Suzuki Miyaura
Mostrando 1-12 de 16 artigos, teses e dissertações.
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1. 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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2. 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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3. Suzuki-Miyaura Coupling between 3-Iodolawsone and Arylboronic Acids. Synthesis of Lapachol Analogues with Antineoplastic and Antileishmanial Activities
A series of 2-hydroxy-3-arylnaphthalene-1,4-diones (3-aryllawsones) were synthesized by Suzuki-Miyaura cross coupling reaction of 3-iodolawsone with arylboronic acids/esters. The hydroxylated resulting products were transformed into their corresponding N,N-diethyl carbamates. The antineoplastic and antileishmanial activities of the compounds were evaluated a
J. Braz. Chem. Soc.. Publicado em: 2017-08
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4. 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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5. 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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6. EFFECTS OF SOLVENT, BASE, AND TEMPERATURE IN THE OPTIMISATION OF A NEW CATALYTIC SYSTEM FOR SONOGASHIRA CROSS-COUPLING USING NCP PINCER PALLADACYCLE
The optimisation of a new catalyst system using NCP pincer palladacycle
1 was investigated using the experimental design technique. NCP pincer palladacycle1 was previously investigated in Suzuki-Miyaura and Heck-Mizoroki cross-couplings and found to be a highly efficient catalyst precursor. In this study, the effects of the typeQuím. Nova. Publicado em: 2015-06
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7. Synthesis of Biphenyl Tyrosine Via Cross-Coupling Suzuki-Miyaura Reaction Using Aryltrifluoroborate Salts
We reported a fast and easy method for obtaining biarylic units from tyrosine derivatives via Suzuki-Miyaura cross-coupling using a variety of substituted and unsubstituted potassium aryl- and heteroaryltrifluoroborate salts. The scope of the methodology was also extended to the formation of bis-tyrosine linked dipeptide bonds, leading to biologically intere
J. Braz. Chem. Soc.. Publicado em: 2015-04
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8. Desenvolvimento de reator tipo "dip catalyst" para filmes poliméricos contendo nanopartículas de metais de transição
This article describes the development of a new catalytic reactor designed to operate with nanoparticle-embedded polymer thin films. Stabilization of metal nanoparticles in films that serve as catalysts in organic reactions is relatively new; therefore, the development of reactors to facilitate their use is necessary. We describe in detail the preparation of
Quím. Nova. Publicado em: 2014
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9. Acoplamento Suzuki-Miyaura: uso de glicerol para síntese de ésteres arilboronatos e como solvente, e síntese de atropoisômeros
Nesta tese a reação de Suzuki-Miyaura será abordada em três diferentes enfoques: utilização de ésteres glicerolarilboronatos, emprego de glicerol como meio reacional e síntese de atropoisômeros a partir de ligantes nitrogenados N-N¿ quirais. Primeiramente, a reação do glicerol com ácido fenilborônico proporcionou uma mistura de ésteres cíclic
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 2012
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10. Funcionalização de cumarinas via reação de acoplamento de Suzuki-Miyaura de sais de organotrifluoroboratos de potássio / Functionalization of coumarins by Suzuki-Miayura cross-Coupling of potassium organotrifluoroborate salts
As cumarinas são compostos com potente atividade biológica. Foi explorada sua funcionalização, iniciando pela sua bromação, gerando o composto 3-bromocumarina, utilizado como material de partida para as reações de acoplamento do tipo Suzuki-Miyaura, que são uma das reações mais empregadas para a formação de ligação carbono-carbono, a qual util
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 08/04/2011
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11. Estudo teórico de efeitos de solvatação do tetraidrofurano sobre um mecanismo modelo de Suzuki-Miyaura / Theoretical study of the effects of tetrahydrofuran s solvation over a Suzuki-Miyaura s model mechanism
Utilizando a implementação do método da coordenada geradora discretizada nos orbitais atômicos, conjuntos de bases adaptados ao pseudopotencial de caroço SBKJC (conjuntos GBSMCS) foram desenvolvidos, validados e utilizados no estudo de possíveis efeitos de solvatação do tetraidrofurano sobre um mecanismo modelo de Suzuki-Miyaura. As metodologias de v
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 03/02/2011
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12. Synthesis of novel kavain-like derivatives and evaluation of their cytotoxic activity
Reações de acoplamento do tipo Heck, Sonogashira-Hagihara, Suzuki-Miyaura e reação de aldolisação catalizadas por metal foram utilizadas para a obtenção de três séries de δ-valerolactonas substituídas em posições 3, 4, 5 e 6 do anel lactônico. As 26 δ-valerolactonas sintetizadas foram testadas contra três linhagens celulares e cinco delas ex
Journal of the Brazilian Chemical Society. Publicado em: 2009