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Showing 1 to 20 of 60 for “"enantiomeric excess"”.

  1. Progress towards a highly efficient and accurate platform for enantiomeric excess determination

    Enantiomeric excess (ee) determination remains as the bottleneck for high throughput screening of asymmetric catalysts. The work described herein sought to expand on two previously developed ee sensing assays from our lab– an iron based amine assembly and a zinc based multicomponent assembly. To …

    texas Repository record for Progress towards a highly efficient and accurate platform for enantiomeric excess determination (opens in a new tab)

  2. Photoresolvable compounds: Towards a chiroptical-liquid crystalline switch

    … optical properties that determine the degree of enantiomeric excess that one can attain at the photostationary state, the g value. Two strategies to increase the g value were investigated: exciton coupling and energy transfer. Energy transfer was shown to be an efficient strategy in the design of …

    uiuc Repository record for Photoresolvable compounds: Towards a chiroptical-liquid crystalline switch (opens in a new tab)

  3. Asymmetric Syntheses With (-)-Sparteine-Complexed Benzylic and Allylic Organolithium Reagents

    … >20 were obtained, as calculated using the enantiomeric excess of the conjugate addition product.

    uiuc Repository record for Asymmetric Syntheses With (-)-Sparteine-Complexed Benzylic and Allylic Organolithium Reagents (opens in a new tab)

  4. Studies of alpha-lithioamine synthetic equivalents: I. Elaboration of primary amines. II. Detection of an intermediate in the lithiation of a benzylic urea

    … the corresponding products with up to 57% enantiomeric excess. Lithiation of N-tert-butyl-N-benzyl carbamates resulted in rearrangement to phenylglycine derivatives. These related investigations are also discussed.

    uiuc Repository record for Studies of alpha-lithioamine synthetic equivalents: I. Elaboration of primary amines. II. Detection of an intermediate in the lithiation of a benzylic urea (opens in a new tab)

  5. Studies on Resolution of Enantiomeric Dialkylaryl Sulfonium Ions with NMR Shift Reagents

    … shift reagent, is focused on for assessment of enantiomeric excess and resolution of methyl sulfonium ions. A series of alkylmethylphenylsulfonium ions were analyzed, where alkyl is ethyl (I), butyl(H), octyl (III), and benzyl(IY). The praseodymium agent gives base-lined resolution of the ortho …

    wku-diss Repository record for Studies on Resolution of Enantiomeric Dialkylaryl Sulfonium Ions with NMR Shift Reagents (opens in a new tab)

  6. Explorations with optically active, cage-annulated crown ethers.

    … that are capable of differentiating between enantiomeric "guest" molecules during host-guest complexation have been prepared via incorporation of chiral elements into the crown ring skeleton. The ability of these crown ethers to recognize the enantiomers of guest salts, i.e., (+) a-methyl …

    unt Repository record for Explorations with optically active, cage-annulated crown ethers. (opens in a new tab)

  7. The Tandem Inter [4+2]/[3+2] Cycloadditions of Nitroalkenes: The Bridged-Mode

    … that were reduced using nickel boride to provide enantiomerically enriched aminocyclopentanes in good yields and high enantiomeric excess. Additionally, the Lewis acid employed in the $\lbrack 4 + 2\rbrack$ cycloaddition was found to impart a remarkable influence on the stereochemical outcome of …

    uiuc Repository record for The Tandem Inter [4+2]/[3+2] Cycloadditions of Nitroalkenes: The Bridged-Mode (opens in a new tab)

  8. CoMFA Study of Chiral Catalysts

    … 70% of the variance in the observed enantiomeric excess can be attributed to the steric field and the remainder of the variance to the electrostatic field. Suggestions about how to improve the performance of inefficient catalysts are given the thesis.

    iupui Repository record for CoMFA Study of Chiral Catalysts (opens in a new tab)

  9. Total synthesis of (S)-4-hydroxy-[a]-Lapachone

    … 42613 was used to yield the target compound. The enantiomeric excess of the product was determined to be ~98% by using 1H NMR chiral shift analysis. The overall yield is 80/0. The biological activity of (S)-4-hydroxy-alapachone and its acetate are under investigation.

    brock Repository record for Total synthesis of (S)-4-hydroxy-[a]-Lapachone (opens in a new tab)

  10. Enantioselective nickel catalysis : exploiting activated C-H bonds

    … product with the best enantioselectivity (enantiomeric excess ca. 70%), however in low yield.

    mit Repository record for Enantioselective nickel catalysis : exploiting activated C-H bonds (opens in a new tab)

  11. The asymmetric synthesis of amino acids via electrophilic glycinates

    … furnishes the zwitterionic α-amino acids in high enantiomeric excess. Dissolving metal reduction of 134 permits the preparation of unsaturated amino acids while use of erythro-4-t-butoxycarbonyl-5,6-diphenyl-2,3,5,6-tetrahydro-1,4-oxazin-2-one 160 allows the direct preparation of t-BOC protected …

    colostate Repository record for The asymmetric synthesis of amino acids via electrophilic glycinates (opens in a new tab)

  12. Development and Mechanistic Investigation of Indium(III)-Catalysed Hydrosilane Reduction of Imines

    … importance inter alia for the development of enantiomerically pure drugs. The application of computational methods in understanding how enantioselectivity is induced in specific reactions is a powerful time-saving tool for organic chemists. By investigating the reaction pathway, specifically …

    cambridge Repository record for Development and Mechanistic Investigation of Indium(III)-Catalysed Hydrosilane Reduction of Imines (opens in a new tab)

  13. Development of an Intelligent Heart-Cut Liquid Chromatography System for Chiral Analysis of Chemical Processes

    … dimension uses a chiral column to measure the enantiomeric excess (ee) of the chiral analyte and the effluent from the third dimension is re-analyzed via a fourth dimension to determine if any loss of chirality has occurred resulting from the analytical method itself. Performance of the setup …

    york Repository record for Development of an Intelligent Heart-Cut Liquid Chromatography System for Chiral Analysis of Chemical Processes (opens in a new tab)

  14. Chiral expression at the nanoscale origin and recognition of chirality

    … dichroism spectroscopy and NSOM. The small enantiomeric excess achieved in experiments was explained by the limits of chirality determination methods. It was found that crystals formed in enantiomeric excess were of opposite chirality to the SAM they were grown on. This confirms previous …

    birmingham Repository record for Chiral expression at the nanoscale origin and recognition of chirality (opens in a new tab)

  15. Synthesis and utilization of guanidine catalysts for applications directed towards the preparation of butenolide and modified amino acid derivatives

    … for a variety of adducts. Highest enantiomeric excess (ee) was afforded between dibromofuranone and p-chlorobenzaldehyde, affording the syn conformation in 96% ee and the anti in 54% ee, with an overall yield of30%. Attempts to increase asymmetric induction were focused on …

    brock Repository record for Synthesis and utilization of guanidine catalysts for applications directed towards the preparation of butenolide and modified amino acid derivatives (opens in a new tab)

  16. Separation of enantiomers of Baclofen

    … Rearrangement with an overall yield of 40%. The enantiomeric excess of (R)-(".")-Baclofen was 99.7%.

    cape-town Repository record for Separation of enantiomers of Baclofen (opens in a new tab)

  17. Synthesis and Biological Studies of Lanthionine Derivatives

    … at the gram scale and excellent diastereomeric excesses (>99%), without any enrichment step, were obtained in aqueous solution. Biological experiments showed the incorporation of meso-Lan and (R,R)-Lan into PG. Upon this results, [35S]lanthionine diastereomers could be used to study the …

    liege Repository record for Synthesis and Biological Studies of Lanthionine Derivatives (opens in a new tab)

  18. CHIRAL LEWIS BASES ACTIVATION OF TRICHLOROSILYL DERIVATIVES

    … 98:2 syn/anti diastereoisomeric ratio and 89% of enantiomeric excess for the major stereoisomer.

    milano Repository record for CHIRAL LEWIS BASES ACTIVATION OF TRICHLOROSILYL DERIVATIVES (opens in a new tab)

  19. RECENT ADVANCES IN IMINIUM SALT CATALYSED ASYMMETRIC EPOXIDATION

    … containing HPLC traces to show determination of enantiomeric excess of epoxides, and enantioenriched alkene traces.

    east-anglia Repository record for RECENT ADVANCES IN IMINIUM SALT CATALYSED ASYMMETRIC EPOXIDATION (opens in a new tab)

  20. A scalable protocol for the synthesis and use of neomenthyldiphenylphosphine.

    … 4 to afford allylic alcohol 5 in high yield and enantiomeric excess. Several important modifications were made to the initially communicated procedure in order to effectively translate this methodology from the millimole to decimole scale. Allylic alcohol 5 was then ozonolyzed to afford …

    mit Repository record for A scalable protocol for the synthesis and use of neomenthyldiphenylphosphine. (opens in a new tab)

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