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A New Type of Bis(sulfonamide)-Diamine Ligand for a Cu(OTf)2-Catalyzed Asymmetric Friedel–Crafts Alkylation Reaction of Indoles with 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.201000111openalex-snapshot
Development of Diphenylamine‐Linked Bis(imidazoline) Ligands and Their Application in Asymmetric Friedel–Crafts Alkylation of Indole Derivatives with Nitroalkenes
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.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.200901843openalex-snapshot
Catalytic Functionalization of Indoles in a New Dimension
inferredcites →https://doi.org/10.1002/anie.201001484openalex-snapshot
Orthogonal Enantioselectivity Approaches Using Homogeneous and Heterogeneous Catalyst Systems: Friedel–Crafts Alkylation of Indole
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.201000540openalex-snapshot
Monodentate N‐Ligand‐Directed Bifunctional Transition‐Metal Catalysis: Highly Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes
inferredcites →https://doi.org/10.1002/chem.201000964openalex-snapshot
A Highly Effective Bis(sulfonamide)–Diamine Ligand: A Unique Chiral Skeleton for the Enantioselective Cu‐Catalyzed Henry Reaction
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/10.1002/cjoc.201090243openalex-snapshot
Synthesis of Tridentate Ligands Based on Chiral Diamines and Their Application to Enantioselective Friedel‐Crafts Alkylation of Indoles with Nitroalkenes
inferredcites →https://doi.org/10.1002/ejoc.200900683openalex-snapshot
New Thiazoline–Oxazoline Ligands and Their Application in the Asymmetric Friedel–Crafts Reaction
inferredcites →https://doi.org/10.1002/ejoc.200901434openalex-snapshot
Immobilization of Diphenylamine‐Linked Bis(oxazoline) Ligands and Their Application in the Asymmetric Friedel–Crafts Alkylation of Indole Derivatives with Nitroalkenes
inferredcites →https://doi.org/10.1002/ejoc.201100506openalex-snapshot
Enhanced Efficiency of Thiourea Catalysts by External Brønsted Acids in the Friedel–Crafts Alkylation of Indoles
inferredcites →https://doi.org/10.1002/ejoc.201100683openalex-snapshot
The Asymmetric Friedel–Crafts Reaction of Indoles with Fluoroalkylated Nitroalkenes Catalyzed by Chiral Phosphoric Acid
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.2008.11.083openalex-snapshot
Synthesis of 9,9′-biphenanthryl-10,10′-bis(oxazoline)s and their preliminary evaluations in the Friedel–Crafts alkylations of indoles with nitroalkenes
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/cr050521aopenalex-snapshot
Reserpine: A Challenge for Total Synthesis of Natural Products
inferredcites →https://doi.org/10.1021/cr078372eopenalex-snapshot
Catalytic Asymmetric Friedel−Crafts Alkylation Reactions—Copper Showed the Way
inferredcites →https://doi.org/10.1021/ja8063292openalex-snapshot
Catalytic Enantioselective Additions of Indoles to Nitroalkenes
inferredcites →https://doi.org/10.1021/jo00382a012openalex-snapshot
Hapalindoles, antibacterial and antimycotic alkaloids from the cyanophyte Hapalosiphon fontinalis
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/jo101932aopenalex-snapshot
A Highly Diastereo- and Enantioselective Copper(I)-Catalyzed Henry Reaction Using a Bis(sulfonamide)−Diamine Ligand
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/10.1039/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/b512615kopenalex-snapshot
Chemistry and biology of monoterpene indole alkaloid biosynthesis
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/10.1055/s-1995-5007openalex-snapshot
A General Method for the Synthesis of Bridged Indole Alkaloids. Addition of Carbon Nucleophiles to N-Alkylpyridinium Salts
inferredcites →https://doi.org/10.1055/s-2005-865210openalex-snapshot
A Journey Across Recent Advances in Catalytic and Stereoselective Alkylation of Indoles
inferredcites →https://doi.org/10.2174/138527205774370496openalex-snapshot
Novel Routes to Pyrroles, Indoles and Carbazoles - Applications in Natural Product Synthesis

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/10.1002/047084289x.rn01748openalex-snapshot
Nitrostyrene
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/10.1002/9781118560273.ch6openalex-snapshot
Electrophilic Aromatic Substitution
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/ajoc.202200188openalex-snapshot
Enantioselective Synthesis of Chiral 3‐Alkynyl‐3‐Hydroxyindolin‐ 2‐Ones by Zn/bis(Sulfonamide)‐Diamine Catalyzed Asymmetric Addition of Alkynes to Isatins
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.201203095openalex-snapshot
ChemInform Abstract: 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/10.1002/cjoc.201201094openalex-snapshot
Ethylenediamine: A Highly Effective Catalyst for One‐Pot Synthesis of Aryl Nitroalkenes via Henry Reaction and Dehydration
inferred← citeshttps://doi.org/10.1002/ejoc.201200584openalex-snapshot
Enantioselective Friedel–Crafts Alkylation of N‐Methylindoles with Nitroalkenes Catalyzed by Chiral Bifunctional Abietic‐Acid‐Derived Thiourea‐ZnII Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.201300172openalex-snapshot
Synthesis of Nitroalkenes Involving a Cooperative Catalytic Action of Iron(III) and Piperidine: A One‐Pot Synthetic Strategy to 3‐Alkylindoles, 2H‐Chromenes and N‐Arylpyrrole
inferred← citeshttps://doi.org/10.1002/ejoc.201300369openalex-snapshot
Leaving Group and Regioselectivity Switches in the Aminoalkylation Reaction of Indoles and Related Heterocycles with α‐Amido Sulfones
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/10.1007/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.catcom.2012.09.032openalex-snapshot
One-pot synthesis of nitroalkenes via the Henry reaction over amino-functionalized MIL-101 catalysts
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.tetasy.2012.08.015openalex-snapshot
Enhanced efficiency of recyclable C3-symmetric cinchonine-squaramides in the asymmetric Friedel–Crafts reaction of indoles with alkyl trifluoropyruvate
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.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.2021.153153openalex-snapshot
Enantioselective Friedel-Crafts alkylation of indole with nitroalkenes in the presence of bifunctional squaramide organocatalysts
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.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/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/ja400650mopenalex-snapshot
Highly Enantioselective Construction of Trifluoromethylated All-Carbon Quaternary Stereocenters via Nickel-Catalyzed Friedel–Crafts Alkylation Reaction
inferred← citeshttps://doi.org/10.1021/jo3001047openalex-snapshot
Enantioselective Synthesis of 3,4-Dihydropyran Derivatives via Organocatalytic Michael Reaction of α,β-Unsaturated Enones
inferred← citeshttps://doi.org/10.1021/jo400747dopenalex-snapshot
Cu(OTf)2-Catalyzed Asymmetric Friedel–Crafts Alkylation Reaction of Indoles with Arylidene Malonates Using Bis(sulfonamide)-Diamine Ligands
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/10.1038/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/10.1039/9781782621966-00214openalex-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/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/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/c4ob00815dopenalex-snapshot
Facile synthesis of 5H-benzo[b]carbazol-6-yl ketones via sequential reaction of Cu-catalyzed Friedel–Crafts alkylation, iodine-promoted cyclization, nucleophilic substitution and aromatization
inferred← citeshttps://doi.org/10.1039/c4ra11860jopenalex-snapshot
Enhancement of stereoselectivities in asymmetric synthesis using fluorinated solvents, auxiliaries, and catalysts
inferred← citeshttps://doi.org/10.1039/c5ra11798dopenalex-snapshot
Ethylenediamine-functionalized magnetic Fe 3 O 4 @SiO 2 nanoparticles: cooperative trifunctional catalysis for selective synthesis of nitroalkenes
inferred← citeshttps://doi.org/10.1039/c6ob00102eopenalex-snapshot
Approach for 2-(arylthio)imidazoles and imidazo[2,1-b]thiazoles from imidazo[2,1-b][1,3,4]thiadiazoles by ring-opening and -reconstruction
inferred← citeshttps://doi.org/10.1039/c7ob00413copenalex-snapshot
Recent progress in transition-metal-catalyzed enantioselective indole functionalizations
inferred← citeshttps://doi.org/10.1039/d1qo00369kopenalex-snapshot
Dinuclear helicate or mononuclear pincer lanthanide complexes from one ligand: stereo-controlled assembly and catalysis
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
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Urea Activation by an External Brønsted Acid: Breaking Self-Association and Tuning Catalytic Performance
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