| Formation and rearrangement of homoserine depsipeptides and depsiproteins in the α‐ketoacid–hydroxylamine ligation with 5‐oxaproline TG Wucherpfennig, F Rohrbacher, VR Pattabiraman, JW Bode Angewandte Chemie International Edition 53 (45), 12244-12247, 2014 | 54* | 2014 |
| Spontaneous head-to-tail cyclization of unprotected linear peptides with the KAHA ligation F Rohrbacher, G Deniau, A Luther, JW Bode Chemical Science 6 (8), 4889-4896, 2015 | 37 | 2015 |
| Chemical synthesis of a homoserine-mutant of the antibacterial, head-to-tail cyclized protein AS-48 by α-ketoacid–hydroxylamine (KAHA) ligation F Rohrbacher, A Zwicky, JW Bode Chemical science 8 (5), 4051-4055, 2017 | 34 | 2017 |
| Photoprotected Peptide α‐Ketoacids and Hydroxylamines for Iterative and One‐Pot KAHA Ligations: Synthesis of NEDD8 F Thuaud, F Rohrbacher, A Zwicky, JW Bode Helvetica Chimica Acta 99 (11), 868-894, 2016 | 27 | 2016 |
| Chemical protein synthesis with the KAHA ligation F Rohrbacher, TG Wucherpfennig, JW Bode Protein Ligation and Total Synthesis II, 1-31, 2015 | 23 | 2015 |
| Incorporation of acid-labile masking groups for the traceless synthesis of C-terminal peptide α-Ketoacids F Thuaud, F Rohrbacher, A Zwicky, JW Bode Organic letters 18 (15), 3670-3673, 2016 | 21 | 2016 |
| Synthesis and Characterization of Energetic Salts of the (C4N122–) Dianion TM Klapötke, DG Piercey, F Rohrbacher, J Stierstorfer Zeitschrift für anorganische und allgemeine Chemie 638 (14), 2235-2242, 2012 | 20 | 2012 |
| Facile Synthesis of Internal and C‐Terminal Peptide α‐Ketoamides with Fmoc‐Solid Phase Peptide Synthesis F Rohrbacher, A Zwicky, JW Bode Helvetica Chimica Acta 101 (5), e1800039, 2018 | 10 | 2018 |
| Product selectivity in KAHA ligations: ester vs. amide formation with cyclic hydroxylamines F Rohrbacher, S Baldauf, TG Wucherpfennig, JW Bode Synlett 28 (15), 1929-1933, 2017 | 10 | 2017 |
| Myotubularin-related protein 7 activates peroxisome proliferator-activated receptor-gamma P Weidner, M Söhn, T Schroeder, L Helm, V Hauber, T Gutting, J Betge, ... Oncogenesis 9 (6), 59, 2020 | 8 | 2020 |
| (4S)‐3‐[(2S)‐2‐(9H‐Fluoren‐9‐ylmethoxycarbonylamino)propanoyl]‐2,2‐dimethyl‐1,3‐oxazolidine‐4‐carboxylic Acid (Fmoc‐Ala‐Ser‐(ψMe,MePro)‐OH) TG Wucherpfennig, F Rohrbacher Encyclopedia of Reagents for Organic Synthesis, 1-3, 2001 | 2 | 2001 |
| Myotubularin-related-protein-7 inhibits mutant (G12V) K-RAS by direct interaction P Weidner, D Saar, M Söhn, T Schroeder, Y Yu, FG Zöllner, N Ponelies, ... Cancer Letters 588, 216783, 2024 | | 2024 |
| Incorporation of Acid-Labile Masking Groups for the Traceless Synthesis of C-Terminal Peptide α-Ketoacids F Rohrbacher, AÌ Zwicky, JW Bode Organic letters 18 (15), 2016 | | 2016 |
