Статті в журналах з теми "Green chemical reaction"
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Nagieva, I. T., N. I. Ali-zadeh, and T. M. Nagiev. "GAS-PHASE OXIDATION OF 2-PICOLINE BY “GREEN OXIDIZERS” H2O2 AND N2O." Azerbaijan Chemical Journal, no. 4 (November 14, 2023): 13–20. http://dx.doi.org/10.32737/0005-2531-2023-4-13-20.
Повний текст джерелаSahoo, Tejaswini, Jagannath Panda, Jnanaranjan Sahu, Dayananda Sarangi, Sunil K. Sahoo, Braja B. Nanda, and Rojalin Sahu. "Green Solvent: Green Shadow on Chemical Synthesis." Current Organic Synthesis 17, no. 6 (September 25, 2020): 426–39. http://dx.doi.org/10.2174/1570179417666200506102535.
Повний текст джерелаIgarashi, Akira. "Catalytic Reaction Engineering toward Green Chemical Processes." JOURNAL OF CHEMICAL ENGINEERING OF JAPAN 38, no. 10 (2005): 779–84. http://dx.doi.org/10.1252/jcej.38.779.
Повний текст джерелаDe Martino, M. Teresa, Loai K. E. A. Abdelmohsen, Floris P. J. T. Rutjes, and Jan C. M. van Hest. "Nanoreactors for green catalysis." Beilstein Journal of Organic Chemistry 14 (March 29, 2018): 716–33. http://dx.doi.org/10.3762/bjoc.14.61.
Повний текст джерелаPrajapati, Pintu, Avani Sheth, Dhaval M. Patel, Advaita Patel, and Priti Mehta. "Sonochemistry: Non-Classical Way of Synthesis." Journal of Drug Delivery and Therapeutics 9, no. 6-s (December 15, 2019): 229–32. http://dx.doi.org/10.22270/jddt.v9i6-s.3691.
Повний текст джерелаDay, Daniel M., Thomas J. Farmer, Joe Granelli, Janice H. Lofthouse, Julie Lynch, Con R. McElroy, James Sherwood, Seishi Shimizu, and James H. Clark. "Reaction Optimization for Greener Chemistry with a Comprehensive Spreadsheet Tool." Molecules 27, no. 23 (December 2, 2022): 8427. http://dx.doi.org/10.3390/molecules27238427.
Повний текст джерелаLi, Yanlin, Shenghua Chen, Wenyuan Duan, Yanli Nan, Donghai Ding, and Guoqing Xiao. "Research progress of vanadium pentoxide photocatalytic materials." RSC Advances 13, no. 33 (2023): 22945–57. http://dx.doi.org/10.1039/d3ra03648k.
Повний текст джерелаDaglia, M., A. Papetti, and G. Gazzani. "Green and roasted coffee antiradical activity stability in chemical systems." Czech Journal of Food Sciences 22, SI - Chem. Reactions in Foods V (January 1, 2004): S191—S194. http://dx.doi.org/10.17221/10658-cjfs.
Повний текст джерелаDomènech, Xavier, José A. Ayllón, José Peral, and Joan Rieradevall. "How Green Is a Chemical Reaction? Application of LCA to Green Chemistry." Environmental Science & Technology 36, no. 24 (December 2002): 5517–20. http://dx.doi.org/10.1021/es020001m.
Повний текст джерелаCunningham, Michael F. "Green Macromolecular Reaction Engineering." Macromolecular Reaction Engineering 16, no. 3 (June 2022): 2200033. http://dx.doi.org/10.1002/mren.202200033.
Повний текст джерелаSuthar, Madhuri J., Jasmin H. Kumbhani, Keyur D. Bhatt, Prakashbhai V. Bishnoi, and Parimal Chatrabhuji. "Ultrasound-Assisted Synthesis and Characterization of 5-Carbonitrile-Functionalized tetrahydropyrimidine Derivatives with Evaluation of Their Antimicrobial Activity." Oriental Journal Of Chemistry 40, no. 1 (February 24, 2024): 281–87. http://dx.doi.org/10.13005/ojc/400134.
Повний текст джерелаRusling, James F. "Green synthesis via electrolysis in microemulsions." Pure and Applied Chemistry 73, no. 12 (January 1, 2001): 1895–905. http://dx.doi.org/10.1351/pac200173121895.
Повний текст джерелаFeng, Tao, and Hao Li. "Functional Catalyst Molecular Sieves in Green Chemical Applications." Energy Science & Policy 1, no. 2 (December 30, 2023): 1–10. http://dx.doi.org/10.61187/esp.v1i2.51.
Повний текст джерелаHeydari, 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 джерелаDr. D. Valli Sowbhagyam. "Ionic Liquids as Green Solvents: A Comprehensive Review." International Research Journal on Advanced Engineering Hub (IRJAEH) 2, no. 02 (February 29, 2024): 220–24. http://dx.doi.org/10.47392/irjaeh.2024.0035.
Повний текст джерелаLapkin, Alexei A. "Editorial overview- Reaction engineering and Catalysis: Green chemical engineering." Current Opinion in Chemical Engineering 26 (December 2019): A3. http://dx.doi.org/10.1016/j.coche.2019.12.002.
Повний текст джерелаDevi, Barla Karuna, Swathi Naraparaju, Chaganti Soujanya, and Sayan Dutta Gupta. "Green Chemistry and Green Solvents: An Overview." Current Green Chemistry 7, no. 3 (December 2, 2020): 314–25. http://dx.doi.org/10.2174/2213346107999200709132815.
Повний текст джерелаSeyyedi, Behnam, Mohammad Edrisi, Maryam Seyyedi, and Gholamreza Mahdavinia. "A new single step synthesis of copper phthalocyanine green using microwave irradiation effects in functionalisation of C−H bonds in aromatic rings." Pigment & Resin Technology 43, no. 3 (April 29, 2014): 113–17. http://dx.doi.org/10.1108/prt-04-2013-0029.
Повний текст джерелаFirdaus, Maulidan, Nisrina Rahma Firdausi, Desy Nila Rahmana, and Triana Kusumaningsih. "Green Metrics Evaluation on The Cannizzaro Reaction of p-Anisaldehyde and Benzaldehyde Under Solvent-Free Conditions." Jurnal Kimia Valensi 9, no. 2 (December 28, 2023): 288–99. http://dx.doi.org/10.15408/jkv.v9i2.35641.
Повний текст джерелаTang, Christina, and Bridget T. McInnes. "Cascade Processes with Micellar Reaction Media: Recent Advances and Future Directions." Molecules 27, no. 17 (August 31, 2022): 5611. http://dx.doi.org/10.3390/molecules27175611.
Повний текст джерелаAranda, Carmen, and Gonzalo de Gonzalo. "Biocatalyzed Redox Processes Employing Green Reaction Media." Molecules 25, no. 13 (July 1, 2020): 3016. http://dx.doi.org/10.3390/molecules25133016.
Повний текст джерелаFabris, Fabrizio, Markus Illner, Jens-Uwe Repke, Alessandro Scarso, and Michael Schwarze. "Is Micellar Catalysis Green Chemistry?" Molecules 28, no. 12 (June 16, 2023): 4809. http://dx.doi.org/10.3390/molecules28124809.
Повний текст джерелаHamzavi, Seyedeh Fazileh Fazileh, Shahla Jamili, Morteza Yousefzadi, Ali Mashinchian Moradi, and Narges Amrollahi Biuki. "Silver Nanoparticles Supported on Chitosan as a Green and Robust Heterogeneous Catalyst for Direct Synthesis of Nitrogen Heterocyclic Compounds under Green Conditions." Bulletin of Chemical Reaction Engineering & Catalysis 14, no. 1 (April 15, 2019): 51. http://dx.doi.org/10.9767/bcrec.14.1.2105.51-59.
Повний текст джерелаIlia, Gheorghe, Vasile Simulescu, Nicoleta Plesu, Vlad Chiriac, and Petru Merghes. "Wittig and Wittig–Horner Reactions under Sonication Conditions." Molecules 28, no. 4 (February 18, 2023): 1958. http://dx.doi.org/10.3390/molecules28041958.
Повний текст джерелаĀbele, E., R. Ābele, Ļ. Golomba, K. Rubina, J. Višņevska та T. Beresņeva. ""Green Chemical" Methods for the Regioselective Synthesis of 1-Hetarylsulfanyl-ω-Cyanoalkanes". Latvian Journal of Chemistry 49, № 1-4 (1 січня 2010): 278–82. http://dx.doi.org/10.2478/v10161-010-0006-8.
Повний текст джерелаLi, Huan, Feng Qin, Lijuan Huang, Wenjing Jia, Mingliang Zhang, Xin Li, and Zhengyu Shu. "Enzymatic synthesis of 2-phenethyl acetate in water catalyzed by an immobilized acyltransferase from Mycobacterium smegmatis." RSC Advances 12, no. 4 (2022): 2310–18. http://dx.doi.org/10.1039/d1ra07946h.
Повний текст джерелаKidwai, M. "Dry media reactions." Pure and Applied Chemistry 73, no. 1 (January 1, 2001): 147–51. http://dx.doi.org/10.1351/pac200173010147.
Повний текст джерелаHájek, Martin, Aleš Vávra, Héctor de Paz Carmona, and Jaroslav Kocík. "The Catalysed Transformation of Vegetable Oils or Animal Fats to Biofuels and Bio-Lubricants: A Review." Catalysts 11, no. 9 (September 17, 2021): 1118. http://dx.doi.org/10.3390/catal11091118.
Повний текст джерелаMohammed, Tasneem, Aayesha Nasreen, Yahya S. Alqahtani, Ibrahim Ahmed Shaikh, Shakeel Iqubal, Shaik Honey Fathima, and Aejaz A. Khan. "Green Synthesis of Therapeutically Active Heterocyclic Scaffolds: A Review." Science of Advanced Materials 15, no. 6 (June 1, 2023): 725–47. http://dx.doi.org/10.1166/sam.2023.4477.
Повний текст джерелаSaha, Pritam, and Koushik Mukherjee. "Zinc catalyzed, microwave irradiated Sonogashira reaction by Sodium Aluminate (NaAlO2) as a base in water: A Green entente." E3S Web of Conferences 405 (2023): 01008. http://dx.doi.org/10.1051/e3sconf/202340501008.
Повний текст джерелаAjvazi, Njomza, and Stojan Stavber. "Direct Cross-Coupling of Alcohols with O-Nucleophiles Mediated by N-Iodosuccinimide as a Precatalyst under Mild Reaction Conditions." Catalysts 11, no. 7 (July 17, 2021): 858. http://dx.doi.org/10.3390/catal11070858.
Повний текст джерелаYadav, J. S., and H. M. Meshram. "Green twist to an old theme. An eco-friendly approach." Pure and Applied Chemistry 73, no. 1 (January 1, 2001): 199–203. http://dx.doi.org/10.1351/pac200173010199.
Повний текст джерелаZou, Ruonan, Jingbo Yu, and Ping Ying. "Electrochemical Construction of C–S Bond: A Green Approach for Preparing Sulfur-Containing Scaffolds." Pharmaceutical Fronts 06, no. 01 (March 2024): e9-e19. http://dx.doi.org/10.1055/s-0044-1780505.
Повний текст джерелаKeglevich, György, Nóra Zsuzsa Kiss, Zoltán Mucsi, Erzsébet Jablonkai, and Erika Bálint. "The synthesis of phosphinates: traditional versus green chemical approaches." Green Processing and Synthesis 3, no. 2 (April 1, 2014): 103–10. http://dx.doi.org/10.1515/gps-2013-0106.
Повний текст джерелаHou, Qian, Zhao Zhang, Ting Ting Yang, and Yan Zhang. "Green Preparation of an Environment-Responsive Polymer." Advanced Materials Research 750-752 (August 2013): 1235–38. http://dx.doi.org/10.4028/www.scientific.net/amr.750-752.1235.
Повний текст джерелаDujjanutat, Praepilas, Arthit Neramittagapong, and Pakawadee Kaewkannetra. "H2-Assisted Chemical Reaction for Green-Kerosene Production." Defect and Diffusion Forum 364 (June 2015): 104–11. http://dx.doi.org/10.4028/www.scientific.net/ddf.364.104.
Повний текст джерелаPawełczyk, Anna, Katarzyna Sowa-Kasprzak, Dorota Olender, and Lucjusz Zaprutko. "Microwave (MW), Ultrasound (US) and Combined Synergic MW-US Strategies for Rapid Functionalization of Pharmaceutical Use Phenols." Molecules 23, no. 9 (September 15, 2018): 2360. http://dx.doi.org/10.3390/molecules23092360.
Повний текст джерелаRajendran, A. "Silica Sulphuric Acid Catalyzed Fischer Esterification Reaction under Solventless Condition: A Novel Green Chemical Reaction." American Chemical Science Journal 1, no. 1 (January 10, 2011): 28–36. http://dx.doi.org/10.9734/acsj/2011/264.
Повний текст джерелаDugar, Arpita, Anil Kumar, Rameshwar Ameta, and Suresh C. Ameta. "A green chemical approach for nitration of aromatic compounds." Macedonian Journal of Chemistry and Chemical Engineering 28, no. 2 (December 15, 2009): 163. http://dx.doi.org/10.20450/mjcce.2009.206.
Повний текст джерелаMondal, Dipayan, Pankaj Lal Kalar, Shivam Kori, Shovanlal Gayen, and Kalpataru Das. "Recent Developments on Synthesis of Indole Derivatives Through Green Approaches and Their Pharmaceutical Applications." Current Organic Chemistry 24, no. 22 (December 18, 2020): 2665–93. http://dx.doi.org/10.2174/1385272824999201111203812.
Повний текст джерелаLee, Seng Hua, Paridah Md Tahir, Wei Chen Lum, Li Peng Tan, Paiman Bawon, Byung-Dae Park, Syeed SaifulAzry Osman Al Edrus, and Ummi Hani Abdullah. "A Review on Citric Acid as Green Modifying Agent and Binder for Wood." Polymers 12, no. 8 (July 29, 2020): 1692. http://dx.doi.org/10.3390/polym12081692.
Повний текст джерелаFantucci, Hugo, Jaspreet S. Sidhu, and Rafael M. Santos. "Mineral Carbonation as an Educational Investigation of Green Chemical Engineering Design." Sustainability 11, no. 15 (August 1, 2019): 4156. http://dx.doi.org/10.3390/su11154156.
Повний текст джерелаEarle, Martyn J., Natalia V. Plechkova, and Kenneth R. Seddon. "Green synthesis of biodiesel using ionic liquids." Pure and Applied Chemistry 81, no. 11 (October 31, 2009): 2045–57. http://dx.doi.org/10.1351/pac-con-08-11-07.
Повний текст джерелаSharma, Sachin, Gaurav Joshi, Sourav Kalra, Sandeep Singh, and Raj Kumar. "Synthetic Versus Enzymatic Pictet-Spengler Reaction: An Overview." Current Organic Synthesis 15, no. 7 (October 16, 2018): 924–39. http://dx.doi.org/10.2174/1570179415666180613084014.
Повний текст джерелаChavan, Prashant, Suhas Pednekar, Ramesh Chaughule, and Anushree Lokur. "Microwave-assisted Efficient One-pot Synthesis of Nitriles Using Recyclable Magnetite (Fe3O4) Nanoparticles as Catalyst and Water as Solvent: A Greener Approach." Nanoscience & Nanotechnology-Asia 10, no. 4 (August 26, 2020): 507–17. http://dx.doi.org/10.2174/2210681209666190218144322.
Повний текст джерелаJameel, Mahmood S., Azlan Abdul Aziz, and Mohammed Ali Dheyab. "Green synthesis: Proposed mechanism and factors influencing the synthesis of platinum nanoparticles." Green Processing and Synthesis 9, no. 1 (July 28, 2020): 386–98. http://dx.doi.org/10.1515/gps-2020-0041.
Повний текст джерелаSaha, Moumita, and Asish R. Das. "Nanocrystalline ZnO: A Competent and Reusable Catalyst for the Preparation of Pharmacology Relevant Heterocycles in the Aqueous Medium." Current Green Chemistry 7, no. 1 (May 15, 2020): 53–104. http://dx.doi.org/10.2174/2213346107666200218122718.
Повний текст джерелаTagawa, Tomohiko. "Reaction Engineering of Microchannel Catalytic Reactors for Green Process." Applied Mechanics and Materials 625 (September 2014): 285–88. http://dx.doi.org/10.4028/www.scientific.net/amm.625.285.
Повний текст джерелаNagieva, I. T., N. I. Ali-zadeh, and T. М. Nagiev. "COHERENT SYNCHRONIZATION OF PYRIDINE DIMERIZATION REACTIONS AND DECOMPOSITION OF “GREEN OXIDANTS” – H2O2 AND N2O." Azerbaijan Chemical Journal, no. 4 (December 8, 2021): 6–11. http://dx.doi.org/10.32737/0005-2531-2021-4-6-11.
Повний текст джерелаXIA, XINXING, MINGZHU DU, and XIUJUAN GENG. "Removal of silicon from green liquor with carbon dioxide in the chemical recovery process of wheat straw soda pulping." March 2013 12, no. 3 (April 1, 2013): 35–40. http://dx.doi.org/10.32964/tj12.3.35.
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