Synthesis of Functionalized 1, 4-Dioxanes with an Additional (Hetero) Aliphatic Ring
10.1055/s-0037-1610195 · doi-reference
Nickel-Catalyzed Suzuki-Miyaura Coupling of Heteroaryl Ethers with Arylboronic Acids
10.1021/jo4005537 · doi-reference
An efficient Suzuki–Miyaura coupling of aryl sulfamates and boronic acids catalyzed by NiCl2 (dppp)
10.1002/ejoc.201200444 · doi-reference
Rapid Nickel-Catalyzed Suzuki–Miyaura Cross-Couplings of Aryl Carbamates and Sulfamates Utilizing Microwave Heating
10.1021/jo1024464 · doi-reference
Suzuki–Miyaura Coupling of Aryl Carbamates, Carbonates, and Sulfamates
10.1021/ja906477r · doi-reference
Air-Stable Triazine-Based Ni(II) PNP Pincer Complexes As Catalysts for the Suzuki-Miyaura Cross-Coupling
10.1021/acs.orglett.6b01398 · doi-reference
Synthesis and characterizations of Ni-NiO nanoparticles on PDDA-modified graphene for oxygen reduction reaction
10.1186/1556-276x-9-444 · doi-reference
Role of Ni in hetero-architectured NiO/Ni composites for enhanced catalytic performance
10.1039/c7cp01332a · doi-reference
NiCl2Ě6H2O: an efficient catalyst precursor for phosphine-free Heck and Sonogashira cross-coupling reactions
10.1016/j.tet.2015.08.023 · doi-reference
Computational Insight into Nickel-Catalyzed Carbon-Carbon versus Carbon-Boron Coupling Reactions of Primary, Secondary, and Tertiary Alkyl Bromides
10.1002/chem.201500110 · doi-reference
Recent advances in mechanistic studies on Ni catalyzed cross-coupling reactions
10.1016/s1872-2067(14)60217-5 · doi-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 · doi-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 · doi-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 · doi-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 · doi-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 · doi-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 · doi-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 · doi-reference
An air-stable binary Ni(0)-olefin catalyst
10.1038/s41929-019-0392-6 · doi-reference
A Modular, Air-Stable Nickel Precatalyst
10.1021/acs.orglett.5b00766 · doi-reference
Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates
10.1021/ol403209k · doi-reference
Development of an air-stable, broadly applicable nickel source for nickel-catalyzed cross-coupling
10.1021/acscatal.5b00498 · doi-reference
Nickel-Catalyzed Suzuki-Miyaura Reaction of Aryl Fluorides
10.1021/ja207759e · doi-reference
N-Heterocyclic Carbene-Assisted, Bis(phosphine)nickel-Catalyzed Cross-Couplings of Diarylborinic Acids with Aryl Chlorides, Tosylates, and Sulfamates
10.1021/jo501291y · doi-reference
Nickel-catalysed Suzuki-Miyaura cross-coupling reactions of aryl halides with arylboronic acids in ionic liquids
10.1016/j.catcom.2014.08.037 · doi-reference
Nickel-Catalyzed Decarboxylative Cross-Coupling of Perfluorobenzoates with Aryl Halides and Sulfonates
10.1021/acs.orglett.5b00241 · doi-reference
Nickel(0)-Catalyzed Heck Cross-Coupling via Activation of Aryl C-OPiv Bonds
10.1021/ol203322v · doi-reference
C-H arylation and alkenylation of imidazoles by nickel catalysis: solvent-accelerated imidazole C-H activation
10.1039/c5sc02942b · doi-reference
Nickel/N-Heterocyclic Carbene-Catalyzed Suzuki-Miyaura Type Cross-Coupling of Aryl Carbamates
10.1021/acs.joc.6b01627 · doi-reference
Suzuki–Miyaura Cross-Coupling of Aryl Carbamates and Sulfamates: Experimental and Computational Studies
10.1021/ja200398c · doi-reference
