| New generation of biocatalysts for organic synthesis BM Nestl, SC Hammer, BA Nebel, B Hauer Angewandte Chemie International Edition 53 (12), 3070-3095, 2014 | 416 | 2014 |
| Design and evolution of enzymes for non-natural chemistry SC Hammer, AM Knight, FH Arnold Current Opinion in Green and Sustainable Chemistry 7, 23-30, 2017 | 216 | 2017 |
| Anti-Markovnikov alkene oxidation by metal-oxo–mediated enzyme catalysis SC Hammer, G Kubik, E Watkins, S Huang, H Minges, FH Arnold Science 358 (6360), 215-218, 2017 | 196 | 2017 |
| Imine reductase‐catalyzed intermolecular reductive amination of aldehydes and ketones PN Scheller, M Lenz, SC Hammer, B Hauer, BM Nestl ChemCatChem 7 (20), 3239-3242, 2015 | 128 | 2015 |
| Squalene hopene cyclases are protonases for stereoselective Brønsted acid catalysis SC Hammer, A Marjanovic, JM Dominicus, BM Nestl, B Hauer Nature chemical biology 11 (2), 121-126, 2015 | 110 | 2015 |
| Squalene hopene cyclases: highly promiscuous and evolvable catalysts for stereoselective CC and CX bond formation SC Hammer, PO Syrén, M Seitz, BM Nestl, B Hauer Current opinion in chemical biology 17 (2), 293-300, 2013 | 76 | 2013 |
| Engineered Enzymes Enable Selective N‐Alkylation of Pyrazoles With Simple Haloalkanes LL Bengel, B Aberle, AN Egler‐Kemmerer, S Kienzle, B Hauer, ... Angewandte Chemie International Edition 60 (10), 5554-5560, 2021 | 73 | 2021 |
| Asymmetric enzymatic hydration of unactivated, aliphatic alkenes RM Demming, SC Hammer, BM Nestl, S Gergel, S Fademrecht, J Pleiss, ... Angewandte Chemie 131 (1), 179-183, 2019 | 66 | 2019 |
| Biokatalysatoren für die organische Synthese–die neue Generation BM Nestl, SC Hammer, BA Nebel, B Hauer Angewandte Chemie 126 (12), 3132-3158, 2014 | 64 | 2014 |
| Entropy is key to the formation of pentacyclic terpenoids by enzyme‐catalyzed polycyclization PO Syrén, SC Hammer, B Claasen, B Hauer Angewandte Chemie 126 (19), 4945-4949, 2014 | 45 | 2014 |
| Stereoselective Friedel–Crafts alkylation catalyzed by squalene hopene cyclases SC Hammer, JM Dominicus, PO Syrén, BM Nestl, B Hauer Tetrahedron 68 (37), 7624-7629, 2012 | 44 | 2012 |
| Enzymatic control over reactive intermediates enables direct oxidation of alkenes to carbonyls by a P450 iron-oxo species J Soler, S Gergel, C Klaus, SC Hammer, M Garcia-Borràs Journal of the American Chemical Society 144 (35), 15954-15968, 2022 | 40 | 2022 |
| Engineered cytochrome P450 for direct arylalkene-to-ketone oxidation via highly reactive carbocation intermediates S Gergel, J Soler, A Klein, KH Schülke, B Hauer, M Garcia-Borràs, ... Nature Catalysis 6 (7), 606-617, 2023 | 35* | 2023 |
| Selectivity in the cyclization of citronellal introduced by squalene hopene cyclase variants SA Bastian, SC Hammer, N Kreß, BM Nestl, B Hauer ChemCatChem 9 (23), 4364-4368, 2017 | 29 | 2017 |
| Substrate Profiling of Anion Methyltransferases for Promiscuous Synthesis of S‐Adenosylmethionine Analogs from Haloalkanes KH Schülke, F Ospina, K Hörnschemeyer, S Gergel, SC Hammer ChemBioChem 23 (4), e202100632, 2022 | 28 | 2022 |
| Substrate Pre‐Folding and Water Molecule Organization Matters for Terpene Cyclase Catalyzed Conversion of Unnatural Substrates SC Hammer, PO Syrén, B Hauer ChemistrySelect 1 (13), 3589-3593, 2016 | 25 | 2016 |
| Selective Biocatalytic N‐Methylation of Unsaturated Heterocycles F Ospina, KH Schülke, J Soler, A Klein, B Prosenc, M Garcia‐Borràs, ... Angewandte Chemie International Edition 61 (48), e202213056, 2022 | 24 | 2022 |
| New catalytic reactions by enzyme engineering C Klaus, SC Hammer Trends in Chemistry 4 (5), 363-366, 2022 | 18 | 2022 |
| Methylation of unactivated alkenes with engineered methyltransferases to generate non‐natural terpenoids B Aberle, D Kowalczyk, S Massini, AN Egler‐Kemmerer, S Gergel, ... Angewandte Chemie International Edition 62 (26), e202301601, 2023 | 14 | 2023 |
| Biocatalytic alkylation chemistry: Building molecular complexity with high selectivity F Ospina, KH Schülke, SC Hammer ChemPlusChem 87 (1), e202100454, 2022 | 11 | 2022 |
Bettina NestlGroup Leader, University of StuttgartVerified email at itb.uni-stuttgart.de