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Chiral Molecular Tweezers: Synthesis and Reactivity in Asymmetric Hydrogenation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20011015)40:20<3726::aid-anie3726>3.0.co;2-dopenalex-snapshot
Enantioselective Organocatalysis
inferredcites →https://doi.org/10.1002/adsc.200404071openalex-snapshot
The Art of Meeting Palladium Specifications in Active Pharmaceutical Ingredients Produced by Pd‐Catalyzed Reactions
inferredcites →https://doi.org/10.1002/adsc.200900719openalex-snapshot
Chiral Amine Synthesis – Recent Developments and Trends for Enamide Reduction, Reductive Amination, and Imine Reduction
inferredcites →https://doi.org/10.1002/adsc.201100206openalex-snapshot
Highly Active Metal‐Free Catalysts for Hydrogenation of Unsaturated Nitrogen‐Containing Compounds
inferredcites →https://doi.org/10.1002/adsc.201301007openalex-snapshot
Metal‐Free Catalytic Hydrogenation of Imines with Recyclable [2.2]Paracyclophane‐Derived Frustrated Lewis Pairs Catalysts
inferredcites →https://doi.org/10.1002/ange.19360490911openalex-snapshot
Berzelius und die Katalyse. Von Dr. phil. Dr.‐Ing. e. h. A. Mittasch. Zum Gedächtnis der Aufstellung des Katalyse‐Begriffes 1835. 23 Seiten, 1 Figur. Akademische Verlagsgesellschaft m. b. H., Leipzig 1935. Preis br. RM. 1,50
inferredcites →https://doi.org/10.1002/anie.200702908openalex-snapshot
Metal‐Free Catalytic Hydrogenation
inferredcites →https://doi.org/10.1002/anie.200801432openalex-snapshot
Metal‐Free Catalytic Hydrogenation of Enamines, Imines, and Conjugated Phosphinoalkenylboranes
inferredcites →https://doi.org/10.1002/anie.200903708openalex-snapshot
Frustrated Lewis Pairs: Metal‐free Hydrogen Activation and More
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.201004525openalex-snapshot
Enantioselective Hydrogenation with Chiral Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1002/anie.201200963openalex-snapshot
Brønsted Acid Activation Strategy in Transition‐Metal Catalyzed Asymmetric Hydrogenation of N‐Unprotected Imines, Enamines, and N‐Heteroaromatic Compounds
inferredcites →https://doi.org/10.1002/anie.201309253openalex-snapshot
Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen
inferredcites →https://doi.org/10.1002/anie.201405531openalex-snapshot
Metal‐Free Hydrogenation Catalyzed by an Air‐Stable Borane: Use of Solvent as a Frustrated Lewis Base
inferredcites →https://doi.org/10.1002/anie.201406122openalex-snapshot
N‐Methylacridinium Salts: Carbon Lewis Acids in Frustrated Lewis Pairs for σ‐Bond Activation and Catalytic Reductions
inferredcites →https://doi.org/10.1002/anie.201409471openalex-snapshot
A Highly cis‐Selective and Enantioselective Metal‐Free Hydrogenation of 2,3‐Disubstituted Quinoxalines
inferredcites →https://doi.org/10.1002/asia.201200776openalex-snapshot
Reaction of an “Invisible” Frustrated N/B Lewis Pair with Dihydrogen
inferredcites →https://doi.org/10.1002/cctc.201402838openalex-snapshot
Enantioselective Metal‐Free Hydrogenation Catalyzed by Chiral Frustrated Lewis Pairs
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.201300462openalex-snapshot
Frustrated Lewis Pair Chemistry of Chiral (+)‐Camphor‐Based Aminoboranes
inferredcites →https://doi.org/10.1002/ejoc.200900071openalex-snapshot
Suzuki Cross‐Coupling at the Chiral Groove of 1,1′‐Binaphthyl: Stereoconservation versus Deracemization Pathway
inferredcites →https://doi.org/10.1007/128_2012_392openalex-snapshot
Frustrated Lewis Pair Mediated Hydrogenations
inferredcites →https://doi.org/10.1007/128_2012_399openalex-snapshot
Hydrogen Activation by Frustrated Lewis Pairs: Insights from Computational Studies
inferredcites →https://doi.org/10.1016/j.crci.2011.05.008openalex-snapshot
Frustrated Lewis pairs: Reactions with dihydrogen and other “small molecules”
inferredcites →https://doi.org/10.1016/j.jorganchem.2007.08.010openalex-snapshot
Study on the electronic effects on stereoconservativity of Suzuki coupling in chiral groove of binaphthyl
inferredcites →https://doi.org/10.1016/j.tetlet.2011.08.046openalex-snapshot
The development of an approach toward sterically-hindered chiral 2′-aryl-1,1′-binaphthalenes functionalized at position 2
inferredcites →https://doi.org/10.1016/j.tetlet.2014.10.138openalex-snapshot
Metal-free asymmetric hydrogenation and hydrosilylation catalyzed by frustrated Lewis pairs
inferredcites →https://doi.org/10.1021/cr100218mopenalex-snapshot
Transition Metal-Catalyzed Enantioselective Hydrogenation of Enamines and Imines
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/ja00183a068openalex-snapshot
Convenient conversion of aldehydes and ketones into the corresponding alkenes via hydroboration of their enamines. A remarkably simple synthesis of either (Z)- or (E)-alkenes
inferredcites →https://doi.org/10.1021/ja307995fopenalex-snapshot
Activation of Hydrogen and Hydrogenation Catalysis by a Borenium Cation
inferredcites →https://doi.org/10.1021/ja4025808openalex-snapshot
Chiral Dienes as “Ligands” for Borane-Catalyzed Metal-Free Asymmetric Hydrogenation of Imines
inferredcites →https://doi.org/10.1021/ja507536nopenalex-snapshot
A Highly Enantioselective Hydrogenation of Silyl Enol Ethers Catalyzed by Chiral Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1021/ja508829xopenalex-snapshot
Enabling Catalytic Ketone Hydrogenation by Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1021/ja5088979openalex-snapshot
Nonmetal Catalyzed Hydrogenation of Carbonyl Compounds
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/ja9025193openalex-snapshot
Palladium-Catalyzed Asymmetric Dearomatization of Naphthalene Derivatives
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/jo00004a038openalex-snapshot
Hydroboration. 86. Convenient conversion of aldehydes and ketones into the corresponding alkenes via hydroboration of their enamines. A remarkably simple synthesis of either (Z)- or (E)-alkenes
inferredcites →https://doi.org/10.1021/jo00019a043openalex-snapshot
Unusual directive effects in the hydroboration of .beta.,.beta.-disubstituted enamines. Conversion of .alpha.-substituted aldehydes to the corresponding alkenes and .beta.-amino alcohols
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/om980673eopenalex-snapshot
Synthesis, Properties, and Hydroboration Activity of the Highly Electrophilic Borane Bis(pentafluorophenyl)borane, HB(C6F5)21
inferredcites →https://doi.org/10.1021/op400315mopenalex-snapshot
Hydrogenation by Frustrated Lewis Pairs: Main Group Alternatives to Transition Metal Catalysts?
inferredcites →https://doi.org/10.1038/nature08634openalex-snapshot
Main-group elements as transition metals
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/b802575bopenalex-snapshot
“Frustrated Lewis pairs”: a concept for new reactivity and catalysis
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/c2cs35007fopenalex-snapshot
Recent advances in transition metal-catalyzed enantioselective hydrogenation of unprotected enamines
inferredcites →https://doi.org/10.1039/c2dt30536dopenalex-snapshot
Asymmetric hydrogenation of imines with a recyclable chiral frustrated Lewis pair catalyst
inferredcites →https://doi.org/10.1039/c2dt30926bopenalex-snapshot
Hydrogen activation by 2-boryl-N,N-dialkylanilines: a revision of Piers’ ansa-aminoborane
inferredcites →https://doi.org/10.1039/c2ob25339aopenalex-snapshot
“Frustrated Lewis pair” hydrogenations
inferredcites →https://doi.org/10.1039/c3cc47889kopenalex-snapshot
Imine hydrogenation by alkylaluminum catalysts
inferredcites →https://doi.org/10.1073/pnas.0307620101openalex-snapshot
Chiral biphenyl diphosphines for asymmetric catalysis: Stereoelectronic design and industrial perspectives
inferredcites →https://doi.org/10.1126/science.1134230openalex-snapshot
Reversible, Metal-Free Hydrogen Activation
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/10.1002/9780470682531.pat0980openalex-snapshot
Boron‐Based Frustrated L ewis Pairs in Hydrogenation Catalysis
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc2520openalex-snapshot
Small Molecule Activation with Frustrated L ewis P airs
inferred← citeshttps://doi.org/10.1002/9783527814237.ch7openalex-snapshot
Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen
inferred← citeshttps://doi.org/10.1002/9783527822294.ch9openalex-snapshot
Asymmetric (Transfer) Hydrogenation of Imines
inferred← citeshttps://doi.org/10.1002/ange.201504922openalex-snapshot
Diferrocenophosphaborin: A Planar‐Chiral, Redox‐Active and Anion‐Responsive Ambiphilic Ligand
inferred← citeshttps://doi.org/10.1002/ange.201506216openalex-snapshot
Diverting Hydrogenations with Wilkinson's Catalyst towards Highly Reactive Rhodium(I) Species
inferred← citeshttps://doi.org/10.1002/ange.201605645openalex-snapshot
Spontaneous Reduction of a Hydroborane To Generate a B−B Single Bond by the Use of a Lewis Pair
inferred← citeshttps://doi.org/10.1002/ange.201606177openalex-snapshot
Tris(pentafluorophenyl)borane‐Catalyzed Acceptorless Dehydrogenation of N‐Heterocycles
inferred← citeshttps://doi.org/10.1002/ange.201700231openalex-snapshot
Auto‐Tandem Catalysis with Frustrated Lewis Pairs for Reductive Etherification of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1002/ange.201709926openalex-snapshot
Asymmetric Imine Hydroboration Catalyzed by Chiral Diazaphospholenes
inferred← citeshttps://doi.org/10.1002/ange.201808289openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201903763openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201914568openalex-snapshot
Asymmetric Hydrogenation of Ketones and Enones with Chiral Lewis Base Derived Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/ange.202007352openalex-snapshot
Borane‐Catalyzed Chemoselective and Enantioselective Reduction of 2‐Vinyl‐Substituted Pyridines
inferred← citeshttps://doi.org/10.1002/ange.202010633openalex-snapshot
Frustrated Radical Pairs: Insights from EPR Spectroscopy
inferred← citeshttps://doi.org/10.1002/ange.202110102openalex-snapshot
Metal‐Free Phosphorus‐Directed Borylation of C(sp2)−H Bonds
inferred← citeshttps://doi.org/10.1002/ange.202200100openalex-snapshot
Asymmetric Intramolecular Hydroalkoxylation of 2‐Vinylbenzyl Alcohols with Chiral Boro‐Phosphates
inferred← citeshttps://doi.org/10.1002/ange.202213399openalex-snapshot
Chiral Frustrated Lewis Pair@Metal‐Organic Framework as a New Platform for Heterogeneous Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/ange.202305449openalex-snapshot
Borane‐Catalyzed Tandem Cyclization/Hydrosilylation Towards Enantio‐ and Diastereoselective Construction of trans‐2,3‐Disubstituted‐1,2,3,4‐Tetrahydroquinoxalines
inferred← citeshttps://doi.org/10.1002/anie.201504922openalex-snapshot
Diferrocenophosphaborin: A Planar‐Chiral, Redox‐Active and Anion‐Responsive Ambiphilic Ligand
inferred← citeshttps://doi.org/10.1002/anie.201506216openalex-snapshot
Diverting Hydrogenations with Wilkinson's Catalyst towards Highly Reactive Rhodium(I) Species
inferred← citeshttps://doi.org/10.1002/anie.201605645openalex-snapshot
Spontaneous Reduction of a Hydroborane To Generate a B−B Single Bond by the Use of a Lewis Pair
inferred← citeshttps://doi.org/10.1002/anie.201606177openalex-snapshot
Tris(pentafluorophenyl)borane‐Catalyzed Acceptorless Dehydrogenation of N‐Heterocycles
inferred← citeshttps://doi.org/10.1002/anie.201700231openalex-snapshot
Auto‐Tandem Catalysis with Frustrated Lewis Pairs for Reductive Etherification of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1002/anie.201709926openalex-snapshot
Asymmetric Imine Hydroboration Catalyzed by Chiral Diazaphospholenes
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C2‐Symmetric Bicyclic Bisborane Catalysts: Kinetic or Thermodynamic Products of a Reversible Hydroboration of Dienes
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Promoting Frustrated Lewis Pairs for Heterogeneous Chemoselective Hydrogenation via the Tailored Pore Environment within Metal–Organic Frameworks
inferred← citeshttps://doi.org/10.1002/anie.201914568openalex-snapshot
Asymmetric Hydrogenation of Ketones and Enones with Chiral Lewis Base Derived Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/anie.202007352openalex-snapshot
Borane‐Catalyzed Chemoselective and Enantioselective Reduction of 2‐Vinyl‐Substituted Pyridines
inferred← citeshttps://doi.org/10.1002/anie.202010633openalex-snapshot
Frustrated Radical Pairs: Insights from EPR Spectroscopy
inferred← citeshttps://doi.org/10.1002/anie.202110102openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202200100openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202213399openalex-snapshot
Chiral Frustrated Lewis Pair@Metal‐Organic Framework as a New Platform for Heterogeneous Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/anie.202305449openalex-snapshot
Borane‐Catalyzed Tandem Cyclization/Hydrosilylation Towards Enantio‐ and Diastereoselective Construction of trans‐2,3‐Disubstituted‐1,2,3,4‐Tetrahydroquinoxalines
inferred← citeshttps://doi.org/10.1002/asia.201600364openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cctc.201700289openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201500805openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201502278openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201600716openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.202000011openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/3418_2016_173openalex-snapshot
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Heterogeneous Catalysis by Frustrated Lewis Pairs
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inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.11189-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-818429-5.00003-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00041-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00129-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-823144-9.00011-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.adomc.2021.01.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ccr.2016.07.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.checat.2022.09.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.checat.2024.100959openalex-snapshot
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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.tetlet.2016.03.080openalex-snapshot
Pre-organized molecular tweezer stabilized by intramolecular hydrogen bonds: solvent-responsive host–guest complexation
inferred← citeshttps://doi.org/10.1016/j.trechm.2019.01.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.accounts.7b00530openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00561openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6c00004openalex-snapshot
Molecular Tuning Nanoarchitectonics of Azobenzene-Based Pliers Directs Chiral Preference and Reversible Helicity Inversion in Coordinated Molecular Rotors
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00884openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.2c01278openalex-snapshot
Asymmetric Hydrogenation by Relay Catalysis with FLPs and CPAs: Stereodivergent Synthesis of 3-Substituted Flavanones
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02905openalex-snapshot
Asymmetric Reduction of Quinolines: A Competition between Enantioselective Transfer Hydrogenation and Racemic Borane Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02954openalex-snapshot
Asymmetric Transfer Hydrogenation of 2-Substituted Quinoxalines with Regenerable Dihydrophenanthridine
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01273openalex-snapshot
Enantioselective Hydrogenation of Diarylmethanimines for Synthesis of Chiral Diarylmethylamines
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01578openalex-snapshot
Chiral Macrocyclic Borane-Catalyzed Asymmetric Hydrogenation of 2-Substituted Quinolines
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00035openalex-snapshot
Metal-Free Carbonylation Route to a Reactive Borataepoxide System
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03614openalex-snapshot
Synthesis of 2,2′-Dihalobiaryls via Cu-Catalyzed Halogenation of Cyclic Diaryliodonium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03833openalex-snapshot
Hexafluoroisopropanol-Enabled Copper-Catalyzed Asymmetric Halogenation of Cyclic Diaryliodoniums for the Synthesis of Axially Chiral 2,2′-Dihalobiaryls
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01073openalex-snapshot
Controlling the Lewis Acidity and Polymerizing Effectively Prevent Frustrated Lewis Pairs from Deactivation in the Hydrogenation of Terminal Alkynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03286openalex-snapshot
Relay Catalysis by Achiral Borane and Chiral Phosphoric Acid in the Metal-Free Asymmetric Hydrogenation of Chromones
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00843openalex-snapshot
Asymmetric Hydrogenation of Hydrazones with Chiral Boranes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01240openalex-snapshot
Cis-Selective and Highly Enantioselective Hydrogenation of 2,3,4-Trisubstituted Quinolines
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/acs.orglett.5b03307openalex-snapshot
Enantioselective Metal-Free Hydrogenations of Disubstituted Quinolines
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02610openalex-snapshot
Borane-Catalyzed Transfer Hydrogenations of Pyridines with Ammonia Borane
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00941openalex-snapshot
Highly Enantioselective Hydrogenation of Imines Catalyzed by Chiral Macrocyclic Boranes
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00935openalex-snapshot
Asymmetric Transfer Hydrogenations of 2,3-Disubstituted Quinoxalines with Ammonia Borane
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.4c05904openalex-snapshot
Activation and Stabilization of Engineered Amine Dehydrogenase by Fatty Acids for Bioprocess Intensification of Asymmetric Reductive Amination
inferred← citeshttps://doi.org/10.1021/acscatal.5b01299openalex-snapshot
Moisture-Tolerant Frustrated Lewis Pair Catalyst for Hydrogenation of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1021/acscatal.5b01417openalex-snapshot
Facile Protocol for Water-Tolerant “Frustrated Lewis Pair”-Catalyzed Hydrogenation
inferred← citeshttps://doi.org/10.1021/acscatal.8b01037openalex-snapshot
Enantioselective Synthesis of Biaryl Atropisomers via Pd/Norbornene-Catalyzed Three-Component Cross-Couplings
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/acscatal.9b01356openalex-snapshot
Triarylborane-Catalyzed Reductive N-Alkylation of Amines: A Perspective
inferred← citeshttps://doi.org/10.1021/jacs.1c00750openalex-snapshot
Reducing Challenges in Organic Synthesis with Stereoselective Hydrogenation and Tandem Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.4c14514openalex-snapshot
A Borenium-Borane Composite for Exhaustive Reduction of Oxo-Chemicals
inferred← citeshttps://doi.org/10.1021/jacs.6b00819openalex-snapshot
Metal-Free sp 2 -C–H Borylation as a Common Reactivity Pattern of Frustrated 2-Aminophenylboranes
inferred← citeshttps://doi.org/10.1021/jacs.6b07245openalex-snapshot
A Frustrated Lewis Pair Catalyzed Asymmetric Transfer Hydrogenation of Imines Using Ammonia Borane
inferred← citeshttps://doi.org/10.1021/jacs.7b11958openalex-snapshot
Formation of Reactive π-Conjugated Frustrated N/B Pairs by Borane-Induced Propargyl Amine Rearrangement
inferred← citeshttps://doi.org/10.1021/jacs.9b07293openalex-snapshot
Enantioselective Imine Reduction Catalyzed by Phosphenium Ions
inferred← citeshttps://doi.org/10.1038/s41467-018-07695-9openalex-snapshot
Click chemistry enables quantitative chiroptical sensing of chiral compounds in protic media and complex mixtures
inferred← citeshttps://doi.org/10.1038/s41467-021-21600-xopenalex-snapshot
Catalytic asymmetric reductive hydroalkylation of enamides and enecarbamates to chiral aliphatic amines
inferred← citeshttps://doi.org/10.1038/s41929-019-0371-yopenalex-snapshot
Development of heterogeneous catalyst systems for the continuous synthesis of chiral amines via asymmetric hydrogenation
inferred← citeshttps://doi.org/10.1039/9781839162442-00080openalex-snapshot
Borane-based Asymmetric FLP Hydrogenations
inferred← citeshttps://doi.org/10.1039/c5cy01372kopenalex-snapshot
Development of silica-supported frustrated Lewis pairs: highly active transition metal-free catalysts for the Z-selective reduction of alkynes
inferred← citeshttps://doi.org/10.1039/c5dt03815dopenalex-snapshot
Synthesis of 2-(lutidinyl)organoboranes and their reactivities against dihydrogen and pinacol borane
inferred← citeshttps://doi.org/10.1039/c5dt03916aopenalex-snapshot
Reversible hydrogen activation by a bulky haloborane based FLP system
inferred← citeshttps://doi.org/10.1039/c5ra12577dopenalex-snapshot
Photophysical properties of quinoxaline-fused [7]carbohelicene derivatives
inferred← citeshttps://doi.org/10.1039/c6cp05211hopenalex-snapshot
Nuclear spin hyperpolarization with ansa-aminoboranes: a metal-free perspective for parahydrogen-induced polarization
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/c6dt04649eopenalex-snapshot
Replacing C 6 F 5 groups with Cl and H atoms in frustrated Lewis pairs: H 2 additions and catalytic hydrogenations
inferred← citeshttps://doi.org/10.1039/c6nj00557hopenalex-snapshot
Metal-free homolytic hydrogen activation: a quest through density functional theory computations
inferred← citeshttps://doi.org/10.1039/c6ob01172aopenalex-snapshot
Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines
inferred← citeshttps://doi.org/10.1039/c6ob01556eopenalex-snapshot
A metal-free hydrogenation of 3-substituted 2H-1,4-benzoxazines
inferred← citeshttps://doi.org/10.1039/c6ra10785kopenalex-snapshot
Pyrite nanoparticles: an Earth-abundant mineral catalyst for activation of molecular hydrogen and hydrogenation of nitroaromatics
inferred← citeshttps://doi.org/10.1039/c7cc01440fopenalex-snapshot
Controlled ring-opening polymerization of α-amino acid N-carboxy-anhydride by frustrated amine/borane Lewis pairs
inferred← citeshttps://doi.org/10.1039/c7ta00101kopenalex-snapshot
Design of electric field controlled molecular gates mounted on metal–organic frameworks
inferred← citeshttps://doi.org/10.1039/c8cs00277kopenalex-snapshot
FLP catalysis: main group hydrogenations of organic unsaturated substrates
inferred← citeshttps://doi.org/10.1039/c8dt01619dopenalex-snapshot
A strategy for developing metal-free hydrogenation catalysts: a DFT proof-of-principle study
inferred← citeshttps://doi.org/10.1039/c8dt04070bopenalex-snapshot
Design considerations for chiral frustrated Lewis pairs: B/N FLPs derived from 3,5-bicyclic aryl piperidines
inferred← citeshttps://doi.org/10.1039/c8ob00023aopenalex-snapshot
B(C 6 F 5 ) 3 -catalyzed transfer hydrogenations of imines with Hantzsch esters
inferred← citeshttps://doi.org/10.1039/c8ob02446dopenalex-snapshot
Asymmetric hydrogenation of imines with chiral alkene-derived boron Lewis acids
inferred← citeshttps://doi.org/10.1039/c8sc02281jopenalex-snapshot
Four-coordinate triarylborane synthesis via cascade B–Cl/C–B cross-metathesis and C–H bond borylation
inferred← citeshttps://doi.org/10.1039/c9cc02900aopenalex-snapshot
Enantioselective reduction of N -alkyl ketimines with frustrated Lewis pair catalysis using chiral borenium ions
inferred← citeshttps://doi.org/10.1039/c9cs00917eopenalex-snapshot
Electron transfer in the confined environments of metal–organic coordination supramolecular systems
inferred← citeshttps://doi.org/10.1039/c9tc05915fopenalex-snapshot
A memory nanodevice based on Zn-MOF-74: a molecular dynamics study
inferred← citeshttps://doi.org/10.1039/d1cc06964kopenalex-snapshot
Chiral FLP-catalyzed asymmetric hydrogenation of 3-fluorinated chromones
inferred← citeshttps://doi.org/10.1039/d1sc02937aopenalex-snapshot
Pyrimidine-directed metal-free C–H borylation of 2-pyrimidylanilines: a useful process for tetra-coordinated triarylborane synthesis
inferred← citeshttps://doi.org/10.1039/d2dt00655copenalex-snapshot
Evidence for the encounter complex in frustrated Lewis pair chemistry
inferred← citeshttps://doi.org/10.1039/d2ob00602bopenalex-snapshot
Asymmetric hydrogenation of TIPS-protected oximes with chiral boranes
inferred← citeshttps://doi.org/10.1039/d2ob01950gopenalex-snapshot
B(C 6 F 5 ) 3 -catalyzed metal-free hydrogenation of 2-oxazolones
inferred← citeshttps://doi.org/10.1039/d5dt02885jopenalex-snapshot
Design of boron-decorated bimetallic iron complexes related to the active site of [FeFe]-hydrogenases and reactivity with hydride donors
inferred← citeshttps://doi.org/10.1055/a-1681-3972openalex-snapshot
Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides
inferred← citeshttps://doi.org/10.1055/a-1684-5552openalex-snapshot
Hydrogenation of Olefins, Alkynes, Allenes, and Arenes by Borane-Based Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1055/a-1701-7679openalex-snapshot
Synthesis and Applications of Chiral Bicyclic Bisborane Catalysts
inferred← citeshttps://doi.org/10.1055/a-2005-5443openalex-snapshot
Frustrated Lewis Pair Catalyzed Reactions
inferred← citeshttps://doi.org/10.1126/science.aaf7229openalex-snapshot
The broadening reach of frustrated Lewis pair chemistry
inferred← citeshttps://doi.org/10.1126/science.aau5105openalex-snapshot
Frontiers in molecular p-block chemistry: From structure to reactivity
inferred← citeshttps://doi.org/10.26434/chemrxiv.13102307openalex-snapshot
Catalytic Asymmetric Reductive Alkylation of Enamines to Chiral Aliphatic Amines
inferred← citeshttps://doi.org/10.3184/146867817x14954764850469openalex-snapshot
Theoretical Evaluation of the Efficiency of Novel Frustrated Lewis Pairs in thecis-Hydrogenation Reaction of Dimethylacetylene
inferred← citeshttps://doi.org/10.3390/molecules20069575openalex-snapshot
Reactivity of Amine/E(C6F5)3 (E = B, Al) Lewis Pairs toward Linear and Cyclic Acrylic Monomers: Hydrogenation vs. Polymerization
inferred← citeshttps://doi.org/10.3390/molecules200711902openalex-snapshot
Ambiphilic Frustrated Lewis Pair Exhibiting High Robustness and Reversible Water Activation: Towards the Metal-Free Hydrogenation of Carbon Dioxide
inferred← citeshttps://doi.org/10.3390/surfaces7030049openalex-snapshot
Supramolecular Chemistry of Polymer-Based Molecular Tweezers: A Minireview
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.79.1065openalex-snapshot
Enantioselective Cooperative Catalysis within Frustrated Lewis Pair Complexes
inferred← citeshttps://doi.org/10.6023/cjoc202208018openalex-snapshot
Chiral Borane-Catalyzed Enantioselective Reactions
inferred← citeshttps://doi.org/10.70675/164df220z03e7z45daz9affz14d8ecaa04efopenalex-snapshot
Catalyse par les paires de Lewis frustrées et les acides de Lewis de type fluorosulfoxoniums : activation de cycles contraints et autres processus
inferred← citeshttps://doi.org/10.70675/96a7c037z2673z4744z80e3z55fc586f7fc8openalex-snapshot
Accès à des acides de Lewis par Umpolung de bases de Lewis chirales : applications en synthèse asymétrique
inferred← citeshttps://doi.org/10.70675/c09274a2zce90z4fd2z80c9zf39e7ef9f4d0openalex-snapshot
Biphényles à chiralité axiale : vers la synthèse de paires de Lewis frustrées pour la catalyse énantiosélective
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