Thèses sur le sujet « Organic reaction methodology »
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Bhuiyan, Mosharef Hossain. « Synthetic organic reaction new methodology and applications ». Thesis, University of North Bengal, 2003. http://hdl.handle.net/123456789/772.
Texte intégralBiswas, Kinkar. « Development of organic reaction methodology using polymar-supported reagents, focused microwaves and on-water chemistry ». Thesis, University of North Bengal, 2016. http://ir.nbu.ac.in/handle/123456789/2745.
Texte intégralLarson, Shawn E. « Enantioselective Brønsted and Lewis Acid-Catalyzed Reaction Methodology : Aziridines as Building Blocks for Catalytic Asymmetric Induction ». Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/4357.
Texte intégralCavitt, Marchello Alfonzo. « Stress relief : Exercising Lewis acid catalysis for donor-acceptor cyclopropane ring-opening annulations, a basis for new reaction methodologies ». Diss., Georgia Institute of Technology, 2015. http://hdl.handle.net/1853/54448.
Texte intégralPelletier, Sophie Marie-Clémentine. « One-pot nitro-Mannich cascade reactions : new methodologies and synthetic applications ». Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:283641bf-bb4e-48a8-8a28-2e048b8c4ea6.
Texte intégralMartinez, Ariza Guillermo, et Ariza Guillermo Martinez. « Exploiting Molecular Diversity to Access Biologically Relevant Chemotypes ». Diss., The University of Arizona, 2016. http://hdl.handle.net/10150/621718.
Texte intégralJha, Satadru. « Organic reactions methodology : studies on carbon-nitrogen hetero bond forming reactions ». Thesis, University of North Bengal, 2004. http://hdl.handle.net/123456789/745.
Texte intégralBaldwin, I. Craig. « New methodology involving allylic substitution and conjugate addition reactions ». Thesis, Loughborough University, 1996. https://dspace.lboro.ac.uk/2134/27583.
Texte intégralDas, Pralay. « New reactions and methodology : studies on transition metal catalyzed organic transformations ». Thesis, University of North Bengal, 2005. http://hdl.handle.net/123456789/775.
Texte intégralBentley, Scott Alexander. « Asymmetric conjugate addition reactions ». Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:9e619a66-6277-48c2-8a2e-24f8206e52b3.
Texte intégralPerego, Luca Alessandro. « Transition metal-catalyzed reactions : mechanistic studies and methodology developments ». Thesis, Paris Sciences et Lettres (ComUE), 2018. http://www.theses.fr/2018PSLEE003/document.
Texte intégralIn 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
Mondière, Aurélie. « Réactions multicomposants et applications : synthèse de cyclopent[b]indoles et pyrrolo[1,2-a]indoles : synthèse diastéréosélective de lignanes tétrahydrofuraniques trisubstitués ». Phd thesis, Université Claude Bernard - Lyon I, 2010. http://tel.archives-ouvertes.fr/tel-00837814.
Texte intégralMciteka, Lulama Patrick. « Novel applications of Morita-Baylis-Hillman methodology in organic synthesis ». Thesis, Rhodes University, 2013. http://hdl.handle.net/10962/d1007598.
Texte intégralParker, Mariah L. « The Investigation of Oxidative Addition Reactions of Metal Complexes in Cross-Coupling Catalytic Cycles Based on a Unique Methodology of Coupled Ion/Ion-Ion/Molecule Reactions ». VCU Scholars Compass, 2018. https://scholarscompass.vcu.edu/etd/5651.
Texte intégralCui, Wenge Cui Wenge. « Part 1, Glyoxal-guanine DNA adducts, derivatization, structure, stability and new detection methodology ; Part 2, Nitrosation studies of oxazolines and imidazolines and the synthesis of N-cyclopropyl aromatic amines / ». free to MU campus, to others for purchase, 2000. http://wwwlib.umi.com/cr/mo/fullcit?p9998477.
Texte intégralVan, Allen Derek. « Methodology and mechanism : Reinvestigating the Ullmann reaction ». 2004. https://scholarworks.umass.edu/dissertations/AAI3136788.
Texte intégralSrimannarayana, Malempati. « Topics In Synthetic Methodology : From Heterocycles To Hydride Transfers ». Thesis, 2009. https://etd.iisc.ac.in/handle/2005/1992.
Texte intégralSrimannarayana, Malempati. « Topics In Synthetic Methodology : From Heterocycles To Hydride Transfers ». Thesis, 2009. http://etd.iisc.ernet.in/handle/2005/1992.
Texte intégralMoulins, Jonathan. « Synthesis of Heterocycles via Chemoselective Geminal Acylation of 2-Methoxyoxazolidines, E/Z Isomerization in the Metathesis of Allyl Alcohol Derivatives with a First-Generation Ruthenium Catalyst, and Interception of Nazarov Reaction Intermediates of Allenyl Vinyl Ketones with Arenes ». 2013. http://hdl.handle.net/10222/37454.
Texte intégral(10730742), Henry J. Hamann. « Amine-Boranes : Synthesis and Applications ». Thesis, 2021.
Trouver le texte intégralLi, Jian-yuan. « The modification of brucine derivatives as chiral ligands and its application in the asymmetric synthesis ». Thesis, 2014. http://hdl.handle.net/1805/6464.
Texte intégralThe modification of brucine derivatives as chiral ligands and the use of a multifaceted chiral ligand, brucine diol, under different reaction conditions to produce various optical isomers is described. In Chapter 1, the generation of a number of brucine derivatives is described. Taking the advantage of brucine-diol’s excellent molecular recognition capability for multiple organic functional groups, we focused on the synthetic modifications of brucine-diol and the synthesis of brucine N-oxide. We also produced various brucine derivatives with different functional moieties in good yields and selectivities. In Chapter 2, we described the investigation of brucine N-oxide catalyzed Morita-Baylis-Hillman (MBH) reaction of alkyl/aryl ketones. Brucine N-oxide was used as a nucleophilic organic catalyst in the MBH reaction of alkyl vinyl ketone. In addition, asymmetric MBH reactions of alkyl vinyl ketones with aldehydes were investigated using a dual catalysis of brucine N-oxide and proline. In this dual catalyst system, proline was found to form iminium intermediates with electron-deficient aryl aldehydes, while the N-oxide activated vinyl ketones provided enolates through the conjugate addition. Our dual catalysis approach also allowed the development of MBH reaction of aryl vinyl ketones. In Chapter 3, brucine diol-copper complex catalyzed asymmetric conjugate addition of glycine (ket)imines to nitroalkenes is discussed. Stereodivergent catalytic asymmetric conjugate reactions for glycine (ket)imines with nitroalkenes were achieved using various chiral catalysts derived from a single chiral source, brucine diol. Both syn- and anti-conjugate addition products were obtained with high diastereoselectivity and enantioselectivity. In Chapter 4, enantiodivergent production of endo-pyrrolidines from glycine (ket)imines using brucine diol-copper complex is described. The [3+2] cycloaddition reaction of glycine imines and activated alkenes was performed to produce endo-pyrrolidines. The reversal of enantioselectivity was observed for endo-pyrrolidines between concerted and stepwise reaction pathways. The three new brucine derivatives produced in this study would potentially work as organocatalysts and chiral ligands with metal ion in asymmetric synthesis. The brucine diol-metal complex catalyzed reactions laid a good foundation for catalytic asymmetric reactions, where a single chiral source was used to control the absolute and the relative stereochemical outcomes of reactions. Understanding the molecular-level interactions between catalyst and substrates will provide insightful mechanistic details for the stereodivergent approaches in asymmetric catalysis.