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Showing 1 to 20 of 76 for “"Boronic acid"”.

  1. Tetracycline-7-boronic acid

    The objective of this study is the preparation of a tetracycline-boron-10 derivative which is stable under biological conditions. The boron-10 should then provide a concentration of material capable of accepting thermal neutrons, thus producing localized high-energy alpha radiation. The fact that …

    u-pacific Repository record for Tetracycline-7-boronic acid (opens in a new tab)

  2. Synthesis and Application of Boronic Acid Derivatives

    Boronic acids are attractive synthetic intermediates and have been shown to be effective as inhibitors of various enzymes. In this project, the overarching goal is the selective inhibition of a protease present in the mitochondria known as human ClpXP. To study the potential selective inhibition of …

    vt Repository record for Synthesis and Application of Boronic Acid Derivatives (opens in a new tab)

  3. Photoredox C–C Cross-Coupling Reactions using Boronic Acid Derivatives

    … as reagents in organic synthesis, the use of boronic acid derivatives to generate carbon-centred radicals remains elusive. This dissertation explores the utilisation of photoredox catalysis to generate carbon radicals from boronic acid derivatives and subsequently engage them in C–C …

    cambridge Repository record for Photoredox C–C Cross-Coupling Reactions using Boronic Acid Derivatives (opens in a new tab)

  4. A kinetic investigation of boronic acid/diol interactions and pattern-based recognition of [alpha]-chiral carboxylates

    Amine-functionalized boronic acids have revolutionized the field of carbohydrate sensing in recent years. Capable of rapidly and reversibly forming cyclic boronate esters with of 1,2- and 1,3-diols, polyols, catechols, and α-hydroxycarboxylic acids, boronic acids have found applications spanning …

    texas Repository record for A kinetic investigation of boronic acid/diol interactions and pattern-based recognition of [alpha]-chiral carboxylates (opens in a new tab)

  5. Click Chemistry on DNA and Targeting RNA structure with Peptide Boronic Acids

    … via redox pathways have provided nucleic acid researchers access to the efficiency and quantitative nature of the click reaction. The majority of ligation procedures in the literature are performed in solution after DNA assembly and modification with alkyne reporter groups. However, …

    vt Repository record for Click Chemistry on DNA and Targeting RNA structure with Peptide Boronic Acids (opens in a new tab)

  6. Targeting HIV-1 RNAs with Medium Sized Branched Peptides Featuring Boron and Acridine-Branched Peptide Library Design, Synthesis, High-Throughput Screening and Validation

    … screening of a 3.3.4 branched peptide boronic acids (BPBAs) library that bind selectively to the tertiary structure of RRE IIB. The library comprised of 46,656 unique sequences. We demonstrate that our highest affinity BPBA (BPBA1) selectively binds RRE IIB in the presence of competitor …

    vt Repository record for Targeting HIV-1 RNAs with Medium Sized Branched Peptides Featuring Boron and Acridine-Branched Peptide Library Design, Synthesis, High-Throughput Screening and Validation (opens in a new tab)

  7. Thiol-Norbornene Hydrogels With Tunable Mechanical Properties for Engineered Extracellular Matrices

    … was designed to yield dynamically adaptable boronic ester bonds via partial enzymatic reaction. Thiol-norborne hydrogel was made to contain hydroxyl phenol as well as boronic acid residues within its network. MT, in this case was used to oxidize the hydroxy phenol moieties into DOPA, which …

    iupui Repository record for Thiol-Norbornene Hydrogels With Tunable Mechanical Properties for Engineered Extracellular Matrices (opens in a new tab)

  8. Examination of UV-Cross-Linkable Di-Block Copolymer Strategy for Functionalized Reaction Surface on Microelectrode Arrays

    … coating for the array. Finally, a copolymer with boronic acid functionality, PCEMA-b-BoSt was made in order to test the versatility of the boronic acid as a starting material for building other functionalities. The boronic acid derived polymer performs better than the previous coating in terms of …

    wustl Repository record for Examination of UV-Cross-Linkable Di-Block Copolymer Strategy for Functionalized Reaction Surface on Microelectrode Arrays (opens in a new tab)

  9. Transmetalation from boronic esters to arylpalladium complexes without prior hydrolysis – mechanistic studies and preparative applications in the anhydrous, Suzuki-Miyaura cross-coupling reaction

    … pre-transmetalation intermediates incorporating boronic esters have been characterized, proving the competency of boronic esters to undergo transmetalation without prior hydrolysis. Boronic ester structure was found to have a significant impact on both pretransmetalation intermediate speciation …

    uiuc Repository record for Transmetalation from boronic esters to arylpalladium complexes without prior hydrolysis – mechanistic studies and preparative applications in the anhydrous, Suzuki-Miyaura cross-coupling reaction (opens in a new tab)

  10. Shape-switching studies with cyclophanes and indicator displacement assays with boronic acids

    … of indicator displacement assays (IDAs) with a boronic acid receptor, used for the differentiation of Z and E alkene mixtures. An IDA protocol was developed which is ammenable to high-throughput screening and can successfully identify Z and E alkene mixtures with an average absolute error of …

    qu-belfast Repository record for Shape-switching studies with cyclophanes and indicator displacement assays with boronic acids (opens in a new tab)

  11. Synthetic routes to hydroxyaucanebobonic acids and their derivatives

    … of synthetic routes leading to hydroxyalkaneboronic acids, which were expected to display some useful and interesting biological and chemical properties, has been carried out with reference to reaction sequences involving the hydroboration of alkenes and interaction of Grignard reagents with …

    greenwich Repository record for Synthetic routes to hydroxyaucanebobonic acids and their derivatives (opens in a new tab)

  12. Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link

    … and the wide variety of commercially available boronic acid substrates. Despite the popularity of the Suzuki-Miyaura reaction, the precise manner in which the organic fragment is transferred from boron to palladium has remained elusive for over 30 years. The work described in this dissertation …

    uiuc Repository record for Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link (opens in a new tab)

  13. Saccharide recognition : boronic acids as receptors in polymeric networks

    In this thesis entitled “Saccharide Recognition - Boronic acids as Receptors in Polymeric Networks” different aspects of boronic acid synthesis, their analysis and incorporation or attachment to different polymeric networks and characterisation thereof were investigated. The following key aspects …

    potsdam-diss Repository record for Saccharide recognition : boronic acids as receptors in polymeric networks (opens in a new tab)

  14. Catalytic and Biological Applications of Benzoxaborolones

    Though first isolated 150 years ago, boronic acids have historically been neglected species. The more recent advent of transition metal-catalyzed reactions has led to an explosion in their use as building blocks, which in turn has led to their application in many other contexts as synthetic methods …

    mit Repository record for Catalytic and Biological Applications of Benzoxaborolones (opens in a new tab)

  15. A synthesis of a homologous series of aryl mono- and diboronic acids

    <p>Many attempts have been made to prepare aryl boronic acids and their esters which show a preferential affinity for tumor tissues for use in radiation therapy of neoplatic disorders (1,2). The data of Soloway, as extended and refined by Hansch and his coworkers, successfully correlates the low …

    u-pacific Repository record for A synthesis of a homologous series of aryl mono- and diboronic acids (opens in a new tab)

  16. Developing test strips for naked-eye detection of alpha-hydroxy acids using indicator-displacement assays: an application of molecular recognition

    … Two examples are the dihydroxylation of maleic acid and fumaric acid catalyzed by osmium tetroxide in water, and the hydrolysis of D-dimethyl tartrate. The assay employed a receptor that has 1,3,5-trisubstituted-2,4,6- triethylbenzene scaffold incorporating boronic acid and guanidinium moieties …

    texas Repository record for Developing test strips for naked-eye detection of alpha-hydroxy acids using indicator-displacement assays: an application of molecular recognition (opens in a new tab)

  17. Luminescent Iridium(III) Cyclometalated Complexes: Host-Guest Chemistry and Application as Sensors

    … displayed the highest solubility in oleic acid (as an example of fatty acid that present in fingerprints). A boronic acid group (B(OH)2) was introduced to the bpy ligand to form B(OH)2-Ir-H, which was used as a sensor for peroxide detection, based on the ability of hydrogen peroxide (H2O2) …

    unsw Repository record for Luminescent Iridium(III) Cyclometalated Complexes: Host-Guest Chemistry and Application as Sensors (opens in a new tab)

  18. Part I: synthesis and cross-coupling of the C1-C12 primary organoborane building block of amphotericin B; Part II: site- and stereoretentive cross-coupling of unactivated secondary boronic acids inspired by amphotericin B

    … idealized limit, a collection of off-the-shelf boronic acid-based building blocks having all of the required functional groups pre-installed in the correct oxidation states and with the desired stereochemical relationships are readily assembled using only a single cross-coupling reaction …

    uiuc Repository record for Part I: synthesis and cross-coupling of the C1-C12 primary organoborane building block of amphotericin B; Part II: site- and stereoretentive cross-coupling of unactivated secondary boronic acids inspired by amphotericin B (opens in a new tab)

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