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Mostrando 241 - 260 Resultados de 21,955 Para Buscar '"Suzuki"', tiempo de consulta: 0.42s Limitar resultados
  1. 241
    “…This light-controllable solubility was exploited to affect the catalytic activity in the Suzuki coupling reaction. The effect of the substrate and catalyst concentration and light intensity on the proceeding and outcome of the reaction was studied. …”
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    A photoresponsive palladium complex of an azopyridyl-triazole ligand: light-controlled solubility drives catalytic activity in the Suzuki coupling reaction
  2. 242
    “…The 3-aryl-1-phosphinoimidazo[1,5-a]pyridine ligands were evaluated in palladium-catalyzed sterically-hindered biaryl and heterobiaryl Suzuki–Miyaura cross-coupling reactions.…”
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    Synthesis of 3-aryl-1-phosphinoimidazo[1,5-a]pyridine ligands for use in Suzuki–Miyaura cross-coupling reactions
  3. 243
    “…The influences of the cyclometalated ligand at the Ir(iii) center on the photophysical and electrochemical properties as well as photocatalytic activity for the Suzuki–Miyaura coupling reaction under mild conditions were evaluated. …”
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    Photoaccelerated energy transfer catalysis of the Suzuki–Miyaura coupling through ligand regulation on Ir(iii)–Pd(ii) bimetallic complexes
  4. 244
    “…A large 1,3-phenylene-bridged hexameric naphthalene wheel N6 and a heptameric wheel N7 were synthesized simply by Suzuki–Miyaura coupling via one-pot reaction from monomers. …”
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    1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C(60)
  5. 245
    “…In pure water, the catalytic activity of nanocatalyst [C(60)-TEG(S)/PdCl(2)] for Suzuki–Miyaura cross-coupling reaction was investigated under different reaction conditions. …”
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    Highly efficient and recyclable water-soluble fullerene-supported PdCl(2) nanocatalyst in Suzuki–Miyaura cross-coupling reaction
  6. 246
    “…[Image: see text] We report here a mechanistically distinct approach to achieve Suzuki–Miyaura-type cross-couplings between alkyl iodides and aryl organoborons. …”
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    Merging Halogen-Atom Transfer (XAT) and Copper Catalysis for the Modular Suzuki–Miyaura-Type Cross-Coupling of Alkyl Iodides and Organoborons
  7. 247
    “…An efficient method for the C-C bond formation via water soluble Na(2)PdCl(4)/sSPhos mediated Suzuki-Miyaura cross-coupling reaction of DNA-conjugated aryl iodide with (het)aryl boronic acids has been developed. …”
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    DNA-Compatible Suzuki-Miyaura Cross-Coupling Reaction of Aryl Iodides With (Hetero)Aryl Boronic Acids for DNA-Encoded Libraries
  8. 248
    “…Moreover, the prepared catalyst could be reused at least 10 times in the Suzuki–Miyaura coupling reaction with high yield.…”
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    One-step synthesis of PdCu@Ti(3)C(2) with high catalytic activity in the Suzuki–Miyaura coupling reaction
  9. 249
    “…The investigation of the catalytic activity of these new ligands in the demanding palladium‐catalyzed Suzuki–Miyaura coupling of o‐dibromoarenes with fluorophenylboronic acid underlined the importance of the amino ester dicyclohexylphosphinoferrocene for avoiding the deleterious homocoupling and arene oligomerization side‐reactions that were otherwise observed with the other phosphine ligands.…”
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    Hybrid Phosphine/Amino‐Acid Ligands Built on Phenyl and Ferrocenyl Platforms: Application in the Suzuki Coupling of o‐Dibromobenzene with Fluorophenylboronic Acid
  10. 250
    “…The robustness of the PG and the ability of the LMWG to reduce Pd(II) in situ to generate naked Pd(0) nanoparticles (PdNPs) combine within these gel beads to give them potential as practical catalysts for Suzuki–Miyaura cross-coupling reactions. The optimized gel beads demonstrate good reusability, green metrics, and most importantly the ability to sustain stirring, improving reaction times and energy consumption compared to previous examples. …”
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    Mechanically Robust Hybrid Gel Beads Loaded with “Naked” Palladium Nanoparticles as Efficient, Reusable, and Sustainable Catalysts for the Suzuki–Miyaura Reaction
  11. 251
    Publicado 1996
    Procedimiento de la Conferencia Libro
    Nihongo kyojuho wakushoppu /
  12. 252
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    Overcoming exponential scaling with system size in Trotter-Suzuki implementations of constrained Hamiltonians: 2+1 U(1) lattice gauge theories
  13. 253
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    Rapid plugged flow synthesis of nucleoside analogues via Suzuki-Miyaura coupling and heck Alkenylation of 5-Iodo-2’-deoxyuridine (or cytidine)
  14. 254
    “…In view of this, we have synthesized novel 3-aryl-N-methyl-1,2,5,6-tetrahydropyridine derivatives 5a-k by Suzuki coupling and screened the efficacy of these derivatives for their AChE inhibitor activity.…”
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    Synthesis of Novel 3-Aryl-N-Methyl-1,2,5,6-Tetrahydropyridine Derivatives by Suzuki coupling: As Acetyl Cholinesterase Inhibitors
  15. 255
    “…A stereoselective and 1,4-benzoquinone-mediated palladium(II)-catalyzed Heck/Suzuki domino reaction involving metal coordinating cyclic methylamino vinyl ethers and a number of electronically diverse arylboronic acids has been developed and studied. …”
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    Development of Stereocontrolled Palladium(II)-Catalyzed Domino Heck/Suzuki β,α-Diarylation Reactions with Chelating Vinyl Ethers and Arylboronic Acids
  16. 256
    “…In the present study, in situ Mössbauer and magnetic circular dichroism spectroscopic studies combined with inorganic syntheses and reaction studies are employed to evaluate the in situ formed iron species and identify the active catalytic species in iron–SciOPP catalyzed Suzuki–Miyaura and Kumada cross-couplings of phenyl nucleophiles and secondary alkyl halides. …”
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    Iron(II) Active Species in Iron–Bisphosphine Catalyzed Kumada and Suzuki–Miyaura Cross-Couplings of Phenyl Nucleophiles and Secondary Alkyl Halides
  17. 257
    “…The Suzuki–Miyaura cross-coupling has been widely recognized as one of the most important methods for the construction of C–C bonds. …”
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    Suzuki–Miyaura cross-coupling of amides and esters at room temperature: correlation with barriers to rotation around C–N and C–O bonds
  18. 258
    “…The Suzuki–Miyaura (SM) reaction is one of the most important methods for C−C bond formation in chemical synthesis. …”
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    A Zinc Catalyzed C(sp(3))−C(sp(2)) Suzuki–Miyaura Cross‐Coupling Reaction Mediated by Aryl‐Zincates
  19. 259
    “…Correction for ‘Palladium-scavenging self-assembled hybrid hydrogels – reusable highly-active green catalysts for Suzuki–Miyaura cross-coupling reactions’ by Petr Slavík et al., Chem. …”
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    Correction: Palladium-scavenging self-assembled hybrid hydrogels – reusable highly-active green catalysts for Suzuki–Miyaura cross-coupling reactions
  20. 260
    “…A revised modular approach to various synthetic (–)‐trans‐Δ(8)‐THC derivatives through late‐stage Suzuki–Miyaura cross‐coupling reactions is disclosed. …”
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    A Revised Modular Approach to (–)‐trans‐Δ(8)‐THC and Derivatives Through Late‐Stage Suzuki–Miyaura Cross‐Coupling Reactions
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