Literatura académica sobre el tema "Organic synthesis, Catalysis, and methodology development"
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Artículos de revistas sobre el tema "Organic synthesis, Catalysis, and methodology development"
De Vreese, Rob y Matthias D’hooghe. "N-Heterocyclic carbene/Brønsted acid cooperative catalysis as a powerful tool in organic synthesis". Beilstein Journal of Organic Chemistry 8 (14 de marzo de 2012): 398–402. http://dx.doi.org/10.3762/bjoc.8.43.
Texto completoDzieszkowski, Krzysztof y Zbigniew Rafiński. "N-Heterocyclic Carbene Catalysis under Oxidizing Conditions". Catalysts 8, n.º 11 (16 de noviembre de 2018): 549. http://dx.doi.org/10.3390/catal8110549.
Texto completoLübken, Dennis, Marius Saxarra y Markus Kalesse. "Tris(acetylacetonato) Iron(III): Recent Developments and Synthetic Applications". Synthesis 51, n.º 01 (27 de noviembre de 2018): 161–77. http://dx.doi.org/10.1055/s-0037-1610393.
Texto completoBiswas, Swapan Kumar. "Recent development of Silver-catalyzed Oxo- and Aza cyclization". International Journal of Experimental Research and Review 26 (30 de diciembre de 2021): 90–98. http://dx.doi.org/10.52756/ijerr.2021.v26.007.
Texto completoKoskinen, Ari M. P. "Chirospecific synthesis: Catalysis and chiral pool hand in hand". Pure and Applied Chemistry 83, n.º 3 (16 de enero de 2011): 435–43. http://dx.doi.org/10.1351/pac-con-10-10-09.
Texto completoYeung, Ying-Yeung. "Cluster Preface: Organosulfur and Organoselenium Compounds in Catalysis". Synlett 30, n.º 14 (19 de agosto de 2019): 1643–45. http://dx.doi.org/10.1055/s-0039-1690021.
Texto completoCortón, Pablo, Paula Novo, Vanesa López-Sobrado, Marcos D. García, Carlos Peinador y Elena Pazos. "Solid-Phase Zincke Reaction for the Synthesis of Peptide-4,4′-bipyridinium Conjugates". Synthesis 52, n.º 04 (30 de julio de 2019): 537–43. http://dx.doi.org/10.1055/s-0039-1690016.
Texto completoKim, Nari, Calvin C. H. Cheng y M. Cynthia Goh. "Universal aqueous synthesis of ultra-small polymer-templated nanoparticles: synthesis optimization methodology for counterion-collapsed poly(acrylic acid)". Canadian Journal of Chemistry 96, n.º 1 (enero de 2018): 44–50. http://dx.doi.org/10.1139/cjc-2017-0444.
Texto completoFeng, Liang, Kun-Yu Wang, Xiu-Liang Lv, Tian-Hao Yan y Hong-Cai Zhou. "Hierarchically porous metal–organic frameworks: synthetic strategies and applications". National Science Review 7, n.º 11 (5 de noviembre de 2019): 1743–58. http://dx.doi.org/10.1093/nsr/nwz170.
Texto completoScheffer, John R. "2000 Alfred Bader Award LectureIn the footsteps of Pasteur: asymmetric induction in the photochemistry of crystalline ammonium carboxylate salts". Canadian Journal of Chemistry 79, n.º 4 (1 de abril de 2001): 349–57. http://dx.doi.org/10.1139/v01-060.
Texto completoTesis sobre el tema "Organic synthesis, Catalysis, and methodology development"
Birrell, James Andrew. "I. Enantioselective Acylation of Silyl Ketene Acetals through Fluoride Anion-Binding Catalysis II. Development of a Practical Method for the Synthesis of Highly Enantioenriched Trans-1,2-Amino Alcohols". Thesis, Harvard University, 2013. http://dissertations.umi.com/gsas.harvard:11037.
Texto completoChemistry and Chemical Biology
Chen, Andrew. "New Radical Reactivity at the Interface of Synthetic Methodology Development and Computational Modeling". The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1593586492097279.
Texto completoPerego, Luca Alessandro. "Transition metal-catalyzed reactions : mechanistic studies and methodology developments". Thesis, Paris Sciences et Lettres (ComUE), 2018. http://www.theses.fr/2018PSLEE003/document.
Texto completoIn this thesis, the mechanism of three organic reactions catalyzed by palladium and copper complexes has been elucidated by the use of both experimental and theoretical methods. The first reaction is the synthesis of amides from haloarenes, isocyanides and water as an example of the broad family of palladium-catalyzed imidoylative couplings. Multiple roles of the isocyanide as both a ligand and a substrate in the different steps of the catalytic cycle have been disclosed. The second transformation is the palladium-catalyzed ring opening of benzofurans leading to indoles. Optimal conditions for this transformation have been found and the key aspects of its mechanism clarified. The last reaction, which is the main topic of this thesis, is the addition of amines to allenes catalyzed by copper salts (hydroamination). A characterization of the catalytically active copper(I) species and insight from theoretical calculations suggested how to extend this reaction to other substrates (allenamides, N-allenylazoles, N-allenylsulfonamides) under mild and efficient conditions
Aparece, Mark Docto. "Synthesis of Organoboron Compounds via a Palladium-Induced 1,2-Metallate Shift Mechanism:". Thesis, Boston College, 2020. http://hdl.handle.net/2345/bc-ir:108927.
Texto completoThis dissertation describes the development of various palladium-catalyzed syntheses of organoboron compounds with the 1,2-metallate shift of organoboron “ate” complexes as a common mechanistic feature. Chapter one discusses the history of the 1,2-metallate shift with a focus on reactions promoted by transition metals, followed by my work on the palladium-catalyzed, enantioselective, halide-tolerant conjunctive cross-coupling reaction to enable the use of Grignard reagents and arylbromides. Chapter two discusses the attempt to engage allylic electrophiles in the conjunctive cross-coupling reaction and the discovery and optimization of the vinylidenation reaction to access 1,1-disubstituted boryl alkenes. Unlike other palladium-catalyzed reactions that proceed by a 1,2-metallate shift, the vinylidenation proceeds by a β-hydride elimination rather than a reductive elimination as the final step in the catalytic cycle. Chapter three discusses the development of the enantioselective conjunctive cross-coupling of propargylic electrophiles to access enantioenriched β-boryl allenes. Methanol additive was found to improve both the yield and enantioselectivity of the reaction. 1H NMR studies show that methanol exchanges with the pinacol ligand on the boron “ate” complex
Thesis (PhD) — Boston College, 2020
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Lamb, Alan David. "Asymmetric synthesis of heterocycles via cation-directed cyclizations and rearrangements". Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:4c0cf06c-d461-42a4-b4d8-a2a2bd961435.
Texto completoBrogan, Samantha. "Development of new methodology for the synthesis of fluorine-containing compounds". Thesis, University of Edinburgh, 2013. http://hdl.handle.net/1842/7887.
Texto completoKarim, Rehana. "Development of radical synthetic methodology using solid-phase organic synthesis". Thesis, Loughborough University, 2003. https://dspace.lboro.ac.uk/2134/34406.
Texto completoEmmett, Edward J. "Development of catalytic methods to exploit sulfur dioxide in organic synthesis". Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:be60729b-5467-4758-8d88-9dff3a2d5810.
Texto completoXu, Chongsong. "Development of functionalized spiroligomers for metal-binding and asymmetric catalysis". Diss., Temple University Libraries, 2019. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/595512.
Texto completoPh.D.
This thesis describes the synthesis of functionalized spiroligomers and their applications in metal binding, metal-mediated catalysis, and organocatalysis. By synthesizing a family of functionalized bis-amino acids achieved from reductive alkylation, the Schafmeister group has developed access to highly functionalized and shape programmable structures named “spiroligomers.” The rigid backbones of spiroligomers are good at organizing the orientations of functional groups on their side chains. This property enables them as promising candidates for catalysts. Firstly we synthesized a few spiroligomer dimers presenting metal-binding groups such as terpys and bipys. With the right orientation of metal binding groups controlled by adjusting the stereocenter of the spiroligomer, macrocyclic “square” complexes with metals were obtained. The crystal structures of these intriguing complexes were solved. This work rendered the first structurally, spectroscopically and electronically characterized metal-spiroligomer complexes as well as the first crystal structure of spiroligomer. Secondly, the question of whether metal-binding spiroligomers are able to catalyze certain reactions became our major concern. We developed a binuclear copper catalyst that could accelerate a phosphate ester rearrangement, and that demonstrated that when the two copper binding terpyridine groups were best able to approach each other, they accelerated the rearrangement more than 1,000 times faster than the background reaction. Other molecules that did not properly organize the two copper atoms demonstrate considerably slower reaction rates. At last, catalysts based on spiroligomers without metals are also of interests. By displaying two hydrophobic groups in various directions on a monomeric spiroligomer (also can be regarded as a proline derivative), we observed variable activities and enantioselectivities in the catalysis of asymmetric Michael addition (up to 94% ee at -40 °C for one organocatalyst).
Temple University--Theses
Stevens, Kiri. "Methodology for the synthesis of NP25302 and other bioactive natural products". Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:ae18879e-d75e-4280-ba55-1ae08e64034f.
Texto completoLibros sobre el tema "Organic synthesis, Catalysis, and methodology development"
Development Of Novel Hydrogenbond Donor Catalysts. Springer Verlag, Japan, 2012.
Buscar texto completoInokuma, Tsubasa. Development of Novel Hydrogen-Bond Donor Catalysts. Springer London, Limited, 2013.
Buscar texto completoInokuma, Tsubasa. Development of Novel Hydrogen-Bond Donor Catalysts. Springer, 2013.
Buscar texto completoInokuma, Tsubasa. Development of Novel Hydrogen-Bond Donor Catalysts. Springer, 2015.
Buscar texto completoDavis, Fred J., ed. Polymer Chemistry. Oxford University Press, 2004. http://dx.doi.org/10.1093/oso/9780198503095.001.0001.
Texto completoSkiba, Grzegorz. Fizjologiczne, żywieniowe i genetyczne uwarunkowania właściwości kości rosnących świń. The Kielanowski Institute of Animal Physiology and Nutrition, Polish Academy of Sciences, 2020. http://dx.doi.org/10.22358/mono_gs_2020.
Texto completoCapítulos de libros sobre el tema "Organic synthesis, Catalysis, and methodology development"
Hargaden, Gráinne C. y Patrick J. Guiry. "Development of the Asymmetric Nozaki-Hiyama-Kishi Reaction". En Innovative Catalysis in Organic Synthesis, 279–307. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527646586.ch13.
Texto completoDoraiswamy, L. K. "Homogeneous Catalysis". En Organic Synthesis Engineering. Oxford University Press, 2001. http://dx.doi.org/10.1093/oso/9780195096897.003.0014.
Texto completoHartwig, John. "Design and Serendipity in the Discovery and Development of Homogeneous Catalysts for Organic Synthesis". En Catalysis of Organic Reactions, 15–21. CRC Press, 2008. http://dx.doi.org/10.1201/9781420070774.ch2.
Texto completoTellis, J. C. "1.2.1 General Principles of Transition-Metal/Photocatalyst Dual Catalysis". En Dual Catalysis in Organic Synthesis 1. Stuttgart: Georg Thieme Verlag, 2020. http://dx.doi.org/10.1055/sos-sd-231-00087.
Texto completoTheodorakis, Emmanuel A., Taotao Ling, Eric J. Rueden, Erwan Poupon y Sun Hee Kim. "Chapter 4 Quinone sesquiterpenes: A challenge for the development of a new synthetic methodology". En Strategies and Tactics in Organic Synthesis, 111–31. Elsevier, 2004. http://dx.doi.org/10.1016/s1874-6004(04)80027-3.
Texto completoBenkoski, Léa y Tristan H. Lambert. "Construction of Multiple Stereocenters". En Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0039.
Texto completoTaber, Douglass F. "Preparation of Heterocycles: The Boukouvalas Synthesis of (−)-Auxofuran". En Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0065.
Texto completoDoraiswamy, L. K. "Membrane-Assisted Reactor Engineering". En Organic Synthesis Engineering. Oxford University Press, 2001. http://dx.doi.org/10.1093/oso/9780195096897.003.0033.
Texto completoRoush, William R. "Evolution of a Strategy for the Synthesis of Olivomycin a: Development of Methodology for the Diastereo- and Enantioselective Synthesis of Carbohydrates from Acyclic Precursors". En Strategies and Tactics in Organic Synthesis, 323–67. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-092429-8.50015-5.
Texto completoPatel, Helina y Akshaya Gupte. "Laccase Catalysis". En Biotechnology, 2054–89. IGI Global, 2019. http://dx.doi.org/10.4018/978-1-5225-8903-7.ch084.
Texto completoActas de conferencias sobre el tema "Organic synthesis, Catalysis, and methodology development"
Ma, Dawei. "Target Synthesis Directed Methodology Development". En 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-speech6.
Texto completoCaixeta, Vanessa y Ulrika Westerlind. "Development of Methodology for Glycopeptide Enrichment". En 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20138512588.
Texto completoContreras-Navarrete, José de Jesús, Francisco Gabriel Granados-Martínez, Alejandro Durán-Navarro, Lada Domratcheva-Lvova, Nelly Flores-Ramírez, Carmen Judith Gutiérrez-García, Omar Aguilar-García y María de Lourdes Mondragón Sánchez. "Taguchi Experimental Design in Carbon Nanomaterials Synthesis". En ASME 2016 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/imece2016-65731.
Texto completoTioni, Estevan y Pascal Rousseaux. "BRINGING TOGETHER MICROWAVE ASSISTED SYNTHESIS AND CHEMICAL ENGINEERING PRINCIPLES". En Ampere 2019. Valencia: Universitat Politècnica de València, 2019. http://dx.doi.org/10.4995/ampere2019.2019.9901.
Texto completoСтарожилов, В. Т. "ZONING AND STRUCTURAL ORGANIZATION OF ORGANIC LANDSCAPE AREAS OF THE PACIFIC LANDSCAPE BELT OF RUSSIA". En Геосистемы Северо-Восточной Азии. Crossref, 2021. http://dx.doi.org/10.35735/tig.2021.17.72.023.
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