| Year |
Citation |
Score |
| 2024 |
Schnitzer T, Schnurr M, Zahrt AF, Sakhaee N, Denmark SE, Wennemers H. Machine Learning to Develop Peptide Catalysts-Successes, Limitations, and Opportunities. Acs Central Science. 10: 367-373. PMID 38435528 DOI: 10.1021/acscentsci.3c01284 |
0.303 |
|
| 2024 |
Hiebert P, Antoniazzi G, Aronoff M, Werner S, Wennemers H. A Lysyl Oxidase-Responsive Collagen Peptide Illuminates Collagen Remodeling in Wound Healing. Matrix Biology : Journal of the International Society For Matrix Biology. PMID 38382767 DOI: 10.1016/j.matbio.2024.02.006 |
0.74 |
|
| 2024 |
Möhler JS, Pickl M, Reiter T, Simić S, Rackl JW, Kroutil W, Wennemers H. Peptide and Enzyme Catalysts Work in Concert in Stereoselective Cascade Reactions - Oxidation Followed by Conjugate Addition. Angewandte Chemie (International Ed. in English). e202319457. PMID 38235524 DOI: 10.1002/anie.202319457 |
0.79 |
|
| 2023 |
Vela-Gallego S, Lewandowski B, Möhler J, Puente A, Gil-Cantero D, Wennemers H, de la Escosura A. Modifying the Catalytic Activity of Lipopeptide Assemblies with Nucleobases. Chemistry (Weinheim An Der Bergstrasse, Germany). e202303395. PMID 37877614 DOI: 10.1002/chem.202303395 |
0.702 |
|
| 2023 |
Schnurr M, Rackl JW, Wennemers H. Overcoming Deactivation of Amine-Based Catalysts: Access to Fluoroalkylated γ-Nitroaldehydes. Journal of the American Chemical Society. 145: 23275-23280. PMID 37845230 DOI: 10.1021/jacs.3c08198 |
0.774 |
|
| 2023 |
Beweries T, Buchmeiser MR, Bugden FE, Champness NR, Chanbasha B, Costas M, Echeverria J, Eisenstein O, Ferguson C, Goodall JC, Gramage-Doria R, Greenhalgh M, Gyton M, Ham R, Kennepohl P, ... ... Wennemers H, et al. Make - underpinning concepts of the synthesis of systems where non-covalent interactions are important: general discussion. Faraday Discussions. PMID 37486614 DOI: 10.1039/d3fd90012f |
0.641 |
|
| 2023 |
Beweries T, Buchmeiser MR, Champness NR, Costas M, Duhme-Klair A, Echeverría J, Eisenstein O, Ferguson CTJ, Goodall JC, Gramage-Doria R, Gyton M, Ham R, Herres-Pawlis S, Johnson CL, Kennepohl P, ... ... Wennemers H, et al. Manipulate - techniques to manipulate the surroundings of a synthetic catalyst to control activity and selectivity: general discussion. Faraday Discussions. PMID 37436131 DOI: 10.1039/d3fd90013d |
0.669 |
|
| 2023 |
Lewandowski B, Schäfer RJB, Cotter E, Harangozo D, Wennemers H. Catalytic templated length-controlled oligomerization. Faraday Discussions. PMID 37185626 DOI: 10.1039/d3fd00002h |
0.687 |
|
| 2022 |
Schnitzer T, Rackl JW, Wennemers H. Stereoselective peptide catalysis in complex environments - from river water to cell lysates. Chemical Science. 13: 8963-8967. PMID 36091207 DOI: 10.1039/d2sc02044k |
0.797 |
|
| 2022 |
Vastakaite G, Grünenfelder C, Wennemers H. Peptide-Catalyzed Stereoselective Conjugate Addition Reaction of Aldehydes to C-Substituted Maleimides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35089626 DOI: 10.1002/chem.202200215 |
0.327 |
|
| 2021 |
Wennemers H, Nicholls LDM. Synergistic Peptide and Gold Catalysis: Enantioselective Addition of Branched Aldehydes to Allenamides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34496089 DOI: 10.1002/chem.202103197 |
0.357 |
|
| 2021 |
Aronoff MR, Hiebert P, Hentzen NB, Werner S, Wennemers H. Imaging and targeting LOX-mediated tissue remodeling with a reactive collagen peptide. Nature Chemical Biology. PMID 34253910 DOI: 10.1038/s41589-021-00830-6 |
0.737 |
|
| 2021 |
Wennemers H. Peptides - Molecular Allrounders. Chimia. 75: 525-529. PMID 34233818 DOI: 10.2533/chimia.2021.525 |
0.313 |
|
| 2020 |
Wennemers H, Möhler JS, Schnitzer T. Amine Catalysis with Substrates Bearing N-Heterocyclic Moieties Enabled by Control over the Enamine Pyramidalization Direction. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32573875 DOI: 10.1002/Chem.202002966 |
0.373 |
|
| 2020 |
Wennemers H, Li M, Puschmann R, Herdlitschka A, Fiedler D. Delivery of myo-inositol hexakisphosphate to the cell nucleus with a proline-based cell penetrating peptide. Angewandte Chemie (International Ed. in English). PMID 32558101 DOI: 10.1002/Anie.202006770 |
0.314 |
|
| 2020 |
Schnitzer T, Wennemers H. Deactivation of Secondary Amine Catalysts via Aldol Reaction-Amine Catalysis under Solvent-Free Conditions. The Journal of Organic Chemistry. PMID 32329616 DOI: 10.1021/Acs.Joc.0C00665 |
0.412 |
|
| 2020 |
Wennemers H, Aronoff MR, Egli J, Schmitt A. Alkylation of g-Azaproline Creates Conformationally Adaptable Proline Derivatives for pH-Responsive Collagen Triple Helices. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32043659 DOI: 10.1002/Chem.201905768 |
0.777 |
|
| 2020 |
Hentzen NB, Islami V, Köhler M, Zenobi R, Wennemers H. A Lateral Salt Bridge for the Specific Assembly of an ABC-Type Collagen Heterotrimer. Journal of the American Chemical Society. PMID 31971793 DOI: 10.1021/Jacs.9B13037 |
0.301 |
|
| 2020 |
Schnitzer T, Möhler JS, Wennemers H. Effect of the enamine pyramidalization direction on the reactivity of secondary amine organocatalysts Chemical Science. 11: 1943-1947. DOI: 10.1039/C9Sc05410C |
0.302 |
|
| 2020 |
Schnitzer T, Ganzoni RL, Wennemers H. Impact of the β-turn hydrogen bond on the trans/cis ratio and the performance of the peptide catalyst H-dPro-Pro-Glu-NH2 Tetrahedron. 131184. DOI: 10.1016/J.Tet.2020.131184 |
0.406 |
|
| 2019 |
Herdlitschka A, Lewandowski B, Wennemers H. Organic Molecular Weaves. Chimia. 73: 450-454. PMID 38549205 DOI: 10.2533/chimia.2019.450 |
0.65 |
|
| 2019 |
Köhler M, Marchand A, Hentzen NB, Egli J, Begley AI, Wennemers H, Zenobi R. Temperature-controlled electrospray ionization mass spectrometry as a tool to study collagen homo- and heterotrimers. Chemical Science. 10: 9829-9835. PMID 32015805 DOI: 10.1039/C9Sc03248G |
0.322 |
|
| 2019 |
Egli J, Schnitzer T, Dietschreit JCB, Ochsenfeld C, Wennemers H. Why Proline? Influence of Ring-Size on the Collagen Triple Helix. Organic Letters. PMID 31682124 DOI: 10.1021/Acs.Orglett.9B03528 |
0.305 |
|
| 2019 |
Ochs NAK, Lewandowska U, Zajaczkowski W, Corra S, Reger S, Herdlitschka A, Schmid S, Pisula W, Müllen K, Bäuerle P, Wennemers H. Oligoprolines guide the self-assembly of quaterthiophenes. Chemical Science. 10: 5391-5396. PMID 31191896 DOI: 10.1039/C8Sc05742G |
0.707 |
|
| 2019 |
Schäfer RJB, Aronoff MR, Wennemers H. Recent Advances in Bioorthogonal Reactions. Chimia. 73: 308-312. PMID 30975262 DOI: 10.2533/Chimia.2019.308 |
0.754 |
|
| 2019 |
Egli J, Siebler C, Köhler M, Zenobi R, Wennemers H. Hydrophobic Moieties Bestow Fast-Folding and Hyperstability on Collagen Triple Helices. Journal of the American Chemical Society. PMID 30920819 DOI: 10.1021/Jacs.8B13871 |
0.314 |
|
| 2019 |
Aronoff MR, Egli J, Menichelli M, Wennemers H. γ-Azaproline Confers pH Responsiveness and Functionalizability on Collagen Triple Helices. Angewandte Chemie (International Ed. in English). PMID 30633447 DOI: 10.1002/Anie.201813048 |
0.761 |
|
| 2019 |
Ritler A, Shoshan M, Deupi X, Wilhelm P, Schibli R, Wennemers H, Behe M. Elucidating the structure-activity relationship of the pentaglutamic acid sequence of minigastrin with the cholecystokinin receptor subtype 2. Bioconjugate Chemistry. PMID 30608664 DOI: 10.1021/Acs.Bioconjchem.8B00849 |
0.725 |
|
| 2019 |
Herdlitschka A, Lewandowski B, Wennemers H. Organic Molecular Weaves Chimia International Journal For Chemistry. 73: 450-454. DOI: 10.2533/Chimia.2019.450 |
0.653 |
|
| 2019 |
Loosli S, Foletti C, Papmeyer M, Wennemers H. Synthesis of 4-(Arylmethyl)proline Derivatives Synlett. 30: 508-510. DOI: 10.1055/S-0037-1611672 |
0.33 |
|
| 2019 |
Schnitzer T, Wennemers H. Effect of
β
3
‐Amino Acids on the Performance of the Peptidic Catalyst H‐
d
Pro‐Pro‐Glu‐NH
2 Helvetica Chimica Acta. 102. DOI: 10.1002/Hlca.201900070 |
0.38 |
|
| 2019 |
Foletti C, Trapp N, Loosli S, Lewandowski B, Wennemers H. 4‐Naphthylmethyl Proline Forms a Channel Structure Helvetica Chimica Acta. 102: e1900052. DOI: 10.1002/Hlca.201900052 |
0.646 |
|
| 2019 |
Shoshan MS, Vonderach T, Hattendorf B, Wennemers H. Cover Picture: Peptide‐Coated Platinum Nanoparticles with Selective Toxicity against Liver Cancer Cells (Angew. Chem. Int. Ed. 15/2019) Angewandte Chemie International Edition. 58: 4745-4745. DOI: 10.1002/Anie.201902737 |
0.71 |
|
| 2019 |
Shoshan MS, Vonderach T, Hattendorf B, Wennemers H. Titelbild: Peptide‐Coated Platinum Nanoparticles with Selective Toxicity against Liver Cancer Cells (Angew. Chem. 15/2019) Angewandte Chemie. 131: 4795-4795. DOI: 10.1002/Ange.201902737 |
0.709 |
|
| 2018 |
Shoshan MS, Vonderach T, Hattendorf B, Wennemers H. Peptide-Coated Platinum Nanoparticles with Selective Toxicity against Liver Cancer Cells. Angewandte Chemie (International Ed. in English). PMID 30561882 DOI: 10.1002/Anie.201813149 |
0.743 |
|
| 2018 |
Rigling C, Kisunzu JK, Duschmalé J, Häussinger D, Wiesner M, Ebert MO, Wennemers H. Conformational Properties of a Peptidic Catalyst: Insights from NMR Spectroscopic Studies. Journal of the American Chemical Society. PMID 30106584 DOI: 10.1021/Jacs.8B05459 |
0.453 |
|
| 2018 |
Wennemers H, Lewandowska U, Corra S, Zajaczkowski W, Ochs NAK, Shoshan MS, Tanabe J, Stappert S, Yashima E, Pisula W, Müllen K. Positional Isomers of Chromophore-Peptide Conjugates Self-Assemble Into Different Morphologies. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29893493 DOI: 10.1002/Chem.201801545 |
0.781 |
|
| 2018 |
Wennemers H, Schnitzer T. Effect of γ-Substituted Proline Derivatives on the Performance of the Peptidic Catalyst H-dPro-Pro-Glu-NH2 Synthesis. 50: 4377-4382. DOI: 10.1055/S-0037-1609547 |
0.426 |
|
| 2017 |
Lewandowska U, Zajaczkowski W, Corra S, Tanabe J, Borrmann R, Benetti EM, Stappert S, Watanabe K, Ochs NAK, Schaeublin R, Li C, Yashima E, Pisula W, Müllen K, Wennemers H. A triaxial supramolecular weave. Nature Chemistry. 9: 1068-1072. PMID 29064493 DOI: 10.1038/Nchem.2823 |
0.711 |
|
| 2017 |
Schnitzer T, Wennemers H. Influence of the Trans/Cis Conformer Ratio on the Stereoselectivity of Peptidic Catalysts. Journal of the American Chemical Society. PMID 29043799 DOI: 10.1021/Jacs.7B06194 |
0.443 |
|
| 2017 |
Raines RT, Wennemers H. Peptides on the Rise. Accounts of Chemical Research. 50: 2419. PMID 29037047 DOI: 10.1021/Acs.Accounts.7B00471 |
0.533 |
|
| 2017 |
Corra S, Shoshan MS, Wennemers H. Peptide mediated formation of noble metal nanoparticles-controlling size and spatial arrangement. Current Opinion in Chemical Biology. 40: 138-144. PMID 28961470 DOI: 10.1016/J.Cbpa.2017.09.005 |
0.781 |
|
| 2017 |
Dobitz S, Aronoff MR, Wennemers H. Oligoprolines as Molecular Entities for Controlling Distance in Biological and Material Sciences. Accounts of Chemical Research. PMID 28885830 DOI: 10.1021/Acs.Accounts.7B00340 |
0.77 |
|
| 2017 |
Hentzen NB, Smeenk LEJ, Witek J, Riniker S, Wennemers H. Cross-Linked Collagen Triple Helices by Oxime Ligation. Journal of the American Chemical Society. PMID 28872857 DOI: 10.1021/Jacs.7B07498 |
0.326 |
|
| 2017 |
Schnitzer T, Wiesner M, Krattiger P, Revell JD, Wennemers H. Is more better? A comparison of tri- and tetrapeptidic catalysts. Organic & Biomolecular Chemistry. PMID 28590473 DOI: 10.1039/C7Ob01039G |
0.397 |
|
| 2017 |
Wennemers H, Siebler C, Egli J, Maryasin B, Erdmann RS, Bergande C, Ochsenfeld C. pH-Responsive Aminoproline-Containing Collagen Triple Helices. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28398637 DOI: 10.1002/Chem.201701134 |
0.307 |
|
| 2017 |
Wennemers H, Schnitzer T. Thieme Chemistry Journals Awardees – Where Are They Now? A Stereoselective Tripeptide Catalyst for Conjugate Addition Reactions of Acetophenones to Dicyanoolefins Synlett. 28: 1282-1286. DOI: 10.1055/S-0036-1588964 |
0.406 |
|
| 2017 |
Engl OD, Saadi J, Cosimi E, Wennemers H. Synthesis of Monothiomalonates - Versatile Thioester Enolate Equivalents for C-C Bond Formations Helvetica Chimica Acta. 100: e1700196. DOI: 10.1002/Hlca.201700196 |
0.77 |
|
| 2016 |
Cosimi E, Saadi J, Wennemers H. Stereoselective Synthesis of α-Fluoro-γ-nitro Thioesters under Organocatalytic Conditions. Organic Letters. 18: 6014-6017. PMID 27934387 DOI: 10.1021/Acs.Orglett.6B02795 |
0.344 |
|
| 2016 |
Cosimi E, Engl OD, Saadi J, Ebert MO, Wennemers H. Stereoselective Organocatalyzed Synthesis of α-Fluorinated β-Amino Thioesters and Their Application in Peptide Synthesis. Angewandte Chemie (International Ed. in English). PMID 27632946 DOI: 10.1002/Anie.201607146 |
0.787 |
|
| 2016 |
Garbuio L, Lewandowski B, Wilhelm P, Ziegler L, Yulikov M, Wennemers H, Jeschke G. Corrigendum: Shape Persistence of Polyproline II Helical Oligoprolines. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 12587. PMID 27546179 DOI: 10.1002/Chem.201601204 |
0.644 |
|
| 2016 |
Grünenfelder CE, Kisunzu JK, Trapp N, Kastl R, Wennemers H. Crystal Structures of Peptidic Catalysts of the H-DPro-Pro-Xaa Type. Biopolymers. PMID 27403581 DOI: 10.1002/Bip.22912 |
0.373 |
|
| 2016 |
Grünenfelder CE, Kisunzu JK, Wennemers H. Peptide-Catalyzed Stereoselective Conjugate Addition Reactions of Aldehydes to Maleimide. Angewandte Chemie (International Ed. in English). PMID 27254460 DOI: 10.1002/Anie.201602230 |
0.442 |
|
| 2016 |
Corra S, Lewandowska U, Benetti EM, Wennemers H. Size-Controlled Formation of Noble-Metal Nanoparticles in Aqueous Solution with a Thiol-Free Tripeptide. Angewandte Chemie (International Ed. in English). PMID 27098442 DOI: 10.1002/Anie.201510337 |
0.736 |
|
| 2016 |
Saadi J, Wennemers H. Enantioselective aldol reactions with masked fluoroacetates. Nature Chemistry. 8: 276-80. PMID 26892561 DOI: 10.1038/Nchem.2437 |
0.333 |
|
| 2016 |
Lewandowska U, Zajaczkowski W, Pisula W, Ma Y, Li C, Müllen K, Wennemers H. Effect of Structural Modifications on the Self-Assembly of Oligoprolines Conjugated with Sterically Demanding Chromophores. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26891419 DOI: 10.1002/Chem.201504952 |
0.343 |
|
| 2016 |
Corra S, Lewandowska U, Benetti EM, Wennemers H. Cover Picture: Size-Controlled Formation of Noble-Metal Nanoparticles in Aqueous Solution with a Thiol-Free Tripeptide (Angew. Chem. Int. Ed. 30/2016) Angewandte Chemie International Edition. 55: 8459-8459. DOI: 10.1002/Anie.201604536 |
0.699 |
|
| 2016 |
Corra S, Lewandowska U, Benetti EM, Wennemers H. Titelbild: Size-Controlled Formation of Noble-Metal Nanoparticles in Aqueous Solution with a Thiol-Free Tripeptide (Angew. Chem. 30/2016) Angewandte Chemie. 128: 8599-8599. DOI: 10.1002/Ange.201604536 |
0.698 |
|
| 2015 |
Siebler C, Maryasin B, Kuemin M, Erdmann RS, Rigling C, Grünenfelder C, Ochsenfeld C, Wennemers H. Importance of dipole moments and ambient polarity for the conformation of Xaa-Pro moieties - a combined experimental and theoretical study. Chemical Science. 6: 6725-6730. PMID 30154996 DOI: 10.1039/C5Sc02211H |
0.307 |
|
| 2015 |
Garbuio L, Lewandowski B, Wilhelm P, Ziegler L, Yulikov M, Wennemers H, Jeschke G. Shape Persistence of Polyproline II Helical Oligoprolines. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 10747-53. PMID 26089127 DOI: 10.1002/Chem.201501190 |
0.676 |
|
| 2015 |
Engl OD, Fritz SP, Wennemers H. Stereoselective Organocatalytic Synthesis of Oxindoles with Adjacent Tetrasubstituted Stereocenters. Angewandte Chemie (International Ed. in English). PMID 26033441 DOI: 10.1002/Anie.201502976 |
0.785 |
|
| 2015 |
Wilhelm P, Lewandowski B, Trapp N, Wennemers H. Correction to "A crystal structure of an oligoproline PPII-helix, at last". Journal of the American Chemical Society. 137: 2786. PMID 25686510 DOI: 10.1021/Jacs.5B00969 |
0.645 |
|
| 2015 |
Siebler C, Trapp N, Wennemers H. Crystal structure of (4S)-aminoproline: conformational insight into a pH-responsive proline derivative. Journal of Peptide Science : An Official Publication of the European Peptide Society. 21: 208-11. PMID 25581874 DOI: 10.1002/Psc.2734 |
0.318 |
|
| 2015 |
Garbuio L, Lewandowski B, Wilhelm P, Ziegler L, Yulikov M, Wennemers H, Jeschke G. Shape Persistence of Polyproline II Helical Oligoprolines Chemistry - a European Journal. 21: 10747-10753. DOI: 10.1002/chem.201501190 |
0.623 |
|
| 2014 |
Wilhelm P, Lewandowski B, Trapp N, Wennemers H. A crystal structure of an oligoproline PPII-helix, at last. Journal of the American Chemical Society. 136: 15829-32. PMID 25368901 DOI: 10.1021/Ja507405J |
0.673 |
|
| 2014 |
Lewandowska U, Zajaczkowski W, Chen L, Bouillière F, Wang D, Koynov K, Pisula W, Müllen K, Wennemers H. Hierarchical supramolecular assembly of sterically demanding π-systems by conjugation with oligoprolines. Angewandte Chemie (International Ed. in English). 53: 12537-41. PMID 25303332 DOI: 10.1002/Anie.201408279 |
0.322 |
|
| 2014 |
Engl OD, Fritz SP, Käslin A, Wennemers H. Organocatalytic route to dihydrocoumarins and dihydroquinolinones in all stereochemical configurations. Organic Letters. 16: 5454-7. PMID 25290528 DOI: 10.1021/Ol502697S |
0.788 |
|
| 2014 |
Lewandowski B, Wennemers H. Asymmetric catalysis with short-chain peptides. Current Opinion in Chemical Biology. 22: 40-6. PMID 25277500 DOI: 10.1016/J.Cbpa.2014.09.011 |
0.735 |
|
| 2014 |
Kolarovic A, Käslin A, Wennemers H. Stereoselective synthesis of indolines via organocatalytic thioester enolate addition reactions. Organic Letters. 16: 4236-9. PMID 25100030 DOI: 10.1021/Ol501936N |
0.334 |
|
| 2014 |
Arakawa Y, Fritz SP, Wennemers H. Organocatalytic stereoselective synthesis of acyclic γ-nitrothioesters with all-carbon quaternary stereogenic centers. The Journal of Organic Chemistry. 79: 3937-45. PMID 24758496 DOI: 10.1021/Jo500403Q |
0.343 |
|
| 2014 |
Duschmalé J, Kohrt S, Wennemers H. Peptide catalysis in aqueous emulsions. Chemical Communications (Cambridge, England). 50: 8109-12. PMID 24752700 DOI: 10.1039/C4Cc01759E |
0.425 |
|
| 2014 |
Bahlinger A, Fritz SP, Wennemers H. Stereoselective metal-free synthesis of β-amino thioesters with tertiary and quaternary stereogenic centers. Angewandte Chemie (International Ed. in English). 53: 8779-83. PMID 24644150 DOI: 10.1002/Anie.201310532 |
0.332 |
|
| 2013 |
Siebler C, Erdmann RS, Wennemers H. From azidoproline to functionalizable collagen. Chimia. 67: 891-5. PMID 24594333 DOI: 10.2533/Chimia.2013.891 |
0.358 |
|
| 2013 |
Digennaro A, Wennemers H, Joshi G, Schmid S, Mena-Osteritz E, Bäuerle P. Chiral suprastructures of asymmetric oligothiophene-hybrids induced by a single proline. Chemical Communications (Cambridge, England). 49: 10929-31. PMID 24129329 DOI: 10.1039/C3Cc44861D |
0.354 |
|
| 2013 |
Kastl R, Arakawa Y, Duschmalé J, Wiesner M, Wennemers H. Peptide-catalyzed 1,4-addition reactions of aldehydes to nitroolefins. Chimia. 67: 279-82. PMID 23967706 DOI: 10.2533/Chimia.2013.279 |
0.438 |
|
| 2013 |
Kastl R, Wennemers H. Peptide-catalyzed stereoselective conjugate addition reactions generating all-carbon quaternary stereogenic centers. Angewandte Chemie (International Ed. in English). 52: 7228-32. PMID 23729292 DOI: 10.1002/Anie.201301583 |
0.376 |
|
| 2013 |
Erdmann RS, Wennemers H. Conformational stability of triazolyl functionalized collagen triple helices. Bioorganic & Medicinal Chemistry. 21: 3565-8. PMID 23548629 DOI: 10.1016/J.Bmc.2013.02.046 |
0.344 |
|
| 2013 |
Held C, Hübner H, Kling R, Nagel YA, Wennemers H, Gmeiner P. Impact of the proline residue on ligand binding of neurotensin receptor 2 (NTS2)-selective peptide-peptoid hybrids. Chemmedchem. 8: 772-8. PMID 23532897 DOI: 10.1002/Cmdc.201300054 |
0.339 |
|
| 2013 |
Arakawa Y, Wennemers H. Enamine catalysis in flow with an immobilized peptidic catalyst. Chemsuschem. 6: 242-5. PMID 23161643 DOI: 10.1002/Cssc.201200740 |
0.399 |
|
| 2013 |
Duschmalé J, Wiest J, Wiesner M, Wennemers H. Effects of internal and external carboxylic acids on the reaction pathway of organocatalytic 1,4-addition reactions between aldehydes and nitroolefins Chemical Science. 4: 1312-1318. DOI: 10.1039/C2Sc21832A |
0.34 |
|
| 2013 |
Schillinger EK, Kümin M, Digennaro A, Mena-Osteritz E, Schmid S, Wennemers H, Bäuerle P. Guiding suprastructure chirality of an oligothiophene by a single amino Acid Chemistry of Materials. 25: 4511-4521. DOI: 10.1021/Cm4020767 |
0.331 |
|
| 2013 |
Seebach D, Sun X, Ebert MO, Schweizer WB, Purkayastha N, Beck AK, Duschmalé J, Wennemers H, Mukaiyama T, Benohoud M, Hayashi Y, Reiher M. Stoichiometric reactions of enamines derived from diphenylprolinol silyl ethers with nitro olefins and lessons for the corresponding organocatalytic conversions - A survey Helvetica Chimica Acta. 96: 799-852. DOI: 10.1002/Hlca.201300079 |
0.384 |
|
| 2013 |
Arakawa Y, Wennemers H. Cover Picture: Enamine Catalysis in Flow with an Immobilized Peptidic Catalyst (ChemSusChem 2/2013) Chemsuschem. 6: 211-211. DOI: 10.1002/Cssc.201390006 |
0.387 |
|
| 2012 |
Erdmann RS, Wennemers H. Effect of sterically demanding substituents on the conformational stability of the collagen triple helix. Journal of the American Chemical Society. 134: 17117-24. PMID 22992124 DOI: 10.1021/Ja3066418 |
0.307 |
|
| 2012 |
Nagel L, Budke C, Erdmann RS, Dreyer A, Wennemers H, Koop T, Sewald N. Influence of sequential modifications and carbohydrate variations in synthetic AFGP analogues on conformation and antifreeze activity. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 12783-93. PMID 22930587 DOI: 10.1002/Chem.201202119 |
0.351 |
|
| 2012 |
Wennemers H. Peptides as asymmetric catalysts and templates for the controlled formation of Ag nanoparticles. Journal of Peptide Science : An Official Publication of the European Peptide Society. 18: 437-41. PMID 22653734 DOI: 10.1002/Psc.2422 |
0.449 |
|
| 2012 |
Erdmann RS, Wennemers H. Conformational stability of collagen triple helices functionalized in the Yaa position by click chemistry. Organic & Biomolecular Chemistry. 10: 1982-6. PMID 22266764 DOI: 10.1039/C2Ob06720J |
0.351 |
|
| 2012 |
Duschmalé J, Wennemers H. Adapting to substrate challenges: peptides as catalysts for conjugate addition reactions of aldehydes to α,β-disubstituted nitroolefins. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 1111-20. PMID 22189758 DOI: 10.1002/Chem.201102484 |
0.424 |
|
| 2012 |
Clerici P, Wennemers H. Mono thiomalonates as thioester enolate equivalents--enantioselective 1,4-addition reactions to nitroolefins under mild conditions. Organic & Biomolecular Chemistry. 10: 110-3. PMID 22068641 DOI: 10.1039/C1Ob06638B |
0.336 |
|
| 2012 |
Kramer RA, Bleicher KH, Wennemers H. Design and synthesis of nucleoproline amino acids for the straightforward preparation of chiral and conformationally constrained nucleopeptides Helvetica Chimica Acta. 95: 2621-2634. DOI: 10.1002/Hlca.201200557 |
0.397 |
|
| 2011 |
Wennemers H. Asymmetric catalysis with peptides. Chemical Communications (Cambridge, England). 47: 12036-41. PMID 21993353 DOI: 10.1039/C1Cc15237H |
0.434 |
|
| 2011 |
Nagel YA, Kuemin M, Wennemers H. Functionalizable oligoprolines as molecular scaffolds. Chimia. 65: 264-7. PMID 21678776 DOI: 10.2533/Chimia.2011.264 |
0.327 |
|
| 2011 |
Arakawa Y, Wiesner M, Wennemers H. Asymmetric Addition of Aldehydes to Nitroalkenes with anImmobilized Peptide Synfacts. 2011: 1026-1026. DOI: 10.1055/S-0030-1260898 |
0.392 |
|
| 2011 |
Messerer M, Wennemers H. Reversing the enantioselectivity of a peptidic catalyst by changing the solvent Synlett. 499-502. DOI: 10.1055/S-0030-1259523 |
0.377 |
|
| 2011 |
Arakawa Y, Wiesner M, Wennemers H. Efficient recovery and reuse of an immobilized peptidic organocatalyst Advanced Synthesis and Catalysis. 353: 1201-1206. DOI: 10.1002/Adsc.201100118 |
0.431 |
|
| 2010 |
Gademann K, Pfaltz A, Wegner HA, Wennemers H, Woggon WD, Chougnet A. Synthesis and catalysis. Chimia. 64: 859-66. PMID 21268993 DOI: 10.2533/Chimia.2010.859 |
0.328 |
|
| 2010 |
Erdmann RS, Wennemers H. Functionalizable collagen model peptides. Journal of the American Chemical Society. 132: 13957-9. PMID 20849115 DOI: 10.1021/Ja103392T |
0.371 |
|
| 2010 |
Wiesner M, Upert G, Angelici G, Wennemers H. Enamine catalysis with low catalyst loadings--high efficiency via kinetic studies. Journal of the American Chemical Society. 132: 6-7. PMID 19791790 DOI: 10.1021/Ja9068112 |
0.386 |
|
| 2010 |
Wiesner M, Wennemers H. Peptide-catalyzed conjugate addition reactions of aldehydes to nitroolefins Synthesis. 1568-1571. DOI: 10.1055/S-0029-1218651 |
0.412 |
|
| 2010 |
Krattiger P, Nassif N, Völkel A, Mastai Y, Wennemers H, Cölfen H. Investigation of active crystal morphogenesis peptide sequences from peptide libraries by crystallization on peptide functionalized beads Colloids and Surfaces a: Physicochemical and Engineering Aspects. 354: 218-225. DOI: 10.1016/J.Colsurfa.2009.09.031 |
0.348 |
|
| 2009 |
Wiesner M, Neuburger M, Wennemers H. Tripeptides of the type H-D-Pro-Pro-Xaa-NH2 as catalysts for asymmetric 1,4-addition reactions: structural requirements for high catalytic efficiency. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 10103-9. PMID 19697376 DOI: 10.1002/Chem.200901021 |
0.429 |
|
| 2009 |
Belser K, Vig Slenters T, Pfumbidzai C, Upert G, Mirolo L, Fromm KM, Wennemers H. Silver nanoparticle formation in different sizes induced by peptides identified within split-and-mix libraries. Angewandte Chemie (International Ed. in English). 48: 3661-4. PMID 19373811 DOI: 10.1002/Anie.200806265 |
0.336 |
|
| 2009 |
Erdmann RS, Wennemers H. Synthesis of fmoc-pro-hyp(TBDPS)-gly-OH and its application as a versatile building block for the preparation of collagen model peptides Synthesis. 143-147. DOI: 10.1055/S-0028-1083281 |
0.41 |
|
| 2008 |
Wennemers H, Raines RT. Peptides and peptidomimetics as prototypes. Current Opinion in Chemical Biology. 12: 690-1. PMID 18992842 DOI: 10.1016/J.Cbpa.2008.10.015 |
0.559 |
|
| 2008 |
Wiesner M, Revell JD, Tonazzi S, Wennemers H. Peptide catalyzed asymmetric conjugate addition reactions of aldehydes to nitroethylene--a convenient entry into gamma2-amino acids. Journal of the American Chemical Society. 130: 5610-1. PMID 18386927 DOI: 10.1021/Ja801027S |
0.415 |
|
| 2008 |
Wiesner M, Revell JD, Wennemers H. Tripeptides as efficient asymmetric catalysts for 1,4-addition reactions of aldehydes to nitroolefins--a rational approach. Angewandte Chemie (International Ed. in English). 47: 1871-4. PMID 18228232 DOI: 10.1002/Anie.200704972 |
0.352 |
|
| 2008 |
Wiesner M, Revell JD, Wennemers H. Tripeptides: Efficient Catalysts for 1,4-Addition Reactions to Nitroolefins Synfacts. 2008: 417-417. DOI: 10.1055/S-2008-1042835 |
0.351 |
|
| 2008 |
Faul CFJ, Krattiger P, Smarsly BM, Wennemers H. Ionic self-assembled molecular receptor-based liquid crystals with tripeptide recognition capabilities Journal of Materials Chemistry. 18: 2962-2967. DOI: 10.1039/B802690D |
0.306 |
|
| 2008 |
Revell J, Wennemers H. Investigating Sequence Space: How Important is the Spatial Arrangement of Functional Groups in the Asymmetric Aldol Reaction Catalyst H-Pro-Pro-Asp-NH2? Advanced Synthesis & Catalysis. 350: 1046-1052. DOI: 10.1002/Adsc.200800053 |
0.389 |
|
| 2007 |
Lubkoll J, Wennemers H. Mimicry of polyketide synthases--enantioselective 1,4-addition reactions of malonic acid half-thioesters to nitroolefins. Angewandte Chemie (International Ed. in English). 46: 6841-4. PMID 17680584 DOI: 10.1002/Anie.200702187 |
0.31 |
|
| 2007 |
Revell JD, Wennemers H. Peptidic catalysts developed by combinatorial screening methods. Current Opinion in Chemical Biology. 11: 269-78. PMID 17548237 DOI: 10.1016/J.Cbpa.2007.05.015 |
0.424 |
|
| 2007 |
Wennemers H. Peptides as asymmetric catalysts for aldol reactions Chimia. 61: 276-278. DOI: 10.2533/Chimia.2007.276 |
0.434 |
|
| 2007 |
Lubkoll J, Wennemers H. Enantioselective 1,4-Addition Reactions of Malonic Acid Half-Thioesters to Nitroolefins Synfacts. 2007: 1206-1206. DOI: 10.1055/S-2007-991242 |
0.31 |
|
| 2007 |
Aprile C, Giacalone F, Gruttadauria M, Marculescu AM, Noto R, Revell JD, Wennemers H. New ionic liquid-modified silica gels as recyclable materials for l-proline- or H-Pro-Pro-Asp-NH2-catalyzed aldol reaction Green Chemistry. 9: 1328-1334. DOI: 10.1039/B709471J |
0.311 |
|
| 2007 |
Revell JD, Wennemers H. Functional group requirements within the peptide H-Pro-Pro-Asp-NH2 as a catalyst for aldol reactions Tetrahedron. 63: 8420-8424. DOI: 10.1016/J.Tet.2007.06.010 |
0.394 |
|
| 2006 |
Grun J, Revell JD, Conza M, Wennemers H. Peptide-polyethylene glycol conjugates: synthesis and properties of peptides bearing a C-terminal polyethylene glycol chain. Bioorganic & Medicinal Chemistry. 14: 6197-201. PMID 16784872 DOI: 10.1016/J.Bmc.2006.05.079 |
0.399 |
|
| 2006 |
Revell JD, Gantenbein D, Krattiger P, Wennemers H. Solid-supported and pegylated H-Pro-Pro-Asp-NHR as catalysts for asymmetric aldol reactions. Biopolymers. 84: 105-13. PMID 16245260 DOI: 10.1002/Bip.20393 |
0.353 |
|
| 2005 |
Krattiger P, Kovasy R, Revell JD, Ivan S, Wennemers H. Increased structural complexity leads to higher activity: peptides as efficient and versatile catalysts for asymmetric aldol reactions. Organic Letters. 7: 1101-3. PMID 15760149 DOI: 10.1021/Ol0500259 |
0.451 |
|
| 2005 |
Nold M, Koch K, Wennemers H. Acid-rich peptides are prone to damage under fenton conditions - Split-and-mix libraries for the detection of selective peptide cleavage Synthesis. 1455-1458. DOI: 10.1055/S-2005-865329 |
0.361 |
|
| 2005 |
Krattiger P, Wennemers H. Water-soluble diketopiperazine receptors - Selective recognition of arginine-rich peptides Synlett. 706-708. DOI: 10.1055/S-2005-862395 |
0.349 |
|
| 2005 |
Krattiger P, Kovàsy R, Revell JD, Wennemers H. Using catalyst-substrate coimmobilization for the discovery of catalysts for asymmetric aldol reactions in split-and-mix libraries Qsar and Combinatorial Science. 24: 1158-1163. DOI: 10.1002/Qsar.200540009 |
0.374 |
|
| 2004 |
Nold M, Wennemers H. Peptide damage under Fenton conditions is sequence-dependent. Chemical Communications (Cambridge, England). 1800-1. PMID 15306890 DOI: 10.1039/B407321E |
0.37 |
|
| 2003 |
Krattiger P, McCarthy C, Pfaltz A, Wennemers H. Catalyst-substrate coimmobilization: a strategy for catalysts discovery in split-and-mix libraries. Angewandte Chemie (International Ed. in English). 42: 1722-4. PMID 12707888 DOI: 10.1002/Anie.200250422 |
0.33 |
|
| 2003 |
Wennemers H, Nold MC, Conza MM, Kulicke KJ, Neuburger M. Flexible but with a defined turn-influence of the template on the binding properties of two-armed receptors. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 442-8. PMID 12532293 DOI: 10.1002/Chem.200390046 |
0.32 |
|
| 2003 |
Wennemers H. Peptide receptors - From selective molecular recognition towards catalytic activity Chimia. 57: 237-240. DOI: 10.2533/000942903777679352 |
0.388 |
|
| 2002 |
Conza M, Wennemers H. Selective binding of two-armed diketopiperazine receptors to side-chain-protected peptides. The Journal of Organic Chemistry. 67: 2696-8. PMID 11950321 DOI: 10.1021/Jo016152+ |
0.327 |
|
| 2001 |
Wennemers H, Conza M, Nold M, Krattiger P. Diketopiperazine receptors: a novel class of highly selective receptors for binding small peptides. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 3342-7. PMID 11531120 DOI: 10.1002/1521-3765(20010803)7:15<3342::Aid-Chem3342>3.0.Co;2-7 |
0.356 |
|
| 2001 |
Wennemers H. Combinatorial chemistry: a tool for the discovery of new catalysts. Combinatorial Chemistry & High Throughput Screening. 4: 273-85. PMID 11375742 DOI: 10.2174/1386207013331138 |
0.3 |
|
| 1997 |
Gasparrini F, Misiti D, Still WC, Villani C, Wennemers H. Enantioselective and Diastereoselective Binding Study of Silica Bound Macrobicyclic Receptors by HPLC. The Journal of Organic Chemistry. 62: 8221-8224. PMID 11671938 |
0.465 |
|
| 1996 |
Maletic M, Wennemers H, McDonald DQ, Breslow R, Still WC. Selective binding of the dipeptides L-Phe-D-Pro and D-Phe-L- Pro to β- cyclodextrin Angewandte Chemie - International Edition in English. 35: 1490-1492. DOI: 10.1002/Anie.199614901 |
0.503 |
|
| 1996 |
Maletic M, Wennemers H, McDonald DQ, Breslow R, Still WC. Selektive Wechselwirkung der DipeptideL-Phe-D-Pro undD-Phe-L-Pro mit β-Cyclodextrin Angewandte Chemie. 108: 1594-1596. DOI: 10.1002/Ange.19961081311 |
0.503 |
|
| 1995 |
Wennemers H, Yoon SS, Still WC. Cyclooligomeric receptors based on trimesic acid and 1,2-diamines. Minimal structure for sequence-selective peptide binding Journal of Organic Chemistry. 60: 1108-1109. DOI: 10.1021/Jo00110A007 |
0.578 |
|
| 1994 |
Wennemers H, Still WC. Peptide complexation in water. Sequence-Selective binding with simple dye molecules Tetrahedron Letters. 35: 6413-6416. DOI: 10.1016/S0040-4039(00)78233-5 |
0.558 |
|
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