The topological and stereochemical complexity inherent in molecular scaffolds with high sp³ character imparts beneficial physical and biological properties relative to sp²-rich compounds, but also amplifies selectivity and reactivity challenges for their efficient synthesis. Modular strategies for the rapid and selective construction of stereodefined sp³-rich molecules would enable access to a broad range of chemical space and advance a significant frontier in organic synthesis. The Paradine group will focus on the discovery of selective catalytic methods for the efficient construction of sp³-rich molecules, with a specific focus on C‒C bond formation. A particular priority will be placed on transformations that utilize simple starting materials and lead to a significant increase in molecular complexity. We are interested both in the development of catalytic synthetic methodologies that exert precise control over reaction outcomes (i.e. enantioselectivity, site-selectivity, chemoselectivity, diastereoselectivity), and fundamental studies that seek to understand the factors that contribute to highly selective transformations.

This research provides ample opportunities for applications to catalysis, total synthesis, medicinal chemistry, and other areas. Collaborations with colleagues across disciplines will be sought out to realize the full potential of my group's research. Students in our group will gain expertise in organic synthesis and reaction discovery. In addition, students will learn techniques in physical and mechanistic organic chemistry, spectroscopic characterization of organic compounds, and the synthesis and investigation of transition metal complexes.