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Guido-Garcia, Fabiola. "The biogeochemistry of iodine". Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/the-biogeochemistry-of-iodine(031a6229-1a96-4068-9764-8291bafb0cad).html.
Pełny tekst źródłaKhan, Zulfiqar Ali. "Novel iodine mediated carbocyclisations and hypervalent iodine(III) reagents". Thesis, Cardiff University, 2010. http://orca.cf.ac.uk/54137/.
Pełny tekst źródłaUntoro, Juliawati. "Use of oral iodized oil to control iodine deficiency in Indonesia /". Online version, 1999. http://bibpurl.oclc.org/web/35068.
Pełny tekst źródłaMowbray, Andrew Paul. "The surface chemistry of iodine and iodine compounds on indium antimonide(001)". Thesis, University of Nottingham, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334804.
Pełny tekst źródłaSinghania, Amit. "Studies on catalytic decomposition of hydrogen iodide for hydrogen production in thermochemical sulphur-iodine (SI) cycle". Thesis, IIT Delhi, 2016. http://localhost:8080/xmlui/handle/12345678/7084.
Pełny tekst źródłaHassan, Shetaya Waleed Hares Abdou. "Iodine dynamics in soil". Thesis, University of Nottingham, 2011. http://eprints.nottingham.ac.uk/12261/.
Pełny tekst źródłaFisher, Christopher John. "Structure and surface reactions of iodine and cadmium iodide on fcc(111) metal surfaces". Thesis, University of Nottingham, 1999. http://eprints.nottingham.ac.uk/13744/.
Pełny tekst źródłaWu, Yichen. "Hypervalent Iodine as Directing Tool in Iodine-Retentive Transformation of C-H Bonds". Doctoral thesis, Universitat Rovira i Virgili, 2017. http://hdl.handle.net/10803/461093.
Pełny tekst źródłaLa química del yodo hipervalente es una potente y versátil herramienta en síntesis orgánica. En particular, los compuestos orgánicos de yodo(III) se han utilizado como oxidantes de 2 electrones, así como agentes de transferencia de grupos en diversos procesos oxidantes de funcionalización. Salvo unas pocas excepciones, estas transformaciones van acompañadas por la pérdida del fragmento yodobenceno. Una opción menos explorada, pero sintéticamente atractiva, consiste en la incorporación tanto del grupo orgánico como del átomo de yodo en el producto final. Este enfoque presenta un claro interés sintético dado que la retención del átomo de yodo posibilita su posterior derivatización. A lo largo de esta Memoria se muestran distintas reacciones de acoplamiento dirigidas por el yodo partiendo de compuestos de yodo trivalente como sustratos. En primer lugar, se describe un nuevo método de α-arilación directa de cetonas en ausencia de metales. La transferencia del grupo arilo tiene lugar vía acoplamiento orto al yodo, y se basa en la activación in situ del átomo de yodo. Este procedimiento presenta buena tolerancia a los distintos grupos funcionales del areno. La selectividad orto se relacionó, mediante cálculos DFT, con un mecanismo de reorganización yodonio-Claisen con una barrera de activación inusualmente baja. Se ha desarrollado también una nueva vía de acceso para reacciones de bencilación regioselectiva del anillo aromático del ArI(OAc)2 con benciltrimetilsilano. Es interesante destacar que este proceso el acoplamiento carbono-carbono tiene lugar selectivamente en la posición para respecto del átomo de yodo. En último lugar, se presenta una nueva estrategia para la “yodoarilación” oxidante de imidazoles. Este procedimiento se basa en la activación del anillo NH-imidazólico con ArI(OAc)2, seguida por una transferencia 1,3 I-a-N del grupo arilo para la obtención de N1-aril-5-yodoimidazoles. El impacto sintético de la transformación emana de la inherente capacidad de los N1-arilo-5-iodo-imidazoles de actuar como precursores para diversos derivados 1,5-sustituidos de imidazol.
The chemistry of organic hypervalent iodine compounds has been a potent and versatile toolbox in organic synthesis. In particular, organic λ3-iodanes have been utilized as terminal 2-electron oxidants, as well as group transfer agents in a wide range oxidative functionalization processes. With few exceptions, such transformations are accompanied by the liberation of the parent organoiodine fragment. A less explored, but synthetically attractive possibility consists in incorporating both the organic group and the iodine atom into the final product. Such approach presents a clear synthetic appeal, given that the iodine retention opens the door for downstream derivatization. This thesis describes a series of such “iodine-directed” coupling reaction employing organo-λ3-iodanes as substrates. In one approach, a new method for direct metal-free α-arylation of ketones is described. The aryl transfer takes place via the coupling ortho to iodine, and is based on in situ hypervalent activation of the iodine atom. The protocol shows good functional group compatibility on the arene core. The ortho-selectivity was rationalized by DFT calculations through an unusual low-barrier “iodonio-Claisen¨ process. We also developed a new approach for regioselective benzylation of the ArI(OAc)2 cores using benzyltrimethylsilane. Interestingly, the carbon-carbon coupling now takes place selectively at para position to the iodine atom. Finally, an approach for oxidative “iodoarylation” of imidazoles was uncovered. The procedure relies on an efficient activation of the parent NH-imidazole with ArI(OAc)2, followed by copper-catalyzed intramolecular 1,3 I-to-N aryl transfer to constitute the synthetically challenging N1-aryl-5-iodoimidazoles. The importance of this manifold resides in the ability of the 5-iodoimidazoles to act as precursors for a range of 1,5-substituted imidazoles.
Sattarzadeh, Masoud. "Determination of iron & iodine absorption from iron and iodine double-fortified salt". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq28793.pdf.
Pełny tekst źródłaVandevijvere, Stefanie. "Optimizing iodine nutrition in Belgium: a selective, progressive and monitored approach to control iodine deficiency". Doctoral thesis, Universite Libre de Bruxelles, 2012. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209599.
Pełny tekst źródłatackle iodine deficiency. It was however only during the last few years that an effort was
undertaken in order to eliminate iodine deficiency as a public health problem in Belgium. In autumn 1998, a nation-wide study among children clearly showed mild iodine deficiency in
Belgium, but no action was taken before 2009. It was only in the framework of the first
National Nutrition and Health Plan 2005-2010 that iodine deficiency was formally recognized
as a public health problem. An agreement between the Ministry of Health and the bakery
sector in April 2009 aimed to encourage and increase the use of iodised salt in the
production of bread. A selective and progressive approach was used in order to keep control
and to avoid a too rapid increase of iodine intake or an excessive iodine intake among the
population. It was calculated that the net yearly savings after installation of such a program
amount to at least 14 million Euros a year.
A recent national survey among school-aged children in autumn 2010 showed a clear and
significant improvement in iodine status compared to more than 10 years ago, suggesting
iodine sufficiency among school-aged children. The median urinary iodine concentration was
however at the lower end of the optimal range and seasonal effects were not taken into
account. The improvement was at least partly linked to the increasing use of iodised salt in
the bakery industry. However, some further silent iodine prophylaxis might also have
occurred, due to changing dietary habits (milk and fish consumption). Pregnant women and
women of child-bearing age in Belgium were found to still suffer from mild iodine deficiency
according to the current recommendations. This is at least partly linked to their lower
consumption of milk and dairy drinks compared to children and due to the higher iodine
requirements during pregnancy. Although the use of iodine-containing supplements among
pregnant women was found to be quite high in Belgium compared to other European
countries, because of the low iodine status among women of child-bearing age, women
became pregnant with a suboptimal iodine status.
In view of these findings, a further increase in the use of iodised instead of non-iodised
household salt and iodised salt by the bakers is recommended. In addition, one should put
efforts in increasing awareness among the public and among health professionals with
regard to iodine-rich food sources and with regard to the use of iodine-containing
supplements starting before conception and continuing during lactation.
In order to further improve iodine status in Belgium and sustain an optimal iodine status
over time, a legal framework is necessary. Mandatory fortification of all household salt and
bread is recommended, while non-iodised alternatives could still be offered upon specific
request. A rigorous monitoring program is indispensable, including vulnerable groups such as
pregnant and lactating women and infants. In addition, sustainability is a key issue as iodine
deficiency re-emerged in several industrial countries due to lack of interest, regulations and
monitoring. Political willing, salt reduction measures, changes in dietary habits among the
population and changes in industrial practices all may affect iodine status in Belgium in the
future. Therefore the strategy of controlling iodine deficiency needs to be directed and
monitored by a Belgian Scientific Committee for the Control of iodine deficiency disorders.
Doctorat en Sciences biomédicales et pharmaceutiques
info:eu-repo/semantics/nonPublished
Booth, James L. "On the ortho - para enhancement of molecular iodine by selective laser excitation". Thesis, University of British Columbia, 1985. http://hdl.handle.net/2429/24484.
Pełny tekst źródłaScience, Faculty of
Physics and Astronomy, Department of
Graduate
Smit, B. S. "Cellular radiotoxicity of iodine-123". Thesis, Stellenbosch : Stellenbosch University, 2000. http://hdl.handle.net/10019.1/51646.
Pełny tekst źródłaENGLISH ABSTRACT: The Auger electron emitter iodine-123 was examined in the form of 4- [12311iodoantipyrineand as [12311Nal for its effectiveness in killing cells of different sensitivity to photon irradiation. Micronucleus assays showed that 4- [12311iodoantipyrineis two to three times more effective in cell inactivation than C2311Nai.This can be attributed to the fact that antipyrine, for reason of its lipid solubility, can enter cells and can reach the cell nucleus, whereas C231]Nai is excluded from the cytoplasm. The differential targeting of intra- and extracellular compartments was confirmed by radionuclide uptake experiments. In the nucleus, Auger decay conceivably is located on the DNA where it may invoke high-LET irradiation damage. Irradiation damage by [12311Naisl by long range y-irradiation and hence low-LET. Results of the present study demonstrate however that the enhancement of MN-frequency seen with 4-[123I]iodoantipyrine over [12311Nalis similar for all cell lines and that the narrowing of MN-response expected for 4- [12311iodoantipyrinedoes not occur. Experiments with the free radical scavenger, DMSO, indicated nearly identical dose reduction factors for both iodine-123 carriers. These two observations strongly suggest that the cell inactivation by 4- [12311iodoantipyrine is not by high-LET direct ionisation of DNA, but due to an indirect effect. The indirect radiation effect of Auger decay in the nucleus is attributed to shielding of DNA by histones. Such a protection mechanism is not unrealistic if it is realised that histones and DNA associate in a 1: 1 weight ratio and that higher order folding of the nucleosome chain into solenoids, loops, and chromatids generates considerable protein density. In the nucleosome core, the histone acta mer measures 7 nm and closely approximates the 10 nm dimention of the Auger electron range. It is suggested that the interlacing of protein density with DNA density suppresses direct ionisation from Auger decay at the DNA and directs the majority of Auger decay to the histones.
AFRIKAANSE OPSOMMING: Die Auger-elektron-uitstraler, jodium-123, is ondersoek in die vorm van 4- [123l]jodoantipirien en [12311Nal om die effektiwiteit te bepaal waarmee dit selle met verskillende grade van sensitiwiteit vir fotonbestraling doodmaak. Mikrokerntellings toon aan dat 4-[123I]jodoantipirien selle twee tot drie maal meer effektief inaktiveer as [12311Nal.Dit kan toegeskryf word aan die feit dat antipirien, as gevolg van sy vetoplosbaarheidseienskappe, die selle kan binnedring en die kern bereik, teenoor [12311Nalwat uitgesluit word uit die sitoplasma. Die differensiële blootstelling van intra- en ekstrasellulere gebiede is bevestig deur radionukliedopname eksperimente. In die selkern vind Auger verval waarskynlik by die DNA plaas waar dit hoë-LET stralingskade veroorsaak. Stralingskade afkomstig van [1231]Nalis deur langafstand y-strale en dus lae-LET. Die resultate van die huidige studie bewys egter dat die verhoogde mikrokernfrekwensie van 4-[12311jodoantipirienteenoor [1231]Nal dieselfde is vir al die sellyne en dat die vernouïng van mikrokernreaksie soos verwag met 4- [12311jodoantipirien, nie plaasvind nie. Eksperimente met die vryradikaalopruimer, DMSO, dui op feitlik identiese dosis-modifiseringsfaktore vir beide jodium-123 draers. Hierdie twee waarnemings is 'n besliste aanduiding dat die selinaktivering deur 4-[12311jodoantipiriennie deur hoë-LET direkte ionisering van DNA plaasvind nie, maar eerder deur indirekte stralingsaksie. Die indirekte stralingseffek van Augerverval in die kern kan toegeskryf word aan afskerming van DNA deur histone. So 'n beskermingsmeganisme is nie onrealisties nie, as in ag geneem word dat histone en DNA in 'n 1: 1 gewigsverhouding assosieer en dat hoër orde vouïng van die nukleosoomketting tot solenoïede, lusse en chromatiede 'n beduidende protïendigtheid genereer. In die nukleosoomkern is die histoon-oktameer ongeveer 7 nm in deursnit en dus vergelykbaar met die 10 nm reikafstand van die Auger elektrone. Dit word voorgestel dat die ineengeweefdheid van die protien-digtheid met die DNA-digtheid die direkte ionisering van die DNA tydens Auger verval onderdruk en dat die meeste van die Auger verval in die histone plaasvind.
Yodle, Chan. "Iodine speciation in marine aerosol". Thesis, University of East Anglia, 2015. https://ueaeprints.uea.ac.uk/56772/.
Pełny tekst źródłaLightowler, Helen. "Iodine in the vegan diet". Thesis, London South Bank University, 1997. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.336909.
Pełny tekst źródłaParthipan, Rajendran. "Aqueous chemistry of iodine in seawater: Potential chemical sources of iodine in the marine atmosphere". Thesis, University of York, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.488743.
Pełny tekst źródłaShea, James Christopher 1964. "Hyperfine structure in the microwave spectra of the iodine fluorides iodine heptafluoride and iodine pentafluoride and of the weakly bound complex hydrochloric acid...nitrous oxide". Thesis, The University of Arizona, 1989. http://hdl.handle.net/10150/277178.
Pełny tekst źródłaBabicheva, Rosalie. "Radiation doses to family members of patients treated with Iodine-131 therapy". Connect to full text, 2001. http://hdl.handle.net/2123/5318.
Pełny tekst źródłaTitle from title screen (viewed Aug. 11, 2009) Includes tables. Submitted in fulfilment of the requirements for the degree of Master of Applied Science to the Faculty of Health Sciences. Includes bibliographical references. Also available in print form.
Fong, Ka-wah Martin. "Adaptation of a simplified method for urinary iodine for studying the iodine status of local Chinese". Click to view the E-thesis via HKUTO, 2004. http://sunzi.lib.hku.hk/hkuto/record/B31971726.
Pełny tekst źródłaFong, Ka-wah Martin, i 方家華. "Adaptation of a simplified method for urinary iodine for studying the iodine status of local Chinese". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B31971726.
Pełny tekst źródłaBowley, Hannah E. "Iodine dynamics in the terrestrial environment". Thesis, University of Nottingham, 2013. http://eprints.nottingham.ac.uk/13241/.
Pełny tekst źródłaNahavandi, Mona. "Iodine induced structures on Cu(100)". Thesis, KTH, Skolan för informations- och kommunikationsteknik (ICT), 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-102816.
Pełny tekst źródłaThompson, Clare. "The role of iodine in autoimmunity". Thesis, University of Cambridge, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.615656.
Pełny tekst źródłaChang, Ching-Chih, i Ching-Chih Chang. "Iodine-129 as an Oceanic Tracer". Diss., The University of Arizona, 2016. http://hdl.handle.net/10150/621856.
Pełny tekst źródłaMacDonald, Samantha Marie. "Iodine chemistry in the remote troposphere". Thesis, University of Leeds, 2013. http://etheses.whiterose.ac.uk/6356/.
Pełny tekst źródłaTheiss, Frederick L. "Removal of iodine using LDH technology". Thesis, Queensland University of Technology, 2016. https://eprints.qut.edu.au/100206/11/Frederick_Theiss_Thesis.pdf.
Pełny tekst źródłaCATANOSO, MARCELA F. "Purificação de sup(123)I e sup(131)I para marcação de biomoléculas". reponame:Repositório Institucional do IPEN, 2011. http://repositorio.ipen.br:8080/xmlui/handle/123456789/10025.
Pełny tekst źródłaMade available in DSpace on 2014-10-09T14:03:04Z (GMT). No. of bitstreams: 0
Dissertação (Mestrado)
IPEN/D
Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP
Babicheva, Rosalie. "Radiation doses to family members of patients treated with Iodine-131 therapy". Master's thesis, School of Medical Radiation Sciences, Faculty of Health Sciences, 2001. http://hdl.handle.net/2123/5318.
Pełny tekst źródłaTitle from title screen (viewed Aug. 11, 2009) Includes tables. Submitted in fulfilment of the requirements for the degree of Master of Applied Science to the Faculty of Health Sciences. Includes bibliographical references. Also available in print form.
Jia, Zhiyu. "Transformations promoted by the hypervalent iodine reagents". Doctoral thesis, Universitat Autònoma de Barcelona, 2014. http://hdl.handle.net/10803/134832.
Pełny tekst źródłaMalmedy, Florence. "Stereoselective transformations using chiral hypervalent iodine reagents". Thesis, Cardiff University, 2016. http://orca.cf.ac.uk/93576/.
Pełny tekst źródłaZhou, Xiang. "Electric field induced predissociation of molecular iodine". Thesis, University of British Columbia, 1991. http://hdl.handle.net/2429/29903.
Pełny tekst źródłaScience, Faculty of
Physics and Astronomy, Department of
Graduate
Nugraha, Tutun. "Iodine retention on stainless steel sampling lines". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ28825.pdf.
Pełny tekst źródłaFurman, Scott Anthony. "Surface chemistry of iodine on platinum (111)". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/NQ36639.pdf.
Pełny tekst źródłaJianping, Lin. "Iodine speciation in the Yarra River estuary /". Connect to thesis, 1992. http://eprints.unimelb.edu.au/archive/00000216.
Pełny tekst źródłaEdmunds, J. J. "Novel fluorination reactions via hypervalent iodine reagents". Thesis, Imperial College London, 1988. http://hdl.handle.net/10044/1/47045.
Pełny tekst źródłaAntien, Kevin. "Développement de nouveaux réactifs iodés hypervalents chiraux hélicéniques. Synthèse collective stéréodivergente d’alcaloïdes de Securinega". Thesis, Bordeaux, 2018. http://www.theses.fr/2018BORD0349/document.
Pełny tekst źródłaHypervalent iodine chemistry has been arousing the interest of the scientific community for the last 30 years. Research efforts are now mainly directed towards applications in asymmetric synthesis, notably through the use of chiral organoiodine scaffolds. To this end, solely central and axial chiralities have been exploited to construct such objects. The use of achiral iodanes (i.e. hypervalent organoiodine compounds) in asymmetric synthesis has been largely neglected by the community. Helical chirality in organic synthesis is mainly found in polyaromatic compounds known as helicenes. These molecules exhibit fascinating structural, electronic and chiroptical properties. They are the center of considerable attention across many fields of research, spanning from asymmetric catalysis to organic light-emitting diodes. Helical chirality has never been exploited in the field of hypervalent iodine chemistry. In the first part of this doctoral work, a methodology for the asymmetric oxygenative dearomatization of phenols by an achiral 3-iodane in the presence of a Cinchona-alkaloid-based phase transfer agent was developed. The second part of this manuscript details the synthesis of a new helicenic organoiodine compound and its application to oxygenative phenol dearomatization reactions. In the last chapter of this doctoral dissertation is described the total, collective and stereodivergent synthesis of 12 Securinega alkaloids. These natural products are commonly found in plants belonging to the genera Securinega (Flueggea), Phyllanthus, Margaritaria and Breynia of the Phyllanthaceae family. Even after little less than half a century of research, the real biogenetic pathway used by nature to construct these molecules is still only partly understood. The chemical synthesis developed in this doctoral work provides a better understanding of the biosynthetic mechanism. It was established in the course of this work that a key aldol condensation step could shed light upon the stereodivergence observed in nature
Kar, Adwitiya. "Novel 125 I production and recovery system". [College Station, Tex. : Texas A&M University, 2007. http://hdl.handle.net/1969.1/ETD-TAMU-1534.
Pełny tekst źródłaRomero, Segura Rafael Martín. "Development of hypervalent iodine(iii)-mediated chemical reactions". Doctoral thesis, Universitat Rovira i Virgili, 2017. http://hdl.handle.net/10803/402470.
Pełny tekst źródłaLos reactivos de iodo hipervalente representan una herramienta muy poderosa para la realización de diferentes oxidaciones libres de metal. Se llevaron a cabo estudios mecanísticos incluyendo experimentos físico-orgánicos de control respecto a la diaminación intermolecular de alquenos, demostrando la veracidad de los cálculos DFT previamente realizados. Esta información resultó crucial para el desarrollo de una pionera diaminación enantioselectiva de estirenos catalizada por iodo(III). Uno de los mayores logros es el diseño de un nuevo catalizador de iodo quiral basado en el ácido láctico como fuente económica de información estereoquímica. La optimización del catalizador incluye un aumento crucial de electrondensidad en el núcleo de iodo y la presencia del grupo amida en la cadena de lactato quiral. Entre los diferentes oxidantes terminales probados, mCPBA resultó ser el más eficiente, dando buenos rendimientos y una enantioselectividad sin precedentes, siendo ésta siempre superior al 90% ee. Esta reacción puede extenderse a alquenos terminales e internos que contengan la estructura de estireno. Este logro representa uno de los resultados más avanzados en la diaminación asimétrica de alquenos. En un estudio adicional, se consiguió una nueva formación de enlaces carbono-boro. Aquí, la borilación de sales de diariliodonio fue posible tras la identificación de un contraión apropiado en el reactivo de diariliodonio. Gracias a la generación in situ de un umpolung en el centro de boro, su arilación por el reactivo hipervalente es posible. Con esta finalidad, se sintetizaron diferentes acetatos de diariliodonio y se demostró la gran aplicabilidad de esta metodología en la transferencia de grupos aromáticos. Este protocolo representa uno de los pocos procesos económicos de borilación en ausencia de metal.
Hypervalent iodine(III) reagents represent a powerful tool for the realisation of different metal-free oxidation reactions. Mechanistic studies including physical-organic control experiments concerning the oxidative iodine(III)-mediated intermolecular diamination of alkens were carried out, demonstrating the veracity of previous DFT calculations. This information provided crucial insight for the development of a pioneering iodine(III)-catalysed enantioselective diamination of styrenes. The design of a novel chiral iodine catalyst based on lactic acid as economic chiral information source represents the key accomplishment. Catalyst optimisation involves a crucial electrondensity enhancement at the iodine core and a secondary amide motive in the chiral lactate side chain. Among different terminal oxidants, conventional mCPBA emerged as the most efficient one leading to good yields and unprecedented enantioselectivities of above 90% ee. The scope of the reaction comprises terminal and internal alkenes within the styrene motif. It represents the state of the art in asymmetric diamination of alkenes. In an additional study, a novel carbon-boron bond formation was accomplished. Here, borylation of diaryliodonium salts was encountered feasible upon identification of a suitable counterion in the diaryliodonium reagent. By generating an in situ umpolung at the boron centre, its arylation by the hypervalent reagent becomes viable. To this end, different diaryliodonium acetates were synthesised, thereby successfully demonstrating a broad applicability of this new methodology regarding the transferable aromatic group. This protocol adds to the still scarce number of economic borylation reactions under metal-free conditions.
Narayanan, Anandhi. "Global model for iodine behaviour in reactor containment". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0020/MQ53344.pdf.
Pełny tekst źródłaPage, Thomas Keri. "Synthesis and reactivity of chiral hypervalent iodine compounds". Thesis, Cardiff University, 2009. http://orca.cf.ac.uk/54874/.
Pełny tekst źródłaFiltness, Michael Jane. "Investigating the early solar system using iodine-129". Thesis, University of Manchester, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.497443.
Pełny tekst źródłaPoulton, Miriam. "Iodine deficiency in the Northern Punjab of Pakistan". Thesis, University College London (University of London), 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267658.
Pełny tekst źródłaPruenglampoo, Sakda. "Dietary iodine intake during pregnancy and birth outcome". Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243117.
Pełny tekst źródłaJegasothy, Shankar. "Kinetic studies on polymer-supported hypervalent iodine oxidants". Thesis, University of Cambridge, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.615044.
Pełny tekst źródłaJi, Chen. "Salt intake and iodine status around the world". Thesis, University of Warwick, 2013. http://wrap.warwick.ac.uk/57708/.
Pełny tekst źródłaBruzzese, John Reed. "Development of an Electric Discharge Oxygen-Iodine Laser". The Ohio State University, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=osu1308228482.
Pełny tekst źródłaAtkinson, Helen. "Iodine in sea ice and the polar atmosphere". Thesis, University of East Anglia, 2011. https://ueaeprints.uea.ac.uk/40451/.
Pełny tekst źródłaPikelnaya, Olga. "Reactive iodine species at North American coastal sites". Diss., Restricted to subscribing institutions, 2008. http://proquest.umi.com/pqdweb?did=1773833421&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.
Pełny tekst źródłaGurung, Ras Kumari. "INVESTIGATIONS OF HYPERVALENT IODINE COMPOUNDS IN ORGANIC TRANSFORMATIONS". OpenSIUC, 2015. https://opensiuc.lib.siu.edu/dissertations/991.
Pełny tekst źródłaBalaji, A. "Analysis Of Solar Pumped Chemical Oxygen Iodine Laser". Thesis, Indian Institute of Science, 2000. https://etd.iisc.ac.in/handle/2005/238.
Pełny tekst źródłaBalaji, A. "Analysis Of Solar Pumped Chemical Oxygen Iodine Laser". Thesis, Indian Institute of Science, 2000. http://hdl.handle.net/2005/238.
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