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Showing 1 to 20 of 73 for “"Lewis-acids"”.

  1. Formation and capture of thiiranium ion intermediates using Lewis acids

    Submission published under a 24 month embargo labeled 'U of I only', the embargo will last until 2017-08-01

    uiuc Repository record for Formation and capture of thiiranium ion intermediates using Lewis acids (opens in a new tab)

  2. Thermodynamics of Molecular Addition Compound Formation Between Amides and Lewis Acids

    Made available in DSpace on 2014-12-05T19:37:48Z (GMT). No. of bitstreams: 1 6104402.pdf: 2471219 bytes, checksum: 7150fa5f304da913bf0ee9390f8bc520 (MD5) Previous issue date: 1961

    uiuc Repository record for Thermodynamics of Molecular Addition Compound Formation Between Amides and Lewis Acids (opens in a new tab)

  3. Reactions at coordinated ligands: redox-active ligands and coordination of Lewis acids

    … of redox-active ligands, ligand protonation and Lewis acid coordination to ligands. The focus is on ligand design rather than substrate or metal optimization with a primary interest in reactivity with dihydrogen. The main thrust of the work has been the investigation of redox-active ligands in …

    uiuc Repository record for Reactions at coordinated ligands: redox-active ligands and coordination of Lewis acids (opens in a new tab)

  4. Lewis Base Activation of Lewis Acids in Asymmetric Aldol Reactions of Silyl Ketene Acetals

    The concept of Lewis base activation of Lewis acids has been effectively reduced to practice for catalysis in the chiral phosphoramide catalyzed/SiCl 4 promoted aldol reaction of silyl ketene acetals and silyl dienol ethers with aldehydes. The weakly acidic species, silicon tetrachloride (SiCl 4), …

    uiuc Repository record for Lewis Base Activation of Lewis Acids in Asymmetric Aldol Reactions of Silyl Ketene Acetals (opens in a new tab)

  5. New Approaches Towards the Asymmetric Allylation of the Formyl and Imino Groups via Strained Silane Lewis Acids

    … functionalities by using strained silanes as Lewis acids. Here in the Laboratory of Professor James L. Leighton, chiral homoallylic alcohols and amines are considered privileged products given their important role as building blocks in natural product synthesis. The new approaches reported …

    columbia-diss Repository record for New Approaches Towards the Asymmetric Allylation of the Formyl and Imino Groups via Strained Silane Lewis Acids (opens in a new tab)

  6. Synthetic and mechanistic investigation of new radical processes: reaction of organic azides with group-XIII Lewis acids

    … with indium trichloride and other group XIII Lewis acids, in particular gallium trichloride, gives rise to strongly coloured, persistent paramagnetic species, whose structure is consistent with the radical cation of the head-to-tail dimer of the aniline corresponding to the starting azide.

    bologna Repository record for Synthetic and mechanistic investigation of new radical processes: reaction of organic azides with group-XIII Lewis acids (opens in a new tab)

  7. Boron Subnaphthalocyanines: The First Unsubstituted Examples, New Boron Lewis Acids, Random Bay Position Halogenation, and Computational Material Screening

    … this, we proposed that a non-halide boron based Lewis acid is required, and that a balance of the Lewis acidity of the boron source and the Lewis basicity of the BsubNc precursor can guide the synthesis of BsubNcs. After achieving this desired outcome, we also explored the application of this …

    toronto-retro Repository record for Boron Subnaphthalocyanines: The First Unsubstituted Examples, New Boron Lewis Acids, Random Bay Position Halogenation, and Computational Material Screening (opens in a new tab)

  8. Applications of novel boron-nitrogen containing heterocycles : design and synthesis o planar-chiral Lewis acids for stereoselective organic synthesis

    Because Lewis acids are very versatile mediators of a variety of stereoselective organic transformations, a great deal of effort has been devoted toward the development of chiral Lewis acids. This thesis describes the design, synthesis, and applications of 1,2-azaborolyl complexes as a novel family …

    mit Repository record for Applications of novel boron-nitrogen containing heterocycles : design and synthesis o planar-chiral Lewis acids for stereoselective organic synthesis (opens in a new tab)

  9. Synthesis and catalytic structure activity relations of hydrophobic zeolites with isolated framework metals that act as water tolerant Lewis acids

    … hydrophobic zeolites results in water-tolerant Lewis acids. This thesis discusses the synthesis, characterization, and structure-activity relations of metal-substituted Beta zeolites in the conversion of oxygenates. Chapter 2 discusses the application of dynamic nuclear polarization (DNP) NMR to …

    mit Repository record for Synthesis and catalytic structure activity relations of hydrophobic zeolites with isolated framework metals that act as water tolerant Lewis acids (opens in a new tab)

  10. Scope, Selectivity, and Mechanism of the Prins Cyclization of Delta,&egr;- and &egr;,zeta-Unsaturated Ketones With Lewis Acids to 1,3-Halohydrins

    Finally, reduction in R:FR increased vertical growth and erectness of both BAS1 gene transformants and control plants, however, overexpression of BAS1 gene induced dwarfism in transgenic creeping bentgrass by delaying vertical shoot growth and altering shoot architecture. True BAS1 transformants …

    uiuc Repository record for Scope, Selectivity, and Mechanism of the Prins Cyclization of Delta,&egr;- and &egr;,zeta-Unsaturated Ketones With Lewis Acids to 1,3-Halohydrins (opens in a new tab)

  11. Stereochemical Course of the Tandem [4+2]/[3+2] Cycloaddition of Nitroalkenes

    … and theoretical studies. Small, soft Lewis acids (such as Me 3Al) promote endo cycloaddition with the vinyl ether reacting in an s-trans conformation. Most other Lewis acids favor exo cycloaddition due either to their size (such as MAPh) or the conformation they force upon the …

    uiuc Repository record for Stereochemical Course of the Tandem [4+2]/[3+2] Cycloaddition of Nitroalkenes (opens in a new tab)

  12. Carbon-Carbon Bonds Formed by Lewis Acid Catalysis or Photoactivation

    … from propargylic alcohols, organoboronates, and Lewis acids. Lewis acids can also be used to facilitate a mild Friedel-Crafts reaction between electron-rich aromatics and allylic or benzylic alcohols. Moreover, these methods can be applied to the synthesis of natural products. Finally, …

    houston Repository record for Carbon-Carbon Bonds Formed by Lewis Acid Catalysis or Photoactivation (opens in a new tab)

  13. A Lewis Acidic Stroll Through the p-Block

    Since the inception of frustrated Lewis pair (FLP) chemistry more than a decade ago, the development of an assortment of main group Lewis acids in the literature has contributed to the enrichment and diversification of FLP reactivity to achieve transition metal-like chemistry. While most of the …

    toronto-retro Repository record for A Lewis Acidic Stroll Through the p-Block (opens in a new tab)

  14. Synthesis and reactivity of early transition metal "Frustrated Lewis Pairs"

    … introduced the new concept of "Frustrated Lewis Pairs" (FLP) wherein sterically demanding Lewis acids and bases do not interact in the expected donor-acceptor fashion, but rather exhibit unique reactivity. To date this concept of FLPs has been limited to main group systems. In this thesis …

    windsor Repository record for Synthesis and reactivity of early transition metal "Frustrated Lewis Pairs" (opens in a new tab)

  15. Part I. Stereochemical Studies on the Addition of Allylsilanes to Aldehydes. Part II. Stereochemical Studies on the Addition of Allylmetal Reagents to Acetals

    … performed to determine the solution structure of Lewis acid-aldehyde complexes. The intramolecular allylmetal-aldehyde reaction was next studied using three different model systems. The first two model systems were investigated to determine the relative disposition of double bonds in the …

    uiuc Repository record for Part I. Stereochemical Studies on the Addition of Allylsilanes to Aldehydes. Part II. Stereochemical Studies on the Addition of Allylmetal Reagents to Acetals (opens in a new tab)

  16. Chiral-Phosphoramide-Catalyzed Enantioselective Allylation Reactions: Mechanistic, Structural and Preparative Studies

    The method of generating chiral Lewis acids with a combination of SiCl 4 and chiral phosphoramides has been applied in the formal hetero-Diels-Alder reaction and modest to high selectivities have been obtained.

    uiuc Repository record for Chiral-Phosphoramide-Catalyzed Enantioselective Allylation Reactions: Mechanistic, Structural and Preparative Studies (opens in a new tab)

  17. Probing the Impact of Solvent on Lewis Acid Catalysis via Fluorescent Lewis Adducts

    … have been developed to measure the strength of a Lewis acid. However, a major challenge for these measurements lies in the complexity that arises from variables, such as solvent and other fundamental interactions, as well as perturbations of Lewis acids as their reaction environment changes. …

    york Repository record for Probing the Impact of Solvent on Lewis Acid Catalysis via Fluorescent Lewis Adducts (opens in a new tab)

  18. Asymmetric synthesis of novel anthracyclinones

    … of novel C9-halogenated anthracyclinones by Lewis acid promoted cyclisations of ortho-methallyl anthraquinonyl chiral dioxanes has been investigated. Tin tetrachloride-N,N-dimethylformamide promoted cyclisation of the dioxane (30) proceeded with excellent stereoselectivity to give an 82% …

    auckland-ms Repository record for Asymmetric synthesis of novel anthracyclinones (opens in a new tab)

  19. Retro-Diels-Alder routes to 4,5 disubstituted cyclopentenones

    … tricyclodecadienones using several Lewis-acid catalysts. 4-Substituted-2 cyclopentenones were isolated in good yield and no double bond rearrangement or decomposition was observed. Similar results were also obtained with the dienones generated from dehydration of β-ketols to give …

    cape-town Repository record for Retro-Diels-Alder routes to 4,5 disubstituted cyclopentenones (opens in a new tab)

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