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Showing 1 to 20 of 53 for “"organolithium"”.

  1. Structural Studies of Organolithium Compounds

    Made available in DSpace on 2014-12-09T17:35:33Z (GMT). No. of bitstreams: 1 6612345.pdf: 2529855 bytes, checksum: af2a6f32ca27ee41dbf3bfe2d30e7e75 (MD5) Previous issue date: 1966

    uiuc Repository record for Structural Studies of Organolithium Compounds (opens in a new tab)

  2. Bonding and Stereochemical Studies of Unsaturated Organolithium Compounds

    Made available in DSpace on 2014-12-10T23:01:15Z (GMT). No. of bitstreams: 1 7212102.pdf: 4304647 bytes, checksum: a7542a08b78334c4eceecd5ce07f8796 (MD5) Previous issue date: 1971

    uiuc Repository record for Bonding and Stereochemical Studies of Unsaturated Organolithium Compounds (opens in a new tab)

  3. The reaction of organolithium reagents with carbon monoxide.

    Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 1969

    mit Repository record for The reaction of organolithium reagents with carbon monoxide. (opens in a new tab)

  4. The Electrophilic Amination of Organolithium Compounds With Methyllithium-Methoxylamines

    Strongly basic aliphatic and benzenoid aromatic organolithium compounds can be stoichiometrically converted to primary amines, upon treatment with two equivalents of a methoxylamine-methyllithium complex, in 14-97% yields, or to secondary amines, either inter- or intramolecularly, upon treatment …

    uiuc Repository record for The Electrophilic Amination of Organolithium Compounds With Methyllithium-Methoxylamines (opens in a new tab)

  5. Structural, Bonding, and Reactivity Studies of Unsaturated Organolithium Compounds

    Made available in DSpace on 2014-12-10T23:02:12Z (GMT). No. of bitstreams: 1 7511599.pdf: 6397672 bytes, checksum: 4f6a1a7b24ae0f91d630dc6fcad030c2 (MD5) Previous issue date: 1974

    uiuc Repository record for Structural, Bonding, and Reactivity Studies of Unsaturated Organolithium Compounds (opens in a new tab)

  6. Condensations of Organolithium and Organomagnesium Reagents With Duryl Ketones

    Made available in DSpace on 2014-12-05T19:37:47Z (GMT). No. of bitstreams: 1 6104345.pdf: 3038861 bytes, checksum: ebc4e31333ea7e7382cef973b4cc13a3 (MD5) Previous issue date: 1961

    uiuc Repository record for Condensations of Organolithium and Organomagnesium Reagents With Duryl Ketones (opens in a new tab)

  7. Rules for ring closure and aspects of organolithium chemistry

    Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 1980

    mit Repository record for Rules for ring closure and aspects of organolithium chemistry (opens in a new tab)

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

    … of racemic cyclic unsaturated esters with the organolithium intermediates derived from lithiation of N-Boc- N-(p-methoxyphenyl)cinnamylamine with n -BuLi/(-)-sparteine was investigated. Kinetic resolution in conjugate addition reactions with alpha,beta-unsaturated lactones proceed with …

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

  9. Mass Spectral and Nuclear Magnetic Resonance Studies of Organolithium Compounds

    Made available in DSpace on 2014-12-09T17:36:37Z (GMT). No. of bitstreams: 1 7013377.pdf: 2724780 bytes, checksum: f4b91d4d1ec5c43c62a615920fa0ac81 (MD5) Previous issue date: 1969

    uiuc Repository record for Mass Spectral and Nuclear Magnetic Resonance Studies of Organolithium Compounds (opens in a new tab)

  10. Computational Studies of Protonated Cyclic Ethers and Benzylic Organolithium Compounds

    Protonated epoxides feature prominently in organic chemistry as reactive intermediates. Gas-phase calculations studying the structure and ring-opening energetics of protonated ethylene oxide, propylene oxide and 2-methyl-1,2-epoxypropane were performed at the B3LYP and MP2 levels (both with the …

    vt Repository record for Computational Studies of Protonated Cyclic Ethers and Benzylic Organolithium Compounds (opens in a new tab)

  11. Kinetics and Mechanism of Organolithium and Organomagnesium Reagent Reactions With Ketones

    Made available in DSpace on 2014-12-10T23:01:29Z (GMT). No. of bitstreams: 1 7317148.pdf: 6299095 bytes, checksum: 77321523282a5ad7528384f2d11a3a67 (MD5) Previous issue date: 1972

    uiuc Repository record for Kinetics and Mechanism of Organolithium and Organomagnesium Reagent Reactions With Ketones (opens in a new tab)

  12. Mechanistic studies of asymmetric induction at benzylic centers of organolithium species

    The mechanisms of asymmetric induction involving the lithiation and substitution of N-benzyl-N-Boc-N-p-methodically amine and N-benzyl-N-Boc-N-3-chloropropyl amine were investigated and are reported here. These two substrates undergo deprotonation with butyllithium in the presence of the chiral …

    uiuc Repository record for Mechanistic studies of asymmetric induction at benzylic centers of organolithium species (opens in a new tab)

  13. I. Enthalpy of Protonation Studies on Selected Organolithium Compounds. Ii. Dipole Stabilized Carbanions in N-Methyl Carboxamides

    Made available in DSpace on 2014-12-13T20:10:04Z (GMT). No. of bitstreams: 1 7714930.pdf: 5080318 bytes, checksum: cf7b65bfc5e248c32aa17b9119ac4f66 (MD5) Previous issue date: 1977

    uiuc Repository record for I. Enthalpy of Protonation Studies on Selected Organolithium Compounds. Ii. Dipole Stabilized Carbanions in N-Methyl Carboxamides (opens in a new tab)

  14. Complex-induced proximity effects in proton transfer and halogen-metal exchange reactions

    … or in a transient high local concentration of organolithium reagent as the organolithium is added to the amide substrate. Differentiation between these two possibilities is achieved by employing reverse addition of the amide substrate to a solution of the organolithium reagent. In cases where …

    uiuc Repository record for Complex-induced proximity effects in proton transfer and halogen-metal exchange reactions (opens in a new tab)

  15. (--)-Sparteine Mediated Asymmetric Synthesis Through Conjugate Addition of Allylic and Benzylic Organolithium Species: Development of a Methodology and Its Application Toward a Total Synthesis

    … In addition, conjugate addition of the allylic organolithium species with N-protected 4-pyridones provides high yields of the corresponding 1,4-addition adduct with high enantiomeric ratios (ers). The reaction is believed to proceed through an N-acyl pyridinium salt formed on reaction of …

    uiuc Repository record for (--)-Sparteine Mediated Asymmetric Synthesis Through Conjugate Addition of Allylic and Benzylic Organolithium Species: Development of a Methodology and Its Application Toward a Total Synthesis (opens in a new tab)

  16. 1. The Endocyclic Restriction Test: Oxygen Transfer From N-Sulfonyl Oxaziridines to Alkenes and Fluorine From N-Fluorosultams to Carbanions. 2. Intra- and Intermolecular Kinetic Isotope Effects in Directed Lithiations

    … transfer from a benzylic or aryl carbon atom to organolithium reagents has been investigated by measuring intra- and intermolecular kinetic isotope effects. The results were more in line with a two-step mechanism where an organolithium base coordinates to the heteroatom of the directing group …

    uiuc Repository record for 1. The Endocyclic Restriction Test: Oxygen Transfer From N-Sulfonyl Oxaziridines to Alkenes and Fluorine From N-Fluorosultams to Carbanions. 2. Intra- and Intermolecular Kinetic Isotope Effects in Directed Lithiations (opens in a new tab)

  17. Enantioselective lateral lithiation-substitution reactions using benzamide directing groups

    Reactions involving organolithium reagents under the influence of the chiral ligand to affect the enantioselective replacement of a carbon-proton bond with a carbon-carbon bond or a carbon-heteroatom bond are described.

    uiuc Repository record for Enantioselective lateral lithiation-substitution reactions using benzamide directing groups (opens in a new tab)

  18. Enantioselective lateral lithiation-substitution of o-ethyl- and o-benzyl-N-pivaloylanilines: Studies of a pathway of stereoinformation transfer

    … intermediate. Electrophilic substitution of the organolithium in the presence of ($-$)-sparteine provides the products with enantiomeric excesses close to 80% for reactions with most electrophiles. The absolute configuration at the benzylic carbon is the same regardless of whether stannyl or …

    uiuc Repository record for Enantioselective lateral lithiation-substitution of o-ethyl- and o-benzyl-N-pivaloylanilines: Studies of a pathway of stereoinformation transfer (opens in a new tab)

  19. FROM BATCH TO FLOW: RETHINK THE WAY OF DOING CHEMISTRY

    … and three chapters on the research projects, organolithium chemistry, photochemistry, alkyl nitrite in α-keto nitrosation reaction. The last section of every chapter is dedicated to the discussion of the result where on water organolithium addition to imines, Pd mediated cross coupling …

    milano Repository record for FROM BATCH TO FLOW: RETHINK THE WAY OF DOING CHEMISTRY (opens in a new tab)

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