Gang Li
Inorganic Chemistry
Assistant Professor

Contact Information
Office Location: ML 359Phone: (435) 797-0604
Email: gang.li@usu.edu
Additional Information:
Educational Background
Biography
Dr. Gang Li received his B.S. in chemistry from Wuhan University in 2010 and his PhD in chemistry from Columbia University in 2015. After doing postdoctoral research at Princeton University and Bristol-Myers Squibb, he joined Utah State University as an assistant professor in August 2019. His research focuses on bioinspired sustainable catalysis by transition metal complexes and their applications in medicinal chemistry
Teaching Interests
Inorganic and bioinorganic chemistry, medicinal chemistry, organometallics, chemical kinetics and reaction mechanisms
Research Interests
Medicinal chemistry, drug diversification, biomimetic catalysis and metalloenzymes, reaction mechanism, synthetic methods
Awards
Bristol-Myers Squibb Postdoctoral Fellowship, 2015
Bristol-Myers Squibb
Reaxys PhD Prize Finalist, 2015
Elsevier, Inc.
George Pegram Awards for Meritorious Achievement in Chemical Research, 2015
Columbia University
Jack Miller Teaching Award, 2012
Columbia University
Faculty Fellowship, 2010
Columbia University
Distinguished Graduate Award, 2010
Wuhan University
- Wan, Y., Li, G., (2025). Tricarbonyl(η5-2,4-cyclopentadien-1-yl)hydrochromium(II): Encyclopedia of Reagents for Organic Synthesis.
- Wan, Y., Tan, L., Wu, K., Li, G., (2022). Bioinspired C(sp3)-H Functionalization by High-Valent Iron/Manganese Oxo Complexes and Applications in Organic Syntheses. Handbook of CH-Functionalization
Publications | Book Chapters
An asterisk (*) at the end of a publication indicates that it has not been peer-reviewed.
Publications | Journal Articles
Academic Journal
- Wu, K., McWhorter, K.L, Ford, A., Tan, L., Waidmann, L.M, Vazquez Hernandez, J.O, Garcia, M.M, Davis, K.M, Li, G., (2025). Cobaloxime Catalyzed Carbene Insertion into N–H Bonds: A Streamlined Route to α-Amino Esters with Mechanistic Insights. Organic Chemistry Frontiers, doi: 10.1039/D5QO01185J
- Tan, L., Wu, K., Li, G., (2025). Cobaloxime-Based Metalloradical Catalysis: A Versatile Strategy for the Synthesis of Cyclopropenes and Oxazoles. Angewandte Chemie, International Edition, e202500667. doi: 10.1002/anie.202500667
- Tan, L., Boehme, M., Papworth, L., Wu, K., Qiu, Y., Li, G., (2024). Highly Diastereoselective Radical Cyclopropanation of Olefins via Cobaloxime‐Based Metalloradical Catalysis. European Journal of Organic Chemistry, 28:3, e202401069. doi: 10.1002/ejoc.202401069
- Tan, L., Wu, K., Li, G., (2023). Rapid Olefin Cyclopropanation Catalyzed by a Bioinspired Cobalt Complex. Chemistry - An Asian Journal, 18:24, e202300873.
- Wan, Y., Ramírez, E., Ford, A., Bustamante, V., Li, G., (2023). Fe-Catalyzed C(sp3)–H Diversification toward γ-Functionalized Amides via Iron Nitrenoid: Mechanistic Insights and Applications. ACS Catalysis, 13:21, 14023–14030.
- Han, J., Tan, L., Wan, Y., Li, G., Anderson, S.N, (2022). C(sp3)–H oxidation and chlorination catalysed by a bioinspired pincer iron(III) complex. Dalton Transactions, 51:31, 11620-11624.
- Wu, W., Li, G., Liu, T.L, (2021). Chloride-mediated electrochemical synthesis of oxazolines. Chem Catalysis, 1:5, 966-967.
- Wang, Y., Zhu, L., Shao, Z., Li, G., Lan, Y., Liu, Q., (2019). Unmasking the Ligand Effect in Manganese-Catalyzed Hydrogenations: Mechanistic Insight and Catalytic Application. Journal of the American Chemical Society, 141:43, 17337-17349.
- Li, G., Kates, P.A, Dilger, A.K, Cheng, P.T, Ewing, W.R, Groves, J.T, (2019). Manganese-Catalyzed Desaturation of N-Acyl Amines and Ethers. ACS Catalysis, 9, 9513-9517.
- Li, G., Dilger, A.K, Cheng, P.T, Ewing, W.R, Groves, J.T, (2018). Selective C−H Halogenation with a Highly Fluorinated Manganese Porphyrin. Angewandte Chemie International Edition, 57:5, 1251-1255.
- Li, G., Kuo, J.L, Han, A., Abuyuan, J.M, Young, L.C, Norton, J.R, Palmer, J.H, (2016). Radical Isomerization and Cycloisomerization Initiated by H• Transfer. Journal of the American Chemical Society, 138:24, 7698-7704.
- Li, G., Estes, D.P, Norton, J.R, Ruccolo, S., Sattler, A., Sattler, W., (2014). Dihydrogen Activation by Cobaloximes with Various Axial Ligands. Inorganic Chemistry, 53:19, 10743-10747.
- Han, A., Spataru, T., Hartung, J., Li, G., Norton, J.R, (2014). Effect of Double-Bond Substituents on the Rate of Cyclization of alpha-Carbomethoxyhex-5-enyl Radicals. The Journal of organic chemistry, 79:5, 1938-1946.
- Norton, J.R, Spataru, T., Camaioni, D.M, Lee, S., Li, G., Choi, J., Franz, J.A, (2014). Kinetics and Mechanism of the Hydrogenation of the CpCr(CO)3•/[CpCr(CO)3]2 Equilibrium to CpCr(CO)3H. Organometallics, 33:10, 2496-2502.
- Li, G., Han, A., Pulling, M.E, Estes, D.P, Norton, J.R, (2012). Evidence for Formation of a Co-H Bond from (H2O)2Co(dmgBF2)2 under H2: Application to Radical Cyclizations. Journal of the American Chemical Society, 134:36, 14662-14665.
- Liu, Q., Li, G., Yi, H., Wu, P., Liu, J., Lei, A., (2011). Pd-Catalyzed Direct and Selective C-H Functionalization: C3-Acetoxylation of Indoles. Chemistry-A European Journal, 17:8, 2353-2357.
- Liu, Q., Li, G., He, J., Liu, J., Li, P., Lei, A., (2010). Palladium-Catalyzed Aerobic Oxidative Carbonylation of Arylboronate Esters under Mild Conditions. Angewandte Chemie International Edition, 49:19, 3371-3374.
- Liu, Q., Lan, Y., Liu, J., Li, G., Wu, Y., Lei, A., (2009). Revealing a Second Transmetalation Step in the Negishi Coupling and Its Competition with Reductive Elimination: Improvement in the Interpretation of the Mechanism of Biaryl Syntheses. Journal of the American Chemical Society, 131:29, 10201-10210.
- Liu, Q., Duan, H., Luo, X., Tang, Y., Li, G., Huang, R., Lei, A., (2008). An Electron-Deficient Diene as Ligand for Palladium-Catalyzed Cross-Coupling Reactions: An Efficient Alkylation of Aryl Iodides by Primary and Secondary Alkylzinc Reagents. Advanced Synthesis & Catalysis, 350:9, 1349-1354.
An asterisk (*) at the end of a publication indicates that it has not been peer-reviewed.
Publications | Other
An asterisk (*) at the end of a publication indicates that it has not been peer-reviewed.