| Biotinylated Rh (III) complexes in engineered streptavidin for accelerated asymmetric C–H activation TK Hyster, L Knörr, TR Ward, T Rovis Science 338 (6106), 500-503, 2012 | 761 | 2012 |
| Rhodium-catalyzed oxidative cycloaddition of benzamides and alkynes via C− H/N− H activation TK Hyster, T Rovis Journal of the American Chemical Society 132 (30), 10565-10569, 2010 | 618 | 2010 |
| A coupling of benzamides and donor/acceptor diazo compounds to form γ-lactams via Rh (III)-catalyzed C–H activation TK Hyster, KE Ruhl, T Rovis Journal of the American Chemical Society 135 (14), 5364-5367, 2013 | 480 | 2013 |
| Pyridine synthesis from oximes and alkynes via rhodium (III) catalysis: Cp* and Cp t provide complementary selectivity TK Hyster, T Rovis Chemical communications 47 (43), 11846-11848, 2011 | 376 | 2011 |
| Accessing non-natural reactivity by irradiating nicotinamide-dependent enzymes with light MA Emmanuel, NR Greenberg, DG Oblinsky, TK Hyster Nature 540 (7633), 414-417, 2016 | 304 | 2016 |
| Photoexcitation of flavoenzymes enables a stereoselective radical cyclization KF Biegasiewicz, SJ Cooper, X Gao, DG Oblinsky, JH Kim, SE Garfinkle, ... Science 364 (6446), 1166-1169, 2019 | 290 | 2019 |
| An improved catalyst architecture for rhodium (III) catalyzed C–H activation and its application to pyridone synthesis TK Hyster, T Rovis Chemical science 2 (8), 1606-1610, 2011 | 220 | 2011 |
| Enantioselective enzyme-catalyzed aziridination enabled by active-site evolution of a cytochrome P450 CC Farwell, RK Zhang, JA McIntosh, TK Hyster, FH Arnold ACS central science 1 (2), 89-93, 2015 | 179 | 2015 |
| Enzyme-controlled nitrogen-atom transfer enables regiodivergent C–H amination TK Hyster, CC Farwell, AR Buller, JA McIntosh, FH Arnold Journal of the American Chemical Society 136 (44), 15505-15508, 2014 | 170 | 2014 |
| Rhodium (III)-catalyzed oxidative carbonylation of benzamides with carbon monoxide Y Du, TK Hyster, T Rovis Chemical communications 47 (44), 12074-12076, 2011 | 168 | 2011 |
| Rh (III)-Catalyzed Intramolecular Hydroarylation, Amidoarylation, and Heck-type Reaction: Three Distinct Pathways Determined by Amide Directing Group TA Davis, TK Hyster, T Rovis Angewandte Chemie (International ed. in English) 52 (52), 14181, 2013 | 164 | 2013 |
| Genetic optimization of metalloenzymes: enhancing enzymes for non‐natural reactions TK Hyster, TR Ward Angewandte Chemie International Edition 55 (26), 7344-7357, 2016 | 151 | 2016 |
| Chemoselectivity in Catalytic C C and C H Bond Activation: Controlling Intermolecular Carboacylation and Hydroarylation of Alkenes MT Wentzel, VJ Reddy, TK Hyster, CJ Douglas Angewandte Chemie 121 (33), 6237-6239, 2009 | 145 | 2009 |
| Enantioselective imidation of sulfides via enzyme-catalyzed intermolecular nitrogen-atom transfer CC Farwell, JA McIntosh, TK Hyster, ZJ Wang, FH Arnold Journal of the American Chemical Society 136 (24), 8766-8771, 2014 | 139 | 2014 |
| Ligand design for Rh (III)-catalyzed C–H activation: an unsymmetrical cyclopentadienyl group enables a regioselective synthesis of dihydroisoquinolones TK Hyster, DM Dalton, T Rovis Chemical science 6 (1), 254-258, 2015 | 136 | 2015 |
| Catalytic promiscuity enabled by photoredox catalysis in nicotinamide-dependent oxidoreductases KF Biegasiewicz, SJ Cooper, MA Emmanuel, DC Miller, TK Hyster Nature chemistry 10 (7), 770-775, 2018 | 134 | 2018 |
| Asymmetric redox-neutral radical cyclization catalysed by flavin-dependent ‘ene’-reductases MJ Black, KF Biegasiewicz, AJ Meichan, DG Oblinsky, B Kudisch, ... Nature chemistry 12 (1), 71-75, 2020 | 130 | 2020 |
| Enantioselective hydrogen atom transfer: discovery of catalytic promiscuity in flavin-dependent ‘ene’-reductases BA Sandoval, AJ Meichan, TK Hyster Journal of the American Chemical Society 139 (33), 11313-11316, 2017 | 115 | 2017 |
| Emerging strategies for expanding the toolbox of enzymes in biocatalysis BA Sandoval, TK Hyster Current Opinion in Chemical Biology 55, 45-51, 2020 | 103 | 2020 |
| Photoenzymatic catalysis enables radical‐mediated ketone reduction in ene‐reductases BA Sandoval, SI Kurtoic, MM Chung, KF Biegasiewicz, TK Hyster Angewandte Chemie 131 (26), 8806-8810, 2019 | 95 | 2019 |
