The novel use of Ni, Co, Cu and Mn heterogeneous catalysts for the Heck reaction
10.1016/s1381-1169(00)00190-4 · doi-reference
A hydrophilic heterogeneous cobalt catalyst for fluoride-free Hiyama, Suzuki, Heck and Hirao cross-coupling reactions in water
10.1039/c9gc03455b · 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 · 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 · 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 · doi-reference
Cobalt schiff base immobilized on a graphene nanosheet with N, O linkage for cross-coupling reaction
10.1021/acs.iecr.8b02979 · 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 · doi-reference
Atom-economical cobalt-catalysed regioselective coupling of epoxides and aziridines with alkenes
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Cobalt-catalyzed coupling of alkyl iodides with alkenes: deprotonation of hydridocobalt enables turnover
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Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative heck reaction
10.1039/c7sc01204g · doi-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 · doi-reference
Microwave assisted template removal of siliceous porous materials
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Insight into the PEG-linked bis-imidazolium bridged framework of mesoporous organosilicas as ion exchangers
10.1016/j.micromeso.2016.05.008 · doi-reference
Cationic Zn-porphyrin immobilized in mesoporous silicas as bifunctional catalyst for CO2 cycloaddition reaction under cocatalyst free conditions
10.1021/acssuschemeng.8b01548 · doi-reference
Hydroisomerization of n-hexane using acidified metal–organic framework and platinum nanoparticles
10.1021/jacs.7b06629 · doi-reference
A confined fabrication of perovskite quantum dots in oriented MOF thin film
10.1021/acsami.6b11712 · doi-reference
Sustainable organometallic catalysis using caffeine-derived NHC–Cu complexes: toward an efficient and green approach to A3-coupling reactions
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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 · 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 · 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 · 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 · 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 · 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 · 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 · doi-reference
N-heterocyclic carbene–palladium (II) complex supported on magnetic mesoporous silica for heck cross-coupling reaction
10.1002/aoc.4904 · doi-reference
Synthesis of dendrimer assisted cobalt nanoparticles and catalytic application in heck coupling reactions in ionic liquid
10.1007/s42452-020-2448-2 · doi-reference
A novel heck reaction catalyzed by co hollow nanospheres in ligand-free condition
10.1039/b617556b · doi-reference
Facile synthesis of co–B amorphous alloy in uniform spherical nanoparticles with enhanced catalytic properties
10.1021/cs300472p · doi-reference
Heck reaction catalyzed by flower-like cobalt nanostructures
10.1016/j.catcom.2009.01.018 · doi-reference
Cobalt-catalyzed Suzuki Biaryl coupling of aryl halides
10.1002/ange.201710053 · doi-reference
Cobalt pincer complex catalyzed Suzuki-Miyaura cross coupling–a green approach
10.1016/j.jorganchem.2016.11.005 · doi-reference
Cobalt-catalyzed cross-coupling reactions of aryl Triflates and Lithium Arylborates
10.1021/acs.joc.9b02105 · doi-reference
Insight into transmetalation enables cobalt-catalyzed Suzuki–Miyaura cross coupling
10.1021/acscentsci.6b00283 · doi-reference
Cobalt-catalyzed cross-coupling reactions of arylboronic esters and aryl halides
10.1021/acs.organomet.7b00726 · 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 · 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 · 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 · doi-reference
Catalytic performance of chitosan-Schiff base supported Pd/co bimetallic catalyst for acrylamide with phenyl halide
10.1002/pat.1420 · 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 · doi-reference
Cobalt 1, 3-diisopropyl-1 H-imidazol-2-ylidene complexes: synthesis, solid-state structures, and quantum chemistry calculations
10.1021/om100680c · doi-reference
