Добірка наукової літератури з теми "Solvent free reaction"
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Статті в журналах з теми "Solvent free reaction"
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 джерелаДисертації з теми "Solvent free reaction"
Chen, Longrui. "Development of Solvent-free Catalyzed Organic Reaction under Mechanochemical Conditions." University of Cincinnati / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1470044218.
Повний текст джерелаMossaraf, Hossain. "Solvent free synthesis of some heterocycles and their applications." Thesis, University of North Bengal, 2017. http://ir.nbu.ac.in/handle/123456789/2621.
Повний текст джерелаGrätz, Sven, Doreen Beyer, Valeriya Tkachova, Sarah Hellmann, Reinhard Berger, Xinliang Feng, and Lars Borchardt. "The mechanochemical Scholl reaction – a solvent-free and versatile graphitization tool." Royal Society of Chemistry, 2018. https://tud.qucosa.de/id/qucosa%3A70655.
Повний текст джерелаAono, Shinji. "Theoretical Study of Electrostatic Solvent Effects within Free Energy Expression and Application to Solvated Reaction." 京都大学 (Kyoto University), 2010. http://hdl.handle.net/2433/126827.
Повний текст джерелаBotti, Luca. "Mechanochemical solvent-free synthesis of Sn-β Zeolite and Ag2O/TiO2 catalysts". Master's thesis, Alma Mater Studiorum - Università di Bologna, 2016. http://amslaurea.unibo.it/11941/.
Повний текст джерелаLiu, Pengyuan. "Development of Ambient Mass Spectrometry for Protein/Peptide Characterization, Solvent-Free Analysis, and Electrochemical Reaction Monitoring." Ohio University / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1419335862.
Повний текст джерелаMachover, Sarah B. "Understanding the Solvent-free Nucleophilic Substitution Reaction Performed in the High Speed Ball Mill (HSBM): Reactions of Secondary Alkyl Halides and Alkali Metal-Halogen Salts." University of Cincinnati / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1307043848.
Повний текст джерелаStrompen, Simon [Verfasser], and Andreas [Akademischer Betreuer] Liese. "Process development of a solvent-free, chemoenzymatic reaction sequence for the enantioselective synthesis of beta-amino acid esters / Simon Strompen. Betreuer: Andreas Liese." Hamburg-Harburg : Universitätsbibliothek der Technischen Universität Hamburg-Harburg, 2012. http://d-nb.info/1048542920/34.
Повний текст джерелаMukherjee, P. "Solvent-free, triphase catalytic oxidation reactions over TS-1/H2O2 system." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2000. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2277.
Повний текст джерелаHopgood, Heather M. "Substitution Reactions in the High Speed Ball Mill." University of Cincinnati / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1479816113315302.
Повний текст джерелаКниги з теми "Solvent free reaction"
Zaikov, G. E. Influence of the solvents on some radical reactions. Edited by Zaikov Gennadiĭ Efremovich. Hauppauge, N.Y: Nova Science Publishers, 2009.
Знайти повний текст джерелаAtkins, Peter. Reactions. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199695126.001.0001.
Повний текст джерелаHumpston, Giles, and David M. Jacobson. Principles of Soldering. ASM International, 2004. http://dx.doi.org/10.31399/asm.tb.ps.9781627083522.
Повний текст джерелаЧастини книг з теми "Solvent free reaction"
Loupy, André. "Solvent-free Reactions." In Modern Solvents in Organic Synthesis, 153–207. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/3-540-48664-x_7.
Повний текст джерелаMohammadi Ziarani, Ghodsi, Fatemeh Mohajer, and Razieh Moradi. "Green Reactions Under Solvent-Free Conditions." In Green Organic Reactions, 63–83. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6897-2_5.
Повний текст джерелаManning, S. C., and R. B. Moore. "Solvent-Free Functionalization of Polypropylene by Reactive Extrusion with Acidic Peroxides." In Solvent-Free Polymerizations and Processes, 248–66. Washington, DC: American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-1998-0713.ch016.
Повний текст джерелаPithawalla, Y. B., and M. Samy El-Shall. "Gas Phase and Cluster Studies of the Early Stages of Cationic Polymerization and the Reactions with Metal Cations." In Solvent-Free Polymerizations and Processes, 232–45. Washington, DC: American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-1998-0713.ch015.
Повний текст джерелаTanko, James M., and N. Kamrudin Suleman. "Solvent Effects in the Reactions of Neutral Free Radicals." In Energetics of Organic Free Radicals, 224–93. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0099-8_8.
Повний текст джерелаGrampp, G., B. Herold, C. Shohoji, and S. Steenken. "The Role of Solvent Dynamics in Inter- and Intramolecular Electron Exchange Reactions." In Organic Free Radicals, 71–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73963-7_36.
Повний текст джерелаJanssen, Leon P. B. M. "Reactive Extrusion for Solvent-Free Processing: Facts and Fantasies." In Integrated Chemical Processes, 391–406. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527605738.ch13.
Повний текст джерелаBraga, Dario, Daniela D'Addario, Lucia Maini, Marco Polito, Stefano Giaffreda, Katia Rubini, and Fabrizia Grepioni. "Applications of Crystal Engineering Strategies in Solvent-free Reactions: Toward a Supramolecular Green Chemistry." In Frontiers in Crystal Engineering, 1–23. Chichester, UK: John Wiley & Sons, Ltd, 2006. http://dx.doi.org/10.1002/0470022612.ch1.
Повний текст джерелаOu, Wenlan, Zhengyu Gong, Qiwen Pan, Ling Zhang, Jianing Dai, and Zhixing Gu. "Verification of Solver for Coupled Simulation of Fluid and Fuel Pin in LFR Based on Openfoam." In Springer Proceedings in Physics, 909–18. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-1023-6_77.
Повний текст джерелаPanunzio, Mauro, Maria Antonietta Lentini, Eileen Campana, Giorgio Martelli, and Paola Vicennati. "Multistep Microwave-Assisted Solvent-Free Organic Reactions: Synthesis of 1,6-Disubstituted-4-Oxo-1,4-Dihydro-Pyridine-3-Carboxylic Acid Benzyl Esters." In Advances in Microwave and Radio Frequency Processing, 386–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/978-3-540-32944-2_41.
Повний текст джерелаТези доповідей конференцій з теми "Solvent free reaction"
Walters, E. A., and J. R. Grover. "Photoionization and Photofragmentation Studies of Van Der Waals Complexes Using VUV Radiation." In Free-Electron Laser Applications in the Ultraviolet. Washington, D.C.: Optica Publishing Group, 1988. http://dx.doi.org/10.1364/fel.1988.sb3.
Повний текст джерелаQiu, Jim. "Physical nitriding reaction of organic metal with solvent-free gallium nitride (GaN)." In Gallium Nitride Materials and Devices XVIII, edited by Hadis Morkoç, Hiroshi Fujioka, and Ulrich T. Schwarz. SPIE, 2023. http://dx.doi.org/10.1117/12.2668731.
Повний текст джерелаScott, T. W., and S. N. Liu. "Picosecond cage recombination measurements of polyatomic free radical pairs." In International Laser Science Conference. Washington, D.C.: Optica Publishing Group, 1986. http://dx.doi.org/10.1364/ils.1986.thl51.
Повний текст джерелаBadajoz, Mercedes, Alicia Chopa, and María Lockhart. "Synthesis of Benzyl Ketones through Indium-Mediated Solvent-Free Reaction of Acid Chlorides with Benzyltins under Ultrasound Irradiation." In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a029.
Повний текст джерелаChatterjee, Rana, Satyajit Samanta, Sougata Santra, and Adinath Majee. "An efficient method for the synthesis of dihydropyrimidines using Brønsted acidic ionic liquid: A solvent and heating free reaction." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018527.
Повний текст джерелаGumbyte, M., R. Kreivaitis та T. Balezentis. "Enzymatic Synthesis of α-Propylene glycol with (9Z)-Octadecenoic Acid by Lipolytic Enzyme". У BALTTRIB 2015. Aleksandras Stulginskis University, 2015. http://dx.doi.org/10.15544/balttrib.2015.08.
Повний текст джерелаKumar, Dinesh. "Modified Algar–Flynn–Oyamada Reaction for the Synthesis of 3-Hydroxy-2-styryl-chromen-4-ones under Solvent-Free Conditions." In International Electronic Conference on Synthetic Organic Chemistry. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13558.
Повний текст джерелаPons, B. Stanley. "Infrared Spectral Electrochemistry of Surface Reactions." In Microphysics of Surfaces, Beams, and Adsorbates. Washington, D.C.: Optica Publishing Group, 1985. http://dx.doi.org/10.1364/msba.1985.tua2.
Повний текст джерелаSANTOS, Maricel del Valle, Alexis Rafael VELEZ, and Ivana Maria MAGARIO. "EFFECT OF MOLAR WEIGHT OF CARBOXYLIC ACIDS ON THE ENZYMATIC ESTERIFICATION OF GLYCEROL." In SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 2021 INTERNATIONAL VIRTUAL CONFERENCE. DR. D. SCIENTIFIC CONSULTING, 2022. http://dx.doi.org/10.48141/sbjchem.21scon.13_abstract_santos.pdf.
Повний текст джерелаMovassagh, Barahman, Akbar Mobaraki, and Babak Karimi. "A novel water-tolerant organosulfonic acid-functionalized silica-coated magnetic nanoparticles as a hydrophobic, recyclable and magnetically separable catalyst for the solvent-free Biginelli reaction." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a009.
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