Добірка наукової літератури з теми "Hydroformylation of Alkenes"
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Статті в журналах з теми "Hydroformylation of Alkenes"
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 джерелаДисертації з теми "Hydroformylation of Alkenes"
Iu, Leo. "New catalysts for branched selective hydroformylation of alkenes." Thesis, University of St Andrews, 2019. http://hdl.handle.net/10023/17068.
Повний текст джерелаOsuna, Anna Maria Banet. "Hydroformylation of higher and functionalised alkenes in supercritical carbon dioxide." Thesis, University of Liverpool, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343988.
Повний текст джерелаAnnis, Alexandra H. "The Development of Rhodium-Catalyzed Asymmetric Hydroformylation of 1-Alkenes to Access Chiral Aldehydes." Thesis, Boston College, 2015. http://hdl.handle.net/2345/bc-ir:104636.
Повний текст джерелаAsymmetric hydroformylation (AHF) is a metal-catalyzed reaction in which CO and H2 are added across an olefin to form a new carbon-carbon bond. AHF has perfect atom-economy and is an ideal way to form a chiral aldehyde. However, the utility of branch selective hydroformylation is limited due to a lack of readily available ligands and restrictions on a wide variety of terminal olefins. Herein, Rh-catalyzed asymmetric hydroformylation of 1-alkenes is reported using commercially available Ph-BPE ligand to generate α-chiral aldehydes. A wide range of terminal olefins were explored and all showed high enantioselectivity (up to 98:2 er) and good regioselectivity (up to 15:1 branched to linear ratio)
Thesis (MS) — Boston College, 2015
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Desset, Simon L. "New strategies for the rhodium-catalysed aqeous-biphasic hydroformylation of medium chain alkenes /." St Andrews, 2009. http://hdl.handle.net/10023/842.
Повний текст джерелаDesset, Simon L. "New strategies for the rhodium-catalysed aqueous-biphasic hydroformylation of medium chain alkenes." Thesis, University of St Andrews, 2009. http://hdl.handle.net/10023/842.
Повний текст джерелаGong, Zhenxin. "Continuous flow homogeneous hydroformylation of 1-octene over supported ionic liquid phase rhodium catalysts using supercritical CO₂." Thesis, University of St Andrews, 2011. http://hdl.handle.net/10023/1877.
Повний текст джерелаBronger, Raymond Petrus Johannes. "Selective hydroformylation of internal alkenes to linear aldehydes novel phosphacyclic diphosphines and their applications /." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2004. http://dare.uva.nl/document/75911.
Повний текст джерелаSun, Xixi. "Scaffolding Catalysis: Towards Regioselective Hydroformylation of Alkenes and Site-Selective Functionalization of Polyhydroxylated Molecules." Thesis, Boston College, 2013. http://hdl.handle.net/2345/3324.
Повний текст джерелаChapter 1. We reported the first synthesis of all-carbon quaternary centers via hydroformylations using a catalytic directing group. With the ability of reversibly and covalently binding to a substrate, and coordinating to a metal center, scaffolding catalyst 1.1 is able to direct the branch-selective hydroformylation of 1,1-disubstituted olefins under mild temperature. Chapter 2. We have designed and synthesized a chiral organocatalyst 2.11. This catalyst is able to covalently bind to one hydroxyl, and utilize the induced intramolecularity to stereoselectively functionalize the other hydroxyl within a cis-1,2-diol via electrophile transfer. Catalyst 2.11 was used in the desymmetrization of meso-1,2-diols under mild conditions (4 C to room temperature), leading to high yields and selectivities for a broad substrate scope. Chapter 3. Catalyst 3.1 and 3.6 were demonstrated to selectively bind to primary hydroxyls over secondary hydroxyls. By combining the binding selectivity with asymmetric catalysis, these scaffolding catalysts were shown to promote the selective silylation of secondary hydroxyls within terminal (S)-1,2-diols. The reversal of substrate bias was further applied to a regiodivergent kinetic resolution of racemic terminal 1,2-diols, producing secondary protected products in synthetically practical levels of enantioselectivity (>95:5 er) and yields (≥40%). Time course studies of this reaction further revealed the optimal condition to form the primary silylated product in high s-factor. Chapter 4. Based on the previous understanding of catalyst 4.5 and 4.6, the exclusive catalyst recognition of cis-1,2-diols within polyhydroxylated molecules was further discovered. This unique functional group display recognition was further allied with the catalyst's ability to stereoselectively differentiate hydroxyls within cis-1,2-diols, enabling the site-selective protection, functionalization, and activation of the inherently less reactive axial hydroxyl groups within carbohydrates. This methodology also enables the selective functionalization of multiple complex molecules, including digoxin, mupirocin, and ribonucleosides, demonstrating the potential power of scaffolding catalysis in the rapid access to valuable synthetic derivatives of polyhydroxylated compounds
Thesis (PhD) — Boston College, 2013
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Guo, Ipin. "Hydroformylation of olefins by water soluble and asymmetric cobalt and platinum complexes." Diss., Virginia Tech, 1991. http://hdl.handle.net/10919/39855.
Повний текст джерелаPh. D.
Du, Toit Judith G. O. "Use of water-soluble phosphine ligands in heterogeneous hydroformylation catalysis : application to long-chain 1-alkenes." Master's thesis, University of Cape Town, 1994. http://hdl.handle.net/11427/22055.
Повний текст джерелаКниги з теми "Hydroformylation of Alkenes"
Naughton, Michael J. The hydroformylation of olefins using supported film catalysts. 1993.
Знайти повний текст джерелаЧастини книг з теми "Hydroformylation of Alkenes"
Breit, Bernhard. "Directed Rhodium-Catalyzed Hydroformylation of Alkenes." In Topics in Organometallic Chemistry, 145–68. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/3418_2007_067.
Повний текст джерелаMika, L. T., and I. T. Horváth. "Hydroformylation of Higher Alkenes." In Water in Organic Synthesis, 1. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-206-00114.
Повний текст джерелаMika, L. T., and I. T. Horváth. "Hydroformylation of Functionalized Alkenes." In Water in Organic Synthesis, 1. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-206-00115.
Повний текст джерела"Asymmetric Hydroformylation of Alkenes." In C-1 Building Blocks in Organic Synthesis 1, edited by van Leeuwen. Stuttgart: Georg Thieme Verlag, 2014. http://dx.doi.org/10.1055/sos-sd-212-00020.
Повний текст джерела"Tandem Hydroformylation of Alkenes." In C-1 Building Blocks in Organic Synthesis 1, edited by van Leeuwen. Stuttgart: Georg Thieme Verlag, 2014. http://dx.doi.org/10.1055/sos-sd-212-00055.
Повний текст джерелаTaber, Douglass. "Selective Reactions of Alkenes." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0023.
Повний текст джерелаFiaud, J. C., and A. Marinetti. "Rhodium-Promoted Hydroformylation of Alkenes." In Organophosphorus Compounds (incl. RO-P and RN-P), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-042-00505.
Повний текст джерела"Synthesis by Hydroformylation of Alkenes." In Category 4, Compounds with Two Carbon Heteroatom Bonds, edited by Brückner. Stuttgart: Georg Thieme Verlag, 2007. http://dx.doi.org/10.1055/sos-sd-025-00196.
Повний текст джерела"Hydroformylation of Alkenes: Industrial Applications." In C-1 Building Blocks in Organic Synthesis 1, edited by van Leeuwen. Stuttgart: Georg Thieme Verlag, 2014. http://dx.doi.org/10.1055/sos-sd-212-00118.
Повний текст джерелаJoule, J. A. "Variation 5: From Alkenes via Hydroformylation." In Science of Synthesis Knowledge Updates KU 2011/1, 1. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-110-00020.
Повний текст джерела