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Christopher Keltie Prier - Publications

Affiliations: 
2014 Chemistry Princeton University, Princeton, NJ 
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15 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Ye Y, Cao J, Oblinsky DG, Verma D, Prier CK, Scholes GD, Hyster TK. Using enzymes to tame nitrogen-centred radicals for enantioselective hydroamination. Nature Chemistry. PMID 36376390 DOI: 10.1038/s41557-022-01083-z  0.361
2019 Cho I, Prier CK, Jia ZJ, Zhang RK, Görbe T, Arnold FH. Enantioselective Aminohydroxylation of Styrenyl Olefins Catalyzed by an Engineered Hemoprotein. Angewandte Chemie (International Ed. in English). PMID 30600873 DOI: 10.1002/Anie.201812968  0.758
2019 Prier CK, Lo MM, Li H, Yasuda N. Stereodivergent Synthesis of 3‐Hydroxyprolines and 3‐Hydroxypipecolic Acids via Ketoreductase‐Catalyzed Dynamic Kinetic Reduction Advanced Synthesis & Catalysis. 361: 5140-5143. DOI: 10.1002/Adsc.201900871  0.736
2018 Prier CK, Kosjek B. Recent preparative applications of redox enzymes. Current Opinion in Chemical Biology. 49: 105-112. PMID 30554005 DOI: 10.1016/J.Cbpa.2018.11.011  0.738
2018 Brandenberg OF, Prier CK, Chen K, Knight AM, Wu Z, Arnold FH. Stereoselective Enzymatic Synthesis of Heteroatom-Substituted Cyclopropanes Acs Catalysis. 8: 2629-2634. DOI: 10.1021/Acscatal.7B04423  0.784
2017 Prier CK, Zhang RK, Buller AR, Brinkmann-Chen S, Arnold FH. Enantioselective, intermolecular benzylic C-H amination catalysed by an engineered iron-haem enzyme. Nature Chemistry. 9: 629-634. PMID 28644476 DOI: 10.1038/Nchem.2783  0.76
2016 Prier CK, Hyster TK, Farwell CC, Huang A, Arnold FH. Asymmetric Enzymatic Synthesis of Allylic Amines: A Sigmatropic Rearrangement Strategy. Angewandte Chemie (International Ed. in English). PMID 26970325 DOI: 10.1002/Anie.201601056  0.787
2015 Prier CK, Arnold FH. Chemomimetic Biocatalysis: Exploiting the Synthetic Potential of Cofactor-Dependent Enzymes To Create New Catalysts. Journal of the American Chemical Society. PMID 26502343 DOI: 10.1021/Jacs.5B09348  0.764
2014 Prier CK, MacMillan DW. Amine α-heteroarylation via photoredox catalysis: a homolytic aromatic substitution pathway. Chemical Science (Royal Society of Chemistry : 2010). 5: 4173-4178. PMID 26236461 DOI: 10.1039/C4Sc02155J  0.746
2014 Prier CK, MacMillan DWC. Amine α-heteroarylation via photoredox catalysis: A homolytic aromatic substitution pathway Chemical Science. 5: 4173-4178. DOI: 10.1039/c4sc02155j  0.745
2013 Prier CK, Rankic DA, MacMillan DW. Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis. Chemical Reviews. 113: 5322-63. PMID 23509883 DOI: 10.1021/Cr300503R  0.747
2011 McNally A, Prier CK, MacMillan DW. Discovery of an α-amino C-H arylation reaction using the strategy of accelerated serendipity. Science (New York, N.Y.). 334: 1114-7. PMID 22116882 DOI: 10.1126/Science.1213920  0.744
2011 Lee J, Berritt S, Prier CK, Joullié MM. Facile ring-opening of azabicyclic [3.1.0]- and [4.1.0]aminocyclopropanes to afford 3-piperidinone and 3-azepinone. Organic Letters. 13: 1083-5. PMID 21271686 DOI: 10.1021/Ol103105Q  0.751
2011 Crowley BM, Potteiger CM, Deng JZ, Prier CK, Paone DV, Burgey CS. Expanding the scope of the Cu assisted Suzuki-Miyaura reaction Tetrahedron Letters. 52: 5055-5059. DOI: 10.1016/J.Tetlet.2011.07.088  0.761
2011 Lee J, Berritt S, Prier CK, Joullie MM. ChemInform Abstract: Facile Ring-Opening of Azabicyclic [3.1.0]- and [4.1.0]Aminocyclopropanes to Afford 3-Piperidinone and 3-Azepinone. Cheminform. 42: no-no. DOI: 10.1002/chin.201123131  0.719
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