Artículos de revistas sobre el tema "Aryls(Heteroaryls) compound"
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Stefanello, Felipe S., Jean C. B. Vieira, Juliane N. Araújo, Vitória B. Souza, Clarissa P. Frizzo, Marcos A. P. Martins, Nilo Zanatta, Bernardo A. Iglesias y Helio G. Bonacorso. "Solution and Solid-State Optical Properties of Trifluoromethylated 5-(Alkyl/aryl/heteroaryl)-2-methyl-pyrazolo[1,5-a]pyrimidine System". Photochem 2, n.º 2 (19 de mayo de 2022): 345–57. http://dx.doi.org/10.3390/photochem2020024.
Texto completoShui, Hongling, Yuhong Zhong, Renshi Luo, Zhanyi Zhang, Jiuzhong Huang, Ping Yang y Nianhua Luo. "Cyclometalated iridium complexes-catalyzed acceptorless dehydrogenative coupling reaction: construction of quinoline derivatives and evaluation of their antimicrobial activities". Beilstein Journal of Organic Chemistry 18 (27 de octubre de 2022): 1507–17. http://dx.doi.org/10.3762/bjoc.18.159.
Texto completoKalam, Sirisha, Rajyalaxmi I y Olivia S. "Synthesis and In vitro P-Glycoprotein Inhibitory Activity of Novel 1,4-Dihydropyridine Derivatives". International Journal of Pharmaceutical Sciences and Nanotechnology 7, n.º 3 (31 de agosto de 2014): 2544–52. http://dx.doi.org/10.37285/ijpsn.2014.7.3.6.
Texto completoMarzo, Leyre, Ignacio Pérez, Francisco Yuste, José Alemán y José Luis García Ruano. "A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes". Chemical Communications 51, n.º 2 (2015): 346–49. http://dx.doi.org/10.1039/c4cc07574a.
Texto completoNarayanaperumal, Senthil, Ricardo S. Schwab, Wystan K. O. Teixeira y Danilo Yano de Albuquerque. "Recent Advances in the Synthesis of Enantiomerically Enriched Diaryl, Aryl Heteroaryl, and Diheteroaryl Alcohols through Addition of Organometallic Reagents to Carbonyl Compounds". Synthesis 52, n.º 13 (16 de marzo de 2020): 1855–73. http://dx.doi.org/10.1055/s-0039-1690847.
Texto completoSaritha, Rajendhiran, Sesuraj Babiola Annes, Subramanian Saravanan y Subburethinam Ramesh. "Carbazole based Electron Donor Acceptor (EDA) catalysis for the synthesis of biaryl and aryl–heteroaryl compounds". Organic & Biomolecular Chemistry 18, n.º 13 (2020): 2510–15. http://dx.doi.org/10.1039/d0ob00282h.
Texto completoSitapara, Sachin M., Jignesh H. Pandya y Chandankumar Pashavan. "An Efficient Synthesis of Novel Triazolo-pyrimidine Derivatives using Copper Catalyzed Click Chemistry (CuAAC) Approach". Asian Journal of Organic & Medicinal Chemistry 7, n.º 2 (2022): 153–58. http://dx.doi.org/10.14233/ajomc.2022.ajomc-p378.
Texto completoGangadurai, Chinnakuzhanthai, Giri Teja Illa y D. Srinivasa Reddy. "FeCl3-catalyzed oxidative decarboxylation of aryl/heteroaryl acetic acids: preparation of selected API impurities". Organic & Biomolecular Chemistry 18, n.º 41 (2020): 8459–66. http://dx.doi.org/10.1039/d0ob01790f.
Texto completoMalik, Ayesha, Nasir Rasool, Iram Kanwal, Muhammad Ali Hashmi, Ameer Fawad Zahoor, Gulraiz Ahmad, Ataf Ali Altaf, Syed Adnan Ali Shah, Sadia Sultan y Zainul Amiruddin Zakaria. "Suzuki–Miyaura Reactions of (4-bromophenyl)-4,6-dichloropyrimidine through Commercially Available Palladium Catalyst: Synthesis, Optimization and Their Structural Aspects Identification through Computational Studies". Processes 8, n.º 11 (23 de octubre de 2020): 1342. http://dx.doi.org/10.3390/pr8111342.
Texto completoSaritha, Rajendhiran, Sesuraj Babiola Annes, Saravanan Subramanian y Subburethinam Ramesh. "Correction: Carbazole based Electron Donor Acceptor (EDA) catalysis for the synthesis of biaryl and aryl–heteroaryl compounds". Organic & Biomolecular Chemistry 18, n.º 15 (2020): 2962. http://dx.doi.org/10.1039/d0ob90043e.
Texto completoKartsev, Victor, Athina Geronikaki, Alexander Zubenko, Anthi Petrou, Marija Ivanov, Jasmina Glamočlija, Marina Sokovic, Lyudmila Divaeva, Anatolii Morkovnik y Alexander Klimenko. "Synthesis and Antimicrobial Activity of New Heteroaryl(aryl) Thiazole Derivatives Molecular Docking Studies". Antibiotics 11, n.º 10 (30 de septiembre de 2022): 1337. http://dx.doi.org/10.3390/antibiotics11101337.
Texto completoMelford C Egbujor, Uchechukwu C Okoro, Samuel A Egu, Pius I Egwuatu, Florence U Eze y Ifeanyi S Amasiatu. "Synthesis and Biological Evaluation of Alanine Derived Bioactive p-Toluenesulphonamide Analogs". International Journal of Research in Pharmaceutical Sciences 11, n.º 4 (19 de octubre de 2020): 6449–58. http://dx.doi.org/10.26452/ijrps.v11i4.3440.
Texto completoLopp, Margus, Eleana Lopušanskaja, Anne Paju y Ivar Järving. "Synthesis of Cyclic 3-Aryl-Substituted 1,2-Dicarbonyl Compounds via Suzuki Cross-Coupling Reactions". Synthesis 50, n.º 09 (12 de febrero de 2018): 1883–90. http://dx.doi.org/10.1055/s-0036-1591543.
Texto completoLan, Jihong, Rongxiang Chen, Fangfang Duo, Menghui Hu y Xiaoyan Lu. "Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals". Molecules 27, n.º 17 (23 de agosto de 2022): 5364. http://dx.doi.org/10.3390/molecules27175364.
Texto completoWang, Cuiying, Chang-Duo Yue, Jia Yuan, Jia-Lian Zheng, Ying Zhang, Hong Yu, Jian Chen et al. "Synthesis of P-chiral phosphine compounds by palladium-catalyzed C–P coupling reactions". Chemical Communications 56, n.º 79 (2020): 11775–78. http://dx.doi.org/10.1039/d0cc05340f.
Texto completoLi, Yabo, Jingran Wang, Zhiwei Wang, Mengmeng Huang, Beiqi Yan, Xiuling Cui, Yusheng Wu y Yangjie Wu. "Palladacycle-catalyzed Suzuki–Miyaura reaction of aryl/heteroaryl halides with MIDA boronates in EtOH/H2O or H2O". RSC Adv. 4, n.º 68 (2014): 36262–66. http://dx.doi.org/10.1039/c4ra07486f.
Texto completoKutchin, Alexander V., Svetlana A. Rubtsova, Olga M. Lezina, Denis V. Sudarikov, Larisa L. Frolova, Irina V. Loginova, Alexey V. Popov y Olga N. Grebyonkina. "Studies on oxidative transformations of thiols, sulfides and alcohols in the presence of chlorine dioxide". Pure and Applied Chemistry 89, n.º 10 (26 de septiembre de 2017): 1379–401. http://dx.doi.org/10.1515/pac-2016-1209.
Texto completoKnochel, Paul, Matthias A. Schade, Sebastian Bernhardt, Georg Manolikakes, Albrecht Metzger, Fabian M. Piller, Christoph J. Rohbogner y Marc Mosrin. "Functionalization of heterocyclic compounds using polyfunctional magnesium and zinc reagents". Beilstein Journal of Organic Chemistry 7 (13 de septiembre de 2011): 1261–77. http://dx.doi.org/10.3762/bjoc.7.147.
Texto completoBegum, Shaheen, V. Anitha Kumari, S. K. Arifa Begum, M. Reddemma, K. Tejaswini y K. Bharathi. "Synthesis and Evaluation of 1,2,4-Triazole Derivatives for Antioxidant, Anti-inflammatory, Cytotoxicity and QSAR Analysis". Asian Journal of Chemistry 35, n.º 1 (27 de diciembre de 2022): 194–202. http://dx.doi.org/10.14233/ajchem.2023.26878.
Texto completoBhatewara, Anjna, Srinivasa Rao Jetti, Tanuja Kadre, Pradeep Paliwal y Shubha Jain. "Microwave-Assisted Synthesis and Biological Evaluation of Dihydropyrimidinone Derivatives as Anti-Inflammatory, Antibacterial, and Antifungal Agents". International Journal of Medicinal Chemistry 2013 (15 de abril de 2013): 1–5. http://dx.doi.org/10.1155/2013/197612.
Texto completoKumar, Dinesh, Gurpreet Singh, Pooja Sharma, Arem Qayum, Girish Mahajan, M. J. Mintoo, Shashank Kumar Singh et al. "4-aryl/heteroaryl-4H-fused Pyrans as Anti-proliferative Agents: Design, Synthesis and Biological Evaluation". Anti-Cancer Agents in Medicinal Chemistry 18, n.º 1 (16 de marzo de 2018): 57–73. http://dx.doi.org/10.2174/1871520617666170918143911.
Texto completoAhmad, Gulraiz, Nasir Rasool, Adeel Mubarik, Ameer Fawad Zahoor, Muhammad Ali Hashmi, Muhammad Zubair, Muhammad Bilal, Mohamed Hussien, Muhammad Saeed Akhtar y Sajjad Haider. "Facile Synthesis of 5-Aryl-N-(pyrazin-2-yl)thiophene-2-carboxamides via Suzuki Cross-Coupling Reactions, Their Electronic and Nonlinear Optical Properties through DFT Calculations". Molecules 26, n.º 23 (2 de diciembre de 2021): 7309. http://dx.doi.org/10.3390/molecules26237309.
Texto completoZonjić, Iva, Lidija-Marija Tumir, Ivo Crnolatac, Filip Šupljika, Livio Racané, Sanja Tomić y Marijana Radić Stojković. "Recognition of ATT Triplex and DNA:RNA Hybrid Structures by Benzothiazole Ligands". Biomolecules 12, n.º 3 (27 de febrero de 2022): 374. http://dx.doi.org/10.3390/biom12030374.
Texto completoRocha, Inaiá O., Yuri G. Kappenberg, Wilian C. Rosa, Clarissa P. Frizzo, Nilo Zanatta, Marcos A. P. Martins, Isadora Tisoco, Bernardo A. Iglesias y Helio G. Bonacorso. "Photophysical, photostability, and ROS generation properties of new trifluoromethylated quinoline-phenol Schiff bases". Beilstein Journal of Organic Chemistry 17 (1 de diciembre de 2021): 2799–811. http://dx.doi.org/10.3762/bjoc.17.191.
Texto completoPoor Heravi, Mohammad Reza y Marjan Ashori. "Boric Acid Catalyzed Convenient Synthesis of Benzimidazoles in Aqueous Media". Journal of Chemistry 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/496413.
Texto completoK, Madhavi y P. Sudeepthi. "Synthesis of Cyanoacetylated Derivatives of Some Heteroaryl Amines as Analgesic and Antioxidant Agents". International Journal of Pharmaceutical Sciences and Nanotechnology 5, n.º 4 (28 de febrero de 2013): 1879–84. http://dx.doi.org/10.37285/ijpsn.2012.5.4.8.
Texto completoPoisson, Thomas, Maria Ivanova, Tatiana Besset y Xavier Pannecoucke. "Palladium-Catalyzed Synthesis of Aryl and Heteroaryl Difluoromethylated Phosphonates". Synthesis 50, n.º 04 (29 de noviembre de 2017): 778–84. http://dx.doi.org/10.1055/s-0036-1589140.
Texto completoBogdanov, Milen G., Meglena I. Kandinska, Darina B. Dimitrova, Blagovesta T. Gocheva y Mariana D. Palamareva. "Preliminary Evaluation of Antimicrobial Activity of Diastereomeric cis/trans-3-Aryl(Heteroaryl)-3,4-dihydroisocoumarin-4-carboxylic Acids". Zeitschrift für Naturforschung C 62, n.º 7-8 (1 de agosto de 2007): 477–82. http://dx.doi.org/10.1515/znc-2007-7-804.
Texto completoMathew, Vinod, J. Keshavayya y V. P. Vaidya. "Synthesis, Characterization and Pharmacological Activities of 3,6-Disubstituted-1,2,4-triazolo [3,4-b]-1,3,4-thiadiazoles and their Dihydro Analogues". E-Journal of Chemistry 4, n.º 3 (2007): 320–42. http://dx.doi.org/10.1155/2007/605058.
Texto completoHurtová, Martina, David Biedermann, Zuzana Osifová, Josef Cvačka, Kateřina Valentová y Vladimír Křen. "Preparation of Synthetic and Natural Derivatives of Flavonoids Using Suzuki–Miyaura Cross-Coupling Reaction". Molecules 27, n.º 3 (31 de enero de 2022): 967. http://dx.doi.org/10.3390/molecules27030967.
Texto completoAverin, Alexei D., Anton S. Abel, Olga K. Grigorova, Gennadij V. Latyshev, Yury N. Kotovshchikov, Alexander Yu Mitrofanov, Alla Bessmertnykh-Lemeune y Irina P. Beletskaya. "Recent achievements in copper catalysis for C–N bond formation". Pure and Applied Chemistry 92, n.º 8 (25 de septiembre de 2020): 1181–99. http://dx.doi.org/10.1515/pac-2020-0301.
Texto completoBaraldi, Pier G., Roberta Budriesi, Barbara Cacciari, Alberto Chiarini, Laura Garuti, Giuseppe Giovanninetti, Alberto Leoni y Marinella Roberti. "Synthesis and Calcium Antagonist Activity of Dialkyl 1,4-Dihydro-2,6-dimethyl-4-(nitrogenous heteroaryl)-3,5-pyridine Dicarboxylates". Collection of Czechoslovak Chemical Communications 57, n.º 1 (1992): 169–78. http://dx.doi.org/10.1135/cccc19920169.
Texto completoDhanawat, Meenakshi, Sumeet Gupta, Rina Das y Dinesh Kumar Mehta. "Assessing the affinity of oxazolidinedione/hydantoin derivatives for the human 5HT1A/2A receptor through homology modeling and docking studies". Journal of University of Shanghai for Science and Technology 23, n.º 09 (4 de septiembre de 2021): 46–66. http://dx.doi.org/10.51201/jusst/21/09505.
Texto completoKatritzky, Alan R., Jianqing Li, Christian V. Stevens y David J. Ager. "AN ALTERNATIVE SYNTHESIS OF ARYL AND HETEROARYL BROMIDES FROM ACTIVATED ARYL HYDROXY COMPOUNDS". Organic Preparations and Procedures International 26, n.º 4 (agosto de 1994): 439–44. http://dx.doi.org/10.1080/00304949409458034.
Texto completoMosallanezhad, Asiyeh y Hamzeh Kiyani. "Green Synthesis of 3-Substituted-4-arylmethylideneisoxazol-5(4H)-one Derivatives Catalyzed by Salicylic Acid". Current Organocatalysis 6, n.º 1 (24 de abril de 2019): 28–35. http://dx.doi.org/10.2174/2213337206666190214161332.
Texto completoBłocka, Aleksandra y Wojciech Chaładaj. "Tandem Pd-Catalyzed Cyclization/Coupling of Non-Terminal Acetylenic Activated Methylenes with (Hetero)Aryl Bromides". Molecules 27, n.º 3 (19 de enero de 2022): 630. http://dx.doi.org/10.3390/molecules27030630.
Texto completoNauš, Petr, Martin Kuchař y Michal Hocek. "Cytostatic and Antiviral 6-Arylpurine Ribonucleosides IX. Synthesis and Evaluation of 6-Substituted 3-Deazapurine Ribonucleosides". Collection of Czechoslovak Chemical Communications 73, n.º 5 (2008): 665–78. http://dx.doi.org/10.1135/cccc20080665.
Texto completoSengmany, Stéphane, Eric Léonel, Rima Rahil y Erwan Le Gall. "Nickel-Catalyzed Electrochemical Reductive Homocouplings of Aryl and Heteroaryl Halides: A Useful Route to Symmetrical Biaryls". Synthesis 50, n.º 01 (12 de septiembre de 2017): 146–54. http://dx.doi.org/10.1055/s-0036-1589100.
Texto completoMahran, Mona, Samia William, Fatem Ramzy y Amira Sembel. "Synthesis and in vitro Evaluation of New Benzothiazole Derivatives as Schistosomicidal Agents". Molecules 12, n.º 3 (26 de marzo de 2007): 622–33. http://dx.doi.org/10.3390/12030622.
Texto completoOmara, Mariam, Mohamed Hagras, Mohamed M. Elsebaie, Nader S. Abutaleb, Hanzada T. Nour El-Din, Maria O. Mekhail, Ahmed S. Attia, Mohamed N. Seleem, Marwa T. Sarg y Abdelrahman S. Mayhoub. "Exploring novel aryl/heteroaryl-isosteres of phenylthiazole against multidrug-resistant bacteria". RSC Advances 13, n.º 29 (2023): 19695–709. http://dx.doi.org/10.1039/d3ra02778c.
Texto completoDharuman, Suresh, Miranda J. Wallace, Stephanie M. Reeve, Jürgen B. Bulitta y Richard E. Lee. "Synthesis and Structure–Activity Relationship of Thioacetamide-Triazoles against Escherichia coli". Molecules 27, n.º 5 (24 de febrero de 2022): 1518. http://dx.doi.org/10.3390/molecules27051518.
Texto completoSechi, Mario, Luciano Sannia, Fabrizio Carta, Michele Palomba, Roberto Dallocchio, Alessandro Dessì, Massimiliano Derudas, Zahrah Zawahir y Nouri Neamati. "Design of Novel Bioisosteres of β-Diketo Acid Inhibitors of HIV-1 Integrase". Antiviral Chemistry and Chemotherapy 16, n.º 1 (febrero de 2005): 41–61. http://dx.doi.org/10.1177/095632020501600105.
Texto completoGhorab, Mostafa M., Mansour S. Al-Said y Reem K. Arafa. "Design, Synthesis and Potential Anti-Proliferative Activity of Some Novel 4-Aminoquinoline Derivatives". Acta Pharmaceutica 64, n.º 3 (1 de septiembre de 2014): 285–97. http://dx.doi.org/10.2478/acph-2014-0030.
Texto completoKATRITZKY, A. R., J. LI, C. V. STEVENS y D. J. AGER. "ChemInform Abstract: An Alternative Synthesis of Aryl and Heteroaryl Bromides from Activated Aryl Hydroxy Compounds." ChemInform 26, n.º 5 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199505089.
Texto completoArasavelli, Ananda Mohan, Ganapavarapu Veera Raghava Sharma y Siddaiah Vidavalur. "Design, synthesis, and anticancer activity of novel aryl/heteroaryl chalcone derivatives". Heterocyclic Communications 22, n.º 1 (1 de febrero de 2016): 1–5. http://dx.doi.org/10.1515/hc-2015-0271.
Texto completoAhmad, Sana, Suvendu Sekhar Dey, Bernard Jousseaume y Thierry Toupance. "Linear or cross-shaped di(cyclopentadienyltitanium) compounds with aryl or heteroaryl spacers". Dalton Trans. 40, n.º 2 (2011): 457–62. http://dx.doi.org/10.1039/c0dt01060j.
Texto completoSutherland, Hamish S., Peter J. Choi, Guo-Liang Lu, Anna C. Giddens, Amy S. T. Tong, Scott G. Franzblau, Christopher B. Cooper, Brian D. Palmer y William A. Denny. "Synthesis and Structure–Activity Relationships for the Anti-Mycobacterial Activity of 3-Phenyl-N-(Pyridin-2-ylmethyl)Pyrazolo[1,5-a]Pyrimidin-7-Amines". Pharmaceuticals 15, n.º 9 (8 de septiembre de 2022): 1125. http://dx.doi.org/10.3390/ph15091125.
Texto completoMicheletti, Gabriele y Carla Boga. "Nucleophile/Electrophile Combinations in Aromatic Substitution: From Wheland to Wheland–Meisenheimer Intermediates Using Strongly Activated Arenes". Synthesis 49, n.º 15 (13 de julio de 2017): 3347–56. http://dx.doi.org/10.1055/s-0036-1588490.
Texto completoAmeur Messaoud, Mohamed Yacine Ameur, Ghenia Bentabed-Ababsa, Ziad Fajloun, Monzer Hamze, Yury S. Halauko, Oleg A. Ivashkevich, Vadim E. Matulis, Thierry Roisnel, Vincent Dorcet y Florence Mongin. "Deprotometalation-Iodolysis and Direct Iodination of 1-Arylated 7-Azaindoles: Reactivity Studies and Molecule Properties". Molecules 26, n.º 20 (19 de octubre de 2021): 6314. http://dx.doi.org/10.3390/molecules26206314.
Texto completoWunderlich, Stefan H y Paul Knochel. "Aluminum Bases for the Highly Chemoselective Preparation of Aryl and Heteroaryl Aluminum Compounds". Angewandte Chemie International Edition 48, n.º 8 (9 de febrero de 2009): 1501–4. http://dx.doi.org/10.1002/anie.200804966.
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