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Showing 1 to 5 of 5 for “"acyl radical"”.

  1. An Acyl Radical Cascade Model for the Total Synthesis of Lyconadin A

    … to 1 based on a novel 7-exo-trig/6-exo-trig acyl radical cascade cyclization. The synthesis of model acyl radical cascade precursor 23 will be presented. Key features of this synthesis include the suppression of competing elimination during the alkylation of a hindered phenethyl bromide and …

    byu Repository record for An Acyl Radical Cascade Model for the Total Synthesis of Lyconadin A (opens in a new tab)

  2. Model Studies Towards the Total Synthesis of Lyconadin A via An Acyl Radical Cascade Reaction

    … synthesis of Lyconadin A was proposed via an acyl radical cascade reaction. To investigate the possibility and stereoselectivity of the cascade cyclization, phenyl selenoester 16 was chosen as a model substrate to study the 7-exo-5-exo radical cyclization. A synthetic route to phenyl …

    byu Repository record for Model Studies Towards the Total Synthesis of Lyconadin A via An Acyl Radical Cascade Reaction (opens in a new tab)

  3. Chiral acyl radicals generated by visible light enable stereoselective access to 3,3-disubstituted oxindoles: application toward the synthesis of (–)- and (+)-physovenine

    Radical species serve as powerful tools for carbon-carbon bond formation in synthetic organic chemistry. Such species can be formed in an efficient and environmentally friendly manner by way of photoredox catalysis, which uses a photocatalyst in conjunction with visible light (typically) to …

    cape-town Repository record for Chiral acyl radicals generated by visible light enable stereoselective access to 3,3-disubstituted oxindoles: application toward the synthesis of (–)- and (+)-physovenine (opens in a new tab)

  4. Studies towards the syntheses of the citreamicins

    … reaction was accomplished. Finally, a novel acyl radical cyclization was employed to construct the pentacyclic core of citreamicin η under mild reaction conditions.

    bu Repository record for Studies towards the syntheses of the citreamicins (opens in a new tab)

  5. Development of New Organic Photoredox Catalysis Driven by Visible Light

    … atom transfer (HAT) to selectively generate acyl radicals from corresponding aldehydes without inducing crossover reactivity of thioesters. In situ formed acyl radicals then react with thiosulfonate S-esters to efficiently produce thioesters. The mild and efficient method exhibits excellent …

    arizona-thes Repository record for Development of New Organic Photoredox Catalysis Driven by Visible Light (opens in a new tab)