| Photo-biocatalysis: biotransformations in the presence of light L Schmermund, V Jurkas, FF Özgen, GD Barone, HC Büchsenschütz, ... Acs Catalysis 9 (5), 4115-4144, 2019 | 246 | 2019 |
| Asymmetric bioreduction of activated alkenes to industrially relevant optically active compounds CK Winkler, G Tasnádi, D Clay, M Hall, K Faber Journal of biotechnology 162 (4), 381-389, 2012 | 182 | 2012 |
| Enzymes revolutionize the bioproduction of value-added compounds: From enzyme discovery to special applications B Wiltschi, T Cernava, A Dennig, MG Casas, M Geier, S Gruber, ... Biotechnology advances 40, 107520, 2020 | 115 | 2020 |
| Chemoenzymatic asymmetric synthesis of pregabalin precursors via asymmetric bioreduction of β-cyanoacrylate esters using ene-reductases CK Winkler, D Clay, S Davies, P O’Neill, P McDaid, S Debarge, J Steflik, ... The Journal of organic chemistry 78 (4), 1525-1533, 2013 | 103 | 2013 |
| Asymmetric bioreduction of alkenes using ene–reductases YersER and KYE1 and effects of organic solvents Y Yanto, CK Winkler, S Lohr, M Hall, K Faber, AS Bommarius Organic letters 13 (10), 2540-2543, 2011 | 89 | 2011 |
| Bioreduction of α-methylcinnamaldehyde derivatives: chemo-enzymatic asymmetric synthesis of Lilial™ and Helional™ C Stueckler, NJ Mueller, CK Winkler, SM Glueck, K Gruber, G Steinkellner, ... Dalton transactions 39 (36), 8472-8476, 2010 | 83 | 2010 |
| Mechanistic studies of fatty acid activation by CYP152 peroxygenases reveal unexpected desaturase activity M Pickl, S Kurakin, FG Cantú Reinhard, P Schmid, A Pöcheim, ... ACS catalysis 9 (1), 565-577, 2018 | 82 | 2018 |
| Regioselective biocatalytic hydroxylation of fatty acids by cytochrome P450s L Hammerer, CK Winkler, W Kroutil Catalysis Letters 148, 787-812, 2018 | 80 | 2018 |
| Identification of promiscuous ene-reductase activity by mining structural databases using active site constellations G Steinkellner, CC Gruber, T Pavkov-Keller, A Binter, K Steiner, C Winkler, ... Nature communications 5 (1), 4150, 2014 | 79 | 2014 |
| Asymmetric Synthesis of (R)‐3‐Hydroxy‐2‐methylpropanoate (‘Roche Ester’) and Derivatives via Biocatalytic CC‐Bond Reduction C Stueckler, CK Winkler, M Bonnekessel, K Faber Advanced Synthesis & Catalysis 352 (14‐15), 2663-2666, 2010 | 79 | 2010 |
| Stereo‐controlled asymmetric bioreduction of α, β‐dehydroamino acid derivatives C Stueckler, CK Winkler, M Hall, B Hauer, M Bonnekessel, K Zangger, ... Advanced Synthesis & Catalysis 353 (7), 1169-1173, 2011 | 54 | 2011 |
| A substrate‐driven approach to determine reactivities of α, β‐unsaturated carboxylic esters towards asymmetric bioreduction G Tasnádi, CK Winkler, D Clay, N Sultana, WMF Fabian, M Hall, K Ditrich, ... Chemistry–A European Journal 18 (33), 10362-10367, 2012 | 52 | 2012 |
| Using deep eutectic solvents to overcome limited substrate solubility in the enzymatic decarboxylation of bio-based phenolic acids AK Schweiger, N Ríos-Lombardía, CK Winkler, S Schmidt, F Morís, ... ACS sustainable chemistry & engineering 7 (19), 16364-16370, 2019 | 45 | 2019 |
| Nitrile as activating group in the asymmetric bioreduction of β‐cyanoacrylic acids catalyzed by ene‐reductases CK Winkler, D Clay, NG Turrini, H Lechner, W Kroutil, S Davies, ... Advanced Synthesis & Catalysis 356 (8), 1878-1882, 2014 | 31 | 2014 |
| NAD (P) H‐Independent Asymmetric C C Bond Reduction Catalyzed by Ene Reductases by Using Artificial Co‐substrates as the Hydrogen Donor CK Winkler, D Clay, M Entner, M Plank, K Faber Chemistry–A European Journal 20 (5), 1403-1409, 2014 | 28 | 2014 |
| Overcoming co‐product inhibition in the nicotinamide independent asymmetric bioreduction of activated C C‐bonds using flavin‐dependent ene‐reductases CK Winkler, D Clay, E van Heerden, K Faber Biotechnology and Bioengineering 110 (12), 3085-3092, 2013 | 28 | 2013 |
| Variants of the Acyltransferase from Mycobacterium smegmatis Enable Enantioselective Acyl Transfer in Water E Jost, M Kazemi, V Mrkonjić, F Himo, CK Winkler, W Kroutil ACS Catalysis 10 (18), 10500-10507, 2020 | 25 | 2020 |
| Asymmetric Synthesis of O‐Protected Acyloins Using Enoate Reductases: Stereochemical Control through Protecting Group Modification CK Winkler, C Stueckler, NJ Mueller, D Pressnitz, K Faber European Journal of Organic Chemistry 2010 (33), 6354-6358, 2010 | 25 | 2010 |
| Trametes versicolor carboxylate reductase uncovered M Winkler, CK Winkler Monatshefte für Chemie-Chemical Monthly 147, 575-578, 2016 | 24 | 2016 |
| Reductive dehalogenation of β-haloacrylic ester derivatives mediated by ene-reductases G Tasnádi, CK Winkler, D Clay, M Hall, K Faber Catalysis Science & Technology 2 (8), 1548-1552, 2012 | 22 | 2012 |
