Статті в журналах з теми "Solvent free reaction"
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Heydari, Somayyeh, Davood Habibi, and Alireza Faraji. "A Green and Efficient Solvent- and Catalyst-Free Ultrasonic Dibenzylation Procedure." Chemistry & Chemical Technology 16, no. 1 (February 20, 2022): 126–32. http://dx.doi.org/10.23939/chcht16.01.126.
Повний текст джерелаAljuboori, Sahar Balkat, Nedaa Abdulhameed Abdulrahim, Shuhad Yassen, and 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 (December 17, 2022): 109–15. http://dx.doi.org/10.54133/ajms.v3i.94.
Повний текст джерелаKarolczak, Stefan, Hugh A. Gillis, Gerald B. Porter, and David C. Walker. "Solvent-dependent rate constants of muonium atom reactions." Canadian Journal of Chemistry 81, no. 2 (February 1, 2003): 175–78. http://dx.doi.org/10.1139/v03-009.
Повний текст джерелаBraga, Dario, Stefano Luca Giaffreda, Fabrizia Grepioni, Michele R. Chierotti, Roberto Gobetto, Giuseppe Palladino, and Marco Polito. "Solvent effect in a “solvent free” reaction." CrystEngComm 9, no. 10 (2007): 879. http://dx.doi.org/10.1039/b711983f.
Повний текст джерелаAway, Kenneth Charles West, and 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, no. 2 (February 1, 1989): 345–49. http://dx.doi.org/10.1139/v89-056.
Повний текст джерелаMiyamoto, Hisakazu, Shotaro Kanetaka, Koichi Tanaka, Kazuhiro Yoshizawa, Shinji Toyota, and Fumio Toda. "Solvent-Free Robinson Annelation Reaction." Chemistry Letters 29, no. 8 (August 2000): 888–89. http://dx.doi.org/10.1246/cl.2000.888.
Повний текст джерелаZhou, Jinkui, and 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, no. 5-6 (May 1, 2001): 841–47. http://dx.doi.org/10.1139/v00-184.
Повний текст джерелаSaikia, Monmi, and Jadab C. Sarma. "Baylis–Hillman reaction under solvent-free conditions — Remarkable rate acceleration and yield enhancement." Canadian Journal of Chemistry 88, no. 12 (December 2010): 1271–76. http://dx.doi.org/10.1139/v10-133.
Повний текст джерелаChoudhuri, Khokan, Arkalekha Mandal, and Prasenjit Mal. "Aerial dioxygen activation vs. thiol–ene click reaction within a system." Chemical Communications 54, no. 30 (2018): 3759–62. http://dx.doi.org/10.1039/c8cc01359d.
Повний текст джерелаAnbu, Nagarjun, Jacob, Kalaiarasi, and Dhakshinamoorthy. "Acetylation of Alcohols, Amines, Phenols, Thiols under Catalyst and Solvent-Free Conditions." Chemistry 1, no. 1 (July 10, 2019): 69–79. http://dx.doi.org/10.3390/chemistry1010006.
Повний текст джерелаJicsinszky, László, and Giancarlo Cravotto. "Toward a Greener World—Cyclodextrin Derivatization by Mechanochemistry." Molecules 26, no. 17 (August 27, 2021): 5193. http://dx.doi.org/10.3390/molecules26175193.
Повний текст джерелаSingh, Girija S. "Greener Approaches to Selected Asymmetric Addition Reactions Relevant to Drug Development." Current Organic Chemistry 25, no. 13 (September 2, 2021): 1497–522. http://dx.doi.org/10.2174/1385272825666210519100457.
Повний текст джерелаRaston, Colin L., and Janet L. Scott. "Chemoselective, solvent-free aldol condensation reaction." Green Chemistry 2, no. 2 (2000): 49–52. http://dx.doi.org/10.1039/a907688c.
Повний текст джерелаCablewski, Teresa, Paul A. Gurr, Peter J. Pajalic, and Christopher R. Strauss. "A solvent-free Jacobs–Gould reaction." Green Chemistry 2, no. 1 (2000): 25–28. http://dx.doi.org/10.1039/a908606d.
Повний текст джерелаPhonchaiya, Sonthi, Bhinyo Panijpan, Shuleewan Rajviroongit, Joanne T. Blanchfield, and Tony Wright. "A Facile Solvent-Free Cannizzaro Reaction." Journal of Chemical Education 86, no. 1 (January 2009): 85. http://dx.doi.org/10.1021/ed086p85.
Повний текст джерелаDu, Rui, Liangliang Han, Zhongqiang Zhou, and Victor Borovkov. "Efficient Synthesis of Novel Quinolinone Derivatives via Catalyst-free Multicomponent Reaction." Letters in Organic Chemistry 17, no. 5 (April 28, 2020): 403–7. http://dx.doi.org/10.2174/1570178616666190828092728.
Повний текст джерелаSharghi, Hashem, and Reza Khalifeh. "Reaction on a solid surface — A simple, economical, and efficient Mannich reaction of azacrown ethers over graphite." Canadian Journal of Chemistry 86, no. 5 (May 1, 2008): 426–34. http://dx.doi.org/10.1139/v08-026.
Повний текст джерелаStolle, Achim, and Bernd Ondruschka. "Solvent-free reactions of alkynes in ball mills: It is definitely more than mixing." Pure and Applied Chemistry 83, no. 7 (April 30, 2011): 1343–49. http://dx.doi.org/10.1351/pac-con-10-09-26.
Повний текст джерелаLam, Solita, Yvonne Puplampu Dove, Adrienne Morris, Ayunna Epps, and Ghislain R. Mandouma. "Cross-Coupling Biarylation of Nitroaryl Chlorides Through High Speed Ball Milling." International Journal for Innovation Education and Research 3, no. 6 (June 30, 2015): 12–35. http://dx.doi.org/10.31686/ijier.vol3.iss6.376.
Повний текст джерелаLi, Xiao Chuan, Shan Shan Gong, and Qi Sun. "Synthesis of Phosphonate-Containing 2-Methyl-1,5-Diaminopentane Derivatives." Advanced Materials Research 1046 (October 2014): 104–7. http://dx.doi.org/10.4028/www.scientific.net/amr.1046.104.
Повний текст джерелаRaiedhah 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, and Faeza Alkorbi Faeza Alkorbi. "Supported Ruthenium Catalysts for Oxidation of Benzyl Alcohol under Solvent Free Conditions." Journal of the chemical society of pakistan 44, no. 4 (2022): 322. http://dx.doi.org/10.52568/001069/jcsp/44.04.2022.
Повний текст джерелаZare, Abdolkarim, and 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, no. 2 (January 11, 2021): 85–90. http://dx.doi.org/10.1515/znb-2020-0098.
Повний текст джерелаMoormann, Widukind, Daniel Langbehn, and Rainer Herges. "Solvent-Free Synthesis of Diazocine." Synthesis 49, no. 15 (July 11, 2017): 3471–75. http://dx.doi.org/10.1055/s-0036-1590685.
Повний текст джерелаYe, X. R., C. Daraio, C. Wang, J. B. Talbot, and S. Jin. "Room Temperature Solvent-Free Synthesis of Monodisperse Magnetite Nanocrystals." Journal of Nanoscience and Nanotechnology 6, no. 3 (March 1, 2006): 852–56. http://dx.doi.org/10.1166/jnn.2006.135.
Повний текст джерелаLoesch-Zhang, Amelia, Cynthia Cordt, Andreas Geissler, and Markus Biesalski. "A Solvent-Free Approach to Crosslinked Hydrophobic Polymeric Coatings on Paper Using Vegetable Oil." Polymers 14, no. 9 (April 27, 2022): 1773. http://dx.doi.org/10.3390/polym14091773.
Повний текст джерелаSoleiman-Beigi, Mohammad, Reza Aryan, Maryam Yousofizadeh, and 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.
Повний текст джерелаBousquet, Till, Mouhamad Jida, Mohamad Soueidan, Rebecca Deprez-Poulain, Francine Agbossou-Niedercorn, and Lydie Pelinski. "Fast and efficient solvent-free Passerini reaction." Tetrahedron Letters 53, no. 3 (January 2012): 306–8. http://dx.doi.org/10.1016/j.tetlet.2011.11.028.
Повний текст джерелаGladysz, John A. "Reaction: Toward Organic-Solvent-free Synthetic Chemistry." Chem 4, no. 9 (September 2018): 2007–8. http://dx.doi.org/10.1016/j.chempr.2018.08.026.
Повний текст джерелаNielsen, Simon Feldbæk, Dan Peters, and Oskar Axelsson. "The Suzuki Reaction Under Solvent-Free Conditions." Synthetic Communications 30, no. 19 (October 2000): 3501–9. http://dx.doi.org/10.1080/00397910008087262.
Повний текст джерелаWaddell, Daniel C., and James Mack. "An environmentally benign solvent-free Tishchenko reaction." Green Chem. 11, no. 1 (2009): 79–82. http://dx.doi.org/10.1039/b810714a.
Повний текст джерелаMotiur Rahman, A. F. M., and Adnan A. Kadi. "Solvent free Cannizzaro reaction applying grindstone technique." Arabian Journal of Chemistry 9 (November 2016): S1373—S1377. http://dx.doi.org/10.1016/j.arabjc.2012.02.010.
Повний текст джерелаMiyamoto, Hisakazu, Shotaro Kanetaka, Koichi Tanaka, Kazuhiro Yoshizawa, Shinji Toyota, and Fumio Toda. "ChemInform Abstract: Solvent-Free Robinson Anellation Reaction." ChemInform 31, no. 51 (December 19, 2000): no. http://dx.doi.org/10.1002/chin.200051046.
Повний текст джерелаGhigo, Giovanni, Matteo Bonomo, Achille Antenucci, Chiara Reviglio, and Stefano Dughera. "Copper-Free Halodediazoniation of Arenediazonium Tetrafluoroborates in Deep Eutectic Solvents-like Mixtures." Molecules 27, no. 6 (March 15, 2022): 1909. http://dx.doi.org/10.3390/molecules27061909.
Повний текст джерелаMarchenko, Roman D., and Andrei S. Potapov. "Synthesis of Bis(1,2,3-triazolyl)alkanes in Superbasic and Solvent-Free Conditions." Molbank 2023, no. 1 (January 13, 2023): M1551. http://dx.doi.org/10.3390/m1551.
Повний текст джерелаMandouma, Ghislain R., Ayunna Epps, and 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, no. 12 (December 31, 2014): 133–49. http://dx.doi.org/10.31686/ijier.vol2.iss12.293.
Повний текст джерелаMiao, Changlin, Zhongming Wang, Lingmei Yang, Huiwen Li, Pengmei Lv, Xinshu Zhuang, Zhenhong Yuan, and Wen Luo. "Lipase-Catalyzed Synthesis of Glycerol-Free Biodiesel from Rapeseed Oil and Dimethyl Carbonate." Journal of Biobased Materials and Bioenergy 14, no. 4 (August 1, 2020): 537–43. http://dx.doi.org/10.1166/jbmb.2020.1973.
Повний текст джерелаRubab, Laila, Ayesha Anum, Sami A. Al-Hussain, Ali Irfan, Sajjad Ahmad, Sami Ullah, Aamal A. Al-Mutairi, and Magdi E. A. Zaki. "Green Chemistry in Organic Synthesis: Recent Update on Green Catalytic Approaches in Synthesis of 1,2,4-Thiadiazoles." Catalysts 12, no. 11 (October 29, 2022): 1329. http://dx.doi.org/10.3390/catal12111329.
Повний текст джерелаSalmar, Siim, Jaak Järv, Tiina Tenno, and Ants Tuulmets. "Role of water in determining organic reactivity in aqueous binary solvents." Open Chemistry 10, no. 5 (October 1, 2012): 1600–1608. http://dx.doi.org/10.2478/s11532-012-0080-8.
Повний текст джерелаKidwai, Mazaahir, Shweta Rastogi, Ruby Thakur, and Shilpi Saxena. "Solvent-Free Synthesis of 2,4,6-Triaryl Pyridines." Zeitschrift für Naturforschung B 59, no. 5 (May 1, 2004): 606–8. http://dx.doi.org/10.1515/znb-2004-0522.
Повний текст джерелаChavelas-Hernández, Leticia, Luis G. Hernández-Vázquez, José D. Bahena-Martínez, Alexa B. Arroyo-Colín, Sinuhe G. Flores-Osorio, Gabriel Navarrete-Vázquez, and 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, no. 1 (December 22, 2023): 34. http://dx.doi.org/10.3390/pr12010034.
Повний текст джерелаSapaev, B., F. E. Saitkulov, A. A. Tashniyazov, and 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.
Повний текст джерелаOlyaei, Abolfazl, Mohsen Vaziri, Reza Razeghi, Shams Bahareh, and 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, no. 4 (2013): 463–68. http://dx.doi.org/10.2298/jsc120506076o.
Повний текст джерелаTahmasbi, Marzieh, Nadiya Koukabi, and Ozra Armandpour. "Sono and nano: A perfect synergy for eco-compatible Biginelli reaction." Heterocyclic Communications 28, no. 1 (January 1, 2022): 1–10. http://dx.doi.org/10.1515/hc-2022-0003.
Повний текст джерелаCai, 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 (August 2009): 1355–58. http://dx.doi.org/10.4028/www.scientific.net/amr.79-82.1355.
Повний текст джерелаKrištofíková, Dominika, Juraj Filo, Mária Mečiarová, and Radovan Šebesta. "Why do thioureas and squaramides slow down the Ireland–Claisen rearrangement?" Beilstein Journal of Organic Chemistry 15 (December 10, 2019): 2948–57. http://dx.doi.org/10.3762/bjoc.15.290.
Повний текст джерелаMa, Xiaofang, Shunxi Li, Samrat Devaramani, Guohu Zhao, and 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, no. 6 (May 20, 2020): 438–42. http://dx.doi.org/10.2174/1570178616666190926104037.
Повний текст джерелаCui, Dong-Xiao, Yue-Dan Li, Jun-Chao Zhu, Yan-Yan Jia, Ai-Dong Wen, and Ping-An Wang. "Highly Efficient Michael Reactions of Nitroolefins by Grinding Means." Current Organic Synthesis 16, no. 3 (June 17, 2019): 449–57. http://dx.doi.org/10.2174/1570179416666190101122150.
Повний текст джерелаChen, Longrui, Betsegaw E. Lemma, Jenna S. Rich, and James Mack. "Freedom: a copper-free, oxidant-free and solvent-free palladium catalysed homocoupling reaction." Green Chem. 16, no. 3 (2014): 1101–3. http://dx.doi.org/10.1039/c3gc41847b.
Повний текст джерелаCrole, David A., Simon J. Freakley, Jennifer K. Edwards, and 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, no. 2190 (June 2016): 20160156. http://dx.doi.org/10.1098/rspa.2016.0156.
Повний текст джерелаBora, Pranjal P., H. Atoholi Sema, Barisha Wahlang, and Ghanashyam Bez. "Rapid synthesis of homoallylic alcohol from aldehyde with allyltributylstannane under solvent-free conditions." Canadian Journal of Chemistry 90, no. 2 (February 2012): 167–72. http://dx.doi.org/10.1139/v11-138.
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