Статті в журналах з теми "Catalysis; Organotin compounds"
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Storozhenko, P. A., K. D. Magdeev, A. A. Grachev, N. I. Kirilina, and V. I. Shiryaev. "Organotin Compounds in Industrial Catalysis. II. Polyurethanes Formation Processes." Kataliz v promyshlennosti 20, no. 3 (May 28, 2020): 203–15. http://dx.doi.org/10.18412/1816-0387-2020-3-203-215.
Повний текст джерелаStorozhenko, P. A., A. V. Veselov, A. A. Grachev, N. I. Kirilina, and V. I. Shiryaev. "Organotin Compounds in Industrial Catalysis. I. (Re)esterification Processes." Kataliz v promyshlennosti 20, no. 3 (May 28, 2020): 190–202. http://dx.doi.org/10.18412/1816-0387-2020-3-190-202.
Повний текст джерелаStorozhenko, P. A., A. A. Grachev, K. D. Magdeev, and V. I. Shiryaev. "Organotin compounds in industrial catalysis: III. Vulcanization of blocked isocyanates and silicones." Kataliz v promyshlennosti 20, no. 6 (November 24, 2020): 413–25. http://dx.doi.org/10.18412/1816-0387-2020-6-413-425.
Повний текст джерелаPlasseraud, Laurent. "Organotin(IV) Complexes Containing Sn–O–Se Moieties: A Structural Inventory." Synthesis 50, no. 18 (June 14, 2018): 3653–61. http://dx.doi.org/10.1055/s-0037-1610164.
Повний текст джерелаWu, Yi-Bo, Bo-Wen Li, Fu-Xiang Li, Jian-Wei Xue, and Zhi-Ping Lv. "Synthesis and characteristics of organotin-based catalysts for acetylene hydrochlorination." Canadian Journal of Chemistry 96, no. 5 (May 2018): 447–52. http://dx.doi.org/10.1139/cjc-2017-0612.
Повний текст джерелаPichler, Johann, Philipp Müller, Ana Torvisco, and Frank Uhlig. "Novel diaminopropyl substituted organotin compounds." Canadian Journal of Chemistry 96, no. 4 (April 2018): 411–18. http://dx.doi.org/10.1139/cjc-2017-0713.
Повний текст джерелаSiwacha, Priyanka, Surbhi Soni, Harish Kumar Sharmaa, and Manoj Kumara. "Synthesis, Characterization and Biological Studies of Some Organotin Compounds: (A-Review)." Oriental Journal Of Chemistry 36, no. 05 (October 25, 2020): 871–78. http://dx.doi.org/10.13005/ojc/360511.
Повний текст джерелаLucas, Christine, Catherine C. Santini, Martina Prinz, Marie-Anne Cordonnier, Jean-Marie Basset, Marie-Françoise Connil, and Bernard Jousseaume. "New optically active organotin compounds for heterogeneous bimetallic catalysis." Journal of Organometallic Chemistry 520, no. 1-2 (August 1996): 101–6. http://dx.doi.org/10.1016/0022-328x(96)06270-5.
Повний текст джерелаAdeyemi, Jerry, and Damian Onwudiwe. "Organotin(IV) Dithiocarbamate Complexes: Chemistry and Biological Activity." Molecules 23, no. 10 (October 9, 2018): 2571. http://dx.doi.org/10.3390/molecules23102571.
Повний текст джерелаAue, Walter A., Bernard J. Flinn, Christopher G. Flinn, Veluppillai Paramasigamani, and Kathleen A. Russell. "Transformation and transmission of organotin compounds inside a gas chromatograph." Canadian Journal of Chemistry 67, no. 3 (March 1, 1989): 402–10. http://dx.doi.org/10.1139/v89-063.
Повний текст джерелаStorozhenko, P. A., A. V. Veselov, A. A. Grachev, N. I. Kirilina, and V. I. Shiryaev. "Organotin Compounds in Industrial Catalysis, Part I: Processes of (Trans)esterification." Catalysis in Industry 12, no. 4 (October 2020): 292–303. http://dx.doi.org/10.1134/s2070050420040078.
Повний текст джерелаStorozhenko, P. A., K. D. Magdeev, A. A. Grachev, N. I. Kirilina, and V. I. Shiryaev. "Organotin Compounds in Industrial Catalysis, Part 2: Processes of Polyurethane Formation." Catalysis in Industry 12, no. 4 (October 2020): 304–15. http://dx.doi.org/10.1134/s207005042004008x.
Повний текст джерелаBuck, Bethany, Alessandro Mascioni, Lawrence Que, and Gianluigi Veglia. "Dealkylation of Organotin Compounds by Biological Dithiols: Toward the Chemistry of Organotin Toxicity." Journal of the American Chemical Society 125, no. 44 (November 2003): 13316–17. http://dx.doi.org/10.1021/ja0354723.
Повний текст джерелаYusof, Enis Nadia Md, Muhammad A. M. Latif, Mohamed I. M. Tahir, Jennette A. Sakoff, Michela I. Simone, Alister J. Page, Abhi Veerakumarasivam, Edward R. T. Tiekink, and Thahira B. S. A. Ravoof. "o-Vanillin Derived Schiff Bases and Their Organotin(IV) Compounds: Synthesis, Structural Characterisation, In-Silico Studies and Cytotoxicity." International Journal of Molecular Sciences 20, no. 4 (February 15, 2019): 854. http://dx.doi.org/10.3390/ijms20040854.
Повний текст джерелаStorozhenko, P. A., A. A. Grachev, K. D. Magdeev, and V. I. Shiryaev. "Organotin Compounds in Industrial Catalysis III: Vulcanization of Blocked Isocyanates and Silicones." Catalysis in Industry 13, no. 2 (April 2021): 132–42. http://dx.doi.org/10.1134/s2070050421020112.
Повний текст джерелаKinart, Wojciech J., and Cezary M. Kinart. "Catalysis of reactions of allyltin compounds and organotin phenoxides by lithium perchlorate." Journal of Organometallic Chemistry 691, no. 8 (April 2006): 1441–51. http://dx.doi.org/10.1016/j.jorganchem.2005.10.038.
Повний текст джерелаKaur, Kulwinder, Raghubir Singh, Varinder Kaur, and Neena Capalash. "Water stable fluorescent organotin(iv) compounds: aggregation induced emission enhancement and recognition of lead ions in an aqueous system." New Journal of Chemistry 46, no. 1 (2022): 148–61. http://dx.doi.org/10.1039/d1nj04612h.
Повний текст джерелаLoganathan, Pushparaj, Renjith S. Pillai, Velusamy Jeevananthan, Ezhumalai David, Nallasamy Palanisami, Nattamai S. P. Bhuvanesh, and Swaminathan Shanmugan. "Assembly of discrete and oligomeric structures of organotin double-decker silsesquioxanes: inherent stability studies." New Journal of Chemistry 45, no. 43 (2021): 20144–54. http://dx.doi.org/10.1039/d1nj03128g.
Повний текст джерелаNeumann, Wilhelm Paul. "Book Review: Organotin Compounds in Organic Synthesis. Edited by Y. Yamamoto." Angewandte Chemie International Edition in English 29, no. 9 (September 1990): 1072–73. http://dx.doi.org/10.1002/anie.199010724.
Повний текст джерелаSomeşan, Adrian-Alexandru, Cristian Silvestru, and Richard A. Varga. "Reactivity of a carbonyl moiety in organotin(iv) compounds: novel Pd(ii) and Cu(ii) complexes supported by organotin(iv) ligands." New Journal of Chemistry 45, no. 8 (2021): 3817–27. http://dx.doi.org/10.1039/d0nj06016j.
Повний текст джерелаSingh, Navjot, Keshav Kumar, Neha Srivastav, Raghubir Singh, Varinder Kaur, Jerry P. Jasinski та Ray J. Butcher. "Exploration of fluorescent organotin compounds of α-amino acid Schiff bases for the detection of organophosphorous chemical warfare agents: quantification of diethylchlorophosphate". New Journal of Chemistry 42, № 11 (2018): 8756–64. http://dx.doi.org/10.1039/c8nj01153b.
Повний текст джерелаSwamy, K. C. Kumara, Charles G. Schmid, Roberta O. Day, and Robert R. Holmes. "Organotin clusters. 6. Tetranuclear organooxotin cage compounds formed with phosphate and phosphonate ligands. A new class of organotin clusters." Journal of the American Chemical Society 112, no. 1 (January 1990): 223–28. http://dx.doi.org/10.1021/ja00157a036.
Повний текст джерелаHolmes, Robert R., K. C. Kumara Swamy, Charles G. Schmid, and Roberta O. Day. "Organotin clusters. 4. Cubic, butterfly, and oxygen-capped clusters of n-butyloxotin phosphinates. A new class of organotin compounds." Journal of the American Chemical Society 110, no. 21 (October 1988): 7060–66. http://dx.doi.org/10.1021/ja00229a019.
Повний текст джерелаBrinkman, Elizabeth A., Karen Salomon, William Tumas, and John I. Brauman. "Electron Affinities and Gas-Phase Acidities of Organogermanium and Organotin Compounds." Journal of the American Chemical Society 117, no. 17 (May 1995): 4905–10. http://dx.doi.org/10.1021/ja00122a022.
Повний текст джерелаStorozhenko, P. A., K. D. Magdeev, A. A. Grachev, and V. I. Shiryaev. "Catalysts for the Direct Synthesis of Organotin Compounds, Part 1: Reactions between Organohalides and Tin Alloys." Catalysis in Industry 13, no. 3 (July 2021): 216–29. http://dx.doi.org/10.1134/s2070050421030107.
Повний текст джерелаStorozhenko, P. A., K. D. Magdeev, A. A. Grachev, and V. I. Shiryaev. "Catalysts in the Direct Synthesis of Organotin Compounds, Part III: Reactions between Carbofunctional Organohalides and Metallic Tin." Catalysis in Industry 14, no. 3 (September 2022): 298–313. http://dx.doi.org/10.1134/s2070050422030047.
Повний текст джерелаStorozhenko, P. A., K. D. Magdeev, A. A. Grachev, and V. I. Shiryaev. "Catalysts in the Direct Synthesis of Organotin Compounds, Part 2: Reactions between Alkyl Halides and Metallic Tin." Catalysis in Industry 13, no. 4 (October 2021): 337–51. http://dx.doi.org/10.1134/s2070050421040127.
Повний текст джерелаWhittleton, Sarah R., Russell J. Boyd, and T. Bruce Grindley. "Homolytic bond-dissociation enthalpies of tin bonds and tin–ligand bond strengths — A computational study." Canadian Journal of Chemistry 87, no. 7 (July 2009): 974–83. http://dx.doi.org/10.1139/v09-033.
Повний текст джерелаHolmes, Robert R., Charles G. Schmid, V. Chandrasekhar, Roberta O. Day, and Joan M. Holmes. "Oxo carboxylate tin ladder clusters. A new structural class of organotin compounds." Journal of the American Chemical Society 109, no. 5 (March 1987): 1408–14. http://dx.doi.org/10.1021/ja00239a022.
Повний текст джерелаGiese, Bernd. "Syntheses with Radicals?C?C Bond Formation via Organotin and Organomercury Compounds [New Synthetic Methods (52)]." Angewandte Chemie International Edition in English 24, no. 7 (June 1985): 553–65. http://dx.doi.org/10.1002/anie.198505531.
Повний текст джерелаJanzen, Michael C., Michael C. Jennings, and Richard J. Puddephatt. "Self-assembly using stannylplatinum(IV) halide complexes as ligands for organotin halides." Canadian Journal of Chemistry 80, no. 11 (November 1, 2002): 1451–57. http://dx.doi.org/10.1139/v02-093.
Повний текст джерелаCelesia, Adriana, Ornella Morana, Tiziana Fiore, Claudia Pellerito, Antonella D’Anneo, Marianna Lauricella, Daniela Carlisi, et al. "ROS-Dependent ER Stress and Autophagy Mediate the Anti-Tumor Effects of Tributyltin (IV) Ferulate in Colon Cancer Cells." International Journal of Molecular Sciences 21, no. 21 (October 30, 2020): 8135. http://dx.doi.org/10.3390/ijms21218135.
Повний текст джерелаCorey, E. J., and Jonathan C. Walker. "Organoiron-mediated oxygenation of allylic organotin compounds. A possible chemical model for enzymatic lipoxygenation." Journal of the American Chemical Society 109, no. 26 (December 1987): 8108–9. http://dx.doi.org/10.1021/ja00260a039.
Повний текст джерелаFish, Richard H. "A Bioorganometallic Chemistry Overview: From Cytochrome P450 Enzyme Metabolism of Organotin Compounds to Organorhodium-Hydroxytamoxifen Complexes with Potential Anti-Cancer Properties; A 37 Year Perspective at the Interface of Organometallic Chemistry and Biology." Australian Journal of Chemistry 63, no. 11 (2010): 1505. http://dx.doi.org/10.1071/ch10239.
Повний текст джерелаHerrmann, Wolfgang A., Josef K. Felixberger, Eberhardt Herdtweck, Adolf Schäfer та Jun Okuda. "Concerning the Role of Organotin Compounds in Olefin Metathesis: Synthesis, Structure, and Lewis Acidity of[(η5-C5Me5)CH3ReCl3]". Angewandte Chemie International Edition in English 26, № 5 (травень 1987): 466–67. http://dx.doi.org/10.1002/anie.198704661.
Повний текст джерелаAntonenko, Taisiya A., Yulia A. Gracheva, Dmitry B. Shpakovsky, Mstislav A. Vorobyev, Dmitrii M. Mazur, Victor A. Tafeenko, Yury F. Oprunenko, et al. "Biological Activity of Novel Organotin Compounds with a Schiff Base Containing an Antioxidant Fragment." International Journal of Molecular Sciences 24, no. 3 (January 19, 2023): 2024. http://dx.doi.org/10.3390/ijms24032024.
Повний текст джерелаLouie, Janis, and John F. Hartwig. "Transmetalation, Involving Organotin Aryl, Thiolate, and Amide Compounds. An Unusual Type of Dissociative Ligand Substitution Reaction." Journal of the American Chemical Society 117, no. 46 (November 1995): 11598–99. http://dx.doi.org/10.1021/ja00151a033.
Повний текст джерелаFan, Binbin, Hongyu Li, Weibin Fan, Jilong Zhang, and Ruifeng Li. "Organotin compounds immobilized on mesoporous silicas as heterogeneous catalysts for direct synthesis of dimethyl carbonate from methanol and carbon dioxide." Applied Catalysis A: General 372, no. 1 (January 5, 2010): 94–102. http://dx.doi.org/10.1016/j.apcata.2009.10.022.
Повний текст джерелаTarasov, D. N., R. P. Tiger, Yu N. Chirkov, S. G. Entelis, and J. J. Tondeur. "Molecular organization of reactants in the kinetics and catalysis of liquid phase reactions: X. Synergism in the combined catalysis of urethane formation by organotin compounds and tertiary amines." Kinetics and Catalysis 41, no. 3 (May 2000): 355–58. http://dx.doi.org/10.1007/bf02755372.
Повний текст джерелаBerrones-Reyes, Jessica C., Blanca M. Muñoz-Flores, Abigail Molina-Paredes, Marisol Ibarra Rodríguez, Alejandro Rodríguez-Ortega, H. V. Rasika Dias, and Víctor M. Jiménez-Pérez. "Fluorescent organotin compounds as dyes in silk fibroin (Bombyx mori): ultrasound-assisted synthesis, chemo-optical characterization, cytotoxicity, and confocal fluorescence microscopy." New Journal of Chemistry 43, no. 13 (2019): 5150–58. http://dx.doi.org/10.1039/c8nj05248d.
Повний текст джерелаSwamy, K. C. Kumara, Charles G. Schmid, Roberta O. Day, and Robert R. Holmes. "Organotin clusters. 5. Crown and extended organooxotin compounds formed with phosphinate ligands. A new class of tetranuclear tin clusters." Journal of the American Chemical Society 110, no. 21 (October 1988): 7067–76. http://dx.doi.org/10.1021/ja00229a020.
Повний текст джерелаDrake, John E., and Jincai Yang. "Synthesis, spectroscopic characterization and structural studies of organotin monothiocarbonates. Crystal structures of Ph3Sn[SCO2Me] and Ph3Sn[SCO2(i-Pr)]." Canadian Journal of Chemistry 78, no. 9 (September 1, 2000): 1214–21. http://dx.doi.org/10.1139/v00-116.
Повний текст джерелаHalvagar, Mohammad Reza, Zohreh Hassanzadeh Fard, and Stefanie Dehnen. "Directed derivatization of organotin sulfide compounds: synthesis and self-assembly of an SnS backpack-like cage and a CuSnS ternary cluster." Chemical Communications 46, no. 26 (2010): 4716. http://dx.doi.org/10.1039/c0cc00889c.
Повний текст джерелаWahba, Haytham M., Michael J. Stevenson, Ahmed Mansour, Jurgen Sygusch, Dean E. Wilcox, and James G. Omichinski. "Structural and Biochemical Characterization of Organotin and Organolead Compounds Binding to the Organomercurial Lyase MerB Provide New Insights into Its Mechanism of Carbon–Metal Bond Cleavage." Journal of the American Chemical Society 139, no. 2 (January 3, 2017): 910–21. http://dx.doi.org/10.1021/jacs.6b11327.
Повний текст джерелаStamenkovic, Jakov, Suzana Cakic, and Goran Nikolic. "Study of the catalytic selectivity of an aqueous two-component polyurethane system by ftir spectroscopy." Chemical Industry 57, no. 11 (2003): 559–62. http://dx.doi.org/10.2298/hemind0311559s.
Повний текст джерелаStorozhenko, P. A., K. D. Magdeev, A. A. Grachev, and V. I. Shiryaev. "Catalysts in the Direct Synthesis of Organotin Compounds. III. Reactions of Carbofunctional Organohalogenides with Metallic Tin." Kataliz v promyshlennosti 21, no. 6 (November 23, 2021): 382–91. http://dx.doi.org/10.18412/1816-0387-2021-6-382-391.
Повний текст джерелаMitchell, Terence N. "Palladium-Catalysed Reactions of Organotin Compounds." Synthesis 1992, no. 09 (1992): 803–15. http://dx.doi.org/10.1055/s-1992-26230.
Повний текст джерелаStorozhenko, P. A., K. D. Magdeev, A. A. Grachev, and V. I. Shiryaev. "Catalysts in the direct synthesis of organotin compounds. I. Reactions of organic halogenides with tin alloys." Kataliz v promyshlennosti 1, no. 1-2 (March 18, 2021): 16–29. http://dx.doi.org/10.18412/1816-0387-2021-1-2-16-29.
Повний текст джерелаSuzuki, Toshimitsu, Toshihiro Ando, Osamu Yamada, and Yoshihisa Watanabe. "Hydroliquefaction of Yallourn coal catalysed by organotin compounds." Fuel 65, no. 6 (June 1986): 786–89. http://dx.doi.org/10.1016/0016-2361(86)90070-0.
Повний текст джерелаHobbs, L. A., and P. J. Smith. "Mono-organotin(IV) compounds as esterification and transesterification catalysts." Applied Organometallic Chemistry 6, no. 1 (February 1992): 95–100. http://dx.doi.org/10.1002/aoc.590060112.
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