Статті в журналах з теми "Esterification Reactivity"
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Zhan, Shaoqi, Xiaochun Tao, Liangzhen Cai, Xiaohui Liu, and Taoping Liu. "The carbon material functionalized with NH2+ and SO3H groups catalyzed esterification with high activity and selectivity." Green Chem. 16, no. 11 (2014): 4649–53. http://dx.doi.org/10.1039/c4gc01395f.
Повний текст джерелаMei, Sheng-Fu, Jin Liu, Zhen Li, Yan Chen, and Jing Zhang. "Reactivity of 2-Phosphonobutane-1,2,4-tricarboxylic Acid Esterification." Asian Journal of Chemistry 26, no. 5 (2014): 1530–32. http://dx.doi.org/10.14233/ajchem.2014.17279.
Повний текст джерелаLi, Chong, Yueping Jiang, Baoshan Huang, Menghang Zhang, Yanhong Feng, and Zhitao Yang. "Preparation and Properties of Jute Fiber Long-Chain Fatty Acid Esters in Supercritical Carbon Dioxide." Materials 12, no. 9 (May 8, 2019): 1499. http://dx.doi.org/10.3390/ma12091499.
Повний текст джерелаRoswanda, Robby, Ilham Ardatul Putra, Maria Mardiastuti, and Didin Mujahidin. "Catalyst Free Hydroxyl Protection of Quinine via Esterification." Key Engineering Materials 811 (July 2019): 3–7. http://dx.doi.org/10.4028/www.scientific.net/kem.811.3.
Повний текст джерелаKastratović, Vlatko, Milica Radulović, and Kristina Kastratović. "Esterification of propanoic acid in the presence of a homogeneous catalyst." Kragujevac Journal of Science, no. 44 (2022): 45–55. http://dx.doi.org/10.5937/kgjsci2244045k.
Повний текст джерелаVázquez, Ester, and Maurizio Prato. "Functionalization of carbon nanotubes for applications in materials science and nanomedicine." Pure and Applied Chemistry 82, no. 4 (March 13, 2010): 853–61. http://dx.doi.org/10.1351/pac-con-09-10-40.
Повний текст джерелаWu, Yan, Shiang He, Dongmei Li, Yang Li, and Hao Wang. "Esterification of naphthenic acids with various structures over tungstophosphoric acid-intercalated layer double hydroxide catalysts with various interlayer spacings." Clay Minerals 56, no. 3 (September 2021): 250–59. http://dx.doi.org/10.1180/clm.2022.3.
Повний текст джерелаKastratovic, Vlatko, and Miljan Bigovic. "Esterification of stearic acid with lower monohydroxylic alcohols." Chemical Industry and Chemical Engineering Quarterly 24, no. 3 (2018): 283–91. http://dx.doi.org/10.2298/ciceq170327040k.
Повний текст джерелаBreitenlechner, Stefan, and Thorsten Bach. "Kinetic Study on the Esterification of Hexanoic Acid with N,N-Dialkylamino Alcohols: Evidence for an Activation by Hydrogen Bonding." Zeitschrift für Naturforschung B 61, no. 5 (May 1, 2006): 583–88. http://dx.doi.org/10.1515/znb-2006-0513.
Повний текст джерелаRabee, Abdallah, Gamal Mekhemer, Amin Osatiashtiani, Mark Isaacs, Adam Lee, Karen Wilson, and Mohamed Zaki. "Acidity-Reactivity Relationships in Catalytic Esterification over Ammonium Sulfate-Derived Sulfated Zirconia." Catalysts 7, no. 7 (July 5, 2017): 204. http://dx.doi.org/10.3390/catal7070204.
Повний текст джерелаNishio, Yuya, Akari Kawazu, Shun Hirano, and Hiroshi Matsubara. "Preparation of fluorous Yamaguchi reagents and evaluation of their reactivity in esterification." Tetrahedron 72, no. 5 (February 2016): 720–25. http://dx.doi.org/10.1016/j.tet.2015.12.026.
Повний текст джерелаErshov, B. G., V. B. Komarov, S. A. Kulyukhin, A. E. Seliverstov та V. N. Bondareva. "Study of the effect of γ-irradiation of industrial grade cellulose on the products of its esterification". Industrial laboratory. Diagnostics of materials 88, № 12 (25 грудня 2022): 28–35. http://dx.doi.org/10.26896/1028-6861-2022-88-12-28-35.
Повний текст джерелаCheng, Yu He, Biao Zhang, Shang Jiang Dai, Han Lin Tong, and Li Xia Li. "Reusable and Efficient Polystryrene-Supported Acidic Ionic Liquid Catalyst for the Synthesis of n-Butyl Acetate." Advanced Materials Research 983 (June 2014): 20–25. http://dx.doi.org/10.4028/www.scientific.net/amr.983.20.
Повний текст джерелаChen, Yaoyao, Chengliang Li, Yongmei Cui, Mingming Sun, Xueshun Jia та Jian Li. "Bu4NI-Catalyzed C–C Bond Cleavage and Oxidative Esterification of Allyl Alcohols with Toluene Derivatives". Synthesis 51, № 19 (16 липня 2019): 3667–74. http://dx.doi.org/10.1055/s-0039-1690105.
Повний текст джерелаHughes, David L., and Robert A. Reamer. "The Effect of Acid Strength on the Mitsunobu Esterification Reaction: Carboxyl vs Hydroxyl Reactivity." Journal of Organic Chemistry 61, no. 9 (January 1996): 2967–71. http://dx.doi.org/10.1021/jo952180e.
Повний текст джерелаKubyshkin, Vladimir, and Nediljko Budisa. "Hydrolysis, polarity, and conformational impact of C-terminal partially fluorinated ethyl esters in peptide models." Beilstein Journal of Organic Chemistry 13 (November 16, 2017): 2442–57. http://dx.doi.org/10.3762/bjoc.13.241.
Повний текст джерелаAdjaoud, Antoine, Reiner Dieden, and Pierre Verge. "Sustainable Esterification of a Soda Lignin with Phloretic Acid." Polymers 13, no. 4 (February 21, 2021): 637. http://dx.doi.org/10.3390/polym13040637.
Повний текст джерелаEcheverri, Marcelo, Amparo Alvarez-Valdés, Francisco Navas, Josefina Perles, Isabel Sánchez-Pérez, and A. G. Quiroga. "Using phosphine ligands with a biological role to modulate reactivity in novel platinum complexes." Royal Society Open Science 5, no. 2 (February 2018): 171340. http://dx.doi.org/10.1098/rsos.171340.
Повний текст джерелаHuang, Chien-Chang, Shih-Han Ho, Jo-Shu Chang, and Pei-Jyuan Gao. "A sulfated/chlorinated Sr–Fe composite oxide as a novel solid and reusable superacid catalyst for oleic acid esterification." New Journal of Chemistry 44, no. 32 (2020): 13669–84. http://dx.doi.org/10.1039/d0nj00525h.
Повний текст джерелаSamateh, Malick, Siddharth Marwaha, Jose K. James, Vikas Nanda, and George John. "Sucralose hydrogels: Peering into the reactivity of sucralose versus sucrose under lipase catalyzed trans-esterification." Carbohydrate Research 521 (November 2022): 108647. http://dx.doi.org/10.1016/j.carres.2022.108647.
Повний текст джерелаMontenegro Hernández, Alejandra, and Jorge Enrique Rodríguez Páez. "Synthesising highly reactive tin oxide using Tin(II)2- ethylhexanoate polynucleation as precursor." Ingeniería e Investigación 29, no. 1 (January 1, 2009): 47–52. http://dx.doi.org/10.15446/ing.investig.v29n1.15142.
Повний текст джерелаDong, Ben, Jiasheng Qian, Mingjie Li, Zheng-Jun Wang, Minyan Wang, Dingyi Wang, Chengkai Yuan, Ying Han, Yue Zhao, and Zhuangzhi Shi. "External oxidant-compatible phosphorus(III)-directed site-selective C–H carbonylation." Science Advances 6, no. 51 (December 2020): eabd1378. http://dx.doi.org/10.1126/sciadv.abd1378.
Повний текст джерелаHeller, Stephen T., and Richmond Sarpong. "On the reactivity of imidazole carbamates and ureas and their use as esterification and amidation reagents." Tetrahedron 67, no. 46 (November 2011): 8851–59. http://dx.doi.org/10.1016/j.tet.2011.09.057.
Повний текст джерелаYujaroen, Duangkamol, Motonobu Goto, Mitsuru Sasaki, and Artiwan Shotipruk. "Esterification of palm fatty acid distillate (PFAD) in supercritical methanol: Effect of hydrolysis on reaction reactivity." Fuel 88, no. 10 (October 2009): 2011–16. http://dx.doi.org/10.1016/j.fuel.2009.02.040.
Повний текст джерелаGhesti, Grace Ferreira, Julio Lemos de Macedo, Vicente Cavalcanti Ibiapina Parente, José Alves Dias, and Sílvia Cláudia Loureiro Dias. "Synthesis, characterization and reactivity of Lewis acid/surfactant cerium trisdodecylsulfate catalyst for transesterification and esterification reactions." Applied Catalysis A: General 355, no. 1-2 (February 2009): 139–47. http://dx.doi.org/10.1016/j.apcata.2008.12.008.
Повний текст джерелаNguyen, Dang T., and Quan T. Pham. "A Theoretical and Experimental Study on Esterification of Citric Acid with the Primary Alcohols and the Hydroxyl Groups of Cellulose Chain (n = 1-2) in Parched Condition." Journal of Chemistry 2020 (November 12, 2020): 1–9. http://dx.doi.org/10.1155/2020/8825456.
Повний текст джерелаTabas, I., S. J. Feinmark, and N. Beatini. "The reactivity of desmosterol and other shellfish- and xanthomatosis-associated sterols in the macrophage sterol esterification reaction." Journal of Clinical Investigation 84, no. 6 (December 1, 1989): 1713–21. http://dx.doi.org/10.1172/jci114354.
Повний текст джерелаJuan, Joon Ching, Jingchang Zhang, and Mohd Ambar Yarmo. "Structure and reactivity of silica-supported zirconium sulfate for esterification of fatty acid under solvent-free condition." Applied Catalysis A: General 332, no. 2 (November 2007): 209–15. http://dx.doi.org/10.1016/j.apcata.2007.08.016.
Повний текст джерелаPatil, Meghshyam K., and Sharekh Shaikh. "Nano-Sized and -Crystalline Sulfated Zirconia Solid Acid Catalysts for Organic Synthesis." Materials Science Forum 757 (May 2013): 69–83. http://dx.doi.org/10.4028/www.scientific.net/msf.757.69.
Повний текст джерелаWang, Lu-Cun, C. M. Friend, Rebecca Fushimi, and Robert J. Madix. "Active site densities, oxygen activation and adsorbed reactive oxygen in alcohol activation on npAu catalysts." Faraday Discussions 188 (2016): 57–67. http://dx.doi.org/10.1039/c5fd00161g.
Повний текст джерелаZahalka, Hayder A., and Yoel Sasson. "Esterification of 1,4-dichlorobutane with sodium formate under solid–liquid phase transfer catalysis. A kinetic study." Canadian Journal of Chemistry 67, no. 2 (February 1, 1989): 245–49. http://dx.doi.org/10.1139/v89-040.
Повний текст джерелаJansen, Jacob H., Adam B. Powell, Sarah E. Specht, Selim Gerislioglu, and Ive Hermans. "Understanding the Structure and Reactivity of Mixed Titanium(IV) Alkoxide and Tin(II)/(IV) Carboxylates as Esterification Catalysts." ACS Sustainable Chemistry & Engineering 10, no. 7 (February 1, 2022): 2484–93. http://dx.doi.org/10.1021/acssuschemeng.1c07633.
Повний текст джерелаThévenet, Sophie, Angelika Wernicke, Stanislaw Belniak, Gérard Descotes, Alain Bouchu, and Yves Queneau. "Esterification of unprotected sucrose with acid chlorides in aqueous medium: kinetic reactivity versus acyl- or alkyloxycarbonyl-group migrations." Carbohydrate Research 318, no. 1-4 (May 1999): 52–66. http://dx.doi.org/10.1016/s0008-6215(99)00079-8.
Повний текст джерелаJoelianingsih, Armansyah H. Tambunan, and Hiroshi Nabetani. "Reactivity of Palm Fatty Acids for the Non-catalytic Esterification in a Bubble Column Reactor at Atmospheric Pressure." Procedia Chemistry 9 (2014): 182–93. http://dx.doi.org/10.1016/j.proche.2014.05.022.
Повний текст джерелаBasiuk, Vladimir A. "Reactivity of Carboxylic Groups on Armchair and Zigzag Carbon Nanotube Tips: A Theoretical Study of Esterification with Methanol." Nano Letters 2, no. 8 (August 2002): 835–39. http://dx.doi.org/10.1021/nl025607n.
Повний текст джерелаHeller, Stephen T., and Richmond Sarpong. "ChemInform Abstract: On the Reactivity of Imidazole Carbamates and Ureas and Their Use as Esterification and Amidation Reagents." ChemInform 43, no. 13 (March 1, 2012): no. http://dx.doi.org/10.1002/chin.201213060.
Повний текст джерелаZoubir, Mohammed, Abdellah Zeroual, Mohammed El Idrissi, Fatima Bkiri, Ahmed Benharref, Noureddine Mazoir, and Abdeslam El Hajbi. "Experimental and theoretical analysis of the reactivity and regioselectivity in esterification reactions of diterpenes (totaradiol, totaratriol, hinikione and totarolone)." Mediterranean Journal of Chemistry 6, no. 4 (April 9, 2017): 98–107. http://dx.doi.org/10.13171/mjc64/01704101226-zeroual.
Повний текст джерелаAsensio, Gregorio, Cecilia Andreu, and J. Alberto Marco. "Influence of structural factors and enzyme type on the reactivity and enantioselectivity of the enzymatic esterification of bicyclicmeso dialcohols." Chemische Berichte 125, no. 10 (October 1992): 2233–38. http://dx.doi.org/10.1002/cber.19921251010.
Повний текст джерелаRajabi, Fatemeh, Chin Hua Chia, Mika Sillanpää, Leonid G. Voskressensky, and Rafael Luque. "Cytosine Palladium Complex Supported on Ordered Mesoporous Silica as Highly Efficient and Reusable Nanocatalyst for One-Pot Oxidative Esterification of Aldehydes." Catalysts 11, no. 12 (December 3, 2021): 1482. http://dx.doi.org/10.3390/catal11121482.
Повний текст джерелаSuota, Maria Juliane, Débora Merediane Kochepka, Marlon Gualberto Ganter Moura, Cleverton Luiz Pirich, Mailson Matos, Washington Luiz Esteves Magalhães, and Luiz Pereira Ramos. "Lignin functionalization strategies and the potential applications of its derivatives – A Review." BioResources 16, no. 3 (July 12, 2021): 6471–511. http://dx.doi.org/10.15376/biores.16.3.suota.
Повний текст джерелаAthmani, Hamza, and Nourreedine Benali-Cherif. "Structure and thermal analysis of amino acids." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C989. http://dx.doi.org/10.1107/s205327331409010x.
Повний текст джерелаXue, Su Ling. "Study on the Properties of Thermoplastic Resin-Based Carbon Fiber Composites Based on the Wrapping Method in the Art Design of Seating." Key Engineering Materials 852 (July 2020): 98–108. http://dx.doi.org/10.4028/www.scientific.net/kem.852.98.
Повний текст джерелаShiryaeva, A. D., S. V. Moiseeva, S. V. Levanova, and I. L. Glazko. "Features of triamyl citrate synthesis." Fine Chemical Technologies 17, no. 6 (January 24, 2023): 483–91. http://dx.doi.org/10.32362/2410-6593-2022-17-6-483-491.
Повний текст джерелаFaggiano, Antonio, Maria Ricciardi, and Antonio Proto. "Catalytic Routes to Produce Polyphenolic Esters (PEs) from Biomass Feedstocks." Catalysts 12, no. 4 (April 18, 2022): 447. http://dx.doi.org/10.3390/catal12040447.
Повний текст джерелаLikhnyovskyi, Ruslan, Yuriy Tsapko, Vitalii Kovalenko, and Natalia Ivashyna. "Regarding the Formation of Wood Material Fire Protection and the Mechanism of its Action." Materials Science Forum 1038 (July 13, 2021): 439–53. http://dx.doi.org/10.4028/www.scientific.net/msf.1038.439.
Повний текст джерелаZdybel, Ewa, Tomasz Zięba, Waldemar Rymowicz, and Ewa Tomaszewska-Ciosk. "Organic Acids of the Microbiological Post-Culture Medium as Substrates to be Used for Starch Modification." Polymers 11, no. 3 (March 12, 2019): 469. http://dx.doi.org/10.3390/polym11030469.
Повний текст джерелаBriand, Glen G., Andreas Decken, Whitney E. M. M. Shannon, and Eric E. Trevors. "Synthesis, structural characterization, and reactivity of (thiolato)bismuth complexes as potential water-tolerant Lewis acid catalysts." Canadian Journal of Chemistry 96, no. 6 (June 2018): 561–69. http://dx.doi.org/10.1139/cjc-2017-0640.
Повний текст джерелаWang, Hui-Hui, Xue-Qin Zhang, Piao Long, Ai-Ping Zhang, Chuan-Fu Liu, and Run-Cang Sun. "Reaction Behavior of Cellulose in the Homogeneous Esterification of Bagasse Modified with Phthalic Anhydride in Ionic Liquid 1-Allyl-3-methylimidazium Chloride." International Journal of Polymer Science 2016 (2016): 1–9. http://dx.doi.org/10.1155/2016/2361284.
Повний текст джерелаASENSIO, G., C. ANDREU, and J. A. MARCO. "ChemInform Abstract: Influence of Structural Factors and Enzyme Type on the Reactivity and Enantioselectivity of the Enzymatic Esterification of Bicyclic meso Dialcohols." ChemInform 24, no. 5 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199305069.
Повний текст джерелаWang, Shuai, and Enrique Iglesia. "Substituent Effects and Molecular Descriptors of Reactivity in Condensation and Esterification Reactions of Oxygenates on Acid–Base Pairs at TiO2 and ZrO2 Surfaces." Journal of Physical Chemistry C 120, no. 38 (September 8, 2016): 21589–616. http://dx.doi.org/10.1021/acs.jpcc.6b07304.
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