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Mostrando 81 - 100 Resultados de 21,955 Para Buscar '"Suzuki"', tiempo de consulta: 0.33s Limitar resultados
  1. 81
    “…[Image: see text] Stable, catalytically active palladium nanoparticles of various average diameters (1.9–7.4 nm) have been synthesized and characterized by X-ray diffraction, spectroscopy, and microscopy techniques to demonstrate remarkable size-dependent and renewed catalytic activity toward the Suzuki–Miyaura coupling reaction in green protocol. …”
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    Size-Dependent Catalytic Activity and Fate of Palladium Nanoparticles in Suzuki–Miyaura Coupling Reactions
  2. 82
    por Knoll, Daniel M., Bräse, Stefan
    Publicado 2018
    “…[Image: see text] We report a new Suzuki cross-coupling protocol for high yielding derivatization of [2.2]paracyclophane with pyridyl and pyrimidyl substituents. …”
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    Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates with Pyridyl and Pyrimidyl Building Blocks
  3. 83
    “…Suzuki cross-coupling reactions catalyzed by palladium are powerful tools for the synthesis of functional organic compounds. …”
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    Palladium-bearing intermetallic electride as an efficient and stable catalyst for Suzuki cross-coupling reactions
  4. 84
    “…In this work, a Ni-catalyzed migratory Suzuki–Miyaura cross-coupling featuring high benzylic or allylic selectivity has been developed. …”
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    Reaction scope and mechanistic insights of nickel-catalyzed migratory Suzuki–Miyaura cross-coupling
  5. 85
    “…Aryl substituted thiazolyl coumarin derivatives were synthesized via Suzuki cross-coupling reaction. A detailed reaction condition optimization revealed that the Pd-PEPPSI-IPent precatalyst in only 2 mol% loading resulted in the desired product with high yield. …”
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    Computational and biological studies of novel thiazolyl coumarin derivatives synthesized through Suzuki coupling
  6. 86
    “…The stereoselective Suzuki–Miyaura cross-coupling of (Z)-β-enamido triflates is demonstrated. …”
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    Ligand-dependent stereoselective Suzuki–Miyaura cross-coupling reactions of β-enamido triflates
  7. 87
    “…Herein, we report the use of the Suzuki–Miyaura cross-coupling reaction for the preparation of a library of synthetic derivatives of flavonoids for biological activity assays. …”
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    Preparation of Synthetic and Natural Derivatives of Flavonoids Using Suzuki–Miyaura Cross-Coupling Reaction
  8. 88
    por Schulte, Robin, Ihmels, Heiko
    Publicado 2022
    “…Thus, the 4,4,5,5-tetramethyl-2-(bicyclo[2.2.1]heptadien-2-yl)-1,3,2-dioxaborolane was prepared and shown to be a suitable substrate for Pd-catalyzed Suzuki–Miyaura coupling reactions with selected haloarenes. …”
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    Borylated norbornadiene derivatives: Synthesis and application in Pd-catalyzed Suzuki–Miyaura coupling reactions
  9. 89
    “…An archazolid natural product fragment that displays dose-dependent inhibition of the vacuolar-type ATPase (VATPase) has been synthesized by a high-yielding Suzuki coupling of two complex subunits. Similarly, a further simplified fragment was prepared and evaluated for VATPase inhibitory activity. …”
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    Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments
  10. 90
    “…A small fenbufen library comprising 18 compounds was prepared via Suzuki Miyara coupling. The five-step preparations deliver 9–17% biphenyl compounds in total yield. …”
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    Antiinflammation Derived Suzuki-Coupled Fenbufens as COX-2 Inhibitors: Minilibrary Construction and Bioassay
  11. 91
    por Li, Jianbin, Huang, Chia-Yu, Li, Chao-Jun
    Publicado 2022
    “…Here, we present a ligand-enabled metallaphotoredox Suzuki-Miyaura cross-coupling protocol for the facile synthesis of diarylmethanes. …”
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    A ligand-enabled metallaphotoredox protocol for Suzuki-Miyaura cross-couplings for the synthesis of diarylmethanes
  12. 92
    “…Here, we report the use of a single-atom Pd catalyst for the classic Suzuki–Miyaura carbon–carbon coupling reaction under phosphine-free and open-air conditions at room temperature. …”
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    Atomically dispersed palladium catalyses Suzuki–Miyaura reactions under phosphine-free conditions
  13. 93
    “…Pd-catalyzed Suzuki–Miyaura cross-coupling is one of the most straightforward and versatile methods for the construction of functionalized arenes and heteroarenes but site-selective cross-coupling of polyhalogenated (hetero)arenes containing identical halogen substituents remains a challenging problem. …”
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    Heterocyclic Suzuki–Miyaura coupling reaction of metalla-aromatics and mechanistic analysis of site selectivity
  14. 94
    por Suzuki, Ichiro, 1935-
    Publicado 1989
    Libro
    Corrosion-resistant coatings technology /
  15. 95
    “…We developed a new catalytic system that efficiently catalyzes Suzuki–Miyaura reactions in water without the need for an organic solvent, as confirmed by NMR. …”
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    Functionalization of Framboidal Phenylboronic Acid-Containing Nanoparticles via Aqueous Suzuki–Miyaura Coupling Reactions
  16. 96
    “…Analysis and screening of aqueous Pd(0) ligand systems has revealed the importance of a guanidine core and the discovery of 1,1-dimethylguanidine as an enhanced ligand for aqueous Suzuki–Miyaura cross-coupling. This novel Pd catalyst system has now allowed the labeling of small molecules, peptides, and proteins with the fluorine-18 prosthetic [(18)F]4-fluorophenylboronic acid. …”
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    Enhanced Aqueous Suzuki–Miyaura Coupling Allows Site-Specific Polypeptide (18)F-Labeling
  17. 97
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    DNA Modification under Mild Conditions by Suzuki–Miyaura Cross-Coupling for the Generation of Functional Probes**
  18. 98
    “…[Image: see text] The carbonylative Suzuki–Miyaura reaction between aryl bromides and arylboronic acid equivalents is herein reported, using base-free conditions and a limited excess of carbon monoxide generated ex situ from stable CO-precursors. …”
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    Carbonylative Suzuki Couplings of Aryl Bromides with Boronic Acid Derivatives under Base-Free Conditions
  19. 99
    “…In this study, we examined hepatic and splenic histopathological findings in the early stage of NASH using the Tsumura Suzuki Obese Diabetes (TSOD) mouse model established for assessing NASH. …”
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    Involvement of splenic iron accumulation in the development of nonalcoholic steatohepatitis in Tsumura Suzuki Obese Diabetes mice
  20. 100
    “…Suzuki–Miyaura cross-coupling reactions of heteroaryl polyhalides with aryl boronates are surveyed. …”
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    Site-selective Suzuki–Miyaura coupling of heteroaryl halides – understanding the trends for pharmaceutically important classes
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