Статті в журналах з теми "Enaminone synthesis"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Enaminone synthesis".
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Chattopadhyay, Amit Kumar, and Stephen Hanessian. "Cyclic enaminones. Part II: applications as versatile intermediates in alkaloid synthesis." Chemical Communications 51, no. 92 (2015): 16450–67. http://dx.doi.org/10.1039/c5cc05892a.
Повний текст джерелаŠtanfel, Urša, Dejan Slapšak, Uroš Grošelj, Franc Požgan, Bogdan Štefane, and 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, no. 2 (January 13, 2021): 400. http://dx.doi.org/10.3390/molecules26020400.
Повний текст джерелаMasaret, Ghada S., and 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, no. 1 (March 20, 2018): 126–36. http://dx.doi.org/10.2174/1570179414666170601121137.
Повний текст джерелаCiber, Luka, Franc Požgan, Helena Brodnik, Bogdan Štefane, Jurij Svete, and Uroš Grošelj. "Synthesis and Catalytic Activity of Organocatalysts Based on Enaminone and Benzenediamine Hydrogen Bond Donors." Catalysts 12, no. 10 (September 28, 2022): 1132. http://dx.doi.org/10.3390/catal12101132.
Повний текст джерелаAgamy, Samia Michel, Mervat Mohammed Abdel-Khalik, Mona Hassan Mohamed, and Mohammed Hilmy Elnagdi. "Enaminones as Building Blocks In Heterocyclic Synthesis: A New One Pot Synthesis of Polyfunctional Substituted Pyridines." Zeitschrift für Naturforschung B 56, no. 10 (October 1, 2001): 1074–78. http://dx.doi.org/10.1515/znb-2001-1016.
Повний текст джерелаLiu, Weibing, Cui Chen та Qing Zhang. "FeCl3-PTSA Co-Catalysed Highly Regio- and Stereo-Selective Synthesis of β-Functionalised Enamine Derivatives". Journal of Chemical Research 36, № 3 (березень 2012): 175–77. http://dx.doi.org/10.3184/174751912x13306054094882.
Повний текст джерелаHassan, Mohamed M., and Mona H. Alhalafi. "Synthesis, Structural Determination, and Antioxidant Activities of Acyclic and Substituted Heterocyclic Phosphonates Linearly Linked 4-hydroxy-2(1H)-quinolinone." Molecules 27, no. 18 (September 13, 2022): 5960. http://dx.doi.org/10.3390/molecules27185960.
Повний текст джерелаSzafraniec, Anna, Marcin Grajda, Hanna Jędrzejewska, Agnieszka Szumna, and 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, no. 20 (October 11, 2020): 7494. http://dx.doi.org/10.3390/ijms21207494.
Повний текст джерелаAl-Romaizan, Abeer N., Nesreen S. Ahmed, and Sherin M. Elfeky. "Design, Synthesis, and Biological Evaluation of Triazolyl- and Triazinyl-Quinazolinediones as Potential Antitumor Agents." Journal of Chemistry 2019 (February 3, 2019): 1–12. http://dx.doi.org/10.1155/2019/9104653.
Повний текст джерелаFilkale, Adelew Estifanos, та 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, № 35 (2020): 15109–21. http://dx.doi.org/10.1039/d0nj00052c.
Повний текст джерелаLi, Yi, Xiaoji Cao, Yunyun Liu, and Jie-Ping Wan. "Regioselective three-component synthesis of 2,3-disubstituted quinolines via the enaminone modified Povarov reaction." Organic & Biomolecular Chemistry 15, no. 45 (2017): 9585–89. http://dx.doi.org/10.1039/c7ob02411h.
Повний текст джерелаWagger, Jernej, David Bevk, Anton Meden, Jurij Svete, and Branko Stanovnik. "Enaminone-Based Synthesis of Dipodazine Derivatives." Helvetica Chimica Acta 89, no. 2 (February 2006): 240–48. http://dx.doi.org/10.1002/hlca.200690026.
Повний текст джерелаŠenica, Luka, Uroš Grošelj, Marta Kasunič, Drago Kočar, Branko Stanovnik, and Jurij Svete. "Synthesis of Enaminone-Based Vinylogous Peptides." European Journal of Organic Chemistry 2014, no. 15 (March 13, 2014): 3067–71. http://dx.doi.org/10.1002/ejoc.201402033.
Повний текст джерелаKnieß, Astrid, Margit Gruner та 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, № 9 (1 вересня 1999): 1133–37. http://dx.doi.org/10.1515/znb-1999-0908.
Повний текст джерелаAmbethkar, Sethurajan, Vediappen Padmini, and Nattamai Bhuvanesh. "A one-pot sequential five-component domino reaction for the expedient synthesis of polysubstituted pyrroles." New Journal of Chemistry 40, no. 5 (2016): 4705–9. http://dx.doi.org/10.1039/c5nj03444b.
Повний текст джерелаWan, Jie-Ping, Youyi Zhou, Yunyun Liu, and Shouri Sheng. "Metal-free oxidative carbonylation on enaminone CC bond for the cascade synthesis of benzothiazole-containing vicinal diketones." Green Chemistry 18, no. 2 (2016): 402–5. http://dx.doi.org/10.1039/c5gc01821h.
Повний текст джерелаKlintworth, Robin, Garreth L. Morgans, Stefania M. Scalzullo, Charles B. de Koning, Willem A. L. van Otterlo, and Joseph P. Michael. "Silica gel and microwave-promoted synthesis of dihydropyrrolizines and tetrahydroindolizines from enaminones." Beilstein Journal of Organic Chemistry 17 (October 13, 2021): 2543–52. http://dx.doi.org/10.3762/bjoc.17.170.
Повний текст джерелаZhong, Shanshan, Yu Lu, Yan Zhang, Yunyun Liu та Jie-Ping Wan. "Synthesis of β,β-diaryl propiophenones via palladium-catalyzed domino arylboronation, elimination and enone hydroarylation of enaminones". Organic & Biomolecular Chemistry 14, № 26 (2016): 6270–73. http://dx.doi.org/10.1039/c6ob01038e.
Повний текст джерелаOlyaei, Abolfazl, Amir Mohamadi, and Nilufar Rahmani. "Green synthesis of new lawsone enaminones and their Z/E(CC)-isomerization induced by organic solvent." RSC Advances 11, no. 21 (2021): 12990–94. http://dx.doi.org/10.1039/d1ra01858b.
Повний текст джерелаBhat, Mashooq Ahmad, Mohamed A. Al-Omar, Ahmed M. Naglah, Atef Kalmouch, and Abdullah Al-Dhfyan. "Synthesis and Characterization of Novel Biginelli Dihydropyrimidinone Derivatives Containing Imidazole Moiety." Journal of Chemistry 2019 (May 13, 2019): 1–7. http://dx.doi.org/10.1155/2019/3131879.
Повний текст джерелаAlshahrani, Saeed, Saied M. Soliman, Abdullah Saleh Alamary, Abdullah Mohammed Al-Majid, Matti Haukka, Sammer Yousuf, and Assem Barakat. "Synthesis of Enaminones-Based Benzo[d]imidazole Scaffold: Characterization and Molecular Insight Structure." Crystals 10, no. 10 (October 21, 2020): 955. http://dx.doi.org/10.3390/cryst10100955.
Повний текст джерелаWu, Wenfeng, Zhuxian Wang, Qun Shen, Qiang Liu, and Huoji Chen. "Fe-Catalyzed enaminone synthesis from ketones and amines." Organic & Biomolecular Chemistry 17, no. 28 (2019): 6753–56. http://dx.doi.org/10.1039/c9ob01137d.
Повний текст джерелаBhat, Mashooq A., Mohamed A. Al-Omar, Ahmed M. Naglah, and Abdullah Al-Dhfyan. "Facile synthesis and anticancer activity of novel dihydropyrimidinone derivatives." Polish Journal of Chemical Technology 24, no. 1 (March 1, 2022): 23–28. http://dx.doi.org/10.2478/pjct-2022-0004.
Повний текст джерелаBhat, Mashooq A., Mohamed A. Al-Omar, Ahmed M. Naglah, and Abdullah Al-Dhfyan. "Biginelli Synthesis of Novel Dihydropyrimidinone Derivatives Containing Phthalimide Moiety." Journal of Chemistry 2020 (March 9, 2020): 1–5. http://dx.doi.org/10.1155/2020/4284628.
Повний текст джерелаShen, Jinhai, Xifa Yang, Fuyuan Wang, Yue Wang, Guolin Cheng та Xiuling Cui. "Base-mediated regiospecific cascade synthesis of N-(2-pyridyl)pyrroles from N-propargylic β-enaminones". RSC Advances 6, № 54 (2016): 48905–9. http://dx.doi.org/10.1039/c6ra08987a.
Повний текст джерелаEdafiogho, Ivan O., Jacqueline A. Moore, Vida A. Farrar, Jesse M. Nicholson, and K. R. Scott. "Synthesis, Reactions, and Preliminary Evaluations of Enaminone Esters." Journal of Pharmaceutical Sciences 83, no. 1 (January 1994): 79–84. http://dx.doi.org/10.1002/jps.2600830119.
Повний текст джерелаWan, Jie-Ping, Chunping Wang, and Yunyun Liu. "Direct synthesis of enaminone functionalized biaryl ethers by CuI-catalyzed O-arylation of enaminone functionalized phenols." Organic & Biomolecular Chemistry 9, no. 19 (2011): 6481. http://dx.doi.org/10.1039/c1ob05947e.
Повний текст джерелаYu, Qing, Yating Zhang та Jie-Ping Wan. "Ambient and aerobic carbon–carbon bond cleavage toward α-ketoester synthesis by transition-metal-free photocatalysis". Green Chemistry 21, № 12 (2019): 3436–41. http://dx.doi.org/10.1039/c9gc01357a.
Повний текст джерелаMahmoud, Huda K., Hanadi A. Katouah, Marwa F. Harras, and Thoraya A. Farghaly. "A New Reactive Ketenaminal: Synthesis, Coupling Reaction, Tautomeric Study, Docking and Antimicrobial Evaluation of the Products." Medicinal Chemistry 16, no. 6 (September 7, 2020): 761–73. http://dx.doi.org/10.2174/1573406415666190716153425.
Повний текст джерелаŠkrlep, Luka, Andreja Čerček-Hočevar, Renata Jakše, Branko Stanovnik, and Jurij Svete. "A Simple Synthesis of 1-Substituted Diethyl Pyrrole-3,4-dicarboxylates." Zeitschrift für Naturforschung B 64, no. 6 (June 1, 2009): 683–88. http://dx.doi.org/10.1515/znb-2009-0614.
Повний текст джерелаShah, Nirav, Nimesh Shah, Manish Patel, and Ranjan Patel. "Design, synthesis and antimicrobial activity of new biquinoline derivatives." Journal of the Serbian Chemical Society 77, no. 3 (2012): 279–86. http://dx.doi.org/10.2298/jsc110630197s.
Повний текст джерелаAl-Saleh, Balkis, Nouria Al-Awadi, Halema Al-kandari, Mervat Mohammed Abdel-Khalik, and Mohamed Hilmy Elnagdi. "Studies with 2H pyranones: Synthesis of new 3-substituted-4-hydroxy-2H-pyran-2-ones." Journal of Chemical Research 2000, no. 1 (January 2000): 16–17. http://dx.doi.org/10.3184/030823400103165725.
Повний текст джерелаWan, Jie-Ping, Chunping Wang, and Yunyun Liu. "ChemInform Abstract: Direct Synthesis of Enaminone Functionalized Biaryl Ethers by CuI-Catalyzed O-Arylation of Enaminone Functionalized Phenols." ChemInform 43, no. 7 (January 23, 2012): no. http://dx.doi.org/10.1002/chin.201207060.
Повний текст джерелаLiang, Xiao, Xin Huang, Mingteng Xiong, Kexin Shen, and Yuanjiang Pan. "Copper(i)-catalyzed N–H olefination of sulfonamides for N-sulfonyl enaminone synthesis." Chemical Communications 54, no. 60 (2018): 8403–6. http://dx.doi.org/10.1039/c8cc04385j.
Повний текст джерелаScapin, 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 (November 10, 2017): 2396–407. http://dx.doi.org/10.3762/bjoc.13.237.
Повний текст джерелаHo, Yuh-Wen, and 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.
Повний текст джерелаTomažin, Urša, Branko Alič, Anja Kristl, Aleš Ručigaj, Uroš Grošelj, Franc Požgan, Matjaž Krajnc, Bogdan Štefane, Urška Šebenik, and Jurij Svete. "Synthesis of polyenaminones by acid-catalysed amino–enaminone ‘click’ polymerisation." European Polymer Journal 108 (November 2018): 603–16. http://dx.doi.org/10.1016/j.eurpolymj.2018.07.048.
Повний текст джерелаEDAFIOGHO, I. O., J. A. MOORE, V. A. FARRAR, J. M. NICHOLSON, and K. R. SCOTT. "ChemInform Abstract: Synthesis, Reactions, and Preliminary Evaluations of Enaminone Esters." ChemInform 25, no. 19 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199419100.
Повний текст джерелаMohammadi, Leila, Mohammad Ali Zolfigol, Mahsa Ebrahiminia, Kenneth P. Roberts, Samira Ansari, Tahereh Azadbakht, and Syed R. Hussaini. "A copper(I)-complexed magnetic nanoparticle catalyst for enaminone synthesis." Catalysis Communications 102 (December 2017): 44–47. http://dx.doi.org/10.1016/j.catcom.2017.08.022.
Повний текст джерелаAbdulsalam, Maysam B., та 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, № 8 (31 серпня 2022): 614–21. http://dx.doi.org/10.53350/pjmhs22168614.
Повний текст джерелаLiu, Ting, Jie-Ping Wan та Yunyun Liu. "Metal-free enaminone C–N bond cyanation for the stereoselective synthesis of (E)- and (Z)-β-cyano enones". Chemical Communications 57, № 72 (2021): 9112–15. http://dx.doi.org/10.1039/d1cc03292e.
Повний текст джерелаKadhom, Hassan J., Ahmed T. Numan та 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, № 02 (25 червня 2022): 640–47. http://dx.doi.org/10.25258/ijddt.12.2.30.
Повний текст джерелаCooper, Melanie M., and John W. Huffman. "Reaction of an enaminone with 1-nitrocyclopentene: synthesis of a triquinane." Journal of the Chemical Society, Chemical Communications, no. 5 (1987): 348. http://dx.doi.org/10.1039/c39870000348.
Повний текст джерелаCimarelli, Cristina, Gianni Palmieri, and Mercedes Camalli. "Stereoselective preparation of enaminone lithium dianions: Synthesis of N,N-dimethylcarbamoylenaminones." Tetrahedron 53, no. 20 (May 1997): 6893–902. http://dx.doi.org/10.1016/s0040-4020(97)00320-7.
Повний текст джерелаShi, Pengfei, Lili Wang, Kehao Chen, Jie Wang, and Jin Zhu. "Co(III)-Catalyzed Enaminone-Directed C–H Amidation for Quinolone Synthesis." Organic Letters 19, no. 9 (April 20, 2017): 2418–21. http://dx.doi.org/10.1021/acs.orglett.7b00968.
Повний текст джерелаChang, Lina, Tao Guo, Ziyi Wang, Shaozhong Wang, and Zhu-Jun Yao. "Azepinoindole Synthesis via a N-Bromosuccinimide-Induced Cycloisomerization of Enaminoester/Enaminone." Journal of Organic Chemistry 82, no. 3 (January 23, 2017): 1567–74. http://dx.doi.org/10.1021/acs.joc.6b02760.
Повний текст джерелаBaškovč, Jernej, David Bevk, Branko Stanovnik, and Jurij Svete. "Bis-enaminone Based Parallel Solution-Phase Synthesis of 1,4-Dihydropyridine Derivatives." Journal of Combinatorial Chemistry 11, no. 3 (May 11, 2009): 500–507. http://dx.doi.org/10.1021/cc900032c.
Повний текст джерелаFarghaly, Thoraya A., Magda A. Abdallah, and Mohamed R. Abdel Aziz. "Synthesis of a NovelTri-enaminone as Building Block for Polyaza-heterocycles." Journal of Heterocyclic Chemistry 54, no. 1 (May 3, 2016): 699–705. http://dx.doi.org/10.1002/jhet.2644.
Повний текст джерелаGajengi, Aravind L., Takehiko Sasaki та 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, № 104 (2016): 101800–101807. http://dx.doi.org/10.1039/c6ra22017g.
Повний текст джерелаŠtanfel, Urša, Tomaž Kotnik, Sebastijan Ričko, Uroš Grošelj, Bogdan Štefane, Klemen Pirnat, Ema Žagar, Boštjan Genorio та Jurij Svete. "Synthesis of Optically and Redox Active Polyenaminones from Diamines and α,α’-Bis[(dimethylamino)methylidene]cyclohexanediones". Polymers 14, № 19 (1 жовтня 2022): 4120. http://dx.doi.org/10.3390/polym14194120.
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