Статті в журналах з теми "C-H Arylation Reactions"
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Dodonova, Jelena, and Sigitas Tumkevicius. "Fused Pyrrolo[2,3-d]pyrimidines (7-Deazapurines) by Palladium-Catalyzed Direct N–H and C–H Arylation Reactions." Synthesis 49, no. 11 (March 2, 2017): 2523–34. http://dx.doi.org/10.1055/s-0036-1588734.
Повний текст джерелаRossi, Renzo, and Maurizio Ciofalo. "Palladium-Catalysed Intermolecular Direct C–H Bond Arylation of Heteroarenes with Reagents Alternative to Aryl Halides: Current State of the Art." Current Organic Chemistry 26, no. 3 (February 2022): 215–74. http://dx.doi.org/10.2174/1385272826666220201124008.
Повний текст джерелаJeyachandran, Rajkumar, Harish Kumar Potukuchi, and Lutz Ackermann. "Copper-catalyzed CuAAC/intramolecular C–H arylation sequence: Synthesis of annulated 1,2,3-triazoles." Beilstein Journal of Organic Chemistry 8 (October 16, 2012): 1771–77. http://dx.doi.org/10.3762/bjoc.8.202.
Повний текст джерелаSingh, Keisham. "Recent Advances in C–H Bond Functionalization with Ruthenium-Based Catalysts." Catalysts 9, no. 2 (February 12, 2019): 173. http://dx.doi.org/10.3390/catal9020173.
Повний текст джерелаDhankhar, Jyoti, and Ilija Čorić. "Direct C–H Arylation." CHIMIA 76, no. 9 (September 21, 2022): 777. http://dx.doi.org/10.2533/chimia.2022.777.
Повний текст джерелаTerai, Seiya, Yuki Sato, Takuya Kochi, and Fumitoshi Kakiuchi. "Efficient synthesis of 3,6,13,16-tetrasubstituted-tetrabenzo[a,d,j,m]coronenes by selective C–H/C–O arylations of anthraquinone derivatives." Beilstein Journal of Organic Chemistry 16 (March 31, 2020): 544–50. http://dx.doi.org/10.3762/bjoc.16.51.
Повний текст джерелаBesson, Thierry, and Corinne Fruit. "Recent Advances in Transition-Metal-Free Late-Stage C-H and N-H Arylation of Heteroarenes Using Diaryliodonium Salts." Pharmaceuticals 14, no. 7 (July 11, 2021): 661. http://dx.doi.org/10.3390/ph14070661.
Повний текст джерелаZhang, Ling, Xiaoyan Lin, Dayun Huang, Xue Liu, and Xiangmei Wu. "Recent Advances in Triarylmethane Synthesis." Synthesis 52, no. 16 (May 14, 2020): 2311–29. http://dx.doi.org/10.1055/s-0040-1707115.
Повний текст джерелаKeske, Eric C., Brandon D. Moore, Olena V. Zenkina, Ruiyao Wang, Gabriele Schatte, and Cathleen M. Crudden. "Highly selective directed arylation reactions via back-to-back dehydrogenative C–H borylation/arylation reactions." Chem. Commun. 50, no. 69 (2014): 9883–86. http://dx.doi.org/10.1039/c4cc02499k.
Повний текст джерелаNgo, Thang Ngoc, Peter Ehlers, Tuan Thanh Dang, Alexander Villinger, and Peter Langer. "Synthesis of indolo[1,2-f]phenanthridines by Pd-catalyzed domino C–N coupling/hydroamination/C–H arylation reactions." Organic & Biomolecular Chemistry 13, no. 11 (2015): 3321–30. http://dx.doi.org/10.1039/c5ob00013k.
Повний текст джерелаGao, Pin, Yu-Rui Gu, and Xin-Hua Duan. "Direct C–H Functionalization of Heteroarenes via Redox-Neutral Radical Process: A Facile Route to C–C Bonds Formation." Synthesis 49, no. 15 (July 6, 2017): 3407–21. http://dx.doi.org/10.1055/s-0036-1588493.
Повний текст джерелаChristodoulou, Michael S., Egle M. Beccalli, and Sabrina Giofrè. "Palladium-Catalyzed Benzodiazepines Synthesis." Catalysts 10, no. 6 (June 6, 2020): 634. http://dx.doi.org/10.3390/catal10060634.
Повний текст джерелаKónya, Krisztina, and Zoltán Sipos. "Synthesis of Benzopyran-Fused Flavone Derivatives via Microwave-Assisted Intramolecular C–H Activation." Synthesis 50, no. 08 (March 7, 2018): 1610–20. http://dx.doi.org/10.1055/s-0036-1591773.
Повний текст джерелаZozik, Yunus, Melike Sevim, Ferruh Lafzi, Haydar Kilic, and Önder Metin. "Magnetically recoverable nickel-palladium alloy nanocatalysts for direct C–H arylation reactions." Dalton Transactions 50, no. 47 (2021): 17515–23. http://dx.doi.org/10.1039/d1dt02985a.
Повний текст джерелаWang, Shoufeng, Shuya Xing, Yingying Zhang, Yafei Fan, Huaiqing Zhao, Jianfeng Wang, Shuxiang Zhang та Wengui Wang. "The Ag-promoted α-C–H arylation of alcohols". RSC Advances 9, № 71 (2019): 41847–50. http://dx.doi.org/10.1039/c9ra09954a.
Повний текст джерелаBabu, Srinivasarao Arulananda, and Arup Dalal. "Pd(II)-Catalyzed Directing-Group-Aided C–H Arylation and Alkylation of Pyrene Core: Synthesis of C1,C2- and C1,C10-Disubstituted Pyrene Motifs." Synthesis 53, no. 18 (March 31, 2021): 3307–24. http://dx.doi.org/10.1055/a-1472-0881.
Повний текст джерелаYemene, Amsalu Efrem, Vishwesh Venkatraman, David Moe Almenningen, Bård Helge Hoff, and Odd Reidar Gautun. "Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation." Molecules 25, no. 10 (May 18, 2020): 2349. http://dx.doi.org/10.3390/molecules25102349.
Повний текст джерелаKeske, Eric C., Brandon D. Moore, Olena V. Zenkina, Ruiyao Wang, Gabriele Schatte, and Cathleen M. Crudden. "ChemInform Abstract: Highly Selective Directed Arylation Reactions via Back-to-Back Dehydrogenative C-H Borylation/Arylation Reactions." ChemInform 46, no. 4 (January 2015): no. http://dx.doi.org/10.1002/chin.201504198.
Повний текст джерелаFujiwara, Yuzo, and Chengguo Jia. "New developments in transition metal-catalyzed synthetic reactions via C-H bond activation." Pure and Applied Chemistry 73, no. 2 (January 1, 2001): 319–24. http://dx.doi.org/10.1351/pac200173020319.
Повний текст джерелаSnieckus, Victor, Livia da Frota, Cédric Schneider, Mauro de Amorim, and Alcides da Silva. "Chemoselective Ruthenium-Catalyzed C–O Bond Activation: Orthogonality of Nickel- and Palladium-Catalyzed Reactions for the Synthesis of Polyaryl Fluorenones." Synlett 28, no. 19 (November 14, 2017): 2587–93. http://dx.doi.org/10.1055/s-0036-1590985.
Повний текст джерелаLiu, Yunyun, Yi Zhang, Meiying Huang, and Jie-Ping Wan. "Step economical synthesis of o-aryl benzamides via C–H activation relayed by the in situ installation of directing group: a multicomponent method." RSC Advances 5, no. 57 (2015): 46192–96. http://dx.doi.org/10.1039/c5ra09078d.
Повний текст джерелаChang, Yu-Chieh, Kun-Mu Lee, Chang-Chieh Ting, and Ching-Yuan Liu. "Step-efficient access to new starburst hole-transport materials with carbazole end-groups for perovskite solar cells via direct C–H/C–Br coupling reactions." Materials Chemistry Frontiers 3, no. 10 (2019): 2041–45. http://dx.doi.org/10.1039/c9qm00309f.
Повний текст джерелаFukuyama, Takahide, Md Taifur Rahman, Hiroshi Mashima, Hideo Takahashi, and Ilhyong Ryu. "Ionic liquids are not innocent in Pd catalysis. C–H arylation of thiazolium and imidazolium ionic liquids with aryl halides." Organic Chemistry Frontiers 4, no. 9 (2017): 1863–66. http://dx.doi.org/10.1039/c7qo00331e.
Повний текст джерелаShchegolkov, Evgeny V., Yanina V. Burgart, Daria A. Matsneva, Sophia S. Borisevich, Renata A. Kadyrova, Iana R. Orshanskaya, Vladimir V. Zarubaev, and Victor I. Saloutin. "Polyfluoroalkylated antipyrines in Pd-catalyzed transformations." RSC Advances 11, no. 56 (2021): 35174–81. http://dx.doi.org/10.1039/d1ra06967e.
Повний текст джерелаZhou, Chun-Ni, Zi-Ang Zheng, George Chang, Yuan-Chao Xiao, Yang-Huan Shen, Gen Li, Yu-Min Zhang, Wang-Ming Peng, Liang Wang, and Biao Xiao. "Phosphorus-Containing Groups Assisted Transition Metal Catalyzed C-H Activation Reactions." Current Organic Chemistry 23, no. 2 (April 23, 2019): 103–35. http://dx.doi.org/10.2174/1385272823666190213113059.
Повний текст джерелаYang, Zhenzhen, Zhenghui Liu, Hongye Zhang, Bo Yu, Yanfei Zhao, Huan Wang, Guipeng Ji, Yu Chen, Xinwei Liu, and Zhimin Liu. "N-Doped porous carbon nanotubes: synthesis and application in catalysis." Chemical Communications 53, no. 5 (2017): 929–32. http://dx.doi.org/10.1039/c6cc09374d.
Повний текст джерелаMcIntyre, Jamie, Irene Mayoral-Soler, Pedro Salvador, Albert Poater, and David J. Nelson. "Insights into mechanism and selectivity in ruthenium(ii)-catalysed ortho-arylation reactions directed by Lewis basic groups." Catalysis Science & Technology 8, no. 12 (2018): 3174–82. http://dx.doi.org/10.1039/c8cy00592c.
Повний текст джерелаWang, Liang, Jun Shen, Sen Yang, Wenjie Liu, Qun Chen, and Mingyang He. "C–H arylation reactions through aniline activation catalysed by a PANI-g-C3N4-TiO2 composite under visible light in aqueous medium." Green Chemistry 20, no. 6 (2018): 1290–96. http://dx.doi.org/10.1039/c8gc00012c.
Повний текст джерелаTanji, Yutaka, Ryo Hamaguchi, Yasushi Tsuji, and Tetsuaki Fujihara. "Pd-Catalyzed intermolecular C–H bond arylation reactions: effect of bulkiness of carboxylate ligands." Chemical Communications 56, no. 27 (2020): 3843–46. http://dx.doi.org/10.1039/d0cc01129k.
Повний текст джерелаCui, Yuxin, Yanxing Jia, and Zhiyao Lu. "Palladium-Catalyzed Domino Heck/C-H Activation/Intermolecular Direct Arylation Reactions." Synthesis 2011, no. 16 (May 26, 2011): 2595–99. http://dx.doi.org/10.1055/s-0030-1260603.
Повний текст джерелаAckermann, Lutz, Andreas Althammer, and Robert Born. "Catalytic Arylation Reactions by CH Bond Activation with Aryl Tosylates." Angewandte Chemie International Edition 45, no. 16 (April 10, 2006): 2619–22. http://dx.doi.org/10.1002/anie.200504450.
Повний текст джерелаKündig, E. Peter, Yixia Jia, Dmitry Katayev, and Masafumi Nakanishi. "Asymmetric Pd-NHC*-catalyzed coupling reactions." Pure and Applied Chemistry 84, no. 8 (July 1, 2012): 1741–48. http://dx.doi.org/10.1351/pac-con-12-02-10.
Повний текст джерелаBrodnik, Helena, Franc Požgan, and Bogdan Štefane. "Synthesis of 8-heteroaryl nitroxoline analogues via one-pot sequential Pd-catalyzed coupling reactions." Organic & Biomolecular Chemistry 14, no. 6 (2016): 1969–81. http://dx.doi.org/10.1039/c5ob02364e.
Повний текст джерелаKim, Seoung-Tae, and Mu-Hyun Baik. "Reductive activation of PdII-precatalysts via decarboxylation of pivalate in direct C–H arylation reactions." Chemical Communications 56, no. 89 (2020): 13868–71. http://dx.doi.org/10.1039/d0cc06085b.
Повний текст джерелаNgo, Thang Ngoc, Frank Janert, Peter Ehlers, Do Huy Hoang, Tuan Thanh Dang, Alexander Villinger, Stefan Lochbrunner, and Peter Langer. "Pd(0)-catalyzed domino C–N coupling/hydroamination/C–H arylation reactions: efficient synthesis and photophysical properties of azaindolo[1,2-f]phenanthridines." Organic & Biomolecular Chemistry 14, no. 4 (2016): 1293–301. http://dx.doi.org/10.1039/c5ob02274f.
Повний текст джерелаPatil, Mahendra. "Mechanism of the t-BuOM (M = K, Na, Li)/DMEDA-Mediated Direct C–H Arylation of Benzene: A Computational Study." Synthesis 52, no. 19 (June 22, 2020): 2883–91. http://dx.doi.org/10.1055/s-0040-1707882.
Повний текст джерелаShen, Rui, Wei Zhu, Xiaodong Yan, Tao Li, Yong Liu, Yunxing Li, Siyuan Dai, and Zhi-Guo Gu. "A porphyrin porous organic polymer with bicatalytic sites for highly efficient one-pot tandem catalysis." Chemical Communications 55, no. 6 (2019): 822–25. http://dx.doi.org/10.1039/c8cc08918c.
Повний текст джерелаZhao, Lingyu, Guodong Shen, Tongxin Zhang, Zhen Wang та Yuhua Liang. "Pd/C-Catalyzed Intramolecular C–H Arylation for the Synthesis of Phenanthridinones and Dibenzo-α-pyrones". SynOpen 01, № 01 (березень 2017): 0129–37. http://dx.doi.org/10.1055/s-0036-1591503.
Повний текст джерелаVerrier, Cécile, Pierrik Lassalas, Laure Théveau, Guy Quéguiner, François Trécourt, Francis Marsais, and Christophe Hoarau. "Recent advances in direct C–H arylation: Methodology, selectivity and mechanism in oxazole series." Beilstein Journal of Organic Chemistry 7 (November 29, 2011): 1584–601. http://dx.doi.org/10.3762/bjoc.7.187.
Повний текст джерелаRocaboy, Ronan, David Dailler, Florian Zellweger, Markus Neuburger, Christophe Salomé, Eric Clot, and Olivier Baudoin. "Domino Pd0 -Catalyzed C(sp3 )-H Arylation/Electrocyclic Reactions via Benzazetidine Intermediates." Angewandte Chemie 130, no. 37 (August 20, 2018): 12307–11. http://dx.doi.org/10.1002/ange.201807097.
Повний текст джерелаRocaboy, Ronan, David Dailler, Florian Zellweger, Markus Neuburger, Christophe Salomé, Eric Clot, and Olivier Baudoin. "Domino Pd0 -Catalyzed C(sp3 )-H Arylation/Electrocyclic Reactions via Benzazetidine Intermediates." Angewandte Chemie International Edition 57, no. 37 (August 20, 2018): 12131–35. http://dx.doi.org/10.1002/anie.201807097.
Повний текст джерелаRossi, Sergio, Fabian Herbrik, Simonetta Resta, and Alessandra Puglisi. "Supported Eosin Y as a Photocatalyst for C-H Arylation of Furan in Batch and Flow." Molecules 27, no. 16 (August 10, 2022): 5096. http://dx.doi.org/10.3390/molecules27165096.
Повний текст джерелаVu Minh, Cuong, Anh Nguyen Thai, Nam Phan Thanh Son, and Tung Nguyen Thanh. "Copper ferrite catalyst for direct arylation of acidic C-H bonds in azoles with aryl aldehydes." Vietnam Journal of Catalysis and Adsorption 10, no. 4 (August 20, 2021): 68–72. http://dx.doi.org/10.51316/jca.2021.070.
Повний текст джерелаChmovzh, Timofey N., Timofey A. Kudryashev, Daria A. Alekhina, and Oleg A. Rakitin. "Palladium-Catalyzed Direct (Het)arylation Reactions of Benzo[1,2-d:4,5-d′]bis([1,2,3]thiadiazole and 4,8-Dibromobenzo[1,2-d:4,5-d′]bis([1,2,3]thiadiazole)." Molecules 28, no. 9 (May 8, 2023): 3977. http://dx.doi.org/10.3390/molecules28093977.
Повний текст джерелаWang, Xiaochen, Yuechen Li, Jianfeng Li, Yuan Zhang, Jinjun Shao, and Yongfang Li. "Direct Arylation Synthesis of Small Molecular Acceptors for Organic Solar Cells." Molecules 28, no. 8 (April 16, 2023): 3515. http://dx.doi.org/10.3390/molecules28083515.
Повний текст джерелаTanji, Yutaka, Naoya Mitsutake, Tetsuaki Fujihara, and Yasushi Tsuji. "Steric Effect of Carboxylate Ligands on Pd-Catalyzed Intramolecular C(sp2 )-H and C(sp3 )-H Arylation Reactions." Angewandte Chemie 130, no. 32 (June 19, 2018): 10471–74. http://dx.doi.org/10.1002/ange.201804566.
Повний текст джерелаTanji, Yutaka, Naoya Mitsutake, Tetsuaki Fujihara, and Yasushi Tsuji. "Steric Effect of Carboxylate Ligands on Pd-Catalyzed Intramolecular C(sp2 )-H and C(sp3 )-H Arylation Reactions." Angewandte Chemie International Edition 57, no. 32 (June 19, 2018): 10314–17. http://dx.doi.org/10.1002/anie.201804566.
Повний текст джерелаMori, Atsunori, Shigeru Matsuda, Masabumi Takahashi, and Daiki Monguchi. "C-H and C-Si Functionalization of Furan Derivatives: Palladium-Catalyzed Homocoupling and Arylation Reactions." Synlett 2009, no. 12 (July 2009): 1941–44. http://dx.doi.org/10.1055/s-0029-1217537.
Повний текст джерелаShahrisa, Aziz, Reza Teimuri-Mofrad, and Mahdi Gholamhosseini-Nazari. "Chemoselective Sequential Reactions for the Synthesis of 12H-Benzo[a]xanthenes and Dihydro-1H-naphtho[1,2-e][1,3]oxazines." Synlett 26, no. 08 (March 12, 2015): 1031–38. http://dx.doi.org/10.1055/s-0034-1380323.
Повний текст джерелаLu, Zhiyao, Yuxin Cui, and Yanxing Jia. "ChemInform Abstract: Palladium-Catalyzed Domino Heck/C-H Activation/Intermolecular Direct Arylation Reactions." ChemInform 42, no. 52 (December 1, 2011): no. http://dx.doi.org/10.1002/chin.201152144.
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