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Cu-Catalyzed Arylation of Phenols: Synthesis of Sterically Hindered and Heteroaryl Diaryl Ethers
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Synthesis of Diaryl Ethers: A Long-Standing Problem Has Been Solved
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Mild Ullmann‐Type Biaryl Ether Formation Reaction by Combination of ortho‐Substituent and Ligand Effects
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Significantly Improved Method for the Pd‐Catalyzed Coupling of Phenols with Aryl Halides: Understanding Ligand Effects
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Three Groups Good, Four Groups Bad? Atropisomerism in ortho‐Substituted Diaryl Ethers
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Enantioselective Synthesis of an Atropisomeric Diaryl Ether
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Catalytic CC, CN, and CO Ullmann‐Type Coupling Reactions
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Ueber eine neue Darstellungsweise von Phenyläthersalicylsäure
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Copper‐ or Iron‐Catalyzed Arylation of Phenols from respectively Aryl Chlorides and Aryl Iodides
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Oligomeric cyanate ester resins: Application of a modified Ullmann synthesis in the preparation of thermosetting polymers
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Heteroatom-linked indanylpyrazines are corticotropin releasing factor type-1 receptor antagonists
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Copper in cross-coupling reactions
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An efficient catalyst system for diaryl ether synthesis from aryl chlorides
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Effect of microwave heating on Ullmann-type heterocycle-aryl ether synthesis using chloro-heterocycles
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Recent Advances in Diaryl Ether Synthesis
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Efficient nucleophilic substitution reactions of pyrimidyl and pyrazyl halides with nucleophiles under focused microwave irradiation
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Tetrahedron report number 163
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The first synthesis of an optically active molecular bevel gear with only two cogs on each wheel
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New N- and O-arylations with phenylboronic acids and cupric acetate
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Copper/Amino Acid Catalyzed Cross-Couplings of Aryl and Vinyl Halides with Nucleophiles
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Orthogonal Cu- and Pd-Based Catalyst Systems for the O- and N-Arylation of Aminophenols
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Palladium-Catalyzed C−O Coupling Involving Unactivated Aryl Halides. Sterically Induced Reductive Elimination To Form the C−O Bond in Diaryl Ethers
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inferredcites →https://doi.org/10.1021/jo0606960openalex-snapshot
Mild and Nonracemizing Conditions for Ullmann-type Diaryl Ether Formation between Aryl Iodides and Tyrosine Derivatives
inferredcites →https://doi.org/10.1021/jo0609982openalex-snapshot
Synthesis and Structure of Cyclic Oligo(p-phenylene oxide)s, −(C6H4O)n− (n = 6−10)
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A β-Keto Ester as a Novel, Efficient, and Versatile Ligand for Copper(I)-Catalyzed C−N, C−O, and C−S Coupling Reactions
inferredcites →https://doi.org/10.1021/jo9012157openalex-snapshot
(2-Pyridyl)acetone-Promoted Cu-Catalyzed O-Arylation of Phenols with Aryl Iodides, Bromides, and Chlorides
inferredcites →https://doi.org/10.1021/ol0350947openalex-snapshot
N,N-Dimethyl Glycine-Promoted Ullmann Coupling Reaction of Phenols and Aryl Halides
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1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols
inferredcites →https://doi.org/10.1021/ol062904gopenalex-snapshot
Cu-Catalyzed N- and O-Arylation of 2-, 3-, and 4-Hydroxypyridines and Hydroxyquinolines
inferredcites →https://doi.org/10.1021/ol0700409openalex-snapshot
Copper-in-Charcoal (Cu/C) Promoted Diaryl Ether Formation
inferredcites →https://doi.org/10.1021/op800266xopenalex-snapshot
Preparation of a Corticotropin-Releasing Factor Antagonist by Nucleophilic Aromatic Substitution and Copper-Mediated Ether Formation
inferredcites →https://doi.org/10.1039/b915249kopenalex-snapshot
Efficient palladium-catalyzed coupling reactions of aryl bromides and chlorides with phenols
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SNAr Bases Macrocyclization via Biaryl Ether Formation: Application in Natural Product Synthesis
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Photochemistry and Photoinduced Toxicity of Acifluorfen, a Diphenyl-Ether Herbicide
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.112openalex-snapshot
A 2,2′-bipyridine-palladacycle catalyzed the coupling of arylboronic acids with nitroarenes
inferred← citeshttps://doi.org/10.1016/j.tet.2015.08.066openalex-snapshot
Copper and l -sodium ascorbate catalyzed hydroxylation and aryloxylation of aryl halides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.08.073openalex-snapshot
Liebeskind–Srogl cross coupling mediated synthesis of verbenachalcone
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.08.059openalex-snapshot
CuI-catalyzed hydroxylation of aryl bromides under the assistance of 5-bromo-2-(1H-imidazol-2-yl)pyridine and related ligands
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.10.149openalex-snapshot
Highly efficient copper catalytic system for the O-arylation of phenol with iodoarene
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.01.063openalex-snapshot
Room temperature Ullmann type C–O and C–S cross coupling of aryl halides with phenol/thiophenol catalyzed by CuO nanoparticles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.11.089openalex-snapshot
Unexpected copper mediated benzyl O→O migration during an Ullmann ether coupling
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.02.073openalex-snapshot
Microwave assisted synthesis of selected diaryl ethers under Cu(I)-catalysis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.04.101openalex-snapshot
CuI mediated synthesis of heterocyclic flavone-benzofuran fused derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.07.099openalex-snapshot
N-Picolinamides as ligands in Ullman type C–O coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153516openalex-snapshot
Copper-catalyzed sp3-sp3 cross-coupling of turbo grignards with benzyl halides
inferred← citeshttps://doi.org/10.1016/j.tgchem.2025.100072openalex-snapshot
Advanced approach to O-alkyl/aryl salicylaldehyde derivatives: Synthesis, characterization, and free-radical homopolymerization for improved thermal stability
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.7b00961openalex-snapshot
Modifying Emission Spectral Bandwidth of Phosphorescent Platinum(II) Complexes Through Synthetic Control
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.9b01617openalex-snapshot
Metal-Assisted Delayed Fluorescent Pd(II) Complexes and Phosphorescent Pt(II) Complex Based on [1,2,4]Triazolo[4,3-a]pyridine-Containing Ligands: Synthesis, Characterization, Electrochemistry, Photophysical Studies, and Application
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.6b01436openalex-snapshot
First Structure–Activity Relationship of 17β-Hydroxysteroid Dehydrogenase Type 14 Nonsteroidal Inhibitors and Crystal Structures in Complex with the Enzyme
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00227openalex-snapshot
Total Syntheses of Lobaric Acid and Its Derivatives from the Antarctic LichenStereocaulon alpinum
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02389openalex-snapshot
Nickel-Catalyzed Cross-Coupling of Aryl 2-Pyridyl Ethers with Organozinc Reagents: Removal of the Directing Group via Cleavage of the Carbon–Oxygen Bonds
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02598openalex-snapshot
Cyanide Ion-Promoted Nucleophilic Displacement of Aromatic Nitro Groups: A Mild, One-Pot, Transition Metal-Free Synthesis of Nitrile-Containing Naphthalimide Aryl Ether Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01357openalex-snapshot
Room-Temperature CuI-Catalyzed N-Arylation of Cyclopropylamine
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01077openalex-snapshot
Aerobic Copper-Catalyzed O-Methylation with Methylboronic Acid
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02849openalex-snapshot
Brønsted Acid Catalyzed Functionalization of Aromatic Alcohols through Nucleophilic Substitution of Hydroxyl Group
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00493openalex-snapshot
Copper-Catalyzed Diaryl Ether Formation from (Hetero)aryl Halides at Low Catalytic Loadings
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02221openalex-snapshot
Rh(III)-Catalyzed Direct ortho-Chalcogenation of Phenols and Anilines
inferred← citeshttps://doi.org/10.1021/acs.joc.7b03020openalex-snapshot
“On Water’’ Promoted Ullmann-Type C–N Bond-Forming Reactions: Application to Carbazole Alkaloids by Selective N-Arylation of Aminophenols
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00020openalex-snapshot
Synthesis of Bioactive 3,4-Dihydro-2 H -naphtho[2,3- b ][1,4]oxazine-5,10-dione and 2,3,4,5-Tetrahydro-1 H -naphtho[2,3- b ]azepine-6,11-dione Derivatives via the Copper-Catalyzed Intramolecular Coupling Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01451openalex-snapshot
Syntheses of Diverse Donor-Substituted Bisbenzofuro[2,3-b:3′,2′-e]pyridines (BBZFPys) via Pd Catalysis, and Their Photophysical Properties
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00997openalex-snapshot
l -(−)-Quebrachitol as a Ligand for Selective Copper(0)-Catalyzed N-Arylation of Nitrogen-Containing Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.oprd.2c00050openalex-snapshot
Cu-Mediated Ullmann-Type Cross-Coupling and Industrial Applications in Route Design, Process Development, and Scale-up of Pharmaceutical and Agrochemical Processes
inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00018openalex-snapshot
Diaryl Ether Formation Merging Photoredox and Nickel Catalysis
inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00183openalex-snapshot
Pd-Catalyzed Etherification of Nitroarenes
inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00377openalex-snapshot
Isomerization-Induced Multiple Reaction Pathways in Platinum-Catalyzed C–H Acylation Reaction of 2-Aryloxypyridines
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00517openalex-snapshot
Regioselective Hydroxylation of Flavonoids by Transition-Metal-Catalyzed C–H Bond Oxidation
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02620openalex-snapshot
CuSO4/N-(9H-carbazol-9-yl)picolinamide-Catalyzed C–O Coupling of (Hetero)Aryl Chlorides with Phenols on Water
inferred← citeshttps://doi.org/10.1021/acsami.3c16260openalex-snapshot
Bis-tridentate Ir(III) Phosphors and Blue Hyperphosphorescence with Suppressed Efficiency Roll-Off at High Brightness
inferred← citeshttps://doi.org/10.1021/acscatal.0c02990openalex-snapshot
Transition-Metal-Catalyzed Denitrative Coupling of Nitroarenes
inferred← citeshttps://doi.org/10.1021/acscatal.5b00050openalex-snapshot
Recent Advances on Ester Synthesis via Transition-Metal Catalyzed C–H Functionalization
inferred← citeshttps://doi.org/10.1021/acsomega.0c00982openalex-snapshot
Introducing an α-Keto Ester Functional Group through Pt-Catalyzed Direct C–H Acylation with Ethyl Chlorooxoacetate
inferred← citeshttps://doi.org/10.1021/ja104264vopenalex-snapshot
Alternative Mechanistic Explanation for Ligand-Dependent Selectivities in Copper-Catalyzed N - and O -Arylation Reactions
inferred← citeshttps://doi.org/10.1021/ja203642nopenalex-snapshot
Total Synthesis and Absolute Stereochemical Assignment of Kibdelone C
inferred← citeshttps://doi.org/10.1021/ja504886xopenalex-snapshot
General Method for Functionalized Polyaryl Synthesis via Aryne Intermediates
inferred← citeshttps://doi.org/10.1021/jacs.5c13469openalex-snapshot
Pd-Catalyzed O-Arylation of Phenols Mediated by a Weak, Soluble Organic Base: Methodology, Mechanism, and Compatibility with Enabling Technologies
inferred← citeshttps://doi.org/10.1021/jacs.7b00049openalex-snapshot
Decarbonylative Diaryl Ether Synthesis by Pd and Ni Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.7b11197openalex-snapshot
Enantioselective Intermolecular C–O Bond Formation in the Desymmetrization of Diarylmethines Employing a Guanidinylated Peptide-Based Catalyst
inferred← citeshttps://doi.org/10.1021/jm500147kopenalex-snapshot
Discovery, Synthesis, and Optimization of Antimalarial 4(1 H )-Quinolone-3-Diarylethers
inferred← citeshttps://doi.org/10.1021/jm500777sopenalex-snapshot
Discovery of Potent and Selective Sirtuin 2 (SIRT2) Inhibitors Using a Fragment-Based Approach
inferred← citeshttps://doi.org/10.1021/jo1022052openalex-snapshot
Transition-Metal-Free O -, S -, and N -Arylation of Alcohols, Thiols, Amides, Amines, and Related Heterocycles
inferred← citeshttps://doi.org/10.1021/jo302089fopenalex-snapshot
Macrocyclizations for Medicinal Chemistry: Synthesis of Druglike Macrocycles by High-Concentration Ullmann Coupling
inferred← citeshttps://doi.org/10.1021/jo400092ropenalex-snapshot
Alkynylated Diazadioxaacenes: Syntheses and Properties
inferred← citeshttps://doi.org/10.1021/ol503224uopenalex-snapshot
Metal-Free Synthesis of ortho-CHO Diaryl Ethers by a Three-Component Sequential Coupling
inferred← citeshttps://doi.org/10.1021/om300636fopenalex-snapshot
Contribution to the Mechanism of Copper-Catalyzed C–N and C–O Bond Formation
inferred← citeshttps://doi.org/10.1039/c0dt00632gopenalex-snapshot
On the origin of copper(i) catalysts from copper(ii) precursors in C–N and C–O cross-couplings
inferred← citeshttps://doi.org/10.1039/c1cc12694fopenalex-snapshot
Chemoselectivity in the Cu-catalyzed O-arylation of phenols and aliphatic alcohols
inferred← citeshttps://doi.org/10.1039/c1gc15481hopenalex-snapshot
O-Alkylation of phenol derivatives via a nucleophilic substitution
inferred← citeshttps://doi.org/10.1039/c2gc16539bopenalex-snapshot
Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids
inferred← citeshttps://doi.org/10.1039/c2gc36776aopenalex-snapshot
Straightforward heterogeneous palladium catalyzed synthesis of aryl ethers and aryl amines via a solvent free aerobic and non-aerobic dehydrogenative arylation
inferred← citeshttps://doi.org/10.1039/c2ra20730copenalex-snapshot
Ligand-free coupling of phenols and alcohols with aryl halides by a recyclable heterogeneous copper catalyst
inferred← citeshttps://doi.org/10.1039/c3ob41332bopenalex-snapshot
Dual catalysis by Cu(i): facile single step click and intramolecular C–O bond formation leading to triazole tethered dihydrobenzodioxines/benzoxazines/benzoxathiines/benzodioxepines
inferred← citeshttps://doi.org/10.1039/c4dt00582aopenalex-snapshot
Possible intermediates of Cu(phen)-catalyzed C–O cross-coupling of phenol with an aryl bromide by in situ ESI-MS and EPR studies
inferred← citeshttps://doi.org/10.1039/c4ob00084fopenalex-snapshot
Pd(ii)-catalyzed oxidative alkoxycarbonylation of 2-phenoxypyridine derivatives with CO and alcohols
inferred← citeshttps://doi.org/10.1039/c5ra10037bopenalex-snapshot
Barberry fruit extract assisted in situ green synthesis of Cu nanoparticles supported on a reduced graphene oxide–Fe 3 O 4 nanocomposite as a magnetically separable and reusable catalyst for the O-arylation of phenols with aryl halides under ligand-free conditions
inferred← citeshttps://doi.org/10.1039/c5ra14758aopenalex-snapshot
A family of ligand and anion dependent structurally diverse Cu( ii ) Schiff-base complexes and their catalytic efficacy in an O -arylation reaction in ethanolic media
inferred← citeshttps://doi.org/10.1039/c6cp00579aopenalex-snapshot
Ether cleavage-triggered degradation of benzyl alkylammonium cations for polyethersulfone anion exchange membranes
inferred← citeshttps://doi.org/10.1039/c6ra04409copenalex-snapshot
Heterogeneous O-arylation of nitroarenes with substituted phenols over a copper immobilized mesoporous silica catalyst
inferred← citeshttps://doi.org/10.1039/c6ra12914eopenalex-snapshot
A review on the advancement of ether synthesis from organic solvent to water
inferred← citeshttps://doi.org/10.1039/c7nj00883jopenalex-snapshot
Analysis of the degradation mechanism of the polyarylene ether anion-exchange membrane for alkaline fuel cell and water-splitting cell applications
inferred← citeshttps://doi.org/10.1039/c7ra09939hopenalex-snapshot
Regioselective C–H chlorination: towards the sequential difunctionalization of phenol derivatives and late-stage chlorination of bioactive compounds
inferred← citeshttps://doi.org/10.1039/c8tc03194kopenalex-snapshot
Blue-emitting bis-tridentate Ir( iii ) phosphors: OLED performances vs. substituent effects
inferred← citeshttps://doi.org/10.1039/d0ob00078gopenalex-snapshot
A modular approach to the bisbenzylisoquinoline alkaloids tetrandrine and isotetrandrine
inferred← citeshttps://doi.org/10.1039/d0qo01150aopenalex-snapshot
Prolinamide plays a key role in promoting copper-catalyzed cycloaddition of azides and alkynes in aqueous media via unprecedented metallacycle intermediates
inferred← citeshttps://doi.org/10.1039/d1dt04371dopenalex-snapshot
Organosulphur and organoselenium compounds as emerging building blocks for catalytic systems for O -arylation of phenols, a C–O coupling reaction
inferred← citeshttps://doi.org/10.1039/d3nj04319copenalex-snapshot
A CuMoO 4 nanocatalyst for C sp 2 –O cross-couplings; easy access to nitrofen derivatives
inferred← citeshttps://doi.org/10.1039/d4cc02331eopenalex-snapshot
Oxalamide ligands with additional coordinating groups for Cu-catalyzed arylation of alcohols and phenols
inferred← citeshttps://doi.org/10.1055/a-1784-1973openalex-snapshot
Copper-Mediated C–O/C–N Bond Formation: A Facile Synthesis of 3-Amidocoumarin, 3-Amidoazacoumarin, and N-Aroylindole Derivatives
inferred← citeshttps://doi.org/10.1055/s-0037-1610655openalex-snapshot
Ligand-Free CuI-Catalyzed Chemoselective S-Arylation of 2-Mercaptobenzimidazole with Aryl Iodides
inferred← citeshttps://doi.org/10.1055/sos-sd-238-00002openalex-snapshot
1.1 Modern Ullmann-Type Couplings
inferred← citeshttps://doi.org/10.1080/00304948.2013.816208openalex-snapshot
Recent Synthetic Developments and Applications of the Ullmann Reaction. A Review
inferred← citeshttps://doi.org/10.1080/00397911.2011.594544openalex-snapshot
Expedient Synthesis of Biologically Potent Aryloxycoumarins and (Aryloxyimino)ethylcoumarins via Copper(II)-Promoted Chan–Lam Coupling Reaction
inferred← citeshttps://doi.org/10.1080/00397911.2014.903421openalex-snapshot
Betti Base as an Efficient Ligand for Copper-Catalyzed Ullmann Coupling of Phenol with Aryl Halides
inferred← citeshttps://doi.org/10.1080/00958972.2021.1914333openalex-snapshot
Preparation and characterization of Cu based on 5,5'-bistetrazole as a recyclable metal-organic framework and application in synthesis of diaryl ether by the Ullmann coupling reaction
inferred← citeshttps://doi.org/10.1080/00958972.2021.2019719openalex-snapshot
Preparation and characterization of a Cu complex based on 2,2′-bipyrimidine as a recyclable metal-organic framework for Suzuki coupling
inferred← citeshttps://doi.org/10.1080/10406638.2021.2019802openalex-snapshot
A Simple and Efficient Ligand-Free Copper-Catalyzed C-N Bond Formation of Aryl (Hetero) Halides and N-Heteroaryl Amines
inferred← citeshttps://doi.org/10.1080/10406638.2022.2112715openalex-snapshot
Preparation of 2-Amino-4-Phenyl-4a,5,6,7-Tetrahydronaphthalene-1,3,3(4H)-Tricarbonitriles Using Prepared CuI Nanoparticles via Green Method by Berberis integerrima (Barberry) Extract
inferred← citeshttps://doi.org/10.1080/10426507.2015.1119135openalex-snapshot
Ullmann diaryl ether synthesis catalyzed by copper (I)/pyridine-functionalized silane
inferred← citeshttps://doi.org/10.1080/17415993.2018.1519566openalex-snapshot
Copper(I) selenophene-2-carboxylate (CuSC) promoted C–S cross-coupling reaction of thiols with aryl iodides
inferred← citeshttps://doi.org/10.1134/s1070363224612791openalex-snapshot
Cu(OAc)2 Catalyzed, Microwave Assisted O-Arylation of Phenols with Haloarenes Using Guanidinium Ionic Liquids as Recyclable System Under Mild Reaction Conditions
inferred← citeshttps://doi.org/10.1155/2012/647386openalex-snapshot
Environmentally Benign Mortar-Pestle-Induced Acylation and O-Alkylation of Aromatic and Heteroaromatic Compounds under Solvent-Free Micellar Conditions and Computation of Their Drug Likeliness Properties
inferred← citeshttps://doi.org/10.1177/0954008320945386openalex-snapshot
Ullmann coupling for low-cost synthesis of anthracene-based polyfluorenes: A photophysical approach
inferred← citeshttps://doi.org/10.1246/cl.180425openalex-snapshot
Cu/Fe/O=PPh 3 -Catalyzed Etherification for the Synthesis of Aryl 3-Benzo[ b ]thienyl Ethers
inferred← citeshttps://doi.org/10.1246/cl.2012.87openalex-snapshot
The First Total Synthesis of Gravicycle
inferred← citeshttps://doi.org/10.1515/epoly-2022-0084openalex-snapshot
A new insight into the reaction mechanism in preparation of poly(phenylene sulfide)
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7844273/v1openalex-snapshot
Harnessing regioselective aryl migration of pyridone-based aryl-λ3‑iodonium salts to access iodine-substituted aryloxypyridines
inferred← citeshttps://doi.org/10.3184/174751912x13247245983221openalex-snapshot
A New Strategy for the One Pot Synthesis of (Aryloxyimino)Ethylcoumarins Promoted by CuCl 2
inferred← citeshttps://doi.org/10.3184/174751916x14597761998193openalex-snapshot
Visible-Light-Mediated Synthesis of Diaryl Ethers from Arylboronic Acids and Diaryliodonium Salts
inferred← citeshttps://doi.org/10.3390/ijms27010110openalex-snapshot
Evaluation of Cytocompatibility and Anti-Inflammatory Activity of Carboxyxanthones Selected by In Silico Studies
inferred← citeshttps://doi.org/10.3390/molecules181214797openalex-snapshot
New Short Strategy for the Synthesis of the Dibenz[b,f]oxepin Scaffold
inferred← citeshttps://doi.org/10.3390/molecules24183234openalex-snapshot
Synthesis and Biological Evaluation of Disubstituted Pyrimidines as Selective 5-HT2C Agonists
inferred← citeshttps://doi.org/10.3390/molecules25245845openalex-snapshot
A Pyranoxanthone as a Potent Antimitotic and Sensitizer of Cancer Cells to Low Doses of Paclitaxel
inferred← citeshttps://doi.org/10.3390/molecules26113370openalex-snapshot
CuI-Catalyzed Coupling Reactions of 4-Iodopyrazoles and Alcohols: Application toward Withasomnine and Homologs
inferred← citeshttps://doi.org/10.3390/molecules28010062openalex-snapshot
Microwave-Assisted Cu-Catalyzed Diaryletherification for Facile Synthesis of Bioactive Prenylated Diresorcinols
inferred← citeshttps://doi.org/10.3390/nano7060149openalex-snapshot
A Recyclable Cu-MOF-74 Catalyst for the Ligand-Free O-Arylation Reaction of 4-Nitrobenzaldehyde and Phenol
inferred← citeshttps://doi.org/10.3390/ph14121311openalex-snapshot
Expanding the Diversity at the C-4 Position of Pyrido[2,3-d]pyrimidin-7(8H)-ones to Achieve Biological Activity against ZAP-70
inferred← citeshttps://doi.org/10.3762/bjoc.8.122openalex-snapshot
Screening of ligands for the Ullmann synthesis of electron-rich diaryl ethers
inferred← citeshttps://doi.org/10.3987/rev-17-869openalex-snapshot
Synthesis of Unsymmetric HetAr–X–HetAr’ Compounds by Rhodium-Catalyzed Heteroaryl Exchange Reactions
inferred← citeshttps://doi.org/10.4236/gsc.2012.24018openalex-snapshot
Environmentally Benign Synthetic Protocol for O-Alkylation of β-Naphthols and Hydroxy Pyridines in Aqueous Micellar Media
inferred← citeshttps://doi.org/10.4236/ijoc.2020.104010openalex-snapshot
Microwave Irradiated Palladium-Catalyzed Cascade Type Cross Coupling of Phenols and Halides for the Synthesis of Polyphenolic Ethers
inferred← citeshttps://doi.org/10.5012/bkcs.2013.34.12.3915openalex-snapshot
Aminophenols as Efficient Ligand for Copper-Catalyzed Ullmann-type Synthesis of Diaryl Ethers
inferred← citeshttps://doi.org/10.70675/6f251c39zce64z4ea6z8194zfcbb1226d97fopenalex-snapshot
Nouvelles méthodes de synthèse pour la formation de liaisons C(aryl)-hétéroatome et C(aryl)-C par réactions de substitution nucléophile aromatique et vinylique
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