Статті в журналах з теми "Hydroformylation of Alkenes"
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Shi, Yukun, Yang Lu, Tongxin Ren, Jie Li, Qiqige Hu, Xiaojing Hu, Baolin Zhu, and Weiping Huang. "Rh Particles Supported on Sulfated g-C3N4: A Highly Efficient and Recyclable Heterogeneous Catalyst for Alkene Hydroformylation." Catalysts 10, no. 11 (November 23, 2020): 1359. http://dx.doi.org/10.3390/catal10111359.
Повний текст джерелаDoyle, MM, WR Jackson, and P. Perlmutter. "The Stereochemistry of Organometallic Compounds. XXXIV. Regioselection in the Hydroformylation of Silylalkenes." Australian Journal of Chemistry 42, no. 11 (1989): 1907. http://dx.doi.org/10.1071/ch9891907.
Повний текст джерелаHood, Drew M., Ryan A. Johnson, Alex E. Carpenter, Jarod M. Younker, David J. Vinyard, and George G. Stanley. "Highly active cationic cobalt(II) hydroformylation catalysts." Science 367, no. 6477 (January 30, 2020): 542–48. http://dx.doi.org/10.1126/science.aaw7742.
Повний текст джерелаYu, Xuetong, Yuxia Ji, Yan Jiang, Rui Lang, Yanxiong Fang, and Botao Qiao. "Recent Development of Single-Atom Catalysis for the Functionalization of Alkenes." Catalysts 13, no. 4 (April 12, 2023): 730. http://dx.doi.org/10.3390/catal13040730.
Повний текст джерелаGeng, Hui-Qing, Tim Meyer, Robert Franke, and Xiao-Feng Wu. "Copper-catalyzed hydroformylation and hydroxymethylation of styrenes." Chemical Science 12, no. 44 (2021): 14937–43. http://dx.doi.org/10.1039/d1sc05474k.
Повний текст джерелаPeral, Daniel, Daniel Herrera, Julio Real, Teresa Flor та J. Carles Bayón. "Strong π-acceptor sulfonated phosphines in biphasic rhodium-catalyzed hydroformylation of polar alkenes". Catalysis Science & Technology 6, № 3 (2016): 800–808. http://dx.doi.org/10.1039/c5cy01004g.
Повний текст джерелаChevry, M., T. Vanbésien, S. Menuel, E. Monflier, and F. Hapiot. "Tetronics/cyclodextrin-based hydrogels as catalyst-containing media for the hydroformylation of higher olefins." Catalysis Science & Technology 7, no. 1 (2017): 114–23. http://dx.doi.org/10.1039/c6cy02070d.
Повний текст джерелаShi, Yukun, Gang Ji, Qiqige Hu, Yang Lu, Xiaojing Hu, Baolin Zhu, and Weiping Huang. "Highly uniform Rh nanoparticles supported on boron doped g-C3N4 as a highly efficient and recyclable catalyst for heterogeneous hydroformylation of alkenes." New Journal of Chemistry 44, no. 1 (2020): 20–23. http://dx.doi.org/10.1039/c9nj05385a.
Повний текст джерелаWu, Lipeng, Qiang Liu, Anke Spannenberg, Ralf Jackstell, and Matthias Beller. "Highly regioselective osmium-catalyzed hydroformylation." Chemical Communications 51, no. 15 (2015): 3080–82. http://dx.doi.org/10.1039/c4cc05626d.
Повний текст джерелаNandakumar, Avanashiappan, Manoj K. Sahoo, and Ekambaram Balaraman. "Reverse-hydroformylation: a missing reaction explored." Organic Chemistry Frontiers 2, no. 10 (2015): 1422–24. http://dx.doi.org/10.1039/c5qo00229j.
Повний текст джерелаKrupčík, Ján, and Dušan Repka. "Analysis of hydroformylation products of higher n-alkenes by capillary gas chromatography." Collection of Czechoslovak Chemical Communications 50, no. 8 (1985): 1808–18. http://dx.doi.org/10.1135/cccc19851808.
Повний текст джерелаTerhorst, M., C. Plass, A. Hinzmann, A. Guntermann, T. Jolmes, J. Rösler, D. Panke, et al. "One-pot synthesis of aldoximes from alkenes via Rh-catalysed hydroformylation in an aqueous solvent system." Green Chemistry 22, no. 22 (2020): 7974–82. http://dx.doi.org/10.1039/d0gc03141k.
Повний текст джерелаBibouche, Bachir, Daniel Peral, Dmitrij Stehl, Viktor Söderholm, Reinhard Schomäcker, Regine von Klitzing, and Dieter Vogt. "Multiphasic aqueous hydroformylation of 1-alkenes with micelle-like polymer particles as phase transfer agents." RSC Advances 8, no. 41 (2018): 23332–38. http://dx.doi.org/10.1039/c8ra04022b.
Повний текст джерелаKämper, Alexander, Peter Kucmierczyk, Thomas Seidensticker, Andreas J. Vorholt, Robert Franke, and Arno Behr. "Ruthenium-catalyzed hydroformylation: from laboratory to continuous miniplant scale." Catalysis Science & Technology 6, no. 22 (2016): 8072–79. http://dx.doi.org/10.1039/c6cy01374k.
Повний текст джерелаImam, Hasan T., Amanda G. Jarvis, Veronica Celorrio, Irshad Baig, Christopher C. R. Allen, Andrew C. Marr, and Paul C. J. Kamer. "Catalytic and biophysical investigation of rhodium hydroformylase." Catalysis Science & Technology 9, no. 22 (2019): 6428–37. http://dx.doi.org/10.1039/c9cy01679a.
Повний текст джерелаLiu, Yan-li, Jian-gui Zhao, Yuan-jiang Zhao, Hui-Min Liu, Hai-yan Fu, Xue-li Zheng, Mao-lin Yuan, Rui-xiang Li, and Hua Chen. "Homogeneous hydroformylation of long chain alkenes catalyzed by water soluble phosphine rhodium complex in CH3OH and efficient catalyst cycling." RSC Advances 9, no. 13 (2019): 7382–87. http://dx.doi.org/10.1039/c8ra08787c.
Повний текст джерелаTakeuchi, Ryo, and Nobuhiro Sato. "Hydroformylation of alkenes having organosilicon substituents." Journal of Organometallic Chemistry 393, no. 1 (August 1990): 1–10. http://dx.doi.org/10.1016/0022-328x(90)87193-h.
Повний текст джерелаKardasheva, Yulia, Maria Terenina, Daniil Sokolov, Natalia Sinikova, Sergey Kardashev, and Eduard Karakhanov. "Hydroformylation of Alkenes over Phosphorous-Free Rhodium Supported on N-Doped Silica." Catalysts 13, no. 5 (April 28, 2023): 818. http://dx.doi.org/10.3390/catal13050818.
Повний текст джерелаZhang, Yang, Michel Sigrist, and Paweł Dydio. "Palladium‐Catalyzed Hydroformylation of Alkenes and Alkynes." European Journal of Organic Chemistry 2021, no. 44 (October 19, 2021): 5985–97. http://dx.doi.org/10.1002/ejoc.202101020.
Повний текст джерелаReek, J., M. Kuil, T. Soltner, and P. van Leeuwen. "Hydroformylation of Internal Alkenes by Encapsulated Rhodium." Synfacts 2006, no. 12 (December 2006): 1262. http://dx.doi.org/10.1055/s-2006-949501.
Повний текст джерелаSharma, Sumeet K., and Raksh V. Jasra. "Aqueous phase catalytic hydroformylation reactions of alkenes." Catalysis Today 247 (June 2015): 70–81. http://dx.doi.org/10.1016/j.cattod.2014.07.059.
Повний текст джерелаCocq, Aurélien, Hervé Bricout, Florence Djedaïni-Pilard, Sébastien Tilloy, and Eric Monflier. "Rhodium-Catalyzed Aqueous Biphasic Olefin Hydroformylation Promoted by Amphiphilic Cyclodextrins." Catalysts 10, no. 1 (January 1, 2020): 56. http://dx.doi.org/10.3390/catal10010056.
Повний текст джерелаZhang, Xiaoli, Juan Wei, and Xiaoming Zhang. "Encapsulated liquid nano-droplets for efficient and selective biphasic hydroformylation of long-chain alkenes." New Journal of Chemistry 43, no. 35 (2019): 14134–38. http://dx.doi.org/10.1039/c9nj02493j.
Повний текст джерелаJackson, W. Roy, Patrick Parlmutter, and Guem-Hee Suh. "Chelation control in the hydroformylation of terminal alkenes." Journal of the Chemical Society, Chemical Communications, no. 10 (1987): 724. http://dx.doi.org/10.1039/c39870000724.
Повний текст джерелаTao, Lin, Mingmei Zhong, Jian Chen, Sanjeevi Jayakumar, Lina Liu, He Li, and Qihua Yang. "Heterogeneous hydroformylation of long-chain alkenes in IL-in-oil Pickering emulsion." Green Chemistry 20, no. 1 (2018): 188–96. http://dx.doi.org/10.1039/c7gc02574b.
Повний текст джерелаMeyer, Wolfgang H., Richard J. Bowen, and David G. Billing. "Tri(3-pyridyl)phosphine as Amphiphilic Ligand in the Rhodium-catalysed Hydroformylation of 1-Hexene." Zeitschrift für Naturforschung B 62, no. 3 (March 1, 2007): 339–45. http://dx.doi.org/10.1515/znb-2007-0306.
Повний текст джерелаBreit, Bernhard, and Wolfgang Seiche. "Self-assembly of bidentate ligands for combinatorial homogeneous catalysis based on an A-T base pair model." Pure and Applied Chemistry 78, no. 2 (January 1, 2006): 249–56. http://dx.doi.org/10.1351/pac200678020249.
Повний текст джерелаAdams, Dave J., James A. Bennett, David J. Cole-Hamilton, Eric G. Hope, Jonathan Hopewell, Jo Kight, Peter Pogorzelec, and Alison M. Stuart. "Rhodium catalysed hydroformylation of alkenes using highly fluorophilic phosphines." Dalton Transactions, no. 24 (2005): 3862. http://dx.doi.org/10.1039/b510766k.
Повний текст джерелаDesset, Simon L., Simon W. Reader, and David J. Cole-Hamilton. "Aqueous-biphasic hydroformylation of alkenes promoted by “weak” surfactants." Green Chemistry 11, no. 5 (2009): 630. http://dx.doi.org/10.1039/b822139a.
Повний текст джерелаWatkins, Avery L., Brian G. Hashiguchi, and Clark R. Landis. "Highly Enantioselective Hydroformylation of Aryl Alkenes with Diazaphospholane Ligands." Organic Letters 10, no. 20 (October 16, 2008): 4553–56. http://dx.doi.org/10.1021/ol801723a.
Повний текст джерелаTominaga, Ken-ichi, and Yoshiyuki Sasaki. "Ruthenium complex-catalyzed hydroformylation of alkenes with carbon dioxide." Catalysis Communications 1, no. 1-4 (November 2000): 1–3. http://dx.doi.org/10.1016/s1566-7367(00)00006-6.
Повний текст джерелаAchonduh, George, Qian Yang, and Howard Alper. "From alkenes to alcohols by cobalt-catalyzed hydroformylation–reduction." Tetrahedron 71, no. 8 (February 2015): 1241–46. http://dx.doi.org/10.1016/j.tet.2015.01.006.
Повний текст джерелаMacDougall, Joanna K., and David J. Cole-Hamilton. "Alcohols as sources of hydrogen in hydroformylation of alkenes." Polyhedron 9, no. 9 (January 1990): 1235–36. http://dx.doi.org/10.1016/s0277-5387(00)86901-6.
Повний текст джерелаWebb, Paul B., Thulani E. Kunene, and David J. Cole-Hamilton. "Continuous flow homogeneous hydroformylation of alkenes using supercritical fluids." Green Chemistry 7, no. 5 (2005): 373. http://dx.doi.org/10.1039/b416713a.
Повний текст джерелаMurzin, Dmitry Yu, Andreas Bernas, and Tapio Salmi. "Kinetic modelling of regioselectivity in alkenes hydroformylation over rhodium." Journal of Molecular Catalysis A: Chemical 315, no. 2 (January 15, 2010): 148–54. http://dx.doi.org/10.1016/j.molcata.2009.06.023.
Повний текст джерелаSharma, Sumeet K., and Raksh V. Jasra. "ChemInform Abstract: Aqueous Phase Catalytic Hydroformylation Reactions of Alkenes." ChemInform 46, no. 21 (May 2015): no. http://dx.doi.org/10.1002/chin.201521286.
Повний текст джерелаBuhling, Armin, Paul C. J. Kamer, and Piet W. N. M. van Leeuwen. "Rhodium catalysed hydroformylation of higher alkenes using amphiphilic ligands." Journal of Molecular Catalysis A: Chemical 98, no. 2 (May 1995): 69–80. http://dx.doi.org/10.1016/1381-1169(95)00014-3.
Повний текст джерелаFuchs, Evelyn, Manfred Keller, and Bernhard Breit. "Phosphabarrelenes as Ligands in Rhodium-Catalyzed Hydroformylation of Internal Alkenes Essentially Free of Alkene Isomerization." Chemistry - A European Journal 12, no. 26 (September 6, 2006): 6930–39. http://dx.doi.org/10.1002/chem.200600180.
Повний текст джерелаDesset, Simon L., David J. Cole-Hamilton, and Douglas F. Foster. "Aqueous-biphasic hydroformylation of higher alkenes promoted by alkylimidazolium salts." Chemical Communications, no. 19 (2007): 1933. http://dx.doi.org/10.1039/b618785d.
Повний текст джерелаWildt, Julia, Anna C. Brezny, and Clark R. Landis. "Backbone-Modified Bisdiazaphospholanes for Regioselective Rhodium-Catalyzed Hydroformylation of Alkenes." Organometallics 36, no. 16 (August 16, 2017): 3142–51. http://dx.doi.org/10.1021/acs.organomet.7b00475.
Повний текст джерелаDeng, Yuchao, Hui Wang, Yuhan Sun, and Xiao Wang. "Principles and Applications of Enantioselective Hydroformylation of Terminal Disubstituted Alkenes." ACS Catalysis 5, no. 11 (October 20, 2015): 6828–37. http://dx.doi.org/10.1021/acscatal.5b01300.
Повний текст джерелаRosales, Merlin, Angel González, Beatríz González, Cristhina Moratinos, Homero Pérez, Johán Urdaneta, and Roberto A. Sánchez-Delgado. "Hydroformylation of alkenes with paraformaldehyde catalyzed by rhodium–phosphine complexes." Journal of Organometallic Chemistry 690, no. 12 (June 2005): 3095–98. http://dx.doi.org/10.1016/j.jorganchem.2005.03.032.
Повний текст джерелаYu, Zhiyong, Meredith S. Eno, Alexandra H. Annis, and James P. Morken. "Enantioselective Hydroformylation of 1-Alkenes with Commercial Ph-BPE Ligand." Organic Letters 17, no. 13 (June 19, 2015): 3264–67. http://dx.doi.org/10.1021/acs.orglett.5b01421.
Повний текст джерелаPolas, Anastasios, James D. E. T. Wilton-Ely, Alexandra M. Z. Slawin, Douglas F. Foster, Petrus J. Steynberg, Michael J. Green, and David J. Cole-Hamilton. "Limonene-derived phosphines in the cobalt-catalysed hydroformylation of alkenes." Dalton Transactions, no. 24 (2003): 4669. http://dx.doi.org/10.1039/b310233e.
Повний текст джерелаPedrós, Marta Giménez, Anna M. Masdeu-Bultó, Jerome Bayardon, and Denis Sinou. "Hydroformylation of Alkenes with Rhodium Catalyst in Supercritical Carbon Dioxide." Catalysis Letters 107, no. 3-4 (March 2006): 205–8. http://dx.doi.org/10.1007/s10562-005-0005-7.
Повний текст джерелаYamane, Motoki, Noriaki Yukimura, Hiroshi Ishiai, and Koichi Narasaka. "Hydroformylation of Monosubstituted Alkenes Catalyzed by W–Rh Bimetallic Complex." Chemistry Letters 35, no. 5 (May 2006): 540–41. http://dx.doi.org/10.1246/cl.2006.540.
Повний текст джерелаKamer, Paul C. J., Annemiek van Rooy, Gerard C. Schoemaker, and Piet W. N. M. van Leeuwen. "In situ mechanistic studies in rhodium catalyzed hydroformylation of alkenes." Coordination Chemistry Reviews 248, no. 21-24 (December 2004): 2409–24. http://dx.doi.org/10.1016/j.ccr.2004.06.006.
Повний текст джерелаIllesinghe, Jayamini, Eva M. Campi, W. Roy Jackson, and Andrea J. Robinson. "Synthesis of Nitrogen Heterocycles by Rhodium-Catalyzed Hydroformylation of Polymer-Attached Amino Alkenes with Syngas." Australian Journal of Chemistry 57, no. 6 (2004): 531. http://dx.doi.org/10.1071/ch03269.
Повний текст джерелаObrecht, Lorenz, Paul C. J. Kamer, and Wouter Laan. "Alternative approaches for the aqueous–organic biphasic hydroformylation of higher alkenes." Catal. Sci. Technol. 3, no. 3 (2013): 541–51. http://dx.doi.org/10.1039/c2cy20538f.
Повний текст джерелаDingwall, Paul, José A. Fuentes, Luke Crawford, Alexandra M. Z. Slawin, Michael Bühl, and Matthew L. Clarke. "Understanding a Hydroformylation Catalyst that Produces Branched Aldehydes from Alkyl Alkenes." Journal of the American Chemical Society 139, no. 44 (October 25, 2017): 15921–32. http://dx.doi.org/10.1021/jacs.7b09164.
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