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Silver-Catalyzed Protodecarboxylation of Heteroaromatic Carboxylic Acids
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Copper‐Catalyzed Protodecarboxylation of Aromatic Carboxylic Acids
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Unique Versatility of Ionic Liquids as Clean Decarboxylation Catalyst Cum Solvent: A Metal‐ and Quinoline‐Free Paradigm towards Synthesis of Indoles, Styrenes, Stilbenes and Arene Derivatives under Microwave Irradiation in Aqueous Conditions
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Dynamic Stereochemistry Transfer in a Transannular Aldol Reaction: Total Synthesis of Hypocrellin A
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The mercury-mediated decarboxylation (Pesci reaction) of naphthoic anhydrides investigated by microwave synthesis
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A new synthesis of furostifoline
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Organocopper intermediates via decarboxylation of cuprous carboxylates
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THE SIMPLE HALOGEN DERIVATIVES OF FURAN
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Two Methods for Directortho-Arylation of Benzoic Acids
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Room Temperature and Phosphine Free Palladium Catalyzed Direct C-2 Arylation of Indoles
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Decarboxylation via Addition of Water to a Carboxyl Group: Acid Catalysis of Pyrrole-2-Carboxylic Acid
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Decarboxylation of indole-2-carboxylic acids: improved procedures
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Products and kinetics of decarboxylation of activated and unactivated aromatic cuprous carboxylates in pyridine and in quinoline
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Decarboxylation of 5-substituted 2-pyridinecarboxylic acids
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Decarboxylation of some 2-substituted pyridinecarboxylic acids
inferredcites →https://doi.org/10.1021/jo00802a019openalex-snapshot
Further evidence as to the nature of the transition state leading to decarboxylation of 2-pyridinecarboxylic acids. Electrical effects in the transition state
inferredcites →https://doi.org/10.1021/jo00975a052openalex-snapshot
Thermal decarboxylation of 2-furoic acids
inferredcites →https://doi.org/10.1021/jo01367a013openalex-snapshot
DECARBOXYLATION AND FORMYLATION OF CERTAIN PYRROLE DERIVATIVES*1
inferredcites →https://doi.org/10.1021/jo015959zopenalex-snapshot
Novel Syntheses of Cis and Trans Isomers of Combretastatin A-4
inferredcites →https://doi.org/10.1021/jo040134lopenalex-snapshot
Efficient Total Syntheses of Phytoalexin and (±)-Paniculidine B and C Based on the Novel Methodology for the Preparation of 1-Methoxyindoles
inferredcites →https://doi.org/10.1021/jo802628zopenalex-snapshot
Microwave-Assisted Cu-Catalyzed Protodecarboxylation of Aromatic Carboxylic Acids
inferredcites →https://doi.org/10.1021/jo962115kopenalex-snapshot
Applications of High-Temperature Aqueous Media for Synthetic Organic Reactions
inferredcites →https://doi.org/10.1021/ol0492602openalex-snapshot
Palladium-Catalyzed Decarboxylation and Decarbonylation under Hydrothermal Conditions: Decarboxylative Deuteration
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Development of a Catalytic Aromatic Decarboxylation Reaction
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Electrophilic substitution at a saturated carbon atom. Part XIV. Consecutive unimolecular mercurydeprotonation and mercurydecarboxylation of pyridioacetic acid ions in aqueous solution
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Synthesis of Biaryls via Catalytic Decarboxylative Coupling
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Ruthenium-Catalyzed Addition of Aromatic Esters at the ortho C–H Bonds to Olefins
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A New Biaryl Synthesis Illustrating a Connection between the Ullmann Biaryl Synthesis and Copper-catalysed Decarboxylation.
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2-Arylthiophenes and 2-Arylfurans by Decarboxylative Couplings of 2-Thenoic and 2-Furoic Acids with Iodoarenes.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Carboxylic Acids as Traceless Directing Groups for Formal meta ‐Selective Direct Arylation
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Palladium‐Catalyzed Decarboxylative CH Bond Arylation of Thiophenes
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Carboxylic Acids as Traceless Directing Groups for the Rhodium(III)‐Catalyzed Decarboxylative CH Arylation of Thiophenes
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The Gold(I)‐Catalysed Protodecarboxylation Mechanism
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Direct CH Amidation of Benzoic Acids to Introduce meta‐ and para‐Amino Groups by Tandem Decarboxylation
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Decarboxylation as the Key Step in C−C Bond‐Forming Reactions
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Advances in Electrochemical Decarboxylative Transformation Reactions
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ChemInform Abstract: Silver‐Catalyzed Protodecarboxylation of Heteroaromatic Carboxylic Acids.
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Tetrasubstituted 2-Imidazolones via Ag(I)-Catalyzed Cycloisomerization of Propargylic Ureas
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Protonated Carbonic Acid and Reactive Intermediates in the Acidic Decarboxylation of Indolecarboxylic Acids
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Palladium-Catalyzed Decarboxylative Cross-Coupling Reactions: A Route for Regioselective Functionalization of Coumarins
inferred← citeshttps://doi.org/10.1021/jo4024478openalex-snapshot
Copper/Silver-Mediated Cascade Reactions for the Construction of 2-Sulfonylbenzo[b]furans from trans-2-Hydroxycinnamic Acids and Sodium Sulfinates
inferred← citeshttps://doi.org/10.1021/jp910498yopenalex-snapshot
A Theoretical Study on C−COOH Homolytic Bond Dissociation Enthalpies
inferred← citeshttps://doi.org/10.1021/ol100001bopenalex-snapshot
Rh(I)-Catalyzed Decarboxylative Transformations of Arenecarboxylic Acids: Ligand- and Reagent-Controlled Selectivity toward Hydrodecarboxylation or Heck−Mizoroki Products
inferred← citeshttps://doi.org/10.1021/ol102158nopenalex-snapshot
Pd-Catalyzed Dearboxylative Heck Coupling with Dioxygen as the Terminal Oxidant
inferred← citeshttps://doi.org/10.1021/ol102974kopenalex-snapshot
Density Functional Theory Study on the Mechanism of Rh-Catalyzed Decarboxylative Conjugate Addition: Diffusion- and Ligand-Controlled Selectivity toward Hydrolysis or β-Hydride Elimination
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/ol300235kopenalex-snapshot
Palladium-Catalyzed Decarboxylative Coupling of Quinolinone-3-Carboxylic Acids and Related Heterocyclic Carboxylic Acids with (Hetero)aryl Halides
inferred← citeshttps://doi.org/10.1021/ol400065jopenalex-snapshot
Direct ortho-Arylation of ortho-Substituted Benzoic Acids: Overriding Pd-Catalyzed Protodecarboxylation
inferred← citeshttps://doi.org/10.1021/ol400197yopenalex-snapshot
Copper Catalyzed Decarboxylative Alkynylation of Quaternary α-Cyano Acetate Salts
inferred← citeshttps://doi.org/10.1021/ol400719dopenalex-snapshot
Direct Benzothiophene Formation via Oxygen-Triggered Intermolecular Cyclization of Thiophenols and Alkynes Assisted by Manganese/PhCOOH
inferred← citeshttps://doi.org/10.1021/ol9027896openalex-snapshot
Synthesis of α,ω-Diarylbutadienes and -Hexatrienes via Decarboxylative Coupling of Cinnamic Acids with Vinyl Bromides under Palladium Catalysis
inferred← citeshttps://doi.org/10.1021/om1000875openalex-snapshot
Unimolecular Reactions of Organocuprates and Organoargentates
inferred← citeshttps://doi.org/10.1021/om200359wopenalex-snapshot
Modeling Solvation of Magnesium Centers by Ether Ligands: Gas-Phase Synthesis and Hydrolysis of the Organomagnesium Cations [CH3Mg(3X-crown-X)]+(X= 4–6)
inferred← citeshttps://doi.org/10.1021/om500493wopenalex-snapshot
Direct versus Water-Mediated Protodecarboxylation of Acetic Acid Catalyzed by Group 10 Carboxylates, [(phen)M(O2CCH3)]+
inferred← citeshttps://doi.org/10.1038/s41467-023-39531-0openalex-snapshot
Rapid planning and analysis of high-throughput experiment arrays for reaction discovery
inferred← citeshttps://doi.org/10.1039/c0cc01029dopenalex-snapshot
Pd-catalyzed cross-coupling of carboxylic acids with nitroethane via combination of decarboxylation and dehydrogenation
inferred← citeshttps://doi.org/10.1039/c0cc01943gopenalex-snapshot
Decarboxylative homocoupling of (hetero)aromatic carboxylic acids
inferred← citeshttps://doi.org/10.1039/c0cc05708hopenalex-snapshot
Decarboxylative biaryl synthesis in a continuous flow reactor
inferred← citeshttps://doi.org/10.1039/c0dt00508hopenalex-snapshot
Gas phase synthesis and reactivity of dimethylaurate
inferred← citeshttps://doi.org/10.1039/c0dt01234copenalex-snapshot
Pd-catalyzed decarboxylative arylation of silyl enol ester sp3β-C–H bond under aerobic conditions
inferred← citeshttps://doi.org/10.1039/c1cc10917kopenalex-snapshot
Decarboxylation of aromatic carboxylic acids by gold( i )- N -heterocyclic carbene (NHC) complexes
inferred← citeshttps://doi.org/10.1039/c1cs15093fopenalex-snapshot
Decarboxylative coupling reactions: a modern strategy for C–C-bond formation
inferred← citeshttps://doi.org/10.1039/c2cc33203eopenalex-snapshot
Copper-catalyzed decarboxylative C(sp2)–C(sp3) coupling reactions via radical mechanism
inferred← citeshttps://doi.org/10.1039/c2cc33306fopenalex-snapshot
Protodecarboxylation of benzoic acids under radical conditions
inferred← citeshttps://doi.org/10.1039/c2cc36720copenalex-snapshot
Arylation of 2-substituted pyridinesvia Pd-catalyzed decarboxylative cross-coupling reactions of 2-picolinic acid
inferred← citeshttps://doi.org/10.1039/c2ob25157dopenalex-snapshot
Selective deuteration of (hetero)aromatic compounds via deutero-decarboxylation of carboxylic acids
inferred← citeshttps://doi.org/10.1039/c2sc20606dopenalex-snapshot
Copper-catalyzed decarboxylative C–N coupling for N-arylation
inferred← citeshttps://doi.org/10.1039/c3cy00580aopenalex-snapshot
Protodecarboxylation of carboxylic acids over heterogeneous silver catalysts
inferred← citeshttps://doi.org/10.1039/c3dt32285hopenalex-snapshot
Fixed-charge phosphine ligands to explore gas-phase coinage metal-mediated decarboxylation reactions
inferred← citeshttps://doi.org/10.1039/c3gc37131jopenalex-snapshot
Iron-catalyzed direct alkenylation of sp3(C–H) bonds via decarboxylation of cinnamic acids under ligand-free conditions
inferred← citeshttps://doi.org/10.1039/c3ob41588kopenalex-snapshot
CuI/1,10-phen/PEG promoted decarboxylation of 2,3-diarylacrylic acids: synthesis of stilbenes under neutral and microwave conditions with an in situ generated recyclable catalyst
inferred← citeshttps://doi.org/10.1039/c3ra41185kopenalex-snapshot
The palladium-catalyzed tandem decarboxylation, carbon–carbon triple bond oxidation and decarbonylative arylation of the benzoxazole C–H bond
inferred← citeshttps://doi.org/10.1039/c4dt00815dopenalex-snapshot
Palladium dichloride adduct of N,N-bis-(diphenylphosphanylmethyl)-2-aminopyridine: synthesis, structure and catalytic performance in the decarboxylative cross-coupling of 4-picolinic acid with aryl bromide
inferred← citeshttps://doi.org/10.1039/c4dt02813aopenalex-snapshot
Acridine based (S,N,S) pincer ligand: designing silver( i ) complexes for the efficient activation of A 3 (aldehyde, alkyne and amine) coupling
inferred← citeshttps://doi.org/10.1039/c4ob01844copenalex-snapshot
Palladium-catalyzed oxidative cross-coupling of azole-4-carboxylates with indoles: an approach to the synthesis of pimprinine
inferred← citeshttps://doi.org/10.1039/c5cc01762aopenalex-snapshot
Peroxide promoted tunable decarboxylative alkylation of cinnamic acids to form alkenes or ketones under metal-free conditions
inferred← citeshttps://doi.org/10.1039/c5nj02792fopenalex-snapshot
A simple protocol for Cu-catalyzed protodecarboxylation of (hetero)aromatic carboxylic acids
inferred← citeshttps://doi.org/10.1039/c5ob00727eopenalex-snapshot
Decarboxylative functionalization of cinnamic acids
inferred← citeshttps://doi.org/10.1039/c5ob01949dopenalex-snapshot
Metal catalyzed defunctionalization reactions
inferred← citeshttps://doi.org/10.1039/c6cs00107fopenalex-snapshot
Ag-catalyzed C–H/C–C bond functionalization
inferred← citeshttps://doi.org/10.1039/c6ra28299gopenalex-snapshot
Pyridine C3-arylation of nicotinic acids accessible via a multicomponent reaction: an entry to all-substituted-3,4-diarylated pyridines
inferred← citeshttps://doi.org/10.1039/c7cc01755copenalex-snapshot
The use of carboxylic acids as traceless directing groups for regioselective C–H bond functionalisation
inferred← citeshttps://doi.org/10.1039/c7cc02392hopenalex-snapshot
A deciduous directing group approach for the addition of aryl and vinyl nucleophiles to maleimides
inferred← citeshttps://doi.org/10.1039/c7cc09934gopenalex-snapshot
Copper-catalyzed decarboxylative regioselective synthesis of 1,5-disubstituted 1,2,3-triazoles
inferred← citeshttps://doi.org/10.1039/c7gc02949gopenalex-snapshot
Decarboxylative reactions with and without light – a comparison
inferred← citeshttps://doi.org/10.1039/c8cc06074fopenalex-snapshot
Merging base-promoted C–C bond cleavage and iron-catalyzed skeletal rearrangement involving C–C/C–H bond activation: synthesis of highly functionalized carbazoles
inferred← citeshttps://doi.org/10.1039/c8ob01806eopenalex-snapshot
Palladium-catalyzed salt-free double decarboxylative aryl allylation
inferred← citeshttps://doi.org/10.1039/c9gc02407gopenalex-snapshot
Transition-metal-free decarboxylative halogenation of 2-picolinic acids with dihalomethane under oxygen conditions
inferred← citeshttps://doi.org/10.1039/d0re00442aopenalex-snapshot
Enone-promoted decarboxylation of trans -4-hydroxy- l -proline in flow: a side-by-side comparison to batch
inferred← citeshttps://doi.org/10.1039/d0sc02609copenalex-snapshot
Organophotoredox/palladium dual catalytic decarboxylative Csp 3 –Csp 3 coupling of carboxylic acids and π-electrophiles
inferred← citeshttps://doi.org/10.1039/d1cc04907kopenalex-snapshot
Nitrous oxide as a diazo transfer reagent: the synthesis of triazolopyridines
inferred← citeshttps://doi.org/10.1039/d1gc00924aopenalex-snapshot
Exploiting a silver–bismuth hybrid material as heterogeneous noble metal catalyst for decarboxylations and decarboxylative deuterations of carboxylic acids under batch and continuous flow conditions
inferred← citeshttps://doi.org/10.1039/d2qo00453dopenalex-snapshot
Decarboxylative amination of benzoic acids bearing electron-donating substituents and nonactivated amines
inferred← citeshttps://doi.org/10.1039/d3nj04195fopenalex-snapshot
Localized surface plasmon resonance assisted photoredox catalysis using newly fabricated copper-nanorods: a decarboxylative approach towards carbon–hydrogen bond formation under visible light
inferred← citeshttps://doi.org/10.1039/d5ob01402fopenalex-snapshot
Iron catalysis enables mild C–Se bond formation via decarboxylative selenylation
inferred← citeshttps://doi.org/10.1055/s-0029-1218742openalex-snapshot
Carbon-Fluorine Bond Formation for the Synthesis of Aryl Fluorides
inferred← citeshttps://doi.org/10.1055/sos-sd-110-00529openalex-snapshot
10.1 Product Class 1: Benzo[b]furans
inferred← citeshttps://doi.org/10.1055/sos-sd-115-00035openalex-snapshot
15.1.4 Pyridines (Update 2016)
inferred← citeshttps://doi.org/10.1080/00304948.2019.1633228openalex-snapshot
Synthesis of Furans – Recent Advances
inferred← citeshttps://doi.org/10.1080/00397911.2019.1570525openalex-snapshot
Application of silver-promoted reactions in the synthesis of five-membered O -heterocycles
inferred← citeshttps://doi.org/10.1111/cbdd.13003openalex-snapshot
A field‐based disparity analysis of new 1,2,5‐oxadiazole derivatives endowed with antiproliferative activity
inferred← citeshttps://doi.org/10.1134/s1990793119030163openalex-snapshot
New Amphiphilic Calix[4]Arene Derivatives with 4,5-Dicarboxytriazolyl Fragments: Synthesis and Use in Micellar Catalysis
inferred← citeshttps://doi.org/10.1177/1469066718795959openalex-snapshot
Formation and reactions of the 1, 8-naphthyridine (napy) ligated geminally dimetallated phenyl complexes [(napy)Cu 2 (Ph)] + , [(napy)Ag 2 (Ph)] + and [(napy)CuAg(Ph)] +
inferred← citeshttps://doi.org/10.1201/b13023-4openalex-snapshot
Valuable Vinylphenols from Rapeseed and Canola
inferred← citeshttps://doi.org/10.1515/gps-2013-0043openalex-snapshot
Microwave heating and conventionally-heated continuous-flow processing as tools for performing cleaner palladium-catalyzed decarboxylative couplings using oxygen as the oxidant – a proof of principle study
inferred← citeshttps://doi.org/10.2174/157017861109140903105543openalex-snapshot
New Synthons of 3-Hydroxyquinoline Derivatives Through SEAr
inferred← citeshttps://doi.org/10.2174/1570179416666181207144430openalex-snapshot
Metal and Non-Metal Catalysts in the Synthesis of Five-Membered S-Heterocycles
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-lxc1vopenalex-snapshot
Copper-Catalyzed Decarboxylative Elimination of Carboxylic Acids to Alkenes
inferred← citeshttps://doi.org/10.3390/catal9121032openalex-snapshot
Recent Organic Transformations with Silver Carbonate as a Key External Base and Oxidant
inferred← citeshttps://doi.org/10.3390/md21040242openalex-snapshot
Challenging Structure Elucidation of Lumnitzeralactone, an Ellagic Acid Derivative from the Mangrove Lumnitzera racemosa
inferred← citeshttps://doi.org/10.6023/cjoc202502006openalex-snapshot
Recent Progress in Traceless Directed Functionalization Reactions of Arylcarboxylic Acids
inferred← citeshttps://doi.org/10.70675/5740e263z6109z44fdzbb8czce907d47990dopenalex-snapshot
Mechanistic insights in the decarboxylation and CO₂ insertion into novel copper (I) complexes
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