On the public citation graph

Palladium Catalyzed C–H Functionalization of O -Arylcarbamates: Selective ortho -Bromination Using NBS

0 signed · 138 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/adsc.200900778openalex-snapshot

Palladium‐Catalyzed Monoselective Halogenation of CH Bonds: Efficient Access to Halogenated Arylpyrimidines using Calcium Halides

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.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.201004426openalex-snapshot

A General Strategy Toward Aromatic 1,2‐Ambiphilic Synthons: Palladium‐Catalyzed ortho ‐Halogenation of PyDipSi‐Arenes

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/chem.200900281openalex-snapshot

Construction of Nitrogen‐Containing Heterocycles by CH Bond Functionalization

inferredcites →https://doi.org/10.1002/ejoc.200701096openalex-snapshot

Suppressing the Anionic Fries Rearrangement of Aryl Dialkylcarbamates; the Isolation of a Crystalline ortho‐Deprotonated Carbamate

inferredcites →https://doi.org/10.1002/ejoc.201001160openalex-snapshot

Copper‐Catalyzed Intramolecular C–H Amination

inferredcites →https://doi.org/10.1007/128_2009_15openalex-snapshot

Pd-Catalyzed C–H Bond Functionalization on the Indole and Pyrrole Nucleus

inferredcites →https://doi.org/10.1007/128_2009_19openalex-snapshot

Metal-Catalyzed Oxidations of C–H to C–N Bonds

inferredcites →https://doi.org/10.1016/j.jorganchem.2010.09.078openalex-snapshot

Palladium-catalyzed C–N bond formation via direct C–H bond functionalization. Recent developments in heterocyclic synthesis

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/10.1016/j.tetlet.2011.04.119openalex-snapshot

Cu(I)/Cu(II)-catalyzed allylic amination of alkenes

inferredcites →https://doi.org/10.1021/ar000209hopenalex-snapshot

Catalytic Functionalization of Arenes and Alkanes via C−H Bond Activation

inferredcites →https://doi.org/10.1021/cr068006fopenalex-snapshot

C−C, C−O, C−N Bond Formation on sp2 Carbon by Pd(II)-Catalyzed Reactions Involving Oxidant Agents

inferredcites →https://doi.org/10.1021/cr900184eopenalex-snapshot

Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

inferredcites →https://doi.org/10.1021/ja00092a058openalex-snapshot

Palladium-catalyzed formation of carbon-nitrogen bonds. Reaction intermediates and catalyst improvements in the hetero cross-coupling of aryl halides and tin amides

inferredcites →https://doi.org/10.1021/ja00096a059openalex-snapshot

Palladium-Catalyzed Aromatic Aminations with in situ Generated Aminostannanes

inferredcites →https://doi.org/10.1021/ja055353iopenalex-snapshot

Combined C−H Functionalization/C−N Bond Formation Route to Carbazoles

inferredcites →https://doi.org/10.1021/ja062856vopenalex-snapshot

Intermolecular Amidation of Unactivated sp2 and sp3 C−H Bonds via Palladium-Catalyzed Cascade C−H Activation/Nitrene Insertion

inferredcites →https://doi.org/10.1021/ja100676ropenalex-snapshot

Palladium-Catalyzed Amination of Aromatic C−H Bonds with Oxime Esters

inferredcites →https://doi.org/10.1021/ja100783copenalex-snapshot

Palladium-Catalyzed Ortho-Arylation of O-Phenylcarbamates with Simple Arenes and Sodium Persulfate

inferredcites →https://doi.org/10.1021/ja1054274openalex-snapshot

On the Mechanism of Palladium-Catalyzed Aromatic C−H Oxidation

inferredcites →https://doi.org/10.1021/ja106364ropenalex-snapshot

Pd-Catalyzed Intermolecular ortho -C−H Amidation of Anilides by N -Nosyloxycarbamate

inferredcites →https://doi.org/10.1021/ja108450mopenalex-snapshot

Palladium-Catalyzed Intermolecular Directed C−H Amidation of Aromatic Ketones

inferredcites →https://doi.org/10.1021/ja1101695openalex-snapshot

Palladium-Catalyzed C−H Aminations of Anilides with N-Fluorobenzenesulfonimide

inferredcites →https://doi.org/10.1021/ja200398copenalex-snapshot

Suzuki−Miyaura Cross-Coupling of Aryl Carbamates and Sulfamates: Experimental and Computational Studies

inferredcites →https://doi.org/10.1021/ja202563wopenalex-snapshot

Pd-Catalyzed Intermolecular C–H Amination with Alkylamines

inferredcites →https://doi.org/10.1021/ja806543sopenalex-snapshot

Oxidative Pd(II)-Catalyzed C−H Bond Amination to Carbazole at Ambient Temperature

inferredcites →https://doi.org/10.1021/ja807129eopenalex-snapshot

Synthesis of β-, γ-, and δ-Lactams via Pd(II)-Catalyzed C−H Activation Reactions

inferredcites →https://doi.org/10.1021/ja904709bopenalex-snapshot

Pd(II)-Catalyzed Amination of C−H Bonds Using Single-Electron or Two-electron Oxidants

inferredcites →https://doi.org/10.1021/ja909818nopenalex-snapshot

Pd(II)-Catalyzed C−H Activation/Aryl−Aryl Coupling of Phenol Esters

inferredcites →https://doi.org/10.1021/jo00041a004openalex-snapshot

Nickel(0)-catalyzed cross coupling of aryl O-carbamates and aryl triflates with Grignard reagents. Directed ortho metalation-aligned synthetic methods for polysubstituted aromatics via a 1,2-dipole equivalent

inferredcites →https://doi.org/10.1021/jo01342a039openalex-snapshot

Nuclear Magnetic Resonance Study of Some N,N-Dimethylcarbamates

inferredcites →https://doi.org/10.1021/jo1015213openalex-snapshot

Iodine-Catalyzed Aminosulfonation of Hydrocarbons by Imidoiodinanes. a Synthetic and Mechanistic Investigation

inferredcites →https://doi.org/10.1021/jo200409hopenalex-snapshot

Copper-Catalyzed Amidation of 2-Phenylpyridine with Oxygen as the Terminal Oxidant

inferredcites →https://doi.org/10.1021/jo801273qopenalex-snapshot

Palladium-Catalyzed Method for the Synthesis of Carbazoles via Tandem C−H Functionalization and C−N Bond Formation

inferredcites →https://doi.org/10.1021/ol0476220openalex-snapshot

Directed ortho Metalation Reaction of Aryl O-Carbamates on Solid Support

inferredcites →https://doi.org/10.1021/ol060747fopenalex-snapshot

A Simple Catalytic Method for the Regioselective Halogenation of Arenes

inferredcites →https://doi.org/10.1021/ol0711117openalex-snapshot

Palladium-Catalyzed C−H Activation/Intramolecular Amination Reaction: A New Route to 3-Aryl/Alkylindazoles

inferredcites →https://doi.org/10.1021/ol201140qopenalex-snapshot

Rhodium-Catalyzed Selective C–H Activation/Olefination of Phenol Carbamates

inferredcites →https://doi.org/10.1021/ol7030944openalex-snapshot

Fine-Tuning of Boron Complexes with Cage-Shaped Ligand Geometry: Rational Design of Triphenolic Ligand as a Template for Structure Control

inferredcites →https://doi.org/10.1021/ol9029534openalex-snapshot

Nickel-Catalyzed Efficient and Practical Suzuki−Miyaura Coupling of Alkenyl and Aryl Carbamates with Aryl Boroxines

inferredcites →https://doi.org/10.1021/om100427sopenalex-snapshot

On the Mechanism of Ligand-Assisted, Copper-Catalyzed Benzylic Amination by Chloramine-T

inferredcites →https://doi.org/10.1039/b916724mopenalex-snapshot

Palladium-catalysed ortho-arylation of carbamate-protected phenols

inferredcites →https://doi.org/10.1039/c003074kopenalex-snapshot

Solvent free catalytic C–H functionalisation

inferredcites →https://doi.org/10.1039/c1cc14108bopenalex-snapshot

Rhodium-catalyzed direct ortho C–H olefination of phenol derivatives

inferredcites →https://doi.org/10.1039/c1cs15082kopenalex-snapshot

Recent advances in the transition metal-catalyzed twofold oxidative C–H bond activation strategy for C–C and C–N bond formation

inferredcites →https://doi.org/10.1039/c1sc00230aopenalex-snapshot

Nickel-catalyzed amination of aryl carbamates and sequential site-selective cross-couplings

inferredcites →https://doi.org/10.1055/s-0028-1087413openalex-snapshot

A New Approach to 3-Substituted Indoles through Palladium-Catalyzed C-H Activation Followed by Intramolecular Amination Reaction of Enamines

inferredcites →https://doi.org/10.1055/s-0031-1289614openalex-snapshot

Non-Cyclizing Direct Transformation of Arene Carbon-Hydrogen Bonds into Carbon-Nitrogen Bonds

inferredcites →https://doi.org/10.1246/cl.2009.328openalex-snapshot

Synthesis of Oxindoles by Palladium-catalyzed C–H Bond Amidation

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.4648007openalex-extracted

Electrochemical Bromination of Electron-Rich Compounds Employing Libr as a “Br” Source

inferred← citeshttps://doi.org/10.1002/9780471264194.fos07552.pub6openalex-snapshot

Palladium( II ) acetate

inferred← citeshttps://doi.org/10.1002/9780471264194.fos07552.pub7openalex-snapshot

Palladium( II ) acetate

inferred← citeshttps://doi.org/10.1002/9781118754887.ch23openalex-snapshot

Chelate‐Assisted Arene C–H Bond Functionalization

inferred← citeshttps://doi.org/10.1002/9783527827992.ch58openalex-snapshot

Bromo‐ and Iodoaromatics

inferred← citeshttps://doi.org/10.1002/adsc.201200902openalex-snapshot

Palladium‐Catalyzed Regioselective Halogenation of Aromatic Azo Compounds

inferred← citeshttps://doi.org/10.1002/adsc.202001033openalex-snapshot

Divergent Halogenation Pathways of 2,2‐Dichlorobut‐3‐yn‐1‐ols to 3‐Chloro‐4‐Iodofurans and α‐Chloro‐γ‐Iodoallenes: Electrophilic versus Pd(II)‐Catalyzed Halogenation Strategies

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.202200060openalex-snapshot

Recent Advances in First‐Row Transition‐Metal‐Mediated C−H Halogenation of (Hetero)arenes and Alkanes

inferred← citeshttps://doi.org/10.1002/ange.201404854openalex-snapshot

Easily Accessible Auxiliary for Palladium‐Catalyzed Intramolecular Amination of C(sp2)H and C(sp3)H Bonds at δ‐ and ε‐Positions

inferred← citeshttps://doi.org/10.1002/ange.201504390openalex-snapshot

Ruthenium‐Catalyzed meta‐Selective CH Bromination

inferred← citeshttps://doi.org/10.1002/ange.201601999openalex-snapshot

Palladium‐Catalyzed Directed para C−H Functionalization of Phenols

inferred← citeshttps://doi.org/10.1002/ange.202010845openalex-snapshot

Dearomatization‐Rearomatization Strategy for ortho‐Selective Alkylation of Phenols with Primary Alcohols

inferred← citeshttps://doi.org/10.1002/ange.202501779openalex-snapshot

A Platform for the Development of Highly Red‐Shifted Azobenzene‐Based Optical Tools

inferred← citeshttps://doi.org/10.1002/anie.201404854openalex-snapshot

Easily Accessible Auxiliary for Palladium‐Catalyzed Intramolecular Amination of C(sp2)H and C(sp3)H Bonds at δ‐ and ε‐Positions

inferred← citeshttps://doi.org/10.1002/anie.201504390openalex-snapshot

Ruthenium‐Catalyzed meta‐Selective CH Bromination

inferred← citeshttps://doi.org/10.1002/anie.201601999openalex-snapshot

Palladium‐Catalyzed Directed para C−H Functionalization of Phenols

inferred← citeshttps://doi.org/10.1002/anie.202010845openalex-snapshot

Dearomatization‐Rearomatization Strategy for ortho‐Selective Alkylation of Phenols with Primary Alcohols

inferred← citeshttps://doi.org/10.1002/anie.202501779openalex-snapshot

A Platform for the Development of Highly Red‐Shifted Azobenzene‐Based Optical Tools

inferred← citeshttps://doi.org/10.1002/asia.201500601openalex-snapshot

RhIII‐Catalyzed C−H Olefination of Benzoic Acids under Mild Conditions using Oxygen as the Sole Oxidant

inferred← citeshttps://doi.org/10.1002/asia.201601413openalex-snapshot

Palladium‐Catalyzed C−H Functionalization of Phenyl 2‐Pyridylsulfonates

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.202000253openalex-snapshot

Rhodium‐Catalyzed ortho ‐Bromination of O‐Phenyl Carbamates Accelerated by a Secondary Amide‐Pendant Cyclopentadienyl Ligand

inferred← citeshttps://doi.org/10.1002/chin.201244084openalex-snapshot

ChemInform Abstract: Palladium Catalyzed C—H Functionalization of O‐Arylcarbamates: Selective ortho‐Bromination Using NBS.

inferred← citeshttps://doi.org/10.1002/cssc.201901951openalex-snapshot

Transition Metal‐Catalyzed Directing‐Group‐Assisted C−H Activation of Phenols

inferred← citeshttps://doi.org/10.1002/ejoc.201300584openalex-snapshot

Metal‐Free Directed ortho C–H Iodination: Synthesis of 2′‐Iodobiaryl‐2‐carbonitriles

inferred← citeshttps://doi.org/10.1002/ejoc.201700660openalex-snapshot

Nickel‐Catalyzed Amination of Aryl Carbamates with Ammonia

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/jccs.202100046openalex-snapshot

Copper porphyrin‐catalyzed C(sp2)—O bond construction via coupling phenols with formamides

inferred← citeshttps://doi.org/10.1002/slct.201902611openalex-snapshot

Acetoxylation and Halogenation of 2‐Arylbenzoxazinones via Palladium‐Catalyzed C(sp 2 )‐H Bond Oxidation

inferred← citeshttps://doi.org/10.1002/slct.202103841openalex-snapshot

Palladium‐Catalyzed Selective o ‐Bromination of Mesoionic 1,3‐Diphenyltetrazolium‐5‐olate: Switching the Directing Group from Nitrogen to Oxygen

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/10.1016/b978-0-08-097742-3.00715-1openalex-snapshot

7.13 Directed Aryl CH Oxidations with Transition Metals

inferred← citeshttps://doi.org/10.1016/j.mcat.2020.110772openalex-snapshot

Regioselective Ortho‐C H sulfenylation of free phenols catalyzed by Co(II)-immobilized on silica-coated magnetic nanoparticles

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.080openalex-snapshot

Palladium-catalyzed ortho-halogenation of diaryl oxime ethers

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.08.069openalex-snapshot

Regioselectivity in free radical bromination of unsymmetrical dimethylated pyridines

inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.154927openalex-snapshot

Electrochemical bromination of electron-rich compounds employing LiBr as a “Br” source

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.joc.0c00831openalex-snapshot

Electrochemically Catalyzed Newman–Kwart Rearrangement: Mechanism, Structure–Reactivity Relationship, and Parallels to Photoredox Catalysis

inferred← citeshttps://doi.org/10.1021/acs.joc.1c01406openalex-snapshot

Cr-Catalyzed Direct ortho-Aminomethylation of Phenols

inferred← citeshttps://doi.org/10.1021/acs.joc.5b00982openalex-snapshot

A Forty Year Odyssey in Metallo–Organic Chemistry

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.6b02693openalex-snapshot

Rhodium(III)-Catalyzed ortho-Alkylation of Phenoxy Substrates with Diazo Compounds via C–H Activation: A Case of Decarboxylative Pyrimidine/Pyridine Migratory Cyclization Rather than Removal of Pyrimidine/Pyridine Directing Group

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

inferred← citeshttps://doi.org/10.1021/acs.joc.7b01542openalex-snapshot

Regioselective Bromination of Thieno[2′,3′:4,5]pyrrolo[1,2-d][1,2,4]triazin-8(7H)-one and Sequential Suzuki Couplings

inferred← citeshttps://doi.org/10.1021/acs.joc.8b01016openalex-snapshot

Cu(II)-Catalyzed Ortho-C–H Nitration of Aryl Ureas By C–H Functionalization

inferred← citeshttps://doi.org/10.1021/acs.joc.8b01176openalex-snapshot

Palladium-Catalyzed Direct Arylation of Polyfluoroarenes for Accessing Tetra-ortho-Substituted Biaryls: Buchwald-type Ligand Having Complementary −PPh2 Moiety Exhibits Better Efficiency

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00646openalex-snapshot

Aerobic Oxidative C–H Olefination of Arylamides with Unactivated Olefins via a Rh(III)-Catalyzed C–H Activation

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03905openalex-snapshot

Rh(III)-Catalyzed Selective Olefination of N-Carboxamide Indoles with Unactivated Olefins at Room Temperature via an Internal Oxidation

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00043openalex-snapshot

Rhodium(III)-CatalyzedOrthoHalogenations ofN-Acylsulfoximines and Synthetic Applications toward Functionalized Sulfoximine Derivatives

inferred← citeshttps://doi.org/10.1021/acscatal.1c05512openalex-snapshot

Role of Brønsted Acids in Promoting Pd(OAc)2-Catalyzed Chlorination of Phenol Carbamates Using N-Chlorosuccinimide

inferred← citeshttps://doi.org/10.1021/acscatal.6b00964openalex-snapshot

Nickel-Catalyzed Reaction of C–H Bonds in Amides with I2: ortho-Iodination via the Cleavage of C(sp2)–H Bonds and Oxidative Cyclization to β-Lactams via the Cleavage of C(sp3)–H Bonds

inferred← citeshttps://doi.org/10.1021/acscatal.8b04098openalex-snapshot

Phenol-Directed C–H Functionalization

inferred← citeshttps://doi.org/10.1021/acscatal.9b01145openalex-snapshot

Copper-Catalyzed Regioselective C–H Amination of Phenol Derivatives with Assistance of Phenanthroline-Based Bidentate Auxiliary

inferred← citeshttps://doi.org/10.1021/acsomega.2c05350openalex-snapshot

Zinc Chloride-Catalyzed Synthesis of Carbamates: An Application for the Synthesis of the Anti-Alzheimer’s Drug Rivastigmine

inferred← citeshttps://doi.org/10.1021/acsomega.8b00441openalex-snapshot

Palladium-Catalyzed Decarboxylative ortho-Acylation of Anilines with Carbamate as a Removable Directing Group

inferred← citeshttps://doi.org/10.1021/ja400659sopenalex-snapshot

Pd(II)-Catalyzed ortho- or meta-C–H Olefination of Phenol Derivatives

inferred← citeshttps://doi.org/10.1021/jacs.3c09290openalex-snapshot

Decarboxylation and Tandem Reduction/Decarboxylation Pathways to Substituted Phenols from Aromatic Carboxylic Acids Using Bimetallic Nanoparticles on Supported Ionic Liquid Phases as Multifunctional Catalysts

inferred← citeshttps://doi.org/10.1021/jacs.7b05155openalex-snapshot

Transition-Metal-Free Decarboxylative Iodination: New Routes for Decarboxylative Oxidative Cross-Couplings

inferred← citeshttps://doi.org/10.1021/jacs.7b06785openalex-snapshot

Cu(II)-Catalyzed ortho-Selective Aminomethylation of Phenols

inferred← citeshttps://doi.org/10.1021/jo400755qopenalex-snapshot

Pd(II)-Catalyzed Aminotetrazole-Directed Ortho-Selective Halogenation of Arenes

inferred← citeshttps://doi.org/10.1021/jo4019683openalex-snapshot

Iridium-Catalyzed Direct Arene C–H Bond Amidation with Sulfonyl- and Aryl Azides

inferred← citeshttps://doi.org/10.1021/ol400565ropenalex-snapshot

Palladium(II)-Catalyzed ortho-Olefination of Benzylic Phosphonic Monoesters

inferred← citeshttps://doi.org/10.1039/c3cc47431copenalex-snapshot

Room-temperature Pd-catalyzed C–H chlorination by weak coordination: one-pot synthesis of 2-chlorophenols with excellent regioselectivity

inferred← citeshttps://doi.org/10.1039/c3ob41548aopenalex-snapshot

Rhodium(iii)-catalyzed ortho-olefination of aryl phosphonates

inferred← citeshttps://doi.org/10.1039/c3ob41558aopenalex-snapshot

Regioselective halogenation of 2-substituted-1,2,3-triazoles via sp2 C–H activation

inferred← citeshttps://doi.org/10.1039/c3qo00010aopenalex-snapshot

Palladium-catalyzed base-accelerated direct C–H bond alkenylation of phenols to synthesize coumarin derivatives

inferred← citeshttps://doi.org/10.1039/c4cc02969kopenalex-snapshot

Storable N-phenylcarbamate palladacycles for rapid functionalization of an alkyne-encoded protein

inferred← citeshttps://doi.org/10.1039/c4ra15461dopenalex-snapshot

Palladium catalyzed ortho-halogenation of 2-arylbenzothiazole and 2,3-diarylquinoxaline

inferred← citeshttps://doi.org/10.1039/c4sc03350gopenalex-snapshot

Rh( iii )-catalyzed C–H olefination of N-pentafluoroaryl benzamides using air as the sole oxidant

inferred← citeshttps://doi.org/10.1039/c5cc02533hopenalex-snapshot

Pd( ii ) catalyzed ortho C–H iodination of phenylcarbamates at room temperature using cyclic hypervalent iodine reagents

inferred← citeshttps://doi.org/10.1039/c5cy00137dopenalex-snapshot

Palladium N-heterocyclic carbene catalyzed regioselective C–H halogenation of 1-aryl-3-methyl-1H-pyrazol-5(4H)-ones using N-halosuccinimides (NXS)

inferred← citeshttps://doi.org/10.1039/c5ob02153gopenalex-snapshot

Efficient, versatile and practical palladium-catalyzed highly regioselective ortho-halogenation of azoxybenzenes

inferred← citeshttps://doi.org/10.1039/c5qo00004aopenalex-snapshot

Transition metal-catalyzed C–H bond functionalizations by the use of diverse directing groups

inferred← citeshttps://doi.org/10.1039/c6ob00169fopenalex-snapshot

Copper( ii )-catalyzed C5 and C7 halogenation of quinolines using sodium halides under mild conditions

inferred← citeshttps://doi.org/10.1039/c7ob01534hopenalex-snapshot

Pd-Catalyzed regioselective C–H halogenation of quinazolinones and benzoxazinones

inferred← citeshttps://doi.org/10.1039/d1nj01998hopenalex-snapshot

Efficient Pd( ii )-catalyzed regioselective ortho -halogenation of arylcyanamides

inferred← citeshttps://doi.org/10.1039/d1ob00506eopenalex-snapshot

Transition-metal-catalyzed ortho -selective C–H functionalization reactions of free phenols

inferred← citeshttps://doi.org/10.1039/d4sc00687aopenalex-snapshot

Csp 2 –H functionalization of phenols: an effective access route to valuable materials via Csp 2 –C bond formation

inferred← citeshttps://doi.org/10.1055/sos-sd-218-00127openalex-snapshot

2.7 C—Hal Bond Formation by Arene C—H Activation

inferred← citeshttps://doi.org/10.3762/bjoc.14.31openalex-snapshot

Palladium-catalyzed ortho-halogenations of acetanilides with N-halosuccinimides via direct sp2 C–H bond activation in ball mills

inferred← citeshttps://doi.org/10.3762/bjoc.18.100openalex-snapshot

Automated grindstone chemistry: a simple and facile way for PEG-assisted stoichiometry-controlled halogenation of phenols and anilines using N -halosuccinimides

inferred← citeshttps://doi.org/10.6023/cjoc202106011openalex-snapshot

Site-Selective C—H Iodination of Phenol Derivatives Using Aryl Iodide as Iodinating Reagent

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.