# Catalytic Cross-Coupling Reactions **Type:** Topics **Canonical URL:** https://scholariq.org/topics/catalytic-cross-coupling-reactions/ ## Facts | Field | Value | | --- | --- | | Description | This cluster of papers focuses on the advances in transition metal-catalyzed cross-coupling reactions, particularly palladium-catalyzed processes, for organic synthesis. It covers topics such as C-C bond formation, homogeneous and heterogeneous catalysis, aryl halides, Suzuki-Miyaura and Heck reactions, and the use of nickel as a catalyst. | | Domain | Physical Sciences | | Field | Chemistry | | OpenAlex ID | t10548 | | Works | 25 | ## Topic papers all Showing 15 of 25. - [Cu-Catalyzed Asymmetric Borylative Cyclization of Cyclohexadienone-Containing 1,6-Enynes](https://scholariq.org/papers/cu-catalyzed-asymmetric-borylative-cyclization-of-cyclohexadienone-containing-1/) - [Catalytic C(sp3)−H Arylation of Free Primary Amines with an exo Directing Group Generated In Situ](https://scholariq.org/papers/catalytic-c-sp-sup-3-sup-h-arylation-of-free-primary-amines-with-an-i-exo-i/) - [In Situ Generation of Palladium Nanoparticles:  A Simple and Highly Active Protocol for Oxygen-Promoted Ligand-Free Suzuki Coupling Reaction of Aryl Chlorides](https://scholariq.org/papers/in-situ-generation-of-palladium-nanoparticles-a-simple-and-highly-active/) - [Synthesis of Noble Metal Nanoparticles Embedded in the Shell Layer of Core−Shell Poly(styrene-co-4-vinylpyridine) Micospheres and Their Application in Catalysis](https://scholariq.org/papers/synthesis-of-noble-metal-nanoparticles-embedded-in-the-shell-layer-of-core-shell/) - [Transition Metal Catalysis in Fluorous Media:  Practical Application of a New Immobilization Principle to Rhodium-Catalyzed Hydroborations of Alkenes and Alkynes](https://scholariq.org/papers/transition-metal-catalysis-in-fluorous-media-practical-application-of-a-new/) - [Cyclopalladated ferrocenylimines: efficient catalysts for homocoupling and Sonogashira reaction of terminal alkynes](https://scholariq.org/papers/cyclopalladated-ferrocenylimines-efficient-catalysts-for-homocoupling-and/) - [Living Polymerization of Conjugated Polar Alkenes Catalyzed by N-Heterocyclic Olefin-Based Frustrated Lewis Pairs](https://scholariq.org/papers/living-polymerization-of-conjugated-polar-alkenes-catalyzed-by-i-n-i/) - [A simple and efficient protocol for a palladium-catalyzed ligand-free Suzuki reaction at room temperature in aqueous DMF](https://scholariq.org/papers/a-simple-and-efficient-protocol-for-a-palladium-catalyzed-ligand-free-suzuki/) - [Aerobic Ligand‐Free Suzuki Coupling Reaction of Aryl Chlorides Catalyzed by In Situ Generated Palladium Nanoparticles at Room Temperature](https://scholariq.org/papers/aerobic-ligand-free-suzuki-coupling-reaction-of-aryl-chlorides-catalyzed-by-i-in/) - [A facile oxidation of boronic acids and boronic esters](https://scholariq.org/papers/a-facile-oxidation-of-boronic-acids-and-boronic-esters/) - [Oxidatively Induced Reductive Elimination: Exploring the Scope and Catalyst Systems with Ir, Rh, and Ru Complexes](https://scholariq.org/papers/oxidatively-induced-reductive-elimination-exploring-the-scope-and-catalyst/) - [Metallabenzene: synthesis, structure, and spectroscopy of a 1-irida-3,5-dimethylbenzene complex](https://scholariq.org/papers/metallabenzene-synthesis-structure-and-spectroscopy-of-a-1-irida-3-5/) - [Remarkable Electronic Effect on Rhodium-Catalyzed Carbonyl Additions and Conjugated Additions with Arylmetallic Reagents](https://scholariq.org/papers/remarkable-electronic-effect-on-rhodium-catalyzed-carbonyl-additions-and/) - [Catalytic Asymmetric Conjugate Protosilylation and Protoborylation of 2-Trifluoromethyl Enynes for Synthesis of Functionalized Allenes](https://scholariq.org/papers/catalytic-asymmetric-conjugate-protosilylation-and-protoborylation-of-2/) - [Chelation versus Non‐Chelation Control in the Stereoselective Alkenyl sp2 C−H Bond Functionalization Reaction](https://scholariq.org/papers/chelation-versus-non-chelation-control-in-the-stereoselective-alkenyl-sp-sup-2/) ## Topic primary papers - [In Situ Generation of Palladium Nanoparticles:  A Simple and Highly Active Protocol for Oxygen-Promoted Ligand-Free Suzuki Coupling Reaction of Aryl Chlorides](https://scholariq.org/papers/in-situ-generation-of-palladium-nanoparticles-a-simple-and-highly-active/) - [Synthesis of Noble Metal Nanoparticles Embedded in the Shell Layer of Core−Shell Poly(styrene-co-4-vinylpyridine) Micospheres and Their Application in Catalysis](https://scholariq.org/papers/synthesis-of-noble-metal-nanoparticles-embedded-in-the-shell-layer-of-core-shell/) - [Cyclopalladated ferrocenylimines: efficient catalysts for homocoupling and Sonogashira reaction of terminal alkynes](https://scholariq.org/papers/cyclopalladated-ferrocenylimines-efficient-catalysts-for-homocoupling-and/) - [A simple and efficient protocol for a palladium-catalyzed ligand-free Suzuki reaction at room temperature in aqueous DMF](https://scholariq.org/papers/a-simple-and-efficient-protocol-for-a-palladium-catalyzed-ligand-free-suzuki/) - [Aerobic Ligand‐Free Suzuki Coupling Reaction of Aryl Chlorides Catalyzed by In Situ Generated Palladium Nanoparticles at Room Temperature](https://scholariq.org/papers/aerobic-ligand-free-suzuki-coupling-reaction-of-aryl-chlorides-catalyzed-by-i-in/) - [Metallabenzene: synthesis, structure, and spectroscopy of a 1-irida-3,5-dimethylbenzene complex](https://scholariq.org/papers/metallabenzene-synthesis-structure-and-spectroscopy-of-a-1-irida-3-5/) - [Remarkable Electronic Effect on Rhodium-Catalyzed Carbonyl Additions and Conjugated Additions with Arylmetallic Reagents](https://scholariq.org/papers/remarkable-electronic-effect-on-rhodium-catalyzed-carbonyl-additions-and/) - [Palladium‐Iminodiacetic Acid Immobilized on pH‐Responsive Polymeric Microspheres: Efficient Quasi‐Homogeneous Catalyst for Suzuki and Heck Reactions in Aqueous Solution](https://scholariq.org/papers/palladium-iminodiacetic-acid-immobilized-on-ph-responsive-polymeric-microspheres/) - [Enabling Deoxygenative C(sp2)-C(sp3) Cross-Coupling for Parallel Medicinal Chemistry](https://scholariq.org/papers/enabling-deoxygenative-c-sp-sup-2-sup-c-sp-sup-3-sup-cross-coupling-for-parallel/) --- Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.