Artículos de revistas sobre el tema "Pyridines"
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McNally, Andrew, Ryan Dolewski y Michael Hilton. "4-Selective Pyridine Functionalization Reactions via Heterocyclic Phosphonium Salts". Synlett 29, n.º 01 (12 de diciembre de 2017): 08–14. http://dx.doi.org/10.1055/s-0036-1591850.
Texto completoCzarnocki, Zbigniew y Piotr Pomarański. "Arylpyridines: A Review from Selective Synthesis to Atropisomerism". Synthesis 51, n.º 03 (14 de diciembre de 2018): 587–611. http://dx.doi.org/10.1055/s-0037-1611365.
Texto completoZhang, Li-Juan, Qun Wu, Jing Sun y Chao-Guo Yan. "Synthesis of functionalized spiro[indoline-3,4’-pyridines] and spiro[indoline-3,4’-pyridinones] via one-pot four-component reactions". Beilstein Journal of Organic Chemistry 9 (2 de mayo de 2013): 846–51. http://dx.doi.org/10.3762/bjoc.9.97.
Texto completoBrugarolas, P., R. Freifelder, S. H. Cheng y O. DeJesus. "Synthesis of meta-substituted [18F]3-fluoro-4-aminopyridine via direct radiofluorination of pyridine N-oxides". Chemical Communications 52, n.º 44 (2016): 7150–52. http://dx.doi.org/10.1039/c6cc02362b.
Texto completoBalkenhohl, Moritz y Paul Knochel. "Regioselective C–H Activation of Substituted Pyridines and other Azines using Mg- and Zn-TMP-Bases". SynOpen 02, n.º 01 (enero de 2018): 0078–95. http://dx.doi.org/10.1055/s-0036-1591966.
Texto completoMallisetty, Naga Mohan, Hanumantharao Ganipisetti, Debendra Majhi y Venkata Nagendra Kumar Putta. "Design, Synthesis of Some New Scaffolds based on Pyrrolyl-Pyridines as Potential Anticancer Agents". Asian Journal of Chemistry 35, n.º 2 (2023): 468–74. http://dx.doi.org/10.14233/ajchem.2023.23974.
Texto completoGad-Elkareem, Mohamed A. M., Azza M. Abdel-Fattah y Mohamed A. A. Elneairy. "Pyrazolo[3,4-b]pyridine in heterocyclic synthesis: synthesis of new pyrazolo[3,4-b]pyridines, imidazo[1',2':1,5]pyrazolo[3,4-b]pyridines, and pyrido[2',3':3,4]pyrazolo[1,5-a]pyrimidines". Canadian Journal of Chemistry 85, n.º 9 (1 de septiembre de 2007): 592–99. http://dx.doi.org/10.1139/v07-089.
Texto completoPreston, Dan, Samantha M. McNeill, James E. M. Lewis, Gregory I. Giles y James D. Crowley. "Enhanced kinetic stability of [Pd2L4]4+ cages through ligand substitution". Dalton Transactions 45, n.º 19 (2016): 8050–60. http://dx.doi.org/10.1039/c6dt00133e.
Texto completoBarlin, GB. "Heterocyclic Amplifiers of Phleomycin. VIII. Mono- Bis-(5'-substituted 1',3',4'-thiadiazol-2'-yl)pyridines and Mono(5'-substituted 1',3',4'-thiadiazol-2'-ylmethyl)pyridines". Australian Journal of Chemistry 38, n.º 10 (1985): 1491. http://dx.doi.org/10.1071/ch9851491.
Texto completoSchmitt, Martine, Jean-Jacques Bourguignon, Gordon B. Barlin y Les P. Davies. "Imidazo[1,2-b]pyridazines. XXIII Some 5-Deaza Analogues. Syntheses of Some 2-Aryl-6-(chloro, methoxy or unsubstituted)-3- (variously substituted)imidazo[1,2-a]pyridines and Their Affinity for Central and Mitochondrial Benzodiazepine Receptor". Australian Journal of Chemistry 50, n.º 7 (1997): 719. http://dx.doi.org/10.1071/c97004.
Texto completoBertuzzi, Giulio, Luca Bernardi y Mariafrancesca Fochi. "Nucleophilic Dearomatization of Activated Pyridines". Catalysts 8, n.º 12 (6 de diciembre de 2018): 632. http://dx.doi.org/10.3390/catal8120632.
Texto completoWójcicka, Anna y Aleksandra Redzicka. "An Overview of the Biological Activity of Pyrrolo[3,4-c]pyridine Derivatives". Pharmaceuticals 14, n.º 4 (11 de abril de 2021): 354. http://dx.doi.org/10.3390/ph14040354.
Texto completoBastrakov, Maxim A., Alexey K. Fedorenko, Alexey M. Starosotnikov, Ivan V. Fedyanin y Vladimir A. Kokorekin. "Synthesis and Facile Dearomatization of Highly Electrophilic Nitroisoxazolo[4,3-b]pyridines". Molecules 25, n.º 9 (8 de mayo de 2020): 2194. http://dx.doi.org/10.3390/molecules25092194.
Texto completoFrohn, Hermann Josef, Thorsten Schroer y Gerald Henkel. "Koordinationsverhalten des Pentafluorphenylxenonium Salzes [C6F5Xe]+[AsF6]- gegenüber Pyridinen unterschiedlicher Basizität / Co-ordinative Behaviour of the Pentafluorophenylxenonium Salt [C6F5Xe]+[AsF6]- to Pyridines of Different Basicity". Zeitschrift für Naturforschung B 50, n.º 12 (1 de diciembre de 1995): 1799–810. http://dx.doi.org/10.1515/znb-1995-1206.
Texto completoKubík, Richard, Stanislav Böhm, Iveta Ruppertová y Josef Kuthan. "Sterically Crowded Heterocycles. III. A General Approach to Imidazo[1,2-a]pyridines by Ferricyanide Oxidation of Quaternary Pyridinium Salts". Collection of Czechoslovak Chemical Communications 61, n.º 1 (1996): 126–38. http://dx.doi.org/10.1135/cccc19960126.
Texto completoNikol’skiy, Vladislav V., Mikhail E. Minyaev, Maxim A. Bastrakov y Alexey M. Starosotnikov. "Mild and efficient synthesis and base-promoted rearrangement of novel isoxazolo[4,5-b]pyridines". Beilstein Journal of Organic Chemistry 20 (14 de mayo de 2024): 1069–75. http://dx.doi.org/10.3762/bjoc.20.94.
Texto completoXin, Zhi Jun, Zhong Jia, Dian He, Jian Ping Liang, Lei Tao, Xue Hu Li y Xi Hong Lu. "Study on N-(pyridin-4-Yl) Salicylamides as Antimycobacterial Agents". Advanced Materials Research 634-638 (enero de 2013): 1371–75. http://dx.doi.org/10.4028/www.scientific.net/amr.634-638.1371.
Texto completoWei, Hongbo y Yun Li. "Quick Access to Pyridines through 6π-3-Azatriene Electrocyclization: Concise Total Synthesis of Suaveoline Alkaloids". Synlett 30, n.º 14 (15 de abril de 2019): 1615–20. http://dx.doi.org/10.1055/s-0037-1611811.
Texto completoForgione, Pat, Fei Chen, Franklin Chacón-Huete y Hassan El-Husseini. "Convenient and Inexpensive Route to Sulfonylated Pyridines via SNAr Reaction of Electron-Rich Pyridines by Iron Catalysis". Synthesis 50, n.º 09 (20 de febrero de 2018): 1914–20. http://dx.doi.org/10.1055/s-0036-1591541.
Texto completoWerstiuk, Nick Henry y Chen Ju. "Protium–deuterium exchange of substituted pyridines in neutral D2O at elevated temperatures". Canadian Journal of Chemistry 67, n.º 1 (1 de enero de 1989): 5–10. http://dx.doi.org/10.1139/v89-002.
Texto completoRazmienė, Beatričė, Eva Řezníčková, Vaida Dambrauskienė, Radek Ostruszka, Martin Kubala, Asta Žukauskaitė, Vladimír Kryštof, Algirdas Šačkus y Eglė Arbačiauskienė. "Synthesis and Antiproliferative Activity of 2,4,6,7-Tetrasubstituted-2H-pyrazolo[4,3-c]pyridines". Molecules 26, n.º 21 (8 de noviembre de 2021): 6747. http://dx.doi.org/10.3390/molecules26216747.
Texto completoHeineking, N., H. Dreizler y R. Schwarz. "Nitrogen and Deuterium Hyperfine Structure in the Rotational Spectra of Pyridine and [4-D] Pyridine". Zeitschrift für Naturforschung A 41, n.º 10 (1 de octubre de 1986): 1210–13. http://dx.doi.org/10.1515/zna-1986-1005.
Texto completoRamesha, Ajjahalli B., Nagarakere C. Sandhya, Chottanahalli S. Pavan Kumar, Mahanthawamy Hiremath, Kempegowda Mantelingu y Kanchugarakoppal S. Rangappa. "A novel approach for the synthesis of imidazo and triazolopyridines from dithioesters". New Journal of Chemistry 40, n.º 9 (2016): 7637–42. http://dx.doi.org/10.1039/c6nj01038e.
Texto completoBakke, J. M. "Nitropyridines: Synthesis and reactions". Pure and Applied Chemistry 75, n.º 10 (1 de enero de 2003): 1403–15. http://dx.doi.org/10.1351/pac200375101403.
Texto completoPrek, Benjamin, Uroš Grošelj, Marta Kasunič, Silvo Zupančič, Jurij Svete y Branko Stanovnik. "Reactions of Methyl Ketones and (Hetero)arylcarboxamides with N,N-Dimethylacetamide Dimethyl Acetal. A Simple Metal-Free Synthesis of 2,4,6-Trisubstituted Pyridines". Australian Journal of Chemistry 68, n.º 2 (2015): 184. http://dx.doi.org/10.1071/ch14349.
Texto completoComparini, Lucrezia Margherita y Mauro Pineschi. "Recent Progresses in the Catalytic Stereoselective Dearomatization of Pyridines". Molecules 28, n.º 17 (22 de agosto de 2023): 6186. http://dx.doi.org/10.3390/molecules28176186.
Texto completoShen, Qun, Huoji Chen, Ling Qin, Hui-bin Wu y Lidong Weng. "Aerobic Iron(III)-Catalyzed Direct Thiolation of Imidazo[1,2-a]pyridine with Thiols". SynOpen 04, n.º 02 (abril de 2020): 17–22. http://dx.doi.org/10.1055/s-0040-1707517.
Texto completoYakovenko, G. G. y M. V. Vovk. "Convenient approaches to the synthesis of 6-amino- and 6-oxoimidazo[4,5-b]pyrazolo[3,4-e]pyridines". Journal of Organic and Pharmaceutical Chemistry 19, n.º 1(73) (15 de marzo de 2021): 10–15. http://dx.doi.org/10.24959/ophcj.21.224583.
Texto completoYang, Kai, Cai-Bo Chen, Zhao-Wen Liu, Zhen-Lin Li, Yu Zeng y Zhao-Yang Wang. "C3-Alkylation of Imidazo[1,2-a]pyridines via Three-Component Aza-Friedel–Crafts Reaction Catalyzed by Y(OTf)3". Molecules 29, n.º 15 (24 de julio de 2024): 3463. http://dx.doi.org/10.3390/molecules29153463.
Texto completoLaxmi, Dandamudi Sri, Suryadevara V. Vardhini, Venkata R. Guttikonda, Mandava V. B. Rao y Manojit Pal. "Synthesis of 2-substituted Furo[3,2-b]pyridines Under Pd/C-Cu Catalysis Assisted by Ultrasound: Their Evaluation as Potential Cytotoxic Agents". Anti-Cancer Agents in Medicinal Chemistry 20, n.º 8 (24 de julio de 2020): 932–40. http://dx.doi.org/10.2174/1871520620666200311102304.
Texto completoŚliwa, Wanda y Małgorzata Deska. "Platinum(II) Complexes of Pyridines. A Review". Collection of Czechoslovak Chemical Communications 64, n.º 3 (1999): 435–58. http://dx.doi.org/10.1135/cccc19990435.
Texto completoDonaire-Arias, Ana, Ana Maria Montagut, Raimon Puig de la Bellacasa, Roger Estrada-Tejedor, Jordi Teixidó y José I. Borrell. "1H-Pyrazolo[3,4-b]pyridines: Synthesis and Biomedical Applications". Molecules 27, n.º 7 (30 de marzo de 2022): 2237. http://dx.doi.org/10.3390/molecules27072237.
Texto completoMu, Bing, Yusheng Wu, Jingya Li, Dapeng Zou, Junbiao Chang y Yangjie Wu. "An unprecedented Pd-catalyzed decarboxylative coupling reaction of aromatic carboxylic acids in aqueous medium under air: synthesis of 3-aryl-imidazo[1,2-a]pyridines from aryl chlorides". Organic & Biomolecular Chemistry 14, n.º 1 (2016): 246–50. http://dx.doi.org/10.1039/c5ob02112j.
Texto completoCai, Xiao-hua, Hai-jun Yang y Guo-lin Zhang. "Aromatization of 1,4-dihydropyridines with selenium dioxide". Canadian Journal of Chemistry 83, n.º 3 (1 de marzo de 2005): 273–75. http://dx.doi.org/10.1139/v05-058.
Texto completoGhotekar, Bhausaheb K., Muddassar A. Kazi, Madhukar N. Jachak y Raghunath B. Toche. "Effect of substituents on absorption and fluorescence properties of pyrazolo[3,4-b]pyrrolo[2,3-d]pyridines". Canadian Journal of Chemistry 86, n.º 11 (1 de noviembre de 2008): 1070–76. http://dx.doi.org/10.1139/v08-155.
Texto completoGrinberga, S., A. Krauze, L. Krasnova y G. Duburs. "Synthesis of 4-Benzo[1,3]Dioxol-5-Ylthieno-[2,3-b]Pyridines". Latvian Journal of Chemistry 51, n.º 1-2 (1 de enero de 2012): 143–48. http://dx.doi.org/10.2478/v10161-012-0002-2.
Texto completoZhu, Jingyun, Ziyue Chen, Meng He, Daoxin Wang, Liangsen Li, Junchao Qi, Renyi Shi y Aiwen Lei. "Metal-free electrochemical C3-sulfonylation of imidazo[1,2-a]pyridines". Organic Chemistry Frontiers 8, n.º 14 (2021): 3815–19. http://dx.doi.org/10.1039/d1qo00348h.
Texto completoVolkov, Pavel A., Anton A. Telezhkin, Kseniya O. Khrapova, Nina I. Ivanova, Alexander I. Albanov, Nina K. Gusarova y Boris A. Trofimov. "Metal-free SHN cross-coupling of pyridines with phosphine chalcogenides: polarization/deprotonation/oxidation effects of electron-deficient acetylenes". New Journal of Chemistry 45, n.º 14 (2021): 6206–19. http://dx.doi.org/10.1039/d1nj00245g.
Texto completoMa, Dongge, Yan Yan, Hongwei Ji, Chuncheng Chen y Jincai Zhao. "Photocatalytic activation of pyridine for addition reactions: an unconventional reaction feature between a photo-induced hole and electron on TiO2". Chemical Communications 51, n.º 98 (2015): 17451–54. http://dx.doi.org/10.1039/c5cc07123b.
Texto completoLi, Bin, Nana Shen, Yujie Yang, Xinying Zhang y Xuesen Fan. "Synthesis of naphtho[1′,2′:4,5]imidazo[1,2-a]pyridines via Rh(iii)-catalyzed C–H functionalization of 2-arylimidazo[1,2-a]pyridines with cyclic 2-diazo-1,3-diketones featuring with a ring opening and reannulation". Organic Chemistry Frontiers 7, n.º 7 (2020): 919–25. http://dx.doi.org/10.1039/d0qo00073f.
Texto completoYang, Chunxia, Wei Zhao, Zhiguo Cheng, Baomin Luo y Dongqin Bi. "Catalytic system for pyridine oxidation to N-oxides under mild conditions based on polyoxomolybdate". RSC Advances 5, n.º 46 (2015): 36809–12. http://dx.doi.org/10.1039/c5ra05196g.
Texto completoKona, Sridevi, Rama Suresh Ravi, Manab Chakravarty y Venkata N. R. Chava. "Phosphine-Free Palladium-Catalyzed Direct C-3 Arylation of 2-Phenylimidazo[1,2-a]pyridine Using Silver(I) Carboxylate". Journal of Chemistry 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/305934.
Texto completoArnestad, Berit, Jan M. Bakke, Ingrid Hegbom, Eli Ranes, Bente Nielsen, Ruby I. Nielsen, Carl Erik Olsen et al. "Direct Nitration of Pyridine and Substituted Pyridines." Acta Chemica Scandinavica 50 (1996): 556–57. http://dx.doi.org/10.3891/acta.chem.scand.50-0556.
Texto completoAbdelrazek, Fathy M., Sobhi M. Gomha, Mohamed E. B. Shaaban, Kamal A. Rabee, Heba N. El-Shemy, Abanoub M. Abdallah y Peter Metz. "One-Pot Three-Component Synthesis and Molecular Docking of Some Novel 2-Thiazolyl Pyridines as Potent Antimicrobial Agents". Mini-Reviews in Medicinal Chemistry 19, n.º 6 (7 de marzo de 2019): 527–38. http://dx.doi.org/10.2174/1389557518666181019124104.
Texto completoKrutošíková, Alžbeta y Róbert Sleziak. "Synthesis of 2-Arylfuro[3,2-c]pyridines and Their Derivatives". Collection of Czechoslovak Chemical Communications 61, n.º 11 (1996): 1627–36. http://dx.doi.org/10.1135/cccc19961627.
Texto completoGrisez, Tom, Nitha Panikkassery Ravi, Mathy Froeyen, Dominique Schols, Luc Van Meervelt, Steven De Jonghe y Wim Dehaen. "Synthesis of a 3,7-Disubstituted Isothiazolo[4,3-b]pyridine as a Potential Inhibitor of Cyclin G-Associated Kinase". Molecules 29, n.º 5 (22 de febrero de 2024): 954. http://dx.doi.org/10.3390/molecules29050954.
Texto completoMotevalli, Kourosh, Zahra Yaghoubi y Roghieh Mirzazadeh. "Microwave-Assisted, One-Pot Three Component Synthesis of 2-PhenylH-imidazo[1,2-α]pyridine". E-Journal of Chemistry 9, n.º 3 (2012): 1047–52. http://dx.doi.org/10.1155/2012/198615.
Texto completoLi, Bin, Nana Shen, Xinying Zhang y Xuesen Fan. "Synthesis of fused imidazo[1,2-a]pyridines derivatives through cascade C(sp2)–H functionalizations". Organic & Biomolecular Chemistry 17, n.º 41 (2019): 9140–50. http://dx.doi.org/10.1039/c9ob01744e.
Texto completoShen, Yang-Lin, Jun-Ling Jin, Yun-Peng Xie y Xing Lu. "tert-Butyl thiol and pyridine ligand co-protected 50-nuclei clusters: the effect of pyridines on Ag–SR bonds". Dalton Transactions 49, n.º 36 (2020): 12574–80. http://dx.doi.org/10.1039/d0dt02003f.
Texto completoBhatt, Keval, Dhara Patel, Mrudangsinh Rathod, Ashish Patel y Drashti Shah. "Efficient Synthesis and Characterization of 6-substituted-N-p-tolyl-imidazo[1,2- a]pyridine-8-carboxamide: A Promising Scaffold for Drug Development". Current Organic Chemistry 27, n.º 22 (diciembre de 2023): 1978–84. http://dx.doi.org/10.2174/0113852728269243231206044929.
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