On the public citation graph

Copper-catalysed ortho -selective C–H bond functionalization of phenols and naphthols with α-aryl-α-diazoesters

https://doi.org/10.1039/d0cc04495d
0 signed · 127 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/ajoc.201800472openalex-snapshot
Gold‐Catalyzed Site‐Selective C−H Bond Functionalization with Diazo Compounds
inferredcites →https://doi.org/10.1002/anie.200390037openalex-snapshot
The Catalytic Intermolecular Orthoarylation of Phenols
inferredcites →https://doi.org/10.1002/anie.201006139openalex-snapshot
Removable Directing Groups in Organic Synthesis and Catalysis
inferredcites →https://doi.org/10.1002/anie.201209455openalex-snapshot
Enantioselective Copper‐Catalyzed Intramolecular Phenolic OH Bond Insertion: Synthesis of Chiral 2‐Carboxy Dihydrobenzofurans, Dihydrobenzopyrans, and Tetrahydrobenzooxepines
inferredcites →https://doi.org/10.1002/anie.201304268openalex-snapshot
The Cross‐Dehydrogenative Coupling of CH Bonds: A Versatile Strategy for CC Bond Formations
inferredcites →https://doi.org/10.1002/anie.201306824openalex-snapshot
Enantioselective Palladium(II) Phosphate Catalyzed Three‐Component Reactions of Pyrrole, Diazoesters, and Imines
inferredcites →https://doi.org/10.1002/anie.201403729openalex-snapshot
Synthesis of Extended π‐Systems through C–H Activation
inferredcites →https://doi.org/10.1002/anie.201403894openalex-snapshot
Direct Functionalization with Complete and Switchable Positional Control: Free Phenol as a Role Model
inferredcites →https://doi.org/10.1002/anie.201404946openalex-snapshot
Chemoselective Carbophilic Addition of α‐Diazoesters through Ligand‐Controlled Gold Catalysis
inferredcites →https://doi.org/10.1002/anie.201502324openalex-snapshot
Direct Synthesis of 5‐Aryl Barbituric Acids by Rhodium(II)‐Catalyzed Reactions of Arenes with Diazo Compounds
inferredcites →https://doi.org/10.1002/anie.201504483openalex-snapshot
Enantioselective Palladium‐Catalyzed CH Functionalization of Indoles Using an Axially Chiral 2,2′‐Bipyridine Ligand
inferredcites →https://doi.org/10.1002/anie.201601750openalex-snapshot
Iron and Manganese Catalysts for the Selective Functionalization of Arene C(sp2)−H Bonds by Carbene Insertion
inferredcites →https://doi.org/10.1002/anie.201601999openalex-snapshot
Palladium‐Catalyzed Directed para C−H Functionalization of Phenols
inferredcites →https://doi.org/10.1002/anie.201607893openalex-snapshot
Ligand‐Accelerated Direct C−H Arylation of BINOL: A Rapid One‐Step Synthesis of Racemic 3,3′‐Diaryl BINOLs
inferredcites →https://doi.org/10.1002/anie.201608937openalex-snapshot
(C6F5)3B Catalyzed Chemoselective and ortho‐Selective Substitution of Phenols with α‐Aryl α‐Diazoesters
inferredcites →https://doi.org/10.1002/anie.201609401openalex-snapshot
Copper/P(tBu)3‐Mediated Regiospecific Synthesis of Fused Furans and Naphthofurans
inferredcites →https://doi.org/10.1002/anie.201611809openalex-snapshot
Highly para‐Selective C−H Alkylation of Benzene Derivatives with 2,2,2‐Trifluoroethyl α‐Aryl‐α‐Diazoesters
inferredcites →https://doi.org/10.1002/anie.201709384openalex-snapshot
Selective Functionalization of Aromatic C(sp2)−H Bonds in the Presence of Benzylic C(sp3)−H Bonds by Electron‐Deficient Carbenoids Generated from 4‐Acyl‐1‐Sulfonyl‐1,2,3‐Triazoles
inferredcites →https://doi.org/10.1002/anie.201804829openalex-snapshot
Cu‐Catalyzed Cross‐Dehydrogenative ortho‐Aminomethylation of Phenols
inferredcites →https://doi.org/10.1002/anie.201811729openalex-snapshot
Chemoselective Borane‐Catalyzed Hydroarylation of 1,3‐Dienes with Phenols
inferredcites →https://doi.org/10.1002/anie.201901762openalex-snapshot
Electrooxidative and Regioselective C−H Azolation of Phenol and Aniline Derivatives
inferredcites →https://doi.org/10.1007/s11434-015-0874-0openalex-snapshot
Gold carbene chemistry from diazo compounds
inferredcites →https://doi.org/10.1016/j.tet.2017.03.055openalex-snapshot
P(NMe2)3-promoted ortho-selective arylation of phenols with diaryliodonium triflates via rhodium catalysis
inferredcites →https://doi.org/10.1016/j.tet.2019.05.040openalex-snapshot
Gold-catalyzed chemoselective formal (3+2)-Annulation reaction between β-naphthols and methyl aryldiazoacetate
inferredcites →https://doi.org/10.1021/acs.chemrev.5b00121openalex-snapshot
Modern Organic Synthesis with α-Diazocarbonyl Compounds
inferredcites →https://doi.org/10.1021/acs.chemrev.7b00382openalex-snapshot
Transition-Metal-Catalyzed Cross-Couplings through Carbene Migratory Insertion
inferredcites →https://doi.org/10.1021/acs.jpca.9b11991openalex-snapshot
How CuCl and CuCl2 Insert into C–N Bonds of Diazo Compounds: An Electronic Structure and Mechanistic Study
inferredcites →https://doi.org/10.1021/acs.orglett.7b03390openalex-snapshot
Gold-Catalyzed Controllable C2-Functionalization of Benzofurans with Aryl Diazoesters
inferredcites →https://doi.org/10.1021/acs.orglett.9b01214openalex-snapshot
Rhenium-Catalyzed Regioselective ortho-Alkenylation and [3 + 2 + 1] Cycloaddition of Phenols with Internal Alkynes
inferredcites →https://doi.org/10.1021/acscatal.8b04098openalex-snapshot
Phenol-Directed C–H Functionalization
inferredcites →https://doi.org/10.1021/ar300051uopenalex-snapshot
Transition-Metal-Catalyzed Enantioselective Heteroatom–Hydrogen Bond Insertion Reactions
inferredcites →https://doi.org/10.1021/ar300340kopenalex-snapshot
Novel Multicomponent Reactions via Trapping of Protic Onium Ylides with Electrophiles
inferredcites →https://doi.org/10.1021/ar5004626openalex-snapshot
Bidentate, Monoanionic Auxiliary-Directed Functionalization of Carbon–Hydrogen Bonds
inferredcites →https://doi.org/10.1021/cr040079gopenalex-snapshot
BINOL: A Versatile Chiral Reagent
inferredcites →https://doi.org/10.1021/cr078364yopenalex-snapshot
Coinage Metal Catalyzed C−H Bond Functionalization of Hydrocarbons
inferredcites →https://doi.org/10.1021/cr300153jopenalex-snapshot
Ruthenium(II)-Catalyzed C–H Bond Activation and Functionalization
inferredcites →https://doi.org/10.1021/cr500410yopenalex-snapshot
Copper-Catalyzed C–H Functionalization Reactions: Efficient Synthesis of Heterocycles
inferredcites →https://doi.org/10.1021/cr5006414openalex-snapshot
Catalytic Silylation of Unactivated C–H Bonds
inferredcites →https://doi.org/10.1021/cr900239nopenalex-snapshot
Catalytic Carbene Insertion into C−H Bonds
inferredcites →https://doi.org/10.1021/ja01141a047openalex-snapshot
The Copper-catalyzed Decomposition of Diazoketones1
inferredcites →https://doi.org/10.1021/ja026108ropenalex-snapshot
GaCl3-Catalyzed Ortho-Ethynylation of Phenols
inferredcites →https://doi.org/10.1021/ja0607739openalex-snapshot
Catalytic Enantioselective O−H Insertion Reactions
inferredcites →https://doi.org/10.1021/ja074729kopenalex-snapshot
Highly Enantioselective Insertion of Carbenoids into O−H Bonds of Phenols: An Efficient Approach to Chiral α-Aryloxycarboxylic 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/ja1093309openalex-snapshot
Rhodium(II)-Catalyzed Enantioselective C−H Functionalization of Indoles
inferredcites →https://doi.org/10.1021/ja204924jopenalex-snapshot
Silanol: A Traceless Directing Group for Pd-Catalyzed o-Alkenylation of Phenols
inferredcites →https://doi.org/10.1021/ja302710vopenalex-snapshot
Dehydrative C–H Alkylation and Alkenylation of Phenols with Alcohols: Expedient Synthesis for Substituted Phenols and Benzofurans
inferredcites →https://doi.org/10.1021/ja305771yopenalex-snapshot
Rh-Catalyzed Intermolecular Carbenoid Functionalization of Aromatic C–H Bonds by α-Diazomalonates
inferredcites →https://doi.org/10.1021/ja402274gopenalex-snapshot
A Coupling of Benzamides and Donor/Acceptor Diazo Compounds To Form γ-Lactams via Rh(III)-Catalyzed C–H Activation
inferredcites →https://doi.org/10.1021/ja503163kopenalex-snapshot
Highly Site-Selective Direct C–H Bond Functionalization of Phenols with α-Aryl-α-diazoacetates and Diazooxindoles via Gold Catalysis
inferredcites →https://doi.org/10.1021/ja504797xopenalex-snapshot
Role of Sterically Demanding Chiral Dirhodium Catalysts in Site-Selective C–H Functionalization of Activated Primary C–H Bonds
inferredcites →https://doi.org/10.1021/ja8015878openalex-snapshot
Silyl-Directed, Iridium-Catalyzed ortho -Borylation of Arenes. A One-Pot ortho -Borylation of Phenols, Arylamines, and Alkylarenes
inferredcites →https://doi.org/10.1021/ja904791yopenalex-snapshot
TBDPS and Br-TBDPS Protecting Groups as Efficient Aryl Group Donors in Pd-Catalyzed Arylation of Phenols and Anilines
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/jacs.5b05086openalex-snapshot
Catalytic Asymmetric Arylation of α-Aryl-α-diazoacetates with Aniline Derivatives
inferredcites →https://doi.org/10.1021/jacs.7b06785openalex-snapshot
Cu(II)-Catalyzed ortho-Selective Aminomethylation of Phenols
inferredcites →https://doi.org/10.1021/jacs.7b10349openalex-snapshot
Rh(III)-Catalyzed Redox-Neutral Unsymmetrical C–H Alkylation and Amidation Reactions of N-Phenoxyacetamides
inferredcites →https://doi.org/10.1021/jo030157kopenalex-snapshot
Catalytic Intermolecular Ortho-Arylation of Phenols
inferredcites →https://doi.org/10.1021/ol202977jopenalex-snapshot
Enantioselective Carbenoid Insertion into Phenolic O–H Bonds with a Chiral Copper(I) Imidazoindolephosphine Complex
inferredcites →https://doi.org/10.1038/nature06485openalex-snapshot
Catalytic C–H functionalization by metal carbenoid and nitrenoid insertion
inferredcites →https://doi.org/10.1038/nchem.1406openalex-snapshot
Highly enantioselective trapping of zwitterionic intermediates by imines
inferredcites →https://doi.org/10.1038/nmat2969openalex-snapshot
Managing the scarcity of chemical elements
inferredcites →https://doi.org/10.1039/c2cs15323hopenalex-snapshot
Recent advances in copper-catalyzed dehydrogenative functionalization via a single electron transfer (SET) process
inferredcites →https://doi.org/10.1039/c2cs35096copenalex-snapshot
From C(sp2)–H to C(sp3)–H: systematic studies on transition metal-catalyzed oxidative C–C formation
inferredcites →https://doi.org/10.1039/c4cc07026gopenalex-snapshot
Orthogonal selectivity with cinnamic acids in 3-substituted benzofuran synthesis through C–H olefination of phenols
inferredcites →https://doi.org/10.1039/c5cc08880aopenalex-snapshot
Gold-catalyzed construction of two adjacent quaternary stereocenters via sequential C–H functionalization and aldol annulation
inferredcites →https://doi.org/10.1039/c5cs00821bopenalex-snapshot
Gold-catalyzed transformations of α-diazocarbonyl compounds: selectivity and diversity
inferredcites →https://doi.org/10.1039/c5ob01196eopenalex-snapshot
Copper-catalyzed trifluoromethylation of alkenes: synthesis of trifluoromethylated benzoxazines
inferredcites →https://doi.org/10.1039/c5sc04319kopenalex-snapshot
Origins of unique gold-catalysed chemo- and site-selective C–H functionalization of phenols with diazo compounds
inferredcites →https://doi.org/10.1039/c6cc01958gopenalex-snapshot
Gold and diazo reagents: a fruitful tool for developing molecular complexity
inferredcites →https://doi.org/10.1039/c6cc04034aopenalex-snapshot
Gold-catalysed facile access to indene scaffolds via sequential C–H functionalization and 5-endo-dig carbocyclization
inferredcites →https://doi.org/10.1039/c7cc05649dopenalex-snapshot
Gold-catalyzed para-selective C–H bond alkylation of benzene derivatives with donor/acceptor-substituted diazo compounds
inferredcites →https://doi.org/10.1039/c8cc03288bopenalex-snapshot
Cp*Ir( iii )-catalyzed C–H/N–H functionalization of sulfoximines for the synthesis of 1,2-benzothiazines at room temperature
inferredcites →https://doi.org/10.1039/c9sc01657kopenalex-snapshot
Ligand and counteranion enabled regiodivergent C–H bond functionalization of naphthols with α-aryl-α-diazoesters
inferredcites →https://doi.org/10.1039/c9sc02189bopenalex-snapshot
Bis(imino)pyridine iron complexes for catalytic carbene transfer reactions
inferredcites →https://doi.org/10.1039/d0cc01118eopenalex-snapshot
Gold-catalyzed intermolecular [4+1] spiroannulation via site-selective aromatic C(sp 2 )–H functionalization and dearomatization of phenol derivatives
inferredcites →https://doi.org/10.6023/cjoc201702020openalex-snapshot
Development of Transition-Metal-Catalyzed C(sp2)-H Functionalization of Arenes with Diazo Compounds

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.4669910openalex-extracted
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0085openalex-snapshot
Site‐Selective CH Functionalization with Diazo Compounds (Carbenes)
inferred← citeshttps://doi.org/10.1002/adsc.202100181openalex-snapshot
Triflic Acid‐Catalyzed Chemo‐ and Site‐Selective C−H Bond Functionalization of Phenols With 1,3‐Dienes
inferred← citeshttps://doi.org/10.1002/adsc.70420openalex-snapshot
O 2 ‐Mediated Cu‐Catalyzed Dehydrogenative Sulfilimination of Tyrosines and Bioactive Phenols
inferred← citeshttps://doi.org/10.1002/ange.202116171openalex-snapshot
Dearomative Cyclopropanation of Naphthols via Cyclopropene Ring‐Opening
inferred← citeshttps://doi.org/10.1002/anie.202116171openalex-snapshot
Dearomative Cyclopropanation of Naphthols via Cyclopropene Ring‐Opening
inferred← citeshttps://doi.org/10.1002/asia.202300693openalex-snapshot
Exploring the Divergent Reactivity of Vinyl Radicals Emanating from Alkynes and Thiols via Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/chem.202202820openalex-snapshot
Efficient Synthesis of Diaryl Quaternary Centers by Rh(II)/Xantphos Catalyzed Relay C−H Functionalization and Allylic Alkylation
inferred← citeshttps://doi.org/10.1002/chem.202301595openalex-snapshot
B(C6F5)3‐Catalyzed [2+3]‐Cyclative o,m‐diC‐H Functionalization of Phenols
inferred← citeshttps://doi.org/10.1002/cmtd.202500108openalex-snapshot
Chemo‐Divergent Friedel–Crafts Alkylation and Friedel–Crafts Acylation of Arenes with α ‐Diazo Ketones Tuned by Reaction Conditions
inferred← citeshttps://doi.org/10.1002/slct.202201180openalex-snapshot
Visible‐Light Aided C−H activation: Metal/Base‐Free Generation of C−C bonds using Porphyrin Photocatalyst
inferred← citeshttps://doi.org/10.1007/s11426-021-1003-9openalex-snapshot
Synthesis of structurally diversified BINOLs and NOBINs via palladium-catalyzed C-H arylation with diazoquinones
inferred← citeshttps://doi.org/10.1016/j.gresc.2021.10.001openalex-snapshot
Borane-catalysed S–H insertion reaction of thiophenols and thiols with α-aryl-α-diazoesters
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115351openalex-snapshot
Copper-catalyzed regioselective C−H alkylation of phenol derivatives with unactivated alkyl chlorides: Manifesting a Cu(I)/Cu(III) pathway
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00903openalex-snapshot
Divergent Gold Catalysis: Unlocking Molecular Diversity through Catalyst Control
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01992openalex-snapshot
Visible-Light-Promoted Oxidative Annulation of Naphthols and Alkynes: Synthesis of Functionalized Naphthofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01185openalex-snapshot
Highly Site-Selective Direct C–H Bond Functionalization of Unactivated Arenes with Propargyl α-Aryl-α-diazoacetates via Scandium Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01258openalex-snapshot
Rh(III)-Catalyzed C8-Spiroannulation of 1-Aminonaphthalenes with Maleimides
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04065openalex-snapshot
Dearomatization/Deiodination of o-Iodophenolic Compounds with α,β-Unsaturated Imines for Accessing Benzofuran Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04182openalex-snapshot
Three-Component Ruthenium-Catalyzed meta-C–H Alkylation of Phenol Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04322openalex-snapshot
Cu-Catalyzed Synthesis of Benzoxazole with Phenol and Cyclic Oxime
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00477openalex-snapshot
Highly Stereoselective Synthesis of Tetrasubstituted Vinyl Selenides via Rhodium-Catalyzed [1,4]-Acyl Migration of Selenoesters and Diazo Compounds
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03969openalex-snapshot
Rhodium-Catalyzed C(sp2)–O Cross Couplings of Diazo Quinones with Phenols to Construct Diaryl Ethers
inferred← citeshttps://doi.org/10.1021/acscatal.4c03131openalex-snapshot
Cesium and Phenoxide Interaction Enabled by Rh Overrides the Innate Solvent-Mediated Chemoselectivity
inferred← citeshttps://doi.org/10.1021/acscatal.5c08077openalex-snapshot
Carbene-Protected Copper Nanocluster for Highly Efficient Difunctionalization of C(sp 2 )–H and O–H Bonds
inferred← citeshttps://doi.org/10.1021/acscentsci.2c00004openalex-snapshot
Overcoming O–H Insertion to Para-Selective C–H Functionalization of Free Phenols: Rh(II)/Xantphos Catalyzed Geminal Difunctionalization of Diazo Compounds
inferred← citeshttps://doi.org/10.1039/d0ra06518hopenalex-snapshot
Progress and prospects in copper-catalyzed C–H functionalization
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/d1ob00820jopenalex-snapshot
Brønsted acid catalysed chemo- and ortho -selective aminomethylation of phenol
inferred← citeshttps://doi.org/10.1039/d1ob01035bopenalex-snapshot
B(C 6 F 5 ) 3 -catalyzed O–H insertion reactions of diazoalkanes with phosphinic acids
inferred← citeshttps://doi.org/10.1039/d1ob01286jopenalex-snapshot
A mild and practical method for deprotection of aryl methyl/benzyl/allyl ethers with HPPh 2 and t BuOK
inferred← citeshttps://doi.org/10.1039/d1qo00276gopenalex-snapshot
Iron-catalysed chemo- and ortho -selective C–H bond functionalization of phenols with α-aryl-α-diazoacetates
inferred← citeshttps://doi.org/10.1039/d1qo00805fopenalex-snapshot
A direct synthesis method towards spirocyclic indazole derivatives via Rh( iii )-catalyzed C–H activation and spiroannulation
inferred← citeshttps://doi.org/10.1039/d1qo01184gopenalex-snapshot
Regiospecific and site-selective C–H allylation of phenols with vinyldiazo compounds catalyzed by In( iii )
inferred← citeshttps://doi.org/10.1039/d1qo01265gopenalex-snapshot
Catalyst-free synthesis of α,α-disubstituted carboxylic acid derivatives under ambient conditions via a Wolff rearrangement reaction
inferred← citeshttps://doi.org/10.1039/d1ra08771aopenalex-snapshot
Bakuchiol – a natural meroterpenoid: structure, isolation, synthesis and functionalization approaches
inferred← citeshttps://doi.org/10.1039/d2cc06744gopenalex-snapshot
B(C 6 F 5 ) 3 -catalyzed cyclopropanation of 3-alkenyl-oxindoles with diazomethanes
inferred← citeshttps://doi.org/10.1039/d2qo00475eopenalex-snapshot
Site-selective rhodium carbene transfer of 2 hydroxy-β-nitrostyrenes with diazo compounds En route to 2-alkylated benzofurans
inferred← citeshttps://doi.org/10.1039/d3ob01548copenalex-snapshot
Borane catalyzed transesterification of tert -butyl esters using α-aryl α-diazoesters
inferred← citeshttps://doi.org/10.1039/d3qo00125copenalex-snapshot
A rhodium-catalyzed ylide formation/Smiles rearrangement reaction of chalcogenide ether and triazoles
inferred← citeshttps://doi.org/10.1039/d4ob00162aopenalex-snapshot
Facile Friedel–Crafts alkylation of arenes under solvent-free conditions
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/10.1039/d5cc00594aopenalex-snapshot
Copper-catalyzed chemoselective C–H functionalization/dearomatization sequence: direct access to indole-based spirocyclic scaffolds
inferred← citeshttps://doi.org/10.1039/d5cc01846copenalex-snapshot
Substrate-controlled regioselective C(sp 2 )–H sulfonylation of ortho -aminophenols
inferred← citeshttps://doi.org/10.1055/a-2134-0352openalex-snapshot
Recent Progress on Copper-Catalyzed C–C Bond Formation via C(sp2)–H Insertions Using Diazo and Related Compounds
inferred← citeshttps://doi.org/10.1055/a-2851-2548openalex-snapshot
Highly Chemo- and Site-Selective Aromatic C–H Bond Functionalization of Phenols with α-Aryl-α-diazoketones via Gold Catalysis
inferred← citeshttps://doi.org/10.1055/s-0040-1706426openalex-snapshot
Copper-Catalyzed ortho-Functionalization of Naphthols and Phenols
inferred← citeshttps://doi.org/10.3390/molecules28041767openalex-snapshot
Theoretical Study on the Copper-Catalyzed ortho-Selective C-H Functionalization of Naphthols with α-Phenyl-α-Diazoesters
inferred← citeshttps://doi.org/10.3390/molecules28083397openalex-snapshot
Recent Advances in Regioselective C–H Bond Functionalization of Free Phenols
inferred← citeshttps://doi.org/10.6023/cjoc202601038openalex-snapshot
Bismuth-Catalyzed X—H Insertion of Diaryl Diazomethanes
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.