Nuclear magnetic resonance (NMR) spectroscopy is the most valuable spectroscopic tool for those who make and/or structurally characterize biomedically relevant organic, organometallic, and polymeric compounds. Access to high quality NMR data is critical to research progress in each of these fields. The modern capabilities of the requested upgrade to our current 500 MHz NMR spectrometer will greatly enhance progress in a myriad of biomedically-motivated projects currently under study at Minnesota. Specifically, the types of projects that will benefit from this instrument include the synthesis of antitumor agents, antibiotics, vaccines, and other bioactive compounds;creation of new sensors for monitoring levels of clinically relevant electrolytes;exploration of important enzyme pathways and functions;bioinorganic studies of models of metalloenzymes;development of new organometallic-based methods applicable to the (asymmetric) synthesis of pharmaceutical agents;determination of structures of new biologically active natural and unnatural products;design of new contrast agents for imaging;the development of new polymer-based vehicles and strategies for both drug and gene delivery;studies of polymeric artificial tissues;and exploratio of carbohydrate-based dendrimers and polymers for use as novel 'theranostic'agents. More specifically, we request funds to upgrade our existing 500 MHz NMR spectrometer with a new console, state-of-the-art probe and automatic sample changer. This spectrometer will be housed in the NMR Laboratory in the Department of Chemistry, where it will be used to perform one- and two-dimensional multinuclear experiments on small and large molecules being synthesized and studied for biomedical research purposes here at the University of Minnesota. This facility serves the needs of nearly 300 researchers, approximately half of whom are in the research groups of the Major and Minor Users in this application. We expect our large user base to benefit tremendously from the versatility afforded by the requested upgrade. Given the combined features of the new probe, which includes automatic tuning and matching capabilities, and autosampler, we will be able to generate, with minimal operator intervention, high quality spectral data for any sequence of experiment(s) with any sample type (small molecules or macromolecules;organic or inorganic;1H, 13C, 19F, 31P, 2H, 15N, 17O, 11B, 51V, 119Sn, 59Co, or 29Si). This is very powerful. These capabilities far exceed what we can do with our current instrument. With this upgrade we will obtain higher quality data and more data. As a direct consequence, both the pace of discovery and depth of understanding will be advanced.

National Institute of Health (NIH)
Office of The Director, National Institutes of Health (OD)
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
Application #
Study Section
Special Emphasis Panel (ZRG1-BCMB-U (30))
Program Officer
Levy, Abraham
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
University of Minnesota Twin Cities
Schools of Arts and Sciences
United States
Zip Code
McClintock, Maria K; Fahnhorst, Grant W; Hoye, Thomas R et al. (2018) Engineering the production of dipicolinic acid in E. coli. Metab Eng 48:208-217
Pearce, Adam J; See, Xin Yi; Tonks, Ian A (2018) Oxidative nitrene transfer from azides to alkynes via Ti(ii)/Ti(iv) redox catalysis: formal [2+2+1] synthesis of pyrroles. Chem Commun (Camb) 54:6891-6894
Jayaraman, Ashish; Mahanthappa, Mahesh K (2018) Counterion-Dependent Access to Low-Symmetry Lyotropic Sphere Packings of Ionic Surfactant Micelles. Langmuir 34:2290-2301
Wang, Yuanxian; Hoye, Thomas R (2018) Intramolecular Capture of HDDA-Derived Benzynes: (i) 6- to 12-Membered Ring Formation, (ii) Internally (vis-à-vis Remotely) Tethered Traps, and (iii) Role of the Rate of Trapping by the Benzynophile. Org Lett 20:88-91
Carlson, Angela S; Calcanas, Cristian; Brunner, Ryan M et al. (2018) Regiocontrolled Wacker Oxidation of Cinnamyl Azides. Org Lett 20:1604-1607
Chiu, Hsin-Chun; Tonks, Ian A (2018) Trimethylsilyl-Protected Alkynes as Selective Cross-Coupling Partners in Titanium-Catalyzed [2+2+1] Pyrrole Synthesis. Angew Chem Int Ed Engl 57:6090-6094
Xiao, Xiao; Woods, Brian P; Xiu, Wen et al. (2018) Benzocyclobutadienes: An Unusual Mode of Access Reveals Unusual Modes of Reactivity. Angew Chem Int Ed Engl 57:9901-9905
Wang, Yuanxian; Hoye, Thomas R (2018) Isomerizations of Propargyl 3-Acylpropiolates via Reactive Allenes. Org Lett 20:4425-4429
Ott, Amy A; Packard, Mary H; Ortuño, Manuel A et al. (2018) Evidence for a Sigmatropic and an Ionic Pathway in the Winstein Rearrangement. J Org Chem 83:8214-8224
Divakaran, Anand; Talluri, Siva K; Ayoub, Alex M et al. (2018) Molecular Basis for the N-Terminal Bromodomain-and-Extra-Terminal-Family Selectivity of a Dual Kinase-Bromodomain Inhibitor. J Med Chem 61:9316-9334

Showing the most recent 10 out of 48 publications