
Eric Nacsa
· Professor of ChemistryPennsylvania State University · Chemistry
Active 2012–2024
About
Shabnam Akhtari is a professor at the Pennsylvania State University, based in the 339 McAllister Building. Her research interests include Number Theory, Geometry of Numbers, and Diophantine Analysis. Her work focuses on these areas within mathematics, contributing to the understanding of their underlying structures and properties.
Research topics
- Combinatorial chemistry
- Organic chemistry
- Chemistry
- Computer Science
- Biochemistry
- Stereochemistry
- Programming language
Selected publications
Chemical Science · 2024 · 27 citations
Senior authorCorresponding- Computer Science
- Combinatorial chemistry
- Chemistry
, without requiring directing or electronically activating groups) for the first time. Key advances also included the introduction of synthetically diversifiable alkyl groups featuring different degrees of substitution, good diastereocontrol in both cyclic and acyclic settings, the addition of biologically valuable heteroarenes featuring Lewis basic nitrogen atoms as well as simple benzenes, and the generation of either tertiary or quaternary benzylic centers. The synthetic potential of this transformation was demonstrated by leveraging it as the key step in a concise synthesis of oliceridine, a new painkiller that received FDA approval in 2020.
Journal of the American Chemical Society · 2023 · 40 citations
Senior authorCorresponding- Chemistry
- Organic chemistry
- Combinatorial chemistry
An electrochemical approach has been leveraged to underpin a new conceptual platform for dehydration reactions, which has been demonstrated in the context of esterification. Esters were prepared from the corresponding acid and alcohol partners at room temperature without acid or base additives and without consuming stoichiometric reagents. This methodology therefore addresses key complications that plague esterification and dehydration reactions more broadly and that represent a leading challenge in synthetic chemistry.
2023 · 2 citations
Senior authorCorresponding- Combinatorial chemistry
- Chemistry
- Stereochemistry
A free-radical cascade approach has enabled the develop-ment of a synthetically versatile alkyl–arylation of olefins. This transformation engages an excellent range of olefins, from mono- to tetrasubstituted, without requiring directing or electronically activating groups. Further synthetic advantages, such as the facile generation of quaternary cen-ters and the introduction of heteroaryl groups with Lewis basic nitrogen atoms, also complement transition-metal-catalyzed alkyl–arylation. Vicinal stereoarrays were gener-ated with high levels of diastereoselectivity. The synthetic potential of this transformation was demonstrated by serving as the key step in a concise synthesis of oliceridine, a new painkiller that received FDA approval in 2020.
Recent grants
Alcohols as Latent Alkylating Agents Using Photoredox Organocatalysis
NIH · $116k · 2017–2019
Frequent coauthors
- 13 shared
Tristan H. Lambert
Cornell University
- 3 shared
Jaxon L. Barney
Pennsylvania State University
- 3 shared
Dylan J. Babcock
Pennsylvania State University
- 3 shared
Ayush Sharma
Pennsylvania State University
- 3 shared
Andrew J. Wolfram
Pennsylvania State University
- 3 shared
Santino M. Servagno
Pennsylvania State University
- 2 shared
Shannon P. Wetzler
University of Michigan–Ann Arbor
- 2 shared
Jonathan P. Litz
University of Washington
Education
- 2015
Ph.D., Chemistry
Columbia University
- 2010
B.Sc., Chemistry
Harvey Mudd College
Awards & honors
- NIH Maximizing Investigators’ Research Award (NIGMS R35 MIRA…
- NSF Faculty Early Career Development Program (CAREER) Award…
- ACS PRF New Doctoral Investigator (2022–2023)
- NIH Ruth L. Kirschstein NRSA Postdoctoral Fellowship (F32) (…
- Arun Guthikonda Memorial Graduate Fellowship, Columbia Unive…
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