Статті в журналах з теми "Arylation coupling"
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Maiti, Debabrata, Sumon Basak, and Jyoti Prasad Biswas. "Transition-Metal-Catalyzed C–H Arylation Using Organoboron Reagents." Synthesis 53, no. 18 (April 19, 2021): 3151–79. http://dx.doi.org/10.1055/a-1485-4666.
Повний текст джерелаBarde, E., A. Guérinot та J. Cossy. "α-Arylation of Amides from α-Halo Amides Using Metal-Catalyzed Cross-Coupling Reactions". Synthesis 51, № 01 (7 грудня 2018): 178–84. http://dx.doi.org/10.1055/s-0037-1611358.
Повний текст джерелаHuang, Qing, Liangxian Liu, Jiayi Zhu, Yu Chen, Feng Lin, and Baoshuang Wang. "Highly Regioselective Arylation of 1,2,3-Triazole N-Oxides with Sodium Arenesulfinates via Palladium-Catalyzed Desulfitative Cross-Coupling Reaction." Synlett 26, no. 08 (March 5, 2015): 1124–30. http://dx.doi.org/10.1055/s-0034-1380186.
Повний текст джерелаFischer, Carolin, and Burkhard Koenig. "Palladium- and copper-mediated N-aryl bond formation reactions for the synthesis of biological active compounds." Beilstein Journal of Organic Chemistry 7 (January 14, 2011): 59–74. http://dx.doi.org/10.3762/bjoc.7.10.
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 джерелаWei, Xiao-Hong, Gang-Wei Wang, and Shang-Dong Yang. "Enantioselective synthesis of arylglycine derivatives by direct C–H oxidative cross-coupling." Chemical Communications 51, no. 5 (2015): 832–35. http://dx.doi.org/10.1039/c4cc07361d.
Повний текст джерелаEl Abbouchi, Abdelmoula, Jamal Koubachi, Nabil El Brahmi, and Said El Kazzouli. "Direct arylation and Suzuki-Miyaura coupling of imidazo[1,2-a]pyridines catalyzed by (SIPr)Pd(allyl)Cl complex under microwave-irradiation." Mediterranean Journal of Chemistry 9, no. 5 (November 27, 2019): 347–54. http://dx.doi.org/10.13171/mjc1911271124sek.
Повний текст джерелаZhu, Hui, Xing Liu, Cai-Zhu Chang, and Zhi-Bing Dong. "Copper-Catalyzed C–S Cross-Coupling Reaction: S-Arylation of Arylthioureas." Synthesis 49, no. 23 (August 22, 2017): 5211–16. http://dx.doi.org/10.1055/s-0036-1590879.
Повний текст джерелаMayhugh, Amy L., and Christine K. Luscombe. "Room-temperature Pd/Ag direct arylation enabled by a radical pathway." Beilstein Journal of Organic Chemistry 16 (March 13, 2020): 384–90. http://dx.doi.org/10.3762/bjoc.16.36.
Повний текст джерелаCao, Zhi-Chao, Da-Gang Yu, Ru-Yi Zhu, Jiang-Bo Wei, and Zhang-Jie Shi. "Direct cross-coupling of benzyl alcohols to construct diarylmethanes via palladium catalysis." Chemical Communications 51, no. 13 (2015): 2683–86. http://dx.doi.org/10.1039/c4cc10084k.
Повний текст джерелаRaina, Gaurav, Prakash Kannaboina, Nagaraju Mupparapu, Sushil Raina, Qazi Naveed Ahmed, and Parthasarathi Das. "Programmed synthesis of triarylnitroimidazoles via sequential cross-coupling reactions." Organic & Biomolecular Chemistry 17, no. 8 (2019): 2134–47. http://dx.doi.org/10.1039/c9ob00144a.
Повний текст джерелаMarquise, Nada, Vincent Dorcet, Floris Chevallier, and Florence Mongin. "Synthesis of substituted azafluorenones from dihalogeno diaryl ketones by palladium-catalyzed auto-tandem processes." Org. Biomol. Chem. 12, no. 41 (2014): 8138–41. http://dx.doi.org/10.1039/c4ob01629g.
Повний текст джерелаWang, Xiaochen, Kai Wang, and Mingfeng Wang. "Synthesis of conjugated polymers via an exclusive direct-arylation coupling reaction: a facile and straightforward way to synthesize thiophene-flanked benzothiadiazole derivatives and their copolymers." Polymer Chemistry 6, no. 10 (2015): 1846–55. http://dx.doi.org/10.1039/c4py01627k.
Повний текст джерелаJin, Rongwei, Charles Beromeo Bheeter, and Henri Doucet. "Hindered aryl bromides for regioselective palladium-catalysed direct arylation at less favourable C5-carbon of 3-substituted thiophenes." Beilstein Journal of Organic Chemistry 10 (May 27, 2014): 1239–45. http://dx.doi.org/10.3762/bjoc.10.123.
Повний текст джерелаFaradhiyani, Alanna, Qiao Zhang, Keisuke Maruyama, Junpei Kuwabara, Takeshi Yasuda, and Takaki Kanbara. "Synthesis of bithiazole-based semiconducting polymers via Cu-catalysed aerobic oxidative coupling." Materials Chemistry Frontiers 2, no. 7 (2018): 1306–9. http://dx.doi.org/10.1039/c7qm00584a.
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 джерелаPacheco-Benichou, Alexandra, Thierry Besson, and Corinne Fruit. "Diaryliodoniums Salts as Coupling Partners for Transition-Metal Catalyzed C- and N-Arylation of Heteroarenes." Catalysts 10, no. 5 (April 28, 2020): 483. http://dx.doi.org/10.3390/catal10050483.
Повний текст джерелаMu, Yucheng, Xiaodong Tan, Yemin Zhang, Xiaobi Jing та Zhuangzhi Shi. "Pd(ii)-catalyzed β-C–H arylation of O-methyl ketoximes with iodoarenes". Organic Chemistry Frontiers 3, № 3 (2016): 380–84. http://dx.doi.org/10.1039/c5qo00438a.
Повний текст джерелаMahindra, Amit, and Rahul Jain. "Regiocontrolled palladium-catalyzed and copper-mediated C–H bond functionalization of protectedl-histidine." Org. Biomol. Chem. 12, no. 23 (2014): 3792–96. http://dx.doi.org/10.1039/c4ob00430b.
Повний текст джерелаChen, Chunxiang, Daniel Hernández Maldonado, Damien Le Borgne, Fabienne Alary, Barbara Lonetti, Benoît Heinrich, Bertrand Donnio, and Kathleen I. Moineau-Chane Ching. "Synthesis of benzothiadiazole-based molecules via direct arylation: an eco-friendly way of obtaining small semi-conducting organic molecules." New Journal of Chemistry 40, no. 9 (2016): 7326–37. http://dx.doi.org/10.1039/c6nj00847j.
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 джерелаZhang, Lei, and Xile Hu. "Nickel catalysis enables convergent paired electrolysis for direct arylation of benzylic C–H bonds." Chemical Science 11, no. 39 (2020): 10786–91. http://dx.doi.org/10.1039/d0sc01445a.
Повний текст джерелаZu, Weisai, Shuai Liu, Xin Jia, and Liang Xu. "Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan–Evans–Lam reactions." Organic Chemistry Frontiers 6, no. 9 (2019): 1356–60. http://dx.doi.org/10.1039/c8qo01313f.
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 джерелаMendis, Shehani N., та Jon A. Tunge. "Decarboxylative dearomatization and mono-α-arylation of ketones". Chemical Communications 52, № 49 (2016): 7695–98. http://dx.doi.org/10.1039/c6cc03672d.
Повний текст джерелаWashington, Jack B., Michele Assante, Chunhui Yan, David McKinney, Vanessa Juba, Andrew G. Leach, Sharon E. Baillie, and Marc Reid. "Trialkylammonium salt degradation: implications for methylation and cross-coupling." Chemical Science 12, no. 20 (2021): 6949–63. http://dx.doi.org/10.1039/d1sc00757b.
Повний текст джерелаSmari, Imen, Liqin Zhao, Kedong Yuan, Hamed Ben Ammar, and Henri Doucet. "Reactivity of bromofluorenes in palladium-catalysed direct arylation of heteroaromatics." Catal. Sci. Technol. 4, no. 10 (2014): 3723–32. http://dx.doi.org/10.1039/c4cy00771a.
Повний текст джерелаNageswar Rao, D., Sk Rasheed, Ram A. Vishwakarma, and Parthasarathi Das. "Copper-catalyzed sequential N-arylation of C-amino-NH-azoles." Chem. Commun. 50, no. 85 (2014): 12911–14. http://dx.doi.org/10.1039/c4cc05628k.
Повний текст джерелаPaul, Sanjay, Hari Datta Khanal, Chayan Dhar Clinton, Sung Hong Kim, and Yong Rok Lee. "Pd(TFA)2-catalyzed direct arylation of quinoxalinones with arenes." Organic Chemistry Frontiers 6, no. 2 (2019): 231–35. http://dx.doi.org/10.1039/c8qo01250d.
Повний текст джерелаLiu, Shuai, Weisai Zu, Jinli Zhang, and Liang Xu. "Chemoselective N-arylation of aminobenzamides via copper catalysed Chan–Evans–Lam reactions." Organic & Biomolecular Chemistry 15, no. 44 (2017): 9288–92. http://dx.doi.org/10.1039/c7ob02491f.
Повний текст джерелаCorrea, Arkaitz, Béla Fiser та Enrique Gómez-Bengoa. "Iron-catalyzed direct α-arylation of ethers with azoles". Chemical Communications 51, № 69 (2015): 13365–68. http://dx.doi.org/10.1039/c5cc05005g.
Повний текст джерелаSiva Reddy, A., K. Ranjith Reddy, D. Nageswar Rao, Chaitanya K. Jaladanki, Prasad V. Bharatam, Patrick Y. S. Lam, and Parthasarathi Das. "Copper(ii)-catalyzed Chan–Lam cross-coupling: chemoselective N-arylation of aminophenols." Organic & Biomolecular Chemistry 15, no. 4 (2017): 801–6. http://dx.doi.org/10.1039/c6ob02444k.
Повний текст джерелаChen, Yuanguang, Fangyu Du, Fengyang Chen, Qifan Zhou та Guoliang Chen. "Methyl-α-d-glucopyranoside as Green Ligand for Selective Copper-Catalyzed N-Arylation". Synthesis 51, № 24 (14 жовтня 2019): 4590–600. http://dx.doi.org/10.1055/s-0039-1690702.
Повний текст джерелаSeifert, Sabine, David Schmidt, and Frank Würthner. "A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides." Organic Chemistry Frontiers 3, no. 11 (2016): 1435–42. http://dx.doi.org/10.1039/c6qo00421k.
Повний текст джерелаSharma, Alpesh K., Hemant Joshi, Renu Bhaskar, Satyendra Kumar, and Ajai K. Singh. "Palladacycles of sulfated and selenated Schiff bases of ferrocene-carboxaldehyde as catalysts for O-arylation and Suzuki–Miyaura coupling." Dalton Transactions 46, no. 8 (2017): 2485–96. http://dx.doi.org/10.1039/c7dt00083a.
Повний текст джерелаShu, Bing, Xiao-Tong Wang, Zi-Xuan Shen, Tong Che, Mei Zhong, Jia-Lin Song, Hua-Jie Kang, Hui Xie, Luyong Zhang та Shang-Shi Zhang. "Iridium-catalyzed arylation of sulfoxonium ylides and arylboronic acids: a straightforward preparation of α-aryl ketones". Organic Chemistry Frontiers 7, № 14 (2020): 1802–8. http://dx.doi.org/10.1039/d0qo00543f.
Повний текст джерелаWagner, Patrick, Maud Bollenbach, Christelle Doebelin, Frédéric Bihel, Jean-Jacques Bourguignon, Christophe Salomé, and Martine Schmitt. "t-BuXPhos: a highly efficient ligand for Buchwald–Hartwig coupling in water." Green Chem. 16, no. 9 (2014): 4170–78. http://dx.doi.org/10.1039/c4gc00853g.
Повний текст джерелаPuthiaraj, Pillaiyar, and Wha-Seung Ahn. "Synthesis of copper nanoparticles supported on a microporous covalent triazine polymer: an efficient and reusable catalyst for O-arylation reaction." Catalysis Science & Technology 6, no. 6 (2016): 1701–9. http://dx.doi.org/10.1039/c5cy01590a.
Повний текст джерелаCong, Zhanqing, Feng Gao, and Hong Liu. "Ni(ii)-catalyzed mono-selective ortho-arylation of unactivated aryl C–H bonds utilizing amino acids as a directing group." RSC Advances 9, no. 19 (2019): 10820–24. http://dx.doi.org/10.1039/c9ra00749k.
Повний текст джерелаLutz, J. Patrick, Stephen T. Chau, and Abigail G. Doyle. "Nickel-catalyzed enantioselective arylation of pyridine." Chemical Science 7, no. 7 (2016): 4105–9. http://dx.doi.org/10.1039/c6sc00702c.
Повний текст джерелаBasu, Souradeep, Alexander H. Sandtorv, and David R. Stuart. "Imide arylation with aryl(TMP)iodonium tosylates." Beilstein Journal of Organic Chemistry 14 (May 11, 2018): 1034–38. http://dx.doi.org/10.3762/bjoc.14.90.
Повний текст джерелаChen, Xin, Yunyun Bian, Baichuan Mo, Peng Sun, Chunxia Chen, and Jinsong Peng. "Copper(ii)-catalyzed synthesis of multisubstituted indoles through sequential Chan–Lam and cross-dehydrogenative coupling reactions." RSC Advances 10, no. 42 (2020): 24830–39. http://dx.doi.org/10.1039/d0ra04592f.
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 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 джерелаYang, Woo-Ram, Yong-Sung Choi, and Jin-Hyun Jeong. "Efficient synthesis of polymethoxyselenoflavones via regioselective direct C–H arylation of selenochromones." Organic & Biomolecular Chemistry 15, no. 14 (2017): 3074–83. http://dx.doi.org/10.1039/c7ob00118e.
Повний текст джерелаMorimoto, Koji, Yusuke Ohnishi, Daichi Koseki, Akira Nakamura, Toshifumi Dohi, and Yasuyuki Kita. "Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling." Organic & Biomolecular Chemistry 14, no. 38 (2016): 8947–51. http://dx.doi.org/10.1039/c6ob01764a.
Повний текст джерелаKumar, K. Anil, Prakash Kannaboina, D. Nageswar Rao, and Parthasarathi Das. "Nickel-catalyzed Chan–Lam cross-coupling: chemoselective N-arylation of 2-aminobenzimidazoles." Organic & Biomolecular Chemistry 14, no. 38 (2016): 8989–97. http://dx.doi.org/10.1039/c6ob01307d.
Повний текст джерелаNasrollahzadeh, Mahmoud. "Advances in Magnetic Nanoparticles-Supported Palladium Complexes for Coupling Reactions." Molecules 23, no. 10 (October 4, 2018): 2532. http://dx.doi.org/10.3390/molecules23102532.
Повний текст джерелаSasmal, Arpan, Thierry Roisnel, Jitendra K. Bera, Henri Doucet, and Jean-François Soulé. "Reactivity of 3-Bromofuran in Pd-Catalyzed C–H Bond Arylation toward the Synthesis of 2,3,5-Triarylfurans." Synthesis 51, no. 17 (May 7, 2019): 3241–49. http://dx.doi.org/10.1055/s-0037-1611819.
Повний текст джерелаGao, Hui, Xinyu Chen, Pei-Long Wang, Meng-Meng Shi, Ling-Long Shang, Heng-Yi Guo, Hongji Li, and Pinhua Li. "Electrochemical benzylic C–H arylation of xanthenes and thioxanthenes without a catalyst and oxidant." Organic Chemistry Frontiers 9, no. 7 (2022): 1911–16. http://dx.doi.org/10.1039/d1qo01925b.
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