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1

Hoffmann, Eric. "The oxidative coupling of phenols using stoichiometric metal oxidants." Thesis, Nelson Mandela Metropolitan University, 2005. http://hdl.handle.net/10948/180.

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The oxidative coupling of 2,6-di-t-butylphenol under mild reaction conditions is well documented and the subject of many patents. However, the coupling of other monoand di- substituted phenols is not as well documented and thus there is scope for further investigation for providing a convenient, environmentally friendly and economically viable method for the oxidative coupling of these phenols. In this study, the oxidative coupling of a variety of alkylated phenolic substrates, 2-tbutylphenol, 2,6-di-t-butylphenol, 2,4 -di-t-butylphenol and ,4-dimethylphenol, using a range of different oxidizi
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2

Setälä, Harri. "Regio- and stereoselectivity of oxidative coupling reaction of phenols : spirodienones as construction units in ligin /." [Espoo, Finland] : VTT, 2008. http://www.vtt.fi/inf/pdf/publications/2008/P689.pdf.

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3

Fürtges, Leon [Verfasser], and Michael [Akademischer Betreuer] Müller. "Oxidative phenol coupling in ascomycetes: regioselectivity of coupling enzymes." Freiburg : Universität, 2018. http://d-nb.info/1163945870/34.

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4

Fukuoka, Tokuma. "Synthesis of novel functional polymeric materials via oxidative coupling of phenols by peroxidase and its model complex." 京都大学 (Kyoto University), 2005. http://hdl.handle.net/2433/144883.

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5

Denizot, Natacha. "Couplages oxydants entre indoles et phénols pour la synthèse de benzofuroindolines naturelles." Thesis, Université Paris-Saclay (ComUE), 2015. http://www.theses.fr/2015SACLS147/document.

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Le noyau benzofuro[2,3-b]indoline est une structure complexe que l’on retrouve dans différentes substances naturelles telles que l’azonazine, la voacalgine A, la bipleiophylline ou encore le diazonamide A. Ces produits naturels possèdent une activité biologique intéressante et plus particulièrement le diazonamide A avec un IC50 inférieur à 15ng/mL sur plusieurs lignées cellulaires cancéreuses. De plus, certaines de ces substances n’ont jamais été synthétisées à ce jour. Lors de la biogénèse de ces composés, il est supposé que le motif benzofuroindoline est créé par un couplage oxydant entre un
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6

Beaud, Rodolphe. "Hydroarylation régiosélective d’indoles pour l’accès aux motifs 3 - arylindolines : études et applications d’une nouvelle réactivité de l’indole." Thesis, Paris 11, 2014. http://www.theses.fr/2014PA112308/document.

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Le diazonamide A, molécule naturelle extraite d’une ascidie marine, présente une activité antitumorale très importante (IC₅₀ < 5 nM) selon un mode d’action tout à fait original. Des études ont en effet prouvé que cette molécule inhibait une enzyme, l’Ornithine-d-aminotransferase, intervenant dans la réplication cellulaire des cellules cancéreuses faisant d’elle un poison du fuseau mitotique très sélectif. Cette molécule présente en son sein un cœur benzofuroindoline qui serait issu, d’un point de vue biogénétique, d’un couplage oxydant entre un noyau indole et un noyau phénol. Afin de dével
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7

Lee, Kerri-Ann S. "Oxidative coupling of sinapic acid." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/mq23377.pdf.

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8

Ji, Jianhua. "Regioselective Coupling Reactions of Diiodophenol Derivatives." Thesis, University of North Texas, 1994. https://digital.library.unt.edu/ark:/67531/metadc277926/.

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Palladium catalyzed reactions of derivatives of 2,4-diiodophenol are explored. Coupling reactions with a series of terminal alkynes and formylation are found to be efficient and regioselective. Coupling with stananne reagents and alkenes do not work. The nature of the oxygen protecting group is critical. The phytotoxic natural product, Eutypine, is synthesized by using regioselective formylation and alkyne coupling. An approach to the plant antimicrobial compound Plicatin B is examined.
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9

Hargreaves, J. S. J. "The catalysed oxidative coupling of methane." Thesis, University of Liverpool, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303659.

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10

You, Shaochun. "CuCl₂-induced oxidative coupling of Anions /." Bern, 1992. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.

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11

Kimkes, Peter. "Oxidative coupling polymerization of primary aromatic diamines." [S.l. : [Groningen : s.n.] ; University of Groningen] [Host], 2008. http://irs.ub.rug.nl/ppn/.

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12

Higashimura, Hideyuki. "Radical-controlled oxidative polymerization of phenols : a new methodology for polymer synthesis." 京都大学 (Kyoto University), 2005. http://hdl.handle.net/2433/144858.

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13

Lapena-Rey, Nieves. "Oxidative coupling of methane in ceramic electrochemical reactors." Thesis, Imperial College London, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.394407.

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14

Russell, Wendy R. "Substituent effects on the oxidative coupling of phenylpropanoids." Thesis, University of Aberdeen, 1997. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=215553.

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Incorporation of phenylpropanoids into the plant polymer lignin occurs by a radical coupling mechanism catalysed by the enzyme peroxidase. Generation of the parent radical requires reduction of the enzyme intermediate compound I, which can be monitored by electron spin resonance (ESR) spectroscopy. It was found that the substituted cinnamyl alcohols were more easily oxidised than their corresponding acids and esters. For all phenylpropanoids, ease of oxidation increased with methoxyl substitution. The dehydrodimers, which represent the products of initial coupling, showed a similar trend with
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15

Kienle, Marcel. "Oxidative and Transition-Metal Catalyzed Cross-Coupling Reactions, Preparation and Coupling of S-Heterocycles." Diss., lmu, 2010. http://nbn-resolving.de/urn:nbn:de:bvb:19-113699.

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16

Tsang, S. C. "An investigation of the catalytic oxidative coupling of methane." Thesis, University of Reading, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.277111.

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17

Serres, Thomas. "Oxidative Coupling of Methane followed by Oligomerization to Liquids." Thesis, Lyon 1, 2013. http://www.theses.fr/2013LYO10229.

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Les importantes réserves de gaz naturel – avérées ou potentielles – font de cet hydrocarbure un substitut plausible du pétrole pour la production d'hydrocarbures liquides. Cependant la plupart des réserves de gaz découvertes à l'heure actuelle sont de taille réduite et dispersées loin des sites de transformation ou de consommation. Le couplage du réformage (RM) et du couplage oxydant du méthane (OCM) dans un réacteur à microcanaux permettrait de rendre viable l'exploitation de ces réserves grâce à des coûts opératoires de transformation du gaz naturel réduits par rapport aux usines actuelles.
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18

Zhang, Yi Qun. "Methane oxidative coupling over fluoride/oxide catalysts : a dissertation." HKBU Institutional Repository, 1993. http://repository.hkbu.edu.hk/etd_ra/15.

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19

Drouhin, Pauline. "Copper(II)-mediated oxidative coupling routes to nitrogen-heterocycles." Thesis, University of York, 2015. http://etheses.whiterose.ac.uk/9095/.

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Nitrogen-containing heterocycles have attracted considerable attention owing to their prevalence in numerous natural substances as well as their extensive applications in biology and pharmacology. In recent years, great efforts have been devoted to the elaboration of novel synthetic methodologies for the construction of N-heterocycles such as oxindoles and indoles. Reported in 2009 by the Taylor group, access to oxindole scaffolds has been successfully demonstrated via a copper(II)-mediated oxidative coupling approach. Following the same principle, the extension of this method to the formation
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20

Deakin, Sherine Jane. "Antioxidant effects of phytochemicals in conditions of oxidative stress : impact on endothelial cell survival and function." Thesis, University of Aberdeen, 2010. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=165549.

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Two dietary polyphenols, delphinidin and resveratrol, were selected for this study; delphinidin, an anthocyanin flavonoid, was found to elicit cardioprotective properties from a pilot study and resveratrol, a stilbene flavonoid, one of the most studied of the polyphenols and was chosen as a worthy comparator. <i>In vitro</i> studies using cultured endothelial cells exposed to a variety of reactive oxygen species (ROS) were used to determine if delphinidin and resveratrol could protect these cells from oxidative damage. It was found that physiological concentrations of delphinidin protected the
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21

Palaty, Jan. "Oxidative coupling of dibenzylbutanolides catalyzed by plant cell culture extracts." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/29710.

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This thesis aims to develop a new and inexpensive synthetic route to the anti-cancer drug etoposide (6) via 4'-demethylpodophyllotoxin (4) or 4'-demethylepipodophyllotoxin (5) involving the oxidative coupling of a dibenzylbutanolide catalyzed by a cell-free extract (CFE) from plant cell culture. This step was studied in depth using the Catharanthus roseus CFE-catalyzed biotransformation of frans-2-(3,5-dimethoxy-4-hydroxybenzyl)-3-(3-hydroxy-4-methoxybenzyl)butanolide (58) to 1-(3,5-dimethoxy-4-hydroxyphenyl)-6-hydroxy-3-hydroxymethyl-7-methoxy-1,2,3,4-tetrahydro-2-naphthoic acid γ lactone (5
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22

Driscoll, Sharon Anne. "Oxidative coupling of methane over alkali-promoted manganese molybdate catalysts /." The Ohio State University, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487847761306923.

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23

Graf, P. O. "Combining oxidative coupling and reforming of methane vision or utopia? /." Enschede : University of Twente [Host], 2009. http://doc.utwente.nl/60460.

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24

Hamid, Hamzah b. Abd. "Oxidative coupling of methane on samaria and on mixed oxide catalysts." Thesis, University of Hull, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.335155.

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25

Zhang, Xiankuan. "Studies of methane oxidative coupling with practical catalysts and model systems." Thesis, University of Cambridge, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386819.

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26

Bailey, Aaron D. "On the Mechanism of Oxidative Coupling of 1,4-Diaminobenzene with Resorcinol." University of Cincinnati / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1468335277.

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27

Kurosawa, Shutaro. "Supercritical Processing of Electrically Conducting Polymers." Diss., Georgia Institute of Technology, 2004. http://hdl.handle.net/1853/4988.

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Thick composites (~ 3 mm in thickness) of polypyrrole with electrically insulating porous (polystyrene) and nonporous (polymethyl methacrylate) substrates were prepared using a two-step batch method. In the two-step method, impregnation of volatile (iodine) or nonvolatile (ferric chloride) oxidant in the substrate is followed by in-situ polymerization of pyrrole. Conductivities as high as 10-1 S/cm were obtained in this work in the case of composites of polypyrrole and porous, crosslinked polystyre. Use of the nonvolatile oxidant (ferric chloride) resulted in higher conducting polymer yield, a
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28

Robinson, Matthew Peter. "Ortho-substituted arylsilanes in oxidative gold catalysis." Thesis, University of Edinburgh, 2018. http://hdl.handle.net/1842/31394.

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Organometallic compounds derived from tin, boron, and zinc, have been used extensively in transition metal-catalysed cross-coupling, and continue to hold status as the go-to reagents to form new carbon-carbon bonds. Recently, organosilicon compounds have emerged as an attractive alternative to these established reagents, benefitting from low toxicity, low cost, and general ease of handling. While the fundamental reactivity of arylsilane reagents (Ar-SiR3) is well known, their role in transition metal-catalysed reactions is generally less well studied. This thesis comprises an investigation int
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29

Pintori, Didier Gil. "Novel benzyne insertion reactions & medium-ring synthesis by oxidative C-H coupling." Thesis, University of Edinburgh, 2011. http://hdl.handle.net/1842/5669.

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This thesis is divided into two main chapters, which are focused on two separated and uncorrelated research areas. The first part of this thesis is dedicated to the research I carried out in benzyne chemistry and the second part is focused on catalytic C-H bond activation. In the first place, a novel insertion reaction of arynes into the nitrogen-carbonyl σ-bond of amides has been investigated as a rapid and powerful approach for the preparation of valuable ortho-disubstituted arenes. Readily available aromatic amides undergo smooth insertion when treated with O-triflatophenyl silane aryne pre
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30

Lindh, Jonas. "Palladium(II)-Catalyzed Coupling Reactions." Doctoral thesis, Uppsala universitet, Avdelningen för organisk farmaceutisk kemi, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-130031.

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Sustainable chemical processes are becoming increasingly important in all fields of synthetic chemistry. Catalysis can play an important role in developing environmentally benign chemical processes, and transition metals have an important role to play in the area of green chemistry. In particular, palladium(II) catalysis includes many key features for successful green chemistry methods, as demonstrated by a number of eco-friendly oxidation reactions catalyzed by palladium(II). The aim of the work presented in this thesis was to develop novel and greener palladium(II)-catalyzed coupling reactio
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31

Nilsson, Johan. "Studies on Oxidative Couplings in H-Phosphonate Chemistry." Doctoral thesis, Stockholm : Institutionen för organisk kemi, Univ, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-203.

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32

Correia, Camille. "Oxidative C-C bond formation via metal-catalyzed coupling of two C-H bonds." Thesis, McGill University, 2013. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=114441.

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This thesis describes the formation of new C-C bonds from the direct oxidative coupling of two C-H bonds, through the use of metal catalysts for activation. First, three different oxidative Cross-Dehydrogenative-Coupling (CDC) reactions will be presented. Initially, through the use of an organic co-catalyst, N-hydroxyphthalimide (NHPI), oxygen could be utilized as the terminal oxidant for the metal catalyzed alkylation of benzylic C-H bonds with 1,3-dicarbonyls and ketones in Chapter 2. The reaction was found to be feasible for a variety of
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33

Devenport, Christopher. "Synthetic strategies for the application of anodic coupling to the pursuit of analgetic compounds." Thesis, University of Bath, 1989. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328590.

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34

Evans, Anthony Steven. "Mechanism of the Heck reaction: nature of oxidative addition and migratory insertion." Thesis, Texas A&M University, 2004. http://hdl.handle.net/1969.1/1130.

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The mechanism of carbon coupling reactions is traditionally represented in a very broad schematic. This thesis seeks to explore the mechanism of these reactions by focusing on Heck olefination. The Heck reaction has become a powerful tool in synthetic labs but the mechanism of this reaction has remained a topic of debate since the reaction's discovery. The catalytic cycle that has come to be accepted, while accurate in its own right, is not nearly as detailed as the complexity of the various stages of the Heck reaction suggest it should be. This study seeks to elucidate the nature of the o
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35

Evans, Anthony Steven. "Mechanism of the Heck reaction: nature of oxidative addition and alkene insertion." Thesis, Texas A&M University, 2004. http://hdl.handle.net/1969.1/1130.

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The mechanism of carbon coupling reactions is traditionally represented in a very broad schematic. This thesis seeks to explore the mechanism of these reactions by focusing on Heck olefination. The Heck reaction has become a powerful tool in synthetic labs but the mechanism of this reaction has remained a topic of debate since the reaction's discovery. The catalytic cycle that has come to be accepted, while accurate in its own right, is not nearly as detailed as the complexity of the various stages of the Heck reaction suggest it should be. This study seeks to elucidate the nature of the o
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36

Giguère-Bisson, Maxime. "Investigation of transition metal-catalyzed oxidative amidation of aldehydes and aldehyde-alkyne-amine coupling reactions." Thesis, McGill University, 2011. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=103659.

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This thesis describes the investigation of various amino acids derivatives as reagents for copper-catalyzed, silver-catalyzed and iron-catalyzed reactions and the investigation of an enantioselective cobalt-catalyzed aldehyde-alkyne-amine (A3) coupling reaction. The first part focuses on the large-scale optimization of the oxidative amidation of aldehydes in the presence of amine hydrochloride salts as well as our effort to enhance the reaction scope by the use of amino acids derivatives and short peptides. This is then followed by the development of an enantioselective cobalt-catalyzed A3-cou
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37

He, Hong. "The oxidative coupling of methane over BaX2/La2O3, LaOX, and BaCO3/LaOX (X=halogen) catalysts." HKBU Institutional Repository, 1996. http://repository.hkbu.edu.hk/etd_ra/58.

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38

Burgos, William David. "Reversible and irreversible adsorption of naphthalene and α-naphthol to soil". Diss., Virginia Tech, 1995. http://hdl.handle.net/10919/38186.

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Experiments were performed with naphthalene and a-naphthol to compare the processes involved in the sorption of a polycyclic aromatic hydrocarbon (PAH) and its metabolite, respectively, and to assess the bioavailability of these two compounds adsorbed to two sandy soils with different organic carbon contents. Adsorption conditions were varied to estimate the extent that biologically-mediated and chemically-induced oxidative coupling, and rate-limited diffusive processes contributed to the apparent irreversible adsorption of these compounds. The purposes of this research were to: (1) investigat
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39

Fleischer, Vinzenz [Verfasser], Reinhard [Akademischer Betreuer] Schomäcker, Ulrich [Gutachter] Nieken, Robert [Gutachter] Schlögl, and Reinhard [Gutachter] Schomäcker. "Oxidative coupling of methane : resolution of the surface and gas phase contributions to the mechanism of the oxidative coupling of methane at Na2WO4-Mn-SiO2-catalyst / Vinzenz Fleischer ; Gutachter: Ulrich Nieken, Robert Schlögl, Reinhard Schomäcker ; Betreuer: Reinhard Schomäcker." Berlin : Technische Universität Berlin, 2017. http://d-nb.info/1156346746/34.

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40

Bhandari, Alok. "Factors affecting binding of chlorophenols to soil." Diss., Virginia Tech, 1995. http://hdl.handle.net/10919/39390.

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Synthetic substituted phenols can become incorporated into soil organic matter by processes similar to natural humification. Biological, (enzyme-catalyzed), and abiotic, (mineral surface catalyzed), reactions have been implicated in these processes which result in the nonextractable binding of phenolic contaminants to soil organic matter. Experiments conducted with phenol, 4-monochlorophenol (MCP), 2,4,6-trichlorophenol (TCP), and pentachlorophenol (PCP) indicated a statistically significant difference in the degree of nonextractable binding in oxic and anoxic environments. Soils were e
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41

Salerno-Paredes, Daniel [Verfasser], and Günter [Akademischer Betreuer] Wozny. "Optimal Synthesis of Downstream Processes using the Oxidative Coupling of Methane Reaction / Daniel Salerno-Paredes. Betreuer: Günter Wozny." Berlin : Universitätsbibliothek der Technischen Universität Berlin, 2013. http://d-nb.info/1031280235/34.

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42

Bumbliauskinė, Jankauskaitė Lina. "Study of Perilla L. species and varieties cultivation, phytochemical composition and biological effect." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2011. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20110309_111240-41438.

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Perilla L. are significant for multi-pharmacological effect. The aim of this work is to study Perilla L. growth and develop¬ment tendencies, productivity; composition of biologically active compounds and their variations during the vegetation period, and the biological effect of the extracts; to select perspective plants for cultivation in Lithuania and for production of medicinal preparations. The objectives of the Study: To investigate and determine growth dynamics of Perilla L. species and varieties during the vegetation period and to assess the influence of climate conditions on the vegeta
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43

Peter, Martin G., Svend Olav Andersen, Rudolf Hartmann, Merle Miessner, and Peter Roepstorff. "Catecholamine-protein conjugates : isolation of 4-phenylphenoxazin-2-ones from oxidative coupling of N-acetyldopamine with alipathic amino acids." Universität Potsdam, 1992. http://opus.kobv.de/ubp/volltexte/2008/1757/.

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4-Phenylphenoxazinones were isolated after biomimetic oxidation, using diphenoloxidases of insect cuticle, mushroom tyrosinase, or after autoxidation of N-acetyldopamine (Image ) in the presence of β-alanine, β-alanine methyl ester or N-acetyl-L-lysine. They are formed presumably by addition of 2-aminoalkyl-5-alkylphenols to the o-quinone of biphenyltetrol which, in turn, arises from oxidative coupling of. The structures of present the first examples for the assembly of reasonably stable intermediates in the rather complex process of chemical modifications of aliphatic amino acid residues by o
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44

Jašo, Stanislav [Verfasser], and Günter [Akademischer Betreuer] Wozny. "Modeling and Design of the Fluidized Bed Reactor for the Oxidative Coupling of Methane / Stanislav Jašo. Betreuer: Günter Wozny." Berlin : Universitätsbibliothek der Technischen Universität Berlin, 2012. http://d-nb.info/1028912943/34.

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45

Guo, Wusheng. "Part I. Hypervalent iodine species: reagents and intermediates in oxidative processes Part II. Water-soluble metal nanoparticles (Rh, Au) in catalysis." Doctoral thesis, Universitat Autònoma de Barcelona, 2014. http://hdl.handle.net/10803/283353.

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Els reactius de iode hipervalent són oxidants eficients en diverses transformacions oxidatives. Kita havia utilitzat el sistema PIFA/BF3·Et2O per assolir acoblaments oxidatius arè-arè. El nostre grup va extendre aquesta metodologia a l’acoblament oxidatiu directe de quatre components (four-component direct oxidative coupling) en el que estaven implicats binaftalè i arens. Seguint amb el nostre interés en aquest tema, en aquesta tesi hem preparat diversos tris-, tetra- i hexanaftalens arilats, compostos que tenen potencial interès en les àrees dels colorants i dels dispositius òptics orgànics.
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46

Paloschi, Rozileia Simoni. "Acoplamento não oxidativo de metano sobre metais suportados em solidos microporosos." [s.n.], 2002. http://repositorio.unicamp.br/jspui/handle/REPOSIP/267578.

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Orientador: Gustavo Paim Valença<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia Quimica<br>Made available in DSpace on 2018-07-31T19:58:48Z (GMT). No. of bitstreams: 1 Paloschi_RozileiaSimoni_M.pdf: 2623823 bytes, checksum: 569787d9b56d1368559be20011050e5e (MD5) Previous issue date: 2002<br>Resumo: A conversão catalítica de metano para combustível liquido ou outros produtos químicos é de grande interesse e muitas tentativas de utilização têm sido feitas para ativar metano em condições não oxidativas e convertê-lo em hidrocarbonetos grandes e compostos
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47

Blackwell, D. T. "Studies on carbon-carbon bond formation : copper mediated oxidative coupling of alkenyl silanes and efforts towards a direct catalytic enolate SN2 alkylation reaction." Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.596704.

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This thesis describes two research projects aimed at the design and development of new methods for the construction of carbon-carbon bonds. The first focused on attempts to extend previous work within the Spring Group on the formation of biaryl-containing medium rings <i>via</i> the oxidative coupling of organocuprates to the formation of dienyl and alkenyl medium rings. It was found that functionalised alkenylsilanes bearing a pendant coordinating group could be prepared with good control over the geometry of the alkene, and undergo stereospecific fluoride-mediated transmetalation to copper f
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48

Bogle, Katherine Mary. "An organocatalytic oxidative coupling strategy for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine." Thesis, University of Manchester, 2011. https://www.research.manchester.ac.uk/portal/en/theses/an-organocatalytic-oxidative-coupling-strategy-for-the-synthesis-of-arylated-quaternary-stereocentres-and-its-application-in-the-total-synthesis-of-powelline-and-buphanidrine(4038d899-f157-4ac5-904b-128553be92ff).html.

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The synthesis of compounds containing α-arylated quaternary stereogenic centres is a significant synthetic challenge. This thesis describes the development of an organocatalytic methodology for the direct construction of this motif through the Michael addition of carbon-centered pro-nucleophiles to highly reactive and unstable ortho-benzoquinones. Proof-of-principle for the base catalysed Michael addition to ortho-quinones was established with stable 1,2-naphthoquinone (Chapter 2), however typical orthobenzoquinones were found to be too unstable to use in this process. Accordingly an oxidative
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Khalaf, Eyada. "Phenolic-Linked Antioxidant and Anti-Hyperglycemic Properties of Selected Cereal, Pseudo-Cereal, and Millet Using In Vitro Screening Methods." Thesis, North Dakota State University, 2018. https://hdl.handle.net/10365/29281.

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Abstract:
Improving diversity of food systems by targeting whole grain cereals, pseudo-cereals, and millets is essential to enhance nutritional qualities beyond macro and micronutrient balance and to address emerging global food and nutritional security-linked public health challenges. However, human health relevant nutritional parameters of whole grains vary widely among species, genotypes, growing conditions, and further due to different processing methods. Therefore, it is important to screen human health relevant nutritional parameters of these whole grains prior to targeting them for wider public h
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50

Langfeld, Kirsten [Verfasser], and Reinhard [Akademischer Betreuer] Schomäcker. "Impact of Synthesis Methods and Oxidizing Agents on the Catalytic Performance of Various Catalysts in the Oxidative Coupling of Methane / Kirsten Langfeld. Betreuer: Reinhard Schomäcker." Berlin : Universitätsbibliothek der Technischen Universität Berlin, 2012. http://d-nb.info/1021219967/34.

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