Now showing items 4300-4319 of 4765

    • Syntese av klorerte fettsyrer til bruk som standarder i miljøanalyser 

      Lauknes, Kristian (Master thesis; Mastergradsoppgave, 2007-06-20)
      Mettede C-16 og C-18 klorerte fettsyrer ble syntetisert til bruk som miljøstandarder. De mettede klorerte fettsyrene hører sammen med en ny type miljøgift nemlig klorerte fettsyrer (ClFA). Dette er en type miljøgift som man per dags dato ikke har så mye kunnskap om, men som er blitt påvist i en rekke forskjellige fiskearter. Hvilken effekt de vil ha på mennesker eller andre pattedyr på toppen av ...
    • Synthesis and biological evaluation of new dipicolylamine zinc chelators as metallo-β-lactamase inhibitors 

      Prandina, Anthony; Radix, Sylvie; Le Borgne, Marc; Jordheim, Lars Petter; Bousfiha, Zineb; Fröhlich, Christopher; Leiros, Hanna-Kirsti S.; Samuelsen, Ørjan; Frøvold, Espen; Rongved, Pål; Åstrand, Ove Alexander Høgmoen (Journal article; Tidsskriftartikkel; Peer reviewed, 2019-02-02)
      Antibiotics are key drugs in modern healthcare, especially in hospitals, where multiresistant bacteria resides and is a potential threat to human health. In the present work, a new series of adjuvants working synergistically with the carbapenem meropenem, in which a selective zinc-chelating agent was covalently linked to the small bacterial peptide D-Ala-D-Ala, was synthesized and tested against ...
    • Synthesis and inhibitor design of carbapenemase inhibitors 

      Akhter, Sundus (Doctoral thesis; Doktorgradsavhandling, 2018-05-24)
      The efficiency of bacteria in acquiring resistance for their survival ensures a never-ending war against resistance. The only tactic to curtail the resistance crisis is to keep pace with it, e.g. by continuous development of new antibiotics with activity against resistant bacteria or revival of existing agents by inhibiting the mechanisms of resistance. β-lactams are the largest and most widely used ...
    • Synthesis and Molecular Structure of a Copper Octaiodocorrole 

      Thomassen, Ivar Kristian; McCormick, Laura J.; Ghosh, Abhik (Journal article; Tidsskriftartikkel; Peer reviewed, 2018-05-09)
      Although rather delicate on account of their propensity to undergo deiodination, β-octaiodoporphyrinoids are of considerable interest as potential precursors to novel β-octasubstituted macrocycles. Presented herein are early results of our efforts to synthesize β-octaiodocorrole derivatives. Oxidative condensation of 3,4-diiodopyrrole and aromatic aldehydes failed to yield free-base octaiodocorroles. ...
    • Synthesis and molecular structure of perhalogenated rhenium-oxo corroles 

      Alemayehu, Abraham B.; Einrem, Rune F.; McCormick‑McPherson, Laura J.; Settineri, Nicholas S.; Ghosh, Abhik (Journal article; Tidsskriftartikkel; Peer reviewed, 2020-11-12)
      As part of our efforts to develop rhenium-oxo corroles as photosensitizers for oxygen sensing and photodynamic therapy, we investigated the potential <i>β</i>-perhalogenation of five ReO <i>meso</i>-tris(<i>para</i>-X-phenyl)corroles, Re[T<i>p</i>XPC](O) (X = CF<sub>3</sub>, H, F, CH<sub>3</sub>, and OCH<sub>3</sub>), with elemental chlorine and bromine. With Cl<sub>2</sub>, <i>β</i>-octachlorinated ...
    • Synthesis of 5,7-diarylindoles via Suzuki-Miyaura coupling in water 

      Elumalai, Vijayaragavan; Hansen, Jørn H (Journal article; Tidsskriftartikkel; Peer reviewed, 2021-11-16)
      The synthesis of novel 5,7-diaryl and diheteroaryl indoles has been explored via efficient double Suzuki–Miyaura coupling. The method notably employs a low catalyst loading of Pd(PPh<sub>3</sub>)<sub>4</sub> (1.5 mol%/coupling) and water as the reaction solvent to obtain 5,7-diarylated indoles without using N-protecting groups in up to 91% yield. The approach is also suitable for N-protected and ...
    • Synthesis of 5-,6-, and 7-membered heterocycles from barbituric acid derivatives 

      Guyader, David (Master thesis; Mastergradsoppgave, 2011-06-10)
      SUMMARY A new procedure has been developed for the synthesis of barbituric acid derivatives. The reactions were performed under solvent free conditions without any catalyst. Employing this synthetic route, a large number of chalconoids and 5-,6-, and 7-membered heterocycles have been successfully synthesized in a very short time. The chalconoids have been synthesized from a barbituric derivative ...
    • Synthesis of a novel class of antitubercular peptidomimetics based on β-aminoboronates. 

      Gorovoy, Alexey (Doctoral thesis; Doktorgradsavhandling, 2012-11-16)
      The unique properties of antimicrobial peptides have attracted the attention of chemists since the 1970’s. This class of compounds provides additional tools in the treatment of infections and the work described in this thesis was therefore focused on the synthesis of short peptidomimetics on the basis of modified amino acids and evaluation of their antimicrobial activity. The compounds of choice ...
    • Synthesis of Indoles and Pyrroles Utilizing Iridium Carbenes Generated from Sulfoxonium Ylides 

      Vaitla, Janakiram; Bayer, Annette; Hopmann, Kathrin Helen (Journal article; Tidsskriftartikkel; Peer reviewed, 2017-03-20)
      Metal carbenes can undergo a myriad of synthetic transformations. Sulfur ylides are potential safe precursors of metal carbenes. Herein, we report cascade reactions that involve carbenoids derived from sulfoxonium ylides for the efficient and regioselective synthesis of indoles and pyrroles. The tandem action of iridium and Brønsted acid catalysts enables rapid assembly of the heterocycles from ...
    • Synthesis of phorbazoles and breitfussins analogues 

      Abdelhady, Ahmed Mossad Mohamed (Master thesis; Mastergradsoppgave, 2016-05-18)
      Breitfussins are a group of a closely related heterocyclic compounds. They consist of a tetracyclic structure with an indole, an oxazole and a pyrrole. The breitfussins exhibit interesting biological activity and analogues synthesis and biological evaluation is ongoing. Phorbazoles have a structural similarity with breitfussins in which a phenol replaces the indole. As a part of this, synthesis of ...
    • Synthesis of Potential Metallo-beta-Lactamase Inhibitors 

      Paulsen, Britt (Master thesis; Mastergradsoppgave, 2011-11-15)
    • Synthesis of Potential Metallo-β-Lactamase Inhibitors 

      Paulsen, Marianne Hagensen (Master thesis; Mastergradsoppgave, 2012-06-04)
      Oppgaven omhandler syntesen av mulige metallo-beta-lactamaser inhibitorer.
    • Synthesis of Sterically Hindered Macrocyclic Ligands via Demetalation of Metallocorroles 

      Capar, Jan (Doctoral thesis; Doktorgradsavhandling, 2016-06-07)
      Despite important developments in synthetic corrole chemistry, the field has long been handicapped by the lack of procedures for demetalation of metallocorroles. This thesis presents general demetalation methods for metallocorroles. A reductive demetalation method was developed using concentrated H2SO4 with 5-200 equivalent of FeCl2 or SnCl2 as a reducing agent. The method proved to be quite general ...
    • Synthesis of thiol-appended gold and rhenium corroles as potential nanoconjugants for gold nanoparticles 

      Engedal Johannessen, Krister (Master thesis; Mastergradsoppgave, 2023-06-10)
      Photodynamic therapy (PDT) today is an established treatment for a variety of cancers as well as various dermatological conditions, macular degeneration and bacterial and other infections. Treatment involves the administration of a photosensitizer, typically a porphyrin, followed by irradiation with light. The photoexcited sensitizer transfers its excess energy to oxygen in the affected tissue, ...
    • Synthesis of XTH inhibitors 

      Pettersen, Martin (Master thesis; Mastergradsoppgave, 2019-05-15)
      XTH er en gruppe enzymer som ble oppdaget tidlig på 90 tallet og muligens er involvert i Cuscuta infeksjonen av tomater. En nylig studie gjort ved arktisk og marin biologi UIT viser at Brilliant Blue R250 fungerer som en god inhibitor mot disse enzymene. I dette prosjektet ble det fokusert på å syntetisere strukturelt like molekyler for å potensielt øke vannløseligheten og inhibitoraktiviteten. ...
    • Synthesis of β-substituted β-aminoboronates 

      Thomassen, Ivar Kristian (Master thesis; Mastergradsoppgave, 2013-05)
      Recent work at the University of Tromsø has uncovered new α-substituted α- and β-aminoboron containing peptidomimetics that shows antimicrobial, antifungal and antitubercular activity in addition to kinase inhibition and promotion. As a continuation of this work a new approach for the synthesis of β-substituted β-aminoboronates has been developed. The approach involves the non-stereospecific ...
    • Synthesis, Spectroscopy, Electrochemistry and DFT of Electron-Rich Ferrocenylsubphthalocyanines 

      Conradie, Jeanet; Swarts, Petrus (Journal article; Tidsskriftartikkel; Peer reviewed, 2020-06-01)
      A series of novel ferrocenylsubphthalocyanine dyads Y-BSubPc(H)<sub>12</sub> with ferrocenylcarboxylic acids Y-H = (FcCH<sub>2</sub>CO<sub>2</sub>-H), (Fc(CH<sub>2</sub>)<sub>3</sub>CO<sub>2</sub>-H) or (FcCO(CH<sub>2</sub>)<sub>2</sub>CO<sub>2</sub>-H) in the axial position were synthesized from the parent Cl-BSubPc(H)<sub>12</sub> via an activated triflate-SubPc intermediate. UV/Vis data revealed ...
    • Synthetic analogs of stryphnusin isolated from the marine sponge Stryphnus fortis inhibit acetylcholinesterase with no effect on muscle function or neuromuscular transmission 

      Moodie, Lindon; Zuzek, Monika; Frangez, Robert; Andersen, Jeanette hammer; Hansen, Espen; Olsen, Elisabeth Klungerbo; Cergolj, Marija; Sepcic, Kristina; Hanssen, Kine Østnes; Svenson, Johan (Journal article; Tidsskriftartikkel; Peer reviewed, 2016-11-09)
      The marine secondary metabolite stryphnusin (1) was isolated from the boreal sponge Stryphnus fortis, collected off the Norwegian coast. Given its resemblance to other natural acetylcholinesterase antagonists, it was evaluated against electric eel acetylcholinesterase and displayed inhibitory activity. A library of twelve synthetic phenethylamine analogs, 2a–7a and 2b–7b, containing tertiary and ...
    • Synthetic aperture radar compact polarimetry for sea ice surveillance 

      Espeseth, Martine Mostervik (Master thesis; Mastergradsoppgave, 2015-06-26)
      The focus of this thesis is to investigate the use of synthetic aperture radar (SAR) compact polarimetry for studies of sea ice. Data obtained from quad-polarimetric SAR systems have already been studied extensively for sea ice monitoring. This thesis focuses on finding parallels to quad-polarimetric features from the compact-polarimetric data. This is achieved through the reconstruction of a pseudo ...
    • Synthetic Aperture Radar Remote Sensing of Operational Platform Produced Water Releases 

      Skrunes, Stine; Johansson, Malin; Brekke, Camilla (Journal article; Tidsskriftartikkel; Peer reviewed, 2019-12-03)
      Oil spill detection services based on satellite synthetic aperture radar (SAR) frequently detect oil slicks close to platforms due to legal releases of produced water. Separating these slicks from larger releases, e.g., due to accidental leakage is challenging. The aim of this work is to investigate the SAR characteristics of produced water, including the typical appearance in HH/VV data, possible ...