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References from Nickel(II) Nanoparticles Immobilized on EDTA-Modified Fe3O4@SiO2 Nanospheres as Efficient and Recyclable Catalysts for Ligand-Free Suzuki–Miyaura Coupling of Aryl Carbamates and Sulfamates. Local targets link to admitted publications; unresolved targets remain external evidence.
Structure and Interaction of Nanoparticle-Protein Complexes
10.1021/acs.langmuir.8b00110 · 2018 · External reference
Nanotechnology, governance, and public deliberation: what role for the social sciences?
10.1177/1075547005281531 · 2005 · External reference
Surface modification of inorganic nanoparticles for development of organic-inorganic nanocomposites-A review
10.1016/j.progpolymsci.2013.02.003 · 2013 · External reference
Greener Biogenic Approach for the Synthesis of Palladium Nanoparticles Using Papaya Peel: An Eco-Friendly Catalyst for C-C Coupling Reaction
10.1021/acsomega.8b00039 · 2018 · External reference
Nanopalladium on Magnetic Ionic Nanoparticle Network (MINN) as an Efficient and Recyclable Catalyst with High Ionic Density and Dispersibility
10.1021/acssuschemeng.8b04566 · 2018 · External reference
Organic phase syntheses of magnetic nanoparticles and their applications
10.1021/acs.chemrev.5b00687 · 2016 · External reference
Biocompatible magnetic core-shell nanocomposites for engineered magnetic tissues
10.1039/c6nr00224b · 2016 · External reference
Preparation and analysis of Fe3O4 magnetic nanoparticles used as targeted-drug carriers
10.1016/s1004-9541(08)60104-4 · 2008 · External reference
Fe3O4@SiO2/Schiff base/Pd complex as an efficient heterogeneous and recyclable nanocatalyst for chemoselective N-arylation of O-alkyl primary carbamates
10.1039/c6ra17268g · 2016 · External reference
Multifunctional mesoporous composite microspheres with well-designed nanostructure: a highly integrated catalyst system
10.1021/ja1025744 · 2010 · External reference
Silica-decorated magnetic nanocomposites for catalytic applications
10.1016/j.ccr.2015.01.001 · 2015 · External reference
Core–shell Fe3O4 polydopamine nanoparticles serve multipurpose as drug carrier, catalyst support and carbon adsorbent
10.1021/am402585y · 2013 · External reference
Core-Shell Nanoparticle-Enhanced Raman Spectroscopy
10.1021/acs.chemrev.6b00596 · 2017 · External reference
Core/shell nanoparticles: classes, properties, synthesis mechanisms, characterization, and applications
10.1021/cr100449n · 2011 · External reference
Magnetically recoverable nanocatalysts
10.1021/cr100230z · 2011 · External reference
Fast-growing field of magnetically recyclable nanocatalysts
10.1021/cr500134h · 2014 · External reference
Palladium-catalyzed cross-coupling reactions of organoboron compounds
10.1021/cr00039a007 · 1995 · External reference
Enantiospecific and Iterative Suzuki-Miyaura Cross-Couplings
10.1021/jacs.7b08326 · 2017 · External reference
Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts
10.1039/c3cs35521g · 2013 · External reference
Designing Pd and Ni catalysts for cross-coupling reactions by minimizing off-cycle species
10.1021/acscatal.8b00230 · 2018 · External reference
Overcoming Halide Inhibition of Suzuki-Miyaura Couplings with Biaryl Monophosphine-Based Catalysts
10.1021/acs.oprd.9b00255 · 2019 · External reference
Amine-Functionalized Graphene Oxide-Stabilized Pd Nanoparticles (Pd@APGO): A Novel and Efficient Catalyst for the Suzuki and Carbonylative Suzuki-Miyaura Coupling Reactions
10.1021/acsomega.8b03023 · 2019 · External reference
Highly efficient method for Suzuki reactions in aqueous media
10.1021/acsomega.8b00469 · 2018 · External reference
Selective Synthesis of (Benzyl)biphenyls by Successive Suzuki-Miyaura Coupling of Phenylboronic Acids with 4-Bromobenzyl Acetate under Air Atmosphere
10.1021/acsomega.7b01450 · 2017 · External reference
Photo-Assisted Synthesis of a Pd-Ag@CQD Nanohybrid and Its Catalytic Efficiency in Promoting the Suzuki-Miyaura Cross-Coupling Reaction under Ligand-Free and Ambient Conditions
10.1021/acsomega.7b01504 · 2017 · External reference
Synthesis of Biaryls via a Nickel(0)-Catalyzed Cross-Coupling Reaction of Chloroarenes with Arylboronic Acids
10.1021/jo9707848 · 1997 · External reference
Synthesis and Characterization of Magnetic Zeolite Y-Palladium-Nickel Ferrite by Ultrasonic Irradiation and Investigating Its Catalytic Activity in Suzuki-Miyaura Cross-Coupling Reactions
10.1021/acsomega.9b00666 · 2019 · External reference
Ligand-controlled chemoselective C (acyl)–O bond vs C (aryl)–C bond activation of aromatic esters in nickel catalyzed C (sp2)–C(sp3) cross-couplings
10.1021/jacs.7b12865 · 2018 · External reference
Combined Theoretical and Experimental Studies of Nickel-Catalyzed Cross-Coupling of Methoxyarenes with Arylboronic Esters via C-O Bond Cleavage
10.1021/jacs.7b04279 · 2017 · External reference
Nickel-catalyzed cross-coupling of aryl phosphates with arylboronic acids
10.1021/jo2000034 · 2011 · External reference
Retention or inversion in stereospecific nickel-catalyzed cross-coupling of benzylic carbamates with arylboronic esters: control of absolute stereochemistry with an achiral catalyst
10.1021/ja311783k · 2013 · External reference
4-Dodecylbenzenesulfonic acid (DBSA) promoted solvent-free diversity-oriented synthesis of primary carbamates, S-thiocarbamates and ureas
10.1039/c5ra14528g · 2015 · External reference
Eco-Efficient Ultrasonic-Responsive Synthesis of Primary O-Alkyl and O-Aryl Thiocarbamates Using Brønsted Acid Ionic Liquid [H-NMP][HSO4] in Aqueous Media at Room Temperature
10.1002/slct.201800107 · 2018 · External reference
Synthesis of primary thiocarbamates by silica sulfuric acid as effective reagent under solid-state and solution conditions
10.1016/j.molstruc.2012.05.033 · 2012 · External reference
N,N-DiethylO-Carbamate: Directed Metalation Group and Orthogonal Suzuki–Miyaura Cross-Coupling Partner
10.1021/ja907700e · 2009 · External reference
C-O/C-H Coupling of Polyfluoroarenes with Aryl Carbamates by Cooperative Ni/Cu Catalysis
10.1021/acs.orglett.6b00819 · 2016 · External reference
Nickel-Catalyzed Cross-Couplings Involving Carbon–Oxygen Bonds
10.1021/cr100259t · 2011 · External reference
Selective Synthesis of Secondary Arylcarbamates via Efficient and Cost Effective Copper-Catalyzed Mono Arylation of Primary Carbamates with Aryl Halides and Arylboronic Acids
10.1007/s10562-017-2277-0 · 2018 · External reference
Ureas as safe carbonyl sources for the synthesis of carbamates with deep eutectic solvents (DESs) as efficient and recyclable solvent/catalyst systems
10.1039/c8nj02624f · 2018 · External reference
Highly efficient synthesis of alkyl and aryl primary thiocarbamates and dithiocarbamates under metal- and solvent-free conditions
10.1007/s11030-018-9831-6 · 2018 · External reference
Nickel/N-Heterocyclic Carbene-Catalyzed Suzuki-Miyaura Type Cross-Coupling of Aryl Carbamates
10.1021/acs.joc.6b01627 · 2016 · External reference
C-H arylation and alkenylation of imidazoles by nickel catalysis: solvent-accelerated imidazole C-H activation
10.1039/c5sc02942b · 2015 · External reference
Nickel(0)-Catalyzed Heck Cross-Coupling via Activation of Aryl C-OPiv Bonds
10.1021/ol203322v · 2012 · External reference
Nickel-Catalyzed Decarboxylative Cross-Coupling of Perfluorobenzoates with Aryl Halides and Sulfonates
10.1021/acs.orglett.5b00241 · 2015 · External reference
Nickel-catalysed Suzuki-Miyaura cross-coupling reactions of aryl halides with arylboronic acids in ionic liquids
10.1016/j.catcom.2014.08.037 · 2015 · External reference
N-Heterocyclic Carbene-Assisted, Bis(phosphine)nickel-Catalyzed Cross-Couplings of Diarylborinic Acids with Aryl Chlorides, Tosylates, and Sulfamates
10.1021/jo501291y · 2014 · External reference
Nickel-Catalyzed Suzuki-Miyaura Reaction of Aryl Fluorides
10.1021/ja207759e · 2011 · External reference
Development of an air-stable, broadly applicable nickel source for nickel-catalyzed cross-coupling
10.1021/acscatal.5b00498 · 2015 · External reference
Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates
10.1021/ol403209k · 2014 · External reference
A Modular, Air-Stable Nickel Precatalyst
10.1021/acs.orglett.5b00766 · 2015 · External reference
An air-stable binary Ni(0)-olefin catalyst
10.1038/s41929-019-0392-6 · 2020 · External reference
Mechanistic Study of an Improved Ni Precatalyst for Suzuki-Miyaura Reactions of Aryl Sulfamates: Understanding the Role of Ni(I) Species
10.1021/jacs.6b11412 · 2017 · External reference
Metal-Free Regioselective Monocyanation of Hydroxy-, Alkoxy-, and Benzyloxyarenes by Potassium Thiocyanate and Silica Sulfuric Acid as a Cyanating Agent
10.1021/acs.joc.8b02191 · 2019 · External reference
A Fe3O4@ SiO2/Schiff Base/Pd Complex as an Efficient Heterogeneous and Recyclable Nanocatalyst for One-Pot Domino Synthesis of Carbamates and Unsymmetrical Ureas
10.1002/ejoc.201901140 · 2019 · External reference
An Fe3O4@SiO2/Schiff base/Cu (ii) complex as an efficient recyclable magnetic nanocatalyst for selective mono N-arylation of primary O-alkyl thiocarbamates and primary O-alkyl carbamates with aryl halides and arylboronic acids
10.1039/c9nj00028c · 2019 · External reference
Superparamagnetic Fe3O4 Nanoparticles in a Deep Eutectic Solvent: An Efficient and Recyclable Catalytic System for the Synthesis of Primary Carbamates and Monosubstituted Ureas
10.1002/ejoc.201800581 · 2018 · External reference
One-pot synthesis of 1-and 5-substituted 1H-tetrazoles using 1, 4-dihydroxyanthraquinone–copper (II) supported on superparamagnetic Fe3O4@SiO2 magnetic porous nanospheres as a recyclable catalyst
10.1002/aoc.3518 · 2016 · External reference
Palladium nanoparticles immobilized on EDTA-modified Fe3O4@SiO2 nanospheres as an efficient and magnetically separable catalyst for Suzuki and Sonogashira cross-coupling reactions
10.1002/aoc.4302 · 2018 · External reference
Suzuki–Miyaura Cross-Coupling of Aryl Carbamates and Sulfamates: Experimental and Computational Studies
10.1021/ja200398c · 2011 · External reference
Recent advances in mechanistic studies on Ni catalyzed cross-coupling reactions
10.1016/s1872-2067(14)60217-5 · 2015 · External reference
Computational Insight into Nickel-Catalyzed Carbon-Carbon versus Carbon-Boron Coupling Reactions of Primary, Secondary, and Tertiary Alkyl Bromides
10.1002/chem.201500110 · 2015 · External reference
NiCl2Ě6H2O: an efficient catalyst precursor for phosphine-free Heck and Sonogashira cross-coupling reactions
10.1016/j.tet.2015.08.023 · 2015 · External reference
Role of Ni in hetero-architectured NiO/Ni composites for enhanced catalytic performance
10.1039/c7cp01332a · 2017 · External reference
Synthesis and characterizations of Ni-NiO nanoparticles on PDDA-modified graphene for oxygen reduction reaction
10.1186/1556-276x-9-444 · 2014 · External reference
Air-Stable Triazine-Based Ni(II) PNP Pincer Complexes As Catalysts for the Suzuki-Miyaura Cross-Coupling
10.1021/acs.orglett.6b01398 · 2016 · External reference
Suzuki–Miyaura Coupling of Aryl Carbamates, Carbonates, and Sulfamates
10.1021/ja906477r · 2009 · External reference
Rapid Nickel-Catalyzed Suzuki–Miyaura Cross-Couplings of Aryl Carbamates and Sulfamates Utilizing Microwave Heating
10.1021/jo1024464 · 2011 · External reference
An efficient Suzuki–Miyaura coupling of aryl sulfamates and boronic acids catalyzed by NiCl2 (dppp)
10.1002/ejoc.201200444 · 2012 · External reference
Nickel-Catalyzed Suzuki-Miyaura Coupling of Heteroaryl Ethers with Arylboronic Acids
10.1021/jo4005537 · 2013 · External reference
Synthesis of Functionalized 1, 4-Dioxanes with an Additional (Hetero) Aliphatic Ring
10.1055/s-0037-1610195 · 2018 · External reference
