phosphane/borane Lewis pair
inferred← citeshttps://doi.org/10.1016/j.poly.2019.06.045openalex-snapshot
Hydrogen activation by isomeric aromatic phosphabenzene: A theoretical study
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.10.138openalex-snapshot
Metal-free asymmetric hydrogenation and hydrosilylation catalyzed by frustrated Lewis pairs
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00168openalex-snapshot
Thermodynamic Hydricity of Transition Metal Hydrides
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00352openalex-snapshot
Polymerization of Polar Monomers Mediated by Main-Group Lewis Acid–Base Pairs
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c00911openalex-snapshot
Energy Decomposition Analysis of Lewis Acid/Base Adducts and Frustrated Lewis Pairs: The Use of EOrb/ESteric Ratios as a Reaction Parameter
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.3c02263openalex-snapshot
Double Bond Cleavage in Small Molecules Using a Geminal Sc/P Lewis Pair
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.9b00501openalex-snapshot
Carbones and Heavier Ylidones (EL2) in Frustrated Lewis Pair Chemistry: Influence of the Nature of EL2 on Dihydrogen Activation
inferred← citeshttps://doi.org/10.1021/acs.jpca.7b11851openalex-snapshot
Surprisingly Flexible Oxonium/Borohydride Ion Pair Configurations
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.jpcc.4c05333openalex-snapshot
Theoretical Investigation of the Steric Effects on Alkyne Semihydrogenation Catalyzed by Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1021/acs.macromol.9b00652openalex-snapshot
Living and Chemoselective (Co)polymerization of Polar Divinyl Monomers Mediated by Bulky Lewis Pairs
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.7b00819openalex-snapshot
Frustrated Lewis Pair Behavior of an Open, Noninteracting Phosphane/Borane Pair at a Rigid Organic Framework: Exploring Decisive Factors for FLP Activity
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00841openalex-snapshot
Synthesis of Half-Titanocenes Containing Anionic N-Heterocyclic Carbenes That Contain a Weakly Coordinating Borate Moiety, Cp′TiX2(WCA-NHC), and Their Use as Catalysts for Ethylene (Co)polymerization
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01373openalex-snapshot
One-Step Conversion of Potassium Organotrifluoroborates to Metal Organoborohydrides
inferred← citeshttps://doi.org/10.1021/acscatal.6b03313openalex-snapshot
Tuning Catalytic Activity in the Hydrogenation of Unactivated Olefins with Transition-Metal Oxos as the Lewis Base Component of Frustrated Lewis Pairs
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/acssuschemeng.3c00497openalex-snapshot
Metal-Free Supramolecular Reduction of Nitro Compounds into the Cucurbit[7]uril Cavity: Testing the Enabling Technique in Aqueous Media
inferred← citeshttps://doi.org/10.1021/ja3110076openalex-snapshot
Reactions of a Cationic Geminal Zr+/P Pair with Small Molecules
inferred← citeshttps://doi.org/10.1021/ja400338eopenalex-snapshot
Noninteracting, Vicinal Frustrated P/B-Lewis Pair at the Norbornane Framework: Synthesis, Characterization, and Reactions
inferred← citeshttps://doi.org/10.1021/ja408385hopenalex-snapshot
Remarkable Behavior of a Bifunctional Alkynylborane Zirconocene Complex toward Donor Ligands and Acetylenes
inferred← citeshttps://doi.org/10.1021/ja4118335openalex-snapshot
Reaction of a Bridged Frustrated Lewis Pair with Nitric Oxide: A Kinetics Study
inferred← citeshttps://doi.org/10.1021/ja413060uopenalex-snapshot
Internal Adduct Formation of Active Intramolecular C4-bridged Frustrated Phosphane/Borane Lewis Pairs
inferred← citeshttps://doi.org/10.1021/ja5028293openalex-snapshot
Frustrated Lewis Pair Modification by 1,1-Carboboration: Disclosure of a Phosphine Oxide Triggered Nitrogen Monoxide Addition to an Intramolecular P/B Frustrated Lewis Pair
inferred← citeshttps://doi.org/10.1021/ja5068146openalex-snapshot
Formation of Unsaturated Vicinal Zr+/P Frustrated Lewis Pairs by the Unique 1,1-Carbozirconation Reactions
inferred← citeshttps://doi.org/10.1021/ja5077525openalex-snapshot
Hydrogen Activation by an Aromatic Triphosphabenzene
inferred← citeshttps://doi.org/10.1021/ja512658mopenalex-snapshot
Chiral Molecular Tweezers: Synthesis and Reactivity in Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1021/jacs.0c08599openalex-snapshot
Direct Conversion of N -Alkylamines to N -Propargylamines through C–H Activation Promoted by Lewis Acid/Organocopper Catalysis: Application to Late-Stage Functionalization of Bioactive Molecules
inferred← citeshttps://doi.org/10.1021/jacs.0c13200openalex-snapshot
Enantioselective Synthesis of N-Alkylamines through β-Amino C–H Functionalization Promoted by Cooperative Actions of B(C6F5)3 and a Chiral Lewis Acid Co-Catalyst
inferred← citeshttps://doi.org/10.1021/jacs.2c07688openalex-snapshot
Taming PH3: State of the Art and Future Directions in Synthesis
inferred← citeshttps://doi.org/10.1021/jacs.4c09012openalex-snapshot
Synthesis and Photochemical Uncaging of Alkene-Protected, Polymer-Bound Vicinal Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1021/jacs.5b00546openalex-snapshot
Organocatalytic Diboration Involving “Reductive Addition” of a Boron–Boron σ-Bond to 4,4′-Bipyridine
inferred← citeshttps://doi.org/10.1021/jacs.5b02078openalex-snapshot
Tunable Luminescence of Bithiophene-Based Flexible Lewis Pairs
inferred← citeshttps://doi.org/10.1021/jacs.5c07140openalex-snapshot
Net Oxidative Addition of H 2 to {M II } 2+ (M = Pd, Pt) by Heterolysis and Protic Rebound
inferred← citeshttps://doi.org/10.1021/jacs.6b00325openalex-snapshot
Selective Oxidation of an Active Intramolecular Amine/Borane Frustrated Lewis Pair with Dioxygen
inferred← citeshttps://doi.org/10.1021/jacs.6b00705openalex-snapshot
Transition-Metal Oxos as the Lewis Basic Component of Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1021/jacs.8b05176openalex-snapshot
Remote Stereochemistry of a Frustrated Lewis Pair Provides Thermal and Photochemical Control of Reactivity
inferred← citeshttps://doi.org/10.1021/jacs.8b13757openalex-snapshot
Enantioselective Conia-Ene-Type Cyclizations of Alkynyl Ketones through Cooperative Action of B(C6F5)3, N-Alkylamine and a Zn-Based Catalyst
inferred← citeshttps://doi.org/10.1021/jacs.9b08662openalex-snapshot
Catalytic Deuterium Incorporation within Metabolically Stable β-Amino C–H Bonds of Drug Molecules
inferred← citeshttps://doi.org/10.1021/om4004225openalex-snapshot
An Enamine/HB(C6F5)2 Adduct as a Dormant State in Frustrated Lewis Pair Chemistry
inferred← citeshttps://doi.org/10.1021/om400769yopenalex-snapshot
Reactions of (Diphenylphosphinomethyl)zirconocene Chloride with B(C6F5)3: Competition between P/B and P/Zr+ Frustrated Lewis Pair Reactions
inferred← citeshttps://doi.org/10.1021/om401118nopenalex-snapshot
Ancillary Metal Centers in Frustrated Lewis Pair Chemistry: Ruthenium Acetylide as a Lewis Base in the Activation of CO2, Aldehyde, and Alkyne
inferred← citeshttps://doi.org/10.1021/om5011512openalex-snapshot
Establishing the Hydride Donor Abilities of Main Group Hydrides
inferred← citeshttps://doi.org/10.1021/om501288topenalex-snapshot
Fine Tuning of the Substituents on the N-Geminal Phosphorus/Silicon-Based Lewis Pairs for the Synthesis of Z-Type Silyliminophosphoranylalkenes
inferred← citeshttps://doi.org/10.1021/om501312aopenalex-snapshot
Frustrated Lewis Pair Behavior of [Cp2ZrOCR2CH2PPh2]+ Cations
inferred← citeshttps://doi.org/10.1038/s41557-024-01588-9openalex-snapshot
Phosphorus-mediated hydrogenation catalysis
inferred← citeshttps://doi.org/10.1039/c3cc47769jopenalex-snapshot
Ethene/alkyne exchange reaction at an intramolecular frustrated Lewis pair
inferred← citeshttps://doi.org/10.1039/c3cc47889kopenalex-snapshot
Imine hydrogenation by alkylaluminum catalysts
inferred← citeshttps://doi.org/10.1039/c4sc03675aopenalex-snapshot
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis
inferred← citeshttps://doi.org/10.1039/c5cc07954copenalex-snapshot
Cooperative reaction chemistry derived from a borata-diene framework
inferred← citeshttps://doi.org/10.1039/c5dt00921aopenalex-snapshot
B(C 6 F 5 ) 3 mediated arene hydrogenation/transannulation of para-methoxyanilines
inferred← citeshttps://doi.org/10.1039/c5dt03055bopenalex-snapshot
Phosphole formation by 1,1-carboboration – reactions of bis-alkynyl phosphanes with a frustrated P/B Lewis pair
inferred← citeshttps://doi.org/10.1039/c5dt03796dopenalex-snapshot
Pyridinium–phosphonium dications: highly electrophilic phosphorus-based Lewis acid catalysts
inferred← citeshttps://doi.org/10.1039/c5ob00634aopenalex-snapshot
Direct synthesis of a geminal zwitterionic phosphonium/hydridoborate system – developing an alternative tool for generating frustrated Lewis pair hydrogen activation systems
inferred← citeshttps://doi.org/10.1039/c5ob01602aopenalex-snapshot
Enamine/butadienylborane cycloaddition in the frustrated Lewis pair regime
inferred← citeshttps://doi.org/10.1039/c6dt00857gopenalex-snapshot
Nitro-redox reactions at a frustrated borane/phosphane Lewis pair
inferred← citeshttps://doi.org/10.1039/c6dt02202bopenalex-snapshot
Chiral carbene–borane adducts: precursors for borenium catalysts for asymmetric FLP hydrogenations
inferred← citeshttps://doi.org/10.1039/c6dt04725dopenalex-snapshot
Borane-catalyzed indole synthesis through intramolecular hydroamination
inferred← citeshttps://doi.org/10.1039/c7dt00777aopenalex-snapshot
Quantification of Lewis acid induced Brønsted acidity of protogenic Lewis bases
inferred← citeshttps://doi.org/10.1039/c7dt01693jopenalex-snapshot
Influence of intramolecular vs. intermolecular phosphonium-borohydrides in catalytic hydrogen, hydride, and proton transfer reactions
inferred← citeshttps://doi.org/10.1039/c7dt01726jopenalex-snapshot
FLP reactivity of [Ph 3 C] + and ( o -tolyl) 3 P and the capture of a Staudinger reaction intermediate
inferred← citeshttps://doi.org/10.1039/c7sc04394eopenalex-snapshot
Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs
inferred← citeshttps://doi.org/10.1039/c8cc09777aopenalex-snapshot
Aromaticity can enhance the reactivity of P-donor/borole frustrated Lewis pairs
inferred← citeshttps://doi.org/10.1039/c8sc01089gopenalex-snapshot
Solid state frustrated Lewis pair chemistry
inferred← citeshttps://doi.org/10.1039/c9ra01468copenalex-snapshot
Mechanistic insight into the catalytic hydrogenation of nonactivated aldehydes with a Hantzsch ester in the presence of a series of organoboranes: NMR and DFT studies
inferred← citeshttps://doi.org/10.1039/d1dt00459jopenalex-snapshot
Reaction of carbon oxides with an ethylene-bridged PH/B Lewis pair
inferred← citeshttps://doi.org/10.1055/a-2742-1904openalex-snapshot
Metal-Free Reagents and Catalysts for C–C Multiple Bond Reduction
inferred← citeshttps://doi.org/10.1055/sos-sd-142-00193openalex-snapshot
42.12.8 Alkylphosphonium Salts (Update 2022)
inferred← citeshttps://doi.org/10.1055/sos-sd-245-00090openalex-snapshot
2.2 Chemoselective Hydrogenation of Arenes
inferred← citeshttps://doi.org/10.1063/1.4916066openalex-snapshot
Solid-state EPR strategies for the structural characterization of paramagnetic NO adducts of frustrated Lewis pairs (FLPs)
inferred← citeshttps://doi.org/10.1073/pnas.1407484111openalex-snapshot
Metal-free transfer hydrogenation of olefins via dehydrocoupling catalysis
inferred← citeshttps://doi.org/10.1126/science.aaf7229openalex-snapshot
The broadening reach of frustrated Lewis pair chemistry
inferred← citeshttps://doi.org/10.2139/ssrn.6024727openalex-snapshot
Organic Superbases in Lewis Pair Catalyzed Hydrogenations of Imines
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.79.632openalex-snapshot
N-Phosphine Oxide-Substituted Imidazolylidenes (PoxIms) as Multifunctional Multipurpose N-Heterocyclic Carbenes
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