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Synthesis of Xylyl-Linked Bis-Benzimidazolium Salts and Their Application in the Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling Reaction of Aryl Chlorides

https://doi.org/10.3390/catal11070817
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The 42 checked references that resolve
resolves10.1021/cr00039a007
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
resolves10.1016/S0040-4020(97)10233-2
Catalytic cross-coupling reactions in biaryl synthesis
resolves10.1016/S0022-328X(98)01055-9
Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998
resolves10.1002/adsc.200404165
A Novel Thiourea Ligand Applied in the Pd‐Catalyzed Heck, Suzuki and Suzuki Carbonylative Reactions
resolves10.1246/cl.2011.894
Cross-coupling Reactions of Organoboranes: An Easy Method for C–C Bonding
resolves10.1021/cr00028a008
Transformations of Chloroarenes, Catalyzed by Transition-Metal Complexes
resolves10.1002/1521-3773(20021115)41:22<4176::AID-ANIE4176>3.0.CO;2-U
Palladium-Catalyzed Coupling Reactions of Aryl Chlorides
resolves10.1021/cr0505268
Selected Patented Cross-Coupling Reaction Technologies
resolves10.1016/j.ccr.2015.01.017
When cross-coupling partners meet indolylphosphines
resolves10.1002/(SICI)1521-3765(20000515)6:10<1773::AID-CHEM1773>3.0.CO;2-P
Polymer-Supported Carbene Complexes of Palladium: Well-Defined, Air-Stable, Recyclable Catalysts for the Heck Reaction
resolves10.1016/S0022-328X(03)00754-X
Metal complexes of acyclic diaminocarbenes: links between N-heterocyclic carbene (NHC)- and Fischer-carbene complexes
resolves10.1016/S0022-328X(97)00736-5
Chelating N-heterocyclic carbene ligands in palladium-catalyzed heck-type reactions
resolves10.1016/S0040-4039(99)02133-4
Palladium-bisimidazol-2-ylidene complexes as catalysts for general and efficient Suzuki cross-coupling reactions of aryl chlorides with arylboronic acids
resolves10.1023/B:CATL.0000034283.73893.4b
Palladium-Catalyzed Suzuki–Miyaura Reaction Using Saturated N-Heterocarbene Ligands
resolves10.1081/SCC-200036594
Suzuki–Miyaura Reaction of Unactivated Aryl Chlorides Using Benzimidazol‐2‐Ylidene Ligands
resolves10.1002/hc.20034
Palladium‐catalyzed Suzuki reaction using 1,3‐dialkylbenzimidazol‐2‐ylidene ligands in aqueous media
resolves10.1016/j.tet.2005.03.043
A new dimeric bidentated NHC–Pd(II) complex from trans-cyclohexane-1,2-diamine for Suzuki reaction and Heck reaction
resolves10.1016/j.tet.2005.09.010
A novel cis-chelated Pd(II)–NHC complex for catalyzing Suzuki and Heck-type cross-coupling reactions
resolves10.1002/aoc.1039
Use of bis(benzimidazolium)–palladium system as a convenient catalyst for Heck and Suzuki coupling reactions of aryl bromides and chlorides
resolves10.1021/om800069p
Cyclometalated cis-Chelated Bidentate N-Heterocyclic Carbene Palladium Complexes: Synthetic, Structural, and Catalytic Studies
resolves10.1016/j.tetlet.2009.03.140
Use of a silicon carbide multi-well plate in conjunction with microwave heating for rapid ligand synthesis, formation of palladium complexes, and catalyst screening in a Suzuki coupling
resolves10.1002/aoc.1633
Synthesis and microwave‐assisted catalytic activity of novel bis‐benzimidazole salts bearing furfuryl and thenyl moieties in Heck and Suzuki cross‐coupling reactions
resolves10.1002/ejic.201200940
Palladium(II) Complexes with Chelating Biscarbene Ligands in the Catalytic Suzuki–Miyaura Cross‐Coupling Reaction
resolves10.1021/om400825e
Chiral 1,2-Cyclohexane-Bridged Bis-NHC Palladium Catalysts for Asymmetric Suzuki–Miyaura Coupling: Synthesis, Characterization, and Steric Effects on Enantiocontrol
resolves10.1021/om500878f
Support-Free Palladium–NHC Catalyst for Highly Recyclable Heterogeneous Suzuki–Miyaura Coupling in Neat Water
resolves10.1039/C9DT02147G
Synthesis and structural characterization of 20-membered macrocyclic rings bearing <i>trans</i> -chelating bis(N-heterocyclic carbene) ligands and the catalytic activity of their palladium( <scp>ii</scp> ) complexes
resolves10.1002/aoc.3896
Bis‐benzimidazolium‐palladium system catalyzed Suzuki‐Miyaura coupling reaction of aryl bromides under mild conditions
resolves10.1039/C8RA04094J
An efficient class of bis-NHC salts: applications in Pd-catalyzed reactions under mild reaction conditions
resolves10.1021/cb300665u
Synthesis and Assessment of Glycosaminoglycan Priming Activity of Cluster-xylosides for Potential Use as Proteoglycan Mimetics
resolves10.1016/j.tetlet.2013.08.046
Coumarin–TPA derivative: a reaction-based ratiometric fluorescent probe for Cu(I)
resolves10.1002/chem.201902458
Gold(I) Complexes Stabilized by Nine‐ and Ten‐Membered N‐Heterocyclic Carbene Ligands
resolves10.1021/acs.organomet.7b00502
Addition of E–H (E = N, P, C, O, S) Bonds to Heterocumulenes Catalyzed by Benzimidazolin-2-iminato Actinide Complexes
resolves10.1021/ja0709167
Highly Stereoselective Formal [3 + 3] Cycloaddition of Enals and Azomethine Imines Catalyzed by <i>N</i>-Heterocyclic Carbenes
resolves10.1039/C5CC08507A
One-pot sequential 1,2-addition, Pd-catalysed cross-coupling of organolithium reagents with Weinreb amides
resolves10.1002/anie.201409982
Transition‐Metal‐Free Intramolecular Carbene Aromatic Substitution/Büchner Reaction: Synthesis of Fluorenes and [6,5,7]Benzo‐fused Rings
resolves10.1016/j.jorganchem.2012.01.015
Suzuki cross-coupling catalyzed by palladium (II) complexes bearing 1-aryl-3,4,5,6-tetrahydropyrimidine ligands
resolves10.1002/ejoc.201402919
Nickel‐Catalyzed Desulfitative Suzuki–Miyaura Cross‐Coupling of <i>N</i>,<i>N</i>‐Disulfonylmethylamines and Arylboronic Acids
resolves10.1021/acs.joc.9b02554
Palladium-Catalyzed Hiyama Coupling of Benzylic Ammonium Salts via C–N Bond Cleavage
resolves10.1002/adsc.201801586
Nickel‐Catalyzed C(<i>sp</i><sup>2</sup>)−C(<i>sp</i><sup>3</sup>) Kumada Cross‐Coupling of Aryl Tosylates with Alkyl Grignard Reagents
resolves10.1039/c2cc16790e
Transition-metal-free highly chemo- and regioselective arylation of unactivated arenes with aryl halides over recyclable heterogeneous catalysts
resolves10.1055/s-0036-1589059
Suzuki–Miyaura Cross-Coupling Reactions in Acetic Acid Employing Sydnone-Derived Catalyst Systems
resolves10.1002/anie.201208025
Decarboxylative Cross‐Coupling of Mesylates Catalyzed by Copper/Palladium Systems with Customized Imidazolyl Phosphine Ligands
The 1 reference without a DOI — listed, not checked
no DOI — not checkedNovel tetrahydropyrimidinium/palladium system as a convenient catalysts: Suzuki coupling reactions of aryl chlorides
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