Coupling Reactions
Mostrando 1-12 de 210 artigos, teses e dissertações.
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1. Desenvolvimento de software e interface para o controle por retroalimentação atrasada em sistemas eletroquímicos
In this paper, we show the development of a LabVIEW algorithm able to apply the delayed feedback control on oscillatory electrochemical reactions. The coupling of the control and the experiments was carried out by a real-time apparatus, measuring the faradaic current and, in sequence, applying a calculated circuit voltage as an analog output. The setup was u
Quím. Nova. Publicado em: 2021-06
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2. PMMA-SiO2 Organic-Inorganic Hybrid Coating Application to Ti-6Al-4V Alloy Prepared through the Sol-Gel Method
Siloxane-poly(methyl methacrylate) (PMMA) hybrid was synthesized based on the sol-gel method and applied to Ti-6Al-4V through dip-coating. The structural feature of the hybrid was subjected to Fourier-transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TG); its morphological properties were analyzed through scanning electron microscope (SE
J. Braz. Chem. Soc.. Publicado em: 2020-02
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3. Palladium Nanoparticles Supported on β-cyclodextrin Functionalised Poly(amido amine)s and their Application in Suzuki-Miyaura Cross-Coupling Reactions
Herein, the synthesis, characterization and catalytic application of an organic-inorganic, palladium (Pd)-containing hybrid material, poly(amidoamine)-cyclodextrin (Pd@PAAs-CD), is reported as an efficient catalyst for Suzuki-Miyaura coupling reactions. The structure of Pd@PAAs-CD was confirmed by Fourier transform infrared spectroscopy (FTIR), transmission
J. Braz. Chem. Soc.. Publicado em: 12/08/2019
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4. New Palladacycle-Derived Acylhydrazones as Pre-catalysts in Mirozoki-Heck Coupling and Oxyarylations
ABSTRACT New acylhydrazone-based palladacycles are prepared and evaluated as pre-catalysts in Mirozoki-Heck and oxyarylation reactions.
An. Acad. Bras. Ciênc.. Publicado em: 14/05/2018
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5. MÉTODOS AMBIENTALMENTE AMIGÁVEIS PARA A IODAÇÃO REGIOSSELETIVA DA 3,7,3’,4’-TETRAMETOXI-QUERCETINA
Halogenated compounds are valuable substrates for the field of organic synthesis and more specifically as reagents for coupling reactions. Environmental friendly procedures for regioselective iodination is the aim of this study, using four different methods previously described in the literature, that embrace green chemistry concepts, to obtain the 6- and 8-
Quím. Nova. Publicado em: 2018-05
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6. Cellulose Oxidation and the Use of Carboxyl Cellulose Metal Complexes in Heterogeneous Catalytic Systems to Promote Suzuki-Miyaura Coupling and C-O Bond Formation Reaction
This work shows the modification of microcrystalline cellulose by the selective oxidation of primary hydroxyl groups to carboxylate groups by a 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO)-mediated system and its application as a heterogeneous ligand by ionic exchange with catalytic metals ions such as palladium, nickel and copper. Afterwards is desc
J. Braz. Chem. Soc.. Publicado em: 2017-11
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7. Microwave Assisted Synthesis of Novel Six-Membered 4-C, 4-O and 4-S Lactams Derivatives: Characterization and in vitro Biological Evaluation of Cytotoxicity and Anticoagulant Activity
A series of six-membered lactam derivatives containing C, O and S atoms in position 4 were synthesized using microwave methodology through coupling reactions. The novel compounds were synthesized following two step reaction to yield fifteen derivatives. The final derivative N-(4-(3-oxotiomorpholin)phenyl) hexanamide was selectively toxic to the HCT-116 cell
J. Braz. Chem. Soc.. Publicado em: 2017-02
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8. PdCl2 Immobilized in Polyacrylamide: a Low Cost and Eco-Friendly Catalyst for Suzuki-Miyaura Reactions
PdCl2 immobilized in polyacrylamide (PAM), named Pd/PAM, produced at an extremely low cost, was found to be an efficient catalyst for Suzuki-Miyaura cross-coupling reactions. Iodo- and bromoarenes may couple with phenylboronic acid under eco-friendly conditions (i.e., phosphine-free and with ethanol as the solvent) to give excellent product yields. Aryl chlo
J. Braz. Chem. Soc.. Publicado em: 2016-04
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9. Coupling DLLME-CE for the Stereoselective Analysis of Venlafaxine and Its Main Metabolites after Biotransformation by Fungi
Fungal biotransformations have become very important in the study of chiral drugs because the reactions performed by these microorganisms may be enantioselective. However, analyses of analytes present in liquid culture medium have proved to be very difficult due to the complexity of this matrix. The aim of this work was to couple dispersive liquid-liquid mic
J. Braz. Chem. Soc.. Publicado em: 2015-09
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10. Palladium Nanoparticles Supported on Poly(
N -vinylpyrrolidone)-Grafted Silica as an Efficient Catalyst for Copper-Free Sonogashira and Suzuki Cross-Coupling ReactionsPalladium catalyst based on polyvinylpyrrolidone-silica hybrid support was prepared and exhibited excellent activity and stability in copper, amine and phosphine-free Sonogashira-Hagihara and Suzuki-Miyaura cross-coupling reactions. The polymeric catalyst was applied efficiently in the coupling reactions of chloro (as well as iodo) and bromoarenes. Elemen
J. Braz. Chem. Soc.. Publicado em: 2015-08
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11. Agarose-Alumina Composite Supported Palladium Catalyst for Suzuki Coupling Reactions
The palladium catalyst supported on agarose-alumina composite and its utilization in the Suzuki reaction have been investigated. The agarose-alumina composite was prepared and modified with organofunctional groups by reacting with the coupling reagent 3-aminopropyltriethoxysilane (APTES) through Al−O−Si bonds. Palladium was efficiently loaded on the comp
J. Braz. Chem. Soc.. Publicado em: 2015-04
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12. Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
A grande capacidade do paládio de formar ligações carbono-carbono entre substratos apropriadamente funcionalizados permitiu que os químicos orgânicos efetuassem transformações antes impossíveis ou alcançáveis somente através de rotas muito longas. Neste contexto, uma das mais elegantes e importantes aplicações das reações de acoplamento cruzad
J. Braz. Chem. Soc.. Publicado em: 2014-12