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Organic Base-Mediated Carboxylation of (Hetero)aromatic Compounds Using Supercritical Carbon Dioxide (scCO2)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Synthetic Organic Chemistry in Supercritical Fluids
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Aluminum‐Catalyzed Formation of Functional 1,3,2‐Dioxathiolane 2‐Oxides from Sulfur Dioxide: An Easy Entry towards N‐Substituted Aziridines
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CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals
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Microwave‐Assisted Kolbe‐Schmitt Synthesis Using Ionic Liquids or Dimcarb as Reactive Solvents
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Flow Chemistry of the Kolbe‐Schmitt Synthesis from Resorcinol: Process Intensification by Alternative Solvents, New Reagents and Advanced Reactor Engineering
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Carboxylation of Phenols with CO2 at Atmospheric Pressure
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C−H Carboxylation of Aromatic Compounds through CO2 Fixation
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Studies on the Structure and Biosynthesis of Tridentoquinone and Related Meroterpenoids from the Mushroom Suillus tridentinus (Boletales)
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AlMe3‐Mediated Regio‐ and Chemoselective Reactions of Indole with Carbamoyl Electrophiles
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A Green Alternative for the Conversion of Arylboronic Acids/Esters into Phenols Promoted by a Reducing Agent, Sodium Sulfite
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Ueber eine neue Darstellungsmethode und einige bemerkenswerte Eigenschaften der Salicylsäure
inferredcites →https://doi.org/10.1002/prac.18850310130openalex-snapshot
Beitrag zur Kenntniss der Kolbe'schen Salicylsäure Synthese
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Improving Pharmaceutical Product Development and Manufacturing: Impact on Cost of Drug Development and Cost of Goods Sold of Pharmaceuticals
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Selective syntheses using cyclodextrins as catalysts
inferredcites →https://doi.org/10.1016/j.apcata.2008.03.037openalex-snapshot
K2CO3-catalyzed direct synthesis of salicylic acid from phenol and supercritical CO2
inferredcites →https://doi.org/10.1016/j.bmcl.2018.03.019openalex-snapshot
Design, synthesis, and evaluation of simple phenol amides as ERRγ agonists
inferredcites →https://doi.org/10.1016/j.cattod.2006.02.019openalex-snapshot
An environmentally friendly hydroformylation using carbon dioxide as a reactant catalyzed by immobilized Ru-complex in ionic liquids
inferredcites →https://doi.org/10.1016/j.cep.2019.107532openalex-snapshot
Are supercritical fluids solvents for the future?
inferredcites →https://doi.org/10.1016/j.cogsc.2018.11.006openalex-snapshot
The greening of solvents: Towards sustainable organic synthesis
inferredcites →https://doi.org/10.1016/j.ejmech.2017.11.054openalex-snapshot
Design, synthesis, and biological evaluation of a series of resorcinol-based N-benzyl benzamide derivatives as potent Hsp90 inhibitors
inferredcites →https://doi.org/10.1016/j.molcata.2004.06.009openalex-snapshot
Ruthenium-catalyzed one-pot hydroformylation of alkenes using carbon dioxide as a reactant
inferredcites →https://doi.org/10.1016/j.molcata.2008.07.017openalex-snapshot
Efficient regioselective carboxylation of phenol to salicylic acid with supercritical CO2 in the presence of aluminium bromide
inferredcites →https://doi.org/10.1016/j.molstruc.2020.127875openalex-snapshot
Synthesis, anticancer evaluation and molecular docking studies of 2,5-bis(indolyl)-1,3,4-oxadiazoles, Nortopsentin analogues
inferredcites →https://doi.org/10.1016/j.tet.2015.08.040openalex-snapshot
An efficient method for syntheses of functionalized 6-bulkysubstituted salicylates under microwave irradiation
inferredcites →https://doi.org/10.1016/j.tet.2015.12.028openalex-snapshot
Me2AlCl-mediated carboxylation, ethoxycarbonylation, and carbamoylation of indoles
inferredcites →https://doi.org/10.1016/j.tetlet.2007.05.132openalex-snapshot
The improved Kolbe–Schmitt reaction using supercritical carbon dioxide
inferredcites →https://doi.org/10.1016/j.tetlet.2009.05.076openalex-snapshot
Carboxylation of indoles and pyrroles with CO2 in the presence of dialkylaluminum halides
inferredcites →https://doi.org/10.1016/j.ultsonch.2015.05.019openalex-snapshot
Conversion of carbon dioxide to resorcylic acid under ultrasonication by Kolbe–Schmitt reaction
inferredcites →https://doi.org/10.1016/s0196-8904(96)00297-xopenalex-snapshot
Carbon dioxide utilisation in the chemical industry
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Synthesis of a Series of Diaminoindoles
inferredcites →https://doi.org/10.1021/jacs.5b05477openalex-snapshot
Hydroxyl-Directed Cross-Coupling: A Scalable Synthesis of Debromohamigeran E and Other Targets of Interest
inferredcites →https://doi.org/10.1021/jm100060bopenalex-snapshot
Discovery of (2,4-Dihydroxy-5-isopropylphenyl)-[5-(4-methylpiperazin-1-ylmethyl)-1,3-dihydroisoindol-2-yl]methanone (AT13387), a Novel Inhibitor of the Molecular Chaperone Hsp90 by Fragment Based Drug Design
inferredcites →https://doi.org/10.1021/jm501745fopenalex-snapshot
Discovery of Highly Selective Brain-Penetrant Vasopressin 1a Antagonists for the Potential Treatment of Autism via a Chemogenomic and Scaffold Hopping Approach
inferredcites →https://doi.org/10.1021/jo01369a006openalex-snapshot
A STUDY OF THE KOLBE-SCHMITT REACTION. II. THE CARBONATION OF PHENOLS
inferredcites →https://doi.org/10.1021/ol050580aopenalex-snapshot
Radester, a Novel Inhibitor of the Hsp90 Protein Folding Machinery
inferredcites →https://doi.org/10.1021/ol3025082openalex-snapshot
Base-Mediated Carboxylation of Unprotected Indole Derivatives with Carbon Dioxide
inferredcites →https://doi.org/10.1021/ol4003465openalex-snapshot
Palladium-Catalyzed Synthesis of Aromatic Carboxylic Acids with Silacarboxylic Acids
inferredcites →https://doi.org/10.1021/op015507oopenalex-snapshot
An Efficient Large-Scale Process for the Human Leukocyte Elastase Inhibitor, DMP 7771
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Large-Scale Applications of Amide Coupling Reagents for the Synthesis of Pharmaceuticals
inferredcites →https://doi.org/10.1038/nature22316openalex-snapshot
Remote carboxylation of halogenated aliphatic hydrocarbons with carbon dioxide
inferredcites →https://doi.org/10.1038/s41467-017-02088-wopenalex-snapshot
Structural absorption by barbule microstructures of super black bird of paradise feathers
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Continuous reactions in supercritical fluids; a cleaner, more selective synthesis of thymol in supercritical CO2
inferredcites →https://doi.org/10.1039/b703488copenalex-snapshot
Key green chemistry research areas—a perspective from pharmaceutical manufacturers
inferredcites →https://doi.org/10.1039/c1cs15083aopenalex-snapshot
Towards mild metal-catalyzed C–H bond activation
inferredcites →https://doi.org/10.1039/c5gc00611bopenalex-snapshot
Perspectives on the replacement of harmful organic solvents in analytical methodologies: a framework toward the implementation of a generation of eco-friendly alternatives
inferredcites →https://doi.org/10.1039/c5ra00358jopenalex-snapshot
Green chemistry approaches as sustainable alternatives to conventional strategies in the pharmaceutical industry
inferredcites →https://doi.org/10.1039/c8gc00008eopenalex-snapshot
Pressurized CO 2 as a carboxylating agent for the biocatalytic ortho -carboxylation of resorcinol
inferredcites →https://doi.org/10.1039/c9cc04550copenalex-snapshot
Kolbe–Schmitt type reaction under ambient conditions mediated by an organic base
inferredcites →https://doi.org/10.1039/jr9520003503openalex-snapshot
671. The carboxylation of resorcinol and the separation of β-and γ-resorcylic acid by ion-exchange chromatography
inferredcites →https://doi.org/10.1080/00397911.2019.1711415openalex-snapshot
A convenient and efficient H2SO4-promoted regioselective monobromination of phenol derivatives using N-bromosuccinimide
inferredcites →https://doi.org/10.1139/v70-222openalex-snapshot
Orientation in nitration and sulfonation of 2,5-dimethylbenzoic acid
inferredcites →https://doi.org/10.3390/nano11010190openalex-snapshot
First Phenol Carboxylation with CO2 on Carbon Nanostructured C@Fe-Al2O3 Hybrids in Aqueous Media under Mild Conditions
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Exploring Green Solvents and Solvent-Free Conditions for Sustainable Organocatalysis
inferred← citeshttps://doi.org/10.1002/ange.202522503openalex-snapshot
A Para‐Selective Kolbe–Schmitt Reaction
inferred← citeshttps://doi.org/10.1002/anie.202522503openalex-snapshot
A Para‐Selective Kolbe–Schmitt Reaction
inferred← citeshttps://doi.org/10.1007/s13369-026-11442-4openalex-snapshot
TPA–Imidazolium@FeCl4 DES as an Eco-Friendly Catalyst and Electrolyte for the Synthesis of Salicylic Acid Derivatives Via Electro-Chemical Kolbe-Schmitt Reaction and Evaluation of Their Anticancer Potential
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The difference of reaction mechanism between 2, 4-di-tert-butylphenol and 2, 6-di-tert-butylphenol in the synthesis of salicylic acid
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