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101por Corral, Jorge A., López, María I., Esquivel, Dolores, Mora, Manuel, Jiménez-Sanchidrián, César, Romero-Salguero, Francisco J.“…All Pd-supported samples were active in the Suzuki cross-coupling reaction between bromobenzene and phenylboronic acid.…”
Publicado 2013
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103“…These results extend the scope of the already very versatile Suzuki–Miyaura reaction toward the synthesis of very electron-poor products, making these more readily accessible. …”
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104por Qiu, Li, McCaffrey, Ryan, Jin, Yinghua, Gong, Yu, Hu, Yiming, Sun, Hongliang, Park, Wounjhang, Zhang, Wei“…When provided with a protective cage shell with minimum surface coverage, such PdNPs are capable of catalyzing organic reactions, showing high catalytic activity in Suzuki–Miyaura coupling reactions.…”
Publicado 2017
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105Post-transcriptional labeling by using Suzuki–Miyaura cross-coupling generates functional RNA probes“…Taken together, this simple approach of generating functional RNA ON probes by Suzuki–Miyaura coupling will be a very important addition to the resources and tools available for analyzing RNA motifs.…”
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106por Zhang, Sheng‐Yan, Yu, Kai, Guo, Yu‐Shuang, Mou, Rui‐Qi, Lu, Xiao‐Fan, Guo, Dian‐Shun“…These catalysts can efficiently catalyze copper‐free Sonogashira, Suzuki and Heck coupling reactions of various aryl iodides, bromides, and chlorides in aqueous media under phosphine‐ligand‐ and organic‐base‐free conditions. …”
Publicado 2018
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107“…The setup for photocatalytic Suzuki reactions triggered by Pd–Azo–POP under conventional batch reaction mode as well as in a prototypal continuous flow system has also been provided in addition to the detailed catalytic data including (1)H and (13)C NMR spectra of the obtained products. …”
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108“…An efficient arylation of SEM-protected pyrroles by the Suzuki–Miyaura coupling reaction has been developed. …”
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109“…The present report implements a decarbonylative version with loss of carbon monoxide (CO) that enables to directly engage carboxylic acids in a Suzuki-Miyaura cross-coupling to produce biaryls as a general method with high cross-coupling selectivity using a well-defined Pd(0)/(II) catalytic cycle. …”
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110“…Palladium-catalyzed Suzuki–Miyaura cross-coupling or aryl halides is widely employed in the synthesis of many important molecules in synthetic chemistry, including pharmaceuticals, polymers and functional materials. …”
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111“…[Image: see text] An improved method for the nickel-catalyzed Suzuki–Miyaura cross-coupling of alkenyl ethers is reported. …”
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112por Khan, Mujeeb, Shaik, Mohammed Rafi, Adil, Syed Farooq, Kuniyil, Mufsir, Ashraf, Muhammad, Frerichs, Hajo, Sarif, Massih Ahmad, Siddiqui, Mohammed Rafiq H., Al–Warthan, Abdulrahman, Labis, Joselito P., Islam, Mohammad Shahidul, Tremel, Wolfgang, Tahir, Muhammad Nawaz“…The kinetics of the catalytic reaction (Suzuki coupling) using HRG-Py-Pd nanocomposite was monitored using gas chromatography (GC).…”
Publicado 2020
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113“…Methods: A total of 126 patients in different Suzuki stages (II, III, IV, and V) of iMMD who underwent bypass surgery from April 2013 to August 2020 were included in this retrospective study. …”
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114“…Herein we report that biogenic palladium nanoparticles generated by the sulfate-reducing bacterium Desulfovibrio alaskensis G20 catalyse the ligand-free Suzuki Miyaura reaction of abiotic substrates. The reaction is highly efficient (>99% yield, 0.5 mol% Pd), occurs under mild conditions (37 °C, aqueous media) and can be accelerated within biocompatible micelles at the cell membrane to yield products containing challenging biaryl bonds. …”
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115por Nikoshvili, Linda Zh., Shkerina, Kristina N., Bykov, Alexey V., Sidorov, Alexander I., Vasiliev, Alexander L., Sulman, Mikhail G., Kiwi-Minsker, Lioubov“…This work addresses the Suzuki cross-coupling between 4-bromoanisole (BrAn) and phenylboronic acid (PBA) in an environmentally benign ethanol–water solvent catalysed by mono- (Pd) and bimetallic (PdAu, PdCu, PdZn) nanoparticles (NPs) stabilised within hyper-cross-linked polystyrene (HPS) bearing tertiary amino groups. …”
Publicado 2021
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117por Vincent, Cooper A., Long, Evan T., Jones, Holly C., Young, Jeffrey C., Spiegel, P. Clint, O’Neil, Gregory W.“…Correction for ‘Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments’ by Cooper T. …”
Publicado 2019
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118Enabling Suzuki–Miyaura coupling of Lewis-basic arylboronic esters with a nonprecious metal catalystpor Haibach, Michael C., Ickes, Andrew R., Tcyrulnikov, Sergei, Shekhar, Shashank, Monfette, Sebastien, Swiatowiec, Rafal, Kotecki, Brian J., Wang, Jason, Wall, Amanda L., Henry, Rodger F., Hansen, Eric C.“…The high cost and negative environmental impact of precious metal catalysts has led to increased demand for nonprecious alternatives for widely practiced reactions such as the Suzuki–Miyaura coupling (SMC). Ni-catalyzed versions of this reaction have failed to achieve high reactivity with Lewis-basic arylboron nucleophiles, especially pinacolboron esters. …”
Publicado 2022
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119por Riva, Laura, Nicastro, Gloria, Liu, Mingchong, Battocchio, Chiara, Punta, Carlo, Sacchetti, Alessandro“…The new composite turned to be an efficient heterogeneous pre-catalyst for promoting Suzuki–Miyaura coupling reactions between aryl halides and phenyl boronic acid in water, obtaining yields higher than 90% in 30 min, by operating in a microwave reactor at 100 °C and with just 2% w/w of CNS-Pd catalyst with respect to aryl halides (4.5‰ for Pd). …”
Publicado 2022
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