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Showing 1 to 11 of 11 for “"Aldimines"”.

  1. New Strategies and Transformations for the alpha-Functionalization of Amines to Access Chiral Amines

    … B6 transamination process: forming ketimines or aldimines to increase the acidities of alpha-C–H protons of amines, thereby enabling the alpha-C–H deprotonation accessible under mild reaction conditions for further derivation. Based on this known process mechanism, we first explored the umpolung …

    duke Repository record for New Strategies and Transformations for the alpha-Functionalization of Amines to Access Chiral Amines (opens in a new tab)

  2. Sustainable catalysis using iron based catalysts for hydrofunctionalization of c=x (x = o, n) unsaturated bonds

    … based iron complexes for the hydrosilylation of aldimines. Conversion of aldimines into amines is one of the most important chemical reactions in synthetic organic chemistry. Amines have been widely used for the production of bulk and fine chemicals, such as dyes, agrochemicals, pharmaceuticals, …

    tdl Repository record for Sustainable catalysis using iron based catalysts for hydrofunctionalization of c=x (x = o, n) unsaturated bonds (opens in a new tab)

  3. Part I: Design, synthesis, and studies of novel age-inhibitors and age-breakers; Part II: Novel synthetic methods for organofluorine compound

    … trifluoromethylation of aromatic N-tosyl aldimines with electron-withdrawing as well as electron-donating groups on the aryl ring. We have synthesized a series of novel purine-based triazole derivatives as potential CDK-inhibitors and characterized their structures using high-field …

    must-thes Repository record for Part I: Design, synthesis, and studies of novel age-inhibitors and age-breakers; Part II: Novel synthetic methods for organofluorine compound (opens in a new tab)

  4. NATURAL PRODUCT INSPIRED METHODOLOGIES: ADVANCES IN DIASTEREOSELECTIVE N-SULFINYL IMINE AND TRIFLUOROPYRUVIC ACID REACTIONS

    … worked well with a diverse set of N-sulfinyl aldimines and ketimines with 50-99% yield and 3:1 to 98:2 diastereoselectivity. A one-pot protocol was developed to access 1,2 amino alcohols with high diastereoselectivity. With a good understanding of the diastereoselective reaction with NSMD and …

    temple Repository record for NATURAL PRODUCT INSPIRED METHODOLOGIES: ADVANCES IN DIASTEREOSELECTIVE N-SULFINYL IMINE AND TRIFLUOROPYRUVIC ACID REACTIONS (opens in a new tab)

  5. Simulating biochemical physics with computers

    … for the decarboxylations of the external aldimines both in water and in DDC are calculated. The contributions of DDC to the rate enhancement of the reaction are elucidated. The reaction mechanism of L-dopa decarboxylation in DDC is proposed. The third part is to study the structural …

    umn Repository record for Simulating biochemical physics with computers (opens in a new tab)

  6. Development and application of carbon-carbon bond forming methodologies

    … addition of carbon nucleophiles to prochiral aldimines was developed. This transformation capitalizes on the inherent properties of boron to promote a ligand exchange with chiral diols generating a chiral nucleophile in situ. Mechanistic studies were carried out to gamer a better understanding …

    bu Repository record for Development and application of carbon-carbon bond forming methodologies (opens in a new tab)

  7. Mirroring Enzymes: The Role of H-Bonding In HQuin-BAM Catalyzed Asymmetric Aza-Henry Reactions: A DFT Study into the Reactivity, Mechanism, and Origins of Selectivity

    … addition to a range of electronically different aldimines, revealed that the origins of stereoselectivity were controlled by a delicate balance of different factors such as steric, orbital interactions, and the extent of distortion in the catalyst and substrates. The structural analysis of …

    brock Repository record for Mirroring Enzymes: The Role of H-Bonding In HQuin-BAM Catalyzed Asymmetric Aza-Henry Reactions: A DFT Study into the Reactivity, Mechanism, and Origins of Selectivity (opens in a new tab)

  8. Copper(I) Hydride-Catalyzed Transformations of π-Electrophiles

    … detailed. Aromatic and aliphatic N-phosphinoyl aldimines possessing a variety of functional groups are coupled with both terminal and internal enynes under mild conditions. The resulting homopropargylic amines are produced in high yields, with moderate diastereoselectivities and generally high …

    mit Repository record for Copper(I) Hydride-Catalyzed Transformations of π-Electrophiles (opens in a new tab)

  9. METHODOLOGY DEVELOPMENT OF N-SULFINYL METALLOENAMINES AND ASYMMETRIC TOTAL SYNTHESIS OF (+)-EPIIBOGAMINE

    … as a surrogate for poorly reacting N-sulfinyl aldimines in the DM3 reaction. This silyl-modified DM3 reaction enabled the shortest asymmetric total synthesis of (+)-epiibogamine in 7 steps. This isoquinuclidine intermediate would also provide access to (+)-dihydrocatharanthine and other Iboga …

    temple Repository record for METHODOLOGY DEVELOPMENT OF N-SULFINYL METALLOENAMINES AND ASYMMETRIC TOTAL SYNTHESIS OF (+)-EPIIBOGAMINE (opens in a new tab)