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Synthesis of Heteroaryl Compounds through Cross-Coupling Reaction of Aryl Bromides or Benzyl Halides with Thienyl and Pyridyl Aluminum Reagents
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Palladium in Heterocyclic Chemistry
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2-Pyridyl and 3-pyridylzinc bromides: direct preparation and coupling reaction
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Facile synthesis of 3-arylpyridine derivatives by palladacycle-catalyzed Stille cross-coupling reaction
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Negishi coupling of 2-pyridylzinc bromide—paradigm shift in cross-coupling chemistry?
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Functional polypyridine ligands from copper-mediated room temperature coupling of 4-chloro-2-trimethylsilylpyridine
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Iron-Catalyzed Reactions in Organic Synthesis
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Room-Temperature Hiyama Cross-Couplings of Arylsilanes with Alkyl Bromides and Iodides
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Iron-catalysed Negishi coupling of benzylhalides and phosphates
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Iron(iii) chloride in oxidative C–C coupling reactions
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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ChemInform Abstract: Synthesis of Heteroaryl Compounds Through Cross‐Coupling Reaction of Aryl Bromides or Benzyl Halides with Thienyl and Pyridyl Aluminum Reagents.
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inferred← citeshttps://doi.org/10.1002/ejoc.201900130openalex-snapshot
Transition‐Metal‐Free Heterobiaryl Synthesis via Aryne Coupling
inferred← citeshttps://doi.org/10.1002/ejoc.202300594openalex-snapshot
Pyrazine Derivative as Supramolecular Host for Immobilization of Palladium Nanoparticles for Efficient Suzuki Coupling
inferred← citeshttps://doi.org/10.1007/s10562-024-04662-6openalex-snapshot
Nickel (II) imidazol-2-ylidine Complexes Supported Through Internally Functionalized Amido Linkage Synthesis and Catalytic Studies for Suzuki Miyaura Cross Coupling
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2015.01.009openalex-snapshot
Nickel-catalyzed one-pot synthesis of biaryls from phenols and arylboronic acids via C–O activation using TCT reagent
inferred← citeshttps://doi.org/10.1016/j.tet.2016.02.005openalex-snapshot
PBr3-mediated unexpected reductive deoxygenation of α-aryl-pyridinemethanols: synthesis of arylmethylpyridines
inferred← citeshttps://doi.org/10.1016/j.tet.2016.02.030openalex-snapshot
An approach to heterodiarylmethanes via sp2–sp3 Suzuki−Miyaura cross-coupling
inferred← citeshttps://doi.org/10.1016/j.tet.2017.06.004openalex-snapshot
Nickel-catalyzed cross-coupling of aryl or 2-menaphthyl quaternary ammonium triflates with organoaluminum reagents
inferred← citeshttps://doi.org/10.1016/j.tet.2018.08.050openalex-snapshot
Highly efficient synthesis of 1,2-disubstituted acetylenes derivatives from the cross-coupling reactions of 1-bromoalkynes with organoalane reagents
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132549openalex-snapshot
Simple and efficient nickel-catalyzed cross-coupling reaction of alkenylalanes with alkynyl halides for synthesis of conjugated enynes
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132564openalex-snapshot
Cross-coupling reaction of organoalane reagents with 2-mercaptobenzo-5-membered heterocycles for efficient synthesis of benzo-5-membered heterocycle sulfides
inferred← citeshttps://doi.org/10.1016/j.tet.2024.133850openalex-snapshot
Copper-assisted palladium catalyzed the cross-coupling reaction of Alknylalane reagents with 2-Thiobenzo[d]thiazoles via C–S bond cleavage
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134089openalex-snapshot
Synthesis of the 2-alkynyl benzo[b]furanes/benzo[b]thiophenes from the cross-coupling reaction of benzo[b]furanyl/ benzo[b]thiophene aluminum reagents with gem-dibromoolefin derivatives catalyzed by palladium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.05.083openalex-snapshot
Synthesis and structural characterization of a highly substituted triazine ring comprising a sterically flexible methylene linker and coordinating substituents
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.tetlet.2024.155249openalex-snapshot
Coinage metal-catalyzed or-mediated oxidative heteroarylation of arenes
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00252openalex-snapshot
Palladium-Catalyzed/Copper-Mediated Decarbonylative Cross-Coupling of S-Pyrimidyl Thioesters for Biaryl Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00767openalex-snapshot
Copper-Catalyzed Electrophilic Amination of Organoaluminum Nucleophiles with O-Benzoyl Hydroxylamines
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01410openalex-snapshot
Asymmetric Addition of Pyridyl Aluminum Reagents to Aldehydes Catalyzed by a Titanium(IV) Catalytic System of (R)-H8-BINOLate
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02077openalex-snapshot
General Copper-Catalyzed Coupling of Alkyl-, Aryl-, and Alkynylaluminum Reagents with Organohalides
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02689openalex-snapshot
Synthesis of Benzothiadiazole Derivatives by Applying C–C Cross-Couplings
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01924openalex-snapshot
Copper Catalyzed the Cross-Coupling Reaction of Arylthioaluminum Reagents with Alkynyl Bromides/Terminal Alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02498openalex-snapshot
Nickel-Catalyzed Cyanation of Phenol Derivatives with Zn(CN)2 Involving C–O Bond Cleavage
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01103openalex-snapshot
Palladium-Catalyzed Decarbonylative Suzuki–Miyaura Coupling of Amides To Achieve Biaryls via C–N Bond Cleavage
inferred← citeshttps://doi.org/10.1021/acs.oprd.7b00185openalex-snapshot
Kumada–Corriu Heteroaryl Cross-Coupling for Synthesis of a Pharmaceutical Intermediate: Comparison of Batch Versus Continuous Reaction Modes
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c04175openalex-snapshot
A General and Selective Synthesis of Methylmonochlorosilanes from Di-, Tri-, and Tetrachlorosilanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02323openalex-snapshot
Selective and Serial Suzuki–Miyaura Reactions of Polychlorinated Aromatics with Alkyl Pinacol Boronic Esters
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02933openalex-snapshot
Transmetal-Catalyzed Enantioselective Cross-Coupling Reaction of Racemic Secondary Benzylic Bromides with Organoaluminum Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02923openalex-snapshot
Palladium-Catalyzed Carbonylative Coupling of Aryl Iodides with Alkenylaluminum Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04117openalex-snapshot
Continuous Flow Enables Metallaphotoredox Catalysis in a Medicinal Chemistry Setting: Accelerated Optimization and Library Execution of a Reductive Coupling between Benzylic Chlorides and Aryl Bromides
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04414openalex-snapshot
Palladium-Catalyzed Synthesis of 1,2-Diketones from Aryl Halides and Organoaluminum Reagents Using tert-Butyl Isocyanide as the CO Source
inferred← citeshttps://doi.org/10.1021/acscatal.0c02805openalex-snapshot
N -(Hetero)arylations with Metalated (Hetero)aryls: Recent Advances in First-Row Transition-Metal-Mediated Cross-Couplings
inferred← citeshttps://doi.org/10.1021/acscatal.7b01058openalex-snapshot
Revisitation of Organoaluminum Reagents Affords a Versatile Protocol for C–X (X = N, O, F) Bond-Cleavage Cross-Coupling: A Systematic Study
inferred← citeshttps://doi.org/10.1021/jacs.1c06112openalex-snapshot
The Versatile Reaction Chemistry of an Alpha-Boryl Diazo Compound
inferred← citeshttps://doi.org/10.1021/ol503560eopenalex-snapshot
Nickel-Catalyzed One-Pot Deoxygenation and Reductive Homocoupling of Phenols via C–O Activation Using TCT Reagent
inferred← citeshttps://doi.org/10.1039/c5ra09257dopenalex-snapshot
An efficient and metal free synthesis of benzylpyridines using HI through the deoxygenation reaction
inferred← citeshttps://doi.org/10.1039/c6nj02560aopenalex-snapshot
Benzylation of heterocyclic N-oxides via direct oxidative cross-dehydrogenative coupling with toluene derivatives
inferred← citeshttps://doi.org/10.1039/c7cc00997fopenalex-snapshot
Exhaustive Suzuki–Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol esters
inferred← citeshttps://doi.org/10.1039/c8ra07013jopenalex-snapshot
l -Proline catalyzed one-pot synthesis of polysubstituted pyridine system incorporating benzothiazole moiety via sustainable sonochemical approach
inferred← citeshttps://doi.org/10.1039/d0ra02984jopenalex-snapshot
Palladium-catalyzed cross-coupling reaction of alkenyl aluminums with 2-bromobenzo[ b ]furans
inferred← citeshttps://doi.org/10.1039/d3nj02026fopenalex-snapshot
The cross-coupling reaction of organoalane reagents with 2-methylthiobenzo[ d ]thiazoles via C–S bond cleavage catalyzed by nickel
inferred← citeshttps://doi.org/10.1126/science.aac6936openalex-snapshot
Sustainable Fe–ppm Pd nanoparticle catalysis of Suzuki-Miyaura cross-couplings in water
inferred← citeshttps://doi.org/10.1134/s1070363218040333openalex-snapshot
Arylation of Pyridine with 9,10-Dioxoanthracenyl-1(2)-diazonium Hydrosulfates
inferred← citeshttps://doi.org/10.3390/catal9030300openalex-snapshot
Suzuki–Miyaura Coupling Using Monolithic Pd Reactors and Scaling-Up by Series Connection of the Reactors
inferred← citeshttps://doi.org/10.3390/molecules29030576openalex-snapshot
Recent Progress on the Synthesis of Bipyridine Derivatives
inferred← citeshttps://doi.org/10.3762/bjoc.11.226openalex-snapshot
Copper-mediated synthesis of N -alkenyl-α,β-unsaturated nitrones and their conversion to tri- and tetrasubstituted pyridines
inferred← citeshttps://doi.org/10.3762/bjoc.11.261openalex-snapshot
Copper-catalyzed arylation of alkyl halides with arylaluminum reagents
inferred← citeshttps://doi.org/10.3762/bjoc.12.10openalex-snapshot
Hydroquinone–pyrrole dyads with varied linkers
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