Статті в журналах з теми "C - hetero"
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Zhao, Yating, and Wujiong Xia. "Photochemical C–H bond coupling for (hetero)aryl C(sp2)–C(sp3) bond construction." Organic & Biomolecular Chemistry 17, no. 20 (2019): 4951–63. http://dx.doi.org/10.1039/c9ob00244h.
Повний текст джерелаHucthagowder, Vishwanathan, Chelsea D. Mullins, Rekha Meyer, Rakesh Nagarajan, John F. DiPersio, Ravi Vij, Michael H. Tomasson, and Shashikant Kulkarni. "Resequencing Analysis of the Human Candidate Ras and Receptor Tyrosine Kinase Gene Family In Multiple Myeloma." Blood 116, no. 21 (November 19, 2010): 301. http://dx.doi.org/10.1182/blood.v116.21.301.301.
Повний текст джерелаChoy, Pui Ying, Shun Man Wong, Anant Kapdi, and Fuk Yee Kwong. "Recent developments in palladium-catalysed non-directed coupling of (hetero)arene C–H bonds with C–Z (Z = B, Si, Sn, S, N, C, H) bonds in bi(hetero)aryl synthesis." Organic Chemistry Frontiers 5, no. 2 (2018): 288–321. http://dx.doi.org/10.1039/c7qo00693d.
Повний текст джерелаXiao, Fang, Jin-Hong Lin, Fei Hao, Xing Zheng, Yu Guo, and Ji-Chang Xiao. "Visible light mediated C–H trifluoromethylation of (hetero)arenes." Organic Chemistry Frontiers 9, no. 7 (2022): 1982–85. http://dx.doi.org/10.1039/d2qo00067a.
Повний текст джерелаRan, You, Yudong Yang, Huansha You, and Jingsong You. "RhCl3-Catalyzed Oxidative C–H/C–H Cross-Coupling of (Hetero)aromatic Sulfonamides with (Hetero)arenes." ACS Catalysis 8, no. 3 (January 30, 2018): 1796–801. http://dx.doi.org/10.1021/acscatal.7b04298.
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 джерелаLiu, Yahu, Xuebin Liao, and Lu Hu. "Recent Progress in Methylation of (Hetero)Arenes by Cross-Coupling or C–H Activation." Synlett 29, no. 04 (February 5, 2018): 375–82. http://dx.doi.org/10.1055/s-0037-1609093.
Повний текст джерелаPahovnik, David, Uroš Uršič, Uroš Grošelj, Anton Meden, Jurij Svete, and Branko Stanovnik. "Synthesis of Dimethyl 1-(Hetero)aryl-4-oxo-1,4-dihydropyridazine- 3,5-dicarboxylates from Dimethyl 3-Oxopentane-1,5-dioates." Zeitschrift für Naturforschung B 63, no. 4 (April 1, 2008): 407–14. http://dx.doi.org/10.1515/znb-2008-0407.
Повний текст джерелаArani, A. Ghorbanpour, and R. Kolahchi. "Exact solution for nonlocal axial buckling of linear carbon nanotube hetero-junctions." Proceedings of the Institution of Mechanical Engineers, Part C: Journal of Mechanical Engineering Science 228, no. 2 (March 25, 2013): 366–77. http://dx.doi.org/10.1177/0954406213483647.
Повний текст джерелаGui, Yong-Yuan, Li-Li Liao, Liang Sun, Zhen Zhang, Jian-Heng Ye, Guo Shen, Zhi-Peng Lu, Wen-Jun Zhou, and Da-Gang Yu. "Coupling of C(sp3)–H bonds with C(sp2)–O electrophiles: mild, general and selective." Chemical Communications 53, no. 6 (2017): 1192–95. http://dx.doi.org/10.1039/c6cc09685a.
Повний текст джерелаGuo, Lirong, Fengting Liu, Liying Wang, Hairui Yuan, Lei Feng, Haifeng Lu, and Hongyin Gao. "Transition-metal-free aerobic C–O bond formation via C–N bond cleavage." Organic Chemistry Frontiers 7, no. 9 (2020): 1077–81. http://dx.doi.org/10.1039/d0qo00173b.
Повний текст джерелаWen, Si, Weiwei Lv, Dan Ba, Jing Liu, and Guolin Cheng. "Ruthenium(ii)-catalyzed chemoselective deacylative annulation of 1,3-diones with sulfoxonium ylides via C–C bond activation." Chemical Science 10, no. 39 (2019): 9104–8. http://dx.doi.org/10.1039/c9sc03245b.
Повний текст джерелаIqbal, S. A., J. Pahl, K. Yuan, and M. J. Ingleson. "Intramolecular (directed) electrophilic C–H borylation." Chemical Society Reviews 49, no. 13 (2020): 4564–91. http://dx.doi.org/10.1039/c9cs00763f.
Повний текст джерелаNi, Hui-Qi, Phillippa Cooper, and Keary M. Engle. "Recent advances in palladium-catalyzed (hetero)annulation of CC bonds with ambiphilic organo(pseudo)halides." Chemical Communications 57, no. 62 (2021): 7610–24. http://dx.doi.org/10.1039/d1cc02836g.
Повний текст джерелаTanwar, Lalita, Jonas Börgel, Johannes Lehmann, and Tobias Ritter. "Selective C–H Iodination of (Hetero)arenes." Organic Letters 23, no. 13 (June 11, 2021): 5024–27. http://dx.doi.org/10.1021/acs.orglett.1c01530.
Повний текст джерелаHirano, Koji, and Masahiro Miura. "Copper-mediated oxidative direct C–C (hetero)aromatic cross-coupling." Chemical Communications 48, no. 87 (2012): 10704. http://dx.doi.org/10.1039/c2cc34659a.
Повний текст джерелаWei, Kai-Jie, Zheng-jun Quan, Zhang Zhang, Yu-xia Da, and Xi-cun Wang. "Direct C–H heteroarylation of azoles with 1,2-di(pyrimidin-2-yl)disulfides through C–S cleavage of disulfides." RSC Advances 6, no. 81 (2016): 78059–63. http://dx.doi.org/10.1039/c6ra18997k.
Повний текст джерелаRoy, Sourav, Michael G. B. Drew, Antonio Bauzá, Antonio Frontera та Shouvik Chattopadhyay. "Estimation of conventional C–H⋯π (arene), unconventional C–H⋯π (chelate) and C–H⋯π (thiocyanate) interactions in hetero-nuclear nickel(ii)–cadmium(ii) complexes with a compartmental Schiff base". Dalton Transactions 46, № 16 (2017): 5384–97. http://dx.doi.org/10.1039/c6dt04906k.
Повний текст джерелаChupakhin, O. N., A. V. Shchepochkin, and V. N. Charushin. "Atom- and step-economical nucleophilic arylation of azaaromatics via electrochemical oxidative cross C–C coupling reactions." Green Chemistry 19, no. 13 (2017): 2931–35. http://dx.doi.org/10.1039/c7gc00789b.
Повний текст джерелаIrgashev, Roman A., Arseny A. Karmatsky, Gennady L. Rusinov, and Valery N. Charushin. "A new and convenient synthetic way to 2-substituted thieno[2,3-b]indoles." Beilstein Journal of Organic Chemistry 11 (June 11, 2015): 1000–1007. http://dx.doi.org/10.3762/bjoc.11.112.
Повний текст джерелаYang, Tao, Congshan Zhou, Zan Yang, Jiao Li, Jie Hua та Jianmin Yi. "KI/K2S2O8-Mediated α-C–H Sulfenylation of Carbonyl Compounds with (Hetero)Aryl Thiols". Synlett 28, № 17 (13 липня 2017): 2325–29. http://dx.doi.org/10.1055/s-0036-1588483.
Повний текст джерелаSantiago, Carlos, Nuria Sotomayor, and Esther Lete. "Pd(II)-Catalyzed C-H Acylation of (Hetero)arenes—Recent Advances." Molecules 25, no. 14 (July 16, 2020): 3247. http://dx.doi.org/10.3390/molecules25143247.
Повний текст джерелаCao, Liming, Yu Hua, Hong-Gang Cheng, and Qianghui Zhou. "C–H hetero-functionalization of arenes through palladacyclopentane-type intermediates." Organic Chemistry Frontiers 8, no. 14 (2021): 3883–914. http://dx.doi.org/10.1039/d0qo01350a.
Повний текст джерелаLiu, Xia, Xin Zhao, Fushun Liang, and Baoyi Ren. "t-BuONa-mediated direct C–H halogenation of electron-deficient (hetero)arenes." Organic & Biomolecular Chemistry 16, no. 6 (2018): 886–90. http://dx.doi.org/10.1039/c7ob03081a.
Повний текст джерелаYang, Yudong, Jingbo Lan, and Jingsong You. "Oxidative C–H/C–H Coupling Reactions between Two (Hetero)arenes." Chemical Reviews 117, no. 13 (January 13, 2017): 8787–863. http://dx.doi.org/10.1021/acs.chemrev.6b00567.
Повний текст джерелаQin, Dekun, Jing Wang, Xurong Qin, Chunxia Wang, Ge Gao, and Jingsong You. "Rh(iii)-catalyzed oxime ether-directed heteroarylation of arene through oxidative C–H/C–H cross-coupling." Chemical Communications 51, no. 28 (2015): 6190–93. http://dx.doi.org/10.1039/c5cc00387c.
Повний текст джерелаZhang, Zuxiao, Leah M. Stateman та David A. Nagib. "δ C–H (hetero)arylationviaCu-catalyzed radical relay". Chemical Science 10, № 4 (2019): 1207–11. http://dx.doi.org/10.1039/c8sc04366c.
Повний текст джерелаKona, Chandrababu Naidu, Mahesh N. Patil, and Chepuri V. Ramana. "Gold(i) catalyzed [1,3] O → C rearrangement of benzylvinyl ethers." Organic Chemistry Frontiers 3, no. 4 (2016): 453–56. http://dx.doi.org/10.1039/c5qo00397k.
Повний текст джерелаMIRANDA, E. N. "ON THE CAPACITY OF MULTILAYER NEURAL NETWORKS TRAINED WITH BACKPROPAGATION." International Journal of Neural Systems 10, no. 04 (August 2000): 281–85. http://dx.doi.org/10.1142/s0129065700000247.
Повний текст джерелаKnochel, Paul, Maximilian Hofmayer, Jeffrey Hammann, and Gérard Cahiez. "Iron-Catalyzed C(sp2)–C(sp3) Cross-Coupling Reactions of Di(hetero)arylmanganese Reagents and Primary and Secondary Alkyl Halides." Synlett 29, no. 01 (August 30, 2017): 65–70. http://dx.doi.org/10.1055/s-0036-1590891.
Повний текст джерелаMaurício, Tatiana, Daniela Couto, Diana Lopes, Tiago Conde, Rita Pais, Joana Batista, Tânia Melo, et al. "Differences and Similarities in Lipid Composition, Nutritional Value, and Bioactive Potential of Four Edible Chlorella vulgaris Strains." Foods 12, no. 8 (April 12, 2023): 1625. http://dx.doi.org/10.3390/foods12081625.
Повний текст джерелаTabasso, Silvia, Emanuela Calcio Gaudino, Elisa Acciardo, Maela Manzoli, Agnese Giacomino та Giancarlo Cravotto. "Microwave-Assisted Dehydrogenative Cross Coupling Reactions in γ-valerolactone with a Reusable Pd/β-cyclodextrin Crosslinked Catalyst". Molecules 24, № 2 (14 січня 2019): 288. http://dx.doi.org/10.3390/molecules24020288.
Повний текст джерелаYamada, Tsuyoshi, Jing Jiang, Naoya Ito, Kwihwan Park, Hayato Masuda, Chikara Furugen, Moeka Ishida, Seiya Ōtori, and Hironao Sajiki. "Development of Facile and Simple Processes for the Heterogeneous Pd-Catalyzed Ligand-Free Continuous-Flow Suzuki–Miyaura Coupling." Catalysts 10, no. 10 (October 19, 2020): 1209. http://dx.doi.org/10.3390/catal10101209.
Повний текст джерелаPradhan, Suman, Sandeep Patel, and Indranil Chatterjee. "Nitrosoarene-catalyzed regioselective aromatic C–H sulfinylation with thiols under aerobic conditions." Chemical Communications 56, no. 37 (2020): 5054–57. http://dx.doi.org/10.1039/d0cc01188f.
Повний текст джерелаHirano, Koji, and Masahiro Miura. "ChemInform Abstract: Copper-Mediated Oxidative Direct C-C (Hetero)aromatic Cross-Coupling." ChemInform 44, no. 3 (January 15, 2013): no. http://dx.doi.org/10.1002/chin.201303199.
Повний текст джерелаBhujabal, Yuvraj B., Kamlesh S. Vadagaonkar, and Anant R. Kapdi. "Pd/PTABS: Catalyst for Efficient C−H (Hetero)Arylation of 1,3,4-Oxadiazoles Using Bromo(Hetero)Arenes." Asian Journal of Organic Chemistry 8, no. 2 (January 18, 2019): 289–95. http://dx.doi.org/10.1002/ajoc.201800713.
Повний текст джерелаPacheco-Benichou, Alexandra, Eugénie Ivendengani, Ioannis K. Kostakis, Thierry Besson, and Corinne Fruit. "Copper-Catalyzed C–H Arylation of Fused-Pyrimidinone Derivatives Using Diaryliodonium Salts." Catalysts 11, no. 1 (December 29, 2020): 28. http://dx.doi.org/10.3390/catal11010028.
Повний текст джерелаBarata-Vallejo, Sebastián, and Al Postigo. "Photocatalytic Difluoromethylation Reactions of Aromatic Compounds and Aliphatic Multiple C–C Bonds." Molecules 24, no. 24 (December 6, 2019): 4483. http://dx.doi.org/10.3390/molecules24244483.
Повний текст джерелаRamanavicius, Simonas, Alla Tereshchenko, Renata Karpicz, Vilma Ratautaite, Urte Bubniene, Audrius Maneikis, Arunas Jagminas, and Arunas Ramanavicius. "TiO2-x/TiO2-Structure Based ‘Self-Heated’ Sensor for the Determination of Some Reducing Gases." Sensors 20, no. 1 (December 21, 2019): 74. http://dx.doi.org/10.3390/s20010074.
Повний текст джерелаMoon, Youngtaek, Yujeong Jeong, Daehyuk Kook та Sungwoo Hong. "Rh(iii)-catalyzed direct C–H/C–H cross-coupling of quinones with arenes assisted by a directing group: identification of carbazole quinones as GSKβ inhibitors". Organic & Biomolecular Chemistry 13, № 13 (2015): 3918–23. http://dx.doi.org/10.1039/c4ob02624a.
Повний текст джерелаZhang, Tao, Zi-Yu Zhang, Guowei Kang, Tao Sheng, Jie-Lun Yan, Yuan-Bin Yang, Yuxin Ouyang, and Jin-Quan Yu. "Enantioselective remote methylene C−H (hetero)arylation of cycloalkane carboxylic acids." Science 384, no. 6697 (May 17, 2024): 793–98. http://dx.doi.org/10.1126/science.ado1246.
Повний текст джерелаYin, Xue-Song, Yi-Chen Li, Jun Yuan, Wen-Jia Gu, and Bing-Feng Shi. "Copper(ii)-catalyzed methoxylation of unactivated (hetero)aryl C–H bonds using a removable bidentate auxiliary." Organic Chemistry Frontiers 2, no. 2 (2015): 119–23. http://dx.doi.org/10.1039/c4qo00276h.
Повний текст джерелаDang, C. V., J. Barrett, M. Villa-Garcia, L. M. Resar, G. J. Kato, and E. R. Fearon. "Intracellular leucine zipper interactions suggest c-Myc hetero-oligomerization." Molecular and Cellular Biology 11, no. 2 (February 1991): 954–62. http://dx.doi.org/10.1128/mcb.11.2.954-962.1991.
Повний текст джерелаJafarov, Maarif A., HM Mamedov, and EF Nasirov. "Photo sensivity Hetero junction C-Si/Porous-Si/Zncds." Madridge Journal of Nanotechnology & Nanoscience 4, no. 1 (January 28, 2019): 123–26. http://dx.doi.org/10.18689/mjnn-1000125.
Повний текст джерелаDang, C. V., J. Barrett, M. Villa-Garcia, L. M. Resar, G. J. Kato, and E. R. Fearon. "Intracellular leucine zipper interactions suggest c-Myc hetero-oligomerization." Molecular and Cellular Biology 11, no. 2 (February 1991): 954–62. http://dx.doi.org/10.1128/mcb.11.2.954.
Повний текст джерелаMeucci, Elizabeth A., Shay N. Nguyen, Nicole M. Camasso, Eugene Chong, Alireza Ariafard, Allan J. Canty, and Melanie S. Sanford. "Nickel(IV)-Catalyzed C–H Trifluoromethylation of (Hetero)arenes." Journal of the American Chemical Society 141, no. 32 (August 5, 2019): 12872–79. http://dx.doi.org/10.1021/jacs.9b06383.
Повний текст джерелаHayrapetyan, Davit, Raja K. Rit, Markus Kratz, Kristina Tschulik, and Lukas J. Gooßen. "Electrochemical C−H Cyanation of Electron-Rich (Hetero)Arenes." Chemistry - A European Journal 24, no. 44 (July 10, 2018): 11288–91. http://dx.doi.org/10.1002/chem.201802247.
Повний текст джерелаHamzehloo, Majid, Akram Hosseinian, Saeideh Ebrahimiasl, Aazam Monfared, and Esmail Vessally. "Direct C-H trifluoromethylthiolation of (hetero)arenes: A review." Journal of Fluorine Chemistry 224 (August 2019): 52–60. http://dx.doi.org/10.1016/j.jfluchem.2019.05.004.
Повний текст джерелаBao, Lei, Hongxiang Yang, Beibei Zhan, and Xiaheng Zhang. "Photoinduced Bi-catalyzed C–H trifluoromethylation of (hetero)arenes." Chem Catalysis 4, no. 1 (January 2024): 100877. http://dx.doi.org/10.1016/j.checat.2023.100877.
Повний текст джерелаAlbano, Gianluigi, Angela Punzi, Maria Annunziata M. Capozzi, and Gianluca M. Farinola. "Sustainable protocols for direct C–H bond arylation of (hetero)arenes." Green Chemistry 24, no. 5 (2022): 1809–94. http://dx.doi.org/10.1039/d1gc03168f.
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