Chris Prier
Affiliations: | 2014 | Chemistry | Princeton University, Princeton, NJ |
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| Cho I, Prier CK, Jia ZJ, et al. (2019) Enantioselective Aminohydroxylation of Styrenyl Olefins Catalyzed by an Engineered Hemoprotein. Angewandte Chemie (International Ed. in English) |
| Prier CK, Lo MM, Li H, et al. (2019) Stereodivergent Synthesis of 3‐Hydroxyprolines and 3‐Hydroxypipecolic Acids via Ketoreductase‐Catalyzed Dynamic Kinetic Reduction Advanced Synthesis & Catalysis. 361: 5140-5143 |
| Prier CK, Kosjek B. (2018) Recent preparative applications of redox enzymes. Current Opinion in Chemical Biology. 49: 105-112 |
| Brandenberg OF, Prier CK, Chen K, et al. (2018) Stereoselective Enzymatic Synthesis of Heteroatom-Substituted Cyclopropanes Acs Catalysis. 8: 2629-2634 |
| Prier CK, Zhang RK, Buller AR, et al. (2017) Enantioselective, intermolecular benzylic C-H amination catalysed by an engineered iron-haem enzyme. Nature Chemistry. 9: 629-634 |
| Prier CK, Hyster TK, Farwell CC, et al. (2016) Asymmetric Enzymatic Synthesis of Allylic Amines: A Sigmatropic Rearrangement Strategy. Angewandte Chemie (International Ed. in English) |
| Prier CK, Arnold FH. (2015) Chemomimetic Biocatalysis: Exploiting the Synthetic Potential of Cofactor-Dependent Enzymes To Create New Catalysts. Journal of the American Chemical Society |
| Prier CK, MacMillan DW. (2014) Amine α-heteroarylation via photoredox catalysis: a homolytic aromatic substitution pathway. Chemical Science (Royal Society of Chemistry : 2010). 5: 4173-4178 |
| Prier CK, MacMillan DWC. (2014) Amine α-heteroarylation via photoredox catalysis: A homolytic aromatic substitution pathway Chemical Science. 5: 4173-4178 |
| Prier CK, Rankic DA, MacMillan DW. (2013) Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis. Chemical Reviews. 113: 5322-63 |