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Asymmetric Catalysis of the Friedel−Crafts Reaction with Fluoral by Chiral Binaphthol-Derived Titanium Catalysts through Asymmetric Activation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.199005121openalex-snapshot
Enantioselective Catalysis with a New Zirconium Trichloride Lewis Acid Containing a “Dibornacyclopentadienyl” Ligand
inferredcites →https://doi.org/10.1016/0040-4020(95)00862-3openalex-snapshot
Asymmetric catalysis of carbonyl-ene and aldol reactions with fluoral by chiral binaphthol-derived titanium complex
inferredcites →https://doi.org/10.1016/0040-4039(91)80419-7openalex-snapshot
Remarkably effective and simple syntheses of enantiomerically pure secondary carbinols from achiral ketones
inferredcites →https://doi.org/10.1016/0957-4166(94)80057-xopenalex-snapshot
Selective reductions. 53. Asymmetric reduction of α-fluoromethyl ketones with B-chlorodiisopinocampheylborane and B-isopinocampheyl-9-borabicyclo[3.3.1]nonane. Combined electronic and steric contributions to the enantiocontrol process
inferredcites →https://doi.org/10.1016/0957-4166(94)80059-6openalex-snapshot
Gold(I)-catalyzed asymmetric aldol reactions of fluorinated benzaldehydes with an α-isocyanoacetamide
inferredcites →https://doi.org/10.1016/0957-4166(94)80060-xopenalex-snapshot
Highly stereocontrolled access to trifluoromethylbenzylic alcohols possessing p-substituents by the bakers' yeast reduction
inferredcites →https://doi.org/10.1016/0957-4166(95)00336-nopenalex-snapshot
Highly enantioselective catalysis of the mukaiyama aldol reaction by BINOL-ti perfluorophenoxide and enoxysilacyclobutane
inferredcites →https://doi.org/10.1016/s0040-4020(98)00740-6openalex-snapshot
Catalytic asymmetric synthesis of chiral fluoroorganic compounds
inferredcites →https://doi.org/10.1016/s0040-4039(00)60408-2openalex-snapshot
Asymmetric catalysis of ene-type reaction with fluoral by chiral titanium complex: A semi-empirical and ab-initio analysis of ene reactivity
inferredcites →https://doi.org/10.1016/s0040-4039(00)77013-4openalex-snapshot
Gold(I)-catalyzed asymmetric aldol reaction of methyl isocyanoacetate with fluorinated benzaldehydes
inferredcites →https://doi.org/10.1016/s0040-4039(00)94581-7openalex-snapshot
A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids
inferredcites →https://doi.org/10.1016/s0040-4039(96)02090-4openalex-snapshot
Catalytic asymmetric nitroaldol reaction of α,α-difluoro aldehydes mediated by rare earth-lithium-BINOL complexes
inferredcites →https://doi.org/10.1016/s0040-4039(97)00231-1openalex-snapshot
Asymmetric carbonyl addition reactions to benzyloxyaldehydes by binaphthol-titanium catalyst: Anti- vs. Syn-diastereofacial preference in anomalous nonchelation complexation
inferredcites →https://doi.org/10.1016/s0040-4039(97)01517-7openalex-snapshot
A transition-state model for the mikami enantioselective ene reaction
inferredcites →https://doi.org/10.1016/s0040-4039(97)01658-4openalex-snapshot
Asymmetric Friedel-Crafts reaction mediated by new chiral auxiliaries derived from (1S)-(−)-β-pinene: Enantioselective synthesis of (−)-8-Norethyl, 1′-normethyl Etodolac
inferredcites →https://doi.org/10.1016/s0040-4039(97)01717-6openalex-snapshot
Enantioselective aldol reaction with a bromofluoroketene silyl acetal catalyzed by a chiral Lewis acid
inferredcites →https://doi.org/10.1016/s0957-4166(97)00045-1openalex-snapshot
Importance of chiral activators in the asymmetric catalysis of Diels-Alder reactions by chiral titanium(IV) complexes
inferredcites →https://doi.org/10.1021/bk-1996-0639openalex-snapshot
Biomedical Frontiers of Fluorine Chemistry
inferredcites →https://doi.org/10.1021/ja00166a035openalex-snapshot
Catalytic asymmetric glyoxylate-ene reaction: a practical access to .alpha.-hydroxy esters in high enantiomeric purities
inferredcites →https://doi.org/10.1021/jo00002a082openalex-snapshot
Enantioselective reduction of aryl trifluoromethyl ketones with BINAL-H. A preparation of 2,2,2-trifluoro-1-(9-anthryl)ethanol
inferredcites →https://doi.org/10.1038/385613a0openalex-snapshot
Asymmetric synthesis by enantiomer-selective activation of racemic catalysts
inferredcites →https://doi.org/10.1246/bcsj.54.35openalex-snapshot
Kinetic Studies on Intramolecular Excimer Formation in Dinaphthylalkanes
inferredcites →https://doi.org/10.1351/pac199668030639openalex-snapshot
Asymmetric calysis of carbonyl-ene reactions and related carbon-carbon bond forming reactions
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/10.1002/0471238961.0618090515120108.a01.pub2openalex-snapshot
Friedel‐Crafts Reactions
inferred← citeshttps://doi.org/10.1002/1521-3757(20010105)113:1<164::aid-ange164>3.0.co;2-vopenalex-snapshot
Catalytic Asymmetric Friedel–Crafts Alkylation ofβ,γ-Unsaturatedα-Ketoesters: Enantioselective Addition of Aromatic C−H Bonds to Alkenes
inferred← citeshttps://doi.org/10.1002/1521-3757(20010202)113:3<562::aid-ange562>3.0.co;2-nopenalex-snapshot
Engineering Catalysts for Enantioselective Addition of Diethylzinc to Aldehydes with Racemic Amino Alcohols: Nonlinear Effects in Asymmetric Deactivation of Racemic Catalysts
inferred← citeshttps://doi.org/10.1002/1521-3757(20010917)113:18<3382::aid-ange3382>3.0.co;2-wopenalex-snapshot
Katalysierte asymmetrische Arylierungen
inferred← citeshttps://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.
inferred← citeshttps://doi.org/10.1002/1521-3773(20010202)40:3<544::aid-anie544>3.0.co;2-8openalex-snapshot
Engineering Catalysts for Enantioselective Addition of Diethylzinc to Aldehydes with Racemic Amino Alcohols: Nonlinear Effects in Asymmetric Deactivation of Racemic Catalysts
inferred← citeshttps://doi.org/10.1002/1521-3773(20010917)40:18<3284::aid-anie3284>3.0.co;2-uopenalex-snapshot
Catalyzed Asymmetric Arylation Reactions
inferred← citeshttps://doi.org/10.1002/9780470872215.ch6openalex-snapshot
Transformations of Carbocycles
inferred← citeshttps://doi.org/10.1002/9780470988589.ch7openalex-snapshot
Method for Introduction of Fluorine‐Functionality Into Molecules
inferred← citeshttps://doi.org/10.1002/9781118754887.ch5openalex-snapshot
Catalytic Enantioselective Electrophilic Aromatic Substitutions
inferred← citeshttps://doi.org/10.1002/9783527619405.ch3fopenalex-snapshot
Titanium‐Mediated Reactions
inferred← citeshttps://doi.org/10.1002/9783527619450.ch5openalex-snapshot
C‐H Transformation at Arenes
inferred← citeshttps://doi.org/10.1002/9783527626977.ch3openalex-snapshot
Addition to Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/9783527627325.ch8openalex-snapshot
Modern Arylations of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/9783527675906.ch5openalex-snapshot
Endeavors to Bridge the Gap between Homo‐ and Heterogeneous Asymmetric Catalysis with Organometallics
inferred← citeshttps://doi.org/10.1002/9783527802142.ch2openalex-snapshot
Titanium‐Based Chiral Lewis Acids
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
inferred← citeshttps://doi.org/10.1002/adsc.202200180openalex-snapshot
Asymmetric Organocatalyzed Friedel–Crafts Reaction of Trihaloacetaldehydes and Phenols
inferred← citeshttps://doi.org/10.1002/ange.200301679openalex-snapshot
Neue katalytische Methoden in der stereoselektiven Friedel‐Crafts‐Alkylierung
inferred← citeshttps://doi.org/10.1002/ange.200503305openalex-snapshot
A Copper( II )‐Catalyzed Aza‐Friedel–Crafts Reaction of N‐(2‐Pyridyl)sulfonyl Aldimines: Synthesis of Unsymmetrical Diaryl Amines and Triaryl Methanes
inferred← citeshttps://doi.org/10.1002/anie.200301679openalex-snapshot
New Catalytic Approaches in the Stereoselective Friedel–Crafts Alkylation Reaction
inferred← citeshttps://doi.org/10.1002/anie.200503305openalex-snapshot
A Copper( II )‐Catalyzed Aza‐Friedel–Crafts Reaction of N‐(2‐Pyridyl)sulfonyl Aldimines: Synthesis of Unsymmetrical Diaryl Amines and Triaryl Methanes
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.201000522openalex-snapshot
Catalytic Enantioselective Arylation of Glyoxylate with Arylsilanes: Practical Synthesis of Optically Active Mandelic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/chem.200305707openalex-snapshot
Combinatorial Chemistry Approach to Chiral Catalyst Engineering and Screening: Rational Design and Serendipity
inferred← citeshttps://doi.org/10.1002/chin.200023033openalex-snapshot
ChemInform Abstract: Asymmetric Catalysis of the Friedel—Crafts Reaction with Fluoral by Chiral Binaphthol‐Derived Titanium Catalysts Through Asymmetric Activation.
inferred← citeshttps://doi.org/10.1002/chir.10160openalex-snapshot
Stereospecific substitution at α‐carbon to trifluoromethyl group: Application to optically active fluorinated amino acid syntheses
inferred← citeshttps://doi.org/10.1002/chir.20487openalex-snapshot
Fluorous “racemic” mixture synthesis: Polysaccharide‐based chiral columns for simultaneous demix and enantioseparation of racemic fluorous tagged compounds
inferred← citeshttps://doi.org/10.1002/chir.20982openalex-snapshot
Enantioselective Friedel–Crafts reaction of indoles with trifluoroacetaldehyde catalyzed by Cinchona alkaloids
inferred← citeshttps://doi.org/10.1002/chir.23304openalex-snapshot
A review on Arthrobacter sp. lipase: A versatile biocatalyst for the kinetic resolution to access enantiomerically pure/enriched compounds
inferred← citeshttps://doi.org/10.1002/cjoc.20010190603openalex-snapshot
Engineering Chiral Catalysts through Asymmetric Activation and Super High Throughput Screening (SHTS)
inferred← citeshttps://doi.org/10.1002/cjoc.200790217openalex-snapshot
Solution Structure and Behavior of Benzophenone‐based Achiral Bisphosphine Ligands in Noyori‐Type Ru(II)‐Catalysts
inferred← citeshttps://doi.org/10.1002/ejoc.200600299openalex-snapshot
Complete Chiral Induction from Enantiopure 1,2‐Diamines to Benzophenone‐Based Achiral Bisphosphane Ligands in Noyori‐Type RuII Catalysts
inferred← citeshttps://doi.org/10.1002/ejoc.200700037openalex-snapshot
Fluorous “Racemic” Mixture Synthesis: Simultaneous Strategy for Demixing and Enantioseparation of Racemic Fluorous‐Tagged Products
inferred← citeshttps://doi.org/10.1002/ejoc.200900353openalex-snapshot
Chiral Brønsted‐Acid‐Catalyzed Enantioselective Arylation of Ethyl Trifluoroacetoacetate and Ethyl Trifluoropyruvate
inferred← citeshttps://doi.org/10.1002/ejoc.201001455openalex-snapshot
Enantioselective Friedel–Crafts Alkylation of Thiophenes with Ethyl Glyoxylate: Easy Access to Chiral Secondary Alcohols
inferred← citeshttps://doi.org/10.1002/ejoc.201901049openalex-snapshot
One‐Pot and Reducible‐Functional‐Group‐Tolerant Synthesis of α‐Aryl‐ and α‐Heteroaryl‐α‐Trifluoromethyl Alcohols via Tandem Trifluoroacetylation and MPV Type Reduction
inferred← citeshttps://doi.org/10.1002/jhet.5570380103openalex-snapshot
Convenient substitution of hydroxypyridines with trifluoroacetaldehyde ethyl hemiacetal
inferred← citeshttps://doi.org/10.1002/slct.201700013openalex-snapshot
PTSA‐Catalyzed Reaction of Indoles with 2‐Oxoaldehydes: Synthesis of α,α‐Bis(indol‐3‐yl) Ketones
inferred← citeshttps://doi.org/10.1007/s11426-025-2728-6openalex-snapshot
Trifluoromethylcarbinolation of (hetero)arenes enabled by trifluoromethyl carbyne
inferred← citeshttps://doi.org/10.1016/j.mencom.2018.07.030openalex-snapshot
Room temperature MgI2-catalyzed Friedel–Crafts reaction between electron-rich (het)arenes and ethyl glyoxylate
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.05.038openalex-snapshot
Asymmetric Friedel–Crafts reaction of furans with alkyl glyoxylates catalyzed by (salen)Co(II) complexes
inferred← citeshttps://doi.org/10.1016/j.molcatb.2013.12.014openalex-snapshot
Arthrobacter sp. lipase catalyzed kinetic resolution of BINOL: The effect of substrate immobilization
inferred← citeshttps://doi.org/10.1016/j.tet.2007.10.078openalex-snapshot
C2 and C1 Symmetry of chiral auxiliaries in catalytic reactions on metal complexes
inferred← citeshttps://doi.org/10.1016/j.tet.2008.03.081openalex-snapshot
FeCl3: an efficient catalyst for reactions of electron-rich arenes with imines or aziridines
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.2010.03.019openalex-snapshot
Synthesis and hydrogenation of (E)-γ-aryl-γ-morpholino-α-trifluoromethylated allyl alcohols through the reaction of trifluoroacetaldehyde ethyl hemiacetal with enamines
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.tetasy.2012.11.014openalex-snapshot
Theoretical study of the imidazolidinone catalyzed 1,4-addition of N,N-dimethyl-3-anisidine with α,β-unsaturated butyric aldehyde
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.06.013openalex-snapshot
Catalytic and highly enantioselective Friedel–Crafts type reactions of heteroaromatic compounds with trifluoropyruvate and glyoxylate by a dicationic palladium complex
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.02.054openalex-snapshot
Rapid and convenient synthesis of aryl- and heteroaryl-α-hydroxy-α-trifluoromethyl acetate via Friedel–Crafts alkylation under solvent- and catalyst-free conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.02.009openalex-snapshot
Lewis and Brönsted acid catalyzed Friedel–Crafts hydroxyalkylation of mucohalic acids: a facile synthesis of functionalized γ-aryl γ-butenolides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.06.028openalex-snapshot
Friedel–Crafts alkylation of a cage enone: synthesis of aralkyl substituted tetracyclo[5.3.1.0[2,6].0[4,8]]undeca-9,11-diones and the formation of fascinating novel cage compounds with pyrrole and thiophene using Montmorillonite K-10
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.01.058openalex-snapshot
Unexpected transformation of quinones to spirolactones and to naturally occurring naphthalenic compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.01.015openalex-snapshot
First asymmetric organocatalyzed domino Friedel–Crafts/lactonization reaction in the enantioselective synthesis of the GABAB receptor modulator (S)-BHFF
inferred← citeshttps://doi.org/10.1016/s0022-1139(02)00044-1openalex-snapshot
Convenient synthesis of α-trifluoromethyl amines via aminofluoroalkylation of arenes with N-trimethylsilyl α-trifluoroacetaldehyde hemiaminal
inferred← citeshttps://doi.org/10.1016/s0022-1139(02)00126-4openalex-snapshot
Friedel–Crafts reaction catalyzed by perfluorinated rare earth metals
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)02824-1openalex-snapshot
Furan approach to the synthesis of the A-ring of Vitamin D analogues
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)01400-xopenalex-snapshot
Catalytic enantioselective conjugate addition of indoles to simple α,β-unsaturated ketones
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00414openalex-snapshot
Desymmetrization of Diols by Phosphorylation with a Titanium-BINOLate Catalyst
inferred← citeshttps://doi.org/10.1021/cr0200318openalex-snapshot
Chiral Poisoning and Asymmetric Activation
inferred← citeshttps://doi.org/10.1021/cr030685wopenalex-snapshot
Fluorinated Carbonyl and Olefinic Compounds: Basic Character and Asymmetric Catalytic Reactions
inferred← citeshttps://doi.org/10.1021/cr078004aopenalex-snapshot
Update 1 of: BINOL: A Versatile Chiral Reagent
inferred← citeshttps://doi.org/10.1021/cr078372eopenalex-snapshot
Catalytic Asymmetric Friedel−Crafts Alkylation Reactions—Copper Showed the Way
inferred← citeshttps://doi.org/10.1021/cr100166aopenalex-snapshot
Asymmetric Construction of Stereogenic Carbon Centers Featuring a Trifluoromethyl Group from Prochiral Trifluoromethylated Substrates
inferred← citeshttps://doi.org/10.1021/ja002593jopenalex-snapshot
Catalytic Enantioselective Friedel−Crafts Reactions of Aromatic Compounds with Glyoxylate: A Simple Procedure for the Synthesis of Optically Active Aromatic Mandelic Acid Esters
inferred← citeshttps://doi.org/10.1021/jo001176mopenalex-snapshot
Catalytic, Highly Enantioselective Friedel−Crafts Reactions of Aromatic and Heteroaromatic Compounds to Trifluoropyruvate. A Simple Approach for the Formation of Optically Active Aromatic and Heteroaromatic Hydroxy Trifluoromethyl Esters
inferred← citeshttps://doi.org/10.1021/jo0256235openalex-snapshot
InBr3-Catalyzed Friedel−Crafts Addition of Indoles to Chiral Aromatic Epoxides: A Facile Route to Enantiopure Indolyl Derivatives
inferred← citeshttps://doi.org/10.1021/jo0256787openalex-snapshot
Optically Active Aromatic and Heteroaromatic α-Amino Acids by a One-Pot Catalytic Enantioselective Addition of Aromatic and Heteroaromatic C−H Bonds to α-Imino Esters
inferred← citeshttps://doi.org/10.1021/jo034992dopenalex-snapshot
Highly Enantioselective Friedel−Crafts Reaction of Aromatic Amines with Ethyl Glyoxylate Catalyzed by Chiral Titanium(IV) Complexes: Practical Synthesis of Aminomandelic Acid Derivatives
inferred← citeshttps://doi.org/10.1021/jo052041popenalex-snapshot
Catalytic Enantioselective Friedel−Crafts/Michael Addition Reactions of Indoles to Ethenetricarboxylates
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/jo101155copenalex-snapshot
Furan Approach to Vitamin D Analogues. Synthesis of the A-Ring of Calcitriol and 1α-Hydroxy-3-deoxyvitamin D3
inferred← citeshttps://doi.org/10.1021/jo200020zopenalex-snapshot
Organocatalytic Asymmetric Direct Aldol Reactions of Trifluoroacetaldehyde Ethyl Hemiacetal with Aromatic Methyl Ketones
inferred← citeshttps://doi.org/10.1021/jo3013594openalex-snapshot
NMR Spectroscopic Characterization and DFT Calculations of Zirconium(IV)-3,3′-Br2–BINOLate and Related Complexes Used in an Enantioselective Friedel–Crafts Alkylation of Indoles with α,β-Unsaturated Ketones
inferred← citeshttps://doi.org/10.1021/jp011485wopenalex-snapshot
Vibrational Circular Dichroism of 1,1‘-Binaphthyl Derivatives: Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1021/jp070662bopenalex-snapshot
UV Near-Resonance Raman Spectroscopic Study of 1,1‘-Bi-2-naphthol Solutions
inferred← citeshttps://doi.org/10.1021/ol050568iopenalex-snapshot
N-Heterocyclic Carbene Catalyzed Trifluoromethylation of Carbonyl Compounds
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/ol0626037openalex-snapshot
Catalytic and Highly Enantioselective Friedel−Crafts Alkylation of Aromatic Ethers with Trifluoropyruvate under Solvent-Free Conditions
inferred← citeshttps://doi.org/10.1021/ol102987nopenalex-snapshot
Organocatalytic Enantioselective Friedel−Crafts Reactions of 1-Naphthols with Aldimines
inferred← citeshttps://doi.org/10.1021/ol201669aopenalex-snapshot
Fluoroanalogs of DDT: Superacidic BF3–H2O Catalyzed Facile Synthesis of 1,1,1-Trifluoro-2,2-diarylethanes and 1,1-Difluoro-2,2-diarylethanes
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/ol800927wopenalex-snapshot
Highly Enantioselective Synthesis of 2-Furanyl-hydroxyacetates from Furans via the Friedel−Crafts Reaction
inferred← citeshttps://doi.org/10.1021/ol901906ropenalex-snapshot
Highly Enantioselective Friedel−Crafts Reaction of Thiophenes with Glyoxylates: Formal Synthesis of Duloxetine
inferred← citeshttps://doi.org/10.1039/b009008popenalex-snapshot
Catalytic enantioselective alkylation of heteroaromatic compounds using alkylidene malonates
inferred← citeshttps://doi.org/10.1039/b009669popenalex-snapshot
Studies on aluminium mediated asymmetric Friedel–Crafts hydroxyalkylation reactions of pyridinecarbaldehydes
inferred← citeshttps://doi.org/10.1039/b408728copenalex-snapshot
A Lewis acid-promoted cyclization of ethenetricarboxylate derivative aromatic compounds. Novel syntheses of oxindoles and benzofuranones via Friedel–Crafts intramolecular Michael addition
inferred← citeshttps://doi.org/10.1039/b911534jopenalex-snapshot
Facile preparation of CF3-substituted carbinols with an azine donor and subsequent kinetic resolution through stereoselective Si–O coupling
inferred← citeshttps://doi.org/10.1039/c2nj40871fopenalex-snapshot
Friedel–Crafts hydroxyalkylation through activation of a carbonyl group using AlBr3: an easy access to pyridyl aryl/heteroaryl carbinols
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/c4ob02597kopenalex-snapshot
The cooperative effect of Lewis pairs in the Friedel–Crafts hydroxyalkylation reaction: a simple and effective route for the synthesis of (±)-carbinoxamine
inferred← citeshttps://doi.org/10.1073/pnas.0601687103openalex-snapshot
Cu-catalyzed cross-dehydrogenative coupling: A versatile strategy for C–C bond formations via the oxidative activation of sp 3 C–H bonds
inferred← citeshttps://doi.org/10.1080/00397911.2010.516860openalex-snapshot
TiCl4-Catalyzed Friedel–Crafts Reaction of Trifluoroacetaldehyde Ethyl Hemiacetal (TFAE)
inferred← citeshttps://doi.org/10.1080/00397911.2020.1786121openalex-snapshot
Asymmetric oxidation of sulfides catalyzed by (R)-6,6'-dibromo-BINOL derived titanium complex
inferred← citeshttps://doi.org/10.1088/1674-0068/21/04/367-375openalex-snapshot
DFT Study on the Structure and Racemization Mechanism of 1,1-Binaphthalene-8,8-diol
inferred← citeshttps://doi.org/10.1246/bcsj.74.377openalex-snapshot
Regioselective Substitution of Phenols with Trifluoroacetaldehyde Ethyl Hemiacetal
inferred← citeshttps://doi.org/10.17721/fujcv13i1p98-103openalex-snapshot
Enantioselective Catalyzed Addition of Substituted Indens to Unsaturated Epoxides
inferred← citeshttps://doi.org/10.3390/molecules26092757openalex-snapshot
Recommended Tests for the Self-Disproportionation of Enantiomers (SDE) to Ensure Accurate Reporting of the Stereochemical Outcome of Enantioselective Reactions
inferred← citeshttps://doi.org/10.3987/com-12-12556openalex-snapshot
RUTHENIUM PORPHYRIN CATALYZED FRIEDEL–CRAFTS TYPE REACTION OF ARENES WITH IMINES
inferred← citeshttps://doi.org/10.6023/cjoc202303010openalex-snapshot
Recent Progress in the Construction of Chiral 3-Substituted Indoles by Asymmetric Friedel-Crafts Reactions
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