Artículos de revistas sobre el tema "Enaminone synthesis"
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Chattopadhyay, Amit Kumar y Stephen Hanessian. "Cyclic enaminones. Part II: applications as versatile intermediates in alkaloid synthesis". Chemical Communications 51, n.º 92 (2015): 16450–67. http://dx.doi.org/10.1039/c5cc05892a.
Texto completoŠtanfel, Urša, Dejan Slapšak, Uroš Grošelj, Franc Požgan, Bogdan Štefane y Jurij Svete. "Synthesis of 6,7-Dihydro-1H,5H-pyrazolo[1,2-a]pyrazoles by Azomethine Imine-Alkyne Cycloadditions Using Immobilized Cu(II)-Catalysts". Molecules 26, n.º 2 (13 de enero de 2021): 400. http://dx.doi.org/10.3390/molecules26020400.
Texto completoMasaret, Ghada S. y Thoraya A. Farghaly. "Synthesis of 8,10-disubstituted-triazoloperimidines from (E)-3-(dimethylamino)-1-(8- phenyl-8H-[1,2,4]triazolo[4,3-a]perimidin-10-yl)prop-2-en-1-one and Their Antimicrobial Activity". Current Organic Synthesis 15, n.º 1 (20 de marzo de 2018): 126–36. http://dx.doi.org/10.2174/1570179414666170601121137.
Texto completoCiber, Luka, Franc Požgan, Helena Brodnik, Bogdan Štefane, Jurij Svete y Uroš Grošelj. "Synthesis and Catalytic Activity of Organocatalysts Based on Enaminone and Benzenediamine Hydrogen Bond Donors". Catalysts 12, n.º 10 (28 de septiembre de 2022): 1132. http://dx.doi.org/10.3390/catal12101132.
Texto completoAgamy, Samia Michel, Mervat Mohammed Abdel-Khalik, Mona Hassan Mohamed y Mohammed Hilmy Elnagdi. "Enaminones as Building Blocks In Heterocyclic Synthesis: A New One Pot Synthesis of Polyfunctional Substituted Pyridines". Zeitschrift für Naturforschung B 56, n.º 10 (1 de octubre de 2001): 1074–78. http://dx.doi.org/10.1515/znb-2001-1016.
Texto completoLiu, Weibing, Cui Chen y Qing Zhang. "FeCl3-PTSA Co-Catalysed Highly Regio- and Stereo-Selective Synthesis of β-Functionalised Enamine Derivatives". Journal of Chemical Research 36, n.º 3 (marzo de 2012): 175–77. http://dx.doi.org/10.3184/174751912x13306054094882.
Texto completoHassan, Mohamed M. y Mona H. Alhalafi. "Synthesis, Structural Determination, and Antioxidant Activities of Acyclic and Substituted Heterocyclic Phosphonates Linearly Linked 4-hydroxy-2(1H)-quinolinone". Molecules 27, n.º 18 (13 de septiembre de 2022): 5960. http://dx.doi.org/10.3390/molecules27185960.
Texto completoSzafraniec, Anna, Marcin Grajda, Hanna Jędrzejewska, Agnieszka Szumna y Waldemar Iwanek. "Enaminone Substituted Resorcin[4]arene—Sealing of an Upper-Rim with a Directional System of Hydrogen-Bonds". International Journal of Molecular Sciences 21, n.º 20 (11 de octubre de 2020): 7494. http://dx.doi.org/10.3390/ijms21207494.
Texto completoAl-Romaizan, Abeer N., Nesreen S. Ahmed y Sherin M. Elfeky. "Design, Synthesis, and Biological Evaluation of Triazolyl- and Triazinyl-Quinazolinediones as Potential Antitumor Agents". Journal of Chemistry 2019 (3 de febrero de 2019): 1–12. http://dx.doi.org/10.1155/2019/9104653.
Texto completoFilkale, Adelew Estifanos y Chandni Pathak. "Dinuclear cobalt complexes supported by biphenol and binaphthol-derived bis(salicylaldimine) ligands: synthesis, characterization and catalytic application in β-enaminone synthesis from 1,3-dicarbonyl compounds and aliphatic amines". New Journal of Chemistry 44, n.º 35 (2020): 15109–21. http://dx.doi.org/10.1039/d0nj00052c.
Texto completoLi, Yi, Xiaoji Cao, Yunyun Liu y Jie-Ping Wan. "Regioselective three-component synthesis of 2,3-disubstituted quinolines via the enaminone modified Povarov reaction". Organic & Biomolecular Chemistry 15, n.º 45 (2017): 9585–89. http://dx.doi.org/10.1039/c7ob02411h.
Texto completoWagger, Jernej, David Bevk, Anton Meden, Jurij Svete y Branko Stanovnik. "Enaminone-Based Synthesis of Dipodazine Derivatives". Helvetica Chimica Acta 89, n.º 2 (febrero de 2006): 240–48. http://dx.doi.org/10.1002/hlca.200690026.
Texto completoŠenica, Luka, Uroš Grošelj, Marta Kasunič, Drago Kočar, Branko Stanovnik y Jurij Svete. "Synthesis of Enaminone-Based Vinylogous Peptides". European Journal of Organic Chemistry 2014, n.º 15 (13 de marzo de 2014): 3067–71. http://dx.doi.org/10.1002/ejoc.201402033.
Texto completoKnieß, Astrid, Margit Gruner y Roland Mayer. "Reaktionsverhalten von β-Oxo-carbonsäurederivaten der Anthracenreihe bei der Synthese von Pyrazolen / On the Reaction Behavior of ß-Oxo Carbonic Acid Derivatives of the Anthracene Series in Pyrazole Synthesis". Zeitschrift für Naturforschung B 54, n.º 9 (1 de septiembre de 1999): 1133–37. http://dx.doi.org/10.1515/znb-1999-0908.
Texto completoAmbethkar, Sethurajan, Vediappen Padmini y Nattamai Bhuvanesh. "A one-pot sequential five-component domino reaction for the expedient synthesis of polysubstituted pyrroles". New Journal of Chemistry 40, n.º 5 (2016): 4705–9. http://dx.doi.org/10.1039/c5nj03444b.
Texto completoWan, Jie-Ping, Youyi Zhou, Yunyun Liu y Shouri Sheng. "Metal-free oxidative carbonylation on enaminone CC bond for the cascade synthesis of benzothiazole-containing vicinal diketones". Green Chemistry 18, n.º 2 (2016): 402–5. http://dx.doi.org/10.1039/c5gc01821h.
Texto completoKlintworth, Robin, Garreth L. Morgans, Stefania M. Scalzullo, Charles B. de Koning, Willem A. L. van Otterlo y Joseph P. Michael. "Silica gel and microwave-promoted synthesis of dihydropyrrolizines and tetrahydroindolizines from enaminones". Beilstein Journal of Organic Chemistry 17 (13 de octubre de 2021): 2543–52. http://dx.doi.org/10.3762/bjoc.17.170.
Texto completoZhong, Shanshan, Yu Lu, Yan Zhang, Yunyun Liu y Jie-Ping Wan. "Synthesis of β,β-diaryl propiophenones via palladium-catalyzed domino arylboronation, elimination and enone hydroarylation of enaminones". Organic & Biomolecular Chemistry 14, n.º 26 (2016): 6270–73. http://dx.doi.org/10.1039/c6ob01038e.
Texto completoOlyaei, Abolfazl, Amir Mohamadi y Nilufar Rahmani. "Green synthesis of new lawsone enaminones and their Z/E(CC)-isomerization induced by organic solvent". RSC Advances 11, n.º 21 (2021): 12990–94. http://dx.doi.org/10.1039/d1ra01858b.
Texto completoBhat, Mashooq Ahmad, Mohamed A. Al-Omar, Ahmed M. Naglah, Atef Kalmouch y Abdullah Al-Dhfyan. "Synthesis and Characterization of Novel Biginelli Dihydropyrimidinone Derivatives Containing Imidazole Moiety". Journal of Chemistry 2019 (13 de mayo de 2019): 1–7. http://dx.doi.org/10.1155/2019/3131879.
Texto completoAlshahrani, Saeed, Saied M. Soliman, Abdullah Saleh Alamary, Abdullah Mohammed Al-Majid, Matti Haukka, Sammer Yousuf y Assem Barakat. "Synthesis of Enaminones-Based Benzo[d]imidazole Scaffold: Characterization and Molecular Insight Structure". Crystals 10, n.º 10 (21 de octubre de 2020): 955. http://dx.doi.org/10.3390/cryst10100955.
Texto completoWu, Wenfeng, Zhuxian Wang, Qun Shen, Qiang Liu y Huoji Chen. "Fe-Catalyzed enaminone synthesis from ketones and amines". Organic & Biomolecular Chemistry 17, n.º 28 (2019): 6753–56. http://dx.doi.org/10.1039/c9ob01137d.
Texto completoBhat, Mashooq A., Mohamed A. Al-Omar, Ahmed M. Naglah y Abdullah Al-Dhfyan. "Facile synthesis and anticancer activity of novel dihydropyrimidinone derivatives". Polish Journal of Chemical Technology 24, n.º 1 (1 de marzo de 2022): 23–28. http://dx.doi.org/10.2478/pjct-2022-0004.
Texto completoBhat, Mashooq A., Mohamed A. Al-Omar, Ahmed M. Naglah y Abdullah Al-Dhfyan. "Biginelli Synthesis of Novel Dihydropyrimidinone Derivatives Containing Phthalimide Moiety". Journal of Chemistry 2020 (9 de marzo de 2020): 1–5. http://dx.doi.org/10.1155/2020/4284628.
Texto completoShen, Jinhai, Xifa Yang, Fuyuan Wang, Yue Wang, Guolin Cheng y Xiuling Cui. "Base-mediated regiospecific cascade synthesis of N-(2-pyridyl)pyrroles from N-propargylic β-enaminones". RSC Advances 6, n.º 54 (2016): 48905–9. http://dx.doi.org/10.1039/c6ra08987a.
Texto completoEdafiogho, Ivan O., Jacqueline A. Moore, Vida A. Farrar, Jesse M. Nicholson y K. R. Scott. "Synthesis, Reactions, and Preliminary Evaluations of Enaminone Esters". Journal of Pharmaceutical Sciences 83, n.º 1 (enero de 1994): 79–84. http://dx.doi.org/10.1002/jps.2600830119.
Texto completoWan, Jie-Ping, Chunping Wang y Yunyun Liu. "Direct synthesis of enaminone functionalized biaryl ethers by CuI-catalyzed O-arylation of enaminone functionalized phenols". Organic & Biomolecular Chemistry 9, n.º 19 (2011): 6481. http://dx.doi.org/10.1039/c1ob05947e.
Texto completoYu, Qing, Yating Zhang y Jie-Ping Wan. "Ambient and aerobic carbon–carbon bond cleavage toward α-ketoester synthesis by transition-metal-free photocatalysis". Green Chemistry 21, n.º 12 (2019): 3436–41. http://dx.doi.org/10.1039/c9gc01357a.
Texto completoMahmoud, Huda K., Hanadi A. Katouah, Marwa F. Harras y Thoraya A. Farghaly. "A New Reactive Ketenaminal: Synthesis, Coupling Reaction, Tautomeric Study, Docking and Antimicrobial Evaluation of the Products". Medicinal Chemistry 16, n.º 6 (7 de septiembre de 2020): 761–73. http://dx.doi.org/10.2174/1573406415666190716153425.
Texto completoŠkrlep, Luka, Andreja Čerček-Hočevar, Renata Jakše, Branko Stanovnik y Jurij Svete. "A Simple Synthesis of 1-Substituted Diethyl Pyrrole-3,4-dicarboxylates". Zeitschrift für Naturforschung B 64, n.º 6 (1 de junio de 2009): 683–88. http://dx.doi.org/10.1515/znb-2009-0614.
Texto completoShah, Nirav, Nimesh Shah, Manish Patel y Ranjan Patel. "Design, synthesis and antimicrobial activity of new biquinoline derivatives". Journal of the Serbian Chemical Society 77, n.º 3 (2012): 279–86. http://dx.doi.org/10.2298/jsc110630197s.
Texto completoAl-Saleh, Balkis, Nouria Al-Awadi, Halema Al-kandari, Mervat Mohammed Abdel-Khalik y Mohamed Hilmy Elnagdi. "Studies with 2H pyranones: Synthesis of new 3-substituted-4-hydroxy-2H-pyran-2-ones". Journal of Chemical Research 2000, n.º 1 (enero de 2000): 16–17. http://dx.doi.org/10.3184/030823400103165725.
Texto completoWan, Jie-Ping, Chunping Wang y Yunyun Liu. "ChemInform Abstract: Direct Synthesis of Enaminone Functionalized Biaryl Ethers by CuI-Catalyzed O-Arylation of Enaminone Functionalized Phenols." ChemInform 43, n.º 7 (23 de enero de 2012): no. http://dx.doi.org/10.1002/chin.201207060.
Texto completoLiang, Xiao, Xin Huang, Mingteng Xiong, Kexin Shen y Yuanjiang Pan. "Copper(i)-catalyzed N–H olefination of sulfonamides for N-sulfonyl enaminone synthesis". Chemical Communications 54, n.º 60 (2018): 8403–6. http://dx.doi.org/10.1039/c8cc04385j.
Texto completoScapin, Elisandra, Paulo R. S. Salbego, Caroline R. Bender, Alexandre R. Meyer, Anderson B. Pagliari, Tainára Orlando, Geórgia C. Zimmer et al. "Synthesis, effect of substituents on the regiochemistry and equilibrium studies of tetrazolo[1,5-a]pyrimidine/2-azidopyrimidines". Beilstein Journal of Organic Chemistry 13 (10 de noviembre de 2017): 2396–407. http://dx.doi.org/10.3762/bjoc.13.237.
Texto completoHo, Yuh-Wen y Maw Cherng Suen. "Thioxopyrimidine in Heterocyclic Synthesis I: Synthesis of Some Novel 6-(Heteroatom-substituted)-(thio)pyrimidine Derivatives". Journal of Chemistry 2013 (2013): 1–15. http://dx.doi.org/10.1155/2013/765243.
Texto completoTomažin, Urša, Branko Alič, Anja Kristl, Aleš Ručigaj, Uroš Grošelj, Franc Požgan, Matjaž Krajnc, Bogdan Štefane, Urška Šebenik y Jurij Svete. "Synthesis of polyenaminones by acid-catalysed amino–enaminone ‘click’ polymerisation". European Polymer Journal 108 (noviembre de 2018): 603–16. http://dx.doi.org/10.1016/j.eurpolymj.2018.07.048.
Texto completoEDAFIOGHO, I. O., J. A. MOORE, V. A. FARRAR, J. M. NICHOLSON y K. R. SCOTT. "ChemInform Abstract: Synthesis, Reactions, and Preliminary Evaluations of Enaminone Esters." ChemInform 25, n.º 19 (19 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199419100.
Texto completoMohammadi, Leila, Mohammad Ali Zolfigol, Mahsa Ebrahiminia, Kenneth P. Roberts, Samira Ansari, Tahereh Azadbakht y Syed R. Hussaini. "A copper(I)-complexed magnetic nanoparticle catalyst for enaminone synthesis". Catalysis Communications 102 (diciembre de 2017): 44–47. http://dx.doi.org/10.1016/j.catcom.2017.08.022.
Texto completoAbdulsalam, Maysam B. y Ahmed T. Numan. "Synthesis, Characterization, and Biological Activity of Mixed ligand Complexes from 8-Hydroxyquinoline and new Ligand for β-Enaminone". Pakistan Journal of Medical and Health Sciences 16, n.º 8 (31 de agosto de 2022): 614–21. http://dx.doi.org/10.53350/pjmhs22168614.
Texto completoLiu, Ting, Jie-Ping Wan y Yunyun Liu. "Metal-free enaminone C–N bond cyanation for the stereoselective synthesis of (E)- and (Z)-β-cyano enones". Chemical Communications 57, n.º 72 (2021): 9112–15. http://dx.doi.org/10.1039/d1cc03292e.
Texto completoKadhom, Hassan J., Ahmed T. Numan y Eman M. Atiyah. "Synthesis and Characterization of New Ligand for β-enaminone and its Mixed Ligand Complexes with Some Metal Ions and Evaluation of their Biological Activity". INTERNATIONAL JOURNAL OF DRUG DELIVERY TECHNOLOGY 12, n.º 02 (25 de junio de 2022): 640–47. http://dx.doi.org/10.25258/ijddt.12.2.30.
Texto completoCooper, Melanie M. y John W. Huffman. "Reaction of an enaminone with 1-nitrocyclopentene: synthesis of a triquinane". Journal of the Chemical Society, Chemical Communications, n.º 5 (1987): 348. http://dx.doi.org/10.1039/c39870000348.
Texto completoCimarelli, Cristina, Gianni Palmieri y Mercedes Camalli. "Stereoselective preparation of enaminone lithium dianions: Synthesis of N,N-dimethylcarbamoylenaminones". Tetrahedron 53, n.º 20 (mayo de 1997): 6893–902. http://dx.doi.org/10.1016/s0040-4020(97)00320-7.
Texto completoShi, Pengfei, Lili Wang, Kehao Chen, Jie Wang y Jin Zhu. "Co(III)-Catalyzed Enaminone-Directed C–H Amidation for Quinolone Synthesis". Organic Letters 19, n.º 9 (20 de abril de 2017): 2418–21. http://dx.doi.org/10.1021/acs.orglett.7b00968.
Texto completoChang, Lina, Tao Guo, Ziyi Wang, Shaozhong Wang y Zhu-Jun Yao. "Azepinoindole Synthesis via a N-Bromosuccinimide-Induced Cycloisomerization of Enaminoester/Enaminone". Journal of Organic Chemistry 82, n.º 3 (23 de enero de 2017): 1567–74. http://dx.doi.org/10.1021/acs.joc.6b02760.
Texto completoBaškovč, Jernej, David Bevk, Branko Stanovnik y Jurij Svete. "Bis-enaminone Based Parallel Solution-Phase Synthesis of 1,4-Dihydropyridine Derivatives". Journal of Combinatorial Chemistry 11, n.º 3 (11 de mayo de 2009): 500–507. http://dx.doi.org/10.1021/cc900032c.
Texto completoFarghaly, Thoraya A., Magda A. Abdallah y Mohamed R. Abdel Aziz. "Synthesis of a NovelTri-enaminone as Building Block for Polyaza-heterocycles". Journal of Heterocyclic Chemistry 54, n.º 1 (3 de mayo de 2016): 699–705. http://dx.doi.org/10.1002/jhet.2644.
Texto completoGajengi, Aravind L., Takehiko Sasaki y Bhalchandra M. Bhanage. "Effect of solvent ratio and counter ions on the morphology of copper nanoparticles and their catalytic application in β-enaminone synthesis". RSC Advances 6, n.º 104 (2016): 101800–101807. http://dx.doi.org/10.1039/c6ra22017g.
Texto completoŠtanfel, Urša, Tomaž Kotnik, Sebastijan Ričko, Uroš Grošelj, Bogdan Štefane, Klemen Pirnat, Ema Žagar, Boštjan Genorio y Jurij Svete. "Synthesis of Optically and Redox Active Polyenaminones from Diamines and α,α’-Bis[(dimethylamino)methylidene]cyclohexanediones". Polymers 14, n.º 19 (1 de octubre de 2022): 4120. http://dx.doi.org/10.3390/polym14194120.
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