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On the Mechanism of B(C6F5)3-Catalyzed Direct Hydrogenation of Imines: Inherent and Thermally Induced Frustration

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

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

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Autoinduced Catalysis and Inverse Equilibrium Isotope Effect in the Frustrated Lewis Pair Catalyzed Hydrogenation of Imines

inferred← citeshttps://doi.org/10.1002/chem.201600716openalex-snapshot

Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines

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.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.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.201703644openalex-snapshot

N‐Phosphine Oxide‐Substituted Imidazolylidenes (PoxIms): Multifunctional Multipurpose Carbenes

inferred← citeshttps://doi.org/10.1002/chem.201902452openalex-snapshot

Reversible Activation of Water by an Air‐ and Moisture‐Stable Frustrated Rhodium Nitrogen Lewis Pair

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.202003167openalex-snapshot

Metal‐only Lewis Pairs of Rhodium with s, p and d‐Block Metals

inferred← citeshttps://doi.org/10.1002/chem.202100641openalex-snapshot

Cationic Aluminium Complexes as Catalysts for Imine Hydrogenation

inferred← citeshttps://doi.org/10.1002/chem.202304140openalex-snapshot

Molecular Dihydrogen Activation by (C5Me5)M/N (M=Rh, Ir) Transition Metal Frustrated Lewis Pairs: Reversible Proton Migration to, and Proton Abstraction from, the C5Me5 Ligand

inferred← citeshttps://doi.org/10.1002/chir.23671openalex-snapshot

Asymmetric catalysis by chiral FLPs: A computational mini‐review

inferred← citeshttps://doi.org/10.1002/cphc.201402610openalex-snapshot

The Unexpected Mechanism Underlying the High‐Valent Mono‐Oxo‐Rhenium(V) Hydride Catalyzed Hydrosilylation of CN Functionalities: Insights from a DFT Study

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.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.201000242openalex-snapshot

Reversible Heterolytic Methane Activation of Metal‐Free Closed‐Shell Molecules: A Computational Proof‐of‐Principle Study

inferred← citeshttps://doi.org/10.1002/ejic.201402202openalex-snapshot

Serendipitous Metal‐Catalyzed H–H/Si–H Exchange

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.201001332openalex-snapshot

Scope and Selectivity of Heterogeneous Rh0‐Catalyzed Tandem Dehydrocoupling/Hydrogenation Using Me2NH·BH3 as a Stoichiometric H2 Source

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/hlca.202100044openalex-snapshot

Strained Ruthenium Complexes Bearing Tridentate Guanidine‐Derived Ligands

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.27046openalex-snapshot

Computational investigation of functionalized carbenes on dinitrogen activation

inferred← citeshttps://doi.org/10.1002/nadc.20174055283openalex-snapshot

Reaktivität verstehen, ohne die Katalysatorstruktur zu kennen

inferred← citeshttps://doi.org/10.1002/poc.4588openalex-snapshot

Insight into acrolein activation by P/B intramolecular frustrated Lewis pairs

inferred← citeshttps://doi.org/10.1002/qua.22203openalex-snapshot

Mechanism of hydrogen activation by frustrated Lewis pairs: A molecular orbital approach

inferred← citeshttps://doi.org/10.1002/qua.22901openalex-snapshot

Steric and electronic effects on the heterolytic H2‐splitting by phosphine‐boranes R3B/PR′3(R = C6F5, Ph; R′ = C6H2Me3,tBu, Ph, C6F5, Me, H): A computational study

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/10.1007/128_2012_378openalex-snapshot

Computational Studies of Lewis Acidity and Basicity in Frustrated Lewis Pairs

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_389openalex-snapshot

Quantum Chemistry of FLPs and Their Activation of Small Molecules: Methodological Aspects

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/10.1007/3418_2016_173openalex-snapshot

Chiral Borane-Based Lewis Acids for Metal Free Hydrogenations

inferred← citeshttps://doi.org/10.1007/430_2026_106openalex-snapshot

Heterobimetallic Frustrated Lewis Pairs Based on Transition and Main Group Metals

inferred← citeshttps://doi.org/10.1007/978-3-030-58888-5_7openalex-snapshot

Heterogeneous Catalysis by Frustrated Lewis Pairs

inferred← citeshttps://doi.org/10.1007/978-3-030-58888-5_9openalex-snapshot

Frustrated Lewis Pairs Based on Transition Metals

inferred← citeshttps://doi.org/10.1007/978-90-481-3865-4_6openalex-snapshot

Bifunctional Acid-Base Catalysis

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/s00214-023-02961-6openalex-snapshot

Exploring an intermolecular Ge/B frustrated Lewis pair from a multicentre Zintl Lewis base

inferred← citeshttps://doi.org/10.1007/s00894-018-3776-7openalex-snapshot

Chemical reactivity of the frustrated Lewis pairs in borophosphines: a theoretical analysis of their Lewis acidity, Lewis basicity and Fukui function

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/s12039-021-02010-4openalex-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/s12039-026-02532-9openalex-snapshot

Selective phosphate adsorption from wastewater using dual Lewis acid catalyst: A metal-free approach

inferred← citeshttps://doi.org/10.1007/s13404-017-0219-7openalex-snapshot

Gold-based frustrated Lewis acid/base pairs (FLPs)

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/b978-0-12-820206-7.00129-3openalex-snapshot

Frustrated Lewis Pair Systems

inferred← citeshttps://doi.org/10.1016/bs.adomc.2021.01.001openalex-snapshot

Bimetallic frustrated Lewis pairs

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.ccr.2018.09.014openalex-snapshot

From structure to novel reactivity in frustrated Lewis pairs

inferred← citeshttps://doi.org/10.1016/j.chempr.2017.05.022openalex-snapshot

A Radical Mechanism for Frustrated Lewis Pair Reactivity

inferred← citeshttps://doi.org/10.1016/j.comptc.2018.03.027openalex-snapshot

Density functional reactivity theory characterizing the reactivity of frustrated Lewis pairs

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.2022.139634openalex-snapshot

Unraveling H2O activation by intermolecular frustrated Lewis pair

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.2024.115747openalex-snapshot

Unraveling Lewis acid-base sites in defected MOFs for catalyzing dicyclopentadiene hydrogenation via a DFT study and descriptor exploration

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.molcata.2010.03.001openalex-snapshot

Hydrogenation of carbon-heteroatom unsaturated bonds: An assessment of consistency of density functional methods☆

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.2014.10.138openalex-snapshot

Metal-free asymmetric hydrogenation and hydrosilylation catalyzed by frustrated Lewis pairs

inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154411openalex-snapshot

A computational mechanistic study of the cleavage of sulfur-sulfur bond by Frustrated Lewis Pairs

inferred← citeshttps://doi.org/10.1021/acs.accounts.2c00832openalex-snapshot

Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations

inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00037openalex-snapshot

Dihydrogen Complexation

inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00091openalex-snapshot

Hydrogen and Dihydrogen Bonds in the Reactions of Metal Hydrides

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.1c01543openalex-snapshot

Investigating Tetrel-Based Neutral Frustrated Lewis Pairs for Hydrogen Activation

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.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.4c03214openalex-snapshot

Diverse and Selective Metal–Ligand Cooperative Routes for Activating Non-Functionalized Ketones

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.5c00332openalex-snapshot

Activation of CO, Isocyanides, and Alkynes by Frustrated Lewis Pairs Based on Cp*M/N (M = Rh, Ir) Couples

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.7b00549openalex-snapshot

Trans-Metal-Trapping Meets Frustrated-Lewis-Pair Chemistry: Ga(CH2SiMe3)3-Induced C–H Functionalizations

inferred← citeshttps://doi.org/10.1021/acs.joc.1c02491openalex-snapshot

A Theoretical Study on the Borane-Catalyzed Reductive Amination of Aniline and Benzaldehyde with Dihydrogen: The Origins of Chemoselectivity

inferred← citeshttps://doi.org/10.1021/acs.joc.5b00941openalex-snapshot

Boron-Catalyzed Silylative Reduction of Nitriles in Accessing Primary Amines and Imines

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.5b00567openalex-snapshot

New Insights into Hydrosilylation of Unsaturated Carbon–Heteroatom (C═O, C═N) Bonds by Rhenium(V)–Dioxo Complexes

inferred← citeshttps://doi.org/10.1021/acs.jpca.7b11851openalex-snapshot

Surprisingly Flexible Oxonium/Borohydride Ion Pair Configurations

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.5b01017openalex-snapshot

Activation of C–H Activation: The Beneficial Effect of Catalytic Amount of Triaryl Boranes on Palladium-Catalyzed C–H Activation

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.5b01380openalex-snapshot

A Highly Stereoselective Metal-Free Hydrogenation of Diimines for the Synthesis ofCis-Vicinal Diamines

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.5b01191openalex-snapshot

Screening Lewis Pair Moieties for Catalytic Hydrogenation of CO 2 in Functionalized UiO-66

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.7b04489openalex-snapshot

B(C6F5)3: Catalyst or Initiator? Insights from Computational Studies into Surrogate Silicon Chemistry

inferred← citeshttps://doi.org/10.1021/acscatal.8b01847openalex-snapshot

Switchable C–H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair

inferred← citeshttps://doi.org/10.1021/acscatal.9b01356openalex-snapshot

Triarylborane-Catalyzed Reductive N-Alkylation of Amines: A Perspective

inferred← citeshttps://doi.org/10.1021/acsomega.2c07442openalex-snapshot

Computational Design of Frustrated Lewis Pairs as a Strategy for Catalytic Hydrogen Activation and Hydrogenation Catalyst

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.3c09761openalex-snapshot

B(C6F5)3-Catalyzed Stereoselective 1,2-cis Arabinofuranosylation with a Conformationally Constrained Donor

inferred← citeshttps://doi.org/10.1021/ar500375jopenalex-snapshot

Frustrated Lewis Pairs: From Concept to Catalysis

inferred← citeshttps://doi.org/10.1021/cr100105aopenalex-snapshot

Amine− and Phosphine−Borane Adducts: New Interest in Old Molecules

inferred← citeshttps://doi.org/10.1021/ic2006474openalex-snapshot

Mechanistic Aspects of Bond Activation with Perfluoroarylboranes

inferred← citeshttps://doi.org/10.1021/ic200663vopenalex-snapshot

Metal-Free Catalytic Hydrogenation of Polar Substrates by Frustrated Lewis Pairs

inferred← citeshttps://doi.org/10.1021/ic201290gopenalex-snapshot

Dihydrogen Activation by Frustrated Carbene-Borane Lewis Pairs: An Experimental and Theoretical Study of Carbene Variation

inferred← citeshttps://doi.org/10.1021/ic901590sopenalex-snapshot

Heterolytic Cleavage of Disulfides by Frustrated Lewis Pairs

inferred← citeshttps://doi.org/10.1021/ic902039gopenalex-snapshot

Computationally Designed Metal-Free Hydrogen Activation Site: Reaching the Reactivity of Metal−Ligand Bifunctional Hydrogenation Catalysts

inferred← citeshttps://doi.org/10.1021/ja206394wopenalex-snapshot

Molecular Hydrogen Tweezers: Structure and Mechanisms by Neutron Diffraction, NMR, and Deuterium Labeling Studies in Solid and Solution

inferred← citeshttps://doi.org/10.1021/ja210214ropenalex-snapshot

Preorganized Frustrated Lewis Pairs

inferred← citeshttps://doi.org/10.1021/ja300365sopenalex-snapshot

Facile Activation of H–H and Si–H Bonds by Boranes

inferred← citeshttps://doi.org/10.1021/ja307995fopenalex-snapshot

Activation of Hydrogen and Hydrogenation Catalysis by a Borenium Cation

inferred← citeshttps://doi.org/10.1021/ja311842ropenalex-snapshot

Mechanistic Studies on the Metal-Free Activation of Dihydrogen by Antiaromatic Pentarylboroles

inferred← citeshttps://doi.org/10.1021/ja4025808openalex-snapshot

Chiral Dienes as “Ligands” for Borane-Catalyzed Metal-Free Asymmetric Hydrogenation of Imines

inferred← citeshttps://doi.org/10.1021/ja406761jopenalex-snapshot

Metal-Free Borane-Catalyzed Highly Stereoselective Hydrogenation of Pyridines

inferred← citeshttps://doi.org/10.1021/ja409344wopenalex-snapshot

Experimental Analysis of the Catalytic Cycle of the Borane-Promoted Imine Reduction with Hydrosilanes: Spectroscopic Detection of Unexpected Intermediates and a Refined Mechanism

inferred← citeshttps://doi.org/10.1021/ja5038337openalex-snapshot

Oxidative Addition of σ Bonds to an Al(I) Center

inferred← citeshttps://doi.org/10.1021/ja507536nopenalex-snapshot

A Highly Enantioselective Hydrogenation of Silyl Enol Ethers Catalyzed by Chiral Frustrated Lewis Pairs

inferred← citeshttps://doi.org/10.1021/ja512658mopenalex-snapshot

Chiral Molecular Tweezers: Synthesis and Reactivity in Asymmetric Hydrogenation

inferred← citeshttps://doi.org/10.1021/ja903511sopenalex-snapshot

Reactions of an Intramolecular Frustrated Lewis Pair with Unsaturated Substrates: Evidence for a Concerted Olefin Addition Reaction

inferred← citeshttps://doi.org/10.1021/ja903878zopenalex-snapshot

Rationalizing the Reactivity of Frustrated Lewis Pairs: Thermodynamics of H2 Activation and the Role of Acid−Base Properties

inferred← citeshttps://doi.org/10.1021/ja905369nopenalex-snapshot

Superelectrophilic Intermediates in Nitrogen-Directed Aromatic Borylation

inferred← citeshttps://doi.org/10.1021/ja9061097openalex-snapshot

A Nonmetal Catalyst for Molecular Hydrogen Activation with Comparable Catalytic Hydrogenation Capability to Noble Metal Catalyst

inferred← citeshttps://doi.org/10.1021/jacs.3c07070openalex-snapshot

Frustrated Radical Pairs in Organic Synthesis

inferred← citeshttps://doi.org/10.1021/jacs.5b06794openalex-snapshot

Frustrated Lewis Pairs

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.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.7b09175openalex-snapshot

Non-Metal-Catalyzed Heterodehydrocoupling of Phosphines and Hydrosilanes: Mechanistic Studies of B(C 6 F 5 ) 3 -Mediated Formation of P–Si Bonds

inferred← citeshttps://doi.org/10.1021/jo402195xopenalex-snapshot

Quantum Chemical Study of B(C6F5)3-Catalyzed Hydrosilylation of Carbonyl Group

inferred← citeshttps://doi.org/10.1021/jp105000xopenalex-snapshot

Reactivity of 2,6-Lutidine/BR3and Pyridine/BR3Lewis Pairs (R = F, Me, C6F5): A Density Functional Study

inferred← citeshttps://doi.org/10.1021/om100378yopenalex-snapshot

Frustrated Lewis Pair Reactions at the [3]Ferrocenophane Framework

inferred← citeshttps://doi.org/10.1021/om100949kopenalex-snapshot

Alkene Addition of Frustrated P/B and N/B Lewis Pairs at the [3]Ferrocenophane Framework

inferred← citeshttps://doi.org/10.1021/om200222jopenalex-snapshot

On the “Reverse Gear”Mechanism of the Reversible Dehydrogenation/Hydrogenation of a Nitrogen Heterocycle Catalyzed by a Cp*Ir Complex: A Computational Study

inferred← citeshttps://doi.org/10.1021/om200615nopenalex-snapshot

Frustrated Lewis Pair Reactions With Bis-Acetylenic Substrates: Exploring the Narrow Gap Separating Very Different Competing Reaction Pathways

inferred← citeshttps://doi.org/10.1021/om400634wopenalex-snapshot

Theoretical Study of POCOP-Pincer Iridium(III)/Iron(II) Hydride Catalyzed Hydrosilylation of Carbonyl Compounds: Hydride Not Involved in the Iridium(III) System but Involved in the Iron(II) System

inferred← citeshttps://doi.org/10.1038/nchem.2063openalex-snapshot

Direct observation of a borane–silane complex involved in frustrated Lewis-pair-mediated hydrosilylations

inferred← citeshttps://doi.org/10.1038/s41598-017-16244-1openalex-snapshot

Heterolytic Splitting of Molecular Hydrogen by Frustrated and Classical Lewis Pairs: A Unified Reactivity Concept

inferred← citeshttps://doi.org/10.1038/s42004-021-00576-1openalex-snapshot

A boron-transfer mechanism mediating the thermally induced revival of frustrated carbene–borane pairs from their shelf-stable adducts

inferred← citeshttps://doi.org/10.1039/9781839162442-00095openalex-snapshot

Structural Variations of FLPs

inferred← citeshttps://doi.org/10.1039/b905137fopenalex-snapshot

On the possibility of catalytic reduction of carbonyl moieties with tris(pentafluorophenyl)borane and H2: a computational study

inferred← citeshttps://doi.org/10.1039/b909620eopenalex-snapshot

Metal-free hydrogen activation and hydrogenation of imines by 1,8-bis(dipentafluorophenylboryl)naphthalene

inferred← citeshttps://doi.org/10.1039/b917304hopenalex-snapshot

Facile syntheses of dissymmetric ferrocene-functionalized Lewis acids and acid–base pairs

inferred← citeshttps://doi.org/10.1039/b917840fopenalex-snapshot

Theoretical study of H 2 splitting and storage by boron–nitrogen-based systems: a bimolecular case and some qualitative aspects

inferred← citeshttps://doi.org/10.1039/b921941bopenalex-snapshot

Computational design of metal-free catalysts for catalytic hydrogenation of imines

inferred← citeshttps://doi.org/10.1039/b923196jopenalex-snapshot

Frustrated Lewis pairs: reactivities of TMS protected amines and phosphines in the presence of B(C 6 F 5 ) 3

inferred← citeshttps://doi.org/10.1039/b927087fopenalex-snapshot

Synthetic methods : Part (ii) Oxidation and reduction methods

inferred← citeshttps://doi.org/10.1039/bk9781849731386-00074openalex-snapshot

Phosphonium salts and P-ylides

inferred← citeshttps://doi.org/10.1039/c001399dopenalex-snapshot

Catalytic metal-free ketone hydrogenation: a computational experiment

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