Member of Yale faculty since 2006.
Research Interests
- Organic Chemistry
- Chemical Biology
- Synthetic Chemistry
Member of Yale faculty since 2006.
Carole Velleca
carole.velleca@yale.edu
CRB 110
Complex molecule synthesis is one of the key disciplines of modern chemical research. The development of new methods for the synthesis and derivatization of such structures is a multi-dimensional activity involving reaction design, development, and application. Research in our group focuses on each of these aspects of chemical synthesis. Utilizing the architecture and design principles presented by biologically relevant structures and processes, we seek to discover new reactions and to apply new principles to the selective synthesis of complex molecules.
As part of this program, we bring to bear the full arsenal of modern synthetic chemistry. Employing rational design, combinatorial screening and a constantly evolving collective intuition, we are working to discover new chemical transformations that enable the rapid synthesis of stereochemically complex structures. In addition, we are investigating the development of new catalysts for the selective functionalization of these molecules.
A particular interest is in the catalytic modification of natural products. These studies are enabling access to an expansive set of biologically inspired natural product analogs. A key component of all of this work is the determination of the fundamental molecular interactions that are responsible for reaction selectivities. As a result, mechanistic analysis is at the heart of many of our studies.
B.A./M.A. Harvard University, 1989
Ph.D. Harvard University, 1994
NSF Postdoctoral Fellow, California Institute of Technology, 1994-96
A. K. Turek, M. H. Sak, S. J. Miller. Kinetic Analysis of a Cysteine-Derived Thiyl-Catalyzed Asymmetric Vinylcyclopropane Cycloaddition Reflects Numerous Attractive Noncovalent Interactions. J. Am. Chem. Soc. 2021, 143, 16173-16183.
J. Hwang, B. Q. Mercado, S. J. Miller. Chirality-Matched Catalyst-Controlled Macrocyclization Reactions. PNAS. 2021, 118, e2113122118.
Yuk-Cheung Chan, M. H. Sak, S. A. Frank, S. J. Miller. Tunable and Cooperative Catalysis for Enantioselective Pictet-Spengler Reaction with Varied Nitrogen-Containing Heterocyclic Carboxaldehydes. Angew. Chem. Int. Ed. 2021, 60, 24573-24581.
Y. Tang, S. J. Miller. Catalytic Enantioselective Synthesis of Pyridyl Sulfoximines. J. Am. Chem. Soc. 2021, 143, 9230-9235.
A. L. Featherston, Y. Kwon, M. M. Pompeo, O. D. Engl, D. K. Leahy, S. J. Miller. Catalytic Asymmetric and Stereodivergent Oligonucleotide Synthesis. Science. 2021, 371, 702-707.
A leader in the field of organic chemistry, Miller has received international recognition for his work in the synthesis of stereochemically complex…
A leader in the field of organic chemistry, Miller has received international recognition for his work in the synthesis of stereochemically complex…
The Yale Chemistry National Science Foundation Fellows are Noah Bartfield, Daniel Chabeda, Nia Harmon, Jenna Molas, Tyler Myers, and Natalie Williams.
The organic chemist pioneered the discovery and development of new catalysts for complex molecular synthesis and derivation in chemical syntheses.