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Articoli di riviste sul tema "Palladium-copper cooperative catalysis"

Autore: Grafiati
Pubblicato: 7 settembre 2024

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1

Semba, Kazuhiko, e Yoshiaki Nakao. "Arylboration of Alkenes by Cooperative Palladium/Copper Catalysis". Journal of the American Chemical Society 136, n. 21 (14 maggio 2014): 7567–70. http://dx.doi.org/10.1021/ja5029556.

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2

Semba, Kazuhiko, Megumi Yoshizawa, Yasuhiro Ohtagaki e Yoshiaki Nakao. "Arylboration of Internal Alkynes by Cooperative Palladium/Copper Catalysis". Bulletin of the Chemical Society of Japan 90, n. 12 (15 dicembre 2017): 1340–43. http://dx.doi.org/10.1246/bcsj.20170226.

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3

Semba, Kazuhiko, Yasuhiro Ohtagaki e Yoshiaki Nakao. "1,2-Arylboration of aliphatic alkenes by cooperative palladium/copper catalysis". Tetrahedron Letters 72 (maggio 2021): 153059. http://dx.doi.org/10.1016/j.tetlet.2021.153059.

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4

Semba, Kazuhiko, e Yoshiaki Nakao. "ChemInform Abstract: Arylboration of Alkenes by Cooperative Palladium/Copper Catalysis." ChemInform 45, n. 50 (27 novembre 2014): no. http://dx.doi.org/10.1002/chin.201450174.

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5

Shintani, Ryo, Hiroki Kurata e Kyoko Nozaki. "Intermolecular Three-Component Arylsilylation of Alkynes under Palladium/Copper Cooperative Catalysis". Journal of Organic Chemistry 81, n. 8 (7 aprile 2016): 3065–69. http://dx.doi.org/10.1021/acs.joc.6b00587.

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6

Ohgi, Akito, Kazuhiko Semba, Tamejiro Hiyama e Yoshiaki Nakao. "Silicon-based Cross-coupling of Aryl Tosylates by Cooperative Palladium/Copper Catalysis". Chemistry Letters 45, n. 8 (5 agosto 2016): 973–75. http://dx.doi.org/10.1246/cl.160439.

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7

Semba, Kazuhiko, Ryohei Kameyama e Yoshiaki Nakao. "Hydrogenative Cross-coupling of Internal Alkynes and Aryl Iodides by Palladium/Copper Cooperative Catalysis". Chemistry Letters 47, n. 2 (5 febbraio 2018): 213–16. http://dx.doi.org/10.1246/cl.170961.

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8

Labre, Flavien, Yves Gimbert, Pierre Bannwarth, Sandra Olivero, Elisabet Duñach e Pierre Y. Chavant. "Application of Cooperative Iron/Copper Catalysis to a Palladium-Free Borylation of Aryl Bromides with Pinacolborane". Organic Letters 16, n. 9 (16 aprile 2014): 2366–69. http://dx.doi.org/10.1021/ol500675q.

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9

Semba, Kazuhiko, Naoki Ohta e Yoshiaki Nakao. "Carboallylation of Electron-Deficient Alkenes with Organoboron Compounds and Allylic Carbonates by Cooperative Palladium/Copper Catalysis". Organic Letters 21, n. 12 (3 giugno 2019): 4407–10. http://dx.doi.org/10.1021/acs.orglett.9b00915.

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10

Hoshi, Takashi, Yuka Shishido, Ayumi Suzuki, Yuki Sasaki, Hisahiro Hagiwara e Toshio Suzuki. "Suzuki–Miyaura Coupling Reactions Using Low Loading of Ligand-activated Palladium Catalyst by Cooperative Copper Catalysis". Chemistry Letters 47, n. 6 (5 giugno 2018): 780–83. http://dx.doi.org/10.1246/cl.180185.

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11

Semba, Kazuhiko, Kenta Ariyama, Hong Zheng, Ryohei Kameyama, Shigeyoshi Sakaki e Yoshiaki Nakao. "Reductive Cross-Coupling of Conjugated Arylalkenes and Aryl Bromides with Hydrosilanes by Cooperative Palladium/Copper Catalysis". Angewandte Chemie International Edition 55, n. 21 (15 aprile 2016): 6275–79. http://dx.doi.org/10.1002/anie.201511975.

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12

Semba, Kazuhiko, Kenta Ariyama, Hong Zheng, Ryohei Kameyama, Shigeyoshi Sakaki e Yoshiaki Nakao. "Reductive Cross-Coupling of Conjugated Arylalkenes and Aryl Bromides with Hydrosilanes by Cooperative Palladium/Copper Catalysis". Angewandte Chemie 128, n. 21 (15 aprile 2016): 6383–87. http://dx.doi.org/10.1002/ange.201511975.

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13

Jeganmohan, Masilamani, Sivakolundu Bhuvaneswari e Chien-Hong Cheng. "A Cooperative Copper- and Palladium-Catalyzed Three-Component Coupling of Benzynes, Allylic Epoxides, and Terminal Alkynes". Angewandte Chemie International Edition 48, n. 2 (2 gennaio 2009): 391–94. http://dx.doi.org/10.1002/anie.200804873.

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14

Sheng, Jie, Congbin Fan e Jie Wu. "Generation of 4-substituted coumarins via C–H bond activation under palladium bromide–copper(I) bromide cooperative catalysis". Tetrahedron 69, n. 48 (dicembre 2013): 10230–34. http://dx.doi.org/10.1016/j.tet.2013.10.043.

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15

Labre, Flavien, Yves Gimbert, Pierre Bannwarth, Sandra Olivero, Elisabet Dunach e Pierre Y. Chavant. "ChemInform Abstract: Application of Cooperative Iron/Copper Catalysis to a Palladium-Free Borylation of Aryl Bromides with Pinacolborane." ChemInform 45, n. 45 (23 ottobre 2014): no. http://dx.doi.org/10.1002/chin.201445203.

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16

Song, Liangliang, Sander Claessen e Erik V. Van der Eycken. "Pyridine-Enabled C–N Bond Activation for the Rapid Construction of Amides and 4-Pyridylglyoxamides by Cooperative Palladium/Copper Catalysis". Journal of Organic Chemistry 85, n. 12 (22 maggio 2020): 8045–54. http://dx.doi.org/10.1021/acs.joc.0c00845.

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17

Li, Yuan, Shaozhong Qiu, Ling Fan e Guodong Yin. "Cooperative Palladium and Copper Catalysis: One‐pot Synthesis of Diamino‐Substituted Naphthalenes from Aryl Halides, 1,4‐Bis(trimethylsilyl)butadiyne and Amines". ChemCatChem 12, n. 4 (2 gennaio 2020): 1230–35. http://dx.doi.org/10.1002/cctc.201901745.

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18

Jin, Ming, Wei Ren, Dang-Wei Qian e Shang-Dong Yang. "Direct Allylic C(sp3)-H Alkylation with 2-Naphthols via Cooperative Palladium and Copper Catalysis: Construction of Cyclohexadienones with Quaternary Carbon Centers". Organic Letters 20, n. 22 (26 ottobre 2018): 7015–19. http://dx.doi.org/10.1021/acs.orglett.8b02910.

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19

Sun, Fenggang, Miao Li, Congfa He, Bin Wang, Bin Li, Xianwei Sui e Zhenhua Gu. "Cleavage of the C(O)–S Bond of Thioesters by Palladium/Norbornene/Copper Cooperative Catalysis: An Efficient Synthesis of 2-(Arylthio)aryl Ketones". Journal of the American Chemical Society 138, n. 24 (13 giugno 2016): 7456–59. http://dx.doi.org/10.1021/jacs.6b02495.

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20

Lesieur, Mathieu, Yannick D. Bidal, Faïma Lazreg, Fady Nahra e Catherine S. J. Cazin. "Versatile Relay and Cooperative Palladium(0)N-Heterocyclic Carbene/Copper(I)N-Heterocyclic Carbene Catalysis for the Synthesis of Tri- and Tetrasubstituted Alkenes". ChemCatChem 7, n. 14 (26 giugno 2015): 2108–12. http://dx.doi.org/10.1002/cctc.201500268.

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21

Lesieur, Mathieu, Yannick D. Bidal, Faima Lazreg, Fady Nahra e Catherine S. J. Cazin. "ChemInform Abstract: Versatile Relay and Cooperative Palladium(0) N-Heterocyclic Carbene/Copper(I) N-Heterocyclic Carbene Catalysis for the Synthesis of Tri- and Tetrasubstituted Alkenes." ChemInform 46, n. 47 (novembre 2015): no. http://dx.doi.org/10.1002/chin.201547074.

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22

Sheng, Jie, Congbin Fan e Jie Wu. "ChemInform Abstract: Generation of 4-Substituted Coumarins via C-H Bond Activation under Palladium Bromide-Copper(I) Bromide Cooperation Catalysis." ChemInform 45, n. 17 (10 aprile 2014): no. http://dx.doi.org/10.1002/chin.201417152.

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23

"Palladium/Copper Cooperative Catalysis for C–H Arylation of Five-Membered Heterocycles". Synfacts 17, n. 05 (20 aprile 2021): 0531. http://dx.doi.org/10.1055/s-0040-1720486.

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24

Shintani, Ryo, Hiroki Kurata e Kyoko Nozaki. "ChemInform Abstract: Intermolecular Three-Component Arylsilylation of Alkynes under Palladium/Copper Cooperative Catalysis." ChemInform 47, n. 34 (agosto 2016). http://dx.doi.org/10.1002/chin.201634183.

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25

Li, Yuan, Jin Wu, Hui Li, Qian Sun, Lixue Xiong e Guodong Yin. "Highly regio- and stereoselective synthesis of bis-sulfanyl substituted conjugated dienes by copper–palladium cooperative catalysis". Organic Chemistry Frontiers, 2021. http://dx.doi.org/10.1039/d0qo01256d.

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Abstract (sommario):
An efficient one-pot method for the synthesis of (Z,Z)-isomers of 1,4-bis(sulfanyl)-1,4-diaryl-1,3-butadienes by the cooperative catalysis of Cu(Xantphos)I/Pd(OAc)2 and a base has been developed.
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26

Semba, Kazuhiko, Kenta Ariyama, Hong Zheng, Ryohei Kameyama, Shigeyoshi Sakaki e Yoshiaki Nakao. "ChemInform Abstract: Reductive Cross-Coupling of Conjugated Arylalkenes and Aryl Bromides with Hydrosilanes by Cooperative Palladium/Copper Catalysis." ChemInform 47, n. 39 (settembre 2016). http://dx.doi.org/10.1002/chin.201639047.

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27

Sun, Fenggang, Miao Li, Congfa He, Bin Wang, Bin Li, Xianwei Sui e Zhenhua Gu. "ChemInform Abstract: Cleavage of the C(O)-S Bond of Thioesters by Palladium/Norbornene/Copper Cooperative Catalysis: An Efficient Synthesis of 2-(Arylthio)aryl Ketones." ChemInform 47, n. 50 (novembre 2016). http://dx.doi.org/10.1002/chin.201650071.

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