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An Improved Catalyst System for Aromatic Carbon−Nitrogen Bond Formation: The Possible Involvement of Bis(Phosphine) Palladium Complexes as Key Intermediates

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Outgoing claims: the papers this work cites, builds on, or argues with.

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A Simple Catalytic Method for the Conversion of Aryl Bromides to Arylamines
inferredcites →https://doi.org/10.1016/0022-328x(87)87181-4openalex-snapshot
Principles and Applications of Organotransition Metal Chemistry
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/10.1021/ja00096a059openalex-snapshot
Palladium-Catalyzed Aromatic Aminations with in situ Generated Aminostannanes
inferredcites →https://doi.org/10.1021/ja00121a030openalex-snapshot
A Rare, Low-Valent Alkylamido Complex, a Diphenylamido Complex, and Their Reductive Elimination of Amines by Three-Coordinate Intermediates
inferredcites →https://doi.org/10.1021/ja00124a026openalex-snapshot
Oxidative Addition of Aryl Bromide after Dissociation of Phosphine from a Two-Coordinate Palladium(0) Complex, Bis(tri-o-tolylphosphine)Palladium(0)
inferredcites →https://doi.org/10.1021/jo951844hopenalex-snapshot
Palladium-Catalyzed Amination of Aryl Iodides
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

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/anie.200461327openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200703763openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200705209openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200800497openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201102543openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201105228openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201202348openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201204633openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201310457openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201406479openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201408651openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201502822openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201604268openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201807775openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201904795openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202216863openalex-snapshot
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Selective N‐Alkylation of Arylamines with Alkyl Chloride in Ionic Liquids: Scope and Applications
inferred← citeshttps://doi.org/10.1002/ejoc.201400159openalex-snapshot
Unsymmetrical Bisphosphines for the Amidation of Aryl Chlorides: A Kinetic Study
inferred← citeshttps://doi.org/10.1002/ejoc.201403428openalex-snapshot
A Tuned Bicyclic Proazaphosphatrane for Catalytically Enhanced N‐Arylation Reactions with Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/ejoc.201500030openalex-snapshot
Efficient and Versatile Buchwald–Hartwig Amination of (Hetero)aryl Chlorides Using the Pd–PEPPSI‐IPr(NMe2)2 Precatalyst in the Presence of Carbonate Base
inferred← citeshttps://doi.org/10.1002/ejoc.201700585openalex-snapshot
Pd‐Catalyzed Amination of Functionalized 6‐Bromo‐pyridinyl‐1,2,4‐triazine Complexant Scaffolds
inferred← citeshttps://doi.org/10.1002/hc.21055openalex-snapshot
C–N Coupling of 1,2‐Dihydro‐2,2,4‐trimethylquinoline Derivatives via a Silver(I)‐Catalyzed Direct Functionalization of a C–H Bond
inferred← citeshttps://doi.org/10.1002/hlca.202100173openalex-snapshot
Pd/Gorlos‐Phos‐Catalyzed Chemoselective Amination of Bromophenyl Chlorides with Primary Arylamines
inferred← citeshttps://doi.org/10.1002/ijch.201900143openalex-snapshot
Shuttling Catalyst: Facilitating C−C Bond Formation via Cross‐Couplings with a Thermoresponsive Polymeric Ligand
inferred← citeshttps://doi.org/10.1002/ijch.201900167openalex-snapshot
In Praise of Basic Research as a Vehicle to Practical Applications: Palladium‐Catalyzed Coupling to Form Carbon‐Nitrogen Bonds
inferred← citeshttps://doi.org/10.1002/ijch.201900171openalex-snapshot
Cu(II)‐CatalyzedOrtho‐Selective Amination of Simple Phenols withO‐Benzoylhydroxylamines
inferred← citeshttps://doi.org/10.1002/jhet.5570370319openalex-snapshot
Synthesis of heterocycles from molecular nitrogen as a nitrogen source
inferred← citeshttps://doi.org/10.1002/marc.200390018openalex-snapshot
Instrumentation for Combinatorial and High‐Throughput Polymer Research: A Short Overview
inferred← citeshttps://doi.org/10.1002/marc.200400429openalex-snapshot
Synthesis of Poly(arylene ether amine)s from a Monomer Containing an Electron‐Donating Amine Group in a Nucleophilic Aromatic Substitution Reaction
inferred← citeshttps://doi.org/10.1002/nadc.19970450209openalex-snapshot
Organische Chemie 1996
inferred← citeshttps://doi.org/10.1002/pi.5695openalex-snapshot
Triphenylamine and some of its derivatives as versatile building blocks for organic electronic applications
inferred← citeshttps://doi.org/10.1002/pola.20377openalex-snapshot
Syntheses of helical polymers through the combination of axially dissymmetric segments
inferred← citeshttps://doi.org/10.1002/pola.22499openalex-snapshot
Synthesis and characterization of a series of 2‐aminopyridine nickel(II) complexes and their catalytic properties toward ethylene polymerization
inferred← citeshttps://doi.org/10.1002/slct.201500016openalex-snapshot
8‐(4‐aminophenyl)BODIPYs as fluorescent pH probes: facile synthesis, computational study and lysosome imaging
inferred← citeshttps://doi.org/10.1002/slct.201600581openalex-snapshot
Synthesis of Chiral C 2 ‐Symmetric Bimetallic Zinc Complexes of Amido‐Oxazolinates and Their Application in Copolymerization of CO 2 and Cyclohexene Oxide
inferred← citeshttps://doi.org/10.1002/slct.201903963openalex-snapshot
Heterogeneous Direct Acylation Strategy to Diaryl Ketones and Their Application to 1, 3‐Dihydroisobenzofurans
inferred← citeshttps://doi.org/10.1002/slct.202103940openalex-snapshot
Goldberg Coupling of Thiazole Substituted Aryl Bromide Demands Stoichiometric Copper Compared to Oxazole
inferred← citeshttps://doi.org/10.1007/3418_2012_56openalex-snapshot
Palladium-Catalyzed sp2 C–N Bond Forming Reactions: Recent Developments and Applications
inferred← citeshttps://doi.org/10.1007/7081_006openalex-snapshot
Microwave-Assisted Synthesis and Functionalization of 2-Pyridones, 2-Quinolones and Other Ring-Fused 2-Pyridones
inferred← citeshttps://doi.org/10.1007/7081_2010_36openalex-snapshot
Metal-Catalyzed Cross-Coupling Reactions for Indoles
inferred← citeshttps://doi.org/10.1007/978-1-4939-9585-1_8openalex-snapshot
Methods to Generate an Array of Novel Rexinoids by SAR on a Potent Retinoid X Receptor Agonist: A Case Study with NEt-TMN
inferred← citeshttps://doi.org/10.1007/s10562-023-04432-wopenalex-snapshot
Palladium N-Heterocyclic Carbene Pre-catalysts Bearing Different Ancillary Ligands for the Buchwald–Hartwig Amination of Cyclic Secondary Amines with Aryl Chlorides
inferred← citeshttps://doi.org/10.1007/s11030-013-9442-1openalex-snapshot
Synthesis and in vitro cytotoxic evaluation of novel $$N$$ -(3,4,5-trimethoxyphenyl)pyridin-2( $$1H$$ )-one derivatives
inferred← citeshttps://doi.org/10.1007/s11172-020-2887-3openalex-snapshot
Stabilization of phosphorus in (1,2,3,4,5-pentaphenylphosphole)palladium
inferred← citeshttps://doi.org/10.1007/s11176-005-0199-9openalex-snapshot
Effect of Steric and Electronic Properties of Palladium Complexes with Bidentate Diphosphine Ligands on the Basis of Diphenyl Oxide on Arylation of Amines
inferred← citeshttps://doi.org/10.1007/s11244-008-9056-5openalex-snapshot
Crossing the Borders Between Homogeneous and Heterogeneous Catalysis: Developing Recoverable and Reusable Catalytic Systems
inferred← citeshttps://doi.org/10.1007/s11696-016-0097-0openalex-snapshot
Triphenylamine-based electroactive compounds: synthesis, properties and application to organic electronics
inferred← citeshttps://doi.org/10.1016/b0-08-043748-6/09090-3openalex-snapshot
Metal Complexes as Catalysts for Carbon-heteroatom Cross-coupling Reactions
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00037-4openalex-snapshot
Vinyl- and Arylnitrogen Compounds
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00137-0openalex-snapshot
C–N Bond Formation through Amination
inferred← citeshttps://doi.org/10.1016/b978-0-12-404598-9.00001-8openalex-snapshot
Reactivity of Thiophenes, Oligothiophenes and Benzothiophenes
inferred← citeshttps://doi.org/10.1016/b978-0-12-815505-9.00004-4openalex-snapshot
Palladacycles as Efficient Precatalysts for Negishi and Buchwald-Hartwig Amination Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00091-3openalex-snapshot
Metal-Catalyzed Amination: C N Bond Formation
inferred← citeshttps://doi.org/10.1016/b978-012141340-8/50005-1openalex-snapshot
COMBINATORIAL SOLID-PHASE SYNTHESIS
inferred← citeshttps://doi.org/10.1016/bs.adioch.2024.05.007openalex-snapshot
Comparative analysis of palladium, nickel and copper phosphane/carbene catalysts in Suzuki–Miyaura couplings: Mechanistic insights and reactivity trends
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106254openalex-snapshot
Development and challenges in the discovery of 5-HT1A and 5-HT7 receptor ligands
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.01.044openalex-snapshot
Pyrazolopyridine antiherpetics: SAR of C2′ and C7 amine substituents
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.03.023openalex-snapshot
5-(3-Bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido[2,3-d]pyrimidin-4-ylamine: structure–activity relationships of 7-substituted heteroaryl analogs as non-nucleoside adenosine kinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.05.043openalex-snapshot
Synthesis of novel substituted 2-phenylpyrazolopyridines with potent activity against herpesviruses
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.07.023openalex-snapshot
Novel potent neuropeptide Y Y5 receptor antagonists: Synthesis and structure–activity relationships of phenylpiperazine derivatives
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.04.059openalex-snapshot
Synthesis and structure–activity relationships of N-(4-amino-2,6-diisopropylphenyl)-N’-(1,4-diarylpiperidine-4-yl)methylureas as anti-hyperlipidemic agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.08.049openalex-snapshot
Design, synthesis and evaluation of monovalent ligands for the asialoglycoprotein receptor (ASGP-R)
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.06.032openalex-snapshot
Discovery of potent, selective, and orally bioavailable quinoline-based dipeptidyl peptidase IV inhibitors targeting Lys554
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.04.066openalex-snapshot
Novel synthetic route for antimalarial benzo[a]phenoxazine derivative SSJ-183 and two active metabolites
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.01.058openalex-snapshot
Synthesis of Nτ-arylhistidine derivatives via direct N-arylation
inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.04.077openalex-snapshot
Synthesis and SAR of highly potent dual 5-HT1A and 5-HT1B antagonists as potential antidepressant drugs
inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.02.049openalex-snapshot
New HIV-1 reverse transcriptase inhibitors based on a tricyclic benzothiophene scaffold: Synthesis, resolution, and inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.04.003openalex-snapshot
Discovery of novel isothiazole inhibitors of the TrkA kinase: Structure–activity relationship, computer modeling, optimization, and identification of highly potent antagonists
inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.12.011openalex-snapshot
3-Hydroxychromones as cyclin-dependent kinase inhibitors: Synthesis and biological evaluation
inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.12.110openalex-snapshot
Solid-phase analogue synthesis of caspase-3 inhibitors via palladium-catalyzed amination of 3-bromopyrazinones
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.09.068openalex-snapshot
Delta agonist hydroxy bioisosteres: The discovery of 3-((1-benzylpiperidin-4-yl){4-[(diethylamino)carbonyl]phenyl}amino)benzamide with improved delta agonist activity and in vitro metabolic stability
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.11.010openalex-snapshot
Highly selective c-Jun N-terminal kinase (JNK) 2 and 3 inhibitors with in vitro CNS-like pharmacokinetic properties prevent neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.01.056openalex-snapshot
Chroman and tetrahydroquinoline ureas as potent TRPV1 antagonists
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.02.075openalex-snapshot
Discovery of 2,4-bis-arylamino-1,3-pyrimidines as insulin-like growth factor-1 receptor (IGF-1R) inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.04.148openalex-snapshot
Syntheses of 2-NBDG analogues for monitoring stereoselective uptake of d-glucose
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.06.094openalex-snapshot
Amine-constrained pyridazinone histamine H3 receptor antagonists
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.11.022openalex-snapshot
Functionalized ferrocenes
inferred← citeshttps://doi.org/10.1016/j.ccr.2006.07.017openalex-snapshot
Preparation of NHC–ruthenium complexes and their catalytic activity in metathesis reaction
inferred← citeshttps://doi.org/10.1016/j.dyepig.2015.03.013openalex-snapshot
Organic sensitizers possessing carbazole donor and indeno[1,2-b] thiophene spacer for efficient dye sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.ejmech.2011.02.024openalex-snapshot
Synthesis and biological evaluation of dibenz[b,f][1,5]oxazocine derivatives for agonist activity at κ-opioid receptor
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.01.027openalex-snapshot
Design, synthesis and pharmacological evaluation of new series of naphthalenic analogues as melatoninergic (MT1/MT2) and serotoninergic 5-HT2C dual ligands (I)
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116459openalex-snapshot
Synthesis and Evaluation of diaryl ether modulators of the leukotriene A4 hydrolase aminopeptidase activity
inferred← citeshttps://doi.org/10.1016/j.eq.2016.10.001openalex-snapshot
N-arilação do imidazol via CuI: um tutorial para otimização de um sistema catalítico através do planejamento experimental
inferred← citeshttps://doi.org/10.1016/j.gresc.2026.03.004openalex-snapshot
Simultaneous construction of C-N axially chiral diarylamines and planar chiral ferrocenes via Pd-catalyzed asymmetric tandem reaction
inferred← citeshttps://doi.org/10.1016/j.ica.2006.03.044openalex-snapshot
Synthesis of tantalum and niobium complexes that contain the diamidoamine ligand, [(3,4,5-F3C6H2NCH2CH2)2NMe]2−, and the triamidoamine ligand, [(3,5-Cl2C6H3NCH2CH2)3N]3−
inferred← citeshttps://doi.org/10.1016/j.jcat.2012.09.002openalex-snapshot
Heterogeneous amination of bromobenzene over titania-supported gold catalysts
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.01.030openalex-snapshot
Synthesis and oxidation of (benzimidazolylidene)Cr(CO)5 complexes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.12.046openalex-snapshot
Preparation of a cobalt-containing P,N-bidentate ligand ligated palladium complex: Its applications in amination and Suzuki cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.08.002openalex-snapshot
Copper(I) catalysis: Synthesis of N,N′-diarylated and N-aryl,N′-formylated chiral C2-symmetric diamines
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.06.043openalex-snapshot
Synthesis of symmetrically and unsymmetrically 3,5-dimethylbenzyl-substituted 1,1′-ferrocene diamines
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2015.07.015openalex-snapshot
Air stable pincer (CNC) N-heterocyclic carbene–cobalt complexes and their application as catalysts for C–N coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.02.023openalex-snapshot
Buchwald-Hartwig reaction: An overview
inferred← citeshttps://doi.org/10.1016/j.mcat.2025.115287openalex-snapshot
Novel supramolecular dimers based on acridine derivatives as photosensitizers for the construction of C N bonds
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