Palladium-catalyzed coupling reactions of aryl chlorides.
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Summary
This review summarizes both the seminal early work and the exciting recent developments in the area of palladium-catalyzed couplings of aryl chlorides.
- Type
- review
- Published
- 2002-11-15
- Cited by
- 2,030
- References
- 19
- OpenAlex
- https://openalex.org/W1973051136
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:45385687
Keywords
Aryl, Palladium, Catalysis, Reactivity (psychology), Combinatorial chemistry
References
- Activation of unreactive bonds and organic synthesis
- Application of Transition Metal Catalysts in Organic Synthesis
- Metal-catalyzed cross-coupling reactions
- Palladium in Heterocyclic Chemistry
- Applied homogeneous catalysis with organometallic compounds
- Dialkylphosphinoimidazoles as New Ligands for Palladium-Catalyzed Coupling Reactions of Aryl Chlorides
- Activation of Unreactive Bonds and Organic Synthesis
- Applied Homogeneous Catalysis with Organometallic Compounds
- Classics in total synthesis
Cited by
- New air-stable planar chiral ferrocenyl monophosphine ligands: Suzuki cross-coupling of aryl chlorides and bromides.
- Pd(0)-Catalyzed carbonylation of 1,1-dichloro-1-alkenes, a new selective access to Z-α-chloroacrylates.
- Nickel-catalyzed cross-coupling of aryl bromides with tertiary Grignard reagents utilizing donor-functionalized N-heterocyclic carbenes (NHCs).
- Controlled Pd(0)/Ad3P-Catalyzed Suzuki Cross-Coupling Polymerization of AB-Type Monomers with Ad3P-Coordinated Acetanilide-Based Palladacycle Complex as Initiator.
- The heck reactions of aryl bromides in ionic liquids medium of n-butyl-n-methylpyrrolidinium trifluoromethanesulfonate
- Synthèse et évaluation pharmacologique d'imidazolidin-2-ones et d'analogues à potentialités immunosuppressives
- Synthesis of flavonoids and flavonoid-based designed multiple ligands for hypertension
- Regioselective Heck Coupling Reactions Focus on Green Chemistry
- A simple and novel amide ligand based on quinoline derivative used for palladium-catalyzed Suzuki coupling reaction
- Cyclometallation, steric and electronic tendencies in a series of Pd(II) complex pre-catalysts bearing imidazole–phenol ligands and effects on Suzuki–Miyaura catalytic efficiencies
- Optimization of Reaction and Substrate Activation in the Stereoselective Cross-Coupling of Chiral 3,3-Diboronyl Amides.
- Applied Cross-Coupling Reactions
- Anionic phosph(in)ito (“phosphoryl”) ligands: Non-classical “actor” phosphane-type ligands in coordination chemistry
- Aryl/heteroaryl pentafluorobenzenesulfonates (ArOPFBs): new electrophilic coupling partners for room temperature Suzuki–Miyaura cross-coupling reactions
- ADVANCES IN SILOXANE-BASED COUPLING TECHNOLOGIES: APPROACHES TOWARD PANCRATISTATIN AND STREPTONIGRIN
- Sterically Controlled Pd-Catalyzed Chemoselective Ketone Synthesis via N-C Cleavage in Twisted Amides.
- A palladium–phosphine catalytic system as an active and recycable precatalyst for Suzuki coupling in water
- Imidazolio-substituted secondary phosphine oxides as potential carbene reagents
- Cyclopalladated ferrocenylimine as an efficient catalyst for the syntheses of diarylmethane derivatives
- Activity and Recyclability Improvement Through Adjusting the Tethering Strategy for Pd-Catalyzed Suzuki–Miyaura Coupling Reaction of Aryl Chlorides
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