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Filtering by: Alternative title ssim SG 63 Remove constraint Alternative title ssim: SG 63 Academic Affiliation Chemistry Remove constraint Academic Affiliation: Chemistry Committee Member Blakemore, Paul R. Remove constraint Committee Member: Blakemore, Paul R.

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  • Synthetic Studies towards Highly Oxygenated Furanyl Diterpenoids

    Creator:
    Goswami, Subir
    Abstract:
    The furanyl diterpenoid family of natural products has drawn the attention of both synthetic organic chemists and pharmacologists due to their complex structural architectures and diverse biological activity. Among them, wortmannin has been most extensively studied for biological activities. All these furanyl diterpenoids consist of a highly strained naptha[1,8-bc]furan core,...
    Resource Type:
    Dissertation
    Full Text:
    dissertation_Pretext-Pages-SG-09.28.2018 AN ABSTRACT OF

  • A Diels-Alder approach to biaryl synthesis

    Creator:
    Ashburn, Bradley O.
    Abstract:
    An expedient approach to the synthesis of a wide range of highly programmable biaryl templates has been accomplished. Utilizing the Diels-Alder [4+2] cycloaddition, a wide range of tri- and tetra-ortho-substituted biaryls have been synthesized in only three to four steps from commercially available materials. We have successfully synthesized entire classes...
    Resource Type:
    Dissertation
    Full Text:
    Experimental…………….…………………..…… 63 TABLE OF CONTENTS (Continued) Page CHAPTER 4 SYNTHESIS OF

  • Computational Investigation and Prediction of Mechanisms and Stereocontrol in Complex Organic Reactions

    Creator:
    Pattawong, Ommidala
    Abstract:
    Complex organic transformations, such as the addition of pyrrole to ketene using planar chiral organocatalyst (*PPY), the four-component anhydride- Manniach reactions, and the site-selective desymmetrization of meso-1,2-diol, are remarkable synthetic reactions that provide high yield and high selectivity. However, the exact mechanism and origins of stereocontrol for theses synthetic organic...
    Resource Type:
    Dissertation
    Full Text:
    ....................................................... 54 4.3.6 The Mechanisms For The Four-Component Reaction ................. 63 4.4 Conclusions