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Catalytic Enantioselective Additions of Indoles to Nitroalkenes
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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/adsc.200505148openalex-snapshot
Guanidine‐Thiourea Bifunctional Organocatalyst for the Asymmetric Henry (Nitroaldol) Reaction
inferredcites →https://doi.org/10.1002/adsc.200606074openalex-snapshot
Recent Progress in Chiral Brønsted Acid Catalysis
inferredcites →https://doi.org/10.1002/anie.200460394openalex-snapshot
“Designer Acids”: Combined Acid Catalysis for Asymmetric Synthesis
inferredcites →https://doi.org/10.1002/anie.200500154openalex-snapshot
Protonated Chiral Catalysts: Versatile Tools for Asymmetric Synthesis
inferredcites →https://doi.org/10.1002/anie.200500227openalex-snapshot
Catalytic Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst
inferredcites →https://doi.org/10.1002/anie.200503132openalex-snapshot
Asymmetric Catalysis by Chiral Hydrogen‐Bond Donors
inferredcites →https://doi.org/10.1002/anie.200603354openalex-snapshot
Indium‐Mediated Asymmetric Allylation of Acylhydrazones Using a Chiral Urea Catalyst
inferredcites →https://doi.org/10.1002/anie.200700298openalex-snapshot
Systematically Probing the Effect of Catalyst Acidity in a Hydrogen‐Bond‐Catalyzed Enantioselective Reaction
inferredcites →https://doi.org/10.1002/anie.200800770openalex-snapshot
Chiral Phosphoric Acid Catalyzed Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes: Cooperative Effect of 3 Å Molecular Sieves
inferredcites →https://doi.org/10.1002/anie.200801373openalex-snapshot
Tandem Catalytic Asymmetric Friedel–Crafts/Henry Reaction: Control of Three Contiguous Acyclic Stereocenters
inferredcites →https://doi.org/10.1002/asia.200700145openalex-snapshot
Organocatalytic Asymmetric Nitroaldol Reaction: Cooperative Effects of Guanidine and Thiourea Functional Groups
inferredcites →https://doi.org/10.1002/asia.200700415openalex-snapshot
Hydrogen‐Bond‐Mediated Asymmetric Catalysis
inferredcites →https://doi.org/10.1002/asia.200800071openalex-snapshot
Asymmetric Friedel–Crafts Alkylation of Electron‐Rich N‐Heterocycles with Nitroalkenes Catalyzed by Diphenylamine‐Tethered Bis(oxazoline) and Bis(thiazoline) ZnII Complexes
inferredcites →https://doi.org/10.1002/chem.200390042openalex-snapshot
Metal‐Free, Noncovalent Catalysis of Diels–Alder Reactions by Neutral Hydrogen Bond Donors in Organic Solvents and in Water
inferredcites →https://doi.org/10.1002/chem.200501076openalex-snapshot
Organocatalysis Mediated by (Thio)urea Derivatives
inferredcites →https://doi.org/10.1002/ejoc.200200635openalex-snapshot
A C 2 ‐Chiral Bis(amidinium) Catalyst for a Diels−Alder Reaction Constituting the Key Step of the Quinkert−Dane Estrone Synthesis
inferredcites →https://doi.org/10.1016/j.tetasy.2008.04.037openalex-snapshot
BINAM and H8-BINAM-based chiral imines and Zn(OTf)2-catalyzed enantioselective Friedel–Crafts alkylation of indoles with nitroalkenes
inferredcites →https://doi.org/10.1016/j.tetlet.2006.07.112openalex-snapshot
Novel axially chiral bis-arylthiourea-based organocatalysts for asymmetric Friedel–Crafts type reactions
inferredcites →https://doi.org/10.1016/j.tetlet.2006.12.081openalex-snapshot
Enantioselective Friedel–Crafts alkylation of indoles with nitroalkenes catalyzed by a bis(oxazoline)–Cu(II) complex
inferredcites →https://doi.org/10.1021/cr068373ropenalex-snapshot
Small-Molecule H-Bond Donors in Asymmetric Catalysis
inferredcites →https://doi.org/10.1021/ja031906iopenalex-snapshot
Chiral Proton Catalysis: A Catalytic Enantioselective Direct Aza-Henry Reaction
inferredcites →https://doi.org/10.1021/ja057848dopenalex-snapshot
Axially Chiral Guanidine as Enantioselective Base Catalyst for 1,4-Addition Reaction of 1,3-Dicarbonyl Compounds with Conjugated Nitroalkenes
inferredcites →https://doi.org/10.1021/ja066808mopenalex-snapshot
Axially Chiral Guanidine as Highly Active and Enantioselective Catalyst for Electrophilic Amination of Unsymmetrically Substituted 1,3-Dicarbonyl Compounds
inferredcites →https://doi.org/10.1021/ja068073ropenalex-snapshot
Chiral Proton Catalysis: Enantioselective Brønsted Acid Catalyzed Additions of Nitroacetic Acid Derivatives as Glycine Equivalents
inferredcites →https://doi.org/10.1021/ja071739copenalex-snapshot
Organocatalysis in Conjugate Amine Additions. Synthesis of β-Amino Acid Derivatives
inferredcites →https://doi.org/10.1021/ja075653vopenalex-snapshot
Enantioselective Aza-Henry Reaction with an N-Sulfinyl Urea Organocatalyst
inferredcites →https://doi.org/10.1021/ja8011808openalex-snapshot
A Diastereo- and Enantioselective Synthesis of α-Substituted syn-α,β-Diamino Acids
inferredcites →https://doi.org/10.1021/ja803370xopenalex-snapshot
Enantioselective Claisen Rearrangements with a Hydrogen-Bond Donor Catalyst
inferredcites →https://doi.org/10.1021/jo0516537openalex-snapshot
Asymmetric Friedel−Crafts Alkylations of Indoles with Nitroalkenes Catalyzed by Zn(II)−Bisoxazoline Complexes
inferredcites →https://doi.org/10.1021/jo070534jopenalex-snapshot
Synthesis of C2-Symmetric Bisamidines: A New Type of Chiral Metal-Free Lewis Acid Analogue Interacting with Carbonyl Groups
inferredcites →https://doi.org/10.1021/jo702154mopenalex-snapshot
Computational Study-Led Organocatalyst Design: A Novel, Highly Active Urea-Based Catalyst for Addition Reactions to Epoxides
inferredcites →https://doi.org/10.1021/jo991372xopenalex-snapshot
Catalysis of a Diels−Alder Reaction by Amidinium Ions
inferredcites →https://doi.org/10.1021/ol047698wopenalex-snapshot
A New Chiral Catalyst for the Enantioselective Strecker Synthesis of α-Amino Acids
inferredcites →https://doi.org/10.1021/ol060586fopenalex-snapshot
Enantioselective Friedel−Crafts Alkylation of Indoles with Nitroalkenes Catalyzed by Bifunctional Tridentate Bis(oxazoline)−Zn(II) Complex
inferredcites →https://doi.org/10.1021/ol071032vopenalex-snapshot
2-Aminopyridinium Ions Activate Nitroalkenes through Hydrogen Bonding
inferredcites →https://doi.org/10.1021/ol071292copenalex-snapshot
Organocatalytic Conjugate Addition of Formaldehyde N,N-Dialkylhydrazones to β,γ-Unsaturated α-Keto Esters
inferredcites →https://doi.org/10.1021/ol990623lopenalex-snapshot
Enantioselective Synthesis of α-Amino Nitriles from N -Benzhydryl Imines and HCN with a Chiral Bicyclic Guanidine as Catalyst
inferredcites →https://doi.org/10.1021/ol991276iopenalex-snapshot
Axially Chiral Amidinium Ions as Inducers of Enantioselectivity in Diels−Alder Reactions
inferredcites →https://doi.org/10.1039/b107298fopenalex-snapshot
Metal-free organocatalysis through explicit hydrogen bonding interactions
inferredcites →https://doi.org/10.1039/b505220copenalex-snapshot
Enantioselective Friedel–Crafts type addition of indoles to nitro-olefins using a chiral hydrogen-bonding catalyst – synthesis of optically active tetrahydro-β-carbolines
inferredcites →https://doi.org/10.1039/b511216hopenalex-snapshot
Recognition and activation by ureas and thioureas: stereoselective reactions using ureas and thioureas as hydrogen-bonding donors
inferredcites →https://doi.org/10.1039/b611138fopenalex-snapshot
Pyridyl thioureas as switchable anion receptors
inferredcites →https://doi.org/10.1055/s-2007-984882openalex-snapshot
Asymmetric Morita-Baylis-Hillman Reaction Catalyzed by Simple Amino Alcohol Derived Thioureas
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Enantioselective Friedel-Crafts Alkylation of 1,3,5-Trimethoxybenzene with Trans-Β-Nitrostyrenes Catalysed by [Cp*Rh{(R)-Prophos}(H2o)][Sbf6]2 (Prophos = Propane-1,2-Diyl-Bis(Diphenylphosphane)
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(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol
inferred← citeshttps://doi.org/10.1002/9780470979525.ch11openalex-snapshot
Addition Reactions: Polar Addition
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub4openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub5openalex-snapshot
Chiral Auxiliaries and Catalysts
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Chiral Auxiliaries and Catalysts
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Chiral Auxiliaries and Catalysts
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Other Reactions For C–C Bond Formation
inferred← citeshttps://doi.org/10.1002/9781118846919.ch6openalex-snapshot
Asymmetric Assisted Catalysis by Multicatalyst System
inferred← citeshttps://doi.org/10.1002/9783527630554.ch6openalex-snapshot
Double Hydrogen Bonding in Asymmetric Organocatalysis: A Mechanistic Perspective
inferred← citeshttps://doi.org/10.1002/9783527637737.ch5openalex-snapshot
Five‐Membered Heterocycles: Indole and Related Systems
inferred← citeshttps://doi.org/10.1002/9783527645824.ch8openalex-snapshot
Hydrogen Bonds as an Alternative Activation
inferred← citeshttps://doi.org/10.1002/9783527658862.ch35openalex-snapshot
Organocatalyzed Asymmetric Arylation and Heteroarylation Reactions
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Facile Creation of 3‐Indolyl‐3‐hydroxy‐2‐oxindoles by an Organocatalytic Enantioselective Friedel–Crafts Reaction of Indoles with Isatins
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Synthesis and Structures of Air‐Stable Binuclear Hafnocene Perfluorobutanesulfonate and Perfluorobenzenesulfonate and their Catalytic Application in CC Bond‐Forming Reactions
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Stereoselective Synthesis of Functionalized Chiral 2‐Nitrocyclohexanecarboxylic Esters via Catalytic Dienamine Addition to β‐Substituted β‐Nitroacrylates
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2,6‐Bis(amido)benzoic Acid with Internal Hydrogen Bond as Brønsted Acid Catalyst for Friedel–Crafts Reaction of Indoles
inferred← citeshttps://doi.org/10.1002/adsc.201500079openalex-snapshot
Organocatalytic Enantioselective Michael Reaction of Malononitrile with β,β‐Disubstituted Nitroalkenes
inferred← citeshttps://doi.org/10.1002/adsc.201500923openalex-snapshot
Enantioselective Copper(II)‐Catalyzed Conjugate Addition of Indoles to β‐Substituted Unsaturated Acyl Phosphonates
inferred← citeshttps://doi.org/10.1002/adsc.201701059openalex-snapshot
Recent Progress in Organocatalytic Asymmetric Domino Transformations
inferred← citeshttps://doi.org/10.1002/adsc.202401458openalex-snapshot
Understanding Chiral Proton Catalysis Using Cinchonium Derivatives in aza‐Michael Additions
inferred← citeshttps://doi.org/10.1002/adsc.70050openalex-snapshot
Pd/BINAP/Peroxide‐Enabled Relay Multicomponent Reactions
inferred← citeshttps://doi.org/10.1002/ajoc.201300246openalex-snapshot
Stereoselective Addition of 1,3‐Diketones to β‐Nitroacrylates Catalyzed by Chiral Metal‐Free Bifunctional Catalysts
inferred← citeshttps://doi.org/10.1002/ange.200901843openalex-snapshot
Katalytische Funktionalisierung von Indolen in einer neuen Dimension
inferred← citeshttps://doi.org/10.1002/ange.200903063openalex-snapshot
Plagiarizing Proteins: Enhancing Efficiency in Asymmetric Hydrogen‐Bonding Catalysis through Positive Cooperativity
inferred← citeshttps://doi.org/10.1002/ange.200904338openalex-snapshot
Iridium‐Catalyzed Regio‐ and Enantioselective N‐Allylation of Indoles
inferred← citeshttps://doi.org/10.1002/ange.201001484openalex-snapshot
Orthogonal Enantioselectivity Approaches Using Homogeneous and Heterogeneous Catalyst Systems: Friedel–Crafts Alkylation of Indole
inferred← citeshttps://doi.org/10.1002/ange.201203852openalex-snapshot
Cooperative Assistance in Bifunctional Organocatalysis: Enantioselective Mannich Reactions with Aliphatic and Aromatic Imines
inferred← citeshttps://doi.org/10.1002/ange.201308196openalex-snapshot
Conjugate‐Base‐Stabilized Brønsted Acids as Asymmetric Catalysts: Enantioselective Povarov Reactions with Secondary Aromatic Amines
inferred← citeshttps://doi.org/10.1002/ange.201501536openalex-snapshot
Catalytic Enantioselective Intramolecular Aza‐Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1002/ange.201612148openalex-snapshot
Catalytic Enantioselective Synthesis of Lactams through Formal [4+2] Cycloaddition of Imines with Homophthalic Anhydride
inferred← citeshttps://doi.org/10.1002/anie.200901843openalex-snapshot
Catalytic Functionalization of Indoles in a New Dimension
inferred← citeshttps://doi.org/10.1002/anie.200903063openalex-snapshot
Plagiarizing Proteins: Enhancing Efficiency in Asymmetric Hydrogen‐Bonding Catalysis through Positive Cooperativity
inferred← citeshttps://doi.org/10.1002/anie.200904338openalex-snapshot
Iridium‐Catalyzed Regio‐ and Enantioselective N‐Allylation of Indoles
inferred← citeshttps://doi.org/10.1002/anie.201001484openalex-snapshot
Orthogonal Enantioselectivity Approaches Using Homogeneous and Heterogeneous Catalyst Systems: Friedel–Crafts Alkylation of Indole
inferred← citeshttps://doi.org/10.1002/anie.201203852openalex-snapshot
Cooperative Assistance in Bifunctional Organocatalysis: Enantioselective Mannich Reactions with Aliphatic and Aromatic Imines
inferred← citeshttps://doi.org/10.1002/anie.201308196openalex-snapshot
Conjugate‐Base‐Stabilized Brønsted Acids as Asymmetric Catalysts: Enantioselective Povarov Reactions with Secondary Aromatic Amines
inferred← citeshttps://doi.org/10.1002/anie.201501536openalex-snapshot
Catalytic Enantioselective Intramolecular Aza‐Diels–Alder Reactions
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Catalytic Enantioselective Synthesis of Lactams through Formal [4+2] Cycloaddition of Imines with Homophthalic Anhydride
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Enantioselective synthesis and biological investigation of tetrahydro‐β‐carboline‐based HDAC6 inhibitors with improved solubility
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DFT Study of Chiral‐Phosphoric‐Acid‐Catalyzed Enantioselective Friedel–Crafts Reaction of Indole with Nitroalkene: Bifunctionality and Substituent Effect of Phosphoric Acid
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Gold(I)‐Mediated Thiourea Organocatalyst Activation: A Synergic Effect for Asymmetric Catalysis
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Asymmetric Friedel–Crafts Reaction of 4,7‐Dihydroindoles with Nitroolefins by Chiral Brønsted Acids under Low Catalyst Loading
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Physical Organic Study of Structure–Activity–Enantioselectivity Relationships in Asymmetric Bifunctional Thiourea Catalysis: Hints for the Design of New Organocatalysts
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Monodentate N‐Ligand‐Directed Bifunctional Transition‐Metal Catalysis: Highly Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes
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Synthesis of Functionalized Indoles with a Trifluoromethyl‐Substituted Stereogenic Tertiary Carbon Atom Through an Enantioselective Friedel–Crafts Alkylation with β‐Trifluoromethyl‐α,β‐enones
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Enantioselective Synthesis of Tetrahydrocarbazoles through a Michael Addition/Ciamician–Plancher Rearrangement Sequence: Asymmetric Synthesis of a Potent Constrained Analogue of MS‐245
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ChemInform Abstract: Catalytic Enantioselective Additions of Indoles to Nitroalkenes.
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Friedel‐Crafts Alkylation of Indoles with Nitroalkenes Catalyzed by Zn(II)‐Thiourea Complex
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Organocatalyzed Asymmetric Friedel–Crafts Reactions
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Accelerating Amine‐Catalyzed Asymmetric Reactions by Intermolecular Cooperative Thiourea/Oxime Hydrogen‐Bond Catalysis
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An efficient and clean Michael addition of indoles to electron‐deficient olefins under solvent‐ and catalyst‐free condition
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Structural considerations for charge‐enhanced Brønsted acid catalysts
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Effects of Brønsted acid cocatalysts on the activities and selectivities of charge‐enhanced thiourea organocatalysts in Friedel–Crafts and oxa‐Pictet–Spengler reactions
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Organocatalytic Asymmetric Cascade Reaction of γ‐Substituted Deconjugated Butenolides with o‐Formyl‐β‐nitrostyrene
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Novel Access to Known and Unknown Thiourea Catalyst via a Multicomponent‐Reaction Approach
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Applications of Helical‐Chiral Pyridines as Organocatalysts in Asymmetric Synthesis
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Electrophilic Substitution Reactions of Indoles
inferred← citeshttps://doi.org/10.1007/7081_2015_171openalex-snapshot
Chiral Guanidines in Michael Reactions
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Organocatalyzed Conjugate Additions
inferred← citeshttps://doi.org/10.1007/s10562-014-1228-2openalex-snapshot
Chiral Bis(Oxazolinyl)thiophenes for Enantioselective Cu(II)-Catalyzed Friedel–Crafts Alkylation of Indole Derivatives with Nitroalkenes
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Arenes and Hetarenes in Reactions with unsaturated Nitro Compounds (Review)
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4.03 Organocatalytic Asymmetric Nucleophilic Addition to Electron-Deficient Alkenes
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5.33 Hydroarylation Reactions
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Prroles and Their Benzo Derivatives: Reactivity
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Ionic liquid [Dabco-C8][FeCl4] as an efficient and recyclable catalyst for direct C3 alkylation of indoles with electron-deficient olefins
inferred← citeshttps://doi.org/10.1016/j.cclet.2011.04.013openalex-snapshot
Friedel–Crafts alkylation of indoles with nitroalkenes catalyzed by Cu(II)–imine complex
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.06.028openalex-snapshot
Metal-free cascade boron–heteroatom addition and alkylation with diazo compounds
inferred← citeshttps://doi.org/10.1016/j.ccr.2017.01.013openalex-snapshot
Recent developments in enantioselective lanthanide-catalyzed transformations
inferred← citeshttps://doi.org/10.1016/j.cdc.2020.100420openalex-snapshot
Effect of ligand tautomerism on Suzuki reactions
inferred← citeshttps://doi.org/10.1016/j.checat.2025.101577openalex-snapshot
Performance-enhancing asymmetric catalysis unlocks tuning without rebuilding
inferred← citeshttps://doi.org/10.1016/j.chempr.2023.02.020openalex-snapshot
Data science enables the development of a new class of chiral phosphoric acid catalysts
inferred← citeshttps://doi.org/10.1016/j.inoche.2013.11.021openalex-snapshot
A trinuclear Cu2Eu complex catalyzed asymmetric Friedel–Crafts alkylations of indoles with nitroalkenes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.10.031openalex-snapshot
Structure and catalytic activity of organopalladium(II) complexes based on 4,5-dihydro-1H-imidazol-5-one derivatives
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.10.011openalex-snapshot
Organometal-catalyzed asymmetric Friedel-Crafts reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123377openalex-snapshot
Enantioselective Friedel-Crafts alkylation of 1,3,5-trimethoxybenzene with trans-β-nitrostyrenes catalysed by [Cp*Rh{(R)-Prophos}(H2O)][SbF6]2 (Prophos = propane-1,2-diyl-bis(diphenylphosphane)
inferred← citeshttps://doi.org/10.1016/j.molstruc.2015.08.029openalex-snapshot
Raman, IR and DFT studies of mechanism of sodium binding to urea catalyst
inferred← citeshttps://doi.org/10.1016/j.tet.2010.05.104openalex-snapshot
Catalyst free conjugate addition of indoles and pyrroles to nitro alkenes under solvent free condition (SFC): an effective greener route to access 3-(2-nitro-1-phenylethyl)-1H-indole and 2-(2-nitro-1-phenylethyl)-1H-pyrrole derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.116openalex-snapshot
Asymmetric Michael addition of 4H-thiopyran-4-one to nitroolefins catalyzed by diamine mono-N-sulfonamide and its application to concise synthesis of enantiopure multiring heterocycles
inferred← citeshttps://doi.org/10.1016/j.tet.2013.08.040openalex-snapshot
1,1-Diamino-2-nitroethylenes as excellent hydrogen bond donor organocatalysts in the Michael addition of carbon-based nucleophiles to β-nitrostyrenes
inferred← citeshttps://doi.org/10.1016/j.tet.2014.03.068openalex-snapshot
Conformational change in a urea catalyst induced by sodium cation and its effect on enantioselectivity of a Friedel-Crafts reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2014.05.045openalex-snapshot
Direct synthesis of α-ketothioamides from aryl methyl ketones and amines via I2-promoted sp3 C–H functionalization
inferred← citeshttps://doi.org/10.1016/j.tet.2014.10.042openalex-snapshot
Conjugate addition nitro-Mannich reaction of carbon and heteroatom nucleophiles to nitroalkenes
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130757openalex-snapshot
Charge-enhanced thiourea catalysts as hydrogen bond donors for Friedel‒Crafts Alkylations
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.05.003openalex-snapshot
Enantioselective Friedel–Crafts alkylations catalysed by well-defined iridium and rhodium half-sandwich complexes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.05.011openalex-snapshot
Enantioselective Friedel–Crafts alkylation of indoles with β,γ-unsaturated α-ketoesters catalyzed by new squaramide-linked bisoxazoline–Zn(OTf)2 complexes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.07.003openalex-snapshot
Novel 3-C-aminomethyl-hexofuranose-derived thioureas and their testing in asymmetric catalysis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.07.071openalex-snapshot
Friedel–Crafts-type alkylation in aqueous media using resin-supported peptide catalyst having polyleucine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.09.129openalex-snapshot
New architectures in hydrogen bond catalysis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.03.114openalex-snapshot
Pd-catalyzed α-arylation of thioamides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.09.081openalex-snapshot
Pd-catalyzed allylic alkylation of thioamides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.12.031openalex-snapshot
Pd-catalyzed asymmetric α-allylic alkylation of thioamides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.03.099openalex-snapshot
Chiral benzimidazoles as hydrogen bonding organocatalysts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.08.060openalex-snapshot
A multipathway coupled domino strategy: I2-mediated oxidative thionation for direct synthesis of thiobenzamides from miscellaneous substrates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.11.030openalex-snapshot
Effective approach to ureas through organocatalyzed one-pot process
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153153openalex-snapshot
Enantioselective Friedel-Crafts alkylation of indole with nitroalkenes in the presence of bifunctional squaramide organocatalysts
inferred← citeshttps://doi.org/10.1016/j.ultsonch.2010.09.007openalex-snapshot
An efficient synthesis of 3-substituted indole derivates under ultrasound irradiation
inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80008-6openalex-snapshot
Chapter 5.2 Five-membered ring systems: pyrroles and benzo analogs
inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70033-9openalex-snapshot
Chapter 5.2: Five-Membered Ring Systems: Pyrroles and Benzo Analogs
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.9b00893openalex-snapshot
Design and Development of a Heterogeneous Catalyst for the Michael Addition of Malononitrile to 2-Enoylpyridines: Influence of the Primary Amide Decorated Framework on Catalytic Activity and Selectivity
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.7b01593openalex-snapshot
Marbostat-100 Defines a New Class of Potent and Selective Antiinflammatory and Antirheumatic Histone Deacetylase 6 Inhibitors
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00498openalex-snapshot
N-Vinyl and N-Aryl Hydroxypyridinium Ions: Charge-Activated Catalysts with Electron-Withdrawing Groups
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02749openalex-snapshot
Enantioselective Friedel–Crafts Alkylation of Indoles with β,γ-Unsaturated α-Ketoesters Catalyzed by New Copper(I) Catalysts
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01750openalex-snapshot
Multi-Ion Complexes and Competition from Bulky BArF – Anions for Chloride Binding in Ion Pairing Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02411openalex-snapshot
Enantioselective Friedel–Crafts Alkylation between Nitroalkenes and Indoles Catalyzed by Charge Activated Thiourea Organocatalysts
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01552openalex-snapshot
Quantification of Catalytic Activity for Electrostatically Enhanced Thioureas via Reaction Kinetics and UV–vis Spectroscopic Measurement
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02321openalex-snapshot
Cyclopropenium Enhanced Thiourea Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01741openalex-snapshot
Electrostatically Enhanced Phosphoric Acids and Their Applications in Asymmetric Friedel–Crafts Alkylations
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00077openalex-snapshot
Enantioselective Direct Functionalization of Indoles by Pd/Sulfoxide-Phosphine-Catalyzed N-Allylic Alkylation
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03213openalex-snapshot
Electrostatically Enhanced Thioureas
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c05342openalex-snapshot
Chiral Thiourea Catalysts Containing Fluxional Groups: Synthesis of Fluorinated Chiral Building Blocks
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00608openalex-snapshot
Chiral Pyridinium Phosphoramide as a Dual Brønsted Acid Catalyst for Enantioselective Diels–Alder Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03584openalex-snapshot
Catalytic Asymmetric Synthesis of Chiral 2-Vinylindole Scaffolds by Friedel–Crafts Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02862openalex-snapshot
Switchable Chemoselectivity for Organocatalytic, Asymmetric Malononitrile Addition to ortho-Formyl Chalcones
inferred← citeshttps://doi.org/10.1021/acscatal.1c05296openalex-snapshot
Organocatalysis Linked to Charge-Enhanced Acidity with Superelectrophilic Traits
inferred← citeshttps://doi.org/10.1021/acscatal.3c06036openalex-snapshot
Barium Alginate Gel Beads: A Homochiral Porous Material from Brown Algae for Heterogeneous Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.8b04962openalex-snapshot
Design of a Primary-Amide-Functionalized Highly Efficient and Recyclable Hydrogen-Bond-Donating Heterogeneous Catalyst for the Friedel–Crafts Alkylation of Indoles with β-Nitrostyrenes
inferred← citeshttps://doi.org/10.1021/acsomega.2c05022openalex-snapshot
Recent Advances in the Catalytic Asymmetric Friedel–Crafts Reactions of Indoles
inferred← citeshttps://doi.org/10.1021/cr400676vopenalex-snapshot
Synthetic Approaches to 3-(2-Nitroalkyl) Indoles and Their Use to Access Tryptamines and Related Bioactive Compounds
inferred← citeshttps://doi.org/10.1021/ja100539copenalex-snapshot
Helical Chiral 2-Aminopyridinium Ions: A New Class of Hydrogen Bond Donor Catalysts
inferred← citeshttps://doi.org/10.1021/ja1093309openalex-snapshot
Rhodium(II)-Catalyzed Enantioselective C−H Functionalization of Indoles
inferred← citeshttps://doi.org/10.1021/ja309133zopenalex-snapshot
Mechanism and Selectivity of Bioinspired Cinchona Alkaloid Derivatives Catalyzed Asymmetric Olefin Isomerization: A Computational Study
inferred← citeshttps://doi.org/10.1021/ja400650mopenalex-snapshot
Highly Enantioselective Construction of Trifluoromethylated All-Carbon Quaternary Stereocenters via Nickel-Catalyzed Friedel–Crafts Alkylation Reaction
inferred← citeshttps://doi.org/10.1021/ja409214copenalex-snapshot
Acceleration of an Aromatic Claisen Rearrangement via a Designed Spiroligozyme Catalyst that Mimics the Ketosteroid Isomerase Catalytic Dyad
inferred← citeshttps://doi.org/10.1021/ja508804nopenalex-snapshot
Allosteric Regulation of Supramolecular Oligomerization and Catalytic Activity via Coordination-Based Control of Competitive Hydrogen-Bonding Events
inferred← citeshttps://doi.org/10.1021/ja903271topenalex-snapshot
Chiral Arylaminophosphonium Barfates as a New Class of Charged Brønsted Acid for the Enantioselective Activation of Nonionic Lewis Bases
inferred← citeshttps://doi.org/10.1021/ja908814hopenalex-snapshot
Bifunctional Asymmetric Catalysis: Amplification of Brønsted Basicity Can Orthogonally Increase the Reactivity of a Chiral Brønsted Acid
inferred← citeshttps://doi.org/10.1021/ja9097803openalex-snapshot
Acyl Phosphonates: Good Hydrogen Bond Acceptors and Ester/Amide Equivalents in Asymmetric Organocatalysis
inferred← citeshttps://doi.org/10.1021/jacs.5b01805openalex-snapshot
Charge-Enhanced Acidity and Catalyst Activation
inferred← citeshttps://doi.org/10.1021/jacs.5b02071openalex-snapshot
Enantioselective A3Reactions of Secondary Amines with a Cu(I)/Acid–Thiourea Catalyst Combination
inferred← citeshttps://doi.org/10.1021/jacs.5c18359openalex-snapshot
Molecular Weight-Controlled Cationic Polymerization of Tetrahydrofuran Using a Squaramidinium Hydrogen-Bond Donor Catalyst
inferred← citeshttps://doi.org/10.1021/jo200546aopenalex-snapshot
Catalytic Asymmetric Friedel–Crafts/Protonation of Nitroalkenes and N-Heteroaromatics
inferred← citeshttps://doi.org/10.1021/jo201678uopenalex-snapshot
Electrophilicities oftrans-β-Nitrostyrenes
inferred← citeshttps://doi.org/10.1021/jo3024945openalex-snapshot
Organocatalytic Asymmetric Michael Addition of Aliphatic Aldehydes to Indolylnitroalkenes: Access to Contiguous Stereogenic Tryptamine Precursors
inferred← citeshttps://doi.org/10.1021/jo4025368openalex-snapshot
FeCl3 Catalyzed Regioselective C-Alkylation of Indolylnitroalkenes with Amino Group Substituted Arenes
inferred← citeshttps://doi.org/10.1021/jo402605nopenalex-snapshot
Computational Study on the pKaShifts in Proline Induced by Hydrogen-Bond-Donating Cocatalysts
inferred← citeshttps://doi.org/10.1021/jo500158eopenalex-snapshot
Computational Study on the Acidic Constants of Chiral Brønsted Acids in Dimethyl Sulfoxide
inferred← citeshttps://doi.org/10.1021/jo9013029openalex-snapshot
Chiral Bronsted Acid-Catalyzed Asymmetric Friedel−Crafts Alkylation of Pyrroles with Nitroolefins
inferred← citeshttps://doi.org/10.1021/ol1025712openalex-snapshot
Chiral Brønsted Base-Promoted Nitroalkane Alkylation: Enantioselective Synthesis of sec-Alkyl-3-Substituted Indoles
inferred← citeshttps://doi.org/10.1021/ol102899yopenalex-snapshot
Internal Lewis Acid Assisted Hydrogen Bond Donor Catalysis
inferred← citeshttps://doi.org/10.1021/ol1029673openalex-snapshot
Reductive Alkylation of Indoles with Alkynes and Hydrosilanes under Indium Catalysis
inferred← citeshttps://doi.org/10.1021/ol201914ropenalex-snapshot
A New Type of Bis(sulfonamide)-Diamine Ligand for a Cu(OTf)2-Catalyzed Asymmetric Friedel–Crafts Alkylation Reaction of Indoles with Nitroalkenes
inferred← citeshttps://doi.org/10.1021/ol2020847openalex-snapshot
Enantioselective Conjugate Addition of Alkenylboronic Acids to Indole-Appended Enones
inferred← citeshttps://doi.org/10.1021/ol202873dopenalex-snapshot
Boronate Urea Activation of Nitrocyclopropane Carboxylates
inferred← citeshttps://doi.org/10.1021/ol202971mopenalex-snapshot
Cooperative Hydrogen-Bonding Effects in Silanediol Catalysis
inferred← citeshttps://doi.org/10.1021/ol300632popenalex-snapshot
Rh 2 ( S -biTISP) 2 -Catalyzed Asymmetric Functionalization of Indoles and Pyrroles with Vinylcarbenoids
inferred← citeshttps://doi.org/10.1021/ol3030605openalex-snapshot
A General Method for the Enantioselective Synthesis of α-Chiral Heterocycles
inferred← citeshttps://doi.org/10.1021/ol403480vopenalex-snapshot
Asymmetric Friedel–Crafts Alkylation of α-Substituted β-Nitroacrylates: Access to β 2,2 -Amino Acids Bearing Indolic All-Carbon Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1021/ol403773aopenalex-snapshot
Conjugate-Base-Stabilized Brønsted Acids: Catalytic Enantioselective Pictet–Spengler Reactions with Unmodified Tryptamine
inferred← citeshttps://doi.org/10.1021/ol9010882openalex-snapshot
Direct Thionation and Selenation of Amides Using Elemental Sulfur and Selenium and Hydrochlorosilanes in the Presence of Amines
inferred← citeshttps://doi.org/10.1021/om200714zopenalex-snapshot
A Cationic NCN Pincer Platinum(II) Aquo Complex with a Bis(imidazolinyl)phenyl Ligand: Studies toward its Synthesis and Asymmetric Friedel–Crafts Alkylation of Indoles with Nitroalkenes
inferred← citeshttps://doi.org/10.1021/om401125qopenalex-snapshot
Metal–Nitroalkene and aci -Nitro Intermediates in Catalytic Enantioselective Friedel–Crafts Reactions of Indoles with trans -β-Nitrostyrenes
inferred← citeshttps://doi.org/10.1021/om500705sopenalex-snapshot
Syntheses of Enantiopure Bifunctional 2-Guanidinobenzimidazole Cyclopentadienyl Ruthenium Complexes: Highly Enantioselective Organometallic Hydrogen Bond Donor Catalysts for Carbon–Carbon Bond Forming Reactions
inferred← citeshttps://doi.org/10.1038/s41598-023-41921-9openalex-snapshot
Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral Yb(OTf)3–pybox complex
inferred← citeshttps://doi.org/10.1038/s42004-023-01041-xopenalex-snapshot
Non-isocyanate polyurethanes synthesized from terpenes using thiourea organocatalysis and thiol-ene-chemistry
inferred← citeshttps://doi.org/10.1039/9781788016490-00066openalex-snapshot
Catalysis by Networks of Cooperative Hydrogen Bonds
inferred← citeshttps://doi.org/10.1039/9781849731140-00001openalex-snapshot
Nucleophilic Additions to Electron-deficient CC Double Bonds
inferred← citeshttps://doi.org/10.1039/9781849732185-00112openalex-snapshot
Enantioselective Conjugate Addition Reactions via Hydrogen-bonding Activation
inferred← citeshttps://doi.org/10.1039/b817310aopenalex-snapshot
Chiral Brønsted acid catalyzed Friedel–Crafts alkylation reactions
inferred← citeshttps://doi.org/10.1039/b904275jopenalex-snapshot
Asymmetric Friedel–Crafts reaction of N-heterocycles and nitroalkenes catalyzed by imidazoline–aminophenol–Cu complex
inferred← citeshttps://doi.org/10.1039/b907399jopenalex-snapshot
Catalytic enantioselective conjugate addition of fluorobis(phenylsulfonyl)methane to enals: synthesis of chiral monofluoromethyl compounds
inferred← citeshttps://doi.org/10.1039/b923063gopenalex-snapshot
Organocatalytic strategies for the asymmetric functionalization of indoles
inferred← citeshttps://doi.org/10.1039/c2cc35582eopenalex-snapshot
Iminium ion catalysis: the enantioselective Friedel–Crafts alkylation–acetalization cascade of naphthols with α,β-unsaturated cyclic ketones
inferred← citeshttps://doi.org/10.1039/c2cc37073eopenalex-snapshot
Internal Lewis acid assisted ureas: tunable hydrogen bond donor catalysts
inferred← citeshttps://doi.org/10.1039/c2ra20544kopenalex-snapshot
Recent advances in asymmetric organocatalytic conjugate addition of arenes and hetero-arenes
inferred← citeshttps://doi.org/10.1039/c2sc20698fopenalex-snapshot
Chiral ionic Brønsted acid–achiral Brønsted base synergistic catalysis for asymmetric sulfa-Michael addition to nitroolefins
inferred← citeshttps://doi.org/10.1039/c3ob41517aopenalex-snapshot
Urea-catalyzed construction of oxazinanes
inferred← citeshttps://doi.org/10.1039/c3ob42350fopenalex-snapshot
Copper-catalyzed annulation of α-substituted diazoacetates with 2-ethynylanilines: the direct synthesis of C2-functionalized indoles
inferred← citeshttps://doi.org/10.1039/c3sc53542hopenalex-snapshot
Stereoselective construction of all-carbon quaternary center by means of chiral phosphoric acid: highly enantioselective Friedel–Crafts reaction of indoles with β,β-disubstituted nitroalkenes
inferred← citeshttps://doi.org/10.1039/c4cc04586fopenalex-snapshot
Enantioselective N-alkylation of isatins and synthesis of chiral N-alkylated indoles
inferred← citeshttps://doi.org/10.1039/c4cy01456aopenalex-snapshot
Synthesis of a chiral fluorescence active probe and its application as an efficient catalyst in the asymmetric Friedel–Crafts alkylation of indole derivatives with nitroalkenes
inferred← citeshttps://doi.org/10.1039/c4ob00348aopenalex-snapshot
A Friedel–Crafts alkylation mechanism using an aminoindanol-derived thiourea catalyst
inferred← citeshttps://doi.org/10.1039/c4ra03805copenalex-snapshot
An easy access to unsymmetrical ureas: a photocatalytic approach to the Lossen rearrangement
inferred← citeshttps://doi.org/10.1039/c6cs00239kopenalex-snapshot
Asymmetric Brønsted acid catalysis with chiral carboxylic acids
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