Дисертації з теми "Aryl Compounds"
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Leyva-Ramos, Elisa. "The temperature dependent photochemistry of aryl azides and aryl diazo compounds /." The Ohio State University, 1986. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487267024997622.
Повний текст джерелаLeary, Edmund. "Single Molecule Conductance of Dithiahexyl-Aryl Compounds." Thesis, University of Liverpool, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.507724.
Повний текст джерелаRoss, Jennifer Nicola. "Alkoxy- substituted aryl- and benzyl- organotin compounds." Thesis, University of Aberdeen, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324880.
Повний текст джерелаKhashoqji, Moayad. "Structural characterisation of novel poly-aryl compounds." Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/structural-characterisation-of-novel-polyaryl-compounds(3fb1fac6-548a-4afc-8ac2-5a14885b0ba4).html.
Повний текст джерелаRowland, Keith E. (Keith Edward). "An NMR Investigation of Aryl Mercury Compounds." Thesis, North Texas State University, 1987. https://digital.library.unt.edu/ark:/67531/metadc500453/.
Повний текст джерелаGuena, Thierry. "Electrochemistry of aryl carbonyl compounds in flow cells." Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243180.
Повний текст джерелаHeaton, Julie N. "Generation and reactions of aryl and alkyl thionitroso compounds." Thesis, Durham University, 1992. http://etheses.dur.ac.uk/6129/.
Повний текст джерелаAprahamian, Steve Lawrence. "Rearrangement-displacement of aryl(chloromethyl)diphenylsilanes with nucleophiles /." The Ohio State University, 1986. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487265555439529.
Повний текст джерелаAl-Harthy, Farida. "Separation of aryl nitro-compounds by HPLC on monolithic columns." Thesis, Loughborough University, 2009. https://dspace.lboro.ac.uk/2134/8683.
Повний текст джерелаNg, Fei-yeung, and 吳飛洋. "Structure and properties of self-assembled coordination compounds: homoleptic d10-metal aryl/alkylacetylides, ruthenium n-heterocyclesand picolinates." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B37878566.
Повний текст джерелаNg, Fei-yeung. "Structure and properties of self-assembled coordination compounds : homoleptic d10-metal aryl/alkylacetylides, ruthenium n-heterocycles and picolinates." View the Table of Contents & Abstract, 2006. http://sunzi.lib.hku.hk/hkuto/record/B36587126.
Повний текст джерелаKhan, Imtiaz. "Enolate-directed catalytic C-H functionalization of 2-aryl-1,3-dicarbonyl compounds." Thesis, University of Nottingham, 2015. http://eprints.nottingham.ac.uk/30261/.
Повний текст джерела楊小雯 and Siu-man Yeung. "The synthesis and reactions of 3H-pyrroles bearing methyl and aryl groups." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1991. http://hub.hku.hk/bib/B31210119.
Повний текст джерелаOtsuka, Shinya. "Studies on Catalytic Transformations of Organosulfur Compounds via C-S Bond Cleavage." Kyoto University, 2019. http://hdl.handle.net/2433/242625.
Повний текст джерелаWieczysty, Martin David. "C-H functionalisation of 2-aryl cyclic 1,3-dicarbonyl compounds ; Enantioselective Rh(I)-catalysed cyclisation of arylboron compounds onto ketones." Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/18741.
Повний текст джерелаTatton, Matthew R. "New methods for the synthesis of aromatic compounds." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:52a95189-d8ea-432f-aefd-4f9ae7ef996a.
Повний текст джерелаBaeza, Mario Ivan. "Synthesis and characterization of acetylenic derivatives of the actinide extractant (aryl)-N,N-di-(alkyl)carbamoylmethylphosphine oxide (CMPO)." To access this resource online via ProQuest Dissertations and Theses @ UTEP, 2008. http://0-proquest.umi.com.lib.utep.edu/login?COPT=REJTPTU0YmImSU5UPTAmVkVSPTI=&clientId=2515.
Повний текст джерелаLibot, Cecile. "The influence of cathode material on the reduction of aryl carbonyl compounds : formation of radicals." Thesis, University of Southampton, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.313211.
Повний текст джерелаMohammad, Reza Farmahin Farahani. "Prediction of the Sensitivity of Avian Species to the Embryotoxic Effects of Dioxin-like Compounds." Thèse, Université d'Ottawa / University of Ottawa, 2013. http://hdl.handle.net/10393/23696.
Повний текст джерелаSriramulu, Phenahas Gandu. "On-Metal Synthesis of Some Aryl Substituted Rhenium ┫ Cyclopenta[C] Pyridazyl Complexes." TopSCHOLAR®, 2010. http://digitalcommons.wku.edu/theses/197.
Повний текст джерелаLi, Wanfei. "Chemical synthesis of anti-HIV compounds based on the aryl naphthalene lignans identified from justicia plants." HKBU Institutional Repository, 2019. https://repository.hkbu.edu.hk/etd_oa/685.
Повний текст джерелаAngulo-Escalante, Miguel Angel 1962. "Inhibition of thioredoxin signalling by alkyl and aryl 2-imidazolyl disulfide compounds as potential antitumor agents." Diss., The University of Arizona, 1998. http://hdl.handle.net/10150/282694.
Повний текст джерелаJayatissa, Kuruppu Lilanthi. "A Metal-Free Approach to Biaryl Compounds: Carbon-Carbon Bond Formation from Diaryliodonium Salts and Aryl Triolborates." PDXScholar, 2015. https://pdxscholar.library.pdx.edu/open_access_etds/2229.
Повний текст джерелаZhang, Ye. "Development of amide-derived P,O-ligands for Suzuki cross-coupling of aryl chlorides and the asymmetric version /." View abstract or full-text, 2005. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202005%20ZHANG.
Повний текст джерелаMeyer, Andreas Uwe [Verfasser], and Burkhard [Akademischer Betreuer] König. "Organic Photoredox Catalysis: Oxidation of Sulfur Containing Compounds and Reduction of Aryl Halides / Andreas Uwe Meyer ; Betreuer: Burkhard König." Regensburg : Universitätsbibliothek Regensburg, 2018. http://d-nb.info/1159375747/34.
Повний текст джерелаRahman, Obaidur. "[11C]Carbon Monoxide and Aryl Triflates in Palladium-Mediated Carbonylation Reactions : Synthetic approaches to [11C]Carbonyl Compounds and [11C]Amines." Doctoral thesis, Uppsala universitet, Kemiska institutionen, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4157.
Повний текст джерелаUrgin, Karene. "Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques." Thesis, Paris Est, 2010. http://www.theses.fr/2010PEST1094.
Повний текст джерелаHeteroaromatic rings are present in various biological and pharmacological active molecules. Substituted aryl-pyridazines have given rise to considerable interest because of their diverse pharmacological properties (antibacterial, anti-inflammatory, cardiovascular drugs…). Moreover, structures which contain pyridazines are used in supramolecular chemistry for their applications through self-assembly processes in the presence of metal ions.In order to elaborate building blocks containing pyridazine rings such as aryl or heteroaryl-pyridazines, we turned our intention on the development of complementary methods involving organometallic reagents. Transition metal-catalyzed cross-coupling reaction of organometallic compounds with organic halides is one of the most powerful methods for the generation of C-C bonds.We chose to develop the most straightforward method involves heterocoupling reaction of aryl/heteroaryl compounds under electrochemical conditions (sacrificial anode process) associated to a nickel catalysis. However some limitations have been pointed out when 3,6-dihalogenopyridazines are involved in the cross-coupling reaction. An electrochemical study was investigated in order to propose some mechanistic considerations. A second part of this work consisted in the study of arylzinc and triarylbismuths reagents toward 3,6-dihalogenopyridazines
Perry, Philip J. "Synthesis and biological evaluation of novel cytotoxic heterocylic compounds : furo[2,3-b]naphthoquinones and 2-aryl-4H-3,1-benzoxazin-4-ones." Thesis, De Montfort University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.391202.
Повний текст джерелаCui, Chunming. "Aluminum (I, II, III) Compounds with Multidentate Ligands: Syntheses, Reactivity, and Structures." Doctoral thesis, [S.l. : s.n.], 2001. http://webdoc.sub.gwdg.de/diss/2001/cui/cui.pdf.
Повний текст джерелаLindstedt, Erik. "Metal-Free O- and C-Arylation with Diaryliodonium Salts." Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-140944.
Повний текст джерелаAt the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 3: Manuscript.
Walker, Kelcey Manae Becker. "Inhibitory actions of Ah receptor agonists and indole-containing compounds in breast cancer cell lines and mouse models." Texas A&M University, 2002. http://hdl.handle.net/1969.1/2433.
Повний текст джерелаLarsson, Malin. "Computational methods for analyzing dioxin-like compounds and identifying potential aryl hydrocarbon receptor ligands : multivariate studies based on human and rodent in vitro data." Doctoral thesis, Umeå universitet, Kemiska institutionen, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-139487.
Повний текст джерелаRahman, Obaidur. "[11C]Carbon Monoxide and Aryl Triflates in Palladium-Mediated Carbonylation Reactions : Synthetic approaches to [11C]Carbonyl Compounds and [11C]Amines." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4157.
Повний текст джерелаManoso, Amy Slover. "Hypercoordinate silicon compounds In organic synthesis improved methods for the synthesis of aryl(trialkoxy)silane derivatives ; and trimethylsilyl cyanide as a cyanide source for nucleophilic substitution /." College Park, Md. : University of Maryland, 2004. http://hdl.handle.net/1903/1664.
Повний текст джерелаThesis research directed by: Chemistry. Title from t.p. of PDF. Includes bibliographical references. Published by UMI Dissertation Services, Ann Arbor, Mich. Also available in paper.
Milton, Edward J. "Pd catalysed C-C & C-O bond formation using bis-(dialkyl/diarylphosphino)ferrocene ligands." Thesis, University of St Andrews, 2010. http://hdl.handle.net/10023/1022.
Повний текст джерелаFelipe-Blanco, Diego. "Salicylic Acid-Catalyzed Radical Arylations from In-situ Formed Arenediazonium Salts." Doctoral thesis, Universidad de Alicante, 2020. http://hdl.handle.net/10045/112757.
Повний текст джерелаSvensson, Akusjärvi Emma [Verfasser]. "Mechanistic Investigations of the Direct Arylation of Pyridine N-oxides with Bromoarenes and Structure-Reactivity Relationship of Aryl Palladium Complexes in Transmetalations with Organoboron Compounds / Emma Svensson Akusjärvi." Berlin : Freie Universität Berlin, 2018. http://d-nb.info/1176635034/34.
Повний текст джерелаBielawski, Marcin. "Efficient and High-Yielding Routes to Diaryliodonium Salts." Licentiate thesis, Stockholm : Department of Organic Chemistry, Stockholm University, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-7969.
Повний текст джерелаFindik, Hamide. "Potassium Permanganate/ Carboxylic Acid/ Organic Solvent: A Powerful Reagent For C-c Bond Formation, Aryl Coupling Reactions And Enone Oxidation Ipso-nitration Of Arylboronic Acids With Silver Nitrite/ Tmscl." Phd thesis, METU, 2009. http://etd.lib.metu.edu.tr/upload/12610472/index.pdf.
Повний текст джерела-acetoxylation of enones and the a-acetoxylation of aromatic ketones were carried out with potassium permanganate and acetic acid, in which acetoxylation products were obtained in 74-96% yields. The same reaction was carried out with carboxylic acids other than acetic acid, which furnished corresponding acyloxy ketones with the same regioselectivity. For the first time, formyloxylation products were synthesized in a 61-85% yield by using formic acid. The potassium permanganate and acetic acid method was also used for aryl coupling reactions. The reaction of arylboronic acids and aryl hydrazines in benzene with potassium permanganate and acetic acid in turn furnished biaryls in a 85-96% yield. We showed that potassium permanganate/carboxylic acid/organic solvent behaves as manganese(III) acetate. In the second part of the thesis, ipso-nitration of arylboronic acids with AgNO2/ TMSCl was performed. Nitration of aromatic compounds is one of the most extensively studied reactions, and nitroaryl moieties play key roles in the physical and chemical properties of many target molecules in organic synthesis. For electrophilic nitration of aromatic compounds, a wide variety of reagents are available to date. Most of them are very strong nitrating agents and often lead to further nitration and mixture of isomers. Since most nitrating agents are oxidants, oxidation of other functional groups can also occur, giving a mixture of products. Thus, a search for milder and selective nitrating agents is a good research goal. In this work, we aimed to apply AgNO2/ TMSCl system to ipso nitration of arylboronic acids.
Monzón, Díaz Gabriel Andrés [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Zincation of heterocycles and aryl nonaflates : directed magnesiation of highly substituted anilines and amino-substituted heterocycles ; synthesis of heterobenzylic zinc compounds ; new generation of iminium salts / Gabriel Andrés Monzón Díaz. Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2012. http://d-nb.info/1025821947/34.
Повний текст джерелаBielawski, Marcin. "Diaryliodonium Salts : Development of Synthetic Methodologies and α-Arylation of Enolates". Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-54738.
Повний текст джерелаRanaivonjatovo, Henri Jacques. "Derives du phosphore et de l'arsenic dicoordonnes doublements lies : diphosphenes, diarsenes et phospha-arsenes." Toulouse 3, 1986. http://www.theses.fr/1986TOU30069.
Повний текст джерелаSmith, S. J. "Novel alkyls, aryls and alkoxides of group 14 and 15 elements." Thesis, University of Sussex, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373133.
Повний текст джерелаCromer, Rémy. "Porphyrines n-substituees : modelisation de l'inhibition d'hemoproteines." Université Louis Pasteur (Strasbourg) (1971-2008), 1986. http://www.theses.fr/1986STR13015.
Повний текст джерелаFigadère, Bruno. "Les composes organomanganeux mixtes : addition 1-2 selective sur des aldehydes ou des cetones portant un groupe fonctionnel, enolisation regioselective de cetones : application en synthese." Paris 6, 1987. http://www.theses.fr/1987PA066371.
Повний текст джерелаKlopper, Reynhardt. "An investigation into the complex formation and potential solvent extraction of Os(IV/III) with N, N - dialkyl - N′- acyl(aroyl)thioureas." Thesis, Stellenbosch : University of Stellenbosch, 2006. http://hdl.handle.net/10019.1/2762.
Повний текст джерелаThis study involved the preliminary investigation into the potential liquid-liquid extraction of Os(IV/III) from hydrochloric acid solutions with ligands of type N,N-dialkyl-N′-acyl(aroyl)thioureas (HL), and ultimate selective pre-concentration and separation of Os(IV/III) from the other platinum group metals. Investigations have also been focused towards understanding the speciation of Os(IV) in hydrochloric acid medium. A series of osmium complexes with ligands of type HL have been synthesised and characterised. This has been done with a view towards understanding the interaction of Os(IV/III) with the HL ligands, and what the resultant stereochemical influences would be on the solvent extraction capabilities of the ligands. The structures of two novel osmium-containing compounds have been verified by means of X-ray crytallography. Firstly, the ion pair OsCl6[(C4H9)4N]2 was obtained as a result of liquid-liquid extraction experiments. Secondly, the only known example (in our knowledge) of an Os(III) - N,N-dialkyl-N′- aroylthiourea complex, in this case tris(N,N-diethyl-N’-benzoylthioureato)osmium(III), was successfully synthesised and characterised. Lastly, preliminary studies into the substitution reactions of ruthenium-polypyridine complexes with N,N-dialkyl-N′-acyl(aroyl)thioureas were conducted. A series of cis-bis(2,2′-bipyridine)(N,N-dialkyl-N′-acyl(aroyl)thioureato)ruthenium(II) complexes have been successfully synthesised and characterised. The electronic absorption behaviour of the formed complexes have been investigated in detail via UV-Vis spectrophotometry.
Maddaluno, Jacques. "Synthèse énantiosélective de composés d'intérêt biologique : approche de polyols vicinaux par aldolisation stéréocontrôlée, approche de bêta-amino esters par addition de Michael stéréocontrôlée sous haute pression." Paris 6, 1986. http://www.theses.fr/1986PA066240.
Повний текст джерелаTrabulsi, Houssam. "Préparation d’iminolactones par cyclisation électrophile d’hydroxamates insaturés : étude de leurs propriétés." Thesis, Paris 11, 2011. http://www.theses.fr/2011PA112052.
Повний текст джерелаThis work deals with the 5-endo halogeno electrophilic cyclization reactions of β,γ-ethylenic hydroxamates to give halolactames and halo cyclic iminolactones.In the first chapter, the reaction of γ-disubstituted β,γ-unsaturated hydroxamates with bis(collidine)bromine(I) hexafluorophosphate is studied. This type of reaction led mainly to the formation of bromo cyclic imidates, which were the thermodynamic products. Unsaturated cyclic imidates were then obtained by reaction with triethylamine. A lactame-iminolactone rearrangement was obtained during those reactions. In a next step we decided to study the diastereoselectivity of the reaction, using optically actif hydroxamates. In the second chapter, we decided to study the reaction of bis(collidine)bromine(I) hexafluorophosphate with γ-aryl β,γ-unsaturated hydroxamates, the corresponding bromo cyclic imidates were also obtained. However, by reaction with triethylamine, these compounds led with good yields, to the formation of 3-cyano-2-propen-1-ones by a Beckmann type fragmentation reaction. In the third chapter, the reaction of γ-mono and disubstituted β,γ-unsaturated imidates with bis(collidine)bromine(I) hexafluorophosphate is studied. The results that we obtained were not sufficient enough to understand the electrophilic cyclization mechanism of these types of substrates
Denis, Alexis. "Fonctionnalisations selectives a l'aide des complexes du palladium : synthese de composes d'interet biologiques, cyclopropanes vinyliques, aryl-3 oxazolidinones-2 (inhibiteurs potentiels de la monoamine oxydase)." Paris 6, 1987. http://www.theses.fr/1987PA066335.
Повний текст джерелаDenys, Goument Colombe. "Dicétones-1,4 thiosubstituées." Rouen, 1988. http://www.theses.fr/1988ROUES023.
Повний текст джерела