Academic literature on the topic 'Mizoroki-Heck cross-coupling'

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Journal articles on the topic "Mizoroki-Heck cross-coupling"

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Jadhav, Sanjay N., and Chandrashekhar V. Rode. "An efficient palladium catalyzed Mizoroki–Heck cross-coupling in water." Green Chemistry 19, no. 24 (2017): 5958–70. http://dx.doi.org/10.1039/c7gc02869e.

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Watson, Allan, Kirsty Wilson, Jane Murray, Helen Sneddon, and Craig Jamieson. "Dimethylisosorbide (DMI) as a Bio-Derived Solvent for Pd-Catalyzed Cross-Coupling Reactions." Synlett 29, no. 17 (2018): 2293–97. http://dx.doi.org/10.1055/s-0037-1611054.

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Palladium-catalyzed bond-forming reactions, such as the ­Suzuki–Miyaura and Mizoroki–Heck reactions, are some of the most broadly utilized reactions within the chemical industry. These reactions frequently employ hazardous solvents; however, to adhere to increasing sustainability pressures and restrictions regarding the use of such solvents, alternatives are highly sought after. Here we demonstrate the utility of dimethyl isosorbide (DMI) as a bio-derived solvent in several benchmark Pd-catalyzed reactions: Suzuki–Miyaura (13 examples, 62–100% yield), Mizoroki–Heck (13 examples, 47–91% yield),
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Wang, Shi-Meng, Hai-Xia Song, Xiao-Yan Wang, Nan Liu, Hua-Li Qin, and Cheng-Pan Zhang. "Palladium-catalyzed Mizoroki–Heck-type reactions of [Ph2SRfn][OTf] with alkenes at room temperature." Chemical Communications 52, no. 80 (2016): 11893–96. http://dx.doi.org/10.1039/c6cc06089g.

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Puthiaraj, Pillaiyar, and Kasi Pitchumani. "Palladium nanoparticles supported on triazine functionalised mesoporous covalent organic polymers as efficient catalysts for Mizoroki–Heck cross coupling reaction." Green Chem. 16, no. 9 (2014): 4223–33. http://dx.doi.org/10.1039/c4gc00412d.

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Moitra, Nirmalya, Ayumi Matsushima, Toshiyuki Kamei, et al. "A new hierarchically porous Pd@HSQ monolithic catalyst for Mizoroki–Heck cross-coupling reactions." New J. Chem. 38, no. 3 (2014): 1144–49. http://dx.doi.org/10.1039/c3nj01433a.

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Matsheku, Asanda C., Richard Tia, Munaka C. Maumela, and Banothile C. E. Makhubela. "Ferrocenylimine Palladium (II) Complexes: Synthesis, Characterization and Application in Mizoroki-Heck and Suzuki-Miyaura Cross-Coupling Reactions." Catalysts 11, no. 7 (2021): 755. http://dx.doi.org/10.3390/catal11070755.

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Carbon-carbon cross-coupling reactions are essential synthetic tools for synthesizing polymers, natural products, agrochemicals, and pharmaceuticals. Therefore, new catalysts that function with greater efficiency and functional group tolerance are being researched. We have prepared new ferrocenylimine monodentate N and P donor ligands and N^N and N^P bidentate chelating ligands (L1 to L4) employed in stabilizing palladium ions for application in Mizoroki-Heck and Suzuki-Miyaura cross-coupling reactions. The ferrocenylimine ligands were successfully synthesized by Schiff base condensation react
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Nejat, Razieh, Ali Reza Mahjoub, Zahra Hekmatian, and Tahereh Azadbakht. "Pd-functionalized MCM-41 nanoporous silica as an efficient and reusable catalyst for promoting organic reactions." RSC Advances 5, no. 21 (2015): 16029–35. http://dx.doi.org/10.1039/c4ra11850b.

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Rangraz, Yalda, Firouzeh Nemati, and Ali Elhampour. "Organoselenium–palladium(ii) complex immobilized on functionalized magnetic nanoparticles as a promising retrievable nanocatalyst for the “phosphine-free” Heck–Mizoroki coupling reaction." New Journal of Chemistry 42, no. 18 (2018): 15361–71. http://dx.doi.org/10.1039/c8nj02433b.

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An air- and moisture-stable organoselenium–palladium complex immobilized on silica-coated magnetic nanoparticles is designed, synthesized and applied as a practical and retrievable catalyst in the Heck–Mizoroki cross-coupling reaction.
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Loska, Rafal, Chandra M Rao Volla, and Pierre Vogel. "Iron-Catalyzed Mizoroki-Heck Cross-Coupling Reaction with Styrenes." Advanced Synthesis & Catalysis 350, no. 18 (2008): 2859–64. http://dx.doi.org/10.1002/adsc.200800662.

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Knowles, Jonathan P., and Andrew Whiting. "The Heck–Mizoroki cross-coupling reaction: a mechanistic perspective." Org. Biomol. Chem. 5, no. 1 (2007): 31–44. http://dx.doi.org/10.1039/b611547k.

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Dissertations / Theses on the topic "Mizoroki-Heck cross-coupling"

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Mabit, Thibaud. "Vers la première synthèse totale de la kidamycine : développement d’une stratégie de synthèse convergente et innovante, et mise au point d’une réaction d’aryl-C-glycosylation stéréospécifique." Thesis, Le Mans, 2018. http://www.theses.fr/2018LEMA1023/document.

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La kidamycine, première molécule de la famille des pluramycines isolée de bactéries Streptomyces pluricolorescens, reste depuis sa découverte en 1956 un défi synthétique pour les chimistes organiciens. Le rempart principal bloquant la synthèse de cette famille de molécules réside dans l'introduction régio- et stéréosélective ainsi que dans l'aménagement fonctionnel de deux unités.Nous nous proposons ici de mettre au point une nouvelle méthodologie d’aryl-C-glycosylation régio- et stéréospécifique par couplage de Mizoroki-Heck inscrite dans une stratégie de synthèse originale et convergente dév
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Milde, Bianca. "(Ethynyl-)Ferrocenyl Phosphine Palladium Complexes and (Bis-)Phosphinoimidazol(e/ium) Compounds and their Application in Homogeneous Catalysis." Doctoral thesis, Universitätsbibliothek Chemnitz, 2012. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-90521.

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Die vorliegende Dissertation beschäftigt sich mit der Synthese, der Charakterisierung und der Anwendung neuartiger Phosphane in homogenkatalytischen Reaktionen. Dabei wurden die Ferrocenyl- und Ferrocenylethinylphosphan-Palladium und Ferrocenylethinylphosphan-Ruthenium Komplexe in der Palladium-vermittelten Mizoroki-Heck- und Suzuki-Miyaura-Reaktion sowie der Ruthenium-katalysierten Synthese von β-Oxopropylestern verwendet. Der Schwerpunkt lag dabei auf der Untersuchung des Einflusses der elektronischen und räumlichen Eigenschaften der Phosphanliganden auf die Aktivität und Produktivität der e
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Lo, Chi Hou, and 羅子豪. "Synthesis of Bidentate C-H Activation Imidazolium Palladium Complexes as Catalysts in Mizoroki-Heck Cross-Coupling Reaction Using Ionic Liquid." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/8d967x.

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Book chapters on the topic "Mizoroki-Heck cross-coupling"

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Barriault, Louis, and Effiette L. O. Sauer. "Asymmetric Cross-coupling and Mizoroki-Heck Reactions." In Quaternary Stereocenters. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527606858.ch7.

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