Zeitschriftenartikel zum Thema „Micellar catalyst“
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Cibulka, Radek, Lenka Baxová, Hana Dvořáková, František Hampl, Petra Ménová, Viktor Mojr, Baptiste Plancq und 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, Nr. 6 (2009): 973–93. http://dx.doi.org/10.1135/cccc2009030.
Broxton, 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, Nr. 7 (1998): 541. http://dx.doi.org/10.1071/c98053.
Steven, Alan. „Micelle-Mediated Chemistry in Water for the Synthesis of Drug Candidates“. Synthesis 51, Nr. 13 (21.05.2019): 2632–47. http://dx.doi.org/10.1055/s-0037-1610714.
Kuimov, Vladimir A., Svetlana F. Malysheva, Natalia A. Belogorlova, Ruslan I. Fattakhov, Alexander I. Albanov und 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, Nr. 4 (11.04.2023): 720. http://dx.doi.org/10.3390/catal13040720.
Augustine, Rimesh, Dae-Kyoung Kim, Ho An Kim, Jae Ho Kim und 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, Nr. 11 (01.11.2020): 6959–67. http://dx.doi.org/10.1166/jnn.2020.18822.
Tang, Christina, und Bridget T. McInnes. „Cascade Processes with Micellar Reaction Media: Recent Advances and Future Directions“. Molecules 27, Nr. 17 (31.08.2022): 5611. http://dx.doi.org/10.3390/molecules27175611.
Wood, Alex B., Daniel E. Roa, Fabrice Gallou und Bruce H. Lipshutz. „α-Arylation of (hetero)aryl ketones in aqueous surfactant media“. Green Chemistry 23, Nr. 13 (2021): 4858–65. http://dx.doi.org/10.1039/d1gc01572a.
Razak, Norazizah Abd, und 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.
Schwarze, M., M. Schmidt, L. A. T. Nguyen, A. Drews, M. Kraume und R. Schomäcker. „Micellar enhanced ultrafiltration of a rhodium catalyst“. Journal of Membrane Science 421-422 (Dezember 2012): 165–71. http://dx.doi.org/10.1016/j.memsci.2012.07.017.
LINDKVIST, Björn, Rolf WEINANDER, Lars ENGMAN, Marc KOETSE, Jan B. F. N. ENGBERTS und Ralf MORGENSTERN. „Glutathione transferase mimics: micellar catalysis of an enzymic reaction“. Biochemical Journal 323, Nr. 1 (01.04.1997): 39–43. http://dx.doi.org/10.1042/bj3230039.
Jin, Bo, Fabrice Gallou, John Reilly und Bruce H. Lipshutz. „ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors“. Chemical Science 10, Nr. 12 (2019): 3481–85. http://dx.doi.org/10.1039/c8sc05618h.
Khan, Mohammad Niyaz, und Ibrahim Isah Fagge. „Kinetics and Mechanism of Cationic Micelle/Flexible Nanoparticle Catalysis: A Review“. Progress in Reaction Kinetics and Mechanism 43, Nr. 1 (März 2018): 1–20. http://dx.doi.org/10.3184/146867818x15066862094905.
Tasca, Elena, Giorgio La Sorella, Laura Sperni, Giorgio Strukul und Alessandro Scarso. „Micellar promoted multi-component synthesis of 1,2,3-triazoles in water at room temperature“. Green Chemistry 17, Nr. 3 (2015): 1414–22. http://dx.doi.org/10.1039/c4gc02248c.
Belousova, I. A., T. M. Prokopyeva, N. G. Razumova, T. S. Gaidash und V. A. Mikhailov. „Turnover in acyl substrates destruction in organized microheterogeneous systems“. Vestnik NovSU, Nr. 3 (2023): 346–56. http://dx.doi.org/10.34680/2076-8052.2023.3(132).346-356.
Takale, Balaram S., Ruchita R. Thakore, Sachin Handa, Fabrice Gallou, John Reilly und Bruce H. Lipshutz. „A new, substituted palladacycle for ppm level Pd-catalyzed Suzuki–Miyaura cross couplings in water“. Chemical Science 10, Nr. 38 (2019): 8825–31. http://dx.doi.org/10.1039/c9sc02528f.
Akporji, Nnamdi, Ruchita R. Thakore, Margery Cortes-Clerget, Joel Andersen, Evan Landstrom, Donald H. Aue, Fabrice Gallou und 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, Nr. 20 (2020): 5205–12. http://dx.doi.org/10.1039/d0sc00968g.
Pasricha, Sharda. „Aqueous Phase Bromination by Micellar Solution of Sodium Dodecyl Sulfate (SDS): An Undergraduate Chemistry Experiment“. Current Catalysis 10, Nr. 3 (Dezember 2021): 214–18. http://dx.doi.org/10.2174/2211544710666211119100631.
Ahanthem, Dini, Devi Prasan Ojha, Francis A. S. Chipem und 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, Nr. 11 (29.11.2020): 823–31. http://dx.doi.org/10.2174/1570178616666190701102542.
Schwarze, Michael, Anke Rost, Thomas Weigel und Reinhard Schomäcker. „Selection of systems for catalyst recovery by micellar enhanced ultrafiltration“. Chemical Engineering and Processing: Process Intensification 48, Nr. 1 (Januar 2009): 356–63. http://dx.doi.org/10.1016/j.cep.2008.04.014.
Liang, Chunshuang, und Shimei Jiang. „Fluorescence light-up detection of cyanide in water based on cyclization reaction followed by ESIPT and AIEE“. Analyst 142, Nr. 24 (2017): 4825–33. http://dx.doi.org/10.1039/c7an01479a.
Yusuf, Osman, Raisuddin Ali, Abdullah H. Alomrani, Aws Alshamsan, Abdullah K. Alshememry, Abdulaziz M. Almalik, Afsaneh Lavasanifar und 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, Nr. 9 (04.05.2021): 2690. http://dx.doi.org/10.3390/molecules26092690.
Schmidt, Fabian, Bastian Zehner, Marlene Kaposi, Markus Drees, János Mink, Wolfgang Korth, Andreas Jess und Mirza Cokoja. „Activation of hydrogen peroxide by the nitrate anion in micellar media“. Green Chemistry 23, Nr. 5 (2021): 1965–71. http://dx.doi.org/10.1039/d0gc03497e.
Drennan, Catherine E., Rachelle J. Hughes, Vincent C. Reinsborough und Oladega O. Soriyan. „Article“. Canadian Journal of Chemistry 76, Nr. 2 (01.02.1998): 152–57. http://dx.doi.org/10.1139/v97-226.
Kulič, Jiří, und Aleš Ptáček. „Alkaline Hydrolysis of 4-Nitrophenyl Acetate and Diphenyl (4-Nitrophenyl) Phosphate Catalyzed by Iodosoarenesulfonic Acids“. Collection of Czechoslovak Chemical Communications 59, Nr. 6 (1994): 1392–99. http://dx.doi.org/10.1135/cccc19941392.
Houyi, N., S. Taichenc und L. Ganzuo. „PREPARATION OF MONODISPERSE NICKEL (COBALT) BOR1DE CATALYST USING REVERSED MICELLAR SYSTEM“. Journal of Dispersion Science and Technology 13, Nr. 6 (Dezember 1992): 647–56. http://dx.doi.org/10.1080/01932699208943344.
Király, Zoltán, Bernadett Veisz, Imre Dékány, Ágnes Mastalir und Zsolt Rázga. „Preparation of an organophilic palladium montmorillonite catalyst in a micellar system“. Chemical Communications, Nr. 19 (1999): 1925–26. http://dx.doi.org/10.1039/a905321b.
Yousif, Dawod, Silvia Tombolato, Elmehdi Ould Maina, Riccardo Po, Paolo Biagini, Antonio Papagni und Luca Vaghi. „Micellar Suzuki Cross-Coupling between Thiophene and Aniline in Water and under Air“. Organics 2, Nr. 4 (16.12.2021): 415–23. http://dx.doi.org/10.3390/org2040025.
Yu, Xiaoqian, Artjom Herberg und Dirk Kuckling. „Micellar Organocatalysis Using Smart Polymer Supports: Influence of Thermoresponsive Self-Assembly on Catalytic Activity“. Polymers 12, Nr. 10 (01.10.2020): 2265. http://dx.doi.org/10.3390/polym12102265.
Dahadha, Adnan A., Mohammed Hassan, Tamara Mfarej, Razan Bani Issa, Mohamed J. Saadh, Mohammad Al-Dhoun, Mohammad Abunuwar und 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 (01.07.2022): 1–11. http://dx.doi.org/10.1155/2022/2609478.
Broxton, TJ, JR Christie und RPT Chung. „Micellar Catalysis of Organic Reactions. XXVI. SNAr Reactions of Azide Ions“. Australian Journal of Chemistry 42, Nr. 6 (1989): 855. http://dx.doi.org/10.1071/ch9890855.
Kulič, Jiří, und Aleš Ptáček. „Catalyzed Alkaline Hydrolysis of Substituted Phenyl Acetates“. Collection of Czechoslovak Chemical Communications 58, Nr. 8 (1993): 1798–802. http://dx.doi.org/10.1135/cccc19931798.
Gebicka, Lidia, und Monika Jurgas-Grudzinska. „Activity and Stability of Catalase in Nonionic Micellar and Reverse Micellar Systems“. Zeitschrift für Naturforschung C 59, Nr. 11-12 (01.12.2004): 887–91. http://dx.doi.org/10.1515/znc-2004-11-1220.
Oranli, Levent, Pratap Bahadur und Gérard Riess. „Hydrodynamic studies on micellar solutions of styrene–butadiene block copolymers in selective solvents“. Canadian Journal of Chemistry 63, Nr. 10 (01.10.1985): 2691–96. http://dx.doi.org/10.1139/v85-447.
Wasylishen, Roderick E., Jan C. T. Kwak, Zhisheng Gao, Elisabeth Verpoorte, J. Bruce MacDonald und Ross M. Dickson. „NMR studies of hydrocarbons solubilized in aqueous micellar solutions“. Canadian Journal of Chemistry 69, Nr. 5 (01.05.1991): 822–33. http://dx.doi.org/10.1139/v91-122.
Zehner, Bastian, Wolfgang Korth, Fabian Schmidt, Mirza Cokoja und Andreas Jess. „Kinetics of Epoxidation of Cyclooctene with Ionic Liquids Containing Tungstate as Micellar Catalyst“. Chemical Engineering & Technology 44, Nr. 12 (05.11.2021): 2374–81. http://dx.doi.org/10.1002/ceat.202100102.
Huang, Xin, Zeyuan Dong, Junqiu Liu, Shizhong Mao, Jiayun Xu, Guimin Luo und Jiacong Shen. „Selenium-Mediated Micellar Catalyst: An Efficient Enzyme Model for Glutathione Peroxidase-like Catalysis“. Langmuir 23, Nr. 3 (Januar 2007): 1518–22. http://dx.doi.org/10.1021/la061727p.
Schmidt, Marcel, Saskia Schreiber, Luise Franz, Hauke Langhoff, Ashkan Farhang, Moritz Horstmann, Hans-Joachim Drexler, Detlef Heller und Michael Schwarze. „Hydrogenation of Itaconic Acid in Micellar Solutions: Catalyst Recycling with Cloud Point Extraction?“ Industrial & Engineering Chemistry Research 58, Nr. 7 (17.09.2018): 2445–53. http://dx.doi.org/10.1021/acs.iecr.8b03313.
Yin, 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, Nr. 15 (2013): 7046. http://dx.doi.org/10.1039/c3nr01938a.
Quentel, François, Guillaume Passard und Frederic Gloaguen. „A Binuclear Iron-Thiolate Catalyst for Electrochemical Hydrogen Production in Aqueous Micellar Solution“. Chemistry - A European Journal 18, Nr. 42 (11.09.2012): 13473–79. http://dx.doi.org/10.1002/chem.201201884.
Broxton, Trevor J., und 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, Nr. 5 (01.05.1993): 670–73. http://dx.doi.org/10.1139/v93-090.
Nabid, Mohammad Reza, und 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 (Januar 2014): 183–90. http://dx.doi.org/10.1016/j.apcata.2013.09.016.
Kumar, Dileep, Malik Abdul Rub und 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, Nr. 7 (Juli 2020): 200775. http://dx.doi.org/10.1098/rsos.200775.
Poša, Mihalj. „Self-Association of the Anion of 7-Oxodeoxycholic Acid (Bile Salt): How Secondary Micelles Are Formed“. International Journal of Molecular Sciences 24, Nr. 14 (24.07.2023): 11853. http://dx.doi.org/10.3390/ijms241411853.
Venkateswaran, Krishnan, Mary V. Barnabas, Bill W. Ng und 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, Nr. 8 (01.08.1988): 1979–83. http://dx.doi.org/10.1139/v88-319.
GOTO, Koichi, Jiro OKAI, Yumiko EJIMA, Takatoshi ITO, Hideo OKAI und Ryuichi UEOKA. „Remarkably Enhanced Enantioselective Hydrolysis of Amino Acid Esters With Tripeptide Catalyst in Micellar Systems.“ NIPPON KAGAKU KAISHI, Nr. 5 (1995): 351–57. http://dx.doi.org/10.1246/nikkashi.1995.351.
Lipshutz, Bruce H., und Subir Ghorai. „PQS: A New Platform for Micellar Catalysis. RCM Reactions in Water, with Catalyst Recycling“. Organic Letters 11, Nr. 3 (05.02.2009): 705–8. http://dx.doi.org/10.1021/ol8027829.
Shrikhande, Janhavi J., Manoj B. Gawande und Radha V. Jayaram. „A catalyst-free N-benzyloxycarbonylation of amines in aqueous micellar media at room temperature“. Tetrahedron Letters 49, Nr. 32 (August 2008): 4799–803. http://dx.doi.org/10.1016/j.tetlet.2008.05.010.
Hájek, Martin, Aleš Vávra, František Skopal, Anna Straková und Miroslav Douda. „The description of catalyst behaviour during transesterification of rapeseed oil – Formation of micellar emulsion“. Renewable Energy 159 (Oktober 2020): 938–43. http://dx.doi.org/10.1016/j.renene.2020.06.082.
Cheng, Mingxing, Tian Shi, Hongyu Guan, Shengtian Wang, Xiaohong Wang und Zijiang Jiang. „Clean production of glucose from polysaccharides using a micellar heteropolyacid as a heterogeneous catalyst“. Applied Catalysis B: Environmental 107, Nr. 1-2 (August 2011): 104–9. http://dx.doi.org/10.1016/j.apcatb.2011.07.002.
Sobhani, Sara, und Zohre Zeraatkar. „A new magnetically recoverable heterogeneous palladium catalyst for phosphonation reactions in aqueous micellar solution“. Applied Organometallic Chemistry 30, Nr. 1 (26.10.2015): 12–19. http://dx.doi.org/10.1002/aoc.3392.