Artículos de revistas sobre el tema "Solvent free reaction"
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Heydari, Somayyeh, Davood Habibi y Alireza Faraji. "A Green and Efficient Solvent- and Catalyst-Free Ultrasonic Dibenzylation Procedure". Chemistry & Chemical Technology 16, n.º 1 (20 de febrero de 2022): 126–32. http://dx.doi.org/10.23939/chcht16.01.126.
Texto completoAljuboori, Sahar Balkat, Nedaa Abdulhameed Abdulrahim, Shuhad Yassen y Heba Hashim Khaleel. "Organic Synthesis under Solvent-free Condition (Green Chemistry): A Mini Literature Review". Al-Rafidain Journal of Medical Sciences ( ISSN: 2789-3219 ) 3 (17 de diciembre de 2022): 109–15. http://dx.doi.org/10.54133/ajms.v3i.94.
Texto completoKarolczak, Stefan, Hugh A. Gillis, Gerald B. Porter y David C. Walker. "Solvent-dependent rate constants of muonium atom reactions". Canadian Journal of Chemistry 81, n.º 2 (1 de febrero de 2003): 175–78. http://dx.doi.org/10.1139/v03-009.
Texto completoBraga, Dario, Stefano Luca Giaffreda, Fabrizia Grepioni, Michele R. Chierotti, Roberto Gobetto, Giuseppe Palladino y Marco Polito. "Solvent effect in a “solvent free” reaction". CrystEngComm 9, n.º 10 (2007): 879. http://dx.doi.org/10.1039/b711983f.
Texto completoAway, Kenneth Charles West y Zhu-Gen Lai. "Solvent effects on SN2 transition state structure. II: The effect of ion pairing on the solvent effect on transition state structure". Canadian Journal of Chemistry 67, n.º 2 (1 de febrero de 1989): 345–49. http://dx.doi.org/10.1139/v89-056.
Texto completoMiyamoto, Hisakazu, Shotaro Kanetaka, Koichi Tanaka, Kazuhiro Yoshizawa, Shinji Toyota y Fumio Toda. "Solvent-Free Robinson Annelation Reaction". Chemistry Letters 29, n.º 8 (agosto de 2000): 888–89. http://dx.doi.org/10.1246/cl.2000.888.
Texto completoZhou, Jinkui y Thomas W. Swaddle. "Pressure effects and solvent dynamics in the electrochemical kinetics of the tris(hexafluoroacetylacetonato)ruthenium(III)/(II) couple in nonaqueous solvents". Canadian Journal of Chemistry 79, n.º 5-6 (1 de mayo de 2001): 841–47. http://dx.doi.org/10.1139/v00-184.
Texto completoSaikia, Monmi y Jadab C. Sarma. "Baylis–Hillman reaction under solvent-free conditions — Remarkable rate acceleration and yield enhancement". Canadian Journal of Chemistry 88, n.º 12 (diciembre de 2010): 1271–76. http://dx.doi.org/10.1139/v10-133.
Texto completoChoudhuri, Khokan, Arkalekha Mandal y Prasenjit Mal. "Aerial dioxygen activation vs. thiol–ene click reaction within a system". Chemical Communications 54, n.º 30 (2018): 3759–62. http://dx.doi.org/10.1039/c8cc01359d.
Texto completoAnbu, Nagarjun, Jacob, Kalaiarasi y Dhakshinamoorthy. "Acetylation of Alcohols, Amines, Phenols, Thiols under Catalyst and Solvent-Free Conditions". Chemistry 1, n.º 1 (10 de julio de 2019): 69–79. http://dx.doi.org/10.3390/chemistry1010006.
Texto completoJicsinszky, László y Giancarlo Cravotto. "Toward a Greener World—Cyclodextrin Derivatization by Mechanochemistry". Molecules 26, n.º 17 (27 de agosto de 2021): 5193. http://dx.doi.org/10.3390/molecules26175193.
Texto completoSingh, Girija S. "Greener Approaches to Selected Asymmetric Addition Reactions Relevant to Drug Development". Current Organic Chemistry 25, n.º 13 (2 de septiembre de 2021): 1497–522. http://dx.doi.org/10.2174/1385272825666210519100457.
Texto completoRaston, Colin L. y Janet L. Scott. "Chemoselective, solvent-free aldol condensation reaction". Green Chemistry 2, n.º 2 (2000): 49–52. http://dx.doi.org/10.1039/a907688c.
Texto completoCablewski, Teresa, Paul A. Gurr, Peter J. Pajalic y Christopher R. Strauss. "A solvent-free Jacobs–Gould reaction". Green Chemistry 2, n.º 1 (2000): 25–28. http://dx.doi.org/10.1039/a908606d.
Texto completoPhonchaiya, Sonthi, Bhinyo Panijpan, Shuleewan Rajviroongit, Joanne T. Blanchfield y Tony Wright. "A Facile Solvent-Free Cannizzaro Reaction". Journal of Chemical Education 86, n.º 1 (enero de 2009): 85. http://dx.doi.org/10.1021/ed086p85.
Texto completoDu, Rui, Liangliang Han, Zhongqiang Zhou y Victor Borovkov. "Efficient Synthesis of Novel Quinolinone Derivatives via Catalyst-free Multicomponent Reaction". Letters in Organic Chemistry 17, n.º 5 (28 de abril de 2020): 403–7. http://dx.doi.org/10.2174/1570178616666190828092728.
Texto completoSharghi, Hashem y Reza Khalifeh. "Reaction on a solid surface — A simple, economical, and efficient Mannich reaction of azacrown ethers over graphite". Canadian Journal of Chemistry 86, n.º 5 (1 de mayo de 2008): 426–34. http://dx.doi.org/10.1139/v08-026.
Texto completoStolle, Achim y Bernd Ondruschka. "Solvent-free reactions of alkynes in ball mills: It is definitely more than mixing". Pure and Applied Chemistry 83, n.º 7 (30 de abril de 2011): 1343–49. http://dx.doi.org/10.1351/pac-con-10-09-26.
Texto completoLam, Solita, Yvonne Puplampu Dove, Adrienne Morris, Ayunna Epps y Ghislain R. Mandouma. "Cross-Coupling Biarylation of Nitroaryl Chlorides Through High Speed Ball Milling". International Journal for Innovation Education and Research 3, n.º 6 (30 de junio de 2015): 12–35. http://dx.doi.org/10.31686/ijier.vol3.iss6.376.
Texto completoLi, Xiao Chuan, Shan Shan Gong y Qi Sun. "Synthesis of Phosphonate-Containing 2-Methyl-1,5-Diaminopentane Derivatives". Advanced Materials Research 1046 (octubre de 2014): 104–7. http://dx.doi.org/10.4028/www.scientific.net/amr.1046.104.
Texto completoRaiedhah Alsaiari, Raiedhah Alsaiari, Moustafa A. Rizk Moustafa A Rizk, Esraa Musa Esraa Musa, Huda Alqahtani Huda Alqahtani, Fatima Alqadri Fatima Alqadri, Mervat Mohamed Mervat Mohamed, Mabkhoot Alsaiari Mabkhoot Alsaiari, Ali Alkorbi Ali Alkorbi, Iman Shedaiwa Iman Shedaiwa y Faeza Alkorbi Faeza Alkorbi. "Supported Ruthenium Catalysts for Oxidation of Benzyl Alcohol under Solvent Free Conditions". Journal of the chemical society of pakistan 44, n.º 4 (2022): 322. http://dx.doi.org/10.52568/001069/jcsp/44.04.2022.
Texto completoZare, Abdolkarim y Manije Dianat. "A highly efficient and green approach for the synthesis of pyrimido[4,5-b]quinolines using N,N-diethyl-N-sulfoethanaminium chloride". Zeitschrift für Naturforschung B 76, n.º 2 (11 de enero de 2021): 85–90. http://dx.doi.org/10.1515/znb-2020-0098.
Texto completoMoormann, Widukind, Daniel Langbehn y Rainer Herges. "Solvent-Free Synthesis of Diazocine". Synthesis 49, n.º 15 (11 de julio de 2017): 3471–75. http://dx.doi.org/10.1055/s-0036-1590685.
Texto completoYe, X. R., C. Daraio, C. Wang, J. B. Talbot y S. Jin. "Room Temperature Solvent-Free Synthesis of Monodisperse Magnetite Nanocrystals". Journal of Nanoscience and Nanotechnology 6, n.º 3 (1 de marzo de 2006): 852–56. http://dx.doi.org/10.1166/jnn.2006.135.
Texto completoLoesch-Zhang, Amelia, Cynthia Cordt, Andreas Geissler y Markus Biesalski. "A Solvent-Free Approach to Crosslinked Hydrophobic Polymeric Coatings on Paper Using Vegetable Oil". Polymers 14, n.º 9 (27 de abril de 2022): 1773. http://dx.doi.org/10.3390/polym14091773.
Texto completoSoleiman-Beigi, Mohammad, Reza Aryan, Maryam Yousofizadeh y Shima Khosravi. "A Combined Synthetic and DFT Study on the Catalyst-Free and Solvent-Assisted Synthesis of 1,3,4-Oxadiazole-2-thiol Derivatives". Journal of Chemistry 2013 (2013): 1–6. http://dx.doi.org/10.1155/2013/476358.
Texto completoBousquet, Till, Mouhamad Jida, Mohamad Soueidan, Rebecca Deprez-Poulain, Francine Agbossou-Niedercorn y Lydie Pelinski. "Fast and efficient solvent-free Passerini reaction". Tetrahedron Letters 53, n.º 3 (enero de 2012): 306–8. http://dx.doi.org/10.1016/j.tetlet.2011.11.028.
Texto completoGladysz, John A. "Reaction: Toward Organic-Solvent-free Synthetic Chemistry". Chem 4, n.º 9 (septiembre de 2018): 2007–8. http://dx.doi.org/10.1016/j.chempr.2018.08.026.
Texto completoNielsen, Simon Feldbæk, Dan Peters y Oskar Axelsson. "The Suzuki Reaction Under Solvent-Free Conditions". Synthetic Communications 30, n.º 19 (octubre de 2000): 3501–9. http://dx.doi.org/10.1080/00397910008087262.
Texto completoWaddell, Daniel C. y James Mack. "An environmentally benign solvent-free Tishchenko reaction". Green Chem. 11, n.º 1 (2009): 79–82. http://dx.doi.org/10.1039/b810714a.
Texto completoMotiur Rahman, A. F. M. y Adnan A. Kadi. "Solvent free Cannizzaro reaction applying grindstone technique". Arabian Journal of Chemistry 9 (noviembre de 2016): S1373—S1377. http://dx.doi.org/10.1016/j.arabjc.2012.02.010.
Texto completoMiyamoto, Hisakazu, Shotaro Kanetaka, Koichi Tanaka, Kazuhiro Yoshizawa, Shinji Toyota y Fumio Toda. "ChemInform Abstract: Solvent-Free Robinson Anellation Reaction." ChemInform 31, n.º 51 (19 de diciembre de 2000): no. http://dx.doi.org/10.1002/chin.200051046.
Texto completoGhigo, Giovanni, Matteo Bonomo, Achille Antenucci, Chiara Reviglio y Stefano Dughera. "Copper-Free Halodediazoniation of Arenediazonium Tetrafluoroborates in Deep Eutectic Solvents-like Mixtures". Molecules 27, n.º 6 (15 de marzo de 2022): 1909. http://dx.doi.org/10.3390/molecules27061909.
Texto completoMarchenko, Roman D. y Andrei S. Potapov. "Synthesis of Bis(1,2,3-triazolyl)alkanes in Superbasic and Solvent-Free Conditions". Molbank 2023, n.º 1 (13 de enero de 2023): M1551. http://dx.doi.org/10.3390/m1551.
Texto completoMandouma, Ghislain R., Ayunna Epps y John Barbas. "Synthesis of Substituted 2,2’-Dinitrobiphenyls by a Novel Solvent-Free High Yielding Ullmann Coupling Biarylation:". International Journal for Innovation Education and Research 2, n.º 12 (31 de diciembre de 2014): 133–49. http://dx.doi.org/10.31686/ijier.vol2.iss12.293.
Texto completoMiao, Changlin, Zhongming Wang, Lingmei Yang, Huiwen Li, Pengmei Lv, Xinshu Zhuang, Zhenhong Yuan y Wen Luo. "Lipase-Catalyzed Synthesis of Glycerol-Free Biodiesel from Rapeseed Oil and Dimethyl Carbonate". Journal of Biobased Materials and Bioenergy 14, n.º 4 (1 de agosto de 2020): 537–43. http://dx.doi.org/10.1166/jbmb.2020.1973.
Texto completoRubab, Laila, Ayesha Anum, Sami A. Al-Hussain, Ali Irfan, Sajjad Ahmad, Sami Ullah, Aamal A. Al-Mutairi y Magdi E. A. Zaki. "Green Chemistry in Organic Synthesis: Recent Update on Green Catalytic Approaches in Synthesis of 1,2,4-Thiadiazoles". Catalysts 12, n.º 11 (29 de octubre de 2022): 1329. http://dx.doi.org/10.3390/catal12111329.
Texto completoSalmar, Siim, Jaak Järv, Tiina Tenno y Ants Tuulmets. "Role of water in determining organic reactivity in aqueous binary solvents". Open Chemistry 10, n.º 5 (1 de octubre de 2012): 1600–1608. http://dx.doi.org/10.2478/s11532-012-0080-8.
Texto completoKidwai, Mazaahir, Shweta Rastogi, Ruby Thakur y Shilpi Saxena. "Solvent-Free Synthesis of 2,4,6-Triaryl Pyridines". Zeitschrift für Naturforschung B 59, n.º 5 (1 de mayo de 2004): 606–8. http://dx.doi.org/10.1515/znb-2004-0522.
Texto completoChavelas-Hernández, Leticia, Luis G. Hernández-Vázquez, José D. Bahena-Martínez, Alexa B. Arroyo-Colín, Sinuhe G. Flores-Osorio, Gabriel Navarrete-Vázquez y Jaime Escalante. "Aza-Michael Additions of Benzylamine to Acrylates Promoted by Microwaves and Conventional Heating Using DBU as Catalyst via Solvent-Free Protocol". Processes 12, n.º 1 (22 de diciembre de 2023): 34. http://dx.doi.org/10.3390/pr12010034.
Texto completoSapaev, B., F. E. Saitkulov, A. A. Tashniyazov y OU Normurodov. "Study of methylation reactions of 2-phenylquinazoline-4-tion with “soft” and “hard” methylation agents and determination of its biological activity". E3S Web of Conferences 258 (2021): 04023. http://dx.doi.org/10.1051/e3sconf/202125804023.
Texto completoOlyaei, Abolfazl, Mohsen Vaziri, Reza Razeghi, Shams Bahareh y Hasan Bagheri. "Novel approach to bis(indolyl)methanes using nickel nanoparticles as a reusable catalyst under solvent-free conditions". Journal of the Serbian Chemical Society 78, n.º 4 (2013): 463–68. http://dx.doi.org/10.2298/jsc120506076o.
Texto completoTahmasbi, Marzieh, Nadiya Koukabi y Ozra Armandpour. "Sono and nano: A perfect synergy for eco-compatible Biginelli reaction". Heterocyclic Communications 28, n.º 1 (1 de enero de 2022): 1–10. http://dx.doi.org/10.1515/hc-2022-0003.
Texto completoCai, Yan Hua. "Studies on Synthesis, Morphology and Theoretical Analysis of Schiff Base Derived From p-Aminobenzoic Acid and p-Hydroxybenzaldehyde by Solvent-Free Reaction Using Jet Milling". Advanced Materials Research 79-82 (agosto de 2009): 1355–58. http://dx.doi.org/10.4028/www.scientific.net/amr.79-82.1355.
Texto completoKrištofíková, Dominika, Juraj Filo, Mária Mečiarová y Radovan Šebesta. "Why do thioureas and squaramides slow down the Ireland–Claisen rearrangement?" Beilstein Journal of Organic Chemistry 15 (10 de diciembre de 2019): 2948–57. http://dx.doi.org/10.3762/bjoc.15.290.
Texto completoMa, Xiaofang, Shunxi Li, Samrat Devaramani, Guohu Zhao y Daqian Xu. "One-Pot, Regioselective Synthesis of Homopropargyl Alcohols using Propargyl Bromide and Carbonyl Compound by the Mg-mediated Reaction under Solvent-free Conditions". Letters in Organic Chemistry 17, n.º 6 (20 de mayo de 2020): 438–42. http://dx.doi.org/10.2174/1570178616666190926104037.
Texto completoCui, Dong-Xiao, Yue-Dan Li, Jun-Chao Zhu, Yan-Yan Jia, Ai-Dong Wen y Ping-An Wang. "Highly Efficient Michael Reactions of Nitroolefins by Grinding Means". Current Organic Synthesis 16, n.º 3 (17 de junio de 2019): 449–57. http://dx.doi.org/10.2174/1570179416666190101122150.
Texto completoChen, Longrui, Betsegaw E. Lemma, Jenna S. Rich y James Mack. "Freedom: a copper-free, oxidant-free and solvent-free palladium catalysed homocoupling reaction". Green Chem. 16, n.º 3 (2014): 1101–3. http://dx.doi.org/10.1039/c3gc41847b.
Texto completoCrole, David A., Simon J. Freakley, Jennifer K. Edwards y Graham J. Hutchings. "Direct synthesis of hydrogen peroxide in water at ambient temperature". Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 472, n.º 2190 (junio de 2016): 20160156. http://dx.doi.org/10.1098/rspa.2016.0156.
Texto completoBora, Pranjal P., H. Atoholi Sema, Barisha Wahlang y Ghanashyam Bez. "Rapid synthesis of homoallylic alcohol from aldehyde with allyltributylstannane under solvent-free conditions". Canadian Journal of Chemistry 90, n.º 2 (febrero de 2012): 167–72. http://dx.doi.org/10.1139/v11-138.
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