Artigos de revistas sobre o tema "Arylation coupling"
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Maiti, Debabrata, Sumon Basak e Jyoti Prasad Biswas. "Transition-Metal-Catalyzed C–H Arylation Using Organoboron Reagents". Synthesis 53, n.º 18 (19 de abril de 2021): 3151–79. http://dx.doi.org/10.1055/a-1485-4666.
Texto completo da fonteBarde, E., A. Guérinot e J. Cossy. "α-Arylation of Amides from α-Halo Amides Using Metal-Catalyzed Cross-Coupling Reactions". Synthesis 51, n.º 01 (7 de dezembro de 2018): 178–84. http://dx.doi.org/10.1055/s-0037-1611358.
Texto completo da fonteHuang, Qing, Liangxian Liu, Jiayi Zhu, Yu Chen, Feng Lin e Baoshuang Wang. "Highly Regioselective Arylation of 1,2,3-Triazole N-Oxides with Sodium Arenesulfinates via Palladium-Catalyzed Desulfitative Cross-Coupling Reaction". Synlett 26, n.º 08 (5 de março de 2015): 1124–30. http://dx.doi.org/10.1055/s-0034-1380186.
Texto completo da fonteFischer, Carolin, e Burkhard Koenig. "Palladium- and copper-mediated N-aryl bond formation reactions for the synthesis of biological active compounds". Beilstein Journal of Organic Chemistry 7 (14 de janeiro de 2011): 59–74. http://dx.doi.org/10.3762/bjoc.7.10.
Texto completo da fonteYemene, Amsalu Efrem, Vishwesh Venkatraman, David Moe Almenningen, Bård Helge Hoff e Odd Reidar Gautun. "Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation". Molecules 25, n.º 10 (18 de maio de 2020): 2349. http://dx.doi.org/10.3390/molecules25102349.
Texto completo da fonteWei, Xiao-Hong, Gang-Wei Wang e Shang-Dong Yang. "Enantioselective synthesis of arylglycine derivatives by direct C–H oxidative cross-coupling". Chemical Communications 51, n.º 5 (2015): 832–35. http://dx.doi.org/10.1039/c4cc07361d.
Texto completo da fonteEl Abbouchi, Abdelmoula, Jamal Koubachi, Nabil El Brahmi e 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, n.º 5 (27 de novembro de 2019): 347–54. http://dx.doi.org/10.13171/mjc1911271124sek.
Texto completo da fonteZhu, Hui, Xing Liu, Cai-Zhu Chang e Zhi-Bing Dong. "Copper-Catalyzed C–S Cross-Coupling Reaction: S-Arylation of Arylthioureas". Synthesis 49, n.º 23 (22 de agosto de 2017): 5211–16. http://dx.doi.org/10.1055/s-0036-1590879.
Texto completo da fonteMayhugh, Amy L., e Christine K. Luscombe. "Room-temperature Pd/Ag direct arylation enabled by a radical pathway". Beilstein Journal of Organic Chemistry 16 (13 de março de 2020): 384–90. http://dx.doi.org/10.3762/bjoc.16.36.
Texto completo da fonteCao, Zhi-Chao, Da-Gang Yu, Ru-Yi Zhu, Jiang-Bo Wei e Zhang-Jie Shi. "Direct cross-coupling of benzyl alcohols to construct diarylmethanes via palladium catalysis". Chemical Communications 51, n.º 13 (2015): 2683–86. http://dx.doi.org/10.1039/c4cc10084k.
Texto completo da fonteRaina, Gaurav, Prakash Kannaboina, Nagaraju Mupparapu, Sushil Raina, Qazi Naveed Ahmed e Parthasarathi Das. "Programmed synthesis of triarylnitroimidazoles via sequential cross-coupling reactions". Organic & Biomolecular Chemistry 17, n.º 8 (2019): 2134–47. http://dx.doi.org/10.1039/c9ob00144a.
Texto completo da fonteMarquise, Nada, Vincent Dorcet, Floris Chevallier e Florence Mongin. "Synthesis of substituted azafluorenones from dihalogeno diaryl ketones by palladium-catalyzed auto-tandem processes". Org. Biomol. Chem. 12, n.º 41 (2014): 8138–41. http://dx.doi.org/10.1039/c4ob01629g.
Texto completo da fonteWang, Xiaochen, Kai Wang e 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, n.º 10 (2015): 1846–55. http://dx.doi.org/10.1039/c4py01627k.
Texto completo da fonteJin, Rongwei, Charles Beromeo Bheeter e 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 (27 de maio de 2014): 1239–45. http://dx.doi.org/10.3762/bjoc.10.123.
Texto completo da fonteFaradhiyani, Alanna, Qiao Zhang, Keisuke Maruyama, Junpei Kuwabara, Takeshi Yasuda e Takaki Kanbara. "Synthesis of bithiazole-based semiconducting polymers via Cu-catalysed aerobic oxidative coupling". Materials Chemistry Frontiers 2, n.º 7 (2018): 1306–9. http://dx.doi.org/10.1039/c7qm00584a.
Texto completo da fonteNgo, Thang Ngoc, Peter Ehlers, Tuan Thanh Dang, Alexander Villinger e 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, n.º 11 (2015): 3321–30. http://dx.doi.org/10.1039/c5ob00013k.
Texto completo da fontePacheco-Benichou, Alexandra, Thierry Besson e Corinne Fruit. "Diaryliodoniums Salts as Coupling Partners for Transition-Metal Catalyzed C- and N-Arylation of Heteroarenes". Catalysts 10, n.º 5 (28 de abril de 2020): 483. http://dx.doi.org/10.3390/catal10050483.
Texto completo da fonteMu, Yucheng, Xiaodong Tan, Yemin Zhang, Xiaobi Jing e Zhuangzhi Shi. "Pd(ii)-catalyzed β-C–H arylation of O-methyl ketoximes with iodoarenes". Organic Chemistry Frontiers 3, n.º 3 (2016): 380–84. http://dx.doi.org/10.1039/c5qo00438a.
Texto completo da fonteMahindra, Amit, e Rahul Jain. "Regiocontrolled palladium-catalyzed and copper-mediated C–H bond functionalization of protectedl-histidine". Org. Biomol. Chem. 12, n.º 23 (2014): 3792–96. http://dx.doi.org/10.1039/c4ob00430b.
Texto completo da fonteChen, Chunxiang, Daniel Hernández Maldonado, Damien Le Borgne, Fabienne Alary, Barbara Lonetti, Benoît Heinrich, Bertrand Donnio e 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, n.º 9 (2016): 7326–37. http://dx.doi.org/10.1039/c6nj00847j.
Texto completo da fonteShchegolkov, Evgeny V., Yanina V. Burgart, Daria A. Matsneva, Sophia S. Borisevich, Renata A. Kadyrova, Iana R. Orshanskaya, Vladimir V. Zarubaev e Victor I. Saloutin. "Polyfluoroalkylated antipyrines in Pd-catalyzed transformations". RSC Advances 11, n.º 56 (2021): 35174–81. http://dx.doi.org/10.1039/d1ra06967e.
Texto completo da fonteZhang, Lei, e Xile Hu. "Nickel catalysis enables convergent paired electrolysis for direct arylation of benzylic C–H bonds". Chemical Science 11, n.º 39 (2020): 10786–91. http://dx.doi.org/10.1039/d0sc01445a.
Texto completo da fonteZu, Weisai, Shuai Liu, Xin Jia e Liang Xu. "Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan–Evans–Lam reactions". Organic Chemistry Frontiers 6, n.º 9 (2019): 1356–60. http://dx.doi.org/10.1039/c8qo01313f.
Texto completo da fonteKónya, Krisztina, e Zoltán Sipos. "Synthesis of Benzopyran-Fused Flavone Derivatives via Microwave-Assisted Intramolecular C–H Activation". Synthesis 50, n.º 08 (7 de março de 2018): 1610–20. http://dx.doi.org/10.1055/s-0036-1591773.
Texto completo da fonteMendis, Shehani N., e Jon A. Tunge. "Decarboxylative dearomatization and mono-α-arylation of ketones". Chemical Communications 52, n.º 49 (2016): 7695–98. http://dx.doi.org/10.1039/c6cc03672d.
Texto completo da fonteWashington, Jack B., Michele Assante, Chunhui Yan, David McKinney, Vanessa Juba, Andrew G. Leach, Sharon E. Baillie e Marc Reid. "Trialkylammonium salt degradation: implications for methylation and cross-coupling". Chemical Science 12, n.º 20 (2021): 6949–63. http://dx.doi.org/10.1039/d1sc00757b.
Texto completo da fonteSmari, Imen, Liqin Zhao, Kedong Yuan, Hamed Ben Ammar e Henri Doucet. "Reactivity of bromofluorenes in palladium-catalysed direct arylation of heteroaromatics". Catal. Sci. Technol. 4, n.º 10 (2014): 3723–32. http://dx.doi.org/10.1039/c4cy00771a.
Texto completo da fonteNageswar Rao, D., Sk Rasheed, Ram A. Vishwakarma e Parthasarathi Das. "Copper-catalyzed sequential N-arylation of C-amino-NH-azoles". Chem. Commun. 50, n.º 85 (2014): 12911–14. http://dx.doi.org/10.1039/c4cc05628k.
Texto completo da fontePaul, Sanjay, Hari Datta Khanal, Chayan Dhar Clinton, Sung Hong Kim e Yong Rok Lee. "Pd(TFA)2-catalyzed direct arylation of quinoxalinones with arenes". Organic Chemistry Frontiers 6, n.º 2 (2019): 231–35. http://dx.doi.org/10.1039/c8qo01250d.
Texto completo da fonteLiu, Shuai, Weisai Zu, Jinli Zhang e Liang Xu. "Chemoselective N-arylation of aminobenzamides via copper catalysed Chan–Evans–Lam reactions". Organic & Biomolecular Chemistry 15, n.º 44 (2017): 9288–92. http://dx.doi.org/10.1039/c7ob02491f.
Texto completo da fonteCorrea, Arkaitz, Béla Fiser e Enrique Gómez-Bengoa. "Iron-catalyzed direct α-arylation of ethers with azoles". Chemical Communications 51, n.º 69 (2015): 13365–68. http://dx.doi.org/10.1039/c5cc05005g.
Texto completo da fonteSiva Reddy, A., K. Ranjith Reddy, D. Nageswar Rao, Chaitanya K. Jaladanki, Prasad V. Bharatam, Patrick Y. S. Lam e Parthasarathi Das. "Copper(ii)-catalyzed Chan–Lam cross-coupling: chemoselective N-arylation of aminophenols". Organic & Biomolecular Chemistry 15, n.º 4 (2017): 801–6. http://dx.doi.org/10.1039/c6ob02444k.
Texto completo da fonteChen, Yuanguang, Fangyu Du, Fengyang Chen, Qifan Zhou e Guoliang Chen. "Methyl-α-d-glucopyranoside as Green Ligand for Selective Copper-Catalyzed N-Arylation". Synthesis 51, n.º 24 (14 de outubro de 2019): 4590–600. http://dx.doi.org/10.1055/s-0039-1690702.
Texto completo da fonteSeifert, Sabine, David Schmidt e Frank Würthner. "A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides". Organic Chemistry Frontiers 3, n.º 11 (2016): 1435–42. http://dx.doi.org/10.1039/c6qo00421k.
Texto completo da fonteSharma, Alpesh K., Hemant Joshi, Renu Bhaskar, Satyendra Kumar e 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, n.º 8 (2017): 2485–96. http://dx.doi.org/10.1039/c7dt00083a.
Texto completo da fonteShu, Bing, Xiao-Tong Wang, Zi-Xuan Shen, Tong Che, Mei Zhong, Jia-Lin Song, Hua-Jie Kang, Hui Xie, Luyong Zhang e Shang-Shi Zhang. "Iridium-catalyzed arylation of sulfoxonium ylides and arylboronic acids: a straightforward preparation of α-aryl ketones". Organic Chemistry Frontiers 7, n.º 14 (2020): 1802–8. http://dx.doi.org/10.1039/d0qo00543f.
Texto completo da fonteWagner, Patrick, Maud Bollenbach, Christelle Doebelin, Frédéric Bihel, Jean-Jacques Bourguignon, Christophe Salomé e Martine Schmitt. "t-BuXPhos: a highly efficient ligand for Buchwald–Hartwig coupling in water". Green Chem. 16, n.º 9 (2014): 4170–78. http://dx.doi.org/10.1039/c4gc00853g.
Texto completo da fontePuthiaraj, Pillaiyar, e 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, n.º 6 (2016): 1701–9. http://dx.doi.org/10.1039/c5cy01590a.
Texto completo da fonteCong, Zhanqing, Feng Gao e 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, n.º 19 (2019): 10820–24. http://dx.doi.org/10.1039/c9ra00749k.
Texto completo da fonteLutz, J. Patrick, Stephen T. Chau e Abigail G. Doyle. "Nickel-catalyzed enantioselective arylation of pyridine". Chemical Science 7, n.º 7 (2016): 4105–9. http://dx.doi.org/10.1039/c6sc00702c.
Texto completo da fonteBasu, Souradeep, Alexander H. Sandtorv e David R. Stuart. "Imide arylation with aryl(TMP)iodonium tosylates". Beilstein Journal of Organic Chemistry 14 (11 de maio de 2018): 1034–38. http://dx.doi.org/10.3762/bjoc.14.90.
Texto completo da fonteChen, Xin, Yunyun Bian, Baichuan Mo, Peng Sun, Chunxia Chen e Jinsong Peng. "Copper(ii)-catalyzed synthesis of multisubstituted indoles through sequential Chan–Lam and cross-dehydrogenative coupling reactions". RSC Advances 10, n.º 42 (2020): 24830–39. http://dx.doi.org/10.1039/d0ra04592f.
Texto completo da fonteBrodnik, Helena, Franc Požgan e Bogdan Štefane. "Synthesis of 8-heteroaryl nitroxoline analogues via one-pot sequential Pd-catalyzed coupling reactions". Organic & Biomolecular Chemistry 14, n.º 6 (2016): 1969–81. http://dx.doi.org/10.1039/c5ob02364e.
Texto completo da fonteTerai, Seiya, Yuki Sato, Takuya Kochi e 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 (31 de março de 2020): 544–50. http://dx.doi.org/10.3762/bjoc.16.51.
Texto completo da fonteYang, Woo-Ram, Yong-Sung Choi e Jin-Hyun Jeong. "Efficient synthesis of polymethoxyselenoflavones via regioselective direct C–H arylation of selenochromones". Organic & Biomolecular Chemistry 15, n.º 14 (2017): 3074–83. http://dx.doi.org/10.1039/c7ob00118e.
Texto completo da fonteMorimoto, Koji, Yusuke Ohnishi, Daichi Koseki, Akira Nakamura, Toshifumi Dohi e Yasuyuki Kita. "Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling". Organic & Biomolecular Chemistry 14, n.º 38 (2016): 8947–51. http://dx.doi.org/10.1039/c6ob01764a.
Texto completo da fonteKumar, K. Anil, Prakash Kannaboina, D. Nageswar Rao e Parthasarathi Das. "Nickel-catalyzed Chan–Lam cross-coupling: chemoselective N-arylation of 2-aminobenzimidazoles". Organic & Biomolecular Chemistry 14, n.º 38 (2016): 8989–97. http://dx.doi.org/10.1039/c6ob01307d.
Texto completo da fonteNasrollahzadeh, Mahmoud. "Advances in Magnetic Nanoparticles-Supported Palladium Complexes for Coupling Reactions". Molecules 23, n.º 10 (4 de outubro de 2018): 2532. http://dx.doi.org/10.3390/molecules23102532.
Texto completo da fonteSasmal, Arpan, Thierry Roisnel, Jitendra K. Bera, Henri Doucet e Jean-François Soulé. "Reactivity of 3-Bromofuran in Pd-Catalyzed C–H Bond Arylation toward the Synthesis of 2,3,5-Triarylfurans". Synthesis 51, n.º 17 (7 de maio de 2019): 3241–49. http://dx.doi.org/10.1055/s-0037-1611819.
Texto completo da fonteGao, Hui, Xinyu Chen, Pei-Long Wang, Meng-Meng Shi, Ling-Long Shang, Heng-Yi Guo, Hongji Li e Pinhua Li. "Electrochemical benzylic C–H arylation of xanthenes and thioxanthenes without a catalyst and oxidant". Organic Chemistry Frontiers 9, n.º 7 (2022): 1911–16. http://dx.doi.org/10.1039/d1qo01925b.
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