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Lewis acid-catalyzed hydrogenation: B(C6F5)3-mediated reduction of imines and nitriles with H2
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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/anie.200400650openalex-snapshot
In the Golden Age of Organocatalysis
inferredcites →https://doi.org/10.1002/anie.200461816openalex-snapshot
A Metal‐Free Transfer Hydrogenation: Organocatalytic Conjugate Reduction of α,β‐Unsaturated Aldehydes
inferredcites →https://doi.org/10.1002/anie.200500827openalex-snapshot
Organocatalytic Hydride Transfers: A New Concept in Asymmetric Hydrogenations
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.200600191openalex-snapshot
A Highly Enantioselective Brønsted Acid Catalyzed Cascade Reaction: Organocatalytic Transfer Hydrogenation of Quinolines and their Application in the Synthesis of Alkaloids
inferredcites →https://doi.org/10.1002/anie.200701215openalex-snapshot
Reactivity of “Frustrated Lewis Pairs”: Three‐Component Reactions of Phosphines, a Borane, and Olefins
inferredcites →https://doi.org/10.1002/anie.200702816openalex-snapshot
Heterolytic H2 Activation by Nonmetals
inferredcites →https://doi.org/10.1002/anie.200702908openalex-snapshot
Metal‐Free Catalytic Hydrogenation
inferredcites →https://doi.org/10.1002/jlac.19616440102openalex-snapshot
Borverbindungen, V Hydrierung von Bortrialkylen und ‐triarylen
inferredcites →https://doi.org/10.1016/j.ica.2006.02.006openalex-snapshot
Pyridine and phosphine reactions with [CPh3][B(C6F5)4]
inferredcites →https://doi.org/10.1016/s0040-4020(02)00974-2openalex-snapshot
B(C 6 F 5 ) 3 catalyzed hydrosilation of enones and silyl enol ethers
inferredcites →https://doi.org/10.1016/s0065-3055(04)52001-4openalex-snapshot
The Chemistry of Perfluoroaryl Boranes
inferredcites →https://doi.org/10.1021/cr000021bopenalex-snapshot
Dihydrogen Bonding: Structures, Energetics, and Dynamics
inferredcites →https://doi.org/10.1021/cr020049iopenalex-snapshot
New Chiral Phosphorus Ligands for Enantioselective Hydrogenation
inferredcites →https://doi.org/10.1021/cr980414zopenalex-snapshot
Catalytic Enantioselective Addition to Imines
inferredcites →https://doi.org/10.1021/ja01483a049openalex-snapshot
HOMOGENEOUS HYDROGENATION CATALYZED BY BORANES
inferredcites →https://doi.org/10.1021/ja016152ropenalex-snapshot
Hydrogenation without a Transition-Metal Catalyst: On the Mechanism of the Base-Catalyzed Hydrogenation of Ketones
inferredcites →https://doi.org/10.1021/ja053247aopenalex-snapshot
Facile Activation of Dihydrogen by an Unsaturated Heavier Main Group Compound
inferredcites →https://doi.org/10.1021/ja0653066openalex-snapshot
Organocatalytic Transfer Hydrogenation of Cyclic Enones
inferredcites →https://doi.org/10.1021/ja067961jopenalex-snapshot
Facile Heterolytic Cleavage of Dihydrogen by Phosphines and Boranes
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/jo01059a056openalex-snapshot
Homogeneous Hydrogenation Catalyzed by Boranes
inferredcites →https://doi.org/10.1021/jo016279zopenalex-snapshot
Highly Efficient B(C 6 F 5 ) 3 -Catalyzed Hydrosilylation of Olefins
inferredcites →https://doi.org/10.1021/jo9624049openalex-snapshot
Highly Regiocontrolled and Efficient Synthesis of Vinyl- and Allylstannanes via Lewis Acids and Pd-Catalyzed Hydrostannation of Allenes: Scope and Limitations
inferredcites →https://doi.org/10.1021/jo991828aopenalex-snapshot
Studies on the Mechanism of B(C 6 F 5 ) 3 -Catalyzed Hydrosilation of Carbonyl Functions
inferredcites →https://doi.org/10.1021/ol006695qopenalex-snapshot
B(C6F5)3-Catalyzed Hydrosilation of Imines via Silyliminium Intermediates
inferredcites →https://doi.org/10.1021/ol0521026openalex-snapshot
Trans- and Cis- Selective Lewis Acid Catalyzed Hydrogermylation of Alkynes
inferredcites →https://doi.org/10.1039/a706187kopenalex-snapshot
Hydrostannation of C–C multiple bonds with Bu3SnH prepared in situ from Bu3SnCl and Et3SiH in the presence of Lewis acid catalysts
inferredcites →https://doi.org/10.1039/b704417hopenalex-snapshot
Tuning Lewis acidity using the reactivity of “frustrated Lewis pairs”: facile formation of phosphine-boranes and cationic phosphonium-boranes
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.4788907openalex-extracted
Construction of Heterogeneous Flps Based on Cofs-Stabilized Boron Cations and Investigation of the Cycloaddition Reaction Performance
inferred← citeshttps://doi.org/10.1002/047084289x.rn01333openalex-snapshot
[2,3,5,6-Tetrafluorophenyl][bis(2,4,6-trimethylphenyl) phosphonium][4-bis(2,3,4,5,6-pentafluorophenyl) borohydride]
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0661openalex-snapshot
Ferrocenes in Frustrated Lewis Pair Chemistry
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0980openalex-snapshot
Boron‐Based Frustrated L ewis Pairs in Hydrogenation Catalysis
inferred← citeshttps://doi.org/10.1002/9781118604755.ch15openalex-snapshot
Enantioselective Organocatalytic Reductions
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc2521openalex-snapshot
Alkaline Earth Catalysis
inferred← citeshttps://doi.org/10.1002/9783527631582.ch11openalex-snapshot
“Frustrated Lewis Pairs”: A Metal‐Free Strategy for Hydrogenation Catalysis
inferred← citeshttps://doi.org/10.1002/9783527651733.ch10openalex-snapshot
New Trends in Organometallic Catalysts
inferred← citeshttps://doi.org/10.1002/9783527681020.ch9openalex-snapshot
Cooperative H 2 Activation by Borane‐Derived Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/9783527811458.vol1-ch10openalex-snapshot
Carbocatalysis: Analyzing the Sources of Organic Transformations
inferred← citeshttps://doi.org/10.1002/9783527814237.ch7openalex-snapshot
Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen
inferred← citeshttps://doi.org/10.1002/adsc.201100206openalex-snapshot
Highly Active Metal‐Free Catalysts for Hydrogenation of Unsaturated Nitrogen‐Containing Compounds
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/ange.200801432openalex-snapshot
Metallfreie katalytische Hydrierung von Enaminen, Iminen und konjugierten Phosphinoalkenylboranen
inferred← citeshttps://doi.org/10.1002/ange.200801675openalex-snapshot
Schlüssiger Nachweis eines SN2‐Si‐Mechanismus in der B(C6F5)3‐ katalysierten Hydrosilylierung von Carbonylverbindungen: Einsichten in die verwandte Hydrierung
inferred← citeshttps://doi.org/10.1002/ange.200802596openalex-snapshot
Hydrogen and Amine Activation by a Frustrated Lewis Pair of a Bulky N‐Heterocyclic Carbene and B(C6F5)3
inferred← citeshttps://doi.org/10.1002/ange.200802705openalex-snapshot
Heterolytic Dihydrogen Activation by a Frustrated Carbene–Borane Lewis Pair
inferred← citeshttps://doi.org/10.1002/ange.200901636openalex-snapshot
Reversible, nicht metallunterstützte Bindung von Kohlendioxid durch frustrierte Lewis‐Paare
inferred← citeshttps://doi.org/10.1002/ange.200903708openalex-snapshot
Frustrierte Lewis‐Paare: metallfreie Wasserstoffaktivierung und mehr
inferred← citeshttps://doi.org/10.1002/ange.200906697openalex-snapshot
Cyclische Allene und Cumulene durch kooperative Addition frustrierter Lewis‐Paare an konjugierte Enine und Diine
inferred← citeshttps://doi.org/10.1002/ange.201001518openalex-snapshot
Expanding the Scope of Metal‐Free Catalytic Hydrogenation through Frustrated Lewis Pair Design
inferred← citeshttps://doi.org/10.1002/ange.201004149openalex-snapshot
Heterolytic SS Bond Cleavage by a Purely Carbogenic Frustrated Lewis Pair
inferred← citeshttps://doi.org/10.1002/ange.201004525openalex-snapshot
Enantioselective Hydrogenation with Chiral Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/ange.201101622openalex-snapshot
Capture of NO by a Frustrated Lewis Pair: A New Type of Persistent N‐Oxyl Radical
inferred← citeshttps://doi.org/10.1002/ange.201104999openalex-snapshot
Heterolytic Cleavage of Dihydrogen by “Frustrated Lewis Pairs” Comprising Bis(2,4,6‐tris(trifluoromethyl)phenyl)borane and Amines: Stepwise versus Concerted Mechanism
inferred← citeshttps://doi.org/10.1002/ange.201203362openalex-snapshot
H2 Activation and Hydride Transfer to Olefins by Al(C6F5)3‐Based Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/ange.201204007openalex-snapshot
Metal‐free Catalytic Olefin Hydrogenation: Low‐Temperature H2 Activation by Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/ange.201205348openalex-snapshot
Metallfreie Hydrierung von elektronenarmen Allenen und Alkenen
inferred← citeshttps://doi.org/10.1002/ange.201301153openalex-snapshot
Phosphastanniran: Ein Phosphor/Zinn(II)‐Lewis‐Paar, das Alkine und Alkene addiert
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.201306243openalex-snapshot
Silver‐Catalyzed Hydrogenation of Aldehydes in Water
inferred← citeshttps://doi.org/10.1002/ange.201309253openalex-snapshot
Metallfreie Hydrierung von ungesättigten Kohlenwasserstoffen mit molekularem Wasserstoff
inferred← citeshttps://doi.org/10.1002/ange.201405531openalex-snapshot
Metal‐Free Hydrogenation Catalyzed by an Air‐Stable Borane: Use of Solvent as a Frustrated Lewis Base
inferred← citeshttps://doi.org/10.1002/ange.201406122openalex-snapshot
N‐Methylacridinium Salts: Carbon Lewis Acids in Frustrated Lewis Pairs for σ‐Bond Activation and Catalytic Reductions
inferred← citeshttps://doi.org/10.1002/ange.201407324openalex-snapshot
B(C6F5)3‐katalysierte Hydrierung von Oximethern ohne Spaltung der N‐O‐Bindung
inferred← citeshttps://doi.org/10.1002/ange.201409246openalex-snapshot
B(C6F5)3‐katalysierte Transferhydrierung von Iminen und verwandten Heteroaromaten mit Cyclohexa‐1,4‐dienen als Wasserstoffquelle
inferred← citeshttps://doi.org/10.1002/ange.201409250openalex-snapshot
Hydrogenations at Room Temperature and Atmospheric Pressure with Mesoionic Carbene‐Stabilized Borenium Catalysts
inferred← citeshttps://doi.org/10.1002/ange.201409471openalex-snapshot
A Highly cis‐Selective and Enantioselective Metal‐Free Hydrogenation of 2,3‐Disubstituted Quinoxalines
inferred← citeshttps://doi.org/10.1002/ange.201502366openalex-snapshot
Chemoselective Silylative Reduction of Conjugated Nitriles under Metal‐Free Catalytic Conditions: β‐Silyl Amines and Enamines
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.201504941openalex-snapshot
B(C6F5)3‐katalysierter Diwasserstofftransfer von einem ungesättigten Kohlenwasserstoff auf einen anderen
inferred← citeshttps://doi.org/10.1002/ange.201606177openalex-snapshot
Tris(pentafluorophenyl)borane‐Catalyzed Acceptorless Dehydrogenation of N‐Heterocycles
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.201610530openalex-snapshot
Selective Metal‐free HB(C6F5)2 Catalyzed Allene Cyclotrimerization: Formation of 1,3,5‐Trimethylenecyclohexane and Its Tris‐hydroboration Product
inferred← citeshttps://doi.org/10.1002/ange.201803804openalex-snapshot
LiAlH4: From Stoichiometric Reduction to Imine Hydrogenation Catalysis
inferred← citeshttps://doi.org/10.1002/ange.201808289openalex-snapshot
C2‐Symmetric Bicyclic Bisborane Catalysts: Kinetic or Thermodynamic Products of a Reversible Hydroboration of Dienes
inferred← citeshttps://doi.org/10.1002/anie.200801432openalex-snapshot
Metal‐Free Catalytic Hydrogenation of Enamines, Imines, and Conjugated Phosphinoalkenylboranes
inferred← citeshttps://doi.org/10.1002/anie.200801675openalex-snapshot
Conclusive Evidence for an S N 2‐Si Mechanism in the B(C 6 F 5 ) 3 ‐Catalyzed Hydrosilylation of Carbonyl Compounds: Implications for the Related Hydrogenation
inferred← citeshttps://doi.org/10.1002/anie.200802596openalex-snapshot
Hydrogen and Amine Activation by a Frustrated Lewis Pair of a Bulky N‐Heterocyclic Carbene and B(C6F5)3
inferred← citeshttps://doi.org/10.1002/anie.200802705openalex-snapshot
Heterolytic Dihydrogen Activation by a Frustrated Carbene–Borane Lewis Pair
inferred← citeshttps://doi.org/10.1002/anie.200901636openalex-snapshot
Reversible Metal‐Free Carbon Dioxide Binding by Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/anie.200903708openalex-snapshot
Frustrated Lewis Pairs: Metal‐free Hydrogen Activation and More
inferred← citeshttps://doi.org/10.1002/anie.200906697openalex-snapshot
Formation of Cyclic Allenes and Cumulenes by Cooperative Addition of Frustrated Lewis Pairs to Conjugated Enynes and Diynes
inferred← citeshttps://doi.org/10.1002/anie.201001518openalex-snapshot
Expanding the Scope of Metal‐Free Catalytic Hydrogenation through Frustrated Lewis Pair Design
inferred← citeshttps://doi.org/10.1002/anie.201004149openalex-snapshot
Heterolytic SS Bond Cleavage by a Purely Carbogenic Frustrated Lewis Pair
inferred← citeshttps://doi.org/10.1002/anie.201004525openalex-snapshot
Enantioselective Hydrogenation with Chiral Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/anie.201101622openalex-snapshot
Capture of NO by a Frustrated Lewis Pair: A New Type of Persistent N‐Oxyl Radical
inferred← citeshttps://doi.org/10.1002/anie.201104999openalex-snapshot
Heterolytic Cleavage of Dihydrogen by “Frustrated Lewis Pairs” Comprising Bis(2,4,6‐tris(trifluoromethyl)phenyl)borane and Amines: Stepwise versus Concerted Mechanism
inferred← citeshttps://doi.org/10.1002/anie.201203362openalex-snapshot
H2 Activation and Hydride Transfer to Olefins by Al(C6F5)3‐Based Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/anie.201204007openalex-snapshot
Metal‐free Catalytic Olefin Hydrogenation: Low‐Temperature H2 Activation by Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/anie.201205348openalex-snapshot
Metal‐Free Hydrogenation of Electron‐Poor Allenes and Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201301153openalex-snapshot
Phosphastannirane: A Phosphorus/Tin(II) Lewis Pair that Undergoes Alkyne and Alkene Addition
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.201306243openalex-snapshot
Silver‐Catalyzed Hydrogenation of Aldehydes in Water
inferred← citeshttps://doi.org/10.1002/anie.201309253openalex-snapshot
Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen
inferred← citeshttps://doi.org/10.1002/anie.201405531openalex-snapshot
Metal‐Free Hydrogenation Catalyzed by an Air‐Stable Borane: Use of Solvent as a Frustrated Lewis Base
inferred← citeshttps://doi.org/10.1002/anie.201406122openalex-snapshot
N‐Methylacridinium Salts: Carbon Lewis Acids in Frustrated Lewis Pairs for σ‐Bond Activation and Catalytic Reductions
inferred← citeshttps://doi.org/10.1002/anie.201407324openalex-snapshot
B(C6F5)3‐Catalyzed Hydrogenation of Oxime Ethers without Cleavage of the NO Bond
inferred← citeshttps://doi.org/10.1002/anie.201409246openalex-snapshot
B(C 6 F 5 ) 3 ‐Catalyzed Transfer Hydrogenation of Imines and Related Heteroarenes Using Cyclohexa‐1,4‐dienes as a Dihydrogen Source
inferred← citeshttps://doi.org/10.1002/anie.201409250openalex-snapshot
Hydrogenations at Room Temperature and Atmospheric Pressure with Mesoionic Carbene‐Stabilized Borenium Catalysts
inferred← citeshttps://doi.org/10.1002/anie.201409471openalex-snapshot
A Highly cis‐Selective and Enantioselective Metal‐Free Hydrogenation of 2,3‐Disubstituted Quinoxalines
inferred← citeshttps://doi.org/10.1002/anie.201502366openalex-snapshot
Chemoselective Silylative Reduction of Conjugated Nitriles under Metal‐Free Catalytic Conditions: β‐Silyl Amines and Enamines
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.201504941openalex-snapshot
B(C6F5)3‐Catalyzed Transfer of Dihydrogen from One Unsaturated Hydrocarbon to Another
inferred← citeshttps://doi.org/10.1002/anie.201606177openalex-snapshot
Tris(pentafluorophenyl)borane‐Catalyzed Acceptorless Dehydrogenation of N‐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.201610530openalex-snapshot
Selective Metal‐free HB(C6F5)2 Catalyzed Allene Cyclotrimerization: Formation of 1,3,5‐Trimethylenecyclohexane and Its Tris‐hydroboration Product
inferred← citeshttps://doi.org/10.1002/anie.201803804openalex-snapshot
LiAlH4: From Stoichiometric Reduction to Imine Hydrogenation Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201808289openalex-snapshot
C2‐Symmetric Bicyclic Bisborane Catalysts: Kinetic or Thermodynamic Products of a Reversible Hydroboration of Dienes
inferred← citeshttps://doi.org/10.1002/asia.201701607openalex-snapshot
Density Functional Theory Mechanistic Study of Boron‐Catalyzed N‐Alkylation of Amines with Formic Acid: Formic Acid Activation by Silylation Reaction
inferred← citeshttps://doi.org/10.1002/cctc.201000038openalex-snapshot
Fullerene‐Mediated Activation of Dihydrogen: A New Method of Metal‐Free Catalytic Hydrogenation
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.201701783openalex-snapshot
Solid Molecular Frustrated Lewis Pairs in a Polyamine Organic Framework for the Catalytic Metal‐free Hydrogenation of Alkenes
inferred← citeshttps://doi.org/10.1002/cctc.202100674openalex-snapshot
LiAlH4‐catalyzed Imine Hydrogenation with Dihydrogen: New DFT Mechanistic Insights
inferred← citeshttps://doi.org/10.1002/cctc.202200144openalex-snapshot
BIAN‐Aluminium‐Catalysed Imine Hydrogenation
inferred← citeshttps://doi.org/10.1002/cctc.202200895openalex-snapshot
Controllable Reactivity Tuned by the Cooperativity in B/P and B/N Intermolecular Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/cctc.202300510openalex-snapshot
Frustrated Lewis Pairs Catalyse the Solvent‐Assisted Synthesis of Azoles from ortho‐Substituted Anilines, CO2 and H2
inferred← citeshttps://doi.org/10.1002/chem.200902322openalex-snapshot
Dispersion‐Oriented Soft Interaction in a Frustrated Lewis Pair and the Entropic Encouragement Effect in its Formation
inferred← citeshttps://doi.org/10.1002/chem.200902369openalex-snapshot
New Strategies to Phosphino–Phosphonium Cations and Zwitterions
inferred← citeshttps://doi.org/10.1002/chem.200903005openalex-snapshot
Borohydrides from Organic Hydrides: Reactions of Hantzsch’s Esters with B(C6F5)3
inferred← citeshttps://doi.org/10.1002/chem.200903483openalex-snapshot
Cyclizations via Frustrated Lewis Pairs: Lewis Acid Induced Intramolecular Additions of Amines to Olefins and Alkynes
inferred← citeshttps://doi.org/10.1002/chem.201001575openalex-snapshot
CC Coupling by Thermolysis of Alkynyl Phosphonium Borates
inferred← citeshttps://doi.org/10.1002/chem.201001814openalex-snapshot
Structure and Dynamic Features of an Intramolecular Frustrated Lewis Pair
inferred← citeshttps://doi.org/10.1002/chem.201100203openalex-snapshot
Synthesis and Reactivity of Alkynyl‐Linked Phosphonium Borates
inferred← citeshttps://doi.org/10.1002/chem.201100286openalex-snapshot
CO2 and Formate Complexes of Phosphine/Borane Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/chem.201100724openalex-snapshot
An Axially Chiral, Electron‐Deficient Borane: Synthesis, Coordination Chemistry, Lewis Acidity, and Reactivity
inferred← citeshttps://doi.org/10.1002/chem.201102438openalex-snapshot
Catalytic Hydrogenation with Frustrated Lewis Pairs: Selectivity Achieved by Size‐Exclusion Design of Lewis Acids
inferred← citeshttps://doi.org/10.1002/chem.201202693openalex-snapshot
Illuminating the Mechanism of the Borane‐Catalyzed Hydrosilylation of Imines with Both an Axially Chiral Borane and Silane
inferred← citeshttps://doi.org/10.1002/chem.201203190openalex-snapshot
Magnesium Catalysis of Imine Hydroboration
inferred← citeshttps://doi.org/10.1002/chem.201203318openalex-snapshot
The Hydride‐Ion Affinity of Borenium Cations and Their Propensity to Activate H2 in Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/chem.201300462openalex-snapshot
Frustrated Lewis Pair Chemistry of Chiral (+)‐Camphor‐Based Aminoboranes
inferred← citeshttps://doi.org/10.1002/chem.201301158openalex-snapshot
Tuning the Lewis Acidity of Boranes in Frustrated Lewis Pair Chemistry: Implications for the Hydrogenation of Electron‐Poor Alkenes
inferred← citeshttps://doi.org/10.1002/chem.201303203openalex-snapshot
Hydrosilylation Induced by N→Si Intramolecular Coordination: Spontaneous Transformation of Organosilanes into 1‐Aza‐Silole‐Type Molecules in the Absence of a Catalyst
inferred← citeshttps://doi.org/10.1002/chem.201304289openalex-snapshot
Ru–η6‐Arene Cations [{(Ph2PC6H4)2B(η6‐Ph)}RuX]+ (X=Cl, H) as Lewis Acids
inferred← citeshttps://doi.org/10.1002/chem.201404242openalex-snapshot
A Combined “Electrochemical–Frustrated Lewis Pair” Approach to Hydrogen Activation: Surface Catalytic Effects at Platinum Electrodes
inferred← citeshttps://doi.org/10.1002/chem.201405014openalex-snapshot
B(C6F5)3‐Mediated Transformations and Hydrogenation of Carbodiimides
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.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.201501535openalex-snapshot
Stoichiometric and Catalytic Inter‐ and Intramolecular Hydroamination of Terminal Alkynes by Frustrated Lewis Pairs
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.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.201504947openalex-snapshot
Spontaneous Double Hydrometallation Induced by N→M Coordination in Organometallic Hydrides of Group 14 Elements
inferred← citeshttps://doi.org/10.1002/chem.201604892openalex-snapshot
Hydrosilylation of RN=CH Imino‐Substituted Pyridines without a Catalyst
inferred← citeshttps://doi.org/10.1002/chem.201700437openalex-snapshot
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.201700477openalex-snapshot
Intermolecular Redox‐Neutral Amine C−H Functionalization Induced by the Strong Boron Lewis Acid B(C 6 F 5 ) 3 in the Frustrated Lewis Pair Regime
inferred← citeshttps://doi.org/10.1002/chem.201803370openalex-snapshot
Cationic Complexes of Boron and Aluminum: An Early 21st Century Viewpoint
inferred← citeshttps://doi.org/10.1002/chem.202001276openalex-snapshot
Semihydrogenation of Alkynes Catalyzed by a Pyridone Borane Complex: Frustrated Lewis Pair Reactivity and Boron–Ligand Cooperation in Concert
inferred← citeshttps://doi.org/10.1002/chem.202100641openalex-snapshot
Cationic Aluminium Complexes as Catalysts for Imine Hydrogenation
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.404242openalex-snapshot
Inside Cover: Modular Synthesis of Linear Bis‐ and Tris‐monodentate Fused [6]Polynorbornane‐Based Ligands and their Assembly into Coordination Cages (Chem. Eur. J. 10/2015)
inferred← citeshttps://doi.org/10.1002/chin.200833044openalex-snapshot
ChemInform Abstract: Lewis Acid Catalyzed Hydrogenation: B(C6F5)3‐Mediated Reduction of Imines and Nitriles with H2.
inferred← citeshttps://doi.org/10.1002/cjoc.202000027openalex-snapshot
Frustrated Lewis Pairs: Discovery and Overviews in Catalysis
inferred← citeshttps://doi.org/10.1002/cphc.200900829openalex-snapshot
High‐Pressure Hydrogen Interactions with Polyaminoborane and Polyiminoborane
inferred← citeshttps://doi.org/10.1002/cphc.201402450openalex-snapshot
How Frustrated Lewis Acid/Base Systems Pass through Transition‐State Regions: H2 Cleavage by [tBu3P/B(C6F5)3]
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.200900194openalex-snapshot
The Role of Amine–B(C6F5)3 Adducts in the Catalytic Reduction of Imines with H2: A Computational Study
inferred← citeshttps://doi.org/10.1002/ejic.200900311openalex-snapshot
“Frustration” of Orbital Interactions in Lewis Base/Lewis Acid Adducts: A Computational Study of H2 Uptake by Phosphanylboranes R2P=BR′2
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.201900516openalex-snapshot
Spontaneous Hydrosilylation of Substituted C=N Imines
inferred← citeshttps://doi.org/10.1002/ejic.202400558openalex-snapshot
Radical‐Driven Imine Hydrogenation Promoted by the Cooperativity of Nickel and a Redox‐Active Ligand
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.200900796openalex-snapshot
B(C6F5)3‐Catalyzed Reduction of Ketones and Imines Using Silicon‐Stereogenic Silanes: Stereoinduction by Single‐Point Binding
inferred← citeshttps://doi.org/10.1002/ejoc.201800944openalex-snapshot
Mechanisms in Frustrated Lewis Pair‐Catalyzed Reactions
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/ejoc.202400613openalex-snapshot
Reduction and Hydrocyanation of Aziridines with C−C Bond Cleavage
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/jcc.26980openalex-snapshot
The reactivity of the trapping reaction of the benzene‐bridged boron/phosphorus‐based frustrated Lewis pair with difluorocarbene and its group 14 analogs: A theoretical investigation
inferred← citeshttps://doi.org/10.1002/slct.202003794openalex-snapshot
Computational Investigation of the Mechanism of FLP Catalyzed H 2 Activation and Lewis Base Assisted Proton Transfer
inferred← citeshttps://doi.org/10.1002/tcr.201600086openalex-snapshot
Cooperative Catalysis of Combined Systems of Transition‐Metal Complexes with Lewis Acids: Theoretical Understanding
inferred← citeshttps://doi.org/10.1007/128_2012_373openalex-snapshot
Intramolecular Frustrated Lewis Pairs: Formation and Chemical Features
inferred← citeshttps://doi.org/10.1007/128_2012_375openalex-snapshot
Paracyclophane Derivatives in Frustrated Lewis Pair Chemistry
inferred← citeshttps://doi.org/10.1007/128_2012_380openalex-snapshot
Carbon-Based Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1007/128_2012_381openalex-snapshot
Discovery of Frustrated Lewis Pairs: Intermolecular FLPs for Activation of Small Molecules
inferred← citeshttps://doi.org/10.1007/128_2012_382openalex-snapshot
New Organoboranes in “Frustrated Lewis Pair” Chemistry
inferred← citeshttps://doi.org/10.1007/128_2012_385openalex-snapshot
Computational Design of Metal-Free Molecules for Activation of Small Molecules, Hydrogenation, and Hydroamination
inferred← citeshttps://doi.org/10.1007/128_2012_391openalex-snapshot
Amine-Borane Mediated Metal-Free Hydrogen Activation and Catalytic Hydrogenation
inferred← citeshttps://doi.org/10.1007/128_2012_392openalex-snapshot
Frustrated Lewis Pair Mediated Hydrogenations
inferred← citeshttps://doi.org/10.1007/128_2012_399openalex-snapshot
Hydrogen Activation by Frustrated Lewis Pairs: Insights from Computational Studies
inferred← citeshttps://doi.org/10.1007/128_2012_402openalex-snapshot
Frustrated Lewis Pairs: From Dihydrogen Activation to Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1007/3418_2016_173openalex-snapshot
Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations
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/10.1007/978-3-642-25258-7_3openalex-snapshot
New Insights into the Molecular Mechanism of H2 Activation
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/s11164-011-0330-yopenalex-snapshot
The reaction mechanisms of boron amidinate and small molecules: a density function theory study
inferred← citeshttps://doi.org/10.1007/s11434-010-0005-xopenalex-snapshot
Encumbering the intramolecular π donation by using a bridge: A strategy for designing metal-free compounds to hydrogen activation
inferred← citeshttps://doi.org/10.1007/s12039-015-0783-4openalex-snapshot
Frustrated Lewis pairs: Design and reactivity
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/10.1016/b978-0-08-097774-4.00136-4openalex-snapshot
Frustrated Lewis Pairs: Activation of H2 and Other Small Molecules
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00931-1openalex-snapshot
H–H Bond Activation
inferred← citeshttps://doi.org/10.1016/b978-0-12-800976-5.00004-7openalex-snapshot
The Mannich Route to Amino-Functionalized [3]Ferrocenophanes
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/b978-0-12-820206-7.00041-xopenalex-snapshot
Frustrated Lewis Pairs in Organic Synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00125-6openalex-snapshot
Recent Development in the Solution-State Chemistry of Boranes and Diboranes
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/bs.adomc.2022.03.004openalex-snapshot
Recent applications of fluorinated arylborane derivatives
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.comptc.2016.04.005openalex-snapshot
Choosing an appropriate model chemistry in a big data context: Application to dative bonding
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.cplett.2023.140405openalex-snapshot
Theoretical prediction of the catalytic efficiency of non-metalated pincer-like phosphorus compounds for the hydrogenation of carbon-monoxide with ammonia-borane
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2025.114317openalex-snapshot
A bulky polymer-supported frustrated Lewis pair: Dihydrogen cleavage with poly(methylenephosphine)-tris(pentafluorophenyl)borane
inferred← citeshttps://doi.org/10.1016/j.ijhydene.2016.03.044openalex-snapshot
Temperature-dependent nature of interaction between hydrogen and copper(II) acetate confined in nanoporous carbon
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.jcat.2025.116445openalex-snapshot
Cationic indium complexes halve H2 partial pressure in CO2 reductive coupling reactions with amines
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.2009.03.023openalex-snapshot
Experimental and theoretical treatment of hydrogen splitting and storage in boron–nitrogen systems
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.jorganchem.2016.02.035openalex-snapshot
Scope and selectivity of B(C6F5)3-catalyzed reactions of the disilane (Ph2SiH)2
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.progpolymsci.2020.101313openalex-snapshot
Polymer-supported Lewis acids and bases: Synthesis and applications
inferred← citeshttps://doi.org/10.1016/j.tet.2014.12.086openalex-snapshot
Frustrated Lewis pairs-assisted reduction of carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.01.099openalex-snapshot
Iron-catalyzed reduction of aromatic aldehydes with paraformaldehyde and H2O as the hydrogen source
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151422openalex-snapshot
Recent topics on reusable immobilized iron nanoparticle pre-catalysts
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00561openalex-snapshot
Metallomimetic Chemistry of Boron
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c01276openalex-snapshot
Progressing the Frustrated Lewis Pair Abilities of N-Heterocyclic Carbene/GaR3 Combinations for Catalytic Hydroboration of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c01809openalex-snapshot
Significant Insight into the Origin of Reaction Barriers Determining Dihydrogen Activation by G13-P-P (G13 = Group 13 Element) and G15-P-Ga (G15 = Group 15 Element) Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.2c03968openalex-snapshot
Influence of the Element and Substituent Effects on the Reactivity of Catching Reactions of Difluorocarbene by Benzene-Bridged and Group-13/Group-15-Based Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.3c01611openalex-snapshot
Reactivity of the Intramolecular Vicinal Group-13/P- and B/Group-15-Based Frustrate Lewis Pairs with Sulfur Dioxide: Mechanistic Insight from DFT
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c04665openalex-snapshot
Hydrophobic B(C6F5)3@R4-MIL-101: A Water-Resistant Heterogeneous Catalyst for Frustrated Lewis Pairs-Mediated Reductive Amination
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c02587openalex-snapshot
Turning the Tables: Ligand-Centered Hydride Shuttling in Organometallic BIP–Al Systems
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.7b01800openalex-snapshot
Activation of C–H Bonds of Alkyl- and Arylnitriles by the TaCl5–PPh3 Lewis Pair
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.0c02680openalex-snapshot
Amide Iridium Complexes As Catalysts for Transfer Hydrogenation Reduction of N-sulfonylimine
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