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Suzuki−Miyaura Coupling of Aryl Tosylates Catalyzed by an Array of Indolyl Phosphine−Palladium Catalysts
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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/10.1002/9783527619405openalex-snapshot
Transition Metals for Organic Synthesis
inferredcites →https://doi.org/10.1002/9783527619535openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/anie.200353015openalex-snapshot
Efficient Palladium‐Catalyzed Coupling of Aryl Chlorides and Tosylates with Terminal Alkynes: Use of a Copper Cocatalyst Inhibits the Reaction
inferredcites →https://doi.org/10.1002/anie.200600442openalex-snapshot
Heck Coupling with Nonactivated Alkenyl Tosylates and Phosphates: Examples of Effective 1,2‐Migrations of the Alkenyl Palladium(II) Intermediates
inferredcites →https://doi.org/10.1002/anie.200802157openalex-snapshot
Palladium‐Catalyzed Amination of Aryl Mesylates
inferredcites →https://doi.org/10.1016/0040-4039(96)01984-3openalex-snapshot
Nickel-catalyzed coupling reaction of lithium organoborates and aryl mesylates possessing an electron withdrawing group
inferredcites →https://doi.org/10.1016/j.tetlet.2006.01.145openalex-snapshot
Ferrocenylmethylphosphines as ligands for room temperature Ni(0)-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl arenesulfonates and aryl chlorides
inferredcites →https://doi.org/10.1016/s0022-328x(02)01264-0openalex-snapshot
Cross-coupling reaction of organoboron compounds via base-assisted transmetalation to palladium(II) complexes
inferredcites →https://doi.org/10.1016/s0022-328x(02)01269-xopenalex-snapshot
Cross-coupling reactions via organoboranes
inferredcites →https://doi.org/10.1016/s0040-4020(98)00809-6openalex-snapshot
Synthesis of biaryls via nickel-catalyzed cross-coupling reaction of arylboronic acids and aryl mesylates
inferredcites →https://doi.org/10.1021/ar050199qopenalex-snapshot
Organotrifluoroborates: Protected Boronic Acids That Expand the Versatility of the Suzuki Coupling Reaction
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/cr0505268openalex-snapshot
Selected Patented Cross-Coupling Reaction Technologies
inferredcites →https://doi.org/10.1021/cr0505674openalex-snapshot
Carbon−Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts
inferredcites →https://doi.org/10.1021/cr0509861openalex-snapshot
Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/ja00088a047openalex-snapshot
A Novel Easily Accessible Chiral Ferrocenyldiphosphine for Highly Enantioselective Hydrogenation, Allylic Alkylation, and Hydroboration Reactions
inferredcites →https://doi.org/10.1021/ja035483wopenalex-snapshot
Expanding Pd-Catalyzed C−N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed Reactions
inferredcites →https://doi.org/10.1021/ja035835zopenalex-snapshot
Oxidative Addition of Aryl Tosylates to Palladium(0) and Coupling of Unactivated Aryl Tosylates at Room Temperature
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/ja038752ropenalex-snapshot
Room-Temperature Ni(0)-Catalyzed Cross-Coupling Reactions of Aryl Arenesulfonates with Arylboronic Acids
inferredcites →https://doi.org/10.1021/ja0580340openalex-snapshot
A General and Long-Lived Catalyst for the Palladium-Catalyzed Coupling of Aryl Halides with Thiols
inferredcites →https://doi.org/10.1021/ja0683180openalex-snapshot
Rationale Behind the Resistance of Dialkylbiaryl Phosphines toward Oxidation by Molecular Oxygen
inferredcites →https://doi.org/10.1021/ja711449eopenalex-snapshot
Palladium-Catalyzed Carbonylation of Aryl Tosylates and Mesylates
inferredcites →https://doi.org/10.1021/ja981318iopenalex-snapshot
Sterically Hindered Chelating Alkyl Phosphines Provide Large Rate Accelerations in Palladium-Catalyzed Amination of Aryl Iodides, Bromides, and Chlorides, and the First Amination of Aryl Tosylates
inferredcites →https://doi.org/10.1021/ja992130hopenalex-snapshot
Highly Active Palladium Catalysts for Suzuki Coupling Reactions
inferredcites →https://doi.org/10.1021/jo00109a044openalex-snapshot
Aryl Mesylates in Metal Catalyzed Homocoupling and Cross-Coupling Reactions. 2. Suzuki-Type Nickel-Catalyzed Cross-Coupling of Aryl Arenesulfonates and Aryl Mesylates with Arylboronic Acids
inferredcites →https://doi.org/10.1021/jo00109a045openalex-snapshot
Aryl Mesylates in Metal-Catalyzed Homocoupling and Cross-Coupling Reactions. 3. A Simple and General Method for the Synthesis of 2,2'-Diaroyl-4,4'-dihydroxybiphenyls
inferredcites →https://doi.org/10.1021/jo00126a047openalex-snapshot
Aryl Mesylates in Metal Catalyzed Homo- and Cross-Coupling Reactions. 4. Scope and Limitations of Aryl Mesylates in Nickel Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/jo049940iopenalex-snapshot
NiCl2(dppe)-Catalyzed Cross-Coupling of Aryl Mesylates, Arenesulfonates, and Halides with Arylboronic Acids
inferredcites →https://doi.org/10.1021/jo051394lopenalex-snapshot
Kumada Coupling of Aryl and Vinyl Tosylates under Mild Conditions
inferredcites →https://doi.org/10.1021/jo051590sopenalex-snapshot
Enol Tosylates as Viable Partners in Pd-Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/jo7019064openalex-snapshot
Palladium-Catalyzed Suzuki−Miyaura Cross-Couplings of Aryl Tosylates with Potassium Aryltrifluoroborates
inferredcites →https://doi.org/10.1021/jo991699yopenalex-snapshot
Simple, Efficient Catalyst System for the Palladium-Catalyzed Amination of Aryl Chlorides, Bromides, and Triflates
inferredcites →https://doi.org/10.1021/ol016526lopenalex-snapshot
NiCl2(PCy3)2: A Simple and Efficient Catalyst Precursor for the Suzuki Cross-Coupling of Aryl Tosylates and Arylboronic Acids
inferredcites →https://doi.org/10.1021/ol048328aopenalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of 2-Indolyldimethylsilanols with Substituted Aryl Halides
inferredcites →https://doi.org/10.1021/ol050117yopenalex-snapshot
Preparation of Enamides via Palladium-Catalyzed Amidation of Enol Tosylates
inferredcites →https://doi.org/10.1021/ol052136dopenalex-snapshot
Regioselective Heck Couplings of α,β-Unsaturated Tosylates and Mesylates with Electron-Rich Olefins
inferredcites →https://doi.org/10.1021/ol061116oopenalex-snapshot
Air-Stable PinP(O)H as Preligand for Palladium-Catalyzed Kumada Couplings of Unactivated Tosylates
inferredcites →https://doi.org/10.1021/ol070898yopenalex-snapshot
Easily Accessible and Highly Tunable Indolyl Phosphine Ligands for Suzuki−Miyaura Coupling of Aryl Chlorides
inferredcites →https://doi.org/10.1021/ol702453qopenalex-snapshot
C−C Bond Formation Catalyzed Heterogeneously by Nickel-on-Graphite (Ni/Cg)
inferredcites →https://doi.org/10.1021/om034187popenalex-snapshot
Oxidative Addition of Aryl Sulfonates to Palladium(0) Complexes of Mono- and Bidentate Phosphines. Mild Addition of Aryl Tosylates and the Effects of Anions on Rate and Mechanism
inferredcites →https://doi.org/10.1039/b410937fopenalex-snapshot
The development of efficient catalysts for palladium-catalyzed coupling reactions of aryl halides
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Palladium( II ) Acetate – Tertiary Phosphine
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ortho,ortho′‐Substituted KITPHOS Monophosphines: Highly Efficient Ligands for Palladium‐Catalyzed CC and CN Bond Formation
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Gold‐Catalyzed Cyclizations: A Comparative Study of ortho,ortho′‐Substituted KITPHOS Monophosphines with their Biaryl Monophosphine Counterpart SPHOS
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Heteroatom Donor‐Decorated Polymer‐Immobilized Ionic Liquid Stabilized Palladium Nanoparticles: Efficient Catalysts for Room‐Temperature Suzuki‐Miyaura Cross‐Coupling in Aqueous Media
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A General and Special Catalyst for Suzuki–Miyaura Coupling Processes
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inferred← citeshttps://doi.org/10.1002/anie.200904306openalex-snapshot
Organotrifluoroborates and Monocoordinated Palladium Complexes as Catalysts—A Perfect Combination for Suzuki–Miyaura Coupling
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inferred← citeshttps://doi.org/10.1002/aoc.3970openalex-snapshot
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Chapter 5.2 Five-membered ring systems: pyrroles and benzo analogs
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inferred← citeshttps://doi.org/10.1021/cr100259topenalex-snapshot
Nickel-Catalyzed Cross-Couplings Involving Carbon−Oxygen Bonds
inferred← citeshttps://doi.org/10.1021/ja200398copenalex-snapshot
Suzuki−Miyaura Cross-Coupling of Aryl Carbamates and Sulfamates: Experimental and Computational Studies
inferred← citeshttps://doi.org/10.1021/jo100846topenalex-snapshot
A General Palladium Catalyst System for Suzuki−Miyaura Coupling of Potassium Aryltrifluoroborates and Aryl Mesylates
inferred← citeshttps://doi.org/10.1021/jo202037xopenalex-snapshot
Ni(COD)2/PCy3 Catalyzed Cross-Coupling of Aryl and Heteroaryl Neopentylglycolboronates with Aryl and Heteroaryl Mesylates and Sulfamates in THF at Room Temperature
inferred← citeshttps://doi.org/10.1021/jo301270topenalex-snapshot
N-Heterocyclic Carbene–Palladium(II)–1-Methylimidazole Complex-Catalyzed Suzuki–Miyaura Coupling of Aryl Sulfonates with Arylboronic Acids
inferred← citeshttps://doi.org/10.1021/ol101592ropenalex-snapshot
Nickel-Catalyzed C−O Activation of Phenol Derivatives with Potassium Heteroaryltrifluoroborates
inferred← citeshttps://doi.org/10.1021/ol1028892openalex-snapshot
A Mild and Efficient Palladium-Catalyzed Cyanation of Aryl Chlorides with K4[Fe(CN)6]
inferred← citeshttps://doi.org/10.1021/ol200128yopenalex-snapshot
Cross-Coupling of Mesylated Phenol Derivatives with Potassium Ammonio- and Amidomethyltrifluoroborates
inferred← citeshttps://doi.org/10.1021/ol2009522openalex-snapshot
Palladium-Catalyzed Decarboxylative Arylation of Potassium Cyanoacetate: Synthesis of α-Diaryl Nitriles from Aryl Halides
inferred← citeshttps://doi.org/10.1021/ol201469ropenalex-snapshot
Cross-Coupling of Mesylated Phenol Derivatives with Potassium Alkoxymethyltrifluoroborates
inferred← citeshttps://doi.org/10.1021/ol301221popenalex-snapshot
Suzuki–Miyaura Cross-Coupling Reactions of Potassium Boc-Protected Aminomethyltrifluoroborate with Aryl and Hetaryl Mesylates
inferred← citeshttps://doi.org/10.1021/ol401021xopenalex-snapshot
Pd-Catalyzed Suzuki–Miyaura Cross-Coupling Reactions between Sulfamates and Potassium Boc-Protected Aminomethyltrifluoroborates
inferred← citeshttps://doi.org/10.1021/ol802493zopenalex-snapshot
Palladium−Indolylphosphine-Catalyzed Hiyama Cross-Coupling of Aryl Mesylates
inferred← citeshttps://doi.org/10.1021/ol9015892openalex-snapshot
A Versatile Catalyst System for Suzuki−Miyaura Cross-Coupling Reactions of C(sp2)-Tosylates and Mesylates
inferred← citeshttps://doi.org/10.1021/om200843fopenalex-snapshot
Ruthenium Complexes of κ(P)- and κ(P)-η6-Coordinated KITPHOS Monophosphines: Efficient Catalysts for the Direct Ortho Arylation of 2-Phenylpyridine andN-Phenylpyrazole with Aryl Chlorides
inferred← citeshttps://doi.org/10.1021/om3011992openalex-snapshot
Electron-Rich Trialkyl-Type Dihydro-KITPHOS Monophosphines: Efficient Ligands for Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling. Comparison with Their Biaryl-Like KITPHOS Monophosphine Counterparts
inferred← citeshttps://doi.org/10.1021/op300236fopenalex-snapshot
Ni- and Fe-Catalyzed Cross-Coupling Reactions of Phenol Derivatives
inferred← citeshttps://doi.org/10.1021/op5002353openalex-snapshot
Aryldiazonium Tetrafluoroborate Salts as Green and Efficient Coupling Partners for the Suzuki–Miyaura Reaction: From Optimisation to Mole Scale
inferred← citeshttps://doi.org/10.1039/c1cc12240aopenalex-snapshot
A versatile palladium catalyst system for Suzuki–Miyaura coupling of alkenyl tosylates and mesylates
inferred← citeshttps://doi.org/10.1039/c1ob05426kopenalex-snapshot
One step entry to P,O- and P,N-type heterocyclic tertiary phosphine ligands and application in Suzuki–Miyaura cross-coupling reactions
inferred← citeshttps://doi.org/10.1039/c1ob05783aopenalex-snapshot
Generation of diverse 2-pyrones via palladium-catalyzed site-selective Suzuki-Miyaura couplings of 3-bromo-4-tosyloxy-2-pyrone
inferred← citeshttps://doi.org/10.1039/c2cc15972dopenalex-snapshot
An efficient palladium–benzimidazolyl phosphine complex for the Suzuki–Miyaura coupling of aryl mesylates: facile ligand synthesis and metal complex characterization
inferred← citeshttps://doi.org/10.1039/c2cy20505jopenalex-snapshot
Direct C–H bond arylations and alkenylations with phenol-derived fluorine-free electrophiles
inferred← citeshttps://doi.org/10.1039/c2ra21667aopenalex-snapshot
Palladium-catalyzed direct arylation of polyfluoroarenes with aryl tosylates and mesylates
inferred← citeshttps://doi.org/10.1039/c3cc41066hopenalex-snapshot
Pd-catalyzed C3-selective arylation of pyridines with phenyl tosylates
inferred← citeshttps://doi.org/10.1039/c3ob40198gopenalex-snapshot
Phthalide: a direct building-block towards P,O and P,N hemilabile ligands. Application in the palladium-catalysed Suzuki–Miyaura cross-coupling of aryl chlorides
inferred← citeshttps://doi.org/10.1039/c3ra22905jopenalex-snapshot
A decade advancement of transition metal-catalyzed borylation of aryl halides and sulfonates
inferred← citeshttps://doi.org/10.1039/c3ra45547eopenalex-snapshot
Chemoselective one-pot synthesis of β-keto sulfones from ketones
inferred← citeshttps://doi.org/10.1039/c4ob00700jopenalex-snapshot
Synthesis of 4-alkynylquinazolines: Pd–Cu-cocatalyzed coupling of quinazoline-4-tosylates with terminal alkynes using N-heterocyclic carbenes as ligands
inferred← citeshttps://doi.org/10.1039/c4qo00103fopenalex-snapshot
Palladium-catalyzed reductive cleavage of tosylated arenes using isopropanol as the mild reducing agent
inferred← citeshttps://doi.org/10.1039/c4ra07455fopenalex-snapshot
Palladium-catalyzed desulfitative cross-coupling of arylsulfinates with arylboronic acids
inferred← citeshttps://doi.org/10.1039/c5nj03038bopenalex-snapshot
1,4-Dihydrophosphinolines and their complexes with group 10 metals
inferred← citeshttps://doi.org/10.1039/c5ob00545kopenalex-snapshot
Divergent synthesis of 4,6-diarylated pyridin-2(1H)-ones from chalcones: novel access to 2,4,6-triaryl pyridines
inferred← citeshttps://doi.org/10.1039/c5ra01363aopenalex-snapshot
Pd-catalyzed desulfitative and denitrogenative Suzuki-type reaction of arylsulfonyl hydrazides
inferred← citeshttps://doi.org/10.1039/c6ra14678copenalex-snapshot
Carbonylative coupling of aryl tosylates/triflates with arylboronic acids under CO atmosphere
inferred← citeshttps://doi.org/10.1039/c7cc06717hopenalex-snapshot
Efficient Ni-catalyzed conversion of phenols protected with 2,4,6-trichloro-1,3,5-triazine (TCT) to olefins
inferred← citeshttps://doi.org/10.1039/c8nj00412aopenalex-snapshot
Synthesis of a class of binaphthyl monophosphine ligands with a naphthofuran skeleton and their applications in Suzuki–Miyaura coupling reactions
inferred← citeshttps://doi.org/10.1039/c8ob01034jopenalex-snapshot
Nickel-catalyzed cyanation of phenol derivatives activated by 2,4,6-trichloro-1,3,5-triazine
inferred← citeshttps://doi.org/10.1039/c9qo01537jopenalex-snapshot
Palladium-catalyzed cross-coupling of (hetero)aryl or alkenyl sulfonates with aryl titanium as the multi-functional reagent
inferred← citeshttps://doi.org/10.1039/c9sc00810aopenalex-snapshot
Conversion of two stereocenters to one or two chiral axes: atroposelective synthesis of 2,3-diarylbenzoindoles
inferred← citeshttps://doi.org/10.1039/d0cy01159bopenalex-snapshot
Palladium-catalyzed cross-couplings by C–O bond activation
inferred← citeshttps://doi.org/10.1039/d0ob01718copenalex-snapshot
An update on the use of sulfinate derivatives as versatile coupling partners in organic chemistry
inferred← citeshttps://doi.org/10.1039/d1nj03706dopenalex-snapshot
Synthesis of ortho -arylated and alkenylated benzamides by palladium-catalyzed denitrogenative cross-coupling reactions of 1,2,3-benzotriazin-4(3 H )-ones with organoboronic acids
inferred← citeshttps://doi.org/10.1039/d3nj00099kopenalex-snapshot
Palladium nanoparticles supported on reduced graphene oxide (Pd@rGO): an efficient heterogeneous catalyst for Suzuki–Miyaura, Heck–Matsuda and Double Suzuki–Miyaura cross-coupling reactions
inferred← citeshttps://doi.org/10.1055/a-1633-8792openalex-snapshot
Direct Copper-Catalyzed C-3 Arylation of Diphenylphosphine Oxide Indoles
inferred← citeshttps://doi.org/10.1107/s2414314617009828openalex-snapshot
Biphenyl-4-yl 4-methylbenzenesulfonate
inferred← citeshttps://doi.org/10.3390/catal5031425openalex-snapshot
Dimethyl-Aluminium Complexes Bearing Naphthyl-Substituted Pyridine-Alkylamides as Pro-Initiators for the Efficient ROP of ε-Caprolactone
inferred← citeshttps://doi.org/10.3987/com-09-s(s)105openalex-snapshot
Stille Cross-Coupling Reactions of Aryl Mesylates and Tosylates Using a Biarylphosphine Based Catalyst System
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