On the public citation graph

Carboxylation and Esterification of Functionalized Arylcopper Reagents

https://doi.org/10.1021/jo047731s
0 signed · 113 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/9780470132388.ch3openalex-snapshot
Tetrakis[iodo(tri‐n‐butylphosphine)copper(I)] and Iodo‐(2,2′‐Bipyridine)‐(Tri‐n‐butylphosphine)copper(I)
inferredcites →https://doi.org/10.1002/ange.19580700102openalex-snapshot
Synthese von Di‐ und Tricarbonsäuren aromatischer Ringsysteme durch Verschiebung von Carboxyl‐Gruppen
inferredcites →https://doi.org/10.1002/anie.196403621openalex-snapshot
Organosodium and Organopotassium Compounds. Part II: Preparation and Synthetic Applications
inferredcites →https://doi.org/10.1002/jlac.18601130120openalex-snapshot
Ueber Synthese der Salicylsäure
inferredcites →https://doi.org/10.1016/0040-4020(89)80072-9openalex-snapshot
New organocopper reagents prepared utilizing highly reactive copper
inferredcites →https://doi.org/10.1016/0960-894x(96)00363-0openalex-snapshot
Novel antifungal 2-aryl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol derivatives with high activity against Aspergillus fumigatus
inferredcites →https://doi.org/10.1016/s0040-4020(02)00830-xopenalex-snapshot
Facile synthesis of ethyl 2-arylpropenoates by cross-coupling reaction using electrogenerated highly reactive zinc
inferredcites →https://doi.org/10.1016/s0040-4039(00)77593-9openalex-snapshot
Remarkably stable ortho-halophenylcopper reagents
inferredcites →https://doi.org/10.1016/s0040-4039(00)91416-3openalex-snapshot
Vinyl acetates from vinyl bromides
inferredcites →https://doi.org/10.1016/s0040-4039(00)93380-xopenalex-snapshot
Preparation of higher order cyano and “non-ate” allyl copper reagents from the reaction of allyl chlorides with a formal copper anion
inferredcites →https://doi.org/10.1016/s0040-4039(00)98797-5openalex-snapshot
SN2′ Substitutions of 1,3-Dichloropropenes with the Functionalized Copper-Zinc Reagents RCu(CN)ZnX
inferredcites →https://doi.org/10.1016/s0040-4039(01)84358-6openalex-snapshot
Organocopper species III. The reaction of copper (I) carboxylates with organyl halides
inferredcites →https://doi.org/10.1016/s0040-4039(01)91965-3openalex-snapshot
Organocopper intermediates in the exchange reaction of aryl halides with salts of copper(I). The possible role of copper(III)
inferredcites →https://doi.org/10.1021/ar50094a004openalex-snapshot
Disodium tetracarbonylferrate, a transition metal analog of a Grignard reagent
inferredcites →https://doi.org/10.1021/cen-v026n031.p2261openalex-snapshot
114th National Meeting American Chemical Society
inferredcites →https://doi.org/10.1021/cr60216a001openalex-snapshot
The Benzyne and Related Intermediates.
inferredcites →https://doi.org/10.1021/ja00012a041openalex-snapshot
Direct formation of functionalized and allylic organocopper reagents derived from a cuprous cyanide lithium bromide complex
inferredcites →https://doi.org/10.1021/ja00039a023openalex-snapshot
Direct formation of highly functionalized allylic organocopper reagents from allylic chlorides and acetates
inferredcites →https://doi.org/10.1021/ja00723a056openalex-snapshot
Facile conversion of alkyl bromides into aldehydes using sodium tetracarbonylferrate(-II)
inferredcites →https://doi.org/10.1021/ja00971a048openalex-snapshot
The Production of Organocopper Intermediates from Radicals in the Reactions of Aromatic Halides and Diazonium Ions with Cuprous Benzoate. New Synthetic Methods for Aryl Benzoates1
inferredcites →https://doi.org/10.1021/ja01303a039openalex-snapshot
The Rates of Alcoholysis of Acyl Chlorides
inferredcites →https://doi.org/10.1021/ja01559a066openalex-snapshot
Central Stimulants. α,α-Disubstituted 2-Piperidinemethanols and 1,1-Disubstituted Heptahydroöxazolo [3,4-a]pyridines
inferredcites →https://doi.org/10.1021/ja01565a037openalex-snapshot
Rates of Solvolysis of the Halophenyldimethylcarbinyl Chlorides. The Effect of Halogen Substituents upon the Rates of Electrophilic Reactions1-3
inferredcites →https://doi.org/10.1021/jo00015a032openalex-snapshot
Direct formation and subsequent substitution of remote ketone-functionalized organocopper reagents
inferredcites →https://doi.org/10.1021/jo00061a024openalex-snapshot
Direct formation and reaction of thienyl-based organocopper reagents
inferredcites →https://doi.org/10.1021/jo00113a013openalex-snapshot
Direct Formation of (Haloaryl)copper Nucleophiles from Haloiodobenzenes and Active Copper
inferredcites →https://doi.org/10.1021/jo00200a064openalex-snapshot
Direct formation of organocopper compounds by oxidative addition of zerovalent copper to organic halides
inferredcites →https://doi.org/10.1021/jo00254a012openalex-snapshot
Preparation of aryl, alkynyl, and vinyl organocopper compounds by the oxidative addition of zerovalent copper to carbon-halogen bonds
inferredcites →https://doi.org/10.1021/jo00267a051openalex-snapshot
Silylcupration-mediated synthesis of 2-substituted allylamines
inferredcites →https://doi.org/10.1021/jo00289a037openalex-snapshot
Homocoupling of alkyl halides and cyclization of .alpha.,.omega.-dihaloalkanes via activated copper
inferredcites →https://doi.org/10.1021/jo00870a018openalex-snapshot
Esterification by alkylation of carboxylate salts. Influence of steric factors and other parameters on reaction rates
inferredcites →https://doi.org/10.1021/om00040a028openalex-snapshot
Formation and substitution of remote ester functionalized organocopper reagents
inferredcites →https://doi.org/10.1039/jr9600000592openalex-snapshot
121. The Ullmann biaryl synthesis. Part V. The influence of ring substituents on the rate of self-condensation of an aryl halide
inferredcites →https://doi.org/10.1080/00397919208021663openalex-snapshot
Direct Formation and Reactions of Allylic Thienyl-Based Organocopper Reagents
inferredcites →https://doi.org/10.1080/00397919408019062openalex-snapshot
Synthetically Useful Mono-Functionalizations of Dihaloarenes via Rieke Metals
inferredcites →https://doi.org/10.1126/science.246.4935.1260openalex-snapshot
Preparation of Organometallic Compounds from Highly Reactive Metal Powders
inferredcites →https://doi.org/10.1246/bcsj.38.330openalex-snapshot
The Reaction of Organolithium Compounds with Nickel Carbonyl

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.4655564openalex-extracted
Recent Progress in the Development of Electrode Materials for Electrochemical Carboxylation with Co2
inferred← citeshttps://doi.org/10.1002/047084289x.rc192.pub2openalex-snapshot
Copper
inferred← citeshttps://doi.org/10.1002/047084289x.rl131.pub2openalex-snapshot
Lithium Naphthalenide
inferred← citeshttps://doi.org/10.1002/9781118662083.cot09-003openalex-snapshot
Formation of Nitriles, Carboxylic Acids, and Derivatives by Carbonylation, Carboxylation, and Related Reactions
inferred← citeshttps://doi.org/10.1002/9783527827992.ch28openalex-snapshot
Carboxylation Reaction Based on the Direct and Indirect Uses of CO 2 : Sustainable Syntheses of CCO 2 , OCO 2 , and NCO 2 Bonds
inferred← citeshttps://doi.org/10.1002/adsc.201100934openalex-snapshot
Carboxylation of Terminal Alkynes with Carbon Dioxide Catalyzed by Poly(N‐Heterocyclic Carbene)‐Supported Silver Nanoparticles
inferred← citeshttps://doi.org/10.1002/ange.200900667openalex-snapshot
Metallkatalysierte Carboxylierung metallorganischer Reagentien mit Kohlendioxid
inferred← citeshttps://doi.org/10.1002/ange.201101341openalex-snapshot
Katalytische Hydrocarboxylierung von Alkenen und Alkinen mit CO2
inferred← citeshttps://doi.org/10.1002/ange.201803186openalex-snapshot
Übergangsmetallkatalysierte Carboxylierungen mit Kohlendioxid
inferred← citeshttps://doi.org/10.1002/ange.202013914openalex-snapshot
Phosphine Carboxylate—Probing the Edge of Stability of a Carbon Dioxide Adduct with Dihydrogenphosphide
inferred← citeshttps://doi.org/10.1002/ange.202214710openalex-snapshot
Site‐Selective Electrochemical C−H Carboxylation of Arenes with CO2
inferred← citeshttps://doi.org/10.1002/anie.200900667openalex-snapshot
Metal‐Catalyzed Carboxylation of Organometallic Reagents with Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/anie.201101341openalex-snapshot
Catalytic Hydrocarboxylation of Alkenes and Alkynes with CO2
inferred← citeshttps://doi.org/10.1002/anie.201803186openalex-snapshot
Transition‐Metal‐Catalyzed Carboxylation Reactions with Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/anie.202013914openalex-snapshot
Phosphine Carboxylate—Probing the Edge of Stability of a Carbon Dioxide Adduct with Dihydrogenphosphide
inferred← citeshttps://doi.org/10.1002/anie.202214710openalex-snapshot
Site‐Selective Electrochemical C−H Carboxylation of Arenes with CO2
inferred← citeshttps://doi.org/10.1002/cctc.201600760openalex-snapshot
Efficient and selective Palladium‐catalyzed Telomerization of 1,3‐Butadiene with Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/cctc.201600943openalex-snapshot
Recent Progress in Metal Catalyzed Direct Carboxylation of Aryl Halides and Pseudo Halides Employing CO2: Opportunities for 11C Radiochemistry
inferred← citeshttps://doi.org/10.1002/chem.201601114openalex-snapshot
Carboxylation of Phenols with CO2 at Atmospheric Pressure
inferred← citeshttps://doi.org/10.1002/chem.202203228openalex-snapshot
Electrocatalytic Reduction of CO2 Coupled with Organic Conversion to Selectively Synthesize High‐Value Chemicals
inferred← citeshttps://doi.org/10.1002/chin.200542094openalex-snapshot
Carboxylation and Esterification of Functionalized Arylcopper Reagents.
inferred← citeshttps://doi.org/10.1002/slct.201803669openalex-snapshot
Nanoporous ZnO Supported CuBr (CuBr/ZnO): An Efficient Catalyst for CO 2 Fixation Reactions
inferred← citeshttps://doi.org/10.1002/slct.202403692openalex-snapshot
Metal‐Free Photooxidation of Toluene Derivatives into the Corresponding Carboxylic Acids and Aldehydes by a HBr/NaOCl·5H 2 O System
inferred← citeshttps://doi.org/10.1002/slct.202505513openalex-snapshot
Expanding the Synthetic Horizon With CO 2 : A C 1 Synthon for Constructing Organic Functionalities and Heterocycles
inferred← citeshttps://doi.org/10.1007/3418_2023_82openalex-snapshot
Copper-Catalyzed C–C Bond Formation via Carboxylation Reactions with CO2
inferred← citeshttps://doi.org/10.1007/s10562-016-1920-5openalex-snapshot
Inserting CO2 into Terminal Alkynes via Bis-(NHC)-Metal Complexes
inferred← citeshttps://doi.org/10.1007/s11244-014-0301-9openalex-snapshot
Making C–C Bonds from Carbon Dioxide via Transition-Metal Catalysis
inferred← citeshttps://doi.org/10.1007/s41061-016-0091-6openalex-snapshot
Synthesis of Carboxylic Acids and Esters from CO2
inferred← citeshttps://doi.org/10.1016/j.apcata.2014.06.004openalex-snapshot
Facile esterification of carboxylic acid using amide functionalized benzimidazolium dicationic ionic liquids
inferred← citeshttps://doi.org/10.1016/j.ccr.2014.09.002openalex-snapshot
Transition metal complex catalyzed carboxylation reactions with CO2
inferred← citeshttps://doi.org/10.1016/j.jcat.2015.09.009openalex-snapshot
Solid poly-N-heterocyclic carbene catalyzed CO2 reduction with hydrosilanes
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115371openalex-snapshot
Recent progress in the development of electrode materials for electrochemical carboxylation with CO2
inferred← citeshttps://doi.org/10.1016/j.tet.2008.03.028openalex-snapshot
Study of the microwave-assisted hydrolysis of nitriles and esters and the implementation of this system in rapid microwave-assisted Pd-catalyzed amination
inferred← citeshttps://doi.org/10.1016/j.tet.2018.09.051openalex-snapshot
Practical selective monohydrolysis of bulky symmetric diesters: Comparing with sonochemistry
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.12.061openalex-snapshot
Practical selective monohydrolysis of bulky symmetric diesters
inferred← citeshttps://doi.org/10.1021/acs.organomet.9b00642openalex-snapshot
Construction of C–Cu Bond: A Useful Strategy in CO2 Conversion
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00836openalex-snapshot
Nickel-Catalyzed Carboxylation of Aryl and Heteroaryl Fluorosulfates Using Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/acscatal.6b02124openalex-snapshot
Metal-Catalyzed Carboxylation of Organic (Pseudo)halides with CO2
inferred← citeshttps://doi.org/10.1021/cm201562popenalex-snapshot
Polymers with Carbazole-Oxadiazole Side Chains as Ambipolar Hosts for Phosphorescent Light-Emitting Diodes
inferred← citeshttps://doi.org/10.1021/cs400443popenalex-snapshot
Copper-Catalyzed Carboxylation of Aryl Iodides with Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/ja803435wopenalex-snapshot
Beyond Aresta’s Complex: Ni- and Pd-Catalyzed Organozinc Coupling with CO2
inferred← citeshttps://doi.org/10.1021/ol200638zopenalex-snapshot
Ligand-Free Ag(I)-Catalyzed Carboxylation of Terminal Alkynes with CO2
inferred← citeshttps://doi.org/10.1021/om300819dopenalex-snapshot
Nickel-Catalyzed Reductive Hydroesterification of Styrenes Using CO2 and MeOH
inferred← citeshttps://doi.org/10.1039/b801381kopenalex-snapshot
Alkali/coinage metals—organolithium, organocuprate chemistry
inferred← citeshttps://doi.org/10.1039/b920163gopenalex-snapshot
Recent developments in carbon dioxide utilization under mild conditions
inferred← citeshttps://doi.org/10.1039/c0cc03890copenalex-snapshot
Direct C–H carboxylation with complexes of the coinage metals
inferred← citeshttps://doi.org/10.1039/c0cs00129eopenalex-snapshot
Transition-metal-catalyzed C–C bond formation through the fixation of carbon dioxide
inferred← citeshttps://doi.org/10.1039/c2cc33848copenalex-snapshot
Carbon dioxide as a carbon source in organic transformation: carbon–carbon bond forming reactions by transition-metal catalysts
inferred← citeshttps://doi.org/10.1039/c4gc00243aopenalex-snapshot
Computational and experimental comparison of diphosphane and diene ligands in the Rh-catalysed carboxylation of organoboron compounds with CO2
inferred← citeshttps://doi.org/10.1039/c4ra00254gopenalex-snapshot
Theoretical insights into copper( i )–NHC-catalyzed C–H carboxylation of terminal alkynes with CO 2 : the reaction mechanisms and the roles of NHC
inferred← citeshttps://doi.org/10.1039/c5cc01153aopenalex-snapshot
Zirconocene-catalyzed sequential ethylcarboxylation of alkenes using ethylmagnesium chloride and carbon dioxide
inferred← citeshttps://doi.org/10.1039/c5dt03794hopenalex-snapshot
1,1′-Bis(di-tert-butylphosphino)ferrocene copper( i ) complex catalyzed C–H activation and carboxylation of terminal alkynes
inferred← citeshttps://doi.org/10.1039/c5ob00200aopenalex-snapshot
Copper-catalysed cross-coupling: an untapped potential
inferred← citeshttps://doi.org/10.1039/c6ob00199hopenalex-snapshot
Copper-catalyzed carboxylation reactions using carbon dioxide
inferred← citeshttps://doi.org/10.1039/c7gc00917hopenalex-snapshot
Incorporation of carbon dioxide into phthalides via ligand-free copper-catalyzed direct carboxylation of benzoxasiloles
inferred← citeshttps://doi.org/10.1039/c7nj03038jopenalex-snapshot
cis -1,2-Bis(diphenylphosphino)ethylene copper( i ) catalyzed C–H activation and carboxylation of terminal alkynes
inferred← citeshttps://doi.org/10.1039/c8nj02286kopenalex-snapshot
Flower-like AgNPs@m-MgO as an excellent catalyst for CO 2 fixation and acylation reactions under ambient conditions
inferred← citeshttps://doi.org/10.1039/c9cc06156hopenalex-snapshot
The dilemma between acid and base catalysis in the synthesis of benzimidazole from o -phenylenediamine and carbon dioxide
inferred← citeshttps://doi.org/10.1039/d1sc02413bopenalex-snapshot
Suppressing carboxylate nucleophilicity with inorganic salts enables selective electrocarboxylation without sacrificial anodes
inferred← citeshttps://doi.org/10.1039/d5gc04497aopenalex-snapshot
Organo-photocatalyzed deoxygenative alkylcarboxylation of olefins with alcohols and CO 2
inferred← citeshttps://doi.org/10.1055/s-0036-1588429openalex-snapshot
Transition-Metal- and Halogen-Free Oxidation of Benzylic sp3 C–H Bonds to Carbonyl Groups Using Potassium Persulfate
inferred← citeshttps://doi.org/10.1055/s-0043-1763755openalex-snapshot
Carboxylation of Alkenes with CO2 via Photocatalytic Cleavage of C=C Double Bonds
inferred← citeshttps://doi.org/10.1055/sos-sd-118-00330openalex-snapshot
18.2.16 Carbon Dioxide, Carbonyl Sulfide, Carbon Disulfide, Isocyanates, Isothiocyanates, Carbodiimides, and Their Selenium, Tellurium, and Phosphorus Analogues (Update 2014)
inferred← citeshttps://doi.org/10.1055/sos-sd-213-00154openalex-snapshot
2.5.4 Carboxylation of Organometallic Reagents
inferred← citeshttps://doi.org/10.1073/pnas.1010962107openalex-snapshot
Copper- and copper– N -heterocyclic carbene-catalyzed C─H activating carboxylation of terminal alkynes with CO 2 at ambient conditions
inferred← citeshttps://doi.org/10.1080/00397910601039226openalex-snapshot
Preparation of Monoalkyl Terephthalates: An Overview
inferred← citeshttps://doi.org/10.3184/030823410x12670951969185openalex-snapshot
Oxidative Esterification of Aldehydes with Alcohols and Phenols in Air
inferred← citeshttps://doi.org/10.3184/174751914x14031774189763openalex-snapshot
2-Iodoxybenzenesulfonic Acid-Catalysed oxidation of Primary and Secondary Alcohols with Oxone in Cetyl Trimethylammonium Bromide Micelles at Room Temperature
inferred← citeshttps://doi.org/10.3390/catal13050811openalex-snapshot
Recent Advances in N-Heterocyclic Carbene Coinage Metal Complexes in A3-Coupling and Carboxylation Reaction
inferred← citeshttps://doi.org/10.3390/catal13121489openalex-snapshot
Recent Advances in Catalyst Design for Carboxylation Using CO2 as the C1 Feedstock
inferred← citeshttps://doi.org/10.3390/catal8070273openalex-snapshot
Highly Efficient Electrocatalytic Carboxylation of 1-Phenylethyl Chloride at Cu Foam Cathode
inferred← citeshttps://doi.org/10.3762/bjoc.10.260openalex-snapshot
Electrocarboxylation: towards sustainable and efficient synthesis of valuable carboxylic acids
inferred← citeshttps://doi.org/10.3987/rev-18-895openalex-snapshot
Recent Advancements in the Synthesis of Half-Esters and Their Applications
inferred← citeshttps://doi.org/10.4018/978-1-5225-8033-1.ch002openalex-snapshot
Conversion of CO2 to High Value Products
inferred← citeshttps://doi.org/10.4028/www.scientific.net/msf.764.1openalex-snapshot
Conversion of Carbon Dioxide into Several Potential Chemical Commodities Following Different Pathways - A Review
inferred← citeshttps://doi.org/10.70675/03ff1123ze99dz4c60z8dc3z268abd7e91d4openalex-snapshot
Développement de nouvelles sondes photoactivables pour la caractérisation des cibles cellulaires du glutathion
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.