Increased structural complexity leads to higher activity: peptides as efficient and versatile catalysts for asymmetric aldol reactions P Krattiger, R Kovasy, JD Revell, S Ivan, H Wennemers Organic letters 7 (6), 1101-1103, 2005 | 332 | 2005 |
Tripeptides as Efficient Asymmetric Catalysts for 1, 4-Addition Reactions of Aldehydes to Nitroolefins–A Rational Approach Angew. Chem. Int. Ed. 2008, 47, 1871-1874. M Wiesner, JD Revell, H Wennemers Angew. Chem. Int. Ed 47, 1871-1874, 2008 | 308 | 2008 |
Asymmetric catalysis with peptides H Wennemers Chemical Communications 47 (44), 12036-12041, 2011 | 246 | 2011 |
Peptide Catalyzed Asymmetric Conjugate Addition Reactions of Aldehydes to Nitroethylene—A Convenient Entry into γ2-Amino Acids M Wiesner, JD Revell, S Tonazzi, H Wennemers Journal of the American Chemical Society 130 (17), 5610-5611, 2008 | 219 | 2008 |
Enamine catalysis with low catalyst loadings-high efficiency via kinetic studies M Wiesner, G Upert, G Angelici, H Wennemers Journal of the American Chemical Society 132 (1), 6-7, 2010 | 212 | 2010 |
Mimicry of Polyketide Synthases–Enantioselective 1, 4-Addition Reactions of Malonic Acid Half-Thioesters to Nitroolefins Angew. Chem. Int. Ed. 2007, 46, 6841-6844. J Lubkoll, H Wennemers Angew. Chem. Int. Ed 46, 6841-6844, 2007 | 208 | 2007 |
A crystal structure of an oligoproline PPII-helix, at last P Wilhelm, B Lewandowski, N Trapp, H Wennemers Journal of the American Chemical Society 136 (45), 15829-15832, 2014 | 172 | 2014 |
Azidoproline containing helices: Stabilization of the polyproline II structure by a functionalizable group M Kümin, LS Sonntag, H Wennemers Journal of the American Chemical Society 129 (3), 466-467, 2007 | 153 | 2007 |
The “azido gauche effect” implications for the conformation of azidoprolines LS Sonntag, S Schweizer, C Ochsenfeld, H Wennemers Journal of the American Chemical Society 128 (45), 14697-14703, 2006 | 144 | 2006 |
Tripeptides of the Type H‐D‐Pro‐Pro‐Xaa‐NH2 as Catalysts for Asymmetric 1,4‐Addition Reactions: Structural Requirements for High Catalytic Efficiency M Wiesner, M Neuburger, H Wennemers Chemistry–A European Journal 15 (39), 10103-10109, 2009 | 141 | 2009 |
Effects of terminal functional groups on the stability of the polyproline II structure: a combined experimental and theoretical study M Kuemin, S Schweizer, C Ochsenfeld, H Wennemers Journal of the American Chemical Society 131 (42), 15474-15482, 2009 | 134 | 2009 |
Enantioselective aldol reactions with masked fluoroacetates J Saadi, H Wennemers Nature chemistry 8 (3), 276-280, 2016 | 132 | 2016 |
Peptide-catalyzed stereoselective conjugate addition reactions generating all-carbon quaternary stereogenic centers. R Kastl, H Wennemers Angewandte Chemie 125 (28), 2013 | 124 | 2013 |
Tuning the cis/trans Conformer Ratio of Xaa–Pro Amide Bonds by Intramolecular Hydrogen Bonds: The Effect on PPII Helix Stability M Kuemin, YA Nagel, S Schweizer, FW Monnard, C Ochsenfeld, ... Angewandte Chemie 122 (36), 6468-6471, 2010 | 118 | 2010 |
Adapting to substrate challenges: peptides as catalysts for conjugate addition reactions of aldehydes to α, β‐disubstituted nitroolefins J Duschmalé, H Wennemers Chemistry–A European Journal 18 (4), 1111-1120, 2012 | 117 | 2012 |
Peptidic catalysts developed by combinatorial screening methods JD Revell, H Wennemers Current opinion in chemical biology 11 (3), 269-278, 2007 | 114 | 2007 |
Solid‐supported and pegylated H–Pro–Pro–Asp–NHR as catalysts for asymmetric aldol reactions JD Revell, D Gantenbein, P Krattiger, H Wennemers Peptide Science: Original Research on Biomolecules 84 (1), 105-113, 2006 | 108 | 2006 |
Catalyst–Substrate Coimmobilization: A Strategy for Catalysts Discovery in Split‐and‐Mix Libraries P Krattiger, C McCarthy, A Pfaltz, H Wennemers Angewandte Chemie International Edition 42 (15), 1722-1724, 2003 | 108 | 2003 |
Diketopiperazine receptors: a novel class of highly selective receptors for binding small peptides H Wennemers, M Conza, M Nold, P Krattiger Chemistry–A European Journal 7 (15), 3342-3347, 2001 | 108 | 2001 |
Synthetic receptors WC Still, G Li, H Wennemers US Patent 6,797,522, 2004 | 106 | 2004 |