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Добірка наукової літератури з теми "Palladium-copper cooperative catalysis"
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Статті в журналах з теми "Palladium-copper cooperative catalysis"
Semba, Kazuhiko, and Yoshiaki Nakao. "Arylboration of Alkenes by Cooperative Palladium/Copper Catalysis." Journal of the American Chemical Society 136, no. 21 (May 14, 2014): 7567–70. http://dx.doi.org/10.1021/ja5029556.
Повний текст джерелаSemba, Kazuhiko, Megumi Yoshizawa, Yasuhiro Ohtagaki, and Yoshiaki Nakao. "Arylboration of Internal Alkynes by Cooperative Palladium/Copper Catalysis." Bulletin of the Chemical Society of Japan 90, no. 12 (December 15, 2017): 1340–43. http://dx.doi.org/10.1246/bcsj.20170226.
Повний текст джерелаSemba, Kazuhiko, Yasuhiro Ohtagaki, and Yoshiaki Nakao. "1,2-Arylboration of aliphatic alkenes by cooperative palladium/copper catalysis." Tetrahedron Letters 72 (May 2021): 153059. http://dx.doi.org/10.1016/j.tetlet.2021.153059.
Повний текст джерелаSemba, Kazuhiko, and Yoshiaki Nakao. "ChemInform Abstract: Arylboration of Alkenes by Cooperative Palladium/Copper Catalysis." ChemInform 45, no. 50 (November 27, 2014): no. http://dx.doi.org/10.1002/chin.201450174.
Повний текст джерелаShintani, Ryo, Hiroki Kurata, and Kyoko Nozaki. "Intermolecular Three-Component Arylsilylation of Alkynes under Palladium/Copper Cooperative Catalysis." Journal of Organic Chemistry 81, no. 8 (April 7, 2016): 3065–69. http://dx.doi.org/10.1021/acs.joc.6b00587.
Повний текст джерелаOhgi, Akito, Kazuhiko Semba, Tamejiro Hiyama, and Yoshiaki Nakao. "Silicon-based Cross-coupling of Aryl Tosylates by Cooperative Palladium/Copper Catalysis." Chemistry Letters 45, no. 8 (August 5, 2016): 973–75. http://dx.doi.org/10.1246/cl.160439.
Повний текст джерелаSemba, Kazuhiko, Ryohei Kameyama, and Yoshiaki Nakao. "Hydrogenative Cross-coupling of Internal Alkynes and Aryl Iodides by Palladium/Copper Cooperative Catalysis." Chemistry Letters 47, no. 2 (February 5, 2018): 213–16. http://dx.doi.org/10.1246/cl.170961.
Повний текст джерелаLabre, Flavien, Yves Gimbert, Pierre Bannwarth, Sandra Olivero, Elisabet Duñach, and Pierre Y. Chavant. "Application of Cooperative Iron/Copper Catalysis to a Palladium-Free Borylation of Aryl Bromides with Pinacolborane." Organic Letters 16, no. 9 (April 16, 2014): 2366–69. http://dx.doi.org/10.1021/ol500675q.
Повний текст джерелаSemba, Kazuhiko, Naoki Ohta, and Yoshiaki Nakao. "Carboallylation of Electron-Deficient Alkenes with Organoboron Compounds and Allylic Carbonates by Cooperative Palladium/Copper Catalysis." Organic Letters 21, no. 12 (June 3, 2019): 4407–10. http://dx.doi.org/10.1021/acs.orglett.9b00915.
Повний текст джерелаHoshi, Takashi, Yuka Shishido, Ayumi Suzuki, Yuki Sasaki, Hisahiro Hagiwara, and Toshio Suzuki. "Suzuki–Miyaura Coupling Reactions Using Low Loading of Ligand-activated Palladium Catalyst by Cooperative Copper Catalysis." Chemistry Letters 47, no. 6 (June 5, 2018): 780–83. http://dx.doi.org/10.1246/cl.180185.
Повний текст джерелаДисертації з теми "Palladium-copper cooperative catalysis"
Panza, Florian. "Fοnctiοnnalisatiοn directe οrthοgοnale métallο-catalysée des sites carbοne-hydrοgène des platefοrmes pharmacοlοgiques à cοeur imidazοisοindοle". Electronic Thesis or Diss., Normandie, 2024. http://www.theses.fr/2024NORMIR11.
Повний текст джерелаFor several decades, chemists constantly seek to push the limits of synthetic strategies by developing ever more efficient and more economical methodologies. In this context, transition metal-catalyzed direct functionalization of C—H bonds is one of the most powerful tools for constructing and funtionalizing simple molecules and ever more complex moieties, with a great diversity of C—H bonds. These strategies also answer the needs for the opening of the chemical space of functionalization. Imidazoisoindole, tricyclic heterocycle composed of an imidazole core, is a very interesting scaffold for biological activity and presents C—H bonds with very diverse properties, but late-functionalization methodology of these structures has yet to be listed in the literature. This work takes place in this context and presents, (I) based on past laboratory experience, a robust methodology to synthetize diversely substituted imidazoisoindoles at high scale by palladium-catalyzed intramolecular C—H activation ; (II) an extension of standard directC2—H functionalization of 1,3-diazole moieties applied to imidazo[5,1-a]isoindoles with a palladium(0)-copper(I) cooperative catalysis ; (III) a new methodology of direct C(sp³)—H palladium-catalyzed mono-functionalization at benzylic position of imidazo[2,1-a]isoindoles ; (IV) a preliminary study of the observed regioselectivity of iridium-catalyzed direct C(sp²)—H borylation of imidazo[2,1-a]isoindoles