Research graph
References from Cobalt (II)/bis-imidazole ethyleneoxy bridged N-heterocyclic carbene on SBA-15 as an active and efficient catalyst for aqueous Heck and Suzuki cross-coupling reactions. Local targets link to admitted publications; unresolved targets remain external evidence.
Pd nanoparticles immobilized on PAMAM-grafted MWCNTs hybrid materials as new recyclable catalyst for Mizoraki–Heck cross-coupling reactions
10.1016/j.apcata.2011.08.021 · 2011 · External reference
Preparation of cobalt-containing ligands with NHC-and/or P-coordinating sites and their application in heck reactions: the formation of an unexpected cobalt-containing Zwitterionic complex
10.1002/ejic.201000271 · 2010 · External reference
Preparation of lignin/glycerol-based bis (cyclic carbonate) for the synthesis of polyurethanes
10.1039/c5gc01340b · 2015 · External reference
Enantioselective nickel-catalyzed Mizoroki–Heck cyclizations to generate quaternary stereocenters
10.1021/acs.orglett.7b01054 · 2017 · External reference
Copper (II) oxide on aluminosilicate mediated heck coupling of styrene with aryl halides in water
10.1039/c3ra23246h · 2013 · External reference
Iron-catalyzed cross-coupling reaction: recyclable heterogeneous iron catalyst for selective olefination of aryl iodides in poly (ethylene glycol) medium
10.1039/c3gc36761d · 2013 · External reference
Pd/cu-free heck and Sonogashira cross-coupling reaction by co nanoparticles immobilized on magnetic chitosan as reusable catalyst
10.1039/c6gc03377f · 2017 · External reference
A decade of exploration of transition-metal-catalyzed cross-coupling reactions: an overview
10.1055/s-0040-1720096 · 2023 · External reference
Recent advances in cobalt-catalyzed cross-coupling reactions
2019 · External reference
Unresolved reference
2026 · External reference
Recent trends of organic synthesis through cobalt metal-based catalysis: a review
10.1039/d6ra04780g · 2026 · External reference
Cobalt-catalyzed aminocarbonylation of alkyl iodides
10.1016/j.jcat.2025.116456 · 2025 · External reference
Multifaceted photocatalysis enables cobalt catalyzed enantioselective C–H activation and APEX reaction for C–N axially chiral molecules
10.1039/d5sc05287d · 2025 · External reference
Exploring cobalt, nickel, and palladium complexes for the hydrogenation reactions: a review
2025 · External reference
Cobalt-catalyzed reductive cross-coupling: a review
10.1007/s11030-024-11017-1 · 2025 · External reference
N-Heterocyclic Carbene Complexes in C–H Activation Reactions
10.1021/acs.chemrev.9b00634 · 2020 · External reference
Well-defined cobalt (I) dihydrogen catalyst: experimental evidence for a co (I)/co (III) redox process in olefin hydrogenation
10.1021/jacs.6b07066 · 2016 · External reference
Mild cobalt-catalyzed Negishi cross-couplings of (hetero) arylzinc reagents with (hetero) aryl halides
10.1002/anie.201510665 · 2016 · External reference
Cobalt-catalyzed coupling of alkenyl triflates with aryl and alkenyl Grignard reagents
10.1246/cl.2008.654 · 2008 · External reference
Stability and reusability of amine-functionalized magnetic-cored dendrimer for heavy metal adsorption
10.1007/s10853-016-0380-z · 2017 · External reference
N-heterocyclic carbenes in materials chemistry
10.1021/acs.chemrev.8b00514 · 2019 · External reference
Co-catalyzed cross-coupling of alkyl halides with tertiary alkyl Grignard reagents using a 1, 3-butadiene additive
10.1021/ja404285b · 2013 · External reference
Cobalt-catalyzed cross-coupling of 3-and 4-Iodopiperidines with Grignard reagents. Chemistry–a
2015 · External reference
A robust and broadly applicable cobalt-catalyzed cross-coupling of functionalized bench-stable Organozinc Pivalates with unsaturated halides
10.1002/anie.201610324 · 2017 · External reference
Magnetically recoverable Fe3O4/CoPd/NC nanocatalyst for high-performance Suzuki-Miyaura cross-coupling reactions
10.1038/s41598-025-34753-2 · 2026 · External reference
Cobalt (III)-catalyzed enantioselective C–H functionalization: ligand innovation and reaction development
10.1021/acs.accounts.5c00013 · 2025 · External reference
Cobalt-catalyzed cross-electrophile coupling of aryl bromides and linear secondary alkyl bromides
10.1039/d5qo01310k · 2026 · External reference
Cobaloxime catalysis: a general platform for Mizoroki-heck-type reactions and catalytic Dehydrohalogenations of Unactivated alkyl chlorides
10.1021/jacs.5c19730 · 2026 · External reference
Dipentaerythritol: a novel additive for the precipitation of dispersed Ni particles in polyols
10.1039/c4ra01464b · 2014 · External reference
Ultrasmall particles and nanocomposites: state of the art
10.1039/c3ra43418d · 2013 · External reference
Efficient hydrodehalogenation of aryl halides catalyzed by Bis (NHC)-Pd (II) complex supported on magnetic mesoporous silica
10.1007/s10562-023-04319-w · 2024 · External reference
Supported Bis-(NHC)-Pd (II) complex: a phosphine-free catalyst supported on magnetic mesoporous silica for the CO-free carbonylation of aryl halides
2024 · External reference
N-heterocyclic carbene complexes of copper, nickel, and cobalt
10.1021/acs.chemrev.8b00505 · 2019 · External reference
NHC-cracker: a platform for the in silico engineering of N-heterocyclic Carbenes for diverse chemical applications
10.1021/acscatal.4c06474 · 2025 · External reference
Redefining metal–ligand interfaces: N-heterocyclic carbene functionalization of metal nanoparticles
10.1002/cphc.202500856 · 2026 · External reference
The latest developments of N-heterocyclic carbenes (NHCs) complexes in cross-coupling chemistry
2022 · External reference
Highly active and stable bis imidazolium-based copper n-heterocyclic carbene modified graphene oxide for O-arylation and N-arylation reactions in water
10.1007/s10562-022-04074-4 · 2023 · External reference
Immobilization of N-heterocyclic carbene compounds: a synthetic perspective
10.1021/acs.chemrev.6b00631 · 2017 · External reference
N-heterocyclic carbene (NHC) organocatalysis: from fundamentals to frontiers
10.1039/d4cs01179a · 2025 · External reference
Recent update on catalytic activity of N-heterocyclic carbene supported on graphene nanosheets: a mini review
10.1016/j.jorganchem.2025.123660 · 2025 · External reference
Recent advances in the synthesis of polymer supported catalysts: a review
10.1007/s42452-025-07106-x · 2025 · External reference
Synthesis and structure of cobalt (II) iodide bearing a bulky N-heterocyclic carbene ligand, and catalytic activation of bromoalkanes
10.1016/j.jorganchem.2012.12.025 · 2013 · External reference
Cobalt 1, 3-diisopropyl-1 H-imidazol-2-ylidene complexes: synthesis, solid-state structures, and quantum chemistry calculations
10.1021/om100680c · 2010 · External reference
Cobalt (II) complexes bearing a bulky N-heterocyclic carbene for catalysis of Kumada–Tamao–Corriu cross-coupling reactions of aryl halides
10.1002/ejic.201200095 · 2012 · External reference
Catalytic performance of chitosan-Schiff base supported Pd/co bimetallic catalyst for acrylamide with phenyl halide
10.1002/pat.1420 · 2010 · External reference
Multi walled carbon nanotubes supported N-heterocyclic carbene–cobalt (ΙΙ) as a novel, efficient and inexpensive catalyst for the Mizoroki–Heck reaction
10.1016/j.catcom.2015.12.027 · 2016 · External reference
Enhanced catalytic performance of silica-supported Pd-NHC complexes in Suzuki-Miyaura coupling reactions
2025 · External reference
Fe3O4@ Boehmite-NH2-CoII NPs: an inexpensive and highly efficient heterogeneous magnetic nanocatalyst for the Suzuki–Miyaura and Heck–Mizoroki cross-coupling reactions
10.1039/c7gc02647a · 2017 · External reference
Highly selective biaryl cross-coupling reactions between aryl halides and aryl Grignard reagents: a new catalyst combination of N-heterocyclic carbenes and iron, cobalt, and nickel fluorides
10.1021/ja9039289 · 2009 · External reference
Cobalt-catalyzed cross-coupling reactions of arylboronic esters and aryl halides
10.1021/acs.organomet.7b00726 · 2017 · External reference
Insight into transmetalation enables cobalt-catalyzed Suzuki–Miyaura cross coupling
10.1021/acscentsci.6b00283 · 2016 · External reference
Cobalt-catalyzed cross-coupling reactions of aryl Triflates and Lithium Arylborates
10.1021/acs.joc.9b02105 · 2019 · External reference
Cobalt pincer complex catalyzed Suzuki-Miyaura cross coupling–a green approach
10.1016/j.jorganchem.2016.11.005 · 2017 · External reference
Cobalt-catalyzed Suzuki Biaryl coupling of aryl halides
10.1002/ange.201710053 · 2017 · External reference
Heck reaction catalyzed by flower-like cobalt nanostructures
10.1016/j.catcom.2009.01.018 · 2009 · External reference
Facile synthesis of co–B amorphous alloy in uniform spherical nanoparticles with enhanced catalytic properties
10.1021/cs300472p · 2012 · External reference
A novel heck reaction catalyzed by co hollow nanospheres in ligand-free condition
10.1039/b617556b · 2007 · External reference
Synthesis of dendrimer assisted cobalt nanoparticles and catalytic application in heck coupling reactions in ionic liquid
10.1007/s42452-020-2448-2 · 2020 · External reference
N-heterocyclic carbene–palladium (II) complex supported on magnetic mesoporous silica for heck cross-coupling reaction
10.1002/aoc.4904 · 2019 · External reference
Polymer containing Pd (II) chelates grafted from SBA-15 for C–C bond formation via the Mizoroki–Heck reaction
10.1007/s11696-024-03486-3 · 2024 · External reference
A new Pd (II) catalyst supported on magnetic SBA-15 for the Mizoroki-Heck coupling reaction
2025 · External reference
Novel hybrid thioamide ligand supported copper nanoparticles on SBA-15: a copper rich robust nanoreactor for green synthesis of triazoles and tetrazoles in water medium
10.1007/s10562-019-03031-y · 2020 · External reference
Carbon coated copper nanostructures as a green and ligand free nanocatalyst for Suzuki cross-coupling reaction
10.1016/j.catcom.2016.12.028 · 2017 · External reference
Highly dispersed copper/ppm palladium nanoparticles as novel magnetically recoverable catalyst for Suzuki reaction under aqueous conditions at room temperature
10.1002/aoc.3743 · 2017 · External reference
Magnetically recoverable gold nanorods as a novel catalyst for the facile reduction of nitroarenes under aqueous conditions
10.1007/s10562-016-1921-4 · 2017 · External reference
Uniform silver nanoparticles on tunable porous N-doped carbon nanospheres for aerobic oxidative synthesis of aryl nitriles from benzylic alcohols
10.1002/aoc.4835 · 2019 · External reference
Eco-friendly N-mono-methylation of anilines with methanol as a sustainable C1 source via hydrogen borrowing: using new caffeine-derived ruthenium–NHC complex as high-efficiency and green catalyst
10.1016/j.inoche.2025.115297 · 2025 · External reference
Well dispersed gold nanoparticles into the multi amine functionalized SBA-15 for green chemical fixation of carbon dioxide to cyclic carbonates under solvent free conditions
2021 · External reference
Sustainable organometallic catalysis using caffeine-derived NHC–Cu complexes: toward an efficient and green approach to A3-coupling reactions
10.1007/s13738-026-03579-8 · 2026 · External reference
A confined fabrication of perovskite quantum dots in oriented MOF thin film
10.1021/acsami.6b11712 · 2016 · External reference
Hydroisomerization of n-hexane using acidified metal–organic framework and platinum nanoparticles
10.1021/jacs.7b06629 · 2017 · External reference
Cationic Zn-porphyrin immobilized in mesoporous silicas as bifunctional catalyst for CO2 cycloaddition reaction under cocatalyst free conditions
10.1021/acssuschemeng.8b01548 · 2018 · External reference
Insight into the PEG-linked bis-imidazolium bridged framework of mesoporous organosilicas as ion exchangers
10.1016/j.micromeso.2016.05.008 · 2016 · External reference
Microwave assisted template removal of siliceous porous materials
10.1039/b202180c · 2002 · External reference
Intraframework metal ion adsorption in ligand-functionalized mesoporous silica
10.1002/1521-4095(20020805)14:15<1053::aid-adma1053>3.0.co;2-x · 2002 · External reference
Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative heck reaction
10.1039/c7sc01204g · 2017 · External reference
Cobalt-catalyzed coupling of alkyl iodides with alkenes: deprotonation of hydridocobalt enables turnover
10.1002/anie.201105235 · 2011 · External reference
Atom-economical cobalt-catalysed regioselective coupling of epoxides and aziridines with alkenes
10.1039/c6cc04410g · 2016 · External reference
Formation of a cobalt (III)− phenoxyl radical complex by acetic acid promoted aerobic oxidation of a co (II) salen complex
10.1021/ic901849e · 2010 · External reference
Mechanisms of cobalt/phosphine-catalyzed cross-coupling reactions. Chemistry–a
2019 · External reference
Cobalt schiff base immobilized on a graphene nanosheet with N, O linkage for cross-coupling reaction
10.1021/acs.iecr.8b02979 · 2019 · External reference
A Co–Cu bimetallic magnetic nanocatalyst with synergistic and bifunctional performance for the base-free Suzuki, Sonogashira, and C–N cross-coupling reactions in water
10.1039/d0dt01846e · 2020 · External reference
Water-dispersible, magnetically recyclable heterogeneous cobalt catalyst for C–C and C–N cross-coupling reactions in aqueous media
10.1021/acsomega.3c10462 · 2024 · External reference
Hybrid Pd0. 1Cu0. 9Co2O4 nano-flakes: a novel, efficient and reusable catalyst for the one-pot heck and Suzuki couplings with simultaneous transesterification reactions under microwave irradiation
10.3389/fchem.2024.1496234 · 2024 · External reference
A hydrophilic heterogeneous cobalt catalyst for fluoride-free Hiyama, Suzuki, Heck and Hirao cross-coupling reactions in water
10.1039/c9gc03455b · 2020 · External reference
The novel use of Ni, Co, Cu and Mn heterogeneous catalysts for the Heck reaction
10.1016/s1381-1169(00)00190-4 · 2000 · External reference
Intraframework metal ion adsorption in ligand-functionalized mesoporous silica
10.1002/1521-4095(20020805)14:15<1053::aid-adma1053>3.0.co;2-x · ExternalCitation · doi-reference
Cobalt-catalyzed Suzuki Biaryl coupling of aryl halides
10.1002/ange.201710053 · ExternalCitation · doi-reference
Cobalt-catalyzed coupling of alkyl iodides with alkenes: deprotonation of hydridocobalt enables turnover
10.1002/anie.201105235 · ExternalCitation · doi-reference
Mild cobalt-catalyzed Negishi cross-couplings of (hetero) arylzinc reagents with (hetero) aryl halides
10.1002/anie.201510665 · ExternalCitation · doi-reference
A robust and broadly applicable cobalt-catalyzed cross-coupling of functionalized bench-stable Organozinc Pivalates with unsaturated halides
10.1002/anie.201610324 · ExternalCitation · doi-reference
Highly dispersed copper/ppm palladium nanoparticles as novel magnetically recoverable catalyst for Suzuki reaction under aqueous conditions at room temperature
10.1002/aoc.3743 · ExternalCitation · doi-reference
Uniform silver nanoparticles on tunable porous N-doped carbon nanospheres for aerobic oxidative synthesis of aryl nitriles from benzylic alcohols
10.1002/aoc.4835 · ExternalCitation · doi-reference
N-heterocyclic carbene–palladium (II) complex supported on magnetic mesoporous silica for heck cross-coupling reaction
10.1002/aoc.4904 · ExternalCitation · doi-reference
Redefining metal–ligand interfaces: N-heterocyclic carbene functionalization of metal nanoparticles
10.1002/cphc.202500856 · ExternalCitation · doi-reference
Preparation of cobalt-containing ligands with NHC-and/or P-coordinating sites and their application in heck reactions: the formation of an unexpected cobalt-containing Zwitterionic complex
10.1002/ejic.201000271 · ExternalCitation · doi-reference
Cobalt (II) complexes bearing a bulky N-heterocyclic carbene for catalysis of Kumada–Tamao–Corriu cross-coupling reactions of aryl halides
10.1002/ejic.201200095 · ExternalCitation · doi-reference
Catalytic performance of chitosan-Schiff base supported Pd/co bimetallic catalyst for acrylamide with phenyl halide
10.1002/pat.1420 · ExternalCitation · doi-reference
Magnetically recoverable gold nanorods as a novel catalyst for the facile reduction of nitroarenes under aqueous conditions
10.1007/s10562-016-1921-4 · ExternalCitation · doi-reference
Novel hybrid thioamide ligand supported copper nanoparticles on SBA-15: a copper rich robust nanoreactor for green synthesis of triazoles and tetrazoles in water medium
10.1007/s10562-019-03031-y · ExternalCitation · doi-reference
Highly active and stable bis imidazolium-based copper n-heterocyclic carbene modified graphene oxide for O-arylation and N-arylation reactions in water
10.1007/s10562-022-04074-4 · ExternalCitation · doi-reference
Efficient hydrodehalogenation of aryl halides catalyzed by Bis (NHC)-Pd (II) complex supported on magnetic mesoporous silica
10.1007/s10562-023-04319-w · ExternalCitation · doi-reference
Stability and reusability of amine-functionalized magnetic-cored dendrimer for heavy metal adsorption
10.1007/s10853-016-0380-z · ExternalCitation · doi-reference
Cobalt-catalyzed reductive cross-coupling: a review
10.1007/s11030-024-11017-1 · ExternalCitation · doi-reference
Polymer containing Pd (II) chelates grafted from SBA-15 for C–C bond formation via the Mizoroki–Heck reaction
10.1007/s11696-024-03486-3 · ExternalCitation · doi-reference
Sustainable organometallic catalysis using caffeine-derived NHC–Cu complexes: toward an efficient and green approach to A3-coupling reactions
10.1007/s13738-026-03579-8 · ExternalCitation · doi-reference
Synthesis of dendrimer assisted cobalt nanoparticles and catalytic application in heck coupling reactions in ionic liquid
10.1007/s42452-020-2448-2 · ExternalCitation · doi-reference
Recent advances in the synthesis of polymer supported catalysts: a review
10.1007/s42452-025-07106-x · ExternalCitation · doi-reference
Pd nanoparticles immobilized on PAMAM-grafted MWCNTs hybrid materials as new recyclable catalyst for Mizoraki–Heck cross-coupling reactions
10.1016/j.apcata.2011.08.021 · ExternalCitation · doi-reference
Heck reaction catalyzed by flower-like cobalt nanostructures
10.1016/j.catcom.2009.01.018 · ExternalCitation · doi-reference
Multi walled carbon nanotubes supported N-heterocyclic carbene–cobalt (ΙΙ) as a novel, efficient and inexpensive catalyst for the Mizoroki–Heck reaction
10.1016/j.catcom.2015.12.027 · ExternalCitation · doi-reference
Carbon coated copper nanostructures as a green and ligand free nanocatalyst for Suzuki cross-coupling reaction
10.1016/j.catcom.2016.12.028 · ExternalCitation · doi-reference
Eco-friendly N-mono-methylation of anilines with methanol as a sustainable C1 source via hydrogen borrowing: using new caffeine-derived ruthenium–NHC complex as high-efficiency and green catalyst
10.1016/j.inoche.2025.115297 · ExternalCitation · doi-reference
Cobalt-catalyzed aminocarbonylation of alkyl iodides
10.1016/j.jcat.2025.116456 · ExternalCitation · doi-reference
Synthesis and structure of cobalt (II) iodide bearing a bulky N-heterocyclic carbene ligand, and catalytic activation of bromoalkanes
10.1016/j.jorganchem.2012.12.025 · ExternalCitation · doi-reference
Cobalt pincer complex catalyzed Suzuki-Miyaura cross coupling–a green approach
10.1016/j.jorganchem.2016.11.005 · ExternalCitation · doi-reference
Recent update on catalytic activity of N-heterocyclic carbene supported on graphene nanosheets: a mini review
10.1016/j.jorganchem.2025.123660 · ExternalCitation · doi-reference
Insight into the PEG-linked bis-imidazolium bridged framework of mesoporous organosilicas as ion exchangers
10.1016/j.micromeso.2016.05.008 · ExternalCitation · doi-reference
The novel use of Ni, Co, Cu and Mn heterogeneous catalysts for the Heck reaction
10.1016/s1381-1169(00)00190-4 · ExternalCitation · doi-reference
Cobalt (III)-catalyzed enantioselective C–H functionalization: ligand innovation and reaction development
10.1021/acs.accounts.5c00013 · ExternalCitation · doi-reference
Immobilization of N-heterocyclic carbene compounds: a synthetic perspective
10.1021/acs.chemrev.6b00631 · ExternalCitation · doi-reference
N-heterocyclic carbene complexes of copper, nickel, and cobalt
10.1021/acs.chemrev.8b00505 · ExternalCitation · doi-reference
N-heterocyclic carbenes in materials chemistry
10.1021/acs.chemrev.8b00514 · ExternalCitation · doi-reference
N-Heterocyclic Carbene Complexes in C–H Activation Reactions
10.1021/acs.chemrev.9b00634 · ExternalCitation · doi-reference
Cobalt schiff base immobilized on a graphene nanosheet with N, O linkage for cross-coupling reaction
10.1021/acs.iecr.8b02979 · ExternalCitation · doi-reference
Cobalt-catalyzed cross-coupling reactions of aryl Triflates and Lithium Arylborates
10.1021/acs.joc.9b02105 · ExternalCitation · doi-reference
Cobalt-catalyzed cross-coupling reactions of arylboronic esters and aryl halides
10.1021/acs.organomet.7b00726 · ExternalCitation · doi-reference
Enantioselective nickel-catalyzed Mizoroki–Heck cyclizations to generate quaternary stereocenters
10.1021/acs.orglett.7b01054 · ExternalCitation · doi-reference
A confined fabrication of perovskite quantum dots in oriented MOF thin film
10.1021/acsami.6b11712 · ExternalCitation · doi-reference
NHC-cracker: a platform for the in silico engineering of N-heterocyclic Carbenes for diverse chemical applications
10.1021/acscatal.4c06474 · ExternalCitation · doi-reference
Insight into transmetalation enables cobalt-catalyzed Suzuki–Miyaura cross coupling
10.1021/acscentsci.6b00283 · ExternalCitation · doi-reference
Water-dispersible, magnetically recyclable heterogeneous cobalt catalyst for C–C and C–N cross-coupling reactions in aqueous media
10.1021/acsomega.3c10462 · ExternalCitation · doi-reference
Cationic Zn-porphyrin immobilized in mesoporous silicas as bifunctional catalyst for CO2 cycloaddition reaction under cocatalyst free conditions
10.1021/acssuschemeng.8b01548 · ExternalCitation · doi-reference
Facile synthesis of co–B amorphous alloy in uniform spherical nanoparticles with enhanced catalytic properties
10.1021/cs300472p · ExternalCitation · doi-reference
Formation of a cobalt (III)− phenoxyl radical complex by acetic acid promoted aerobic oxidation of a co (II) salen complex
10.1021/ic901849e · ExternalCitation · doi-reference
Co-catalyzed cross-coupling of alkyl halides with tertiary alkyl Grignard reagents using a 1, 3-butadiene additive
10.1021/ja404285b · ExternalCitation · doi-reference
Highly selective biaryl cross-coupling reactions between aryl halides and aryl Grignard reagents: a new catalyst combination of N-heterocyclic carbenes and iron, cobalt, and nickel fluorides
10.1021/ja9039289 · ExternalCitation · doi-reference
Cobaloxime catalysis: a general platform for Mizoroki-heck-type reactions and catalytic Dehydrohalogenations of Unactivated alkyl chlorides
10.1021/jacs.5c19730 · ExternalCitation · doi-reference
Well-defined cobalt (I) dihydrogen catalyst: experimental evidence for a co (I)/co (III) redox process in olefin hydrogenation
10.1021/jacs.6b07066 · ExternalCitation · doi-reference
Hydroisomerization of n-hexane using acidified metal–organic framework and platinum nanoparticles
10.1021/jacs.7b06629 · ExternalCitation · doi-reference
Cobalt 1, 3-diisopropyl-1 H-imidazol-2-ylidene complexes: synthesis, solid-state structures, and quantum chemistry calculations
10.1021/om100680c · ExternalCitation · doi-reference
Magnetically recoverable Fe3O4/CoPd/NC nanocatalyst for high-performance Suzuki-Miyaura cross-coupling reactions
10.1038/s41598-025-34753-2 · ExternalCitation · doi-reference
Microwave assisted template removal of siliceous porous materials
10.1039/b202180c · ExternalCitation · doi-reference
A novel heck reaction catalyzed by co hollow nanospheres in ligand-free condition
10.1039/b617556b · ExternalCitation · doi-reference
Iron-catalyzed cross-coupling reaction: recyclable heterogeneous iron catalyst for selective olefination of aryl iodides in poly (ethylene glycol) medium
10.1039/c3gc36761d · ExternalCitation · doi-reference
Copper (II) oxide on aluminosilicate mediated heck coupling of styrene with aryl halides in water
10.1039/c3ra23246h · ExternalCitation · doi-reference
Ultrasmall particles and nanocomposites: state of the art
10.1039/c3ra43418d · ExternalCitation · doi-reference
Dipentaerythritol: a novel additive for the precipitation of dispersed Ni particles in polyols
10.1039/c4ra01464b · ExternalCitation · doi-reference
Preparation of lignin/glycerol-based bis (cyclic carbonate) for the synthesis of polyurethanes
10.1039/c5gc01340b · ExternalCitation · doi-reference
Atom-economical cobalt-catalysed regioselective coupling of epoxides and aziridines with alkenes
10.1039/c6cc04410g · ExternalCitation · doi-reference
Pd/cu-free heck and Sonogashira cross-coupling reaction by co nanoparticles immobilized on magnetic chitosan as reusable catalyst
10.1039/c6gc03377f · ExternalCitation · doi-reference
Fe3O4@ Boehmite-NH2-CoII NPs: an inexpensive and highly efficient heterogeneous magnetic nanocatalyst for the Suzuki–Miyaura and Heck–Mizoroki cross-coupling reactions
10.1039/c7gc02647a · ExternalCitation · doi-reference
Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative heck reaction
10.1039/c7sc01204g · ExternalCitation · doi-reference
A hydrophilic heterogeneous cobalt catalyst for fluoride-free Hiyama, Suzuki, Heck and Hirao cross-coupling reactions in water
10.1039/c9gc03455b · ExternalCitation · doi-reference
A Co–Cu bimetallic magnetic nanocatalyst with synergistic and bifunctional performance for the base-free Suzuki, Sonogashira, and C–N cross-coupling reactions in water
10.1039/d0dt01846e · ExternalCitation · doi-reference
N-heterocyclic carbene (NHC) organocatalysis: from fundamentals to frontiers
10.1039/d4cs01179a · ExternalCitation · doi-reference
Cobalt-catalyzed cross-electrophile coupling of aryl bromides and linear secondary alkyl bromides
10.1039/d5qo01310k · ExternalCitation · doi-reference
Multifaceted photocatalysis enables cobalt catalyzed enantioselective C–H activation and APEX reaction for C–N axially chiral molecules
10.1039/d5sc05287d · ExternalCitation · doi-reference
Recent trends of organic synthesis through cobalt metal-based catalysis: a review
10.1039/d6ra04780g · ExternalCitation · doi-reference
A decade of exploration of transition-metal-catalyzed cross-coupling reactions: an overview
10.1055/s-0040-1720096 · ExternalCitation · doi-reference
Cobalt-catalyzed coupling of alkenyl triflates with aryl and alkenyl Grignard reagents
10.1246/cl.2008.654 · ExternalCitation · doi-reference
Hybrid Pd0. 1Cu0. 9Co2O4 nano-flakes: a novel, efficient and reusable catalyst for the one-pot heck and Suzuki couplings with simultaneous transesterification reactions under microwave irradiation
10.3389/fchem.2024.1496234 · ExternalCitation · doi-reference
