On the public citation graph

Highly Enantioselective Construction of Trifluoromethylated All-Carbon Quaternary Stereocenters via Nickel-Catalyzed Friedel–Crafts Alkylation Reaction

0 signed · 263 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1521-3773(19980302)37:4<388::aid-anie388>3.0.co;2-vopenalex-snapshot
The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters
inferredcites →https://doi.org/10.1002/352760393xopenalex-snapshot
Modern Fluoroorganic Chemistry
inferredcites →https://doi.org/10.1002/9780470281895openalex-snapshot
Bioorganic and Medicinal Chemistry of Fluorine
inferredcites →https://doi.org/10.1002/9781118075647openalex-snapshot
Chiral Drugs
inferredcites →https://doi.org/10.1002/9781444312096openalex-snapshot
Fluorine in Medicinal Chemistry and Chemical Biology
inferredcites →https://doi.org/10.1002/9783527626977openalex-snapshot
Catalytic Asymmetric Friedel–Crafts Alkylations
inferredcites →https://doi.org/10.1002/adsc.200505165openalex-snapshot
Stereoselective Construction of Quaternary Stereocenters
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.200500227openalex-snapshot
Catalytic Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst
inferredcites →https://doi.org/10.1002/anie.200501041openalex-snapshot
Highly Enantioselective Catalytic Fluorination and Chlorination Reactions of Carbonyl Compounds Capable of Two‐Point Binding
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.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/anie.201003172openalex-snapshot
Entropy‐Controlled Catalytic Asymmetric 1,4‐Type Friedel–Crafts Reaction of Phenols Using Conformationally Flexible Guanidine/Bisthiourea Organocatalyst
inferredcites →https://doi.org/10.1002/anie.201004051openalex-snapshot
Transition‐Metal‐Catalyzed Trifluoromethylation of Aryl Halides
inferredcites →https://doi.org/10.1002/anie.201201012openalex-snapshot
Tamed Arene and Heteroarene Trifluoromethylation
inferredcites →https://doi.org/10.1002/anie.201201278openalex-snapshot
Organocatalytic Asymmetric Synthesis of Trifluoromethyl‐substituted Diarylpyrrolines: Enantioselective Conjugate Cyanation of β‐Aryl‐β‐trifluoromethyl‐disubstituted Enones
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.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.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.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
inferredcites →https://doi.org/10.1002/chem.201001546openalex-snapshot
Enantioselective Organocatalytic Synthesis of Fluorinated Molecules
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.200901492openalex-snapshot
Organocatalyzed Asymmetric Friedel–Crafts Reactions
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.2011.01.002openalex-snapshot
Trifluoromethylation of aryl and heteroaryl halides
inferredcites →https://doi.org/10.1016/j.tetasy.2008.11.011openalex-snapshot
Recent advances in enantioselective trifluoromethylation reactions
inferredcites →https://doi.org/10.1021/cr030685wopenalex-snapshot
Fluorinated Carbonyl and Olefinic Compounds: Basic Character and Asymmetric Catalytic Reactions
inferredcites →https://doi.org/10.1021/cr078372eopenalex-snapshot
Catalytic Asymmetric Friedel−Crafts Alkylation Reactions—Copper Showed the Way
inferredcites →https://doi.org/10.1021/cr100166aopenalex-snapshot
Asymmetric Construction of Stereogenic Carbon Centers Featuring a Trifluoromethyl Group from Prochiral Trifluoromethylated Substrates
inferredcites →https://doi.org/10.1021/cr1004293openalex-snapshot
Aromatic Trifluoromethylation with Metal Complexes
inferredcites →https://doi.org/10.1021/cr800221vopenalex-snapshot
Update 1 of: Asymmetric Fluorination, Trifluoromethylation, and Perfluoroalkylation Reactions
inferredcites →https://doi.org/10.1021/cr9003488openalex-snapshot
Perchloric Acid and Its Salts: Very Powerful Catalysts in Organic Chemistry
inferredcites →https://doi.org/10.1021/ja002670aopenalex-snapshot
Lewis Acid-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions of Diazoalkane: Chiral Ligand/Achiral Auxiliary Cooperative Chirality Control
inferredcites →https://doi.org/10.1021/ja027313+openalex-snapshot
Enantioselective Michael Additions of Nitromethane by a Catalytic Double Activation Method Using Chiral Lewis Acid and Achiral Amine Catalysts
inferredcites →https://doi.org/10.1021/ja0421497openalex-snapshot
Enantioselective Addition of Nitrones to Activated Cyclopropanes
inferredcites →https://doi.org/10.1021/ja050800fopenalex-snapshot
Enantioselective Synthesis of Nitroalkanes Bearing All-Carbon Quaternary Stereogenic Centers through Cu-Catalyzed Asymmetric Conjugate Additions
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/ja302691ropenalex-snapshot
Side-Arm-Promoted Highly Enantioselective Ring-Opening Reactions and Kinetic Resolution of Donor–Acceptor Cyclopropanes with Amines
inferredcites →https://doi.org/10.1021/ja3039773openalex-snapshot
Highly Enantioselective Copper-Catalyzed Electrophilic Trifluoromethylation of β-Ketoesters
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/ja973519copenalex-snapshot
Transition-Metal Aqua Complexes of 4,6-Dibenzofurandiyl-2,2‘-bis(4-phenyloxazoline). Effective Catalysis in Diels−Alder Reactions Showing Excellent Enantioselectivity, Extreme Chiral Amplification, and High Tolerance to Water, Alcohols, Amines, and Acids
inferredcites →https://doi.org/10.1021/ja982254eopenalex-snapshot
Highly Endo- and Enantioselective Asymmetric Nitrone Cycloadditions Catalyzed by the Aqua Complex of 4,6-Dibenzofurandiyl-2,2‘-bis(4-phenyl- oxazoline)−Nickel(II) Perchlorate. Transition Structure Based on Dramatic Effect of MS 4A on Selectivities
inferredcites →https://doi.org/10.1021/ja991064gopenalex-snapshot
Asymmetric Conjugate Addition of Thiols to a 3-(2-Alkenoyl)-2-oxazolidinone Catalyzed by the DBFOX/Ph Aqua Complex of Nickel(II) Perchlorate
inferredcites →https://doi.org/10.1021/ja991704fopenalex-snapshot
First Ruthenium-Catalyzed Allylation of Thiols Enables the General Synthesis of Allylic Sulfides
inferredcites →https://doi.org/10.1021/jm800219fopenalex-snapshot
The Many Roles for Fluorine in Medicinal Chemistry
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/jo1024333openalex-snapshot
Enantioselective Friedel−Crafts Alkylation of Indoles with Trifluoroethylidene Malonates by Copper−Bis(oxazoline) Complexes: Construction of Trifluoromethyl-Substituted Stereogenic Tertiary Carbon Center
inferredcites →https://doi.org/10.1021/jo201061fopenalex-snapshot
Asymmetric Cycloaddition Reactions of Diazoesters with 2-Alkenoic Acid Derivatives Catalyzed by Binaphthyldiimine–Ni(II) complexes
inferredcites →https://doi.org/10.1021/jo701561dopenalex-snapshot
Axially Chiral BINIM and Ni(II)-Catalyzed Highly Enantioselective 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides and N-Arylmaleimides
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/ol062675yopenalex-snapshot
Highly Enantioselective and Diastereoselective 1,3-Dipolar Cycloaddition Reactions between Azomethine Imines and 3-Acryloyl-2-oxazolidinone Catalyzed by Binaphthyldiimine−Ni(II) Complexes
inferredcites →https://doi.org/10.1021/ol100171zopenalex-snapshot
Enantioselective Friedel−Crafts Reaction of β-Trifluoromethylated Acrylates with Pyrroles and Its Application to the Synthesis of Trifluorinated Heliotridane
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/ol201316zopenalex-snapshot
Organocatalytic Asymmetric Strecker Reaction of Di- and Trifluoromethyl Ketoimines. Remarkable Fluorine Effect
inferredcites →https://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
inferredcites →https://doi.org/10.1021/ol300274uopenalex-snapshot
High-Pressure Accelerated Asymmetric Organocatalytic Friedel–Crafts Alkylation of Indoles with Enones: Application to Quaternary Stereogenic Centers Construction
inferredcites →https://doi.org/10.1021/ol702003xopenalex-snapshot
Asymmetric Friedel−Crafts Alkylation of Methoxyfuran with Nitroalkenes Catalyzed by Diphenylamine-Tethered Bis(oxazoline)−Zn(II) Complexes
inferredcites →https://doi.org/10.1021/ol8009286openalex-snapshot
A Mild Procedure for the Lewis Acid-Catalyzed Ring-Opening of Activated Cyclopropanes with Amine Nucleophiles
inferredcites →https://doi.org/10.1021/ol901572xopenalex-snapshot
Enantioselective Michael Reactions of β, β-Disubstituted Nitroalkenes: A New Approach to β2,2-Amino Acids with Hetero-Quaternary Stereocenters
inferredcites →https://doi.org/10.1038/nature10108openalex-snapshot
Catalysis for fluorination and trifluoromethylation
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/b704925kopenalex-snapshot
Organocatalytic asymmetric Friedel–Crafts alkylation/cascade reactions of naphthols and nitroolefins
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/10.1039/c0cc02309dopenalex-snapshot
Metal-catalyzed asymmetric conjugate addition reaction: formation of quaternary stereocenters
inferredcites →https://doi.org/10.1039/c1cc12306hopenalex-snapshot
Highly enantioselective yttrium(iii)-catalyzed Friedel–Crafts alkylation of β-trichloro(trifluoro)methyl aryl enones with indoles
inferredcites →https://doi.org/10.1039/c2cc32757kopenalex-snapshot
Practical synthesis of 4,4,4-trifluorocrotonaldehyde: a versatile precursor for the enantioselective formation of trifluoromethylated stereogenic centers via organocatalytic 1,4-additions
inferredcites →https://doi.org/10.1039/c2ob25074hopenalex-snapshot
A heterotrimetallic Pd–Sm–Pd complex for asymmetric Friedel–Crafts alkylations of pyrroles with nitroalkenes
inferredcites →https://doi.org/10.1055/s-0030-1259947openalex-snapshot
Synthesis of Trifluoromethylated and gem-Difluoromethylenated Biologically Interesting Compounds from Fluorine-Containing Synthons
inferredcites →https://doi.org/10.1055/s-2006-926302openalex-snapshot
Catalytic Enantioselective Construction of All-Carbon Quaternary Stereocenters
inferredcites →https://doi.org/10.1073/pnas.0307113101openalex-snapshot
Catalytic asymmetric synthesis of all-carbon quaternary stereocenters
inferredcites →https://doi.org/10.1126/science.1131943openalex-snapshot
Fluorine in Pharmaceuticals: Looking Beyond Intuition
inferredcites →https://doi.org/10.4155/fmc.09.65openalex-snapshot
Fluorine in Medicinal Chemistry: A Century of Progress and a 60-Year Retrospective of Selected Highlights

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/10.1002/9783527819201.ch4openalex-snapshot
Development of a Nickel‐Catalyzed Enantioselective Mizoroki–Heck Coupling
inferred← citeshttps://doi.org/10.1002/adsc.201301027openalex-snapshot
Catalytic Asymmetric Conjugate Addition of Mercaptans to β‐Substituted‐β‐Trifluoromethyl Oxazolidinone Enoates: Access to Chiral Trifluoromethylated Tertiary Thioethers and Thiols
inferred← citeshttps://doi.org/10.1002/adsc.201400977openalex-snapshot
Enantioselective Organocatalyzed Oxa‐Michael–Aldol Cascade Reactions: Construction of Chiral 4H‐Chromenes with a Trifluoromethylated Tetrasubstituted Carbon Stereocenter
inferred← citeshttps://doi.org/10.1002/adsc.201401189openalex-snapshot
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.201600272openalex-snapshot
Friedel–Crafts Reaction of Indoles with Isatin‐Derived β,γ‐Unsaturated α‐Keto Esters Using a BINOL‐Derived Bisoxazoline (BOX)/Copper(II) Complex as Catalyst
inferred← citeshttps://doi.org/10.1002/adsc.201600327openalex-snapshot
High‐Pressure‐Mediated Asymmetric Organocatalytic Hydroxyalkylation of Indoles with Trifluoromethyl Ketones
inferred← citeshttps://doi.org/10.1002/adsc.201700465openalex-snapshot
Organocatalytic Enantioselective Synthesis of Dihydropyrano‐ indole Derivatives Bearing Trifluoromethylated All‐Carbon‐ Substituted Stereocenters
inferred← citeshttps://doi.org/10.1002/adsc.201700975openalex-snapshot
Organocatalytic Enantioselective Synthesis of Trifluoromethyl‐Containing Tetralin Derivatives by Sequential (Hetero)Michael Reaction–Intramolecular Nitrone Cycloaddition
inferred← citeshttps://doi.org/10.1002/adsc.202200918openalex-snapshot
Synthesis of 3‐Aryl Oxindoles having Trifluoromethylated Quaternary Stereocenters via Catalyst Free Arylation
inferred← citeshttps://doi.org/10.1002/adsc.202201353openalex-snapshot
Nickel‐Catalyzed Intermolecular Branched/Linear Regioselective C−H Alkylation of 4‐Oxoquinazolines
inferred← citeshttps://doi.org/10.1002/adsc.202300666openalex-snapshot
Advances in Catalytic Asymmetric Construction of Quaternary Stereogenic Centers by Conjugate Addition to β,β‐Disubstituted Nitroalkenes
inferred← citeshttps://doi.org/10.1002/ajoc.201700570openalex-snapshot
Metal‐Free, Visible‐Light‐Mediated Direct C−H Trifluoromethylation of Hydrazones with NADH Coenzyme Model Catalyst
inferred← citeshttps://doi.org/10.1002/ange.201305075openalex-snapshot
Enantioselective Electrophilic Trifluoromethylthiolation of β‐Ketoesters: A Case of Reactivity and Selectivity Bias for Organocatalysis
inferred← citeshttps://doi.org/10.1002/ange.201306997openalex-snapshot
Chiral‐at‐Metal Octahedral Iridium Catalyst for the Asymmetric Construction of an All‐Carbon Quaternary Stereocenter
inferred← citeshttps://doi.org/10.1002/ange.201307250openalex-snapshot
One‐Pot Tandem Approach to Spirocyclic Oxindoles Featuring Adjacent Spiro‐Stereocenters
inferred← citeshttps://doi.org/10.1002/ange.201403082openalex-snapshot
Remote Enantioselective Friedel–Crafts Alkylations of Furans through HOMO Activation
inferred← citeshttps://doi.org/10.1002/ange.201600619openalex-snapshot
Construction of Quaternary Stereogenic Carbon Centers through Copper‐Catalyzed Enantioselective Allylic Alkylation of Azoles
inferred← citeshttps://doi.org/10.1002/ange.201602542openalex-snapshot
Diastereo‐ and Enantioselective Copper(I)‐Catalyzed Intermolecular [3+2] Cycloaddition of Azomethine Ylides with β‐Trifluoromethyl β,β‐Disubstituted Enones
inferred← citeshttps://doi.org/10.1002/ange.201606955openalex-snapshot
Construction of Quaternary Stereocenters by Nickel‐Catalyzed Heck Cyclization Reactions
inferred← citeshttps://doi.org/10.1002/ange.201706631openalex-snapshot
Palladium‐Catalyzed Suzuki–Miyaura Cross‐Coupling of Secondary α‐(Trifluoromethyl)benzyl Tosylates
inferred← citeshttps://doi.org/10.1002/ange.202208742openalex-snapshot
Catalytic and Stereoselective Transformations with Easily Accessible and Purchasable Allyl and Alkenyl Fluorides
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/ange.202519102openalex-snapshot
Iridium Porphyrin‐Catalyzed Asymmetric Rearrangement of Oxindoles with Aryl Diazoesters: Enantioselective Synthesis of Chiral Tertiary 2‐Indolyl Alcohols
inferred← citeshttps://doi.org/10.1002/anie.201305075openalex-snapshot
Enantioselective Electrophilic Trifluoromethylthiolation of β‐Ketoesters: A Case of Reactivity and Selectivity Bias for Organocatalysis
inferred← citeshttps://doi.org/10.1002/anie.201306997openalex-snapshot
Chiral‐at‐Metal Octahedral Iridium Catalyst for the Asymmetric Construction of an All‐Carbon Quaternary Stereocenter
inferred← citeshttps://doi.org/10.1002/anie.201307250openalex-snapshot
One‐Pot Tandem Approach to Spirocyclic Oxindoles Featuring Adjacent Spiro‐Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.201403082openalex-snapshot
Remote Enantioselective Friedel–Crafts Alkylations of Furans through HOMO Activation
inferred← citeshttps://doi.org/10.1002/anie.201600619openalex-snapshot
Construction of Quaternary Stereogenic Carbon Centers through Copper‐Catalyzed Enantioselective Allylic Alkylation of Azoles
inferred← citeshttps://doi.org/10.1002/anie.201602542openalex-snapshot
Diastereo‐ and Enantioselective Copper(I)‐Catalyzed Intermolecular [3+2] Cycloaddition of Azomethine Ylides with β‐Trifluoromethyl β,β‐Disubstituted Enones
inferred← citeshttps://doi.org/10.1002/anie.201606955openalex-snapshot
Construction of Quaternary Stereocenters by Nickel‐Catalyzed Heck Cyclization Reactions
inferred← citeshttps://doi.org/10.1002/anie.201706631openalex-snapshot
Palladium‐Catalyzed Suzuki–Miyaura Cross‐Coupling of Secondary α‐(Trifluoromethyl)benzyl Tosylates
inferred← citeshttps://doi.org/10.1002/anie.202208742openalex-snapshot
Catalytic and Stereoselective Transformations with Easily Accessible and Purchasable Allyl and Alkenyl Fluorides
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/anie.202519102openalex-snapshot
Iridium Porphyrin‐Catalyzed Asymmetric Rearrangement of Oxindoles with Aryl Diazoesters: Enantioselective Synthesis of Chiral Tertiary 2‐Indolyl Alcohols
inferred← citeshttps://doi.org/10.1002/asia.201600941openalex-snapshot
Asymmetric Construction of Pyrrolidines Bearing a Trifluoromethylated Quaternary Stereogenic Center via CuI‐Catalyzed 1,3‐Dipolar Cycloaddition of Azomethine Ylides with β‐CF3‐β,β‐Disubstituted Nitroalkenes
inferred← citeshttps://doi.org/10.1002/cctc.201500141openalex-snapshot
Enantioselective [3+2] Cyclization of 3‐Isothiocyanato Oxindoles with Trifluoromethylated 2‐Butenedioic Acid Diesters
inferred← citeshttps://doi.org/10.1002/chem.201400026openalex-snapshot
Regio‐ and Enantioselective Synthesis of N‐Allylindoles by Iridium‐Catalyzed Allylic Amination/Transition‐Metal‐Catalyzed Cyclization Reactions
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.201405730openalex-snapshot
Enantioselective Organocatalytic Reduction of β‐Trifluoromethyl Nitroalkenes: An Efficient Strategy for the Synthesis of Chiral β‐Trifluoromethyl Amines
inferred← citeshttps://doi.org/10.1002/chem.201500361openalex-snapshot
Catalytic Asymmetric Synthesis of Enantioenriched Heterocycles Bearing a CCF3 Stereogenic Center
inferred← citeshttps://doi.org/10.1002/chem.201501897openalex-snapshot
Enantio‐ and Diastereoselective Formal Hetero‐Diels–Alder Reactions of Trifluoromethylated Enones Catalyzed by Chiral Primary Amines
inferred← citeshttps://doi.org/10.1002/chem.201503631openalex-snapshot
Lewis Acid Catalyzed Asymmetric Three‐Component Coupling Reaction: Facile Synthesis of α‐Fluoromethylated Tertiary Alcohols
inferred← citeshttps://doi.org/10.1002/chem.201600989openalex-snapshot
Asymmetric Diels–Alder Cycloadditions of Trifluoromethylated Dienophiles Under Trienamine Catalysis
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.201805416openalex-snapshot
Enantioselective C2‐Alkylation of Indoles through a Redox‐Relay Heck Reaction of 2‐Indole Triflates
inferred← citeshttps://doi.org/10.1002/chem.202404152openalex-snapshot
Asymmetric Amination of 1,2‐Diol through Borrowing Hydrogen: Synthesis of Vicinal Amino α‐Tertiary Alcohol
inferred← citeshttps://doi.org/10.1002/chin.201332130openalex-snapshot
ChemInform Abstract: Highly Enantioselective Construction of Trifluoromethylated All‐Carbon Quaternary Stereocenters via Nickel‐Catalyzed Friedel—Crafts Alkylation Reaction.
inferred← citeshttps://doi.org/10.1002/cjoc.201800070openalex-snapshot
Copper(I)‐Catalyzed Asymmetric [3+2]‐Cycloaddition of α ‐Substituted Iminoesters with α ‐Trifluoromethyl α, β ‐Unsaturated Esters
inferred← citeshttps://doi.org/10.1002/cjoc.202100018openalex-snapshot
New Amines and Activation Modes in Asymmetric Aminocatalysis
inferred← citeshttps://doi.org/10.1002/ejoc.201402243openalex-snapshot
Highly Enantioselective Michael Addition of Malonates to β‐CF3‐β‐(3‐Indolyl)nitroalkenes: Construction of Trifluoromethylated All‐Carbon Quaternary Stereogenic Centres
inferred← citeshttps://doi.org/10.1002/ejoc.201403682openalex-snapshot
Remote Amide‐Controlled Gold‐Catalyzed Stereoselective Hydro‐heteroarylation of Acrylamides: Access to Pyrido[3,4‐b]indoles
inferred← citeshttps://doi.org/10.1002/ejoc.201601540openalex-snapshot
Nickel(II)‐Catalyzed Enantioselective 1,3‐Dipolar Cycloaddition of Nitrones with α,β‐Unsaturated Acylcarboxylates
inferred← citeshttps://doi.org/10.1002/ejoc.201700510openalex-snapshot
In Pursuit of β‐Amino‐α‐nitro‐β‐(trifluoromethyl) Ketones: Nitro‐Mannich versus Mannich‐Type Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.202300428openalex-snapshot
Rh‐Catalyzed Hydroheteroarylation of Styrenes: Access to Alkylated Heteroarenes with All‐Carbon Quaternary Centers
inferred← citeshttps://doi.org/10.1002/ejoc.202401168openalex-snapshot
Modern Approaches for Asymmetric Construction of CF3‐All Carbon Quaternary Stereocenters from Prochiral Trifluoromethyl Alkenes
inferred← citeshttps://doi.org/10.1002/ejoc.202500500openalex-snapshot
Substrate Divergent 4π/6π Electrocyclization of CF3‐Quinolone Heterodendralenes
inferred← citeshttps://doi.org/10.1002/jcc.24877openalex-snapshot
Mechanistic investigation inspired “on water” reaction for hydrobromic acid‐catalyzed Friedel–Crafts–type reaction of β‐naphthol and formaldehyde
inferred← citeshttps://doi.org/10.1002/slct.201800113openalex-snapshot
Enantioselective Addition of Cyanide to CF 3 ‐Substituted Alkylidenemalonates: Construction of Trifluoromethylated All‐Carbon Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1002/slct.202102134openalex-snapshot
A Highly Enantioselective Approach to Hydrocarbazole Derivatives Catalyzed by Diphenylmethylidene Bis(oxazoline)‐Ni(II) Complexes
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/s10593-016-1971-yopenalex-snapshot
3-Nitro-2-phenyl-2-(trifluoromethyl)-2H-chromenes: synthesis and reactions with nucleophiles
inferred← citeshttps://doi.org/10.1007/s40242-016-5482-2openalex-snapshot
Iron chloride hexahydrate-catalyzed Friedel-Crafts akylation of cyclic ketene dithioacetals with alcohols
inferred← citeshttps://doi.org/10.1016/b978-0-08-100017-5.00006-6openalex-snapshot
Five-Membered Ring Systems
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/b978-0-32-390644-9.00056-1openalex-snapshot
Olefins Hydrofunctionnalization; Hydroarylation (Vinylation, Alkynylation) of Electron Deficient Olefins
inferred← citeshttps://doi.org/10.1016/b978-0-443-18939-5.00006-8openalex-snapshot
Five-membered ring systems: pyrroles and benzo analogs
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.cclet.2021.10.062openalex-snapshot
Highly enantioselective construction of CF3-bearing all-carbon quaternary stereocenters: Chiral spiro-fused bisoxazoline ligands with 1,1′-binaphthyl sidearm for asymmetric Michael-type Friedel-Crafts reaction
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.jfluchem.2014.10.002openalex-snapshot
Palladium-catalyzed allylation of trifluoromethylated ketene aminoacetals
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2015.01.015openalex-snapshot
A practical synthesis of trifluoromethyl alkyl ketones
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2015.05.011openalex-snapshot
Organocatalytic enantioselective Diels–Alder reaction of 4,4,4-trifluorocrotonaldehyde
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.tet.2014.05.017openalex-snapshot
Highly selective trifluoroacetic ester/ketone metathesis: an efficient approach to trifluoromethyl ketones and esters
inferred← citeshttps://doi.org/10.1016/j.tet.2014.12.020openalex-snapshot
Heteroarylidene-tethered bis(oxazoline) copper complexes catalyzed cascade reaction involving asymmetric Friedel–Crafts alkylation/N-hemiacetalization of indoles with β,γ-unsaturated α-ketoester
inferred← citeshttps://doi.org/10.1016/j.tet.2016.09.002openalex-snapshot
All-carbon quaternary centers in natural products and medicinal chemistry: recent advances
inferred← citeshttps://doi.org/10.1016/j.tet.2018.07.011openalex-snapshot
Critical view on the recent enantioselective synthesis of alcohols, amines and related molecules having tertiary benzylic stereocenter
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131897openalex-snapshot
Mg/BOX complexes as efficient catalysts for the enantioselective Michael addition of malonates to β-trifluoromethyl-α,β-unsaturated ketones and their N-tosyl imines
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.05.005openalex-snapshot
Enantioselective aldol reactions of α,β-unsaturated ketones with trifluoroacetophenone catalyzed by a chiral primary amine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.05.062openalex-snapshot
DBSA-catalyzed Friedel–Crafts alkylation of cyclic ketene dithioacetals with alcohols in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.01.090openalex-snapshot
Base-catalyzed cascade 1,6-sulfur-Michael/Henry reaction of trifluoromethyl-substituted styrylisoxazoles: Diastereoselective synthesis of tetrahydrothiophenes with a trifluoromethylated quaternary center
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152443openalex-snapshot
Organocatalytic enantioselective conjugate addition of nitroalkanes to trifluoromethylated 3-methyleneoxindoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156254openalex-snapshot
Beyond traditional Pictet–Spengler cyclization: aromatic amines as emerging cyclization partners
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00844openalex-snapshot
Further Developments and Applications of Oxazoline-Containing Ligands in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00385openalex-snapshot
Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00336openalex-snapshot
Synthesis of Chiral Bis(3-indolyl)methanes Bearing a Trifluoromethylated All-Carbon Quaternary Stereocenter via Nickel-Catalyzed Asymmetric Friedel–Crafts Alkylation Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02412openalex-snapshot
HFIP as Protonation Reagent and Solvent for Regioselective Alkylation of Indoles with All-Carbon Centers
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02519openalex-snapshot
Visible-Light-Induced Markovnikov Hydroalkoxylation of α-Trifluoromethyl Alkenes with ortho-Diketones
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02848openalex-snapshot
Organocatalytic Asymmetric Synthesis of Dihydrobenzoxazinones Bearing Trifluoromethylated Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01670openalex-snapshot
Catalyst-Free Synthesis of Trifluoromethylated Five- and Seven-Membered Nitrogen-Containing Heterocycles via Aza-Michael Addition and Lactamization of Trifluoroethylene Oxindoles
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00123openalex-snapshot
Enantioselective Friedel–Crafts Alkylation Reactions of 3-Substituted Indoles with Electron-Deficient Alkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00358openalex-snapshot
Lewis Acid Catalyzed Friedel–Crafts Alkylation of Alkenes with Trifluoropyruvates
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00855openalex-snapshot
Synthesis of (Z)-α-Trifluoromethyl Alkenyl Triflate: A Scaffold for Diverse Trifluoromethylated Species
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00930openalex-snapshot
Visible Light-Induced Photoredox Construction of Trifluoromethylated Quaternary Carbon Centers from Trifluoromethylated Tertiary Bromides
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01950openalex-snapshot
Construction of Furan Derivatives with a Trifluoromethyl Stereogenic Center: Enantioselective Friedel–Crafts Alkylations via Formal Trienamine Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01014openalex-snapshot
Enantioselective Conjugate Addition of 2-Acetyl Azaarenes to β,β-Disubstituted Nitroalkene for the Construction of All-Carbon Quaternary Stereocenters
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.8b02405openalex-snapshot
Visible Light-Induced Radical Cyclization of Tertiary Bromides with Isonitriles To Construct Trifluoromethylated Quaternary Carbon Center
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02601openalex-snapshot
Asymmetric Michael Addition of 2-Acetyl Azaarenes to β-CF3-β-(3-indolyl)nitroalkenes Catalyzed by a Cobalt(II)/(imidazoline-oxazoline) Complex
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00465openalex-snapshot
Nickel-Catalyzed Asymmetric Friedel–Crafts Propargylation of 3-Substituted Indoles with Propargylic Carbonates Bearing an Internal Alkyne Group
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00612openalex-snapshot
Activation of Chiral (Salen)TiCl2 Complex by Phosphorane for the Highly Enantioselective Cyanation of Nitroolefins
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03100openalex-snapshot
Iridium-Catalyzed Asymmetric Cascade Allylation/Lactonization of Indole Esters: Access to Chiral Tricyclic Oxazinoindolones
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00656openalex-snapshot
Phosphine-Catalyzed Domino Annulation of γ-Vinyl Allenoates: Synthesis of Tetrahydrofuro[3,2-c]quinoline Derivatives
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.5b01799openalex-snapshot
Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01864openalex-snapshot
Chiral Phosphoric Acid-Catalyzed Enantioselective Pictet–Spengler Reaction for Concise Synthesis of CF3-Substituted Tetrahydro-β-Carbolines
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00781openalex-snapshot
Friedel–Crafts Alkylation of Indoles with p-Quinols: The Role of Hydrogen Bonding of Water for the Desymmetrization of the Cyclohexadienone System
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01317openalex-snapshot
Cu(I)-Catalyzed Enantioselective Friedel–Crafts Alkylation of Indoles with 2-Aryl-N-sulfonylaziridines as Alkylating Agents
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01494openalex-snapshot
Catalytic Enantioselective Conjugate Alkynylation of β-Aryl-β-trifluoromethyl Enones Constructing Propargylic All-Carbon Quaternary Stereogenic Centers
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01498openalex-snapshot
Asymmetric Synthesis of CF3- and Indole-Containing Thiochromanes via a Squaramide-Catalyzed Michael–Aldol Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02540openalex-snapshot
Enantioselective Synthesis of Quaternary Stereocenters via Chromium Catalysis
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.7b03941openalex-snapshot
Rhodium-Catalyzed Asymmetric Arylative Ring-Opening Reactions of Heterobicyclic Alkenes with Anilines
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b04039openalex-snapshot
Asymmetric Construction of Fluoroalkyl Tertiary Alcohols through a Three-Component Reaction of (Bpin)2, 1,3-Enynes, and Fluoroalkyl Ketones Catalyzed by a Copper(I) Complex
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00925openalex-snapshot
Direct Asymmetric Formal [3 + 2] Cycloaddition Reaction of Isocyanoesters with β-Trifluoromethyl β,β -Disubstituted Enones Leading to Optically Active Dihydropyrroles
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00963openalex-snapshot
Asymmetric Synthesis of β-Indolyl Cyclopentanones and Cyclopentylamides with an All-Carbon Quaternary Stereocenter via Chiral Phosphoric Acid Catalyzed Friedel–Crafts Alkylation Reactions
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03758openalex-snapshot
One-Pot Enantioselective Synthesis of 2-Pyrrolidinone Derivatives Bearing a Trifluoromethylated All-Carbon Quaternary Stereocenter
inferred← citeshttps://doi.org/10.1021/acscatal.2c03330openalex-snapshot
Leveraging the Hydroarylation of α-(Trifluoromethyl)styrenes to Access Trifluoromethylated All-Carbon Quaternary Centers
inferred← citeshttps://doi.org/10.1021/acscatal.6b02080openalex-snapshot
Restricted Conformation of a Hydrogen Bond Mediated Catalyst Enables the Highly Efficient Enantioselective Construction of an All-Carbon Quaternary Stereocenter
inferred← citeshttps://doi.org/10.1021/acscatal.6b03015openalex-snapshot
Copper(I)/Ming-Phos-Catalyzed Asymmetric Intermolecular [3 + 2] Cycloaddition of Azomethine Ylides with α-Trifluoromethyl α, β-Unsaturated Esters
inferred← citeshttps://doi.org/10.1021/acscatal.9b01502openalex-snapshot
Chiral Spiro Phosphoric Acid-Catalyzed Friedel–Crafts Conjugate Addition/Enantioselective Protonation Reactions
inferred← citeshttps://doi.org/10.1021/acscatal.9b01811openalex-snapshot
Enantioselective Friedel–Crafts Alkylation Reaction of Indoles with α-Trifluoromethylated β-Nitrostyrenes Catalyzed by Chiral BINOL Metal Phosphate
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/acsorginorgau.5c00039openalex-snapshot
Transfer Hydrogenation of β-Trifluoromethylated Nitroalkenes Catalyzed by Chiral Calcium Phosphate
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/ja403852eopenalex-snapshot
Practical Selective Hydrogenation of α-Fluorinated Esters with Bifunctional Pincer-Type Ruthenium(II) Catalysts Leading to Fluorinated Alcohols or Fluoral Hemiacetals
inferred← citeshttps://doi.org/10.1021/ja507788ropenalex-snapshot
Gold-Catalyzed Hydroarylation of Alkenes with Dialkylanilines
inferred← citeshttps://doi.org/10.1021/jacs.1c12040openalex-snapshot
A New Organocatalytic Desymmetrization Reaction Enables the Enantioselective Total Synthesis of Madangamine E
inferred← citeshttps://doi.org/10.1021/jacs.7b04374openalex-snapshot
Enantioselective Formation of CF3-Bearing All-Carbon Quaternary Stereocenters via C–H Functionalization of Methanol: Iridium Catalyzed Allene Hydrohydroxymethylation
inferred← citeshttps://doi.org/10.1021/jacs.7b12137openalex-snapshot
Enantioselective Regiodivergent Synthesis of Chiral Pyrrolidines with Two Quaternary Stereocenters via Ligand-Controlled Copper(I)-Catalyzed Asymmetric 1,3-Dipolar Cycloadditions
inferred← citeshttps://doi.org/10.1021/jo402212jopenalex-snapshot
Organocatalytic Reactions of α-Trifluoromethylated Esters with Terminal Alkenes at Room Temperature
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/ol500157bopenalex-snapshot
Highly Enantioselective Organocatalyzed Vinylogous Michael-Type Reaction for the Construction of Trifluoromethylated All-Carbon Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1021/ol502941dopenalex-snapshot
Efficient and Highly Enantioselective Construction of Trifluoromethylated Quaternary Stereogenic Centers via High-Pressure Mediated Organocatalytic Conjugate Addition of Nitromethane to β,β-Disubstituted Enones
inferred← citeshttps://doi.org/10.1021/ol503067gopenalex-snapshot
Amide Groups Switch Selectivity: C–H Trifluoromethylation of α,β-Unsaturated Amides and Subsequent Asymmetric Transformation
inferred← citeshttps://doi.org/10.1021/ol5035222openalex-snapshot
Chiral Phosphoric Acid Catalyzed Highly Enantioselective Friedel–Crafts Alkylation Reaction of C3-Substituted Indoles to β,γ-Unsaturated α-Ketimino Esters
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/10.1039/9781782626701-00310openalex-snapshot
Enantioselective Nickel-Catalysed Miscellaneous Reactions
inferred← citeshttps://doi.org/10.1039/c3ob42329hopenalex-snapshot
Enantioselective organocatalytic oxa-Michael addition of oximes to β-CF 3 -β-disubstituted nitroalkenes: efficient synthesis of β-amino-α-trifluoromethyl alcohols
inferred← citeshttps://doi.org/10.1039/c3sc52548aopenalex-snapshot
Effect of the trifluoromethyl group on torquoselectivity in the 4π ring-opening reaction of oxetenes: stereoselective synthesis of tetrasubstituted olefins
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/c4cc07801bopenalex-snapshot
Catalytic highly enantioselective transfer hydrogenation of β-trifluoromethyl nitroalkenes. An easy and general entry to optically active β-trifluoromethyl amines
inferred← citeshttps://doi.org/10.1039/c4ob01144aopenalex-snapshot
Fluorous chiral bisoxazolines: application in copper-catalyzed asymmetric α-hydrophosphonylation
inferred← citeshttps://doi.org/10.1039/c4ob01920bopenalex-snapshot
1,4 Addition of unprotected pyrrole onto chiral acrylamides: toward synthesis of new polypeptidic architectures
inferred← citeshttps://doi.org/10.1039/c4qo00265bopenalex-snapshot
Enantioselective Friedel–Crafts reaction of 4,7-dihydroindoles with β-CF 3 -β-disubstituted nitroalkenes
inferred← citeshttps://doi.org/10.1039/c4ra00701hopenalex-snapshot
Enantioselective synthesis of N-allylindoles via palladium-catalyzed allylic amination/oxidation of indolines
inferred← citeshttps://doi.org/10.1039/c4ra03269aopenalex-snapshot
Bis(oxazoline)-copper catalyzed enantioselective hydrophosphonylation of aldehydes
inferred← citeshttps://doi.org/10.1039/c5cc08480fopenalex-snapshot
An efficient approach for the construction of trifluoromethylated all-carbon quaternary stereocenters: enantioselective Ni( ii )-catalyzed Michael addition of 2-acetyl azaarene to β,β-disubstituted nitroalkenes
inferred← citeshttps://doi.org/10.1039/c5nj01488copenalex-snapshot
A Ce(OTf) 3 /PyBox catalyzed enantioselective Hosomi–Sakurai reaction of aldehydes with allyltrimethylsilane
inferred← citeshttps://doi.org/10.1039/c6ob00119jopenalex-snapshot
The squaramide-catalyzed asymmetric Michael/cyclization tandem reaction for the synthesis of chiral trifluoromethylated hydroxyimino tetrahydrobenzofuranones
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/c6ra00093bopenalex-snapshot
Catalytic asymmetric synthesis of enantioenriched β-nitronitrile bearing a C-CF 3 stereogenic center
inferred← citeshttps://doi.org/10.1039/c7cc03015kopenalex-snapshot
Copper( i )-catalyzed asymmetric exo-selective [3+2] cycloaddition of azomethine ylides with β-trifluoromethyl β,β-disubstituted enones
inferred← citeshttps://doi.org/10.1039/c7ob00413copenalex-snapshot
Recent progress in transition-metal-catalyzed enantioselective indole functionalizations
inferred← citeshttps://doi.org/10.1039/c7ob00595dopenalex-snapshot
Copper-catalysed enantioselective Michael addition of malonic esters to β-trifluoromethyl-α,β-unsaturated imines
inferred← citeshttps://doi.org/10.1039/c7ob00970dopenalex-snapshot
Palladium-catalyzed geometrically selective hydrogenation of (Z)-trifluoromethyl alkenyl triflate: an efficient approach to (Z) or (E)-3,3,3-trifluoropropenyl derivatives
inferred← citeshttps://doi.org/10.1039/c7qo00229gopenalex-snapshot
Asymmetric synthesis of CF 3 - and indole-containing tetrahydro-β-carbolines via chiral spirocyclic phosphoric acid-catalyzed aza-Friedel–Crafts reaction
inferred← citeshttps://doi.org/10.1039/c7qo00291bopenalex-snapshot
Cu( i )-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter
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/c8qo00932eopenalex-snapshot
Regioselective indole C2-alkylation using β-CF 3 -substituted enones under redox neutral Rh( iii ) catalysis
inferred← citeshttps://doi.org/10.1039/c9gc03345aopenalex-snapshot
Metal-free graphene oxide-catalyzed aza-semipinacol rearrangement to prepare 2-(indol-2-yl)phenols and benzofuro[3,2- b ]indolines containing quaternary carbon centers
inferred← citeshttps://doi.org/10.1039/c9qo01203fopenalex-snapshot
The enantioselective construction of trifluoromethylated quaternary stereocenters via the Rh-catalyzed asymmetric dehydrated arylation of unprotected hemiaminals
inferred← citeshttps://doi.org/10.1039/c9sc01446bopenalex-snapshot
Nickel-catalyzed C–H alkylation of indoles with unactivated alkyl chlorides: evidence of a Ni( i )/Ni( iii ) pathway
inferred← citeshttps://doi.org/10.1039/c9sc04858hopenalex-snapshot
Chiral cis -iron( ii ) complexes with metal- and ligand-centered chirality for highly regio- and enantioselective alkylation of N-heteroaromatics
inferred← citeshttps://doi.org/10.1039/d0ob00004copenalex-snapshot
Enantioselective synthesis of trifluoromethyl substituted cyclohexanones via an organocatalytic cascade Michael/aldol reaction
inferred← citeshttps://doi.org/10.1039/d0ob00956copenalex-snapshot
Synthesis and practical applications of 2-(2-nitroalkyl)pyrroles
inferred← citeshttps://doi.org/10.1039/d1ob01238jopenalex-snapshot
Enantioselective Friedel–Crafts reaction of hydroxyarenes with nitroenynes to access chiral heterocycles via sequential catalysis
inferred← citeshttps://doi.org/10.1039/d2qo01982eopenalex-snapshot
Asymmetric synthesis of 7-membered-ring-bridged 3,4-fused tricyclic indoles via Friedel–Crafts alkylation/annulation
inferred← citeshttps://doi.org/10.1039/d4qo00555dopenalex-snapshot
Acid–solvent cluster-catalyzed general and regioselective Friedel–Crafts arylation of alcohols
inferred← citeshttps://doi.org/10.1039/d4qo01942copenalex-snapshot
Organocatalytic enantioselective [2 + 2] cycloadditions towards chiral fused α-trifluoromethyl azetidines
inferred← citeshttps://doi.org/10.1055/a-2921-6973openalex-snapshot
Enantioselective Construction of Trifluoromethylated Quaternary Centers via NHC-Catalyzed Cross-Annulation Reaction
inferred← citeshttps://doi.org/10.1055/s-0040-1719879openalex-snapshot
Chiral Calcium Phosphate Catalyzed Enantioselective Synthesis of All-Carbon Quaternary Center by Friedel–Crafts Alkylation Reaction of Pyrroles and Trifluoromethylated Nitrostyrenes
inferred← citeshttps://doi.org/10.1055/s-0040-1720139openalex-snapshot
Visible-Light-Induced Photoredox Construction of Trifluoromethylated Quaternary All-Carbon Centers and Tertiary Alcohols via C(sp3)–Si Bond Cleavage
inferred← citeshttps://doi.org/10.1093/nsr/nwx058openalex-snapshot
China's flourishing synthetic organofluorine chemistry: innovations in the new millennium
inferred← citeshttps://doi.org/10.1134/s1070428016100018openalex-snapshot
1-Bromo-3,3,3-trifluoro-1-nitropropene: Synthesis and reaction with phenyl azide
inferred← citeshttps://doi.org/10.3184/174751918x15240724383170openalex-snapshot
Michael Addition of Aryl Thiols to 3-(2,2,2-Trifluoroethylidene)Oxindoles under Catalyst-Free Conditions: The Rapid Synthesis of Sulfur-Containing Oxindole Derivatives
inferred← citeshttps://doi.org/10.3390/molecules21060699openalex-snapshot
The Chiral Pool in the Pictet–Spengler Reaction for the Synthesis of β-Carbolines
inferred← citeshttps://doi.org/10.3390/molecules21081000openalex-snapshot
A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst
inferred← citeshttps://doi.org/10.3390/molecules25020414openalex-snapshot
The Pictet-Spengler Reaction Updates Its Habits
inferred← citeshttps://doi.org/10.3390/molecules26237408openalex-snapshot
Exploiting the Chiral Ligands of Bis(imidazolinyl)- and Bis(oxazolinyl)thiophenes—Synthesis and Application in Cu-Catalyzed Friedel–Crafts Asymmetric Alkylation
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.