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High-Yielding, Versatile, and Practical [Rh(III)Cp*]-Catalyzed Ortho Bromination and Iodination of Arenes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9783527612222openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/adsc.200900778openalex-snapshot
Palladium‐Catalyzed Monoselective Halogenation of CH Bonds: Efficient Access to Halogenated Arylpyrimidines using Calcium Halides
inferredcites →https://doi.org/10.1002/adsc.201100232openalex-snapshot
Grignard‐Type Arylation of Aldehydes via a Rhodium‐Catalyzed CH Activation under Mild Conditions
inferredcites →https://doi.org/10.1002/anie.200462884openalex-snapshot
Palladium‐Catalyzed Asymmetric Iodination of Unactivated CH Bonds under Mild Conditions
inferredcites →https://doi.org/10.1002/anie.200705613openalex-snapshot
Pd II ‐Catalyzed Monoselective ortho Halogenation of CH Bonds Assisted by Counter Cations: A Complementary Method to Directed ortho Lithiation
inferredcites →https://doi.org/10.1002/anie.200800924openalex-snapshot
Fluorescent Naphthyl‐ and Anthrylazoles from the Catalytic Coupling of Phenylazoles with Internal Alkynes through the Cleavage of Multiple CH Bonds
inferredcites →https://doi.org/10.1002/anie.200802187openalex-snapshot
Synthesis of Indolines and Tetrahydroisoquinolines from Arylethylamines by Pd II ‐Catalyzed CH Activation Reactions
inferredcites →https://doi.org/10.1002/anie.200806273openalex-snapshot
Palladium(II)‐Catalyzed CH Activation/CC Cross‐Coupling Reactions: Versatility and Practicality
inferredcites →https://doi.org/10.1002/anie.200902996openalex-snapshot
Transition‐Metal‐Catalyzed Direct Arylation of (Hetero)Arenes by CH Bond Cleavage
inferredcites →https://doi.org/10.1002/anie.201006222openalex-snapshot
Rhodium‐Catalyzed Oxidative Olefination of CH Bonds in Acetophenones and Benzamides
inferredcites →https://doi.org/10.1002/anie.201006381openalex-snapshot
The Vinyl Moiety as a Handle for Regiocontrol in the Preparation of Unsymmetrical 2,3‐Aliphatic‐Substituted Indoles and Pyrroles
inferredcites →https://doi.org/10.1002/anie.201007464openalex-snapshot
Rhodium‐Catalyzed Direct Addition of Aryl CH Bonds to N‐Sulfonyl Aldimines
inferredcites →https://doi.org/10.1002/anie.201101606openalex-snapshot
Mild CH Halogenation of Anilides and the Isolation of an Unusual Palladium(I)–Palladium(II) Species
inferredcites →https://doi.org/10.1002/anie.201107334openalex-snapshot
On the Interpretation of Deuterium Kinetic Isotope Effects in CH Bond Functionalizations by Transition‐Metal Complexes
inferredcites →https://doi.org/10.1002/anie.201107842openalex-snapshot
[RhIIICp*]‐Catalyzed Dehydrogenative ArylAryl Bond Formation
inferredcites →https://doi.org/10.1002/asia.201101018openalex-snapshot
Undirected Arene and Chelate‐Assisted Olefin C‐H Bond Activation: [Rh III Cp*]‐Catalyzed Dehydrogenative Alkene–Arene Coupling as a New Pathway for the Selective Synthesis of Highly Substituted Z Olefins
inferredcites →https://doi.org/10.1002/chem.201001363openalex-snapshot
Oxidative Coupling of Aromatic Substrates with Alkynes and Alkenes under Rhodium Catalysis
inferredcites →https://doi.org/10.1002/chem.201101340openalex-snapshot
Rh III ‐Catalyzed Oxidative Olefination of Vinylic CH Bonds: Efficient and Selective Access to Di‐unsaturated α‐Amino Acid Derivatives and Other Linear 1,3‐Butadienes
inferredcites →https://doi.org/10.1016/b978-0-323-95948-3.00001-5openalex-snapshot
Organic reaction mechanism
inferredcites →https://doi.org/10.1016/j.tet.2006.06.075openalex-snapshot
Scope and selectivity in palladium-catalyzed directed C–H bond halogenation reactions
inferredcites →https://doi.org/10.1021/ar200185gopenalex-snapshot
Weak Coordination as a Powerful Means for Developing Broadly Useful C–H Functionalization Reactions
inferredcites →https://doi.org/10.1021/ar200190gopenalex-snapshot
Rhodium Catalyzed Chelation-Assisted C–H Bond Functionalization Reactions
inferredcites →https://doi.org/10.1021/ar800164nopenalex-snapshot
Cross-Dehydrogenative Coupling (CDC): Exploring C−C Bond Formations beyond Functional Group Transformations
inferredcites →https://doi.org/10.1021/cr0509760openalex-snapshot
Aryl−Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation
inferredcites →https://doi.org/10.1021/cr100280dopenalex-snapshot
Catalytic Dehydrogenative Cross-Coupling: Forming Carbon−Carbon Bonds by Oxidizing Two Carbon−Hydrogen Bonds
inferredcites →https://doi.org/10.1021/cr900005nopenalex-snapshot
Rhodium-Catalyzed C−C Bond Formation via Heteroatom-Directed C−H Bond Activation
inferredcites →https://doi.org/10.1021/cr900184eopenalex-snapshot
Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions
inferredcites →https://doi.org/10.1021/ja031543mopenalex-snapshot
A Highly Selective Catalytic Method for the Oxidative Functionalization of C−H Bonds
inferredcites →https://doi.org/10.1021/ja060232jopenalex-snapshot
Highly Selective C−H Functionalization/Halogenation of Acetanilide
inferredcites →https://doi.org/10.1021/ja077866qopenalex-snapshot
Reactivity of Pd(II) Complexes with Electrophilic Chlorinating Reagents: Isolation of Pd(IV) Products and Observation of C−Cl Bond-Forming Reductive Elimination
inferredcites →https://doi.org/10.1021/ja103776uopenalex-snapshot
Rhodium-Catalyzed Oxidative Cycloaddition of Benzamides and Alkynes via C−H/N−H Activation
inferredcites →https://doi.org/10.1021/ja103834bopenalex-snapshot
Rh Catalyzed Olefination and Vinylation of Unactivated Acetanilides
inferredcites →https://doi.org/10.1021/ja104305sopenalex-snapshot
Pyrrole Synthesis via Allylic sp3 C−H Activation of Enamines Followed by Intermolecular Coupling with Unactivated Alkynes
inferredcites →https://doi.org/10.1021/ja109562xopenalex-snapshot
Rhodium(III)-Catalyzed Arylation of Boc-Imines via C−H Bond Functionalization
inferredcites →https://doi.org/10.1021/ja109676dopenalex-snapshot
Rh(III)-Catalyzed Directed C−H Olefination Using an Oxidizing Directing Group: Mild, Efficient, and Versatile
inferredcites →https://doi.org/10.1021/ja110650mopenalex-snapshot
Diverse Strategies toward Indenol and Fulvene Derivatives: Rh-Catalyzed C−H Activation of Aryl Ketones Followed by Coupling with Internal Alkynes
inferredcites →https://doi.org/10.1021/ja201143vopenalex-snapshot
Rhodium(III)-Catalyzed Heterocycle Synthesis Using an Internal Oxidant: Improved Reactivity and Mechanistic Studies
inferredcites →https://doi.org/10.1021/ja203495copenalex-snapshot
Expedient Synthesis of N-Acyl Anthranilamides and β-Enamine Amides by the Rh(III)-Catalyzed Amidation of Aryl and Vinyl C–H Bonds with Isocyanates
inferredcites →https://doi.org/10.1021/ja205228yopenalex-snapshot
Pyridinyl Directed Alkenylation with Olefins via Rh(III)-Catalyzed C–C Bond Cleavage of Secondary Arylmethanols
inferredcites →https://doi.org/10.1021/ja900200gopenalex-snapshot
Palladium-Catalyzed C−H Bond Functionalization with Arylsulfonyl Chlorides
inferredcites →https://doi.org/10.1021/ja9049228openalex-snapshot
Palladium-Catalyzed Aromatic C−H Halogenation with Hydrogen Halides by Means of Electrochemical Oxidation
inferredcites →https://doi.org/10.1021/jo1021184openalex-snapshot
Rhodium-Catalyzed Oxidative 1:1, 1:2, and 1:4 Coupling Reactions of Phenylazoles with Internal Alkynes through the Regioselective Cleavages of Multiple C−H Bonds
inferredcites →https://doi.org/10.1021/jo2002209openalex-snapshot
Oxidative Coupling of NH Isoquinolones with Olefins Catalyzed by Rh(III)
inferredcites →https://doi.org/10.1021/jo200339wopenalex-snapshot
Synthesis of Highly Substituted Acenes through Rhodium-Catalyzed Oxidative Coupling of Arylboron Reagents with Alkynes
inferredcites →https://doi.org/10.1021/jo200509mopenalex-snapshot
Rhodium-Catalyzed Regioselective Olefination Directed by a Carboxylic Group
inferredcites →https://doi.org/10.1021/jo200853jopenalex-snapshot
Selective ortho-Bromination of Substituted Benzaldoximes Using Pd-Catalyzed C–H Activation: Application to the Synthesis of Substituted 2-Bromobenzaldehydes
inferredcites →https://doi.org/10.1021/jo201530ropenalex-snapshot
Rhodium(III)-Catalyzed Oxidative Coupling of 5-Aryl-1 H -pyrazoles with Alkynes and Acrylates
inferredcites →https://doi.org/10.1021/jo901485vopenalex-snapshot
Rhodium-Catalyzed Mono- and Divinylation of 1-Phenylpyrazoles and Related Compounds via Regioselective C−H Bond Cleavage
inferredcites →https://doi.org/10.1021/ol060747fopenalex-snapshot
A Simple Catalytic Method for the Regioselective Halogenation of Arenes
inferredcites →https://doi.org/10.1021/ol070406hopenalex-snapshot
An Efficient Waste-Free Oxidative Coupling via Regioselective C−H Bond Cleavage: Rh/Cu-Catalyzed Reaction of Benzoic Acids with Alkynes and Acrylates under Air
inferredcites →https://doi.org/10.1021/ol1010483openalex-snapshot
Expedient Drug Synthesis and Diversification via ortho-C−H Iodination using Recyclable PdI 2 as the Precatalyst
inferredcites →https://doi.org/10.1021/ol102241fopenalex-snapshot
Rh(III)-Catalyzed Tandem Oxidative Olefination−Michael Reactions between Aryl Carboxamides and Alkenes
inferredcites →https://doi.org/10.1021/ol1022596openalex-snapshot
Rh(III)-Catalyzed Oxidative Coupling of N-Aryl-2-aminopyridine with Alkynes and Alkenes
inferredcites →https://doi.org/10.1021/ol102504bopenalex-snapshot
Rhodium(III)-Catalyzed Synthesis of Isoquinolines from Aryl Ketone O-Acyloxime Derivatives and Internal Alkynes
inferredcites →https://doi.org/10.1021/ol102890kopenalex-snapshot
Rh(III)-Catalyzed Oxidative Coupling of Unactivated Alkenes via C−H Activation
inferredcites →https://doi.org/10.1021/ol200600popenalex-snapshot
Rhodium-Catalyzed Selective Olefination of Arene Esters via C−H Bond Activation
inferredcites →https://doi.org/10.1021/ol201729wopenalex-snapshot
Rhodium-Catalyzed Oxidative ortho-Acylation of Benzamides with Aldehydes: Direct Functionalization of the sp2 C–H Bond
inferredcites →https://doi.org/10.1021/ol202557wopenalex-snapshot
Rh Catalyzed C–H Activation and Oxidative Olefination without Chelate Assistance: On the Reactivity of Bromoarenes
inferredcites →https://doi.org/10.1021/ol203353aopenalex-snapshot
Rh[III]-Catalyzed Direct C–H Amination Using N-Chloroamines at Room Temperature
inferredcites →https://doi.org/10.1021/om070095eopenalex-snapshot
Reactions of Platinum(II) Complexes with Chloride-Based Oxidants: Routes to Pt(III) and Pt(IV) Products
inferredcites →https://doi.org/10.1039/b816707aopenalex-snapshot
Transition metal-catalyzed C–H activation reactions: diastereoselectivity and enantioselectivity
inferredcites →https://doi.org/10.1039/b908581eopenalex-snapshot
Pd-catalyzed oxidative coupling with organometallic reagents via C–H activation
inferredcites →https://doi.org/10.1039/c0cc05557copenalex-snapshot
Copper(ii)-catalyzed ortho-functionalization of 2-arylpyridines with acyl chlorides
inferredcites →https://doi.org/10.1039/c0dt00385aopenalex-snapshot
Solvent-free aromatic C–H functionalisation/halogenation reactions
inferredcites →https://doi.org/10.1039/c1cs15083aopenalex-snapshot
Towards mild metal-catalyzed C–H bond activation
inferredcites →https://doi.org/10.1039/c1ob05636kopenalex-snapshot
Investigating N-methoxy-N′-aryl ureas in oxidative C–H olefination reactions: an unexpected oxidation behaviour
inferredcites →https://doi.org/10.1055/s-2008-1067256openalex-snapshot
Transition-Metal-Catalyzed Carbon-Carbon Bond Formation via Carbon-Hydrogen Bond Cleavage
inferredcites →https://doi.org/10.1246/cl.2010.744openalex-snapshot
Rhodium-catalyzed Oxidative Coupling/Cyclization of Benzamides with Alkynes via C–H Bond Cleavage
inferredcites →https://doi.org/10.2174/1385272033372987openalex-snapshot
Aryl and Heteroaryllithium Compounds by Metal - Halogen Exchange. Synthesis of Carbocyclic and Heterocyclic Systems
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.4187024openalex-extracted
Selective Pyridine-Directed C-H Activations Enabled Synthesis of Pyridine-Pyridone Α-Helix Mimics
inferred← citeshttps://doi.org/10.1002/9781118754887.ch23openalex-snapshot
Chelate‐Assisted Arene C–H Bond Functionalization
inferred← citeshttps://doi.org/10.1002/9781118788981.ch6openalex-snapshot
Homogeneous Transition‐Metal‐Catalyzed C–H Bond Functionalization
inferred← citeshttps://doi.org/10.1002/9783527346028.ch8openalex-snapshot
Theoretical Study of Rh ‐Catalysis
inferred← citeshttps://doi.org/10.1002/9783527687800.ch5openalex-snapshot
Electrophilic Halogenation of Arenes
inferred← citeshttps://doi.org/10.1002/9783527811908.ch19openalex-snapshot
Rhodium( III )‐Catalyzed Non‐annulative Carbon–Hydrogen Bond Functionalization
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0024openalex-snapshot
Rhodium‐Catalyzed CH Halogenation
inferred← citeshttps://doi.org/10.1002/adsc.201200902openalex-snapshot
Palladium‐Catalyzed Regioselective Halogenation of Aromatic Azo Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201300581openalex-snapshot
Nitrogen Dioxide‐Catalyzed Electrophilic Iodination of Arenes
inferred← citeshttps://doi.org/10.1002/adsc.201300999openalex-snapshot
A General Approach towards Catechol and Pyrogallol through Ruthenium‐ and Palladium‐Catalyzed CH Hydroxylation by Weak Coordination
inferred← citeshttps://doi.org/10.1002/adsc.201400197openalex-snapshot
Formal SN‐Type Reactions in Rhodium(III)‐Catalyzed CH Bond Activation
inferred← citeshttps://doi.org/10.1002/adsc.201400198openalex-snapshot
Rhodium‐Catalyzed Direct Oxidative CH Acylation of 2‐Arylpyridines with Terminal Alkynes: A Synthesis of Pyrido[2,1‐a]isoindoles
inferred← citeshttps://doi.org/10.1002/adsc.201400590openalex-snapshot
Sodium Halides as Halogenating Reagents: Rhodium(III)‐Catalyzed Versatile and Practical Halogenation of Aryl Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201400798openalex-snapshot
Rhodium(III)‐Catalyzed ortho‐Arylation of Anilides with Aryl Halides
inferred← citeshttps://doi.org/10.1002/adsc.201400810openalex-snapshot
Arylmethyl Chlorides: New Bifunctional Reagents for Palladium‐Catalyzed ortho‐Chlorination and Acylation of 2‐Arylpyridines
inferred← citeshttps://doi.org/10.1002/adsc.201600177openalex-snapshot
Nickel(II)‐Mediated Regioselective CH Monoiodination of Arenes and Heteroarenes by using Molecular Iodine
inferred← citeshttps://doi.org/10.1002/adsc.201601308openalex-snapshot
Rhodium(III)‐Catalyzed Controllable C−H Bond Functionalization of Benzamides and Vinylidenecyclopropanes: A Directing Group Determined Reaction Pathway
inferred← citeshttps://doi.org/10.1002/adsc.202300971openalex-snapshot
Regioselective Organocatalyzed Monochlorination of Arenes with Electrophilic Chlorosulfoniums
inferred← citeshttps://doi.org/10.1002/ajoc.201300294openalex-snapshot
Synthesis of Substituted Pyrazoles from Vinylhydrozones via Bromoamination and Hydroamination with 2,2,6,6‐Tetramethylpiperidine‐1‐oxyl and N‐Bromosuccinimide
inferred← citeshttps://doi.org/10.1002/ajoc.201402140openalex-snapshot
Palladium‐Catalyzed Desulfinative Iodination of Sodium Sulfinates and Sulfonyl Hydrazides
inferred← citeshttps://doi.org/10.1002/ajoc.201500245openalex-snapshot
Heterogeneous Cu‐MnO Catalyzed Monoselective ortho ‐Halogenation of Aromatic C−H Bonds under Visible Light
inferred← citeshttps://doi.org/10.1002/ajoc.201500294openalex-snapshot
One‐Pot Synthesis of 3‐Iminoisoindolinones by a Rhodium(III)‐Catalyzed and Methanol‐Assisted C−H Cyanation–Cyclization Cascade with N‐Alkoxyl Transfer
inferred← citeshttps://doi.org/10.1002/ajoc.201600028openalex-snapshot
Pd‐Catalyzed Late‐Stage Monoacetoxylation and Monoiodination of 4‐Alkyl‐1,5‐diaryl‐1 H‐pyrazole‐3‐carboxylates via Direct Csp2−H Bond Activation
inferred← citeshttps://doi.org/10.1002/ajoc.201600259openalex-snapshot
RhIII‐Catalyzed Directed C−H Bromination and Iodination to Synthesize Atropisomeric Biaryls
inferred← citeshttps://doi.org/10.1002/ajoc.201700238openalex-snapshot
Palladium‐Catalyzed ortho‐Halogenation of Tertiary Benzamides
inferred← citeshttps://doi.org/10.1002/ajoc.201700620openalex-snapshot
Regioselective Chlorination of Aryl C−H bonds with Hypervalent Iodine(III) Reagent 1‐Chloro‐1,2‐benziodoxol‐3‐one
inferred← citeshttps://doi.org/10.1002/ajoc.201800142openalex-snapshot
Transition‐Metal‐Catalyzed Site‐Selective C−H Halogenation Reactions
inferred← citeshttps://doi.org/10.1002/ajoc.201800452openalex-snapshot
Developments in Cp*CoIII‐Catalyzed C−H Bond Functionalizations
inferred← citeshttps://doi.org/10.1002/ajoc.202200060openalex-snapshot
Recent Advances in First‐Row Transition‐Metal‐Mediated C−H Halogenation of (Hetero)arenes and Alkanes
inferred← citeshttps://doi.org/10.1002/ajoc.70403openalex-snapshot
Copper‑Mediated Ortho ‑C─H Halogenation of Arylaldehydes Enabled by a Transient Directing Group
inferred← citeshttps://doi.org/10.1002/ange.201203269openalex-snapshot
Ohne dirigierende Gruppen: übergangsmetallkatalysierte C‐H‐Aktivierung einfacher Arene
inferred← citeshttps://doi.org/10.1002/ange.201203792openalex-snapshot
Selektive Rhodium(III)‐katalysierte gekreuzte dehydrierende Kupplung von Furan‐ und Thiophenderivaten
inferred← citeshttps://doi.org/10.1002/ange.201204970openalex-snapshot
Rhodium(III)‐Catalyzed Intramolecular Annulation through CH Activation: Total Synthesis of (±)‐Antofine, (±)‐Septicine, (±)‐Tylophorine, and Rosettacin
inferred← citeshttps://doi.org/10.1002/ange.201205723openalex-snapshot
Rhodium‐Catalyzed Direct CH Amination of Benzamides with Aryl Azides: A Synthetic Route to Diarylamines
inferred← citeshttps://doi.org/10.1002/ange.201205734openalex-snapshot
Rhodium(III) und Hexabrombenzol – ein Katalysatorsystem zur gekreuzten dehydrierenden Kupplung einfacher Arene und Heterocyclen mit Arenen mit dirigierenden Gruppen
inferred← citeshttps://doi.org/10.1002/ange.201206191openalex-snapshot
Access to Sultams by Rhodium(III)‐Catalyzed Directed CH Activation
inferred← citeshttps://doi.org/10.1002/ange.201207479openalex-snapshot
Synthesis of ortho‐Acylphenols through the Palladium‐Catalyzed Ketone‐Directed Hydroxylation of Arenes
inferred← citeshttps://doi.org/10.1002/ange.201209887openalex-snapshot
Rhodium(III)‐Catalyzed CC Coupling between Arenes and Aziridines by CH Activation
inferred← citeshttps://doi.org/10.1002/ange.201300176openalex-snapshot
Regio‐ and Chemoselective CH Chlorination/Bromination of Electron‐Deficient Arenes by Weak Coordination and Study of Relative Directing‐Group Abilities
inferred← citeshttps://doi.org/10.1002/ange.201301165openalex-snapshot
Milde Rhodium(III)‐katalysierte direkte C‐H‐Allylierung von Arenen mit Allylcarbonaten
inferred← citeshttps://doi.org/10.1002/ange.201301426openalex-snapshot
Milde Rhodium(III)‐katalysierte Cyclisierung von Amiden mit α,β‐ungesättigten Aldehyden und Ketonen zu Azepinonen: Anwendung in der Synthese des Homoprotoberberin‐Gerüsts
inferred← citeshttps://doi.org/10.1002/ange.201302784openalex-snapshot
Direct CH Amination of Arenes with Alkyl Azides under Rhodium Catalysis
inferred← citeshttps://doi.org/10.1002/ange.201304884openalex-snapshot
Twofold Unsymmetrical CH Functionalization of PyrDipSi‐Substituted Arenes: A General Method for the Synthesis of Substituted meta‐Halophenols
inferred← citeshttps://doi.org/10.1002/ange.201306754openalex-snapshot
[3]Dendralensynthese: Rhodium(III)‐katalysierte Alkenyl‐C‐H‐ Aktivierung und Kupplungsreaktion mit Allenylcarbinolcarbonat
inferred← citeshttps://doi.org/10.1002/ange.201309198openalex-snapshot
Rhodium‐Catalyzed CH Alkynylation of Arenes at Room Temperature
inferred← citeshttps://doi.org/10.1002/ange.201406747openalex-snapshot
Rhodium(III)‐Catalyzed CC and CO Coupling of Quinoline N‐Oxides with Alkynes: Combination of CH Activation with O‐Atom Transfer
inferred← citeshttps://doi.org/10.1002/ange.201502278openalex-snapshot
Diaryliodoniums by Rhodium(III)‐Catalyzed CH Activation: Mild Synthesis and Diversified Functionalizations
inferred← citeshttps://doi.org/10.1002/ange.201504390openalex-snapshot
Ruthenium‐Catalyzed meta‐Selective CH Bromination
inferred← citeshttps://doi.org/10.1002/ange.201607388openalex-snapshot
Highly ortho‐Selective Chlorination of Anilines Using a Secondary Ammonium Salt Organocatalyst
inferred← citeshttps://doi.org/10.1002/ange.201610117openalex-snapshot
Kombination von Cp*RhIII‐katalysierter C‐H‐Aktivierung mit einer Variante der Wagner‐Meerwein‐Umlagerung
inferred← citeshttps://doi.org/10.1002/ange.201611757openalex-snapshot
Synthesis of Active Hexafluoroisopropyl Benzoates through a Hydrogen‐Bond‐Enabled Palladium(II)‐Catalyzed C−H Alkoxycarbonylation Reaction
inferred← citeshttps://doi.org/10.1002/ange.201800549openalex-snapshot
Zum europäischen Verbot von 1,2‐Dichlorethan: Chancen für die Forschung zur C‐H‐Aktivierung
inferred← citeshttps://doi.org/10.1002/ange.201804528openalex-snapshot
Oxidative C−H/C−H Cross‐Coupling Reactions between N‐Acylanilines and Benzamides Enabled by a Cp*‐Free RhCl3/TFA Catalytic System
inferred← citeshttps://doi.org/10.1002/ange.201808159openalex-snapshot
Rhodiumkatalysierte sp2‐ und sp3‐C‐H‐Funktionalisierungen mit entfernbaren dirigierenden Gruppen
inferred← citeshttps://doi.org/10.1002/ange.201809657openalex-snapshot
Synthesis of Polysubstituted Iodoarenes Enabled by Iterative Iodine‐Directed para and ortho C−H Functionalization
inferred← citeshttps://doi.org/10.1002/ange.201908418openalex-snapshot
The Power of Iodane‐Guided C−H Coupling: A Group‐Transfer Strategy in Which a Halogen Works for Its Money
inferred← citeshttps://doi.org/10.1002/ange.202003595openalex-snapshot
A Chemistry for Incorporation of Selenium into DNA‐Encoded Libraries
inferred← citeshttps://doi.org/10.1002/ange.202300905openalex-snapshot
Palladium‐Catalyzed Enantioselective Isodesmic C−H Iodination of Phenylacetic Weinreb Amides
inferred← citeshttps://doi.org/10.1002/ange.202305983openalex-snapshot
Regio‐ and Chemoselective Formal (4+1) Carbocyclization of Chalcones with Internal Alkynes via Rhodium(III) Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202424183openalex-snapshot
Silylation of Aryl and Alkyl Chlorides by a Seven‐Membered Dialkoxysilyl Group Si(pan)Me via an In Situ Generated Silylpotassium
inferred← citeshttps://doi.org/10.1002/anie.201203269openalex-snapshot
Beyond Directing Groups: Transition‐Metal‐Catalyzed CH Activation of Simple Arenes
inferred← citeshttps://doi.org/10.1002/anie.201203792openalex-snapshot
Selective Rhodium(III)‐Catalyzed Cross‐Dehydrogenative Coupling of Furan and Thiophene Derivatives
inferred← citeshttps://doi.org/10.1002/anie.201204970openalex-snapshot
Rhodium(III)‐Catalyzed Intramolecular Annulation through CH Activation: Total Synthesis of (±)‐Antofine, (±)‐Septicine, (±)‐Tylophorine, and Rosettacin
inferred← citeshttps://doi.org/10.1002/anie.201205723openalex-snapshot
Rhodium‐Catalyzed Direct CH Amination of Benzamides with Aryl Azides: A Synthetic Route to Diarylamines
inferred← citeshttps://doi.org/10.1002/anie.201205734openalex-snapshot
Rhodium(III) and Hexabromobenzene—A Catalyst System for the Cross‐Dehydrogenative Coupling of Simple Arenes and Heterocycles with Arenes Bearing Directing Groups
inferred← citeshttps://doi.org/10.1002/anie.201206191openalex-snapshot
Access to Sultams by Rhodium(III)‐Catalyzed Directed CH Activation
inferred← citeshttps://doi.org/10.1002/anie.201207479openalex-snapshot
Synthesis of ortho ‐Acylphenols through the Palladium‐Catalyzed Ketone‐Directed Hydroxylation of Arenes
inferred← citeshttps://doi.org/10.1002/anie.201209887openalex-snapshot
Rhodium(III)‐Catalyzed CC Coupling between Arenes and Aziridines by CH Activation
inferred← citeshttps://doi.org/10.1002/anie.201300176openalex-snapshot
Regio‐ and Chemoselective CH Chlorination/Bromination of Electron‐Deficient Arenes by Weak Coordination and Study of Relative Directing‐Group Abilities
inferred← citeshttps://doi.org/10.1002/anie.201301165openalex-snapshot
Mild Rhodium(III)‐Catalyzed Direct CH Allylation of Arenes with Allyl Carbonates
inferred← citeshttps://doi.org/10.1002/anie.201301426openalex-snapshot
Mild Rhodium(III)‐Catalyzed Cyclization of Amides with α,β‐Unsaturated Aldehydes and Ketones to Azepinones: Application to the Synthesis of the Homoprotoberberine Framework
inferred← citeshttps://doi.org/10.1002/anie.201302784openalex-snapshot
Direct CH Amination of Arenes with Alkyl Azides under Rhodium Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201304884openalex-snapshot
Twofold Unsymmetrical CH Functionalization of PyrDipSi‐Substituted Arenes: A General Method for the Synthesis of Substituted meta‐Halophenols
inferred← citeshttps://doi.org/10.1002/anie.201306754openalex-snapshot
[3]Dendralene Synthesis: Rhodium(III)‐Catalyzed Alkenyl CH Activation and Coupling Reaction with Allenyl Carbinol Carbonate
inferred← citeshttps://doi.org/10.1002/anie.201309198openalex-snapshot
Rhodium‐Catalyzed CH Alkynylation of Arenes at Room Temperature
inferred← citeshttps://doi.org/10.1002/anie.201406747openalex-snapshot
Rhodium(III)‐Catalyzed CC and CO Coupling of Quinoline N‐Oxides with Alkynes: Combination of CH Activation with O‐Atom Transfer
inferred← citeshttps://doi.org/10.1002/anie.201502278openalex-snapshot
Diaryliodoniums by Rhodium(III)‐Catalyzed CH Activation: Mild Synthesis and Diversified Functionalizations
inferred← citeshttps://doi.org/10.1002/anie.201504390openalex-snapshot
Ruthenium‐Catalyzed meta‐Selective CH Bromination
inferred← citeshttps://doi.org/10.1002/anie.201607388openalex-snapshot
Highly ortho ‐Selective Chlorination of Anilines Using a Secondary Ammonium Salt Organocatalyst
inferred← citeshttps://doi.org/10.1002/anie.201610117openalex-snapshot
Combination of Cp*RhIII‐Catalyzed C−H Activation and a Wagner–Meerwein‐Type Rearrangement
inferred← citeshttps://doi.org/10.1002/anie.201611757openalex-snapshot
Synthesis of Active Hexafluoroisopropyl Benzoates through a Hydrogen‐Bond‐Enabled Palladium(II)‐Catalyzed C−H Alkoxycarbonylation Reaction
inferred← citeshttps://doi.org/10.1002/anie.201800549openalex-snapshot
European Restrictions on 1,2‐Dichloroethane: C−H Activation Research and Development Should Be Liberated and not Limited
inferred← citeshttps://doi.org/10.1002/anie.201804528openalex-snapshot
Oxidative C−H/C−H Cross‐Coupling Reactions between N‐Acylanilines and Benzamides Enabled by a Cp*‐Free RhCl3/TFA Catalytic System
inferred← citeshttps://doi.org/10.1002/anie.201808159openalex-snapshot
Rhodium‐Catalyzed C(sp2)‐ or C(sp3)−H Bond Functionalization Assisted by Removable Directing Groups
inferred← citeshttps://doi.org/10.1002/anie.201809657openalex-snapshot
Synthesis of Polysubstituted Iodoarenes Enabled by Iterative Iodine‐Directed para and ortho C−H Functionalization
inferred← citeshttps://doi.org/10.1002/anie.201908418openalex-snapshot
The Power of Iodane‐Guided C−H Coupling: A Group‐Transfer Strategy in Which a Halogen Works for Its Money
inferred← citeshttps://doi.org/10.1002/anie.202003595openalex-snapshot
A Chemistry for Incorporation of Selenium into DNA‐Encoded Libraries
inferred← citeshttps://doi.org/10.1002/anie.202300905openalex-snapshot
Palladium‐Catalyzed Enantioselective Isodesmic C−H Iodination of Phenylacetic Weinreb Amides
inferred← citeshttps://doi.org/10.1002/anie.202305983openalex-snapshot
Regio‐ and Chemoselective Formal (4+1) Carbocyclization of Chalcones with Internal Alkynes via Rhodium(III) Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202424183openalex-snapshot
Silylation of Aryl and Alkyl Chlorides by a Seven‐Membered Dialkoxysilyl Group Si(pan)Me via an In Situ Generated Silylpotassium
inferred← citeshttps://doi.org/10.1002/asia.201601131openalex-snapshot
Rhodium‐Catalyzed Oxidative Benzannulation of N‐Pivaloylanilines with Internal Alkynes through Dual C−H Bond Activation: Synthesis of Highly Substituted Naphthalenes
inferred← citeshttps://doi.org/10.1002/asia.202300788openalex-snapshot
Exploring the Versatility of the Amidation of Aryl Acid Fluorides using the Germylamines R3GeNMe2
inferred← citeshttps://doi.org/10.1002/bkcs.70031openalex-snapshot
Cp * Co ( III )‐catalyzed C – H functionalization of bioactive heterocyclic motifs
inferred← citeshttps://doi.org/10.1002/cctc.201300734openalex-snapshot
Cu‐Mediated Direct Aryl CH Halogenation: a Strategy to Control Mono‐ and Di‐Selectivity
inferred← citeshttps://doi.org/10.1002/cctc.201701182openalex-snapshot
Metal‐Free, Oxidant‐Free, and Controllable Graphene Oxide Catalyzed Direct Iodination of Arenes and Ketones
inferred← citeshttps://doi.org/10.1002/cctc.201800328openalex-snapshot
Copper(II)‐Catalyzed Selective Para Amination of Arylamine with Pyrazole by C−H Functionalization
inferred← citeshttps://doi.org/10.1002/chem.201203856openalex-snapshot
Amino‐Directed Rh III ‐Catalyzed CH Activation Leading to One‐Pot Synthesis of NH Carbazoles
inferred← citeshttps://doi.org/10.1002/chem.201300829openalex-snapshot
Controllable Mono‐/Dialkenylation of Benzyl Thioethers through Rh‐Catalyzed Aryl CH Activation
inferred← citeshttps://doi.org/10.1002/chem.201301168openalex-snapshot
Rhodium‐Catalyzed Synthesis of Amides from Aldehydes and Azides by Chelation‐Assisted CH Bond Activation
inferred← citeshttps://doi.org/10.1002/chem.201301785openalex-snapshot
Copper‐Catalyzed Direct Synthesis of Iodoenamides from Ketoximes
inferred← citeshttps://doi.org/10.1002/chem.201303730openalex-snapshot
Rhodium‐Catalyzed Directed Sulfenylation of Arene CH Bonds
inferred← citeshttps://doi.org/10.1002/chem.201303923openalex-snapshot
Room‐Temperature ortho‐Alkoxylation and ‐Halogenation of N‐Tosylbenzamides by Using Palladium(II)‐Catalyzed CH Activation
inferred← citeshttps://doi.org/10.1002/chem.201402350openalex-snapshot
Iridium‐Catalyzed Isomerization/Bromination of Allylic Alcohols: Synthesis of α‐Bromocarbonyl Compounds
inferred← citeshttps://doi.org/10.1002/chem.201403712openalex-snapshot
Aniline Carbamates: A Versatile and Removable Motif for Palladium‐Catalyzed Directed CH Activation
inferred← citeshttps://doi.org/10.1002/chem.201502234openalex-snapshot
Selective Halogenation Using an Aniline Catalyst
inferred← citeshttps://doi.org/10.1002/chem.201502689openalex-snapshot
Base‐Promoted Coupling of Carbon Dioxide, Amines, and Diaryliodonium Salts: A Phosgene‐ and Metal‐Free Route to O‐Aryl Carbamates
inferred← citeshttps://doi.org/10.1002/chem.201502918openalex-snapshot
Selective Heterogeneous C−H Activation/Halogenation Reactions Catalyzed by Pd@MOF Nanocomposites
inferred← citeshttps://doi.org/10.1002/chem.201503147openalex-snapshot
A Luminescent Nitrogen‐Containing Polycyclic Aromatic Hydrocarbon Synthesized by Photocyclodehydrogenation with Unprecedented Regioselectivity
inferred← citeshttps://doi.org/10.1002/chem.201503791openalex-snapshot
Relayed Regioselective Alkynylation/Olefination of Unsymmetrical Cyclic Diaryliodonium Species Catalyzed by Cu and Pd: Affording Fluorescent Cytotoxic Benzoxazoles
inferred← citeshttps://doi.org/10.1002/chem.201605188openalex-snapshot
Computational Investigation of the Role Played by Rhodium(V) in the Rhodium(III)‐Catalyzed ortho‐Bromination of Arenes
inferred← citeshttps://doi.org/10.1002/chem.201700280openalex-snapshot
Monoprotected l ‐Amino Acid ( l ‐MPAA), Accelerated Bromination, Chlorination, and Iodination of C(sp2)−H Bonds by Iridium(III) Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201703006openalex-snapshot
Transition Metal Catalyzed, Regioselective B(4)‐Halogenation and B(4,5)‐Diiodination of Cage B−H Bonds in o‐Carboranes
inferred← citeshttps://doi.org/10.1002/chem.201804058openalex-snapshot
The Coming of Age in Iodane‐Guided ortho‐C−H Propargylation: From Insight to Synthetic Potential
inferred← citeshttps://doi.org/10.1002/chem.202000253openalex-snapshot
Rhodium‐Catalyzed ortho ‐Bromination of O‐Phenyl Carbamates Accelerated by a Secondary Amide‐Pendant Cyclopentadienyl Ligand
inferred← citeshttps://doi.org/10.1002/chem.202002204openalex-snapshot
IrIII‐Catalyzed Selective ortho‐Monoiodination of Benzoic Acids with Unbiased C−H Bonds
inferred← citeshttps://doi.org/10.1002/chem.202102502openalex-snapshot
Oxidatively Induced Selective Carbon‐Carbon Bond Formation From Isolated Rhodium(III) Complexes
inferred← citeshttps://doi.org/10.1002/chem.202300978openalex-snapshot
Sunlight Induced and Alternative Sc(OTf)3 Catalyzed Remote C−H Halogenation of Indoles
inferred← citeshttps://doi.org/10.1002/chin.201242035openalex-snapshot
ChemInform Abstract: High‐Yielding, Versatile, and Practical [Rh(III)Cp*]‐Catalyzed ortho Bromination and Iodination of Arenes.
inferred← citeshttps://doi.org/10.1002/cjoc.201700726openalex-snapshot
Rh‐catalyzed Transient Directing Group Promoted C—H Amidation of Benzaldehydes Utilizing Dioxazolones
inferred← citeshttps://doi.org/10.1002/cssc.201801287openalex-snapshot
[Cp*RhIII]/Ionic Liquid as a Highly Efficient and Recyclable Catalytic Medium for C−H Amidation
inferred← citeshttps://doi.org/10.1002/ejoc.201700546openalex-snapshot
Amides as Weak Coordinating Groups in Proximal C–H Bond Activation
inferred← citeshttps://doi.org/10.1002/ejoc.201701004openalex-snapshot
Fused Systems Based on 2‐Aminopyrimidines: Synthesis Combining Deprotolithiation‐in situ Zincation with N ‐Arylation Reactions and Biological Properties
inferred← citeshttps://doi.org/10.1002/ejoc.201701573openalex-snapshot
Enabling Efficient Late‐Stage Functionalization of Drug‐Like Molecules with LC‐MS and Reaction‐Driven Data Processing
inferred← citeshttps://doi.org/10.1002/ejoc.201800378openalex-snapshot
Synthesis of Amides from Alcohols and Amines Through a Domino Oxidative Amidation and Telescoped Transamidation Process
inferred← citeshttps://doi.org/10.1002/ejoc.201801097openalex-snapshot
A Visible Light‐Mediated Regioselective Halogenation of Anilides and Quinolines by Using a Heterogeneous Cu‐MnO Catalyst
inferred← citeshttps://doi.org/10.1002/ejoc.202100964openalex-snapshot
Rh(III)‐Catalyzed Selective C7 Halogenation of Indolines
inferred← citeshttps://doi.org/10.1002/ejoc.202200316openalex-snapshot
Quinazoline‐Assisted ortho‐Halogenation with N‐Halosuccinimides through Pd(II)‐Catalyzed C(sp2)−H Activation
inferred← citeshttps://doi.org/10.1002/ejoc.202200348openalex-snapshot
Synthesis of Angucycline/Tetrangulol Derivatives Using Suzuki‐Miyaura Cross‐Coupling and Ring‐Closing Carbonyl‐Olefin Metathesis Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.202200399openalex-snapshot
Copper‐Catalyzed Regioselective Halogenation of Anilides with N‐Fluorobenzenesulfonimide
inferred← citeshttps://doi.org/10.1002/ejoc.202500125openalex-snapshot
Organocatalytic Halogenation of Aromatic and Heteroaromatic Compounds
inferred← citeshttps://doi.org/10.1002/ijch.201700053openalex-snapshot
Group 9 Transition Metal‐Catalyzed C−H Halogenations
inferred← citeshttps://doi.org/10.1002/jlcr.3559openalex-snapshot
Preparation of tritium‐labeled PF‐622, a novel fatty acid amide hydrolase inhibitor
inferred← citeshttps://doi.org/10.1002/slct.201702184openalex-snapshot
Visible Light‐Mediated Installation of Halogen Functionalities into Multiple Bond Systems
inferred← citeshttps://doi.org/10.1002/slct.201801097openalex-snapshot
Advances in Development of C–H Activation/Functionalization Using a Catalytic Directing Group
inferred← citeshttps://doi.org/10.1002/slct.201803053openalex-snapshot
Palladium‐Catalyzed Regioselective C‐H Bond ortho ‐Acetylation and Oxidative Homocoupling of N ‐Arylcarbamates
inferred← citeshttps://doi.org/10.1002/slct.201901456openalex-snapshot
Room‐Temperature C‐H Bromination and Iodination with Sodium Bromide and Sodium Iodide Using N ‐Fluorobenzenesulfonimide as an Oxidant
inferred← citeshttps://doi.org/10.1007/3418_2015_123openalex-snapshot
Rh(III)- and Ir(III)-Catalyzed Direct C–H Bond Transformations to Carbon–Heteroatom Bonds
inferred← citeshttps://doi.org/10.1007/978-4-431-54604-7_7openalex-snapshot
Applications of Cyclometalation Reactions and Five-Membered Ring Products for Synthetic Purposes
inferred← citeshttps://doi.org/10.1007/978-981-16-0432-4_4openalex-snapshot
Theoretical View of Rh-Catalyzed C–H Functionalization for the Construction of C–X Bonds (X = O, N, B, Si, or Halide)
inferred← citeshttps://doi.org/10.1007/s10562-017-2234-yopenalex-snapshot
Isothiocyanate-Directed Ortho-Selective Halogenation of Arenes via C–H Functionalization
inferred← citeshttps://doi.org/10.1007/s10562-018-2324-5openalex-snapshot
Copper(I) Halide for Regioselective Ortho-Halogenation of Directed Arenes
inferred← citeshttps://doi.org/10.1007/s11426-014-5130-yopenalex-snapshot
Some recent advances in transition-metal-catalyzed ortho SP2 C-H functionalization using Ru, Rh, and Pd
inferred← citeshttps://doi.org/10.1007/s40242-015-4512-9openalex-snapshot
Cu-catalyzed aryl C-H halogenation using N-halosuccinimides via assistance of benzoic acid
inferred← citeshttps://doi.org/10.1016/b978-0-12-815675-9.00004-7openalex-snapshot
Imides: A Special Chemical Entity in Rhodium Catalysis
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00122-0openalex-snapshot
Direct C–E (E = Boron, Halogen, Oxygen) Bond Formation Through C–H Activation
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.06.036openalex-snapshot
C–H activation reactions as useful tools for medicinal chemists
inferred← citeshttps://doi.org/10.1016/j.catcom.2012.11.022openalex-snapshot
A simple and effective copper catalyst for the conversion of arylboronic acids to aryl iodides at room temperature
inferred← citeshttps://doi.org/10.1016/j.catcom.2017.01.019openalex-snapshot
A green catalytic method for selective synthesis of iodophenols via aerobic oxyiodination under organic solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.catcom.2019.105784openalex-snapshot
Acid-promoted palladium(II)-catalyzed ortho-halogenation of primary benzamides: En route to halo-arenes
inferred← citeshttps://doi.org/10.1016/j.cclet.2015.07.011openalex-snapshot
Palladium-catalyzed ortho-selective CH bond chlorination of aromatic ketones
inferred← citeshttps://doi.org/10.1016/j.cclet.2019.09.057openalex-snapshot
Palladium-catalyzed meta-C H bond iodination of arenes with I2
inferred← citeshttps://doi.org/10.1016/j.ccr.2019.213024openalex-snapshot
Synthesis of BODIPY dyes through postfunctionalization of the boron dipyrromethene core
inferred← citeshttps://doi.org/10.1016/j.crci.2012.08.003openalex-snapshot
On the selectivity in some Rh(III) catalyzed CH activation cross-couplings
inferred← citeshttps://doi.org/10.1016/j.isci.2019.01.017openalex-snapshot
Electrochemical Oxidative Clean Halogenation Using HX/NaX with Hydrogen Evolution
inferred← citeshttps://doi.org/10.1016/j.isci.2021.102467openalex-snapshot
Iridium-catalyzed C−H methylation and d3-methylation of benzoic acids with application to late-stage functionalizations
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.02.004openalex-snapshot
Direct use of CO2 for O-arylcarbamate synthesis via mild Cu(II)-catalyzed aerobic C-H functionalization in pincer-like macrocyclic systems
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.05.025openalex-snapshot
Quinazoline-directed selective ortho-iodination for the synthesis of 2-(2-iodoaryl)-4-arylquinazolines
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.02.012openalex-snapshot
Comparative computational study on C-C/C-N/C-Br bond formations in Rh(III)-catalyzed C-H functionalizations: Stepwise versus concerted mechanisms
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.03.016openalex-snapshot
Counterion effect and directing group effect in Rh-mediated C H bond activation processes: A theoretical study
inferred← citeshttps://doi.org/10.1016/j.molstruc.2013.10.011openalex-snapshot
Synthesis and structural insights of substituted 2-iodoacetanilides and 2-iodoanilines
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135454openalex-snapshot
Green halogenation of aromatic compounds using environmentally friendly synthesized rod-like metal-organic framework (MIL-88A) catalyst
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.141409openalex-snapshot
An efficient Cu catalyzed regioselective Ortho-nitration approach for the synthesis of 2-nitroarylcyanamides: Molecular docking and ADME studies
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.068openalex-snapshot
Employing a robustness screen: rapid assessment of rhodium(III)-catalysed C–H activation reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.070openalex-snapshot
Palladium-catalyzed picolinamide-directed halogenation of ortho C–H bonds of benzylamine substrates
inferred← citeshttps://doi.org/10.1016/j.tet.2015.03.004openalex-snapshot
Rhodium-catalyzed ortho-selective C–H halogenation of 2-arylbenzo[d]thiazoles using N-halosuccinimides as halogen sources
inferred← citeshttps://doi.org/10.1016/j.tet.2015.08.034openalex-snapshot
Recent advances in the C–H-functionalization of the distal positions in pyridines and quinolines
inferred← citeshttps://doi.org/10.1016/j.tet.2016.01.037openalex-snapshot
Substituent effects on axial chirality in 1-aryl-3,4-dihydroisoquinolines: controlling the rate of bond rotation
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130621openalex-snapshot
Regioselective bromination of aryl ureas with Phenyliodine(III) diacetate and potassium bromide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.12.107openalex-snapshot
Transition-metal-catalyzed ketone-directed ortho-C–H functionalization reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.02.071openalex-snapshot
The direct C–H halogenations of indoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.12.076openalex-snapshot
Surprisingly facile C–H activation in the course of oxime-directed catalytic asymmetric hydroboration
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.150openalex-snapshot
Aerobic oxidative bromination of arenes using an ionic liquid as both the catalyst and the solvent
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.01.003openalex-snapshot
Rapid aerobic iodination of arenes mediated by hypervalent iodine in fluorinated solvents
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.06.019openalex-snapshot
Electrochemical bromination of late stage intermediates and drug molecules
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153074openalex-snapshot
Practical bromination of arylhydroxylamines with SOBr2 towards ortho-bromo-anilides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155019openalex-snapshot
Potassium iodide as iodinating reagent: Rhodium(III)-catalyzed versatile and practical ortho-iodination of benzoic acids
inferred← citeshttps://doi.org/10.1016/s1872-2067(14)60245-xopenalex-snapshot
Rh(III)-catalyzed C–H activation of benzamides: Coupling with quinones
inferred← citeshttps://doi.org/10.1021/acs.chemrev.3c00923openalex-snapshot
The Versatile and Strategic O-Carbamate Directed Metalation Group in the Synthesis of Aromatic Molecules: An Update
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00400openalex-snapshot
Use of Bromine and Bromo-Organic Compounds in Organic Synthesis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00089openalex-snapshot
Modern Transition-Metal-Catalyzed Carbon–Halogen Bond Formation
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.7b00450openalex-snapshot
Solvent Mediating a Switch in the Mechanism for Rhodium(III)-Catalyzed Carboamination/Cyclopropanation Reactions between N-Enoxyphthalimides and Alkenes
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00319openalex-snapshot
Confirmation of the Revised Structure of Samoquasine A and a Proposed Structural Revision of Cherimoline
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01917openalex-snapshot
Catalyst-Controlled Regioselective Chlorination of Phenols and Anilines through a Lewis Basic Selenoether Catalyst
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00048openalex-snapshot
Dual Role of the Rhodium(III) Catalyst in C–H Activation: [4 + 3] Annulation of Amide with Allylic Alcohols to 7-Membered Lactams
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01938openalex-snapshot
Cp*Rh(III)-Catalyzed Regioselective C(sp3)–H Electrophilic Trifluoromethylthiolation of 8-Methylquinolines
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00924openalex-snapshot
Synthesis of Furans via Rhodium(III)-Catalyzed Cyclization of Acrylic Acids with α-Diazocarbonyl Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00689openalex-snapshot
Intramolecular Hydroarylation of Arenes via Imidazole-Directed C–H Activation in Aqueous Methanol Using Rhodium(III) as the Catalyst and Mechanistic Study
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02754openalex-snapshot
Construction of an Angular Tricyclic Benzofuran Skeleton Using the C–H Activation Strategy
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01133openalex-snapshot
Palladium-Catalyzed, Site-Selective C(sp2)8–H Halogenation and Nitration of 4-Quinolone Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00775openalex-snapshot
Palladium-Catalyzed ortho-Olefination of Phenyl Acetic and Phenyl Propylacetic Esters via C–H Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01021openalex-snapshot
Room-Temperature Cu(II)-Catalyzed Chemo- and Regioselective Ortho-Nitration of Arenes via C–H Functionalization
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01304openalex-snapshot
Synthesis of Benzofulvene Derivatives from Diarylacetylenes via Pd(II)-Catalyzed Alkyne-Directed C(sp2)–H Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02129openalex-snapshot
Relative Rate Profiles of Functionalized Iodoarene Catalysts for Iodine(III) Oxidations
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00109openalex-snapshot
Solventless Catalytic C–H and C–X Functionalization without Ball Milling
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00186openalex-snapshot
Copper(II)-Catalyzed Oxidative Cross-Coupling of Anilines, Primary Alkyl Amines, and Sodium Azide Using TBHP: A Route to 2-Substituted Benzimidazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00329openalex-snapshot
Palladium-Catalyzed Carbamate-Directed Regioselective Halogenation: A Route to Halogenated Anilines
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02522openalex-snapshot
Rhodium(III)-Catalyzed C–H Functionalization of 1-(2H)-Phthalazinones at C8
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02731openalex-snapshot
Palladium-Catalyzed, ortho-Selective C–H Halogenation of Benzyl Nitriles, Aryl Weinreb Amides, and Anilides
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