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Catalytic Asymmetric Friedel–Crafts/Protonation of Nitroalkenes and N-Heteroaromatics
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.200500227openalex-snapshot
Catalytic Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst
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/anie.200804221openalex-snapshot
Enantioselective Enolate Protonations: Friedel–Crafts Reactions with α‐Substituted Acrylates
inferredcites →https://doi.org/10.1002/anie.200901843openalex-snapshot
Catalytic Functionalization of Indoles in a New Dimension
inferredcites →https://doi.org/10.1002/anie.201090157openalex-snapshot
Tandem Catalytic Asymmetric Friedel–Crafts/Henry Reaction: Control of Three Contiguous Acyclic Stereocenters
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.200701439openalex-snapshot
A Library of Chiral Imidazoline–Aminophenol Ligands: Discovery of an Efficient Reaction Sphere
inferredcites →https://doi.org/10.1002/chem.200900033openalex-snapshot
Asymmetric Friedel–Crafts Reaction of 4,7‐Dihydroindoles with Nitroolefins by Chiral Brønsted Acids under Low Catalyst Loading
inferredcites →https://doi.org/10.1002/chem.201001623openalex-snapshot
Organocatalytic Asymmetric Synthesis of trans‐1,3‐Disubstituted Tetrahydroisoquinolines via a Reductive Amination/Aza‐Michael Sequence
inferredcites →https://doi.org/10.1002/chir.20189openalex-snapshot
Catalytic enantioselective addition of indoles to arylnitroalkenes: An effective route to enantiomerically enriched tryptamine precursors
inferredcites →https://doi.org/10.1016/j.tet.2007.03.175openalex-snapshot
Catalytic and asymmetric Friedel–Crafts alkylation of indoles with nitroacrylates. Application to the synthesis of tryptophan analogues
inferredcites →https://doi.org/10.1016/j.tet.2008.04.014openalex-snapshot
Improved preparation of alkyl 2-(3-indolyl)-3-nitroalkanoates under fully heterogeneous conditions: stereoselective synthesis of alkyl (E)-2-(3-indolyl)-2-alkenoates
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/10.1016/s0040-4020(01)86957-xopenalex-snapshot
Asymmetric synthesis of unusual amino acids: Synthesis of optically pure isomers of N-indole- (2-mesitylenesulfonyl)-β-methyltryptophan
inferredcites →https://doi.org/10.1016/s0040-4039(00)95356-5openalex-snapshot
Isolation of a new alkaloid “yohambinine” from rauwolfia serpentina benth.
inferredcites →https://doi.org/10.1016/s0957-4166(01)00442-6openalex-snapshot
A new convenient approach to chiral β-aryl(heteroaryl)alkylamines
inferredcites →https://doi.org/10.1016/s0960-894x(03)00073-8openalex-snapshot
Novel and potent human and rat β3-Adrenergic receptor agonists containing substituted 3-indolylalkylamines
inferredcites →https://doi.org/10.1021/cr078372eopenalex-snapshot
Catalytic Asymmetric Friedel−Crafts Alkylation Reactions—Copper Showed the Way
inferredcites →https://doi.org/10.1021/ja100539copenalex-snapshot
Helical Chiral 2-Aminopyridinium Ions: A New Class of Hydrogen Bond Donor Catalysts
inferredcites →https://doi.org/10.1021/ja711080yopenalex-snapshot
Asymmetric Friedel−Crafts Alkylation of Pyrroles with Nitroalkenes Using a Dinuclear Zinc Catalyst
inferredcites →https://doi.org/10.1021/ja8063292openalex-snapshot
Catalytic Enantioselective Additions of Indoles to Nitroalkenes
inferredcites →https://doi.org/10.1021/ja9066354openalex-snapshot
Tandem Asymmetric Aza-Darzens/Ring-Opening Reactions: Dual Functionality from the Silane Lewis Acid
inferredcites →https://doi.org/10.1021/jm00402a026openalex-snapshot
Synthesis and serotonin receptor affinities of a series of enantiomers of .alpha.-methyltryptamines: evidence for the binding conformation of tryptamines at serotonin 5-HT1B receptors
inferredcites →https://doi.org/10.1021/jo00081a025openalex-snapshot
Preparation of .beta.-substituted tryptophan derivatives: comparison of the reactivity of N-methylindole toward aziridine-2-lactones and aziridine-2-carboxylic esters and interpretation of results using MNDO calculations
inferredcites →https://doi.org/10.1021/jo00094a041openalex-snapshot
Cyclic Tautomers of Tryptophan: Enantio- and Diastereoselective Synthesis of .beta.-Substituted and .alpha.,.beta.-Disubstituted Derivatives of Tryptophan
inferredcites →https://doi.org/10.1021/jo00121a010openalex-snapshot
A Versatile Asymmetric Synthesis of .beta.-Branched .alpha.-Amino Acids
inferredcites →https://doi.org/10.1021/jo048776wopenalex-snapshot
Efficient Preparation of 2-Indolyl-1-nitroalkane Derivatives Employing Nitroalkenes as Versatile Michael Acceptors: New Practical Linear Approach to Alkyl 9H-β-Carboline-4-carboxylate
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/jo1025833openalex-snapshot
Easy Access to Fully Functionalized Chiral Tetrahydro-β-Carboline Alkaloids
inferredcites →https://doi.org/10.1021/jo9013029openalex-snapshot
Chiral Bronsted Acid-Catalyzed Asymmetric Friedel−Crafts Alkylation of Pyrroles with Nitroolefins
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/ol100161nopenalex-snapshot
Ag-Catalyzed Diastereo- and Enantioselective Synthesis of β-Substituted Tryptophans from Sulfonylindoles
inferredcites →https://doi.org/10.1021/ol1001818openalex-snapshot
An Enantioselective Approach to Highly Substituted Tetrahydrocarbazoles through Hydrogen Bonding-Catalyzed Cascade Reactions
inferredcites →https://doi.org/10.1021/ol1025712openalex-snapshot
Chiral Brønsted Base-Promoted Nitroalkane Alkylation: Enantioselective Synthesis of sec-Alkyl-3-Substituted Indoles
inferredcites →https://doi.org/10.1021/ol102580nopenalex-snapshot
Enantioselective Conjugate Addition of Oximes to Trisubstituted β-Nitroacrylates: An Organocatalytic Approach to β2,2-Amino Acid Derivatives
inferredcites →https://doi.org/10.1021/op060210hopenalex-snapshot
N,N-Diethyl-(R)-[3-(2-aminopropyl)-1H-indol-7-yloxy]acetamide: Its Process Chemistry Ranging from Enantiocontrolled Construction of the Chiral Amine Side Chain to Regioselective Functionalization of the Aromatic Starting Materials
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/b817310aopenalex-snapshot
Chiral Brønsted acid catalyzed Friedel–Crafts alkylation reactions
inferredcites →https://doi.org/10.1039/b904275jopenalex-snapshot
Asymmetric Friedel–Crafts reaction of N-heterocycles and nitroalkenes catalyzed by imidazoline–aminophenol–Cu complex
inferredcites →https://doi.org/10.1080/00397910903458025openalex-snapshot
Microwave-Assisted Conjugate Addition of Pyrrole on Electron-Deficient Nitro-Olefins
inferredcites →https://doi.org/10.1080/00397919608004608openalex-snapshot
Conformationally Restricted Analogues of Tryptophan: Synthesis of Chiral 3-Amino-4-indolyl-2-piperidones
inferredcites →https://doi.org/10.1161/01.cir.12.2.220openalex-snapshot
Rauwolfia Serpentina in the Treatment of High Blood Pressure
inferredcites →https://doi.org/10.1248/cpb.53.184openalex-snapshot
Discovery of a Novel and Potent Human and Rat .BETA.3-Adrenergic Receptor Agonist, [3-[(2R)-[[(2R)-(3-Chlorophenyl)-2-hydroxyethyl]amino]propyl]-1H-indol-7-yloxy]acetic Acid
inferredcites →https://doi.org/10.5860/choice.37-0939openalex-snapshot
Comprehensive natural products chemistry
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.4868679openalex-extracted
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/10.1002/9780471264194.fos02343.pub6openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub7openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/adsc.201800709openalex-snapshot
β‐Nitroacrylates: A Versatile and Growing Class of Functionalized Nitroalkenes
inferred← citeshttps://doi.org/10.1002/adsc.202000747openalex-snapshot
Diastereoselective Isomerization of (E)‐β‐Nitroenones into β‐Nitro‐β,γ‐Unsaturated Ketones under Microwave Conditions
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/ajoc.201600288openalex-snapshot
Metal‐Templated Asymmetric Catalysis: ( Z )‐1‐Bromo‐1‐Nitrostyrenes as Versatile Substrates for Friedel–Crafts Alkylation of Indoles
inferred← citeshttps://doi.org/10.1002/ajoc.202100427openalex-snapshot
Recent Advances in Metal‐ and Organocatalyzed Asymmetric Functionalization of Pyrroles
inferred← citeshttps://doi.org/10.1002/ange.201208918openalex-snapshot
Catalytic Asymmetric Synthesis of Mixed 3,3′‐Bisindoles and Their Evaluation as Wnt Signaling Inhibitors
inferred← citeshttps://doi.org/10.1002/ange.201704133openalex-snapshot
Enantioselective Reaction of 2H‐Azirines with Phosphite Using Chiral Bis(imidazoline)/Zinc(II) Catalysts
inferred← citeshttps://doi.org/10.1002/anie.201208918openalex-snapshot
Catalytic Asymmetric Synthesis of Mixed 3,3′‐Bisindoles and Their Evaluation as Wnt Signaling Inhibitors
inferred← citeshttps://doi.org/10.1002/anie.201704133openalex-snapshot
Enantioselective Reaction of 2H‐Azirines with Phosphite Using Chiral Bis(imidazoline)/Zinc(II) Catalysts
inferred← citeshttps://doi.org/10.1002/chem.201304456openalex-snapshot
An Imidazoline–Aminophenol (IAP) Nickel Catalyst: Structure and Catalytic Activity in the Enantioselective 1,4‐Addition of 3′‐Indolyl‐3‐Oxindoles to Nitroethylene
inferred← citeshttps://doi.org/10.1002/chem.201601301openalex-snapshot
Temperature Dual Enantioselective Control in a Rhodium‐Catalyzed Michael‐Type Friedel–Crafts Reaction: A Mechanistic Explanation
inferred← citeshttps://doi.org/10.1002/chin.201148110openalex-snapshot
ChemInform Abstract: Catalytic Asymmetric Friedel—Crafts/Protonation of Nitroalkenes and N‐Heteroaromatics.
inferred← citeshttps://doi.org/10.1002/cjoc.202000486openalex-snapshot
Chiral Imidazoline Ligands and Their Applications in Metal‐Catalyzed Asymmetric Synthesis†
inferred← citeshttps://doi.org/10.1002/ejoc.201101722openalex-snapshot
Asymmetric Benzoylation of meso‐Hydrobenzoin Using a Reusable Tripodal Imidazoline–Pyridine–Cu Catalyst
inferred← citeshttps://doi.org/10.1002/hlca.201500128openalex-snapshot
Phenylalanine‐Derived Imidazolines Bearing Heteroaromatic Pendants: Synthesis, Characterization, and Application in the AsymmetricHenryReaction
inferred← citeshttps://doi.org/10.1002/slct.202505483openalex-snapshot
Reactivity of 1‐Aryl‐3‐Nitro‐ and 1‐Aryl‐3‐Bromo‐3‐Nitropropenones With Semicarbazides and Benzohydrazide: Convenient Synthesis of Monohydrazones of α‐Diketones
inferred← citeshttps://doi.org/10.1002/slct.74752openalex-snapshot
Selective Addition of Active Methylene Compounds to Pull‐Pull Nitroenones
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
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14853-xopenalex-snapshot
Prroles and Their Benzo Derivatives: Reactivity
inferred← citeshttps://doi.org/10.1016/j.abb.2013.10.023openalex-snapshot
A novel indole compound, AWT-489, inhibits prostaglandin D2-induced CD55 expression by acting on DP prostanoid receptors as an antagonist in LS174T human colon cancer cells
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2020.110949openalex-snapshot
PLA/β-CD-based fibres loaded with quercetin as potential antibacterial dressing materials
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.mencom.2019.03.005openalex-snapshot
Friedel–Crafts reaction of electron-rich (het)arenes with nitroalkenes
inferred← citeshttps://doi.org/10.1016/j.tet.2015.03.059openalex-snapshot
Asymmetric Friedel–Crafts alkylation of pyrrole with nitroalkenes catalyzed by a copper complex of a bisphenol A-derived Schiff base
inferred← citeshttps://doi.org/10.1016/j.tet.2026.135136openalex-snapshot
Enantioselective Friedel-Crafts alkylation of indoles with cyclic N-sulfonyl ketimino esters catalyzed by Cu(II) complex bearing binaphthyl-proline-imidazoline-based ligands
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.11.007openalex-snapshot
Highly stereoselective imidazolethiones mediated Friedel–Crafts alkylation of indole derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.06.046openalex-snapshot
Asymmetric Friedel–Crafts alkylation of indoles with 2-nitro-3-arylacrylates catalyzed by a metal-templated hydrogen bonding catalyst
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00749openalex-snapshot
HFIP in Organic Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02669openalex-snapshot
Overcoming the Usual Reactivity of β-Nitroenones: Synthesis of Polyfunctionalized Homoallylic Alcohols and Conjugated Nitrotriene Systems
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03731openalex-snapshot
Organocatalytic Asymmetric Friedel–Crafts Reaction of Prochiral 3,4-Fused Pyrroles via a Desymmetrization/Kinetic Resolution Sequence
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/acsomega.0c03485openalex-snapshot
Catalytic Enantioselective Alkylation of Indoles with trans -4-Methylthio-β-Nitrostyrene
inferred← citeshttps://doi.org/10.1021/acsomega.9b04115openalex-snapshot
Lewis Acid-Catalyzed Enantioselective Friedel–Crafts Alkylation of Pyrrole in Water
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/jo300539yopenalex-snapshot
Asymmetric Allylic Alkylation of Pyrroles and 4,7-Dihydroindoles with Alkene–Phosphine Ligands
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Direct Olefination at the C-4 Position of Tryptophan via C–H Activation: Application to Biomimetic Synthesis of Clavicipitic Acid
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
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Metal–Nitroalkene and aci -Nitro Intermediates in Catalytic Enantioselective Friedel–Crafts Reactions of Indoles with trans -β-Nitrostyrenes
inferred← citeshttps://doi.org/10.1039/9781782621966-00214openalex-snapshot
Asymmetric Friedel–Crafts Alkylation Reactions
inferred← citeshttps://doi.org/10.1039/c2ob07192dopenalex-snapshot
Organocatalytic enantioselective Michael addition of a kojic acid derivative to nitro olefins
inferred← citeshttps://doi.org/10.1039/c4cs00209aopenalex-snapshot
Strategies for the asymmetric functionalization of indoles: an update
inferred← citeshttps://doi.org/10.1039/c4sc00265bopenalex-snapshot
MOF catalysis in relation to their homogeneous counterparts and conventional solid catalysts
inferred← citeshttps://doi.org/10.1039/c6qo00273kopenalex-snapshot
Enantioselective β-alkylation of pyrroles with the formation of an all-carbon quaternary stereocenter
inferred← citeshttps://doi.org/10.1039/c7ob00413copenalex-snapshot
Recent progress in transition-metal-catalyzed enantioselective indole functionalizations
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Progress in recent development of stereoselective synthesis of β 2 -amino acid derivatives from β-nitroacrylate derivatives
inferred← citeshttps://doi.org/10.1039/d0ob00956copenalex-snapshot
Synthesis and practical applications of 2-(2-nitroalkyl)pyrroles
inferred← citeshttps://doi.org/10.1039/d4cc03601hopenalex-snapshot
Synthesis of chiral systems featuring the pyrrole unit: a review
inferred← citeshttps://doi.org/10.1107/s2056989023004644openalex-snapshot
Structure of (R,R)-4-bromo-2-{4-[4-bromo-1-(4-toluenesulfonyl)-1H-pyrrol-2-yl]-1,3-dinitrobutan-2-yl}-1-(4-toluenesulfonyl)-1H-pyrrole, another ostensible by-product in the synthesis of geminal-dimethyl hydrodipyrrins
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Catalytic Asymmetric [3+2]-Cycloaddition Reaction for Controlling Multiple Sterogenic Centers on Pyrrolidines
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Chiral Bis(imidazolidine)-containing NCN Pincer Metal Complexes for Cooperative Asymmetric Catalysis
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