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Theses Doctoral

Synthetic Innovations Towards the Total Synthesis of Natural Product Derivatives for Drug Development

Tekle-Smith, Makeda Aislinn

In order to provide scalable, efficient and selective routes towards pharmaceutically relevant compounds, we have focused on improving the economical viability and practicality of strained-silane Lewis acid activation. Towards these goals, the Leighton group has developed a new mode of anion catalysis to activate silane Lewis acids. Weakly coordinating anions have been used to access hyper-coordinate silicon species with unprecedented levels of reactivity, which have facilitated previously unattainable complex fragment couplings. A highly enantioselective and efficient method for anion catalyzed nucleophilic addition to aldehydes has enabled the synthesis of rationally designed, structurally simplified D-ring modified analogs of spongistatin 1. The completion of a step-economical route towards extremely potent, linker-handle equipped spongistatin 1 analogs and their application to targeted drug delivery will be discussed.


This item is currently under embargo. It will be available starting 2021-07-08.

More About This Work

Academic Units
Thesis Advisors
Leighton, James L.
Ph.D., Columbia University
Published Here
August 30, 2019
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