Статті в журналах з теми "Micellar catalyst"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Micellar catalyst".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Cibulka, Radek, Lenka Baxová, Hana Dvořáková, František Hampl, Petra Ménová, Viktor Mojr, Baptiste Plancq, and Serkan Sayin. "Catalytic effect of alloxazinium and isoalloxazinium salts on oxidation of sulfides with hydrogen peroxide in micellar media." Collection of Czechoslovak Chemical Communications 74, no. 6 (2009): 973–93. http://dx.doi.org/10.1135/cccc2009030.
Повний текст джерелаBroxton, Trevor J. "Micellar Catalysis of Organic Reactions. XXXVIII A Study of the Catalytic Effect of Micelles of 3-Hydroxymethyl-1-tetradecylpyridinium Bromide on Amide Hydrolysis and Nucleophilic Aromatic Substitution." Australian Journal of Chemistry 51, no. 7 (1998): 541. http://dx.doi.org/10.1071/c98053.
Повний текст джерелаSteven, Alan. "Micelle-Mediated Chemistry in Water for the Synthesis of Drug Candidates." Synthesis 51, no. 13 (May 21, 2019): 2632–47. http://dx.doi.org/10.1055/s-0037-1610714.
Повний текст джерелаKuimov, Vladimir A., Svetlana F. Malysheva, Natalia A. Belogorlova, Ruslan I. Fattakhov, Alexander I. Albanov, and Boris A. Trofimov. "Triton-X-100 as an Organic Catalyst for One-Pot Synthesis of Arylmethyl-H-phosphinic Acids from Red Phosphorus and Arylmethyl Halides in the KOH/H2O/Toluene Multiphase Superbase System." Catalysts 13, no. 4 (April 11, 2023): 720. http://dx.doi.org/10.3390/catal13040720.
Повний текст джерелаAugustine, Rimesh, Dae-Kyoung Kim, Ho An Kim, Jae Ho Kim, and Il Kim. "Poly(N-isopropylacrylamide)-b-Poly(L-lysine)-b-Poly(L-histidine) Triblock Amphiphilic Copolymer Nanomicelles for Dual-Responsive Anticancer Drug Delivery." Journal of Nanoscience and Nanotechnology 20, no. 11 (November 1, 2020): 6959–67. http://dx.doi.org/10.1166/jnn.2020.18822.
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 джерелаWood, Alex B., Daniel E. Roa, Fabrice Gallou та Bruce H. Lipshutz. "α-Arylation of (hetero)aryl ketones in aqueous surfactant media". Green Chemistry 23, № 13 (2021): 4858–65. http://dx.doi.org/10.1039/d1gc01572a.
Повний текст джерелаRazak, Norazizah Abd, and M. Niyaz Khan. "Kinetics and Mechanism of Nanoparticles-Catalyzed Piperidinolysis of Anionic Phenyl Salicylate." Scientific World Journal 2014 (2014): 1–7. http://dx.doi.org/10.1155/2014/604139.
Повний текст джерелаSchwarze, M., M. Schmidt, L. A. T. Nguyen, A. Drews, M. Kraume, and R. Schomäcker. "Micellar enhanced ultrafiltration of a rhodium catalyst." Journal of Membrane Science 421-422 (December 2012): 165–71. http://dx.doi.org/10.1016/j.memsci.2012.07.017.
Повний текст джерелаLINDKVIST, Björn, Rolf WEINANDER, Lars ENGMAN, Marc KOETSE, Jan B. F. N. ENGBERTS, and Ralf MORGENSTERN. "Glutathione transferase mimics: micellar catalysis of an enzymic reaction." Biochemical Journal 323, no. 1 (April 1, 1997): 39–43. http://dx.doi.org/10.1042/bj3230039.
Повний текст джерелаJin, Bo, Fabrice Gallou, John Reilly, and Bruce H. Lipshutz. "ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors." Chemical Science 10, no. 12 (2019): 3481–85. http://dx.doi.org/10.1039/c8sc05618h.
Повний текст джерелаKhan, Mohammad Niyaz, and Ibrahim Isah Fagge. "Kinetics and Mechanism of Cationic Micelle/Flexible Nanoparticle Catalysis: A Review." Progress in Reaction Kinetics and Mechanism 43, no. 1 (March 2018): 1–20. http://dx.doi.org/10.3184/146867818x15066862094905.
Повний текст джерелаTasca, Elena, Giorgio La Sorella, Laura Sperni, Giorgio Strukul, and Alessandro Scarso. "Micellar promoted multi-component synthesis of 1,2,3-triazoles in water at room temperature." Green Chemistry 17, no. 3 (2015): 1414–22. http://dx.doi.org/10.1039/c4gc02248c.
Повний текст джерелаBelousova, I. A., T. M. Prokopyeva, N. G. Razumova, T. S. Gaidash, and V. A. Mikhailov. "Turnover in acyl substrates destruction in organized microheterogeneous systems." Vestnik NovSU, no. 3 (2023): 346–56. http://dx.doi.org/10.34680/2076-8052.2023.3(132).346-356.
Повний текст джерелаTakale, Balaram S., Ruchita R. Thakore, Sachin Handa, Fabrice Gallou, John Reilly, and Bruce H. Lipshutz. "A new, substituted palladacycle for ppm level Pd-catalyzed Suzuki–Miyaura cross couplings in water." Chemical Science 10, no. 38 (2019): 8825–31. http://dx.doi.org/10.1039/c9sc02528f.
Повний текст джерелаAkporji, Nnamdi, Ruchita R. Thakore, Margery Cortes-Clerget, Joel Andersen, Evan Landstrom, Donald H. Aue, Fabrice Gallou, and Bruce H. Lipshutz. "N2Phos – an easily made, highly effective ligand designed for ppm level Pd-catalyzed Suzuki–Miyaura cross couplings in water." Chemical Science 11, no. 20 (2020): 5205–12. http://dx.doi.org/10.1039/d0sc00968g.
Повний текст джерелаPasricha, Sharda. "Aqueous Phase Bromination by Micellar Solution of Sodium Dodecyl Sulfate (SDS): An Undergraduate Chemistry Experiment." Current Catalysis 10, no. 3 (December 2021): 214–18. http://dx.doi.org/10.2174/2211544710666211119100631.
Повний текст джерелаAhanthem, Dini, Devi Prasan Ojha, Francis A. S. Chipem, and Warjeet S. Laitonjam. "One-pot Pseudo-Domino Three-Component Knoevenagel Condensation Reaction in Water Enabled by Micellar Catalyst: Mechanism and Reactivity." Letters in Organic Chemistry 17, no. 11 (November 29, 2020): 823–31. http://dx.doi.org/10.2174/1570178616666190701102542.
Повний текст джерелаSchwarze, Michael, Anke Rost, Thomas Weigel, and Reinhard Schomäcker. "Selection of systems for catalyst recovery by micellar enhanced ultrafiltration." Chemical Engineering and Processing: Process Intensification 48, no. 1 (January 2009): 356–63. http://dx.doi.org/10.1016/j.cep.2008.04.014.
Повний текст джерелаLiang, Chunshuang, and Shimei Jiang. "Fluorescence light-up detection of cyanide in water based on cyclization reaction followed by ESIPT and AIEE." Analyst 142, no. 24 (2017): 4825–33. http://dx.doi.org/10.1039/c7an01479a.
Повний текст джерелаYusuf, Osman, Raisuddin Ali, Abdullah H. Alomrani, Aws Alshamsan, Abdullah K. Alshememry, Abdulaziz M. Almalik, Afsaneh Lavasanifar та Ziyad Binkhathlan. "Design and Development of D‒α‒Tocopheryl Polyethylene Glycol Succinate‒block‒Poly(ε-Caprolactone) (TPGS−b−PCL) Nanocarriers for Solubilization and Controlled Release of Paclitaxel". Molecules 26, № 9 (4 травня 2021): 2690. http://dx.doi.org/10.3390/molecules26092690.
Повний текст джерелаSchmidt, Fabian, Bastian Zehner, Marlene Kaposi, Markus Drees, János Mink, Wolfgang Korth, Andreas Jess, and Mirza Cokoja. "Activation of hydrogen peroxide by the nitrate anion in micellar media." Green Chemistry 23, no. 5 (2021): 1965–71. http://dx.doi.org/10.1039/d0gc03497e.
Повний текст джерелаDrennan, Catherine E., Rachelle J. Hughes, Vincent C. Reinsborough, and Oladega O. Soriyan. "Article." Canadian Journal of Chemistry 76, no. 2 (February 1, 1998): 152–57. http://dx.doi.org/10.1139/v97-226.
Повний текст джерелаKulič, Jiří, and Aleš Ptáček. "Alkaline Hydrolysis of 4-Nitrophenyl Acetate and Diphenyl (4-Nitrophenyl) Phosphate Catalyzed by Iodosoarenesulfonic Acids." Collection of Czechoslovak Chemical Communications 59, no. 6 (1994): 1392–99. http://dx.doi.org/10.1135/cccc19941392.
Повний текст джерелаHouyi, N., S. Taichenc, and L. Ganzuo. "PREPARATION OF MONODISPERSE NICKEL (COBALT) BOR1DE CATALYST USING REVERSED MICELLAR SYSTEM." Journal of Dispersion Science and Technology 13, no. 6 (December 1992): 647–56. http://dx.doi.org/10.1080/01932699208943344.
Повний текст джерелаKirály, Zoltán, Bernadett Veisz, Imre Dékány, Ágnes Mastalir, and Zsolt Rázga. "Preparation of an organophilic palladium montmorillonite catalyst in a micellar system." Chemical Communications, no. 19 (1999): 1925–26. http://dx.doi.org/10.1039/a905321b.
Повний текст джерелаYousif, Dawod, Silvia Tombolato, Elmehdi Ould Maina, Riccardo Po, Paolo Biagini, Antonio Papagni, and Luca Vaghi. "Micellar Suzuki Cross-Coupling between Thiophene and Aniline in Water and under Air." Organics 2, no. 4 (December 16, 2021): 415–23. http://dx.doi.org/10.3390/org2040025.
Повний текст джерелаYu, Xiaoqian, Artjom Herberg, and Dirk Kuckling. "Micellar Organocatalysis Using Smart Polymer Supports: Influence of Thermoresponsive Self-Assembly on Catalytic Activity." Polymers 12, no. 10 (October 1, 2020): 2265. http://dx.doi.org/10.3390/polym12102265.
Повний текст джерелаDahadha, Adnan A., Mohammed Hassan, Tamara Mfarej, Razan Bani Issa, Mohamed J. Saadh, Mohammad Al-Dhoun, Mohammad Abunuwar, and Nesrin T. Talat. "The Catalytic Influence of Polymers and Surfactants on the Rate Constants of Reaction of Maltose with Cerium (IV) in Acidic Aqueous Medium." Journal of Chemistry 2022 (July 1, 2022): 1–11. http://dx.doi.org/10.1155/2022/2609478.
Повний текст джерелаBroxton, TJ, JR Christie, and RPT Chung. "Micellar Catalysis of Organic Reactions. XXVI. SNAr Reactions of Azide Ions." Australian Journal of Chemistry 42, no. 6 (1989): 855. http://dx.doi.org/10.1071/ch9890855.
Повний текст джерелаKulič, Jiří, and Aleš Ptáček. "Catalyzed Alkaline Hydrolysis of Substituted Phenyl Acetates." Collection of Czechoslovak Chemical Communications 58, no. 8 (1993): 1798–802. http://dx.doi.org/10.1135/cccc19931798.
Повний текст джерелаGebicka, Lidia, and Monika Jurgas-Grudzinska. "Activity and Stability of Catalase in Nonionic Micellar and Reverse Micellar Systems." Zeitschrift für Naturforschung C 59, no. 11-12 (December 1, 2004): 887–91. http://dx.doi.org/10.1515/znc-2004-11-1220.
Повний текст джерелаOranli, Levent, Pratap Bahadur, and Gérard Riess. "Hydrodynamic studies on micellar solutions of styrene–butadiene block copolymers in selective solvents." Canadian Journal of Chemistry 63, no. 10 (October 1, 1985): 2691–96. http://dx.doi.org/10.1139/v85-447.
Повний текст джерелаWasylishen, Roderick E., Jan C. T. Kwak, Zhisheng Gao, Elisabeth Verpoorte, J. Bruce MacDonald, and Ross M. Dickson. "NMR studies of hydrocarbons solubilized in aqueous micellar solutions." Canadian Journal of Chemistry 69, no. 5 (May 1, 1991): 822–33. http://dx.doi.org/10.1139/v91-122.
Повний текст джерелаZehner, Bastian, Wolfgang Korth, Fabian Schmidt, Mirza Cokoja, and Andreas Jess. "Kinetics of Epoxidation of Cyclooctene with Ionic Liquids Containing Tungstate as Micellar Catalyst." Chemical Engineering & Technology 44, no. 12 (November 5, 2021): 2374–81. http://dx.doi.org/10.1002/ceat.202100102.
Повний текст джерелаHuang, Xin, Zeyuan Dong, Junqiu Liu, Shizhong Mao, Jiayun Xu, Guimin Luo, and Jiacong Shen. "Selenium-Mediated Micellar Catalyst: An Efficient Enzyme Model for Glutathione Peroxidase-like Catalysis." Langmuir 23, no. 3 (January 2007): 1518–22. http://dx.doi.org/10.1021/la061727p.
Повний текст джерелаSchmidt, Marcel, Saskia Schreiber, Luise Franz, Hauke Langhoff, Ashkan Farhang, Moritz Horstmann, Hans-Joachim Drexler, Detlef Heller, and Michael Schwarze. "Hydrogenation of Itaconic Acid in Micellar Solutions: Catalyst Recycling with Cloud Point Extraction?" Industrial & Engineering Chemistry Research 58, no. 7 (September 17, 2018): 2445–53. http://dx.doi.org/10.1021/acs.iecr.8b03313.
Повний текст джерелаYin, Hong, Qiushi Wang, Sebastian Geburt, Steffen Milz, Bart Ruttens, Giedrius Degutis, Jan D'Haen, et al. "Controlled synthesis of ultrathin ZnO nanowires using micellar gold nanoparticles as catalyst templates." Nanoscale 5, no. 15 (2013): 7046. http://dx.doi.org/10.1039/c3nr01938a.
Повний текст джерелаQuentel, François, Guillaume Passard, and Frederic Gloaguen. "A Binuclear Iron-Thiolate Catalyst for Electrochemical Hydrogen Production in Aqueous Micellar Solution." Chemistry - A European Journal 18, no. 42 (September 11, 2012): 13473–79. http://dx.doi.org/10.1002/chem.201201884.
Повний текст джерелаBroxton, Trevor J., and Robin A. Coa. "Micellar catalysis of organic reactions. Part 33. Amide hydrolysis in neutral solution in the presence of a copper-containing micelle." Canadian Journal of Chemistry 71, no. 5 (May 1, 1993): 670–73. http://dx.doi.org/10.1139/v93-090.
Повний текст джерелаNabid, Mohammad Reza, and Yasamin Bide. "H40-PCL-PEG unimolecular micelles both as anchoring sites for palladium nanoparticles and micellar catalyst for Heck reaction in water." Applied Catalysis A: General 469 (January 2014): 183–90. http://dx.doi.org/10.1016/j.apcata.2013.09.016.
Повний текст джерелаKumar, Dileep, Malik Abdul Rub, and Abdullah M. Asiri. "Synthesis and characterization of geminis and implications of their micellar solution on ninhydrin and metal amino acid complex." Royal Society Open Science 7, no. 7 (July 2020): 200775. http://dx.doi.org/10.1098/rsos.200775.
Повний текст джерелаPoša, Mihalj. "Self-Association of the Anion of 7-Oxodeoxycholic Acid (Bile Salt): How Secondary Micelles Are Formed." International Journal of Molecular Sciences 24, no. 14 (July 24, 2023): 11853. http://dx.doi.org/10.3390/ijms241411853.
Повний текст джерелаVenkateswaran, Krishnan, Mary V. Barnabas, Bill W. Ng, and David C. Walker. "Residence-time of muonium at micelles: Effect of added micelles on the reactivity of muonium towards ionic solutes in water." Canadian Journal of Chemistry 66, no. 8 (August 1, 1988): 1979–83. http://dx.doi.org/10.1139/v88-319.
Повний текст джерелаGOTO, Koichi, Jiro OKAI, Yumiko EJIMA, Takatoshi ITO, Hideo OKAI, and Ryuichi UEOKA. "Remarkably Enhanced Enantioselective Hydrolysis of Amino Acid Esters With Tripeptide Catalyst in Micellar Systems." NIPPON KAGAKU KAISHI, no. 5 (1995): 351–57. http://dx.doi.org/10.1246/nikkashi.1995.351.
Повний текст джерелаLipshutz, Bruce H., and Subir Ghorai. "PQS: A New Platform for Micellar Catalysis. RCM Reactions in Water, with Catalyst Recycling." Organic Letters 11, no. 3 (February 5, 2009): 705–8. http://dx.doi.org/10.1021/ol8027829.
Повний текст джерелаShrikhande, Janhavi J., Manoj B. Gawande, and Radha V. Jayaram. "A catalyst-free N-benzyloxycarbonylation of amines in aqueous micellar media at room temperature." Tetrahedron Letters 49, no. 32 (August 2008): 4799–803. http://dx.doi.org/10.1016/j.tetlet.2008.05.010.
Повний текст джерелаHájek, Martin, Aleš Vávra, František Skopal, Anna Straková, and Miroslav Douda. "The description of catalyst behaviour during transesterification of rapeseed oil – Formation of micellar emulsion." Renewable Energy 159 (October 2020): 938–43. http://dx.doi.org/10.1016/j.renene.2020.06.082.
Повний текст джерелаCheng, Mingxing, Tian Shi, Hongyu Guan, Shengtian Wang, Xiaohong Wang, and Zijiang Jiang. "Clean production of glucose from polysaccharides using a micellar heteropolyacid as a heterogeneous catalyst." Applied Catalysis B: Environmental 107, no. 1-2 (August 2011): 104–9. http://dx.doi.org/10.1016/j.apcatb.2011.07.002.
Повний текст джерелаSobhani, Sara, and Zohre Zeraatkar. "A new magnetically recoverable heterogeneous palladium catalyst for phosphonation reactions in aqueous micellar solution." Applied Organometallic Chemistry 30, no. 1 (October 26, 2015): 12–19. http://dx.doi.org/10.1002/aoc.3392.
Повний текст джерела