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Selected Patented Cross-Coupling Reaction Technologies
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3 of the 200 references listed on this page are in the Retraction Watch database as retracted (export 2026-11-11): 10.1021/ja034848+ (notice 2006-06-21), 10.1021/ja036157j (notice 2006-06-21), 10.1021/ol035313o (notice 2006-06-15).
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-3773(19980817)37:15<2046::aid-anie2046>3.0.co;2-lopenalex-snapshot
Transition Metal Catalyzed Synthesis of Arylamines and Aryl Ethers from Aryl Halides and Triflates: Scope and Mechanism
inferredcites →https://doi.org/10.1002/(sici)1521-3773(19981231)37:24<3387::aid-anie3387>3.0.co;2-popenalex-snapshot
A Convenient and General Method for Pd-Catalyzed Suzuki Cross-Couplings of Aryl Chlorides and Arylboronic Acids
inferredcites →https://doi.org/10.1002/0471264229.os081.05openalex-snapshot
Palladium Catalyzed Cross‐Coupling of ( Z )‐1‐Heptenyldimethylsilanol with 4‐Iodoanisole: ( Z )‐1‐Heptenyl)‐4‐methoxybenzene
inferredcites →https://doi.org/10.1002/1521-3773(20000901)39:17<2980::aid-anie2980>3.0.co;2-#openalex-snapshot
Odds and Trends: Recent Developments in the Chemistry of Odorants
inferredcites →https://doi.org/10.1002/1521-3773(20010917)40:18<3387::aid-anie3387>3.0.co;2-6openalex-snapshot
Catalytic C−C Bond Formation through Selective Activation of C−F Bonds
inferredcites →https://doi.org/10.1002/1521-3773(20020215)41:4<609::aid-anie609>3.0.co;2-mopenalex-snapshot
Iron-Catalyzed Cross-Coupling Reactions of Alkyl-Grignard Reagents with Aryl Chlorides, Tosylates, and Triflates
inferredcites →https://doi.org/10.1002/1521-3773(20020415)41:8<1290::aid-anie1290>3.0.co;2-yopenalex-snapshot
N-Heterocyclic Carbenes: A New Concept in Organometallic Catalysis
inferredcites →https://doi.org/10.1002/1521-3773(20021115)41:22<4176::aid-anie4176>3.0.co;2-uopenalex-snapshot
Palladium-Catalyzed Coupling Reactions of Aryl Chlorides
inferredcites →https://doi.org/10.1002/9783527612222openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/9783527612222.ch10openalex-snapshot
Organosilicon Compounds in Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/9783527612222.ch5openalex-snapshot
Cross‐Coupling Reactions to sp Carbon Atoms
inferredcites →https://doi.org/10.1002/9783527619535openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/9783527619535.ch13openalex-snapshot
Palladium‐Catalyzed Aromatic Carbon‐Nitrogen Bond Formation
inferredcites →https://doi.org/10.1002/adsc.200404071openalex-snapshot
The Art of Meeting Palladium Specifications in Active Pharmaceutical Ingredients Produced by Pd‐Catalyzed Reactions
inferredcites →https://doi.org/10.1002/adsc.200404156openalex-snapshot
Industrial R&D on Catalytic CC and CN Coupling Reactions: A Personal Account on Goals, Approaches and Results
inferredcites →https://doi.org/10.1002/adsc.200404216openalex-snapshot
Palladium‐Catalyzed CN and CO Coupling–A Practical Guide from an Industrial Vantage Point †
inferredcites →https://doi.org/10.1002/adsc.200404223openalex-snapshot
Nickel‐Catalyzed Cross‐Couplings of Unactivated Alkyl Halides and Pseudohalides with Organometallic Compounds
inferredcites →https://doi.org/10.1002/adsc.200404392openalex-snapshot
The Synthesis of Important Pharmaceutical Building Blocks by Palladium‐Catalyzed Coupling Reaction: Access to Various Arylhydrazines
inferredcites →https://doi.org/10.1002/adsc.200505158openalex-snapshot
Industrial‐Scale Palladium‐Catalyzed Coupling of Aryl Halides and Amines –A Personal Account
inferredcites →https://doi.org/10.1002/anie.198605081openalex-snapshot
The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)]
inferredcites →https://doi.org/10.1002/anie.199423791openalex-snapshot
Fine Feathers Make Fine Birds: The Heck Reaction in Modern Garb
inferredcites →https://doi.org/10.1002/anie.199513481openalex-snapshot
A Simple Catalytic Method for the Conversion of Aryl Bromides to Arylamines
inferredcites →https://doi.org/10.1002/anie.199518441openalex-snapshot
Palladacycles as Structurally Defined Catalysts for the Heck Olefination of Chloro‐ and Bromoarenes
inferredcites →https://doi.org/10.1002/anie.199603861openalex-snapshot
Nonstabilized Alkyl Complexes and Alkyl‐Cyano‐Ate Complexes of Iron( II ) and Cobalt( II ) as New Reagents in Organic Synthesis
inferredcites →https://doi.org/10.1002/anie.200201617openalex-snapshot
Evolution in the Palladium‐Catalyzed Cross‐Coupling of sp‐ and sp 2 ‐Hybridized Carbon Atoms
inferredcites →https://doi.org/10.1002/anie.200250778openalex-snapshot
A Convenient Procedure for the Palladium‐Catalyzed Cyanation of Aryl Halides
inferredcites →https://doi.org/10.1002/anie.200300594openalex-snapshot
Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
inferredcites →https://doi.org/10.1002/anie.200301660openalex-snapshot
Integrated Microfluidic Systems
inferredcites →https://doi.org/10.1002/anie.200460045openalex-snapshot
Readily Available Onio‐Substituted Methyleneiminium Salts: Single Precursors for a Variety of Aminocarbenes
inferredcites →https://doi.org/10.1002/anie.200461189openalex-snapshot
Monoligated Palladium Species as Catalysts in Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/anie.200462560openalex-snapshot
Supported Gold Catalyzes the Homocoupling of Phenylboronic Acid with High Conversion and Selectivity
inferredcites →https://doi.org/10.1002/anie.200490023openalex-snapshot
Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
inferredcites →https://doi.org/10.1002/anie.200500468openalex-snapshot
Palladium‐Catalyzed Intermolecular Alkenylation of Indoles by Solvent‐Controlled Regioselective CH Functionalization
inferredcites →https://doi.org/10.1002/anie.200500589openalex-snapshot
Anilide ortho ‐Arylation by Using CH Activation Methodology
inferredcites →https://doi.org/10.1002/cber.190303602174openalex-snapshot
Ueber eine neue Bildungsweise von Diphenylaminderivaten
inferredcites →https://doi.org/10.1002/cber.19060390298openalex-snapshot
Ueber Phenylirungen bei Gegenwart von Kupfer als Katalysator
inferredcites →https://doi.org/10.1002/cber.19070400498openalex-snapshot
Über Phenylierung von primären aromatischen Aminen
inferredcites →https://doi.org/10.1002/cber.19190520840openalex-snapshot
Das am Ringkohlenstoff gebundene Halogen und sein Ersatz durch andere Substituenten. I. Mitteilung: Ersatz des Halogens durch die Carboxylgruppe
inferredcites →https://doi.org/10.1002/cber.19971300802openalex-snapshot
New Coupling Reactions and Phosphorylations Using Organozinc Reagents
inferredcites →https://doi.org/10.1002/chem.200400582openalex-snapshot
Highly Efficient and Mild Copper‐Catalyzed N‐ and C‐Arylations with Aryl Bromides and Iodides
inferredcites →https://doi.org/10.1002/jhet.5570290436openalex-snapshot
Synthesis of 7‐ and 5,7‐substituted‐6‐fluoro‐2‐methyl‐1,2,3,4‐tetrahydroquinolines: Convenient precursors of quinolone antibacterial agents
inferredcites →https://doi.org/10.1002/jlac.19314880107openalex-snapshot
Fluoranthen und seine Derivate. III. Mitteilung
inferredcites →https://doi.org/10.1016/0040-4039(95)00605-copenalex-snapshot
Palladium-catalyzed synthesis of arylamines from aryl halides. Mechanistic studies lead to coupling in the absence of tin reagents
inferredcites →https://doi.org/10.1016/b978-0-08-052349-1.00072-xopenalex-snapshot
Coupling Reactions Between sp Carbon Centers
inferredcites →https://doi.org/10.1016/j.ccr.2004.09.014openalex-snapshot
Copper in cross-coupling reactions
inferredcites →https://doi.org/10.1016/j.jorganchem.2004.10.037openalex-snapshot
Transition metal catalyzed cross-coupling of aryl Grignard reagents with aryl fluorides via Pd- or Ni-activation of the C–F bond: an efficient synthesis of unsymmetrical biaryls – application of microwave technology in ligand and catalyst screening
inferredcites →https://doi.org/10.1016/j.jorganchem.2005.03.071openalex-snapshot
Successful application of microstructured continuous reactor in the palladium catalysed aromatic amination
inferredcites →https://doi.org/10.1016/j.jorganchem.2005.07.066openalex-snapshot
Contributions to the chemistry of carbenemetal chemistry
inferredcites →https://doi.org/10.1016/j.tet.2005.08.054openalex-snapshot
Non-conventional methodologies for transition-metal catalysed carbon–carbon coupling: a critical overview. Part 1: The Heck reaction
inferredcites →https://doi.org/10.1016/j.tet.2005.11.027openalex-snapshot
Transition metal catalyzed oxidative functionalization of carbon–hydrogen bonds
inferredcites →https://doi.org/10.1016/j.tetlet.2005.04.022openalex-snapshot
Palladium charcoal-catalyzed, ligandless Suzuki reaction by using tetraarylborates in water
inferredcites →https://doi.org/10.1016/j.tetlet.2005.06.085openalex-snapshot
Pd–EDTA as an efficient catalyst for Suzuki–Miyaura reactions in water
inferredcites →https://doi.org/10.1016/j.tetlet.2005.09.001openalex-snapshot
Selective cis-addition of C–H bonds of pyrroles and thiophenes to alkynes catalyzed by a dinuclear palladium complex
inferredcites →https://doi.org/10.1016/s0008-6223(02)00293-2openalex-snapshot
Bioadsorption of Pb(II), Cd(II), and Cr(VI) on activated carbon from aqueous solutions
inferredcites →https://doi.org/10.1016/s0010-8545(98)00073-3openalex-snapshot
Role of dba in the reactivity of palladium(0) complexes generated in situ from mixtures of Pd(dba)2 and phosphines
inferredcites →https://doi.org/10.1016/s0022-328x(00)86239-7openalex-snapshot
Iron catalysis in the reaction of grignard reagents with alkyl halides
inferredcites →https://doi.org/10.1016/s0022-328x(00)92215-0openalex-snapshot
Conversion of disilanes to functional monosilanes
inferredcites →https://doi.org/10.1016/s0022-328x(00)94048-8openalex-snapshot
Synthesis of aryl- and vinyl-substituted acetylene derivatives by the use of nickel and palladium complexes
inferredcites →https://doi.org/10.1016/s0022-328x(00)94049-xopenalex-snapshot
Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives
inferredcites →https://doi.org/10.1016/s0022-328x(00)95116-7openalex-snapshot
Silicon hydrides and nickel complexes
inferredcites →https://doi.org/10.1016/s0022-328x(00)95117-9openalex-snapshot
Silicon hydrides and nickel complexes
inferredcites →https://doi.org/10.1016/s0022-328x(02)01157-9openalex-snapshot
How I came across the silicon-based cross-coupling reaction
inferredcites →https://doi.org/10.1016/s0022-328x(97)00736-5openalex-snapshot
Chelating N-heterocyclic carbene ligands in palladium-catalyzed heck-type reactions
inferredcites →https://doi.org/10.1016/s0022-328x(98)01048-1openalex-snapshot
The palladium-catalysed arylation and vinylation of alkenes—enantioselective fashion
inferredcites →https://doi.org/10.1016/s0022-328x(98)01050-xopenalex-snapshot
Application of palladacycles in Heck type reactions
inferredcites →https://doi.org/10.1016/s0022-328x(98)01054-7openalex-snapshot
Palladium-catalyzed amination of aryl halides and sulfonates
inferredcites →https://doi.org/10.1016/s0022-328x(98)01055-9openalex-snapshot
Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998
inferredcites →https://doi.org/10.1016/s0022-328x(98)01063-8openalex-snapshot
Mechanistic and kinetic studies of palladium catalytic systems
inferredcites →https://doi.org/10.1016/s0040-4020(01)00730-xopenalex-snapshot
Nickel-catalysed sequential amination of aryl- and heteroaryl di- and trichlorides
inferredcites →https://doi.org/10.1016/s0040-4020(99)00788-7openalex-snapshot
Nickel-catalysed couplings of aryl chlorides with secondary amines and piperazines
inferredcites →https://doi.org/10.1016/s0040-4039(00)80145-8openalex-snapshot
Activation of reducing agents. Sodium hydride containing complex reducing agents 25. A one pot one reagent cross-coupling reaction of aryl halides
inferredcites →https://doi.org/10.1016/s0040-4039(00)96298-1openalex-snapshot
Phenylation of aromatic and aliphatic amines by phenyllead triacetate using copper catalysis
inferredcites →https://doi.org/10.1016/s0040-4039(00)96607-3openalex-snapshot
Palladium-mediated silylation of organic halides with disilane/F- reagent
inferredcites →https://doi.org/10.1016/s0040-4039(01)01079-6openalex-snapshot
Nickel-catalysed amination of aryl chlorides using a dihydroimidazoline carbene ligand
inferredcites →https://doi.org/10.1016/s0040-4039(01)01734-8openalex-snapshot
Semi-continuous nanofiltration-coupled Heck reactions as a new approach to improve productivity of homogeneous catalysts
inferredcites →https://doi.org/10.1016/s0040-4039(01)02193-1openalex-snapshot
Palladium-catalyzed coupling of aryl halides with arylhalosilanes in air and water
inferredcites →https://doi.org/10.1016/s0040-4039(01)81015-7openalex-snapshot
Copper salts catalysis of N-phenylation of amines by trivalent organobismuth compounds
inferredcites →https://doi.org/10.1016/s0040-4039(01)87265-8openalex-snapshot
Nucleophilic aromatic substitution a new nickel-catalyzed process and the SRN1 reaction. Improved synthesis of cephalotaxinone
inferredcites →https://doi.org/10.1016/s0040-4039(01)93852-3openalex-snapshot
Palladium-catalyzed cross-coupling reaction of alkenylalkoxysilanes with aryl and alkenyl halides in the presence of a fluoride ion
inferredcites →https://doi.org/10.1016/s0040-4039(98)00503-6openalex-snapshot
New N- and O-arylations with phenylboronic acids and cupric acetate
inferredcites →https://doi.org/10.1016/s0040-4039(98)00504-8openalex-snapshot
New aryl/heteroaryl CN bond cross-coupling reactions via arylboronic acid/cupric acetate arylation
inferredcites →https://doi.org/10.1016/s0040-4039(99)00291-9openalex-snapshot
An efficient copper-catalyzed coupling of aryl halides with imidazoles
inferredcites →https://doi.org/10.1016/s1367-5931(97)80063-4openalex-snapshot
Web alert Mechanisms Analytical techniques
inferredcites →https://doi.org/10.1021/ar00049a001openalex-snapshot
Recent Developments and New Perspectives in the Heck Reaction
inferredcites →https://doi.org/10.1021/ar00083a001openalex-snapshot
Palladium- or nickel-catalyzed cross coupling. A new selective method for carbon-carbon bond formation
inferredcites →https://doi.org/10.1021/ar010065mopenalex-snapshot
Origins, Current Status, and Future Challenges of Green Chemistry
inferredcites →https://doi.org/10.1021/ar020001ropenalex-snapshot
Design and Implementation of New, Silicon-Based, Cross-Coupling Reactions: Importance of Silicon−Oxygen Bonds
inferredcites →https://doi.org/10.1021/ar50082a006openalex-snapshot
Electron-transfer mechanisms for organometallic intermediates in catalytic reactions
inferredcites →https://doi.org/10.1021/ar50120a002openalex-snapshot
Mechanisms of oxidative addition of organic halides to Group 8 transition-metal complexes
inferredcites →https://doi.org/10.1021/ar980063aopenalex-snapshot
Anionic Pd(0) and Pd(II) Intermediates in Palladium-Catalyzed Heck and Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/bk-2000-0767openalex-snapshot
Green Chemical Syntheses and Processes
inferredcites →https://doi.org/10.1021/cr00022a008openalex-snapshot
Preparation and reactions of polyfunctional organozinc reagents in organic synthesis
inferredcites →https://doi.org/10.1021/cr00037a009openalex-snapshot
Regio- and Stereochemical Aspects of the Palladium-Catalyzed Reactions of Silanes
inferredcites →https://doi.org/10.1021/cr000664ropenalex-snapshot
Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction
inferredcites →https://doi.org/10.1021/cr00104a001openalex-snapshot
Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics
inferredcites →https://doi.org/10.1021/cr030009uopenalex-snapshot
Organic Reactions in Aqueous Media with a Focus on Carbon−Carbon Bond Formations: A Decade Update
inferredcites →https://doi.org/10.1021/cr030681ropenalex-snapshot
The Potential of Palladacycles: More Than Just Precatalysts
inferredcites →https://doi.org/10.1021/cr040664hopenalex-snapshot
Iron-Catalyzed Reactions in Organic Synthesis
inferredcites →https://doi.org/10.1021/cr950243nopenalex-snapshot
Comparison of Phosphorus and Silicon: Hypervalency, Stereochemistry, and Reactivity
inferredcites →https://doi.org/10.1021/cr9902704openalex-snapshot
Ligand Bite Angle Effects in Metal-catalyzed C−C Bond Formation
inferredcites →https://doi.org/10.1021/ja0002058openalex-snapshot
Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions
inferredcites →https://doi.org/10.1021/ja00074a018openalex-snapshot
Intimate mechanism of oxidative addition to zerovalent palladium complexes in the presence of halide ions and its relevance to the mechanism of palladium-catalyzed nucleophilic substitutions
inferredcites →https://doi.org/10.1021/ja00092a058openalex-snapshot
Palladium-catalyzed formation of carbon-nitrogen bonds. Reaction intermediates and catalyst improvements in the hetero cross-coupling of aryl halides and tin amides
inferredcites →https://doi.org/10.1021/ja00096a059openalex-snapshot
Palladium-Catalyzed Aromatic Aminations with in situ Generated Aminostannanes
inferredcites →https://doi.org/10.1021/ja00239a032openalex-snapshot
Mechanisms and models for copper mediated nucleophilic aromatic substitution. 2. Single catalytic species from three different oxidation states of copper in an Ullmann synthesis of triarylamines
inferredcites →https://doi.org/10.1021/ja0035295openalex-snapshot
Stille Couplings Catalytic in Tin: The “Sn−O” Approach
inferredcites →https://doi.org/10.1021/ja00449a019openalex-snapshot
Reactions of two-coordinate phosphine platinum(0) and palladium(0) compounds. Ligand exchange and reactivities toward small molecules
inferredcites →https://doi.org/10.1021/ja00479a077openalex-snapshot
A general, selective, and facile method for ketone synthesis from acid chlorides and organotin compounds catalyzed by palladium
inferredcites →https://doi.org/10.1021/ja00735a030openalex-snapshot
Vinylation of Grignard reagents. Catalysis by iron
inferredcites →https://doi.org/10.1021/ja00811a029openalex-snapshot
Organophosphinepalladium complexes as catalysts for vinylic hydrogen substitution reactions
inferredcites →https://doi.org/10.1021/ja01107a047openalex-snapshot
Diaryliodonium Salts. II. The Phenylation of Organic and Inorganic Bases1,2
inferredcites →https://doi.org/10.1021/ja016226zopenalex-snapshot
A General and Efficient Copper Catalyst for the Amidation of Aryl Halides and the N -Arylation of Nitrogen Heterocycles
inferredcites →https://doi.org/10.1021/ja026032zopenalex-snapshot
Fabrication of Hollow Palladium Spheres and Their Successful Application to the Recyclable Heterogeneous Catalyst for Suzuki Coupling Reactions
inferredcites →https://doi.org/10.1021/ja034848+openalex-snapshot
Selective C-Arylation of Free (NH)-Heteroarenes via Catalytic C−H Bond Functionalization
inferredcites →https://doi.org/10.1021/ja035565kopenalex-snapshot
Synthetic, Structural, and Mechanistic Studies on the Oxidative Addition of Aromatic Chlorides to a Palladium (N-Heterocyclic Carbene) Complex: Relevance to Catalytic Amination
inferredcites →https://doi.org/10.1021/ja036157jopenalex-snapshot
Diversity Synthesis via C−H Bond Functionalization: Concept-Guided Development of New C-Arylation Methods for Imidazoles
inferredcites →https://doi.org/10.1021/ja036947topenalex-snapshot
The First General Palladium Catalyst for the Suzuki−Miyaura and Carbonyl Enolate Coupling of Aryl Arenesulfonates
inferredcites →https://doi.org/10.1021/ja042491jopenalex-snapshot
Catalysts for Suzuki−Miyaura Coupling Processes: Scope and Studies of the Effect of Ligand Structure
inferredcites →https://doi.org/10.1021/ja045533copenalex-snapshot
Reevaluation of the Mechanism of the Amination of Aryl Halides Catalyzed by BINAP-Ligated Palladium Complexes
inferredcites →https://doi.org/10.1021/ja0460763openalex-snapshot
CuBr-Catalyzed Efficient Alkynylation of sp3 C−H Bonds Adjacent to a Nitrogen Atom
inferredcites →https://doi.org/10.1021/ja0474493openalex-snapshot
An Extremely Active Catalyst for the Negishi Cross-Coupling Reaction
inferredcites →https://doi.org/10.1021/ja049744topenalex-snapshot
Iron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents
inferredcites →https://doi.org/10.1021/ja050058jopenalex-snapshot
Highly Efficient Copper-Catalyzed Nitro-Mannich Type Reaction: Cross-Dehydrogenative-Coupling between sp 3 C−H Bond and sp 3 C−H Bond
inferredcites →https://doi.org/10.1021/ja050279popenalex-snapshot
Direct C-Arylation of Free (NH)-Indoles and Pyrroles Catalyzed by Ar−Rh(III) Complexes Assembled In Situ
inferredcites →https://doi.org/10.1021/ja0516054openalex-snapshot
CuBr-Catalyzed Direct Indolation of Tetrahydroisoquinolines via Cross-Dehydrogenative Coupling between sp3 C−H and sp2 C−H Bonds
inferredcites →https://doi.org/10.1021/ja0518373openalex-snapshot
Sequential Cross-Coupling of 1,4-Bissilylbutadienes: Synthesis of Unsymmetrical 1,4-Disubstituted 1,3-Butadienes
inferredcites →https://doi.org/10.1021/ja055819xopenalex-snapshot
Catalytic Direct Arylation with Aryl Chlorides, Bromides, and Iodides: Intramolecular Studies Leading to New Intermolecular Reactions
inferredcites →https://doi.org/10.1021/ja056327nopenalex-snapshot
Nickel-Catalyzed Cross-Coupling Reaction of Aryl Fluorides and Chlorides with Grignard Reagents under Nickel/Magnesium Bimetallic Cooperation
inferredcites →https://doi.org/10.1021/ja9608306openalex-snapshot
An Improved Catalyst System for Aromatic Carbon−Nitrogen Bond Formation: The Possible Involvement of Bis(Phosphine) Palladium Complexes as Key Intermediates
inferredcites →https://doi.org/10.1021/ja960937topenalex-snapshot
A Second-Generation Catalyst for Aryl Halide Amination: Mixed Secondary Amines from Aryl Halides and Primary Amines Catalyzed by (DPPF)PdCl2
inferredcites →https://doi.org/10.1021/ja9637098openalex-snapshot
Identification of the Effective Palladium(0) Catalytic Species Generatedin Situfrom Mixtures of Pd(dba)2and Bidentate Phosphine Ligands. Determination of Their Rates and Mechanism in Oxidative Addition
inferredcites →https://doi.org/10.1021/ja983378uopenalex-snapshot
Simple, Highly Active Palladium Catalysts for Ketone and Malonate Arylation: Dissecting the Importance of Chelation and Steric Hindrance
inferredcites →https://doi.org/10.1021/jo00239a056openalex-snapshot
Cross-coupling of organosilanes with organic halides mediated by a palladium catalyst and tris(diethylamino)sulfonium difluorotrimethylsilicate
inferredcites →https://doi.org/10.1021/jo00430a041openalex-snapshot
Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides
inferredcites →https://doi.org/10.1021/jo00865a019openalex-snapshot
Mechanistic studies of iron catalysis in the cross coupling of alkenyl halides and Grignard reagents
inferredcites →https://doi.org/10.1021/jo00893a013openalex-snapshot
Synthesis of olefins. Cross-coupling of alkenyl halides and Grignard reagents catalyzed by iron complexes
inferredcites →https://doi.org/10.1021/jo00896a020openalex-snapshot
Palladium-catalyzed conjugated diene synthesis from vinylic halides and olefinic compounds
inferredcites →https://doi.org/10.1021/jo00979a024openalex-snapshot
Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides
inferredcites →https://doi.org/10.1021/jo010025wopenalex-snapshot
Use of Polymer-Supported Dialkylphosphinobiphenyl Ligands for Palladium-Catalyzed Amination and Suzuki Reactions
inferredcites →https://doi.org/10.1021/jo01047a008openalex-snapshot
The Substitution of Aryl Iodides with Cuprous Acetylides. A Synthesis of Tolanes and Heterocyclics 1
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inferredcites →https://doi.org/10.1021/jo016048sopenalex-snapshot
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Pd/C as a Reusable Catalyst for the Coupling Reaction of Halophenols and Arylboronic Acids in Aqueous Media
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Nickel-on-Charcoal-Catalyzed Aromatic Aminations and Kumada Couplings: Mechanistic and Synthetic Aspects
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P(i-BuNCH2CH2)3N: An Effective Ligand in the Palladium-Catalyzed Amination of Aryl Bromides and Iodides
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A Modified Synthesis of Iodoazidoaryl Prazosin
inferredcites →https://doi.org/10.1021/jo035834popenalex-snapshot
Cross-Coupling and Dehalogenation Reactions Catalyzed by (N-Heterocyclic carbene)Pd(allyl)Cl Complexes
inferredcites →https://doi.org/10.1021/jo0481250openalex-snapshot
Ligand-Free Palladium-Catalyzed Cyanation of Aryl Halides
inferredcites →https://doi.org/10.1021/jo048187qopenalex-snapshot
Masked 3-Aminoindan-1-ones by a Palladium-Catalyzed Three-Component Annulation Reaction
inferredcites →https://doi.org/10.1021/jo048667hopenalex-snapshot
Improved Synthesis of Aryltrialkoxysilanes via Treatment of Aryl Grignard or Lithium Reagents with Tetraalkyl Orthosilicates
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Scope and Limitations of Pd2(dba)3/P(i-BuNCH2CH2)3N-Catalyzed Buchwald−Hartwig Amination Reactions of Aryl Chlorides
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Ortho-Selective Direct Cross-Coupling Reaction of 2-Aryloxazolines and 2-Arylimidazolines with Aryl and Alkenyl Halides Catalyzed by Ruthenium Complexes
inferredcites →https://doi.org/10.1021/jo050274aopenalex-snapshot
Regioselective Synthesis of 1,5-Diaryl-1H-imidazoles by Palladium-Catalyzed Direct Arylation of 1-Aryl-1H-imidazoles
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Efficient Palladium-Catalyzed Homocoupling Reaction and Sonogashira Cross-Coupling Reaction of Terminal Alkynes under Aerobic Conditions
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Efficient Synthesis of a GABA A α 2,3 -Selective Allosteric Modulator via a Sequential Pd-Catalyzed Cross-Coupling Approach
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Mild and Room Temperature C−C Bond Forming Reactions of Nucleoside C-6 Arylsulfonates
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Efforts Directed toward the Synthesis of Colchicine: Application of Palladium-Catalyzed Siloxane Cross-Coupling Methodology
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A Soluble Base for the Copper-Catalyzed Imidazole N-Arylations with Aryl Halides
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Suzuki−Miyaura, α-Ketone Arylation and Dehalogenation Reactions Catalyzed by a Versatile N -Heterocyclic Carbene−Palladacycle Complex
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Cooperative Catalyst Effects in Palladium-Mediated Cyanation Reactions of Aryl Halides and Triflates
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Pd(PhCN)2Cl2/P(t-Bu)3: A Versatile Catalyst for Sonogashira Reactions of Aryl Bromides at Room Temperature
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Suzuki Cross-Coupling Reactions Catalyzed by Palladium Nanoparticles in Aqueous Solution
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A Novel, Highly Selective, and General Methodology for the Synthesis of 1,5-Diene-Containing Oligoisoprenoids of All Possible Geometrical Combinations Exemplified by an Iterative and Convergent Synthesis of Coenzyme Q10
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Activation of Aryl Chlorides for Suzuki Cross-Coupling by Ligandless, Heterogeneous Palladium
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Regioselective Palladium-Catalyzed Arylation of 2-Furaldehyde
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Regioselective Palladium-Catalyzed Arylation of 3-Carboalkoxy Furan and Thiophene
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Sonogashira Coupling Reaction with Diminished Homocoupling
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Cross-Coupling Reactions of Arylsilanols with Substituted Aryl Halides
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Efficient Nickel-Mediated Intramolecular Amination of Aryl Chlorides
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Palladium-Catalyzed Silylation of Aryl Bromides Leading to Functionalized Aryldimethylsilanols
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Cobalt-Catalyzed Arylation of Azole Heteroarenes via Direct C−H Bond Functionalization
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Ligand- and Base-Free Copper(II)-Catalyzed C−N Bond Formation: Cross-Coupling Reactions of Organoboron Compounds with Aliphatic Amines and Anilines
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Palladium-Catalyzed Regioselective Arylation of Imidazo[1,2-a]pyrimidine
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A General and Mild Ullmann-Type Synthesis of Diaryl Ethers
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Hiyama Cross-Coupling of Chloro-, Fluoro-, and Methoxypyridyltrimethylsilanes: Room-Temperature Novel Access to Functional Bi(het)aryl
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Palladium-Catalyzed Cross-Coupling of Aryl Triethylammonium Bis(catechol) Silicates with Aryl Bromides Using Microwave Irradiation
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An Investigation into Causes and Effects of High Cyanide Levels in the Palladium-Catalyzed Cyanation Reaction
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Palladium−Phosphinous Acid-Catalyzed NaOH-Promoted Cross-Coupling Reactions of Arylsiloxanes with Aryl Chlorides and Bromides in Water
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Palladium-Catalyzed Arylation and Heteroarylation of Indolizines
inferredcites →https://doi.org/10.1021/ol051216eopenalex-snapshot
Phosphine Oxides as Preligands in Ruthenium-Catalyzed Arylations via C−H Bond Functionalization Using Aryl Chlorides
inferredcites →https://doi.org/10.1021/ol052063yopenalex-snapshot
Palladium-Catalyzed Coupling Reactions of Bromothiophenes at the C−H Bond Adjacent to the Sulfur Atom with a New Activator System, AgNO3/KF
inferredcites →https://doi.org/10.1021/ol052961uopenalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of (2-Pyridyl)allyldimethylsilanes with Aryl Iodides
inferredcites →https://doi.org/10.1021/ol990614copenalex-snapshot
A New Transformation of Silanols. Palladium-Catalyzed Cross-Coupling with Organic Halides in the Presence of Silver(I) Oxide
inferredcites →https://doi.org/10.1021/ol991186dopenalex-snapshot
Improvements in Cross Coupling Reactions of Hypervalent Siloxane Derivatives
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Rate and Mechanism of Oxidative Addition of Aryl Triflates to Zerovalent Palladium Complexes. Evidence for the Formation of Cationic (.sigma.-Aryl)palladium Complexes
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Rates and Mechanism of the Formation of Zerovalent Palladium Complexes from Mixtures of Pd(OAc)2 and Tertiary Phosphines and Their Reactivity in Oxidative Additions
inferredcites →https://doi.org/10.1021/om00006a053openalex-snapshot
Structural Characterization and Simple Synthesis of {Pd[P(o-Tol)3]2}. Spectroscopic Study and Structural Characterization of the Dimeric Palladium(II) Complexes Obtained by Oxidative Addition of Aryl Bromides and Their Reactivity with Amines
inferredcites →https://doi.org/10.1021/om00045a012openalex-snapshot
Evidence of the formation of zerovalent palladium from Pd(OAc)2 and triphenylphosphine
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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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Bis[2-(diphenylphosphino)phenyl]ether (DPE-Phos)
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Bis-[2-(diphenylphosphino)phenyl]ether (Dpe-Phos)
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Bis-[2-(diphenylphosphino)phenyl]ether (Dpe-Phos)
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Bis(tricyclohexylphosphine)dichloronickel
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Catalysts, Supported
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Copper‐Catalyzed Amination of Aryl and Alkenyl Electrophiles
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Transition‐Metal‐Catalyzed Alkyl–Alkyl Cross‐Coupling Reactions
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Synthesis of Lithium 2‐Pyridyltriolborate and its Cross‐Coupling Reaction with Aryl Halides
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Ruthenium‐Catalyzed Direct Oxidative Alkenylation of Arenes Through Twofold CH Bond Functionalization in Water: Synthesis of Ethyl (E)‐3‐(2‐Acetamido‐4‐Methylphenyl)Acrylate
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Palladium‐Catalyzed Buchwald‐Hartwig Amination and Suzuki‐MiyauraCross‐Coupling Reaction of Aryl Mesylates
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Nickel‐Catalyzed Suzuki–Miyaura Coupling int‐Amyl Alcohol for the Preparation of 5‐(Furan‐3‐yl)pyrimidine
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Palladium‐Catalyzed Buchwald‐Hartwig Amination and Suzuki‐Miyaura Cross‐Coupling Reaction of Aryl Mesylates
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Pharmaceutical Industry: Biocatalysts and Chemocatalysts
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Silver‐Mediated Oxidation Reactions: Recent Advances and New Prospects
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Iron‐Catalyzed Reactions of Grignard Reagents
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Functionalization of Fluorinated Aromatics by Nickel‐Mediated CH and CF Bond Oxidative Addition: Prospects for the Synthesis of Fluorine‐Containing Pharmaceuticals
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Selected Applications of Transition Metal‐Catalyzed Carbon–Carbon Cross‐Coupling Reactions in the Pharmaceutical Industry
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CH Activation of Heteroaromatics
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Nanocatalysts for the Heck Coupling Reactions
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Aryl Carbon–Heteroatom Coupling Reactions Using Nanometal Catalyst
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Formation of Alkanes and Arenes by Coupling Reactions
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Process Chemistry and Copper Catalysis
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Ullmann Condensation Today: Arylation of Alcohols and Thiols with Aryl Halides
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Palladium‐Catalyzed Indole Ring Synthesis
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Transition Metal‐Mediated Carbon–Heteroatom Cross‐Coupling (C—N, C—O, C—S, C—Se, C—Te, C—P, C—As, C—Sb, and C—B Bond Forming Reactions)
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Homogeneous Transition‐Metal‐Catalyzed C–F Activation
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Homogeneous Transition‐Metal‐Catalyzed C–O Bond Activation
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Cyclodehydrogenation in the Synthesis of Graphene‐Type Molecules
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Iron‐Catalyzed Cross‐Coupling Reactions
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Metal‐Catalyzed Direct Arylations (Excluding Palladium)
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Syntheses via C – H Bond Functionalizations
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Tailored Graphene‐Type Molecules by Chemical Synthesis
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Palladium‐Catalyzed Cross‐Coupling Reactions – A General Introduction
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Coupling Reactions Induced by Polymer‐Supported Catalysts
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Palladium‐Catalyzed Aromatic Carbon–Nitrogen Bond Formation
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Cross‐Coupling Reactions to sp Carbon Atoms
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Lithium Compounds in Cross‐Coupling Reactions
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NHC–Copper Complexes and their Applications
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Mechanisms of Metal‐Mediated C–N Coupling Processes: A Synergistic Relationship between Gas‐Phase Experiments and Computational Chemistry
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Stille Polycondensation: A Versatile Synthetic Approach to Functional Polymers
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Chemical Paired Transformations
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Pd ‐Catalyzed C C Bond‐Forming Reactions
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Activation of Amide CN Bonds by Nickel Catalysis
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Supported Ultra Small Palladium on Magnetic Nanoparticles Used as Catalysts for Suzuki Cross‐Coupling and Heck Reactions
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Highly Efficient Alkyne Hydroarylation with Chelating Dicarbene Palladium(II) and Platinum(II) Complexes
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Ligand‐Free Copper‐Catalyzed N‐Arylation of Nitrogen Nucleophiles
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Iron‐Catalyzed CN Cross‐Coupling of Sulfoximines with Aryl Iodides
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Efficient Cross‐Coupling Reactions of Nitrogen Nucleophiles with Aryl Halides in Water
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Intramolecular Palladium‐Catalyzed Direct Arylation vs. Heck Reactions: Synthesis of Pyrroloisoquinolines and Isoindoles
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Nano‐Iron Oxide as a Recyclable Catalyst for Intramolecular CN Cross‐Coupling Reactions under Ligand‐Free Conditions: One‐Pot Synthesis of 1,4‐Dihydroquinoline Derivatives
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Intramolecular Photochemical Cross‐Coupling Reactions of 3‐Acyl‐2‐haloindoles and 2‐Chloropyrrole‐3‐carbaldehydes with Substituted Benzenes
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Nine Times Fluoride can be Good for your Syntheses. Not just Cheaper: Nonafluorobutanesulfonates as Intermediates for Transition Metal‐Catalyzed Reactions
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Recent Applications of Palladium‐Catalyzed Coupling Reactions in the Pharmaceutical, Agrochemical, and Fine Chemical Industries
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Sulfonated N‐Heterocyclic Carbenes for Pd‐Catalyzed Sonogashira and Suzuki–Miyaura Coupling in Aqueous Solvents
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Regioselective Functionalization of the Imidazole Ring via Transition Metal‐Catalyzed CN and CC Bond Forming Reactions
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Dimethyl Sulfoxide/Potassium Hydroxide: A Superbase for the Transition Metal‐Free Preparation of Cross‐Coupling Products
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Ligand‐Free Copper‐Catalyzed Amination of Heteroaryl Halides with Alkyl‐ and Arylamines
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Highly Efficient Suzuki–Miyaura Coupling of Aryl Tosylates and Mesylates Catalyzed by Stable, Cost‐Effective [1,3‐Bis(diphenylphosphino)propane]nickel(II) Chloride [Ni(dppp)Cl2] with only 1 mol% Loading
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Fe3O4@mesoporouspolyaniline: A Highly Efficient and Magnetically Separable Catalyst for Cross‐Coupling of Aryl Chlorides and Phenols
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Multi‐Layered, Covalently Supported Ionic Liquid Phase (mlc‐SILP) as Highly Cross‐Linked Support for Recyclable Palladium Catalysts for the Suzuki Reaction in Aqueous Medium
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Ligand‐Free Buchwald–Hartwig Aromatic Aminations of Aryl Halides Catalyzed by Low‐Leaching and Highly Recyclable Sulfur‐Modified Gold‐Supported Palladium Material
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Copper‐Catalyzed Ultrasound‐Expedited N‐Arylation of Sulfoximines using Diaryliodonium Salts
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Selective Palladium‐Catalyzed Suzuki–Miyaura Reactions of Polyhalogenated Heteroarenes
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Nickel‐Catalyzed Cross‐Coupling of Arene‐ or Heteroarenecarbonitriles with Aryl‐ or Heteroarylmanganese Reagents through CCN Bond Activation
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Thioethers as Directing Group for the Palladium‐Catalyzed Direct Arylation of Arenes
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Room Temperature Palladium‐Catalyzed Decarboxylative Acyl/Aroylation using [Fe(III)(EDTA)(η2‐O2)]3− as Oxidant at Biological pH
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Synthesis of 3‐Arylated 3,4‐Dihydrocoumarins: Combining Continuous Flow Hydrogenation with Laccase‐Catalysed Oxidation
inferred← citeshttps://doi.org/10.1002/adsc.201400176openalex-snapshot
A Sulfur Ylides‐Mediated Domino Benzannulation Strategy to Construct Biaryls, Alkenylated and Alkynylated Benzene Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201400659openalex-snapshot
Copper‐Catalyzed Cross Dehydrogenative Coupling of N,N‐Disubstituted Formamides and Phenols: A Direct Access to Carbamates
inferred← citeshttps://doi.org/10.1002/adsc.201400763openalex-snapshot
Copper‐Catalyzed Oxidative Ring Closure of ortho‐Cyanoanilides with Hypervalent Iodonium Salts: Arylation–Ring Closure Approach to Iminobenzoxazines
inferred← citeshttps://doi.org/10.1002/adsc.201400798openalex-snapshot
Rhodium(III)‐Catalyzed ortho‐Arylation of Anilides with Aryl Halides
inferred← citeshttps://doi.org/10.1002/adsc.201500457openalex-snapshot
Nickel–Copper‐Catalyzed C(sp2)N Cross‐Coupling of Cyclic and Bridged Amides: An Access to Cyclic Enamides and Alkenyl Vince Lactams
inferred← citeshttps://doi.org/10.1002/adsc.201600487openalex-snapshot
Synthesis of Hydroxy‐Substituted p‐Terphenyls and some Larger Oligophenylenes via Palladium on Charcoal Catalyzed Suzuki‐Miyaura Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201700810openalex-snapshot
Recent Advances in Palladium‐Catalyzed Cross‐Coupling Reactions at ppm to ppb Molar Catalyst Loadings
inferred← citeshttps://doi.org/10.1002/adsc.201701563openalex-snapshot
Pd‐PEPPSI: Water‐Assisted Suzuki−Miyaura Cross‐Coupling of Aryl Esters at Room Temperature using a Practical Palladium‐NHC (NHC=N‐Heterocyclic Carbene) Precatalyst
inferred← citeshttps://doi.org/10.1002/adsc.201800333openalex-snapshot
Palladium (II)‐Catalyzed Decarboxylative Cross‐Dehydrogenative Coupling: Direct Synthesis of meta‐Substituted Biaryls from Aromatic Acids
inferred← citeshttps://doi.org/10.1002/adsc.201801586openalex-snapshot
Nickel‐Catalyzed C(sp2)−C(sp3) Kumada Cross‐Coupling of Aryl Tosylates with Alkyl Grignard Reagents
inferred← citeshttps://doi.org/10.1002/adsc.201900334openalex-snapshot
I2/TBHP Mediated Divergent C(sp2)‐P Cleavage of Allenylphosphine Oxides: Substituent‐Controlled Regioselectivity
inferred← citeshttps://doi.org/10.1002/adsc.201900545openalex-snapshot
C−N Cross‐Coupling Reactions Under Mild Conditions Using Singlet Di‐Radical Nickel(II)‐Complexes as Catalyst: N‐Arylation and Quinazoline Synthesis
inferred← citeshttps://doi.org/10.1002/adsc.201901601openalex-snapshot
Biaryl Cross‐Coupling Enabled by Photo‐Induced Electron Transfer
inferred← citeshttps://doi.org/10.1002/adsc.202000122openalex-snapshot
Suzuki‐Miyaura Cross‐Coupling of Amides using Well‐Defined, Air‐Stable [(PR3)2Pd(II)X2] Precatalysts
inferred← citeshttps://doi.org/10.1002/adsc.202000679openalex-snapshot
Direct N‐Alkylation/Fluoroalkylation of Amines Using Carboxylic Acids via Transition‐Metal‐Free Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.202000987openalex-snapshot
Differences in the Performance of Allyl Based Palladium Precatalysts for Suzuki‐Miyaura Reactions
inferred← citeshttps://doi.org/10.1002/adsc.202300371openalex-snapshot
Synthesis of 2‐Perfluoroalkylazuleno[2,1‐d]pyrimidin‐4(3H)‐ones via Brønsted Acid‐Mediated Intramolecular Cyclization and Transformation into Pyrimidines
inferred← citeshttps://doi.org/10.1002/adsc.202300724openalex-snapshot
Catalyst‐Controlled Divergent C3/C5 Site‐Selective C−H Arylation of 2‐Pyridylthiophenes
inferred← citeshttps://doi.org/10.1002/adsc.202301255openalex-snapshot
Palladium‐Catalyzed Chemoselective Amination of Chloro(hetero)aryl Triflates Enabled by Alkyl‐Pyrazole‐Based Phosphine Ligands
inferred← citeshttps://doi.org/10.1002/adsc.202400707openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Aryl Alkyl Selenides with Aryl Bromides: Cross‐Coupling Between Two Electrophiles
inferred← citeshttps://doi.org/10.1002/advs.201500140openalex-snapshot
Facet‐Controlled Synthetic Strategy of Cu 2 O‐Based Crystals for Catalysis and Sensing
inferred← citeshttps://doi.org/10.1002/advs.201801368openalex-snapshot
Synthesis of a Novel Disperse Reactive Dye Involving a Versatile Bridge Group for the Sustainable Coloration of Natural Fibers in Supercritical Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/aesr.202100011openalex-snapshot
Bronze Age of Direct Mechanocatalysis: How Alloyed Milling Materials Advance Coupling in Ball Mills
inferred← citeshttps://doi.org/10.1002/ajoc.201300074openalex-snapshot
Silver‐Nitrate‐Catalyzed N‐Arylation of Amines and O‐Arylations of Phenols and Alcohols
inferred← citeshttps://doi.org/10.1002/ajoc.201300129openalex-snapshot
Direct CH Arylation of Unactivated Arenes with Aryl Halides Promoted by Bis(imino)pyridine Derivatives
inferred← citeshttps://doi.org/10.1002/ajoc.201402181openalex-snapshot
A Direct CH Arylation of Unactivated Arenes Promoted by Mixed Potassium Alkoxides
inferred← citeshttps://doi.org/10.1002/ajoc.201500062openalex-snapshot
Unimolecular 4‐Hydroxypiperidines: New Ligands for Copper‐Catalyzed N‐Arylation
inferred← citeshttps://doi.org/10.1002/ajoc.201600045openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of (Hetero)aryl Chlorides with Aryllithium Compounds
inferred← citeshttps://doi.org/10.1002/ajoc.201700064openalex-snapshot
Pd(PPh3)4‐Catalyzed Buchwald–Hartwig Amination ofAryl Fluorosulfonates with Aryl Amines
inferred← citeshttps://doi.org/10.1002/ajoc.201700238openalex-snapshot
Palladium‐Catalyzed ortho‐Halogenation of Tertiary Benzamides
inferred← citeshttps://doi.org/10.1002/ajoc.201700267openalex-snapshot
Regioselective Metal‐Free C2−H Arylation of Quinoline N ‐Oxides with Aryldiazonium Salts/Anilines under Ambient Conditions
inferred← citeshttps://doi.org/10.1002/ajoc.201700301openalex-snapshot
An Efficient and Environmentally Benign Bentonite–Gold Nanohybrid‐Catalyzed Oxidative Cross‐Coupling of Ketones with Benzylic Primary Alcohols
inferred← citeshttps://doi.org/10.1002/ajoc.201800080openalex-snapshot
Recent Progress in Transition‐Metal‐Free, Base‐Mediated Benzannulation Reactions for the Synthesis of a Diverse Range of Aromatic and Heteroaromatic Compounds
inferred← citeshttps://doi.org/10.1002/ajoc.201800154openalex-snapshot
A Copper‐Catalyzed Domino Reaction of Alkynyl Bromides and Oxazolidine‐2‐thiones: Synthesis of Thiazol‐2‐ones
inferred← citeshttps://doi.org/10.1002/ajoc.201800438openalex-snapshot
Construction of Biaryl Scaffolds from Iodoarenes and C−H Heteroarenes Using an Amide Base Generated in situ from Aminosilane and Fluoride Anion
inferred← citeshttps://doi.org/10.1002/ajoc.201900305openalex-snapshot
1,3,5‐Triphenylpyrazoline‐Based Organocatalysis: Synthesis of Aryl‐Heteroaryl Compounds and Exploiting By‐Product from the Reaction for Alkyne‐Carbonyl Metathesis (ACM) Reaction in One Pot
inferred← citeshttps://doi.org/10.1002/ajoc.202000059openalex-snapshot
A Combination of Biocompatible Room Temperature Ionic Liquid and Palladium Catalyst for Base‐ and Ligand‐Free Suzuki Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ajoc.202000443openalex-snapshot
Palladium‐Catalyzed Direct C−H Arylation of Arenes Promoted by Quaternary Ammonium Salt
inferred← citeshttps://doi.org/10.1002/ajoc.202100301openalex-snapshot
Alkynylazulenes as Building Blocks for Highly Unsaturated Scaffolds
inferred← citeshttps://doi.org/10.1002/ajoc.202100792openalex-snapshot
Copper‐Catalyzed N‐Arylation of Indoles and Anilines with Aryltrialkoxysilanes
inferred← citeshttps://doi.org/10.1002/ajoc.202500263openalex-snapshot
Noncross Coupling Route to Biaryls and Heterobiaryls via Iodoarylation of Arynes
inferred← citeshttps://doi.org/10.1002/ajoc.202500332openalex-snapshot
Advanced Pd–NAPA Precatalysts for Broad‐Scope Kumada–Tamao–Corriu Couplings of Challenging Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/ajoc.202500595openalex-snapshot
Direct C─H Arylation of (Hetero)arenes Using Hantzsch Ester as a Photoredox Catalyst
inferred← citeshttps://doi.org/10.1002/ange.200604988openalex-snapshot
Ein effizienter Dirhodiumkatalysator für die nichtdirigierte Direktarylierung nichtaktivierter Arene
inferred← citeshttps://doi.org/10.1002/ange.200700590openalex-snapshot
Suzuki–Miyaura Coupling Reaction by PdII‐Catalyzed Aromatic CH Bond Activation Directed by an N‐Alkyl Acetamino Group
inferred← citeshttps://doi.org/10.1002/ange.200701282openalex-snapshot
Efficient CuO‐Nanoparticle‐Catalyzed CS Cross‐Coupling of Thiols with Iodobenzene
inferred← citeshttps://doi.org/10.1002/ange.200703299openalex-snapshot
Iron‐Catalyzed N‐Arylation of Nitrogen Nucleophiles
inferred← citeshttps://doi.org/10.1002/ange.200704018openalex-snapshot
Iron‐Catalyzed CO Cross‐Couplings of Phenols with Aryl Iodides
inferred← citeshttps://doi.org/10.1002/ange.200704402openalex-snapshot
Efficient Cobalt‐Catalyzed Formation of Unsymmetrical Biaryl Compounds and Its Application in the Synthesis of a Sartan Intermediate
inferred← citeshttps://doi.org/10.1002/ange.200705558openalex-snapshot
Palladium‐Catalyzed Intermolecular Ene–Yne Coupling: Development of an Atom‐Efficient Mizoroki–Heck‐Type Reaction
inferred← citeshttps://doi.org/10.1002/ange.200705668openalex-snapshot
Iron‐Catalyzed S‐Arylation of Thiols with Aryl Iodides
inferred← citeshttps://doi.org/10.1002/ange.200705976openalex-snapshot
Distannylierung und Silastannylierung in situ generierter Allene
inferred← citeshttps://doi.org/10.1002/ange.200802526openalex-snapshot
Iron‐Mediated Direct Arylation of Unactivated Arenes
inferred← citeshttps://doi.org/10.1002/ange.200803193openalex-snapshot
A General Palladium‐Catalyzed Suzuki–Miyaura Coupling of Aryl Mesylates
inferred← citeshttps://doi.org/10.1002/ange.200804497openalex-snapshot
Katalytische C‐C‐, C‐N‐ und C‐O‐Ullmann‐Kupplungen
inferred← citeshttps://doi.org/10.1002/ange.200804524openalex-snapshot
A Copper‐Catalyzed, pH‐Neutral Construction of High‐Enantiopurity Peptidyl Ketones from Peptidic S‐Acylthiosalicylamides in Air at Room Temperature
inferred← citeshttps://doi.org/10.1002/ange.200900329openalex-snapshot
C(Aryl)‐O‐Aktivierung von Arylcarboxylaten in nickelkatalysierten Biarylsynthesen
inferred← citeshttps://doi.org/10.1002/ange.200901246openalex-snapshot
One‐Step Synthesis of the Benzocyclo[penta‐ to octa‐]isoindole Core
inferred← citeshttps://doi.org/10.1002/ange.200902236openalex-snapshot
Copper‐Catalyzed Cross‐Couplings with Part‐per‐Million Catalyst Loadings
inferred← citeshttps://doi.org/10.1002/ange.200902237openalex-snapshot
On the Role of Metal Contaminants in Catalyses with FeCl3
inferred← citeshttps://doi.org/10.1002/ange.200902996openalex-snapshot
Übergangsmetallkatalysierte direkte Arylierungen von (Hetero)Arenen durch C‐H‐Bindungsbruch
inferred← citeshttps://doi.org/10.1002/ange.200904033openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling of Aryl Halides Using Organotitanium Nucleophiles
inferred← citeshttps://doi.org/10.1002/ange.200906811openalex-snapshot
Pd‐PEPPSI‐IPent: Low‐Temperature Negishi Cross‐Coupling for the Preparation of Highly Functionalized, Tetra‐ortho‐Substituted Biaryls
inferred← citeshttps://doi.org/10.1002/ange.200906996openalex-snapshot
Nickel‐Catalyzed Direct CH Arylation and Alkenylation of Heteroarenes with Organosilicon Reagents
inferred← citeshttps://doi.org/10.1002/ange.201006208openalex-snapshot
Palladium‐katalysierte dehydrierende Kreuzkupplungen von Benzazolen mit Azolen
inferred← citeshttps://doi.org/10.1002/ange.201007187openalex-snapshot
Hoch diastereoselektive eisenvermittelte C(sp2)‐C(sp3)‐Kreuzkupplungen zwischen Aryl‐Grignard‐Reagentien und cyclischen Iodhydrinderivaten
inferred← citeshttps://doi.org/10.1002/ange.201100096openalex-snapshot
Effiziente und selektive Monomethylierung kontra N‐H‐Bindungsaktivierung von Ammoniak: atomares Zink als Abgangsgruppe in einer SN2‐Reaktion von “nacktem” Zn(CH3)+ und NH3
inferred← citeshttps://doi.org/10.1002/ange.201100683openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling of Aryltrimethylammonium Iodides with Organozinc Reagents
inferred← citeshttps://doi.org/10.1002/ange.201103621openalex-snapshot
Nickel‐katalysierte Cycloaddition durch zwei sequenzielle C‐H‐Aktivierungen
inferred← citeshttps://doi.org/10.1002/ange.201103720openalex-snapshot
Carboxylic Acids as Traceless Directing Groups for Formal meta‐Selective Direct Arylation
inferred← citeshttps://doi.org/10.1002/ange.201105020openalex-snapshot
Copper‐Catalyzed Oxidative CO Coupling by Direct CH Bond Activation of Formamides: Synthesis of Enol Carbamates and 2‐Carbonyl‐Substituted Phenol Carbamates
inferred← citeshttps://doi.org/10.1002/ange.201106086openalex-snapshot
Cross‐Coupling of Aryl Grignard Reagents with Aryl Iodides and Bromides through SRN1 Pathway
inferred← citeshttps://doi.org/10.1002/ange.201107017openalex-snapshot
Palladiumkatalysierte Kreuzkupplungen: eine historische Perspektive im Kontext der Nobel‐Preise 2010
inferred← citeshttps://doi.org/10.1002/ange.201200153openalex-snapshot
A General Pd‐Catalyzed Decarboxylative Cross‐Coupling Reaction between Aryl Carboxylic Acids: Synthesis of Biaryl Compounds
inferred← citeshttps://doi.org/10.1002/ange.201203521openalex-snapshot
An Expeditious Route to Eight‐Membered Heterocycles By Nickel‐Catalyzed Cycloaddition: Low‐Temperature C sp 2C sp 3 Bond Cleavage
inferred← citeshttps://doi.org/10.1002/ange.201204798openalex-snapshot
An Efficient Route to Polysubstituted Tetrahydronaphthols: Silver‐Catalyzed [4+2] Cyclization of 2‐Alkylbenzaldehydes and Alkenes
inferred← citeshttps://doi.org/10.1002/ange.201205119openalex-snapshot
Synthese und Anwendung wasserlöslicher NHC‐Übergangsmetall‐Komplexe
inferred← citeshttps://doi.org/10.1002/ange.201207750openalex-snapshot
Mild and General Conditions for Negishi Cross‐Coupling Enabled by the Use of Palladacycle Precatalysts
inferred← citeshttps://doi.org/10.1002/ange.201300587openalex-snapshot
Copper‐Mediated CH/CH Biaryl Coupling of Benzoic Acid Derivatives and 1,3‐Azoles
inferred← citeshttps://doi.org/10.1002/ange.201300917openalex-snapshot
Base‐Catalyzed Synthesis of Substituted Indazoles under Mild, Transition‐Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ange.201302506openalex-snapshot
Einfache und doppelte N‐H‐Aktivierung in NH3 durch [Al2O3].+: Erzeugung des Aminylradikals und von Nitren bei Raumtemperatur
inferred← citeshttps://doi.org/10.1002/ange.201305342openalex-snapshot
Selective Reductive Cleavage of Inert Aryl CO Bonds by an Iron Catalyst
inferred← citeshttps://doi.org/10.1002/ange.201306427openalex-snapshot
Hindered Aryllithium Reagents as Partners in Palladium‐Catalyzed Cross‐Coupling: Synthesis of Tri‐ and Tetra‐ortho‐Substituted Biaryls under Ambient Conditions
inferred← citeshttps://doi.org/10.1002/ange.201306869openalex-snapshot
Nickel‐Catalyzed Cycloaddition of 1,3‐Dienes with 3‐Azetidinones and 3‐Oxetanones
inferred← citeshttps://doi.org/10.1002/ange.201309761openalex-snapshot
Ascorbic Acid as an Initiator for the Direct CH Arylation of (Hetero)arenes with Anilines Nitrosated In Situ
inferred← citeshttps://doi.org/10.1002/ange.201406479openalex-snapshot
Dehydrogenative N‐Incorporation: A Direct Approach to Quinoxaline N‐Oxides under Mild Conditions
inferred← citeshttps://doi.org/10.1002/ange.201407586openalex-snapshot
Copper‐Catalyzed Coupling of Triaryl‐ and Trialkylindium Reagents with Aryl Iodides and Bromides through Consecutive Transmetalations
inferred← citeshttps://doi.org/10.1002/ange.201507128openalex-snapshot
Palladium‐Catalyzed Heteroarylation and Concomitant ortho‐Alkylation of Aryl Iodides
inferred← citeshttps://doi.org/10.1002/ange.201510497openalex-snapshot
Lewis‐Säure‐unterstützte metallkatalysierte Kreuzkupplung: Alkylierung von Arylmethylethern unter C‐O‐Bindungsspaltung ohne β‐Hydrideliminierung
inferred← citeshttps://doi.org/10.1002/ange.201604429openalex-snapshot
Highly Chemoselective Iridium Photoredox and Nickel Catalysis for the Cross‐Coupling of Primary Aryl Amines with Aryl Halides
inferred← citeshttps://doi.org/10.1002/ange.201703667openalex-snapshot
Hydroxamsäuren als chemoselektive (ortho‐Amino)arylierungsreagenzien durch sigmatrope Umlagerung
inferred← citeshttps://doi.org/10.1002/ange.201802813openalex-snapshot
Electron‐Catalyzed Cross‐Coupling of Arylboron Compounds with Aryl Iodides
inferred← citeshttps://doi.org/10.1002/ange.201805961openalex-snapshot
Metal‐Free Synthesis of Pharmaceutically Important Biaryls by Photosplicing
inferred← citeshttps://doi.org/10.1002/ange.201904795openalex-snapshot
The Buchwald–Hartwig Amination After 25 Years
inferred← citeshttps://doi.org/10.1002/ange.201909798openalex-snapshot
NHC‐Coordinated Diphosphene‐Stabilized Gold(I) Hydride and Its Reversible Conversion to Gold(I) Formate with CO2
inferred← citeshttps://doi.org/10.1002/ange.201910395openalex-snapshot
Cu‐Mediated Amination of (Hetero)Aryl C−H bonds with NH Azaheterocycles
inferred← citeshttps://doi.org/10.1002/ange.202006740openalex-snapshot
Transformations of Aryl Ketones via Ligand‐Promoted C−C Bond Activation
inferred← citeshttps://doi.org/10.1002/ange.202008866openalex-snapshot
Efficient Pd‐Catalyzed Direct Coupling of Aryl Chlorides with Alkyllithium Reagents
inferred← citeshttps://doi.org/10.1002/ange.202201543openalex-snapshot
Alternating Current Electrolysis Enabled Formal C−O/O−H Cross‐Metathesis of 4‐Alkoxy Anilines with Alcohols
inferred← citeshttps://doi.org/10.1002/ange.202311100openalex-snapshot
Dual Tunability for Uncatalyzed N‐Alkylation of Primary Amines Enabled by Plasma‐Microdroplet Fusion
inferred← citeshttps://doi.org/10.1002/ange.202405824openalex-snapshot
Consolidation of the Oxidant‐Free Au(I)/Au(III) Catalysis Enabled by the Hemilabile Ligand Strategy
inferred← citeshttps://doi.org/10.1002/ange.202413122openalex-snapshot
Programmable C−N Bond Formation through Radical‐Mediated Chemistry in Plasma‐Microdroplet Fusion
inferred← citeshttps://doi.org/10.1002/ange.202413846openalex-snapshot
C1‐4 Alkylation of Aryl Bromides with Light Alkanes enabled by Metallaphotocatalysis in Flow
inferred← citeshttps://doi.org/10.1002/ange.202505391openalex-snapshot
Reverse Regioselective Dicarbofunctionalization via Anti ‐Michael‐Type Addition
inferred← citeshttps://doi.org/10.1002/ange.202512024openalex-snapshot
A Broadly Applicable Strategy to Aminate Azines Enabled by Electronically Tuned Phosphine Reagents
inferred← citeshttps://doi.org/10.1002/ange.202518983openalex-snapshot
Nickel‐Mediated Synthesis of Fused Heterocycle‐Linked Covalent Organic Frameworks for Self‐Sensitized Photocatalysis
inferred← citeshttps://doi.org/10.1002/ange.3094782openalex-snapshot
Iron Catalyzed Aryl–Aryl Kumada Cross‐Coupling: A Mechanistic and Computational Investigation
inferred← citeshttps://doi.org/10.1002/anie.200604988openalex-snapshot
An Efficient Bimetallic Rhodium Catalyst for the Direct Arylation of Unactivated Arenes
inferred← citeshttps://doi.org/10.1002/anie.200700590openalex-snapshot
Suzuki–Miyaura Coupling Reaction by Pd II ‐Catalyzed Aromatic CH Bond Activation Directed by an N ‐Alkyl Acetamino Group
inferred← citeshttps://doi.org/10.1002/anie.200701282openalex-snapshot
Efficient CuO‐Nanoparticle‐Catalyzed CS Cross‐Coupling of Thiols with Iodobenzene
inferred← citeshttps://doi.org/10.1002/anie.200703299openalex-snapshot
Iron‐Catalyzed N‐Arylation of Nitrogen Nucleophiles
inferred← citeshttps://doi.org/10.1002/anie.200704018openalex-snapshot
Iron‐Catalyzed CO Cross‐Couplings of Phenols with Aryl Iodides
inferred← citeshttps://doi.org/10.1002/anie.200704402openalex-snapshot
Efficient Cobalt‐Catalyzed Formation of Unsymmetrical Biaryl Compounds and Its Application in the Synthesis of a Sartan Intermediate
inferred← citeshttps://doi.org/10.1002/anie.200705558openalex-snapshot
Palladium‐Catalyzed Intermolecular Ene–Yne Coupling: Development of an Atom‐Efficient Mizoroki–Heck‐Type Reaction
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