Статті в журналах з теми "C-Hetero Bond"
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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 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 джерелаRoth-Barton, Jesse, Yit Wooi Goh, Asimo Karnezis та Jonathan M. White. "Structural Studies on α-Pyrone Cycloadducts. Manifestation of the Early Stages of CO2 Extrusion by retro Hetero-Diels - Alder Reaction". Australian Journal of Chemistry 62, № 5 (2009): 407. http://dx.doi.org/10.1071/ch09018.
Повний текст джерелаCorrea, Arkaitz, та Marcos Segundo. "Cross-Dehydrogenative Coupling Reactions for the Functionalization of α-Amino Acid Derivatives and Peptides". Synthesis 50, № 15 (25 червня 2018): 2853–66. http://dx.doi.org/10.1055/s-0037-1610073.
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 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 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 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 джерелаGe, Danhua, and Xue-Qiang Chu. "Multiple-fold C–F bond functionalization for the synthesis of (hetero)cyclic compounds: fluorine as a detachable chemical handle." Organic Chemistry Frontiers 9, no. 7 (2022): 2013–55. http://dx.doi.org/10.1039/d1qo01749g.
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 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.
Повний текст джерелаHagui, Wided, Néji Besbes, Ezzeddine Srasra, Jean-François Soulé, and Henri Doucet. "Direct access to 2-(hetero)arylated pyridines from 6-substituted 2-bromopyridines via phosphine-free palladium-catalyzed C–H bond arylations: the importance of the C6 substituent." RSC Advances 6, no. 21 (2016): 17110–17. http://dx.doi.org/10.1039/c6ra01861k.
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 джерелаSharma, Ruchi, and M. Ramu Yadav. "Recent developments in decarboxylative C(aryl)–X bond formation from (hetero)aryl carboxylic acids." Organic & Biomolecular Chemistry 19, no. 25 (2021): 5476–500. http://dx.doi.org/10.1039/d1ob00675d.
Повний текст джерелаZhou, Ming-Bo, Rui Pi, Fan Teng, Yang Li, and Jin-Heng Li. "Ring-opening formal hetero-[5+2] cycloaddition of 1-tosyl-2,3-dihydro-1H-pyrroles with terminal alkynes: entry to 1-tosyl-2,3-dihydro 2,3-dihydro-1H-azepines." Chemical Communications 55, no. 75 (2019): 11295–98. http://dx.doi.org/10.1039/c9cc05082e.
Повний текст джерелаLi, Mengli, Xing Li, Honghong Chang, Wenchao Gao, and Wenlong Wei. "Palladium-catalyzed direct C–H arylation of pyridine N-oxides with potassium aryl- and heteroaryltrifluoroborates." Organic & Biomolecular Chemistry 14, no. 8 (2016): 2421–26. http://dx.doi.org/10.1039/c5ob02409a.
Повний текст джерелаCui, Bingcun, Guosheng Huang, Jin Liu, Shaofen Jin, Yingxing Zhou, Dongmei Ni, Tingting Liu, Gang Hu, and Xin Yu. "Palladium-Catalyzed ortho-Monoacylation of Arenes with Aldehydes via 1,2,4-Benzotriazine-Directed C–H Bond Activation." Synthesis 52, no. 09 (February 10, 2020): 1407–16. http://dx.doi.org/10.1055/s-0039-1691564.
Повний текст джерелаWelsh, Thomas A., Audrey Laventure, Thomas Baumgartner, and Gregory C. Welch. "Dithienophosphole-based molecular electron acceptors constructed using direct (hetero)arylation cross-coupling methods." Journal of Materials Chemistry C 6, no. 8 (2018): 2148–54. http://dx.doi.org/10.1039/c7tc05631a.
Повний текст джерелаPunji, Benudhar, and Muniyappa Vijaykumar. "Advances in Transition-Metal-Catalyzed C–H Bond Oxygenation of Amides." Synthesis 53, no. 17 (April 13, 2021): 2935–46. http://dx.doi.org/10.1055/a-1481-2584.
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 джерелаFrogley, Benjamin J., and Anthony F. Hill. "Metal coordination to bipyridyl carbynes." Dalton Transactions 49, no. 10 (2020): 3272–83. http://dx.doi.org/10.1039/c9dt04744a.
Повний текст джерелаVarala, Ravi, Vittal Seema, and Narsimhaswamy Dubasi. "Phenyliodine(III)diacetate (PIDA): Applications in Organic Synthesis." Organics 4, no. 1 (December 23, 2022): 1–40. http://dx.doi.org/10.3390/org4010001.
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 джерелаLe Bras, Jean, and Jacques Muzart. "Pd-Catalyzed Intermolecular Dehydrogenative Heck Reactions of Five-Membered Heteroarenes." Catalysts 10, no. 5 (May 19, 2020): 571. http://dx.doi.org/10.3390/catal10050571.
Повний текст джерелаLipp, Benjamin, Alexander Lipp, Heiner Detert, and Till Opatz. "Light-Induced Alkylation of (Hetero)aromatic Nitriles in a Transition-Metal-Free C–C-Bond Metathesis." Organic Letters 19, no. 8 (April 7, 2017): 2054–57. http://dx.doi.org/10.1021/acs.orglett.7b00652.
Повний текст джерелаGuchhait, Sankar, Maneesh Kashyap, and Shuddham Saraf. "Direct C-H Bond Arylation of (Hetero)arenes with Aryl and Heteroarylboronic Acids." Synthesis 2010, no. 07 (January 20, 2010): 1166–70. http://dx.doi.org/10.1055/s-0029-1219234.
Повний текст джерелаBrahim, Mariem, Hamed Ben Ammar, Jean-François Soulé, and Henri Doucet. "Regiocontroled Pd-catalysed C5-arylation of 3-substituted thiophene derivatives using a bromo-substituent as blocking group." Beilstein Journal of Organic Chemistry 12 (October 17, 2016): 2197–203. http://dx.doi.org/10.3762/bjoc.12.210.
Повний текст джерелаKang, Qing-Qing, Wenfeng Wu, Qiang Li, and Wen-Ting Wei. "Photochemical strategies for C–N bond formation via metal catalyst-free (hetero) aryl C(sp2)–H functionalization." Green Chemistry 22, no. 10 (2020): 3060–68. http://dx.doi.org/10.1039/d0gc01088j.
Повний текст джерелаMahajan, Bhushan, Dnyaneshwar Aand, and Ajay K. Singh. "Silver‐Catalyzed Arylation of (Hetero)arenes via Oxidative Benzylic C−C Bond Cleavage of Benzyl Alcohols/ Benzaldehyde." ChemistrySelect 3, no. 43 (November 23, 2018): 12336–40. http://dx.doi.org/10.1002/slct.201803215.
Повний текст джерелаLiu, Kai-Hui, Guang-Qi Hu, Cai-Xia Wang, Fei-Fei Sheng, Jing-Wen Bai, Jian-Guo Gu, and Hong-Hai Zhang. "C–H Bond Functionalization of (Hetero)aryl Bromide Enabled Synthesis of Brominated Biaryl Compounds." Organic Letters 23, no. 15 (July 16, 2021): 5626–30. http://dx.doi.org/10.1021/acs.orglett.1c01613.
Повний текст джерелаVogel, Pierre, and José Angel Sordo Gonzalo. "Expeditious Asymmetric Synthesis of Polypropionates Relying on Sulfur Dioxide-Induced C–C Bond Forming Reactions." Catalysts 11, no. 11 (October 21, 2021): 1267. http://dx.doi.org/10.3390/catal11111267.
Повний текст джерелаShokol, Tetyana, Natalia Gorbulenko, and Volodymyr Khilya. "Synthesis of chromones, annulated with oxygen-containing heterocycles with two hetero atoms at C(7)-C(8) bond." French-Ukrainian Journal of Chemistry 7, no. 1 (2019): 121–39. http://dx.doi.org/10.17721/fujcv7i1p121-139.
Повний текст джерелаDing, Chengrong, Guofu Zhang, Lidi Xuan, and Yiyong Zhao. "Sulfuryl Fluoride Promoted Thiocyanation of Alcohols: A Practical Method for Preparing Thiocyanates." Synlett 31, no. 14 (June 16, 2020): 1413–17. http://dx.doi.org/10.1055/s-0040-1707151.
Повний текст джерелаMao, Wenbin, and Chen Zhu. "C–C Bond (Hetero)arylation of Ring-Fused Benzocyclobutenols and Application in the Assembly of Polycyclic Aromatic Hydrocarbons." Journal of Organic Chemistry 82, no. 17 (August 23, 2017): 9133–43. http://dx.doi.org/10.1021/acs.joc.7b01727.
Повний текст джерелаMa, Changle, Danielle Hagstrom, Soumi Guha Polley, and Suresh Subramani. "Redox-regulated Cargo Binding and Release by the Peroxisomal Targeting Signal Receptor, Pex5." Journal of Biological Chemistry 288, no. 38 (July 31, 2013): 27220–31. http://dx.doi.org/10.1074/jbc.m113.492694.
Повний текст джерелаLi, Yahui, and Xiao‐Feng Wu. "Direct C−H Bond Borylation of (Hetero)Arenes: Evolution from Noble Metal to Metal Free." Angewandte Chemie International Edition 59, no. 5 (January 27, 2020): 1770–74. http://dx.doi.org/10.1002/anie.201914914.
Повний текст джерелаGuchhait, Sankar K., Maneesh Kashyap, and Shuddham Saraf. "ChemInform Abstract: Direct C-H Bond Arylation of (Hetero)arenes with Aryl and Heteroarylboronic Acids." ChemInform 41, no. 31 (July 9, 2010): no. http://dx.doi.org/10.1002/chin.201031099.
Повний текст джерелаRodrigues, Janh, Sumbal Saba, Antônio C. Joussef, Jamal Rafique, and Antonio L. Braga. "KIO3 -Catalyzed C(sp2 )-H Bond Selenylation/Sulfenylation of (Hetero)arenes: Synthesis of Chalcogenated (Hetero)arenes and their Evaluation for Anti-Alzheimer Activity." Asian Journal of Organic Chemistry 7, no. 9 (August 21, 2018): 1819–24. http://dx.doi.org/10.1002/ajoc.201800346.
Повний текст джерелаAlbano, Gianluigi, Gianfranco Decandia, Maria Annunziata M. Capozzi, Nicola Zappimbulso, Angela Punzi, and Gianluca M. Farinola. "Infrared Irradiation‐Assisted Solvent‐Free Pd‐Catalyzed (Hetero)aryl‐aryl Coupling via C−H Bond Activation." ChemSusChem 14, no. 16 (July 22, 2021): 3391–401. http://dx.doi.org/10.1002/cssc.202101070.
Повний текст джерелаAckermann, Lutz. "Metal-catalyzed direct alkylations of (hetero)arenes via C–H bond cleavages with unactivated alkyl halides." Chemical Communications 46, no. 27 (2010): 4866. http://dx.doi.org/10.1039/c0cc00778a.
Повний текст джерелаHagui, Wided, Henri Doucet, and Jean-François Soulé. "Application of Palladium-Catalyzed C(sp2)–H Bond Arylation to the Synthesis of Polycyclic (Hetero)Aromatics." Chem 5, no. 8 (August 2019): 2006–78. http://dx.doi.org/10.1016/j.chempr.2019.06.005.
Повний текст джерелаHagui, Wided, Henri Doucet, and Jean-François Soulé. "Application of Palladium-Catalyzed C(sp2)–H Bond Arylation to the Synthesis of Polycyclic (Hetero)Aromatics." Chem 5, no. 8 (August 2019): 2277. http://dx.doi.org/10.1016/j.chempr.2019.07.004.
Повний текст джерелаRohokale, Rajendra S., Rupali G. Kalshetti, and Chepuri V. Ramana. "Iridium(III)-Catalyzed Alkynylation of 2-(Hetero)arylquinazolin-4-one Scaffolds via C–H Bond Activation." Journal of Organic Chemistry 84, no. 5 (January 28, 2019): 2951–61. http://dx.doi.org/10.1021/acs.joc.8b02738.
Повний текст джерелаDu, Bao-Xin, Zheng-Jun Quan, Yu-Xia Da, Zhang Zhang, and Xi-Cun Wang. "ChemInform Abstract: Chemo-Controlled Cross-Coupling of Di(hetero)aryl Disulfides with Grignard Reagents: C-C vs.C-S Bond Formation." ChemInform 46, no. 33 (July 28, 2015): no. http://dx.doi.org/10.1002/chin.201533208.
Повний текст джерелаSatriani, Igor Levi, Rahmawati Munir, Adrianus Inu Natalisanto, and Dadan Hamdani. "Analysis of ITO/a-Si:H(p)/a-Si:H(i)/c-Si(n)/Al HIT (Heterostructure with Intrinsic Thin Layer) solar cell performances." ELKHA 15, no. 1 (April 18, 2023): 11. http://dx.doi.org/10.26418/elkha.v15i1.61351.
Повний текст джерелаGarcias-Morales, Cesar, David Ortegón-Reyna, and Armando Ariza-Castolo. "Investigation of the role of stereoelectronic effects in the conformation of piperidones by NMR spectroscopy and X-ray diffraction." Beilstein Journal of Organic Chemistry 11 (October 22, 2015): 1973–84. http://dx.doi.org/10.3762/bjoc.11.213.
Повний текст джерелаWalia, Preet Kamal, Manoj Kumar, and Vandana Bhalla. "Tailoring of Hetero-oligophenylene Stabilized Nanohybrid Materials: Potential Tandem Photo-Promoted Systems for C-C and C-X Bond Formation Reactions via C-H Activation." ChemistrySelect 2, no. 13 (May 2, 2017): 3758–68. http://dx.doi.org/10.1002/slct.201700101.
Повний текст джерелаMajee, Suman, Devalina Ray, and Bimal KrishnaBanik. "Samarium-Mediated Asymmetric Synthesis." Catalysts 13, no. 1 (December 24, 2022): 24. http://dx.doi.org/10.3390/catal13010024.
Повний текст джерелаMal, Sourav, Manoranjan Jana, and Satinath Sarkar. "Recent Update on Transition Metal‐Free C(sp 2 )−H Bond Halogenation in (Hetero) Arenes." ChemistrySelect 6, no. 41 (November 2, 2021): 11299–330. http://dx.doi.org/10.1002/slct.202102956.
Повний текст джерелаLu, Ming-Zhu, Ping Lu, Yun-He Xu, and Teck-Peng Loh. "Mild Rh(III)-Catalyzed Direct C–H Bond Arylation of (Hetero)Arenes with Arylsilanes in Aqueous Media." Organic Letters 16, no. 10 (April 30, 2014): 2614–17. http://dx.doi.org/10.1021/ol500754h.
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