Synthesis of Polycyclic Ring Systems Via C-H Bond Insertion and Enantioselective Conjugate Addition

dc.contributor.advisorMay, Jeremy A.
dc.contributor.committeeMemberGilbertson, Scott R.
dc.contributor.committeeMemberDaugulis, Olafs
dc.contributor.committeeMemberBall, Zachary T.
dc.contributor.committeeMemberXu, Shoujun
dc.creatorJansone-Popova, Santa 1985- 2014 2014
dc.description.abstractThis dissertation presents three main projects. The first discusses synthetic strategies towards the total synthesis of the natural product Maoecrystal V. The second part presents an efficient way to construct complex polycyclic ring systems. The third project describes an organocatalytic asymmetric conjugate addition of organoboronates to indole-appended enones. A structurally complex natural product, Maoecrystal V, possesses potent biological activity against the HeLa cancer cell line. An efficient synthetic route would allow access to larger quantities of this compound. Our approach is based on a rhodium-catalyzed bridgehead C-H bond insertion method to construct a γ-lactone. Substitution of the molecule’s methylene hydrogens with deuterium or fluorine atoms allows selective functionalization of the methine C-H bond. Installation of two more rings in the molecule will finish the total synthesis of Maoecrystal V. The alkyne/carbene cascade reaction is highly efficient and predictable in transforming simple, commercially available materials into complex polycyclic molecules, which represent the core structures of many natural products. Subsequently, we discovered an alkyne/carbamate-derived nitrene cascade reaction that leads to the formation of complex polycyclic molecules containing nitrogen atoms. Two products are produced during the reaction and their identity and ratio can be controlled by the relative size of the silyl substituent on the alkyne. Lastly, an efficient method for the organocatalytic conjugate addition of alkenylboronic acids to indole-appended enones was developed. Most importantly, unprotected indoles can be used as substrates, which further increases the applicability of this method.
dc.description.departmentChemistry, Department of
dc.format.digitalOriginborn digital
dc.identifier.citationPortions of this document appear in: Jansone-Popova, Santa, and Jeremy A. May. "Synthesis of bridged polycyclic ring systems via carbene cascades terminating in C–H bond insertion." Journal of the American Chemical Society 134, no. 43 (2012): 17877-17880. DOI: 10.1021/ja308305z. And in: Jansone-Popova, Santa, Phong Q. Le, and Jeremy A. May. "Carbene cascades for the formation of bridged polycyclic rings." Tetrahedron 70, no. 27 (2014): 4118-4127. And in: Lundy, Brian J., Santa Jansone-Popova, and Jeremy A. May. "Enantioselective conjugate addition of alkenylboronic acids to indole-appended enones." Organic letters 13, no. 18 (2011): 4958-4961. The material from this article is from the accepted manuscript of a published work that appeared in final form in Organic Letters. The version of record for that article is available at the following DOI: 10.1021/ol2020847. And in: Vallakati, Ravikrishna, Brian J. Lundy, Santa Jansone�Popova, and Jeremy A. May. "Biomimetic Synthesis and Studies Toward Enantioselective Synthesis of Flindersial Alkaloids." Chirality 27, no. 1 (2015): 14-17. DOI: 10.1002/chir.22134.
dc.rightsThe author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
dc.subjectC-H bond insertion
dc.subjectOrganic synthesis
dc.titleSynthesis of Polycyclic Ring Systems Via C-H Bond Insertion and Enantioselective Conjugate Addition
dc.type.genreThesis of Natural Sciences and Mathematics, Department of of Houston of Philosophy


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