Artykuły w czasopismach na temat „Arylation coupling”
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Maiti, Debabrata, Sumon Basak i Jyoti Prasad Biswas. "Transition-Metal-Catalyzed C–H Arylation Using Organoboron Reagents". Synthesis 53, nr 18 (19.04.2021): 3151–79. http://dx.doi.org/10.1055/a-1485-4666.
Pełny tekst źródłaBarde, E., A. Guérinot i J. Cossy. "α-Arylation of Amides from α-Halo Amides Using Metal-Catalyzed Cross-Coupling Reactions". Synthesis 51, nr 01 (7.12.2018): 178–84. http://dx.doi.org/10.1055/s-0037-1611358.
Pełny tekst źródłaHuang, Qing, Liangxian Liu, Jiayi Zhu, Yu Chen, Feng Lin i Baoshuang Wang. "Highly Regioselective Arylation of 1,2,3-Triazole N-Oxides with Sodium Arenesulfinates via Palladium-Catalyzed Desulfitative Cross-Coupling Reaction". Synlett 26, nr 08 (5.03.2015): 1124–30. http://dx.doi.org/10.1055/s-0034-1380186.
Pełny tekst źródłaFischer, Carolin, i Burkhard Koenig. "Palladium- and copper-mediated N-aryl bond formation reactions for the synthesis of biological active compounds". Beilstein Journal of Organic Chemistry 7 (14.01.2011): 59–74. http://dx.doi.org/10.3762/bjoc.7.10.
Pełny tekst źródłaYemene, Amsalu Efrem, Vishwesh Venkatraman, David Moe Almenningen, Bård Helge Hoff i Odd Reidar Gautun. "Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation". Molecules 25, nr 10 (18.05.2020): 2349. http://dx.doi.org/10.3390/molecules25102349.
Pełny tekst źródłaWei, Xiao-Hong, Gang-Wei Wang i Shang-Dong Yang. "Enantioselective synthesis of arylglycine derivatives by direct C–H oxidative cross-coupling". Chemical Communications 51, nr 5 (2015): 832–35. http://dx.doi.org/10.1039/c4cc07361d.
Pełny tekst źródłaEl Abbouchi, Abdelmoula, Jamal Koubachi, Nabil El Brahmi i 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, nr 5 (27.11.2019): 347–54. http://dx.doi.org/10.13171/mjc1911271124sek.
Pełny tekst źródłaZhu, Hui, Xing Liu, Cai-Zhu Chang i Zhi-Bing Dong. "Copper-Catalyzed C–S Cross-Coupling Reaction: S-Arylation of Arylthioureas". Synthesis 49, nr 23 (22.08.2017): 5211–16. http://dx.doi.org/10.1055/s-0036-1590879.
Pełny tekst źródłaMayhugh, Amy L., i Christine K. Luscombe. "Room-temperature Pd/Ag direct arylation enabled by a radical pathway". Beilstein Journal of Organic Chemistry 16 (13.03.2020): 384–90. http://dx.doi.org/10.3762/bjoc.16.36.
Pełny tekst źródłaCao, Zhi-Chao, Da-Gang Yu, Ru-Yi Zhu, Jiang-Bo Wei i Zhang-Jie Shi. "Direct cross-coupling of benzyl alcohols to construct diarylmethanes via palladium catalysis". Chemical Communications 51, nr 13 (2015): 2683–86. http://dx.doi.org/10.1039/c4cc10084k.
Pełny tekst źródłaRaina, Gaurav, Prakash Kannaboina, Nagaraju Mupparapu, Sushil Raina, Qazi Naveed Ahmed i Parthasarathi Das. "Programmed synthesis of triarylnitroimidazoles via sequential cross-coupling reactions". Organic & Biomolecular Chemistry 17, nr 8 (2019): 2134–47. http://dx.doi.org/10.1039/c9ob00144a.
Pełny tekst źródłaMarquise, Nada, Vincent Dorcet, Floris Chevallier i Florence Mongin. "Synthesis of substituted azafluorenones from dihalogeno diaryl ketones by palladium-catalyzed auto-tandem processes". Org. Biomol. Chem. 12, nr 41 (2014): 8138–41. http://dx.doi.org/10.1039/c4ob01629g.
Pełny tekst źródłaWang, Xiaochen, Kai Wang i 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, nr 10 (2015): 1846–55. http://dx.doi.org/10.1039/c4py01627k.
Pełny tekst źródłaJin, Rongwei, Charles Beromeo Bheeter i 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 (27.05.2014): 1239–45. http://dx.doi.org/10.3762/bjoc.10.123.
Pełny tekst źródłaFaradhiyani, Alanna, Qiao Zhang, Keisuke Maruyama, Junpei Kuwabara, Takeshi Yasuda i Takaki Kanbara. "Synthesis of bithiazole-based semiconducting polymers via Cu-catalysed aerobic oxidative coupling". Materials Chemistry Frontiers 2, nr 7 (2018): 1306–9. http://dx.doi.org/10.1039/c7qm00584a.
Pełny tekst źródłaNgo, Thang Ngoc, Peter Ehlers, Tuan Thanh Dang, Alexander Villinger i 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, nr 11 (2015): 3321–30. http://dx.doi.org/10.1039/c5ob00013k.
Pełny tekst źródłaPacheco-Benichou, Alexandra, Thierry Besson i Corinne Fruit. "Diaryliodoniums Salts as Coupling Partners for Transition-Metal Catalyzed C- and N-Arylation of Heteroarenes". Catalysts 10, nr 5 (28.04.2020): 483. http://dx.doi.org/10.3390/catal10050483.
Pełny tekst źródłaMu, Yucheng, Xiaodong Tan, Yemin Zhang, Xiaobi Jing i Zhuangzhi Shi. "Pd(ii)-catalyzed β-C–H arylation of O-methyl ketoximes with iodoarenes". Organic Chemistry Frontiers 3, nr 3 (2016): 380–84. http://dx.doi.org/10.1039/c5qo00438a.
Pełny tekst źródłaMahindra, Amit, i Rahul Jain. "Regiocontrolled palladium-catalyzed and copper-mediated C–H bond functionalization of protectedl-histidine". Org. Biomol. Chem. 12, nr 23 (2014): 3792–96. http://dx.doi.org/10.1039/c4ob00430b.
Pełny tekst źródłaChen, Chunxiang, Daniel Hernández Maldonado, Damien Le Borgne, Fabienne Alary, Barbara Lonetti, Benoît Heinrich, Bertrand Donnio i 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, nr 9 (2016): 7326–37. http://dx.doi.org/10.1039/c6nj00847j.
Pełny tekst źródłaShchegolkov, Evgeny V., Yanina V. Burgart, Daria A. Matsneva, Sophia S. Borisevich, Renata A. Kadyrova, Iana R. Orshanskaya, Vladimir V. Zarubaev i Victor I. Saloutin. "Polyfluoroalkylated antipyrines in Pd-catalyzed transformations". RSC Advances 11, nr 56 (2021): 35174–81. http://dx.doi.org/10.1039/d1ra06967e.
Pełny tekst źródłaZhang, Lei, i Xile Hu. "Nickel catalysis enables convergent paired electrolysis for direct arylation of benzylic C–H bonds". Chemical Science 11, nr 39 (2020): 10786–91. http://dx.doi.org/10.1039/d0sc01445a.
Pełny tekst źródłaZu, Weisai, Shuai Liu, Xin Jia i Liang Xu. "Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan–Evans–Lam reactions". Organic Chemistry Frontiers 6, nr 9 (2019): 1356–60. http://dx.doi.org/10.1039/c8qo01313f.
Pełny tekst źródłaKónya, Krisztina, i Zoltán Sipos. "Synthesis of Benzopyran-Fused Flavone Derivatives via Microwave-Assisted Intramolecular C–H Activation". Synthesis 50, nr 08 (7.03.2018): 1610–20. http://dx.doi.org/10.1055/s-0036-1591773.
Pełny tekst źródłaMendis, Shehani N., i Jon A. Tunge. "Decarboxylative dearomatization and mono-α-arylation of ketones". Chemical Communications 52, nr 49 (2016): 7695–98. http://dx.doi.org/10.1039/c6cc03672d.
Pełny tekst źródłaWashington, Jack B., Michele Assante, Chunhui Yan, David McKinney, Vanessa Juba, Andrew G. Leach, Sharon E. Baillie i Marc Reid. "Trialkylammonium salt degradation: implications for methylation and cross-coupling". Chemical Science 12, nr 20 (2021): 6949–63. http://dx.doi.org/10.1039/d1sc00757b.
Pełny tekst źródłaSmari, Imen, Liqin Zhao, Kedong Yuan, Hamed Ben Ammar i Henri Doucet. "Reactivity of bromofluorenes in palladium-catalysed direct arylation of heteroaromatics". Catal. Sci. Technol. 4, nr 10 (2014): 3723–32. http://dx.doi.org/10.1039/c4cy00771a.
Pełny tekst źródłaNageswar Rao, D., Sk Rasheed, Ram A. Vishwakarma i Parthasarathi Das. "Copper-catalyzed sequential N-arylation of C-amino-NH-azoles". Chem. Commun. 50, nr 85 (2014): 12911–14. http://dx.doi.org/10.1039/c4cc05628k.
Pełny tekst źródłaPaul, Sanjay, Hari Datta Khanal, Chayan Dhar Clinton, Sung Hong Kim i Yong Rok Lee. "Pd(TFA)2-catalyzed direct arylation of quinoxalinones with arenes". Organic Chemistry Frontiers 6, nr 2 (2019): 231–35. http://dx.doi.org/10.1039/c8qo01250d.
Pełny tekst źródłaLiu, Shuai, Weisai Zu, Jinli Zhang i Liang Xu. "Chemoselective N-arylation of aminobenzamides via copper catalysed Chan–Evans–Lam reactions". Organic & Biomolecular Chemistry 15, nr 44 (2017): 9288–92. http://dx.doi.org/10.1039/c7ob02491f.
Pełny tekst źródłaCorrea, Arkaitz, Béla Fiser i Enrique Gómez-Bengoa. "Iron-catalyzed direct α-arylation of ethers with azoles". Chemical Communications 51, nr 69 (2015): 13365–68. http://dx.doi.org/10.1039/c5cc05005g.
Pełny tekst źródłaSiva Reddy, A., K. Ranjith Reddy, D. Nageswar Rao, Chaitanya K. Jaladanki, Prasad V. Bharatam, Patrick Y. S. Lam i Parthasarathi Das. "Copper(ii)-catalyzed Chan–Lam cross-coupling: chemoselective N-arylation of aminophenols". Organic & Biomolecular Chemistry 15, nr 4 (2017): 801–6. http://dx.doi.org/10.1039/c6ob02444k.
Pełny tekst źródłaChen, Yuanguang, Fangyu Du, Fengyang Chen, Qifan Zhou i Guoliang Chen. "Methyl-α-d-glucopyranoside as Green Ligand for Selective Copper-Catalyzed N-Arylation". Synthesis 51, nr 24 (14.10.2019): 4590–600. http://dx.doi.org/10.1055/s-0039-1690702.
Pełny tekst źródłaSeifert, Sabine, David Schmidt i Frank Würthner. "A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides". Organic Chemistry Frontiers 3, nr 11 (2016): 1435–42. http://dx.doi.org/10.1039/c6qo00421k.
Pełny tekst źródłaSharma, Alpesh K., Hemant Joshi, Renu Bhaskar, Satyendra Kumar i 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, nr 8 (2017): 2485–96. http://dx.doi.org/10.1039/c7dt00083a.
Pełny tekst źródłaShu, Bing, Xiao-Tong Wang, Zi-Xuan Shen, Tong Che, Mei Zhong, Jia-Lin Song, Hua-Jie Kang, Hui Xie, Luyong Zhang i Shang-Shi Zhang. "Iridium-catalyzed arylation of sulfoxonium ylides and arylboronic acids: a straightforward preparation of α-aryl ketones". Organic Chemistry Frontiers 7, nr 14 (2020): 1802–8. http://dx.doi.org/10.1039/d0qo00543f.
Pełny tekst źródłaWagner, Patrick, Maud Bollenbach, Christelle Doebelin, Frédéric Bihel, Jean-Jacques Bourguignon, Christophe Salomé i Martine Schmitt. "t-BuXPhos: a highly efficient ligand for Buchwald–Hartwig coupling in water". Green Chem. 16, nr 9 (2014): 4170–78. http://dx.doi.org/10.1039/c4gc00853g.
Pełny tekst źródłaPuthiaraj, Pillaiyar, i 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, nr 6 (2016): 1701–9. http://dx.doi.org/10.1039/c5cy01590a.
Pełny tekst źródłaCong, Zhanqing, Feng Gao i 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, nr 19 (2019): 10820–24. http://dx.doi.org/10.1039/c9ra00749k.
Pełny tekst źródłaLutz, J. Patrick, Stephen T. Chau i Abigail G. Doyle. "Nickel-catalyzed enantioselective arylation of pyridine". Chemical Science 7, nr 7 (2016): 4105–9. http://dx.doi.org/10.1039/c6sc00702c.
Pełny tekst źródłaBasu, Souradeep, Alexander H. Sandtorv i David R. Stuart. "Imide arylation with aryl(TMP)iodonium tosylates". Beilstein Journal of Organic Chemistry 14 (11.05.2018): 1034–38. http://dx.doi.org/10.3762/bjoc.14.90.
Pełny tekst źródłaChen, Xin, Yunyun Bian, Baichuan Mo, Peng Sun, Chunxia Chen i Jinsong Peng. "Copper(ii)-catalyzed synthesis of multisubstituted indoles through sequential Chan–Lam and cross-dehydrogenative coupling reactions". RSC Advances 10, nr 42 (2020): 24830–39. http://dx.doi.org/10.1039/d0ra04592f.
Pełny tekst źródłaBrodnik, Helena, Franc Požgan i Bogdan Štefane. "Synthesis of 8-heteroaryl nitroxoline analogues via one-pot sequential Pd-catalyzed coupling reactions". Organic & Biomolecular Chemistry 14, nr 6 (2016): 1969–81. http://dx.doi.org/10.1039/c5ob02364e.
Pełny tekst źródłaTerai, Seiya, Yuki Sato, Takuya Kochi i 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 (31.03.2020): 544–50. http://dx.doi.org/10.3762/bjoc.16.51.
Pełny tekst źródłaYang, Woo-Ram, Yong-Sung Choi i Jin-Hyun Jeong. "Efficient synthesis of polymethoxyselenoflavones via regioselective direct C–H arylation of selenochromones". Organic & Biomolecular Chemistry 15, nr 14 (2017): 3074–83. http://dx.doi.org/10.1039/c7ob00118e.
Pełny tekst źródłaMorimoto, Koji, Yusuke Ohnishi, Daichi Koseki, Akira Nakamura, Toshifumi Dohi i Yasuyuki Kita. "Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling". Organic & Biomolecular Chemistry 14, nr 38 (2016): 8947–51. http://dx.doi.org/10.1039/c6ob01764a.
Pełny tekst źródłaKumar, K. Anil, Prakash Kannaboina, D. Nageswar Rao i Parthasarathi Das. "Nickel-catalyzed Chan–Lam cross-coupling: chemoselective N-arylation of 2-aminobenzimidazoles". Organic & Biomolecular Chemistry 14, nr 38 (2016): 8989–97. http://dx.doi.org/10.1039/c6ob01307d.
Pełny tekst źródłaNasrollahzadeh, Mahmoud. "Advances in Magnetic Nanoparticles-Supported Palladium Complexes for Coupling Reactions". Molecules 23, nr 10 (4.10.2018): 2532. http://dx.doi.org/10.3390/molecules23102532.
Pełny tekst źródłaSasmal, Arpan, Thierry Roisnel, Jitendra K. Bera, Henri Doucet i Jean-François Soulé. "Reactivity of 3-Bromofuran in Pd-Catalyzed C–H Bond Arylation toward the Synthesis of 2,3,5-Triarylfurans". Synthesis 51, nr 17 (7.05.2019): 3241–49. http://dx.doi.org/10.1055/s-0037-1611819.
Pełny tekst źródłaGao, Hui, Xinyu Chen, Pei-Long Wang, Meng-Meng Shi, Ling-Long Shang, Heng-Yi Guo, Hongji Li i Pinhua Li. "Electrochemical benzylic C–H arylation of xanthenes and thioxanthenes without a catalyst and oxidant". Organic Chemistry Frontiers 9, nr 7 (2022): 1911–16. http://dx.doi.org/10.1039/d1qo01925b.
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