Journal articles on the topic 'Micellar catalyst'
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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.
Full textBroxton, 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.
Full textSteven, 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.
Full textKuimov, 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.
Full textAugustine, 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.
Full textTang, 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.
Full textWood, Alex B., Daniel E. Roa, Fabrice Gallou, and Bruce H. Lipshutz. "α-Arylation of (hetero)aryl ketones in aqueous surfactant media." Green Chemistry 23, no. 13 (2021): 4858–65. http://dx.doi.org/10.1039/d1gc01572a.
Full textRazak, 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.
Full textSchwarze, 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.
Full textLINDKVIST, 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.
Full textJin, 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.
Full textKhan, 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.
Full textTasca, 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.
Full textBelousova, 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.
Full textTakale, 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.
Full textAkporji, 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.
Full textPasricha, 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.
Full textAhanthem, 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.
Full textSchwarze, 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.
Full textLiang, 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.
Full textYusuf, Osman, Raisuddin Ali, Abdullah H. Alomrani, Aws Alshamsan, Abdullah K. Alshememry, Abdulaziz M. Almalik, Afsaneh Lavasanifar, and 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, no. 9 (May 4, 2021): 2690. http://dx.doi.org/10.3390/molecules26092690.
Full textSchmidt, 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.
Full textDrennan, 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.
Full textKulič, 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.
Full textHouyi, 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.
Full textKirály, 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.
Full textYousif, 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.
Full textYu, 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.
Full textDahadha, 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.
Full textBroxton, 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.
Full textKulič, 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.
Full textGebicka, 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.
Full textOranli, 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.
Full textWasylishen, 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.
Full textZehner, 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.
Full textHuang, 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.
Full textSchmidt, 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.
Full textYin, 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.
Full textQuentel, 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.
Full textBroxton, 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.
Full textNabid, 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.
Full textKumar, 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.
Full textPoša, 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.
Full textVenkateswaran, 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.
Full textGOTO, 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.
Full textLipshutz, 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.
Full textShrikhande, 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.
Full textHájek, 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.
Full textCheng, 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.
Full textSobhani, 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.
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