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Suzuki−Miyaura Reactions of Arenediazonium Salts Catalyzed by Pd(0)/C. One-Pot Chemoselective Double Cross-Coupling Reactions
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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/(sici)1521-3773(19980302)37:4<402::aid-anie402>3.0.co;2-9openalex-snapshot
Electroluminescent Conjugated Polymers—Seeing Polymers in a New Light
inferredcites →https://doi.org/10.1002/1521-3765(20020902)8:17<3901::aid-chem3901>3.0.co;2-eopenalex-snapshot
Synthesis of Monocarbenepalladium(0) Complexes and Their Catalytic Behavior in Cross-Coupling Reactions of Aryldiazonium Salts
inferredcites →https://doi.org/10.1016/0040-4039(96)00699-5openalex-snapshot
Cross-coupling of arenediazonium tetrafluoroborates with arylboronic acids catalysed by palladium
inferredcites →https://doi.org/10.1016/s0040-4039(97)00939-8openalex-snapshot
Cross-coupling reactions of arenediazonium tetrafluoroborates with potassium aryl- or alkenyltrifluoroborates catalyzed by palladium
inferredcites →https://doi.org/10.1016/s0040-4039(98)01003-xopenalex-snapshot
Potassium vinyltrifluoroborate : A stable and efficient vinylating agent of arenediazonium salts using palladium catalysts
inferredcites →https://doi.org/10.1021/cr980079eopenalex-snapshot
Photoalignment of Liquid-Crystal Systems
inferredcites →https://doi.org/10.1021/jo9912451openalex-snapshot
A Novel Regio- and Stereoselective Formal Cross-Coupling Reaction of Unsaturated Silanes with Arenediazonium Tetrafluoroborates
inferredcites →https://doi.org/10.1021/op980079gopenalex-snapshot
Multikilogram-Scale Synthesis of a Biphenyl Carboxylic Acid Derivative Using a Pd/C-Mediated Suzuki Coupling Approach
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781118662083.cot01-002openalex-snapshot
Formation of Alkanes and Arenes by Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527628698.hgc052openalex-snapshot
Coupling Reactions in Water
inferred← citeshttps://doi.org/10.1002/adsc.200800025openalex-snapshot
Efficient and Practical Cross‐Coupling of Arenediazonium Tetrafluoroborate Salts with Boronic Acids Catalyzed by Palladium(0)/Barium Carbonate
inferred← citeshttps://doi.org/10.1002/adsc.200800162openalex-snapshot
Suzuki–Miyaura Cross‐Coupling of 2‐Nitroarenediazonium Tetrafluoroborates: Synthesis of Unsymmetrical 2‐Nitrobiphenyls and Highly Functionalized Carbazoles
inferred← citeshttps://doi.org/10.1002/adsc.200800539openalex-snapshot
Heck Cross‐Coupling of Aryldiazonium Tetrafluoroborate with Acrylates Catalyzed by Palladium on Charcoal
inferred← citeshttps://doi.org/10.1002/adsc.200800783openalex-snapshot
Improved Suzuki–Miyaura Reactions of Aryldiazonium Salts with Boronic Acids by Tuning Palladium on Charcoal Catalyst Properties
inferred← citeshttps://doi.org/10.1002/adsc.200900765openalex-snapshot
Recyclable Heterogeneous Palladium Catalysts in Pure Water: Sustainable Developments in Suzuki, Heck, Sonogashira and Tsuji–Trost Reactions
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One‐Pot Suzuki/Heck Sequence for the Synthesis of (E)‐Stilbenes Featuring a Recyclable Silica‐Supported Palladium Catalyst via a Multi‐Component Reaction in 1,3‐Propanediol
inferred← citeshttps://doi.org/10.1002/adsc.201100226openalex-snapshot
Functionalization of the 3‐Position of Thiophene and Benzo[b]thiophene Moieties by Palladium‐Catalyzed CC Bond Forming Reactions using Diazonium Salts
inferred← citeshttps://doi.org/10.1002/adsc.201100531openalex-snapshot
Aryl Diazonium versus Iodonium Salts: Preparation, Applications and Mechanisms for the Suzuki–Miyaura Cross‐Coupling Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201200929openalex-snapshot
A Deacetylation–Diazotation–Coupling Sequence: Palladium‐ Catalyzed CC Bond Formation with Acetanilides as Formal Leaving Groups
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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.201800343openalex-snapshot
Development of the Applications of Palladium on Charcoal in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/aoc.2877openalex-snapshot
1‐(α‐Aminobenzyl)‐2‐naphthol as phosphine‐free ligand for Pd‐catalyzed Suzuki and one‐pot Wittig‐Suzuki reaction
inferred← citeshttps://doi.org/10.1002/aoc.3076openalex-snapshot
N‐Heterocyclic carbene/phosphite synergistically assisted Pd/C‐catalyzed Suzuki coupling of aryl chlorides
inferred← citeshttps://doi.org/10.1002/aoc.3180openalex-snapshot
Chemoselective one‐pot synthesis of terphenyl derivatives by sequential directed C―H functionalization–Suzuki coupling
inferred← citeshttps://doi.org/10.1002/aoc.3248openalex-snapshot
One‐pot synthesis of polyfluoroterphenyls via palladium‐catalyzed Suzuki–Miyaura coupling of chlorobromobenzene and CH bond functionalization of perfluoroarenes
inferred← citeshttps://doi.org/10.1002/aoc.3346openalex-snapshot
Carboxymethylcellulose‐supported palladium nanoparticles generated in situ from palladium(II) carboxymethylcellulose as an efficient and reusable catalyst for ligand‐ and base‐free Heck–Matsuda and Suzuki–Miyaura couplings
inferred← citeshttps://doi.org/10.1002/aoc.3592openalex-snapshot
Cyclodextrin‐supported palladium complex: A highly active and recoverable catalyst for Suzuki–Miyaura cross‐coupling reaction in aqueous medium
inferred← citeshttps://doi.org/10.1002/aoc.4192openalex-snapshot
Methanol aided synthesis of PdNPs decorated on montmorillonite K 10 and its implication in Suzuki Miyaura type cross coupling reaction under base free condition
inferred← citeshttps://doi.org/10.1002/cctc.201500179openalex-snapshot
Palladium Nanoparticles Supported on Sulfonic Acid Functionalized Silica as Trifunctional Heterogeneous Catalysts for Heck and Suzuki Reactions
inferred← citeshttps://doi.org/10.1002/cctc.201600134openalex-snapshot
Heterogeneous Palladium Catalysts for Suzuki–Miyaura Coupling Reactions Involving Aryl Diazonium Salts
inferred← citeshttps://doi.org/10.1002/chem.201001377openalex-snapshot
A Useful, Reliable and Safer Protocol for Hydrogenation and the Hydrogenolysis of O‐Benzyl Groups: The In Situ Preparation of an Active Pd0/C Catalyst with Well‐Defined Properties
inferred← citeshttps://doi.org/10.1002/chem.201203005openalex-snapshot
A Modular Synthesis of Teraryl‐Based α‐Helix Mimetics, Part 1: Synthesis of Core Fragments with Two Electronically Differentiated Leaving Groups
inferred← citeshttps://doi.org/10.1002/chem.201300347openalex-snapshot
Stabilisation of Carbon‐Supported Palladium Nanoparticles through the Formation of an Alloy with Gold: Application to the Sonogashira Reaction
inferred← citeshttps://doi.org/10.1002/chem.201300858openalex-snapshot
Chelation‐Assisted Cross‐Coupling of Anilines through In Situ Activation as Diazonium Salts with Boronic Acids under Ligand‐, Base‐, and Salt‐Free Conditions
inferred← citeshttps://doi.org/10.1002/chem.201402093openalex-snapshot
Elucidating the Structure–Property Relationships of Donor–π‐Acceptor Dyes for Dye‐Sensitized Solar Cells (DSSCs) through Rapid Library Synthesis by a One‐Pot Procedure
inferred← citeshttps://doi.org/10.1002/chem.201500979openalex-snapshot
Rapid Synthesis of Thiophene‐Based, Organic Dyes for Dye‐Sensitized Solar Cells (DSSCs) by a One‐Pot, Four‐Component Coupling Approach
inferred← citeshttps://doi.org/10.1002/chem.201603626openalex-snapshot
Using Anilines as Masked Cross‐Coupling Partners: Design of a Telescoped Three‐Step Flow Diazotization, Iododediazotization, Cross‐Coupling Process
inferred← citeshttps://doi.org/10.1002/chin.200747088openalex-snapshot
Suzuki—Miyaura Reactions of Arenediazonium Salts Catalyzed by Pd(0)/C. One‐Pot Chemoselective Double Cross‐Coupling Reactions.
inferred← citeshttps://doi.org/10.1002/cjoc.201500446openalex-snapshot
Synthesis of Terphenyl Derivatives by Pd‐Catalyzed Suzuki‐Miyaura Reaction of Dibromobenzene Using 2N2O‐Salen as a Ligand in Aqueous Solution
inferred← citeshttps://doi.org/10.1002/cssc.200800110openalex-snapshot
Heterogeneous Multifunctional Catalysts for Tandem Processes: An Approach toward Sustainability
inferred← citeshttps://doi.org/10.1002/ejoc.201200721openalex-snapshot
Practical Pd/C‐Catalysed Suzuki–Miyaura Reactions for the Preparation of 3‐Aryl‐4‐oxypyridin‐2(1H)‐ones, 3‐Aryl‐2,4‐oxypyridines and 3‐Aryl‐2,4‐oxyquinolines as Useful Intermediates for the Synthesis of Biologically Active Compounds
inferred← citeshttps://doi.org/10.1002/ejoc.201200758openalex-snapshot
Highly Selective Activation of Vinyl C–S Bonds Over Aryl C–S Bonds in the Pd‐Catalyzed Coupling of (E)‐(β‐Trifluoromethyl)vinyldiphenylsulfonium Salts: Preparation of Trifluoromethylated Alkenes and Dienes
inferred← citeshttps://doi.org/10.1007/978-3-031-04398-7_15openalex-snapshot
On the Use of Diazonium Salts in the Design of Catalytic Hybrid Materials and Coatings
inferred← citeshttps://doi.org/10.1007/s41981-021-00160-7openalex-snapshot
Synthesis of arenediazonium salts and Suzuki- Miyaura cross-coupling reaction in microreactors
inferred← citeshttps://doi.org/10.1016/j.apcata.2014.05.019openalex-snapshot
On the peculiar recycling properties of charcoal-supported palladium oxide nanoparticles in Sonogashira reactions
inferred← citeshttps://doi.org/10.1016/j.carbpol.2022.120271openalex-snapshot
A new thioglycolic ester β-cyclodextrin/PdCl2 in water: An accessible catalyst for the Suzuki-Miyaura coupling reaction
inferred← citeshttps://doi.org/10.1016/j.catcom.2018.08.023openalex-snapshot
Oxygen-promoted Suzuki–Miyaura reaction of aryl fluorosulfates and potassium aryltrifluoroborates: Mild and efficient access to biaryls and terphenyls
inferred← citeshttps://doi.org/10.1016/j.catcom.2024.106862openalex-snapshot
Magnetically retractable tea extract stabilized palladium nanoparticles for denitrogenative cross-coupling of aryl bromides with arylhydrazines under green conditions: An alternate route for the biaryls synthesis
inferred← citeshttps://doi.org/10.1016/j.cattod.2011.03.054openalex-snapshot
Palladium-based innovative catalytic procedures: Designing new homogeneous and heterogeneous catalysts for the synthesis and functionalisation of N-containing heteroaromatic compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2008.05.004openalex-snapshot
Potassium permanganate/carboxylic acid/organic solvent: a powerful reagent for enone oxidation and aryl coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2011.06.001openalex-snapshot
Highly selective palladium-catalyzed Suzuki–Miyaura monocoupling reactions of ethene and arene derivatives bearing two or more electrophilic sites
inferred← citeshttps://doi.org/10.1016/j.tet.2011.06.108openalex-snapshot
Pd-catalyzed regiocontrolled Sonogashira and Suzuki cross-coupling reaction of 3,6-dihalogenoimidazo[1,2-a]pyridines: one-pot double-coupling approach
inferred← citeshttps://doi.org/10.1016/j.tet.2013.07.023openalex-snapshot
One-pot synthesis of functionalized p-terphenyl derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2014.09.039openalex-snapshot
Synthesis of EDOT-containing organic dyes via one-pot, four-component Suzuki–Miyaura coupling and the evaluation of their photovoltaic properties
inferred← citeshttps://doi.org/10.1016/j.tet.2018.01.031openalex-snapshot
A convenient and efficient one pot synthesis of unsymmetrically substituted p-terphenyls via a phosphine-free double Suzuki cross-coupling protocol using 1,4-dibromo-2-nitrobenzene as the substrate
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130540openalex-snapshot
Base-free Pd-MOF catalyzed the Suzuki-Miyaura cross-coupling reaction of arenediazonium tetrafluoroborate salts with arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.10.112openalex-snapshot
Unexpected formation of hydroxyborazaphosphonic acid in the reaction of (N-benzyl)benzylideneimine-2-boronic acid with diethyl phosphite
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.05.003openalex-snapshot
Pd(0)/C-catalyzed cross-couplings of acyl chlorides with triarylbismuths as atom-efficient sub-stoichiometric multi-coupling reagents
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.06.084openalex-snapshot
Heterogeneous palladium multi-task catalyst for sequential Heck-reduction–cyclization (HRC) reactions: influence of the support
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.11.053openalex-snapshot
Suzuki–Miyaura cross-coupling of aryldiazonium silica sulfates under mild and heterogeneous conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.09.001openalex-snapshot
Pd-catalyzed cross-coupling reactions of arenediazonium salts with arylsilanes and aryltrifluoroborates in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151491openalex-snapshot
Highly efficient palladium-catalyzed cross-coupling of diarylborinic acids with arenediazoniums for practical diaryl synthesis
inferred← citeshttps://doi.org/10.1016/j.tgchem.2024.100051openalex-snapshot
Pd-catalysed one-pot and three-component sequential chemoselective double cross-coupling: Synthesis of novel 2-aryl-1,3-azoles from 4-bromophenyl tosylate
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00272openalex-snapshot
Dual Role of Acetanilides: Traceless Removal of a Directing Group through Deacetylation/Diazotation and Palladium-Catalyzed C–C-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01910openalex-snapshot
Multibond Forming Tandem Reactions of Anilines via Stable Aryl Diazonium Salts: One-Pot Synthesis of 3,4-Dihydroquinolin-2-ones
inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00264openalex-snapshot
Mechanisms for the Oxidative Addition of Palladium(0) Complexes to Arenediazonium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02380openalex-snapshot
Transition-Metal-Free Cross-Coupling of Aryl andN-Heteroaryl Cyanides with Benzylic Zinc Reagents
inferred← citeshttps://doi.org/10.1021/acsanm.1c01038openalex-snapshot
Palladium Nanoparticles on Covalent Organic Framework Supports as Catalysts for Suzuki–Miyaura Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/cr1002084openalex-snapshot
Heterogeneous Catalysts for the One-Pot Synthesis of Chemicals and Fine Chemicals
inferred← citeshttps://doi.org/10.1021/jo502004ropenalex-snapshot
Covalent Dimers of 1,3-Diphenylisobenzofuran for Singlet Fission: Synthesis and Electrochemistry
inferred← citeshttps://doi.org/10.1021/jo802318popenalex-snapshot
A New Route to Multifunctionalized p-Terphenyls and Heteroaryl Analogues via [5C + 1C(N)] Annulation Strategy
inferred← citeshttps://doi.org/10.1021/la8029787openalex-snapshot
Detonation Nanodiamond: An Organic Platform for the Suzuki Coupling of Organic Molecules
inferred← citeshttps://doi.org/10.1021/ol200752xopenalex-snapshot
Unprecedented Substoichiometric Use of Hazardous Aryl Diazonium Salts in the Heck-Matsuda Reaction via a Double Catalytic Cycle
inferred← citeshttps://doi.org/10.1021/ol801589popenalex-snapshot
Pd-Catalyzed Efficient One-Pot Sequential Cross-Coupling Reactions of Aryl Dihalides
inferred← citeshttps://doi.org/10.1021/om700796gopenalex-snapshot
Synthesis and Structural Characterization of Nickel(II) Complexes Supported by Pyridine-Functionalized N-Heterocyclic Carbene Ligands and Their Catalytic Acitivities for Suzuki Coupling
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/b926547nopenalex-snapshot
Base free aryl coupling of diazonium compounds and boronic esters: self-activation allowing an overall highly practical process
inferred← citeshttps://doi.org/10.1039/c1ob05256jopenalex-snapshot
Suzuki–Miyaura cross coupling reactions with Phenoldiazonium salts
inferred← citeshttps://doi.org/10.1039/c1ob06385eopenalex-snapshot
Pd nanoparticle catalysed one-pot sequential Heck and Suzuki couplings of bromo-chloroarenes in ionic liquids and water
inferred← citeshttps://doi.org/10.1039/c1ob06752dopenalex-snapshot
Suzuki–Miyaura cross-couplings of arenediazonium tetrafluoroborate salts with arylboronic acids catalyzed by aluminium hydroxide-supported palladium nanoparticles
inferred← citeshttps://doi.org/10.1039/c2gc15679bopenalex-snapshot
Suzuki-Miyaura cross-coupling of arenediazonium salts catalyzed by alginate/gellan-stabilized palladium nanoparticles under aerobic conditions in water
inferred← citeshttps://doi.org/10.1039/c3ob40420jopenalex-snapshot
Scope and limitations of the Heck–Matsuda-coupling of phenol diazonium salts and styrenes: a protecting-group economic synthesis of phenolic stilbenes
inferred← citeshttps://doi.org/10.1039/c5cy00907copenalex-snapshot
Pd/C as an efficient heterogeneous catalyst for carbonylative four-component synthesis of 4(3H)-quinazolinones
inferred← citeshttps://doi.org/10.1039/c5ra12512jopenalex-snapshot
Synthesis of benzochromenes and dihydrophenanthridines with helical motifs using Garratt–Braverman and Buchwald–Hartwig reactions
inferred← citeshttps://doi.org/10.1039/c6cy00613bopenalex-snapshot
Highly efficient synthesis of flavones via Pd/C-catalyzed cyclocarbonylation of 2-iodophenol with terminal acetylenes
inferred← citeshttps://doi.org/10.1039/c8cs00453fopenalex-snapshot
Biaryl synthesis with arenediazonium salts: cross-coupling, CH-arylation and annulation reactions
inferred← citeshttps://doi.org/10.1039/c8ob01661eopenalex-snapshot
Temperature-controlled sequential Suzuki–Miyaura reactions for preparing unsymmetrical terphenyls
inferred← citeshttps://doi.org/10.1039/d1sc01351copenalex-snapshot
S( vi ) in three-component sulfonamide synthesis: use of sulfuric chloride as a linchpin in palladium-catalyzed Suzuki–Miyaura coupling
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/10.1039/d5ra03486hopenalex-snapshot
Successive diastereoselective C(sp 3 )–H arylation and Suzuki coupling toward enantioenriched polyaryl unnatural amino acid motifs
inferred← citeshttps://doi.org/10.1039/d5ra05453bopenalex-snapshot
Tea-derived catalysts: a sustainable approach to organic transformations
inferred← citeshttps://doi.org/10.1055/sos-sd-110-00529openalex-snapshot
10.1 Product Class 1: Benzo[b]furans
inferred← citeshttps://doi.org/10.1080/14786419.2020.1791112openalex-snapshot
Heterogeneous Pd/C-catalyzed, ligand free Suzuki–Miyaura coupling reaction furnishes new p-terphenyl derivatives
inferred← citeshttps://doi.org/10.1080/17518253.2019.1677786openalex-snapshot
Flow reactor synthesis of unsymmetrically substitutedp-terphenyls using sequentially selective Suzuki cross-coupling protocols
inferred← citeshttps://doi.org/10.1155/2022/1552334openalex-snapshot
Complex Nanomaterials in Catalysis for Chemically Significant Applications: From Synthesis and Hydrocarbon Processing to Renewable Energy Applications
inferred← citeshttps://doi.org/10.11606/d.60.2017.tde-13122016-083118openalex-snapshot
Aplicação da química de sais de diazônio na modificação estrutural dos fluoróforos do tipo BODIPY
inferred← citeshttps://doi.org/10.3390/catal11091078openalex-snapshot
Recent Advances of Pd/C-Catalyzed Reactions
inferred← citeshttps://doi.org/10.3390/catal6090142openalex-snapshot
Solventless Synthesis of Quaterphenyls and Terphenyls from Chalcones and Allylsulfones under Phase Transfer Catalysis Conditions
inferred← citeshttps://doi.org/10.3390/catal9020111openalex-snapshot
An Amino-Chain Modified β-cyclodextrin: A Supramolecular Ligand for Pd(OAc)2 Acceleration in Suzuki–Miyaura Coupling Reactions in Water
inferred← citeshttps://doi.org/10.3762/bjoc.7.41openalex-snapshot
Studies on Pd/NiFe2O4 catalyzed ligand-free Suzuki reaction in aqueous phase: synthesis of biaryls, terphenyls and polyaryls
inferred← citeshttps://doi.org/10.3987/com-09-s(s)59openalex-snapshot
Synthesis of Fluorinated 2,3-Disubstituted Benzofurans Potential β-Amyloid Aggregation Inhibitors
inferred← citeshttps://doi.org/10.5012/bkcs.2011.32.1.35openalex-snapshot
A Simple and Green Synthesis of Tetrahydrobenzo[α]-xanthen-11-one Using PEG-400 as Efficient and Recyclable Reaction Media
inferred← citeshttps://doi.org/10.5012/bkcs.2011.32.1.359openalex-snapshot
Chemoselective Suzuki Cross-Coupling Reactions of Chiral Pyrrolizines
inferred← citeshttps://doi.org/10.5012/bkcs.2011.32.8.2970openalex-snapshot
One-Pot Homo- and Cross-Coupling Reactions of Arenediazonium Tosylate Salts for the Synthesis of Biaryls and Polyaryls
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