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Asymmetric Friedel−Crafts Alkylations of Indoles with Nitroalkenes Catalyzed by Zn(II)−Bisoxazoline Complexes

https://doi.org/10.1021/jo0516537
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What this work says

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

inferredcites →https://doi.org/10.1002/0471224480openalex-snapshot
The Nitro Group in Organic Synthesis
inferredcites →https://doi.org/10.1002/1099-0690(200206)2002:12<1877::aid-ejoc1877>3.0.co;2-uopenalex-snapshot
Asymmetric Michael Additions to Nitroalkenes
inferredcites →https://doi.org/10.1002/1521-3773(20010105)40:1<160::aid-anie160>3.0.co;2-sopenalex-snapshot
Catalytic Asymmetric Friedel-Crafts Alkylation of beta,gamma-Unsaturated alpha-Ketoesters: Enantioselective Addition of Aromatic C-H Bonds to Alkenes This work was made possible by a grant from the Danish National Research Foundation.
inferredcites →https://doi.org/10.1002/1521-3773(20020703)41:13<2348::aid-anie2348>3.0.co;2-kopenalex-snapshot
Monodentate Chiral Spiro Phosphoramidites: Efficient Ligands for Rhodium-Catalyzed Enantioselective Hydrogenation of Enamides
inferredcites →https://doi.org/10.1002/anie.199507981openalex-snapshot
C2‐Symmetric Cationic Copper( II ) Complexes as Chiral Lewis Acids: Counterion Effects in the Enantioselective Diels–Alder Reaction
inferredcites →https://doi.org/10.1002/anie.200301679openalex-snapshot
New Catalytic Approaches in the Stereoselective Friedel–Crafts Alkylation Reaction
inferredcites →https://doi.org/10.1002/anie.200301692openalex-snapshot
Synthetic Routes towards Enantiomerically Pure β‐Amino Acids
inferredcites →https://doi.org/10.1002/anie.200352175openalex-snapshot
Catalytic Enantioselective Conjugate Reduction of β,β‐Disubstituted Nitroalkenes
inferredcites →https://doi.org/10.1002/hlca.19850680611openalex-snapshot
Asymmetrische Michael‐Additionen. Stereoselektive Alkylierung chiraler, nicht racemischer Enolate durch Nitroolefine. Herstellung enantiomerenreiner γ‐Aminobuttersäure‐ und Bernsteinsäure‐Derivate
inferredcites →https://doi.org/10.1002/hlca.200390317openalex-snapshot
Designing New α,β‐Unsaturated Thioesters for the Catalytic, Enantioselective FriedelCrafts Alkylation of Indoles
inferredcites →https://doi.org/10.1016/0040-4020(94)01100-eopenalex-snapshot
Enantioselective conjugate addition of primary dialkylzinc reagents to 2-aryl- and 2-heteroaryl-nitroolefins mediated by titanium-TADDOLates preparation of enantioenriched 2-aryl-alkylamines
inferredcites →https://doi.org/10.1016/j.tetlet.2003.08.106openalex-snapshot
A new methodology of intramolecular hetero Diels–Alder reaction with β-alkoxy-substituted conjugated nitroalkenes as heterodienes: stereoselective one-pot synthesis of trans-fused bicyclic γ-lactones
inferredcites →https://doi.org/10.1016/s0040-4039(03)01089-xopenalex-snapshot
Conjugate addition of indoles and thiols with electron-deficient olefins catalyzed by Bi(OTf)3
inferredcites →https://doi.org/10.1021/ar960062nopenalex-snapshot
Chiral Bis(oxazoline) Copper(II) Complexes: Versatile Catalysts for Enantioselective Cycloaddition, Aldol, Michael, and Carbonyl Ene Reactions
inferredcites →https://doi.org/10.1021/ja002805copenalex-snapshot
Rhodium-Catalyzed Asymmetric Conjugate Addition of Organoboronic Acids to Nitroalkenes
inferredcites →https://doi.org/10.1021/ja026936kopenalex-snapshot
Sidearm Effect: Improvement of the Enantiomeric Excess in the Asymmetric Michael Addition of Indoles to Alkylidene Malonates
inferredcites →https://doi.org/10.1021/ja029817dopenalex-snapshot
Highly Enantioselective Conjugate Addition of Dialkylzinc Reagents to Acyclic Nitroalkenes: A Catalytic Route to β2-Amino Acids, Aldehydes, and Alcohols
inferredcites →https://doi.org/10.1021/ja036972zopenalex-snapshot
Enantioselective Michael Reaction of Malonates to Nitroolefins Catalyzed by Bifunctional Organocatalysts
inferredcites →https://doi.org/10.1021/ja036985copenalex-snapshot
Enantioselective Indole Friedel−Crafts Alkylations Catalyzed by Bis(oxazolinyl)pyridine−Scandium(III) Triflate Complexes
inferredcites →https://doi.org/10.1021/ja0423217openalex-snapshot
Highly Enantioselective Friedel−Crafts Alkylations of Pyrroles and Indoles with α‘-Hydroxy Enones under Cu(II)-Simple Bis(oxazoline) Catalysis
inferredcites →https://doi.org/10.1021/ja046296gopenalex-snapshot
Catalytic Enantioselective Michael Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes Catalyzed by Well-Defined Chiral Ru Amido Complexes
inferredcites →https://doi.org/10.1021/ja047281lopenalex-snapshot
Highly Enantioselective Conjugate Addition of Malonate and β-Ketoester to Nitroalkenes: Asymmetric C−C Bond Formation with New Bifunctional Organic Catalysts Based on Cinchona Alkaloids
inferredcites →https://doi.org/10.1021/ja052433dopenalex-snapshot
Enantioselective Friedel−Crafts Alkylations of α,β-Unsaturated 2-Acyl Imidazoles Catalyzed by Bis(oxazolinyl)pyridine−Scandium(III) Triflate Complexes
inferredcites →https://doi.org/10.1021/ja992314wopenalex-snapshot
Catalytic Enantioselective Conjugate Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes
inferredcites →https://doi.org/10.1021/jo0353177openalex-snapshot
Lewis Acid Catalysis in Supercritical Carbon Dioxide. Use of Poly(ethylene glycol) Derivatives and Perfluoroalkylbenzenes as Surfactant Molecules Which Enable Efficient Catalysis in ScCO 2
inferredcites →https://doi.org/10.1021/jo035552popenalex-snapshot
Controllable Enantioselective Friedel−Crafts Reaction1 between Indoles and Alkylidene Malonates Catalyzed by Pseudo-C3-Symmetric Trisoxazoline Copper(II) Complexes
inferredcites →https://doi.org/10.1021/jo0487202openalex-snapshot
Can Simple Enones Be Useful Partners for the Catalytic Stereoselective Alkylation of Indoles?
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/ol0059596openalex-snapshot
Enantioselective Copper-Catalyzed Conjugate Addition of Dialkyl Zinc to Nitro-Olefins
inferredcites →https://doi.org/10.1021/ol0488338openalex-snapshot
Efficient Cu-Catalyzed Asymmetric Conjugate Additions of Alkylzinc Reagents to Aromatic and Aliphatic Acyclic Nitroalkenes
inferredcites →https://doi.org/10.1021/ol0491282openalex-snapshot
Highly Enantioselective Copper-Catalyzed Conjugate Addition of Diethylzinc to Nitroalkenes
inferredcites →https://doi.org/10.1039/b009008popenalex-snapshot
Catalytic enantioselective alkylation of heteroaromatic compounds using alkylidene malonates
inferredcites →https://doi.org/10.1039/b313197aopenalex-snapshot
Enantioselective Friedel–Crafts reaction of indoles with arylidene malonates catalyzed by i Pr-bisoxazoline–Cu(OTf) 2
inferredcites →https://doi.org/10.1039/b412653jopenalex-snapshot
The facile and efficient Michael addition of indoles and pyrrole to α,β-unsaturated electron-deficient compounds catalyzed by aluminium dodecyl sulfate trihydrate [Al(DS) 3 ]·3H 2 O in water
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/10.1055/s-2001-18068openalex-snapshot
InCl3-Catalysed Conjugate Addition of Indoles with Electron-Deficient Olefins
inferredcites →https://doi.org/10.1055/s-2002-31970openalex-snapshot
A Practical Indium Tribromide Catalysed Addition of Indoles to Nitroalkenes in Aqueous Media

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)
inferred← citeshttps://doi.org/10.1002/9780470066911.ch8openalex-snapshot
Electrophilic Aromatic Substitution
inferred← citeshttps://doi.org/10.1002/9780470669587.ch6openalex-snapshot
Electrophilic Aromatic Substitution
inferred← citeshttps://doi.org/10.1002/9783527626977.ch2openalex-snapshot
Michael Addition
inferred← citeshttps://doi.org/10.1002/9783527626977.ch6openalex-snapshot
Unactivated Alkenes
inferred← citeshttps://doi.org/10.1002/9783527675944.ch4openalex-snapshot
Zinc‐Catalyzed Friedel–Crafts Reactions
inferred← citeshttps://doi.org/10.1002/9783527675944.ch6openalex-snapshot
Zinc‐Catalyzed CC Bond Formation
inferred← citeshttps://doi.org/10.1002/9783527802142.ch5openalex-snapshot
Zinc‐based Chiral Lewis Acids
inferred← citeshttps://doi.org/10.1002/9783527839278.ch6openalex-snapshot
Chiral MOFs for Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.200600495openalex-snapshot
Asymmetric Friedel–Crafts Alkylations of Indoles with Ethyl Glyoxylate Catalyzed by (S)‐BINOL‐Titanium(IV) Complex: Direct Access to Enantiomerically Enriched 3‐Indolyl(hydroxy)acetates
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An Efficient Enantioselective Method for Asymmetric Friedel–Crafts Alkylation of Indoles with α,β‐Unsaturated Aldehydes
inferred← citeshttps://doi.org/10.1002/adsc.200900357openalex-snapshot
Synthesis of Functionalized Indoles with an α‐Stereogenic Ketone Moiety Through an Enantioselective Friedel–Crafts Alkylation with (E)‐1,4‐Diaryl‐2‐butene‐1,4‐diones
inferred← citeshttps://doi.org/10.1002/adsc.200900669openalex-snapshot
Highly Enantioselective Friedel–Crafts Reaction of Indole with Alkylidenemalonates Catalyzed by Heteroarylidene Malonate‐Derived Bis(oxazoline) Copper(II) Complexes
inferred← citeshttps://doi.org/10.1002/adsc.201000111openalex-snapshot
Development of Diphenylamine‐Linked Bis(imidazoline) Ligands and Their Application in Asymmetric Friedel–Crafts Alkylation of Indole Derivatives with Nitroalkenes
inferred← citeshttps://doi.org/10.1002/adsc.201200547openalex-snapshot
Zinc‐Catalyzed Organic Synthesis: CC, CN, CO Bond Formation Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201300439openalex-snapshot
Synthesis and Structures of Air‐Stable Binuclear Hafnocene Perfluorobutanesulfonate and Perfluorobenzenesulfonate and their Catalytic Application in CC Bond‐Forming Reactions
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.201800067openalex-snapshot
Asymmetric Brominative Dearomatization of Naphthols Catalyzed by Chiral Copper Complexes
inferred← citeshttps://doi.org/10.1002/ange.200701067openalex-snapshot
Chiral Brønsted Acid Catalyzed Enantioselective Friedel–Crafts Reaction of Indoles and α‐Aryl Enamides: Construction of Quaternary Carbon Atoms
inferred← citeshttps://doi.org/10.1002/ange.200703668openalex-snapshot
Asymmetrische Brønsted‐Säure‐Katalyse: enantioselektive nucleophile Substitutionen und 1,4‐Additionen
inferred← citeshttps://doi.org/10.1002/ange.200800770openalex-snapshot
Chiral Phosphoric Acid Catalyzed Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes: Cooperative Effect of 3 Å Molecular Sieves
inferred← citeshttps://doi.org/10.1002/ange.200801373openalex-snapshot
Tandem Catalytic Asymmetric Friedel–Crafts/Henry Reaction: Control of Three Contiguous Acyclic Stereocenters
inferred← citeshttps://doi.org/10.1002/ange.200901843openalex-snapshot
Katalytische Funktionalisierung von Indolen in einer neuen Dimension
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.201101254openalex-snapshot
Asymmetric Binary Acid Catalysis: A Regioselectivity Switch between Enantioselective 1,2‐ and 1,4‐Addition through Different Counteranions of InIII
inferred← citeshttps://doi.org/10.1002/ange.202501566openalex-snapshot
Synthesis of NIR‐II Fluorophores by a C(sp 2 )−C(sp 2 /sp) Coupling Reaction Driven by Charge‐Transfer Interaction
inferred← citeshttps://doi.org/10.1002/anie.200701067openalex-snapshot
Chiral Brønsted Acid Catalyzed Enantioselective Friedel–Crafts Reaction of Indoles and α‐Aryl Enamides: Construction of Quaternary Carbon Atoms
inferred← citeshttps://doi.org/10.1002/anie.200703668openalex-snapshot
Asymmetric Brønsted Acid Catalysis: Enantioselective Nucleophilic Substitutions and 1,4‐Additions
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/anie.200801373openalex-snapshot
Tandem Catalytic Asymmetric Friedel–Crafts/Henry Reaction: Control of Three Contiguous Acyclic Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.200901843openalex-snapshot
Catalytic Functionalization of Indoles in a New Dimension
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.201101254openalex-snapshot
Asymmetric Binary Acid Catalysis: A Regioselectivity Switch between Enantioselective 1,2‐ and 1,4‐Addition through Different Counteranions of InIII
inferred← citeshttps://doi.org/10.1002/anie.202501566openalex-snapshot
Synthesis of NIR‐II Fluorophores by a C(sp 2 )−C(sp 2 /sp) Coupling Reaction Driven by Charge‐Transfer Interaction
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/asia.201000596openalex-snapshot
DFT Study of Chiral‐Phosphoric‐Acid‐Catalyzed Enantioselective Friedel–Crafts Reaction of Indole with Nitroalkene: Bifunctionality and Substituent Effect of Phosphoric Acid
inferred← citeshttps://doi.org/10.1002/asia.201901647openalex-snapshot
KOtBu‐Catalyzed Michael Addition Reactions Under Mild and Solvent‐Free Conditions
inferred← citeshttps://doi.org/10.1002/cctc.201402309openalex-snapshot
Selective N‐Alkylation of Indoles with α,β‐Unsaturated Compounds Catalyzed by a Monomeric Phosphate
inferred← citeshttps://doi.org/10.1002/cctc.201601583openalex-snapshot
Friedel–Crafts Alkylation of Indoles with Nitroalkenes through Hydrogen‐Bond‐Donating Metal–Organic Framework
inferred← citeshttps://doi.org/10.1002/cctc.201800369openalex-snapshot
2D‐2D Nanocomposite of MoS2‐Graphitic Carbon Nitride as Multifunctional Catalyst for Sustainable Synthesis of C3‐Functionalized Indoles
inferred← citeshttps://doi.org/10.1002/cctc.71070openalex-snapshot
Dual Functional Urea Tethered Al(III) MOF as a Robust Heterogeneous Platform for Hydrogen Bond Assisted Friedel‐Crafts Alkylation and Cu(II)‐Mediated Chan–Lam Coupling
inferred← citeshttps://doi.org/10.1002/chem.200700676openalex-snapshot
Superelectrophilicity of the Nitroolefinic Fragment of 4‐Nitrobenzodifuroxan in Michael‐Type Reactions with Indoles: A Kinetic Study in Acetonitrile
inferred← citeshttps://doi.org/10.1002/chem.200701439openalex-snapshot
A Library of Chiral Imidazoline–Aminophenol Ligands: Discovery of an Efficient Reaction Sphere
inferred← citeshttps://doi.org/10.1002/chem.200701908openalex-snapshot
Asymmetric Friedel–Crafts Alkylation of Indoles with Methyl (E)‐2‐Oxo‐4‐aryl‐3‐butenoates Catalyzed by Sc(OTf)3/pybox
inferred← citeshttps://doi.org/10.1002/chem.200802210openalex-snapshot
Enantioselective Friedel–Crafts Alkylation of Indoles with Alkylidene Malonates Catalyzed by N,N′‐Dioxide–Scandium(III) Complexes: Asymmetric Synthesis of β‐Carbolines
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/chem.200902705openalex-snapshot
Chiral Brønsted Acid Directed Iron‐Catalyzed Enantioselective Friedel–Crafts Alkylation of Indoles with β‐Aryl α′‐Hydroxy Enones
inferred← citeshttps://doi.org/10.1002/chem.201000540openalex-snapshot
Monodentate N‐Ligand‐Directed Bifunctional Transition‐Metal Catalysis: Highly Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes
inferred← citeshttps://doi.org/10.1002/chem.201000568openalex-snapshot
Synthesis of Functionalized Indoles with a Trifluoromethyl‐Substituted Stereogenic Tertiary Carbon Atom Through an Enantioselective Friedel–Crafts Alkylation with β‐Trifluoromethyl‐α,β‐enones
inferred← citeshttps://doi.org/10.1002/chem.201404354openalex-snapshot
Highly Enantioselective Ring‐Opening Reactions of Aziridines with Indole and Its Application in the Building of C3‐Halogenated Pyrroloindolines
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/chem.202202441openalex-snapshot
Highly Active La(III)‐Based Metal‐Organic Framework as a Heterogeneous Lewis Acid Catalyst for Friedel‐Crafts Alkylation
inferred← citeshttps://doi.org/10.1002/chin.200622120openalex-snapshot
Asymmetric Friedel—Crafts Alkylations of Indoles with Nitroalkenes Catalyzed by Zn(II)—Bisoxazoline Complexes.
inferred← citeshttps://doi.org/10.1002/cjoc.200790190openalex-snapshot
An Efficient Synthetic Method to Nonnatural α‐ and β‐Tryptophan Analogues via Friedel‐Crafts Alkylation of Indoles with Nitroacrylates
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Conjugate Addition of Indoles to α,β‐Unsaturated Ketones (Chalcones) Catalyzed by KHSO4 under Ultrasonic Conditions
inferred← citeshttps://doi.org/10.1002/cjoc.200990373openalex-snapshot
Fluorapatite: An Effective Solid Base Catalyst for Michael Addition of Indole/pyrrole to Nitroalkenes under Solventless Condition
inferred← citeshttps://doi.org/10.1002/cjoc.201090094openalex-snapshot
Ionic Liquid‐coordinated Ytterbium(III) Sulfonate Catalyzed Michael Addition of Indoles to Electron‐deficient Nitroolefins
inferred← citeshttps://doi.org/10.1002/cjoc.201090243openalex-snapshot
Synthesis of Tridentate Ligands Based on Chiral Diamines and Their Application to Enantioselective Friedel‐Crafts Alkylation of Indoles with Nitroalkenes
inferred← citeshttps://doi.org/10.1002/cjoc.201180480openalex-snapshot
Friedel‐Crafts Alkylation of Indoles with Nitroalkenes Catalyzed by Zn(II)‐Thiourea Complex
inferred← citeshttps://doi.org/10.1002/ejoc.200600646openalex-snapshot
Enantioselective Michael‐Type Friedel–Crafts Reactions of Indoles to Enones Catalyzed by a Chiral Camphor‐Based Brønsted Acid
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New Thiazoline–Oxazoline Ligands and Their Application in the Asymmetric Friedel–Crafts Reaction
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Immobilization of Diphenylamine‐Linked Bis(oxazoline) Ligands and Their Application in the Asymmetric Friedel–Crafts Alkylation of Indole Derivatives with Nitroalkenes
inferred← citeshttps://doi.org/10.1002/ejoc.201100506openalex-snapshot
Enhanced Efficiency of Thiourea Catalysts by External Brønsted Acids in the Friedel–Crafts Alkylation of Indoles
inferred← citeshttps://doi.org/10.1002/ejoc.201100683openalex-snapshot
The Asymmetric Friedel–Crafts Reaction of Indoles with Fluoroalkylated Nitroalkenes Catalyzed by Chiral Phosphoric Acid
inferred← citeshttps://doi.org/10.1002/ejoc.201101335openalex-snapshot
Synthesis of Thiazoline–Oxazoline Ligands and Their Application in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/ejoc.201101648openalex-snapshot
Rhodium‐Catalyzed Asymmetric Addition of Arylboronic Acids to Indolylnitroalkenes
inferred← citeshttps://doi.org/10.1002/ejoc.201200382openalex-snapshot
Asymmetric Friedel–Crafts Alkylation of Indoles with Nitrodienes and 2‐Propargyloxy‐β‐nitrostyrenes Catalyzed by Diphenylamine‐Linked Bis(oxazoline)–Zn(OTf)2 Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.201201288openalex-snapshot
Conjugate Addition of Indoles and Pyrroles to Dihydronitronaphthalenes in Water: Synthesis of 3,4‐Fused Tetrahydro‐β‐carbolines
inferred← citeshttps://doi.org/10.1002/ejoc.201201636openalex-snapshot
Enantioselective Friedel–Crafts Alkylation of Indoles with (E)‐1‐Aryl‐4‐benzyloxybut‐2‐en‐1‐ones Catalyzed by an (R)‐3,3′‐Br2BINOLate–Hafnium(IV) Complex
inferred← citeshttps://doi.org/10.1002/ejoc.201901007openalex-snapshot
A Tandem Asymmetric Friedel–Crafts Alkylation/Michael Addition: Synthesis of Novel Ergoline Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202501247openalex-snapshot
Design and Synthesis of Lactose‐Derived Ligands and Their Application in Asymmetric Friedel–Crafts Alkylation
inferred← citeshttps://doi.org/10.1002/jccs.201900191openalex-snapshot
Development of dipyridine‐based coordinative polymers for reusable heterogeneous catalysts
inferred← citeshttps://doi.org/10.1002/jhet.2861openalex-snapshot
Microwave‐accelerated Conjugate Addition of 2‐Arylindoles to Substituted β‐Nitrostyrenes in the Presence of Ammonium Trifluoroacetate: An Efficient Approach for the Synthesis of a Novel Class of CB1 Cannabinoid Receptor Allosteric Modulators
inferred← citeshttps://doi.org/10.1002/jhet.569openalex-snapshot
An efficient and clean Michael addition of indoles to electron‐deficient olefins under solvent‐ and catalyst‐free condition
inferred← citeshttps://doi.org/10.1002/poc.1469openalex-snapshot
A theoretical and experimental study of the polar Diels–Alder cycloaddition of cyclopentadiene with nitrobenzodifuroxan
inferred← citeshttps://doi.org/10.1002/slct.202504368openalex-snapshot
Pd(II)‐Catalyzed Decarboxylation‐Alkylation of 3‐Formylindoles with Nitroalkenes to Access 3‐(2‐Nitroalkyl)indoles
inferred← citeshttps://doi.org/10.1007/3418_2015_114openalex-snapshot
New Chemistry with Anionic NNN Pincer Ligands
inferred← citeshttps://doi.org/10.1007/7081_2007_073openalex-snapshot
Functionalization of Indole and Pyrrole Cores via Michael-Type Additions
inferred← citeshttps://doi.org/10.1007/7081_2010_52openalex-snapshot
Electrophilic Substitution Reactions of Indoles
inferred← citeshttps://doi.org/10.1007/978-94-007-1454-0_2openalex-snapshot
“Green” Asymmetric Synthesis: The Catalysts
inferred← citeshttps://doi.org/10.1007/s00706-014-1347-xopenalex-snapshot
Graphite as an effective catalyst for Michael addition of indoles to nitroolefins in aqueous alcoholic solution
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/10.1007/s10593-014-1514-3openalex-snapshot
Arenes and Hetarenes in Reactions with unsaturated Nitro Compounds (Review)
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Efficient iron-catalyzed Michael addition of indole to nitroolefins under solvent-free conditions
inferred← citeshttps://doi.org/10.1007/s11426-009-0179-8openalex-snapshot
Modification of diphenylamine-linked bis(oxazoline) ligands: Tuning of electronic effect and rigidity of ligand skeleton
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00311-6openalex-snapshot
3.11 Alkaloid Derived Auxiliaries: Miscellaneous Alkaloids
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00406-7openalex-snapshot
4.04 Metal-Catalyzed Asymmetric Nucleophilic Addition to Electron-Deficient Alkenes
inferred← citeshttps://doi.org/10.1016/j.apcata.2011.03.010openalex-snapshot
Immobilization of 1,5,7-triazabicyclo [4.4.0] dec-5-ene over mesoporous materials: An efficient catalyst for Michael-addition reactions under solvent-free condition
inferred← citeshttps://doi.org/10.1016/j.catcom.2014.04.013openalex-snapshot
Synthesis of chiral benzene-based tetraoxazolines and their application in asymmetric Friedel–Crafts alkylation of indole derivatives with nitroalkenes
inferred← citeshttps://doi.org/10.1016/j.catcom.2017.06.018openalex-snapshot
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.ccr.2021.213926openalex-snapshot
Recent developments in enantioselective zinc-catalyzed transformations
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.09.014openalex-snapshot
Synthesis and biological evaluation of new piplartine analogues as potent aldose reductase inhibitors (ARIs)
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.jcat.2020.03.034openalex-snapshot
New 1D chiral Zr-MOFs based on in situ imine linker formation as catalysts for asymmetric C C coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jcis.2017.01.091openalex-snapshot
Cu3(BTC)2 as a viable heterogeneous solid catalyst for Friedel-Crafts alkylation of indoles with nitroalkenes
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2009.01.004openalex-snapshot
A novel pyrrolidinium ionic liquid with 1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoroethoxy)ethanesulfonate anion as a recyclable reaction medium and efficient catalyst for Friedel–Crafts alkylations of indoles with nitroalkenes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.04.039openalex-snapshot
Synthesis, structural characterization of benzimidazole-functionalized Ni(II) and Hg(II) N-heterocyclic carbene complexes and their applications as efficient catalysts for Friedel–Crafts alkylations
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.mcat.2021.112007openalex-snapshot
Friedel-Crafts alkylation reaction efficiently catalyzed by a di-amide functionalized Zr(IV) metal-organic framework
inferred← citeshttps://doi.org/10.1016/j.poly.2018.12.023openalex-snapshot
Synthesis, crystal structure and investigation of the catalytic and spectroscopic properties of a Zn(II) complex with coumarin-hydrazone ligand
inferred← citeshttps://doi.org/10.1016/j.tet.2007.02.091openalex-snapshot
Catalytic conjugate addition of heterocyclic compounds to α,β-unsaturated carbonyl compounds by hafnium salts and scandium salts
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.tet.2008.09.023openalex-snapshot
Cu(OTf)2/trisoxazoline catalyzed asymmetric Friedel–Crafts reaction of pyrroles with alkylidene malonates
inferred← citeshttps://doi.org/10.1016/j.tet.2008.11.083openalex-snapshot
Synthesis of 9,9′-biphenanthryl-10,10′-bis(oxazoline)s and their preliminary evaluations in the Friedel–Crafts alkylations of indoles with nitroalkenes
inferred← citeshttps://doi.org/10.1016/j.tet.2009.06.071openalex-snapshot
Trisoxazoline/Cu(II)-catalyzed asymmetric intramolecular Friedel–Crafts alkylation reaction of indoles
inferred← citeshttps://doi.org/10.1016/j.tet.2009.07.053openalex-snapshot
Synthesis of highly modular bis(oxazoline) ligands by Suzuki cross-coupling and evaluation as catalytic ligands
inferred← citeshttps://doi.org/10.1016/j.tet.2010.02.054openalex-snapshot
Asymmetric Friedel–Crafts alkylation of activated benzenes with methyl (E)-2-oxo-4-aryl-3-butenoates catalyzed by [Pybox/Sc(OTf)3]
inferred← citeshttps://doi.org/10.1016/j.tet.2011.07.041openalex-snapshot
Tris(pentafluorophenyl)borane [B(C6F5)3]-catalyzed Friedel–Crafts reactions of activated arenes and heteroarenes with α-amidosulfones: the synthesis of unsymmetrical triarylmethanes
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.2014.12.022openalex-snapshot
Chiral zinc catalysts for asymmetric synthesis
inferred← citeshttps://doi.org/10.1016/j.tet.2015.05.013openalex-snapshot
Strong Lewis acids of air-stable binuclear triphenylantimony(V) complexes and their catalytic application in C–C bond-forming reactions
inferred← citeshttps://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
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.2013.11.018openalex-snapshot
Highly enantioselective Friedel–Crafts alkylation of indole with electron deficient trans-β-nitroalkenes using Zn(II)–oxazoline–imidazoline catalysts
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.2015.01.004openalex-snapshot
Highly enantioselective catalytic Friedel–Crafts reactions of cyclic α-alkylidene β-oxo imides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.03.110openalex-snapshot
Highly regioselective Friedel–Crafts alkylation of indoles with α,β-unsaturated N-acylbenzotriazoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.07.112openalex-snapshot
Novel axially chiral bis-arylthiourea-based organocatalysts for asymmetric Friedel–Crafts type reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.10.038openalex-snapshot
FeCl3-catalyzed propargylation of aromatic compounds with propargylic acetates
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.04.011openalex-snapshot
Sulfamic acid-catalyzed Michael addition of indoles and pyrrole to electron-deficient nitroolefins under solvent-free condition
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.07.090openalex-snapshot
Catalytic enantioselective Friedel–Crafts alkylation at the 2-position of indole with simple enones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.09.109openalex-snapshot
Catalyst-free aqueous-mediated conjugative addition of indoles to β-nitrostyrenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.12.093openalex-snapshot
Convenient synthesis of bis(indolyl)alkanes and bis(pyrrolyl)alkanes by Cu(OTf)2-catalyzed addition of indole and pyrrole to acetylenic sulfone
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.12.055openalex-snapshot
Triarylaminium salt facilitated Friedel–Crafts reaction of indoles with enamides and vinyl ethers
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.05.064openalex-snapshot
A highly efficient route to C-3 alkyl-substituted indoles via a metal-free transfer hydrogenation
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/10.1021/acs.inorgchem.9b00665openalex-snapshot
Competing Allosteric Mechanisms for Coordination-Directed Conformational Changes of Chiral Stacking Structures with Aromatic Rings
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01767openalex-snapshot
Synthesis of Bis(oxazoline) Ligands Possessing C-5 gem -Disubstitution and Their Application in Asymmetric Friedel–Crafts Alkylations
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00387openalex-snapshot
Mechanism and Origins of Stereoinduction in an Asymmetric Friedel–Crafts Alkylation Reaction of Chalcone Catalyzed by Chiral N,N′-Dioxide–Sc(III) Complex
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00612openalex-snapshot
Enantioselective Synthesis of 2-Amino-1,1-diarylalkanes Bearing a Carbocyclic Ring Substituted Indole through Asymmetric Catalytic Reaction of Hydroxyindoles with Nitroalkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01406openalex-snapshot
Reactions of 3,3,3-Trihalogeno-1-nitropropenes with Arenes in the Superacid CF3SO3H: Synthesis of (Z)-3,3,3-Trihalogeno-1,2-diarylpropan-1-one Oximes and Study on the Reaction Mechanism
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c04106openalex-snapshot
1,3-Difunctionalization of β-Alkyl Nitroalkenes via Combination of Lewis Base Catalysis and Radical Oxidation
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.9b00747openalex-snapshot
Sodium-Catalyzed Friedel–Crafts Reactions and Mechanistic Insight
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.0c03485openalex-snapshot
Catalytic Enantioselective Alkylation of Indoles with trans -4-Methylthio-β-Nitrostyrene
inferred← citeshttps://doi.org/10.1021/acssuschemeng.3c06108openalex-snapshot
Urea-Tethered Porous Organic Polymer (POP) as an Efficient Heterogeneous Catalyst for Hydrogen Bond Donating Organocatalysis and Continuous Flow Reaction
inferred← citeshttps://doi.org/10.1021/ar5002457openalex-snapshot
Anionic Chiral Tridentate N-Donor Pincer Ligands in Asymmetric Catalysis
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/cr800400zopenalex-snapshot
Recent Applications of Oxazoline-Containing Ligands in Asymmetric Catalysis
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/ja511403topenalex-snapshot
Turning On Catalysis: Incorporation of a Hydrogen-Bond-Donating Squaramide Moiety into a Zr Metal–Organic Framework
inferred← citeshttps://doi.org/10.1021/ja8063292openalex-snapshot
Catalytic Enantioselective Additions of Indoles to Nitroalkenes
inferred← citeshttps://doi.org/10.1021/jo1010137openalex-snapshot
Friedel−Crafts Arylation Reactions of N-Sulfonyl Aldimines or Sulfonamidesulfones with Electron-Rich Arenes Catalyzed by FeCl3·6H2O: Synthesis of Triarylmethanes and Bis-heteroarylarylmethanes
inferred← citeshttps://doi.org/10.1021/jo200546aopenalex-snapshot
Catalytic Asymmetric Friedel–Crafts/Protonation of Nitroalkenes and N-Heteroaromatics
inferred← citeshttps://doi.org/10.1021/jo200733topenalex-snapshot
Asymmetric Synthesis of β2-Tryptophan Analogues via Friedel–Crafts Alkylation of Indoles with a Chiral Nitroacrylate
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/jo801721zopenalex-snapshot
Second-Generation DBFOX Ligands for the Synthesis of β-Substituted α-Amino Acids via Enantioselective Radical Conjugate Additions
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/jo9014613openalex-snapshot
InBr3: A Versatile Catalyst for the Different Types of Friedel−Crafts Reactions
inferred← citeshttps://doi.org/10.1021/ol0602001openalex-snapshot
Asymmetric Friedel−Crafts Addition of Indoles to N -Sulfonyl Aldimines: A Simple Approach to Optically Active 3-Indolyl-methanamine Derivatives
inferred← citeshttps://doi.org/10.1021/ol060586fopenalex-snapshot
Enantioselective Friedel−Crafts Alkylation of Indoles with Nitroalkenes Catalyzed by Bifunctional Tridentate Bis(oxazoline)−Zn(II) Complex
inferred← citeshttps://doi.org/10.1021/ol070483copenalex-snapshot
Gold(I)-Catalyzed Intramolecular Enantioselective Hydroarylation of Allenes with Indoles
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/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/ol702003xopenalex-snapshot
Asymmetric Friedel−Crafts Alkylation of Methoxyfuran with Nitroalkenes Catalyzed by Diphenylamine-Tethered Bis(oxazoline)−Zn(II) Complexes
inferred← citeshttps://doi.org/10.1021/ol8016929openalex-snapshot
Highly Enantioselective Friedel−Crafts Reaction of Indoles with 2-EnoylPyridine 1-Oxides Catalyzed by Chiral Pyridine 2,6-Bis(5′,5′-diphenyloxazoline)−Cu(II) Complexes
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/om801005jopenalex-snapshot
Chiral NCN Pincer Pt(II) and Pd(II) Complexes with 1,3-Bis(2′-imidazolinyl)benzene: Synthesis via Direct Metalation, Characterization, and Catalytic Activity in the Friedel−Crafts Alkylation Reaction
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/10.1039/b610263hopenalex-snapshot
Efficient Friedel–Crafts alkylation of indoles and pyrrole with enones and nitroalkene in water
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/b923063gopenalex-snapshot
Organocatalytic strategies for the asymmetric functionalization of indoles
inferred← citeshttps://doi.org/10.1039/c004037aopenalex-snapshot
Organocatalytic Michael addition of unprotected 3-substituted oxindoles to nitroolefins
inferred← citeshttps://doi.org/10.1039/c0cc02181dopenalex-snapshot
Rhodium-catalyzed asymmetric conjugate alkynylation of nitroalkenes
inferred← citeshttps://doi.org/10.1039/c0ob00709aopenalex-snapshot
FeCl 3 -promoted alkylation of indoles by enamides
inferred← citeshttps://doi.org/10.1039/c2ob25074hopenalex-snapshot
A heterotrimetallic Pd–Sm–Pd complex for asymmetric Friedel–Crafts alkylations of pyrroles with nitroalkenes
inferred← citeshttps://doi.org/10.1039/c2ob25315aopenalex-snapshot
Enantioselective Friedel–Crafts alkylation of indoles with 2-enoylpyridine-N-oxides catalyzed by glucoBOX-Cu(ii) complex
inferred← citeshttps://doi.org/10.1039/c2ob25360gopenalex-snapshot
Asymmetric Friedel–Crafts alkylation of indoles with 3-nitro-2H-chromenes catalyzed by diphenylamine-linked bis(oxazoline) and bis(thiazoline) Zn(II) complexes
inferred← citeshttps://doi.org/10.1039/c3cy00629hopenalex-snapshot
Asymmetric Friedel–Crafts addition of indoles to N-sulfonyl aldimines catalyzed by Cu( ii ) chiral amino alcohol based Schiff base complexes
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/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/c4ra02825bopenalex-snapshot
Solvent and catalyst free route to 3-indolyl glycoconjugates: synthesis of sugar tethered isoxazolines and isoxazoles from 3-indolyl nitroalkanes
inferred← citeshttps://doi.org/10.1039/c8cc03447hopenalex-snapshot
Highly enantioselective Friedel–Crafts alkylation of N , N -dialkylanilines with trans -β-nitrostyrene catalyzed by a homochiral metal–organic framework
inferred← citeshttps://doi.org/10.1039/c9ob00545eopenalex-snapshot
A chiral bicyclic skeleton-tethered bipyridine–Zn(OTf) 2 complex as a Lewis acid: enantioselective Friedel–Crafts alkylation of indoles with nitroalkenes
inferred← citeshttps://doi.org/10.1039/d2nj04542gopenalex-snapshot
Friedel–Crafts alkylation of indoles with β-nitroalkenes using ammonium niobium oxalate as a recyclable catalyst
inferred← citeshttps://doi.org/10.1039/d2qi00206jopenalex-snapshot
Urea-engineering mediated hydrogen-bond donating Friedel–Crafts alkylation of indoles and nitroalkenes in a dual-functionalized microporous metal–organic framework with high recyclability and pore-fitting-induced size-selectivity
inferred← citeshttps://doi.org/10.1039/d4qo00248bopenalex-snapshot
Naphthyridine–2NO, a new C 2 -symmetric rigid tetradentate bimetallic ligand and its application in asymmetric Friedel–Crafts alkylation
inferred← citeshttps://doi.org/10.1039/d4ra08471copenalex-snapshot
Ni( ii )/spiroBox-catalyzed asymmetric Friedel–Crafts alkylation of indoles with nitroalkenes
inferred← citeshttps://doi.org/10.1039/d6cc00711bopenalex-snapshot
Mantis-shaped bifunctional tridentate HoMPy-PI-NO ligands capable of cooperatively activating nucleophiles and electrophiles: empowering asymmetric addition reactions
inferred← citeshttps://doi.org/10.1039/d6cc01883aopenalex-snapshot
Squaramide-functionalized coordination capsule as hydrogen-bond-donor catalyst for efficient Friedel–Crafts alkylation
inferred← citeshttps://doi.org/10.1055/a-1743-4534openalex-snapshot
Synthesis and Applications of Asymmetric Catalysis Using Chiral Ligands Containing Quinoline Motifs
inferred← citeshttps://doi.org/10.1055/b-0035-128263openalex-snapshot
10.13 Product Class 13: Indole and Its Derivatives
inferred← citeshttps://doi.org/10.1055/s-0036-1589068openalex-snapshot
The Friedel–Crafts Reaction of Indoles with Michael Acceptors Catalyzed by Magnesium and Calcium Salts
inferred← citeshttps://doi.org/10.1055/sos-sd-103-00147openalex-snapshot
3.1.11 Organometallic Complexes of Zinc (Update 2014)
inferred← citeshttps://doi.org/10.1080/00397910801989600openalex-snapshot
Mild and Efficient Michael Addition of Activated Olefins to Indoles using TBAB as a Catalyst: Synthesis of 3‐Substituted Indoles
inferred← citeshttps://doi.org/10.1080/00397910902883728openalex-snapshot
Synthesis of 2-Indolyl-1-nitroalkane Derivatives Using Nanocrystalline Titanium(IV) Oxide
inferred← citeshttps://doi.org/10.1080/00397910903398676openalex-snapshot
Sc(OTf)3: A Highly Efficient and Renewable Catalyst for Michael Addition of Indoles to Nitroolefins in Water
inferred← citeshttps://doi.org/10.1080/10426507.2010.536189openalex-snapshot
Chiral Phosphoric Acid Catalyzed Asymmetric Friedel–Crafts Alkylation of Indoles with Nitroolefins
inferred← citeshttps://doi.org/10.1080/10610278.2018.1515488openalex-snapshot
Steric effects of pH switchable, substituted (2-pyridinium)urea organocatalysts: a solution and solid phase study
inferred← citeshttps://doi.org/10.1155/2014/649197openalex-snapshot
Facile and Promising Method for Michael Addition of Indole and Pyrrole to Electron-Deficient trans - β -Nitroolefins Catalyzed by a Hydrogen Bond Donor Catalyst Feist’s Acid and Preliminary Study of Antimicrobial Activity
inferred← citeshttps://doi.org/10.1246/cl.2008.1284openalex-snapshot
Catalytic Conjugate Addition of Indoles to 4-Aryl-4-oxobut-2-enoates by FeCl3
inferred← citeshttps://doi.org/10.2174/138527209789578126openalex-snapshot
The Role of the Indole in Important Organocatalytic Enantioselective Friedel-Crafts Alkylation Reactions
inferred← citeshttps://doi.org/10.2174/1385272819666140809010818openalex-snapshot
Chiral BrOnsted Acid-Catalyzed Friedel-Crafts Reaction of Indoles
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