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Showing 1 to 7 of 7 for “"Pancratistatin"”.

  1. Synthesis of unnatural analogues of pancratistatin and narciclasine

    … towards the synthesis of C-1 analogues of pancratistatin and A-ring heterocyclic analogues of narciclasine are discussed. Evaluation of the new analogues as cancer growth inhibitory agents is also described

    brock Repository record for Synthesis of unnatural analogues of pancratistatin and narciclasine (opens in a new tab)

  2. Mechanism Determination of the Effects of Pancratistatin on Model Mitochondrial Membranes

    … specific cell types, such as cancer cells. Pancratistatin (PST) is an antiviral alkaloid metabolite that has demonstrated directed apoptotic action on various human cancer cell lines while having minimal/no toxic effect on normal cells. However, PST’s mechanism of action remains uncertain. …

    windsor Repository record for Mechanism Determination of the Effects of Pancratistatin on Model Mitochondrial Membranes (opens in a new tab)

  3. Chemistry of oxa- and aza-bicyclic(4.1.0)heptenes, total synthesis of (+)-pancratistatin

    … by a concise enantiocontrolled synthesis of (+)-pancratistatin (9). The key step involved the S<sub>N</sub>2 opening of 7b with the aryl cyanocuprate derived from amide 217 to generate the pivotal cyclization precursor.

    vt Repository record for Chemistry of oxa- and aza-bicyclic(4.1.0)heptenes, total synthesis of (+)-pancratistatin (opens in a new tab)

  4. Total synthesis enabled by nickel-catalyzed transformations: Dearomative carboamination and methylenecyclopropane annulation

    … the completion of the synthesis of the 7-deoxypancratistatin and pancratistatin, we then developed a directed cupration/oxidation reaction to create a direct synthetic connection between the two natural products. Chapter 3 delineates how we improved the dearomative carboamination, ultimately …

    uiuc Repository record for Total synthesis enabled by nickel-catalyzed transformations: Dearomative carboamination and methylenecyclopropane annulation (opens in a new tab)

  5. Controlled synthesis of complex organic molecules and nanomaterials: Engaging chemical properties for biological applications

    Submission original under an indefinite embargo labeled 'Open Access'. The submission was exported from vireo on 2024-09-16 without embargo terms

    uiuc Repository record for Controlled synthesis of complex organic molecules and nanomaterials: Engaging chemical properties for biological applications (opens in a new tab)

  6. Controlled synthesis of complex organic molecules and nanomaterials: Engaging chemical properties for biological applications

    Submission original under an indefinite embargo labeled 'Open Access'. The submission was exported from vireo on 2024-09-16 without embargo terms

    uiuc Repository record for Controlled synthesis of complex organic molecules and nanomaterials: Engaging chemical properties for biological applications (opens in a new tab)