Year |
Citation |
Score |
2023 |
Corkery D, Ursu A, Lucas B, Grigalunas M, Kriegler S, Oliva R, Dec R, Koska S, Pahl A, Sievers S, Ziegler S, Winter R, Wu YW, Waldmann H. Inducin Triggers LC3-Lipidation and ESCRT-Mediated Lysosomal Membrane Repair. Chembiochem : a European Journal of Chemical Biology. e202300579. PMID 37869939 DOI: 10.1002/cbic.202300579 |
0.396 |
|
2023 |
Xie J, Pahl A, Krzyzanowski A, Krupp A, Liu J, Koska S, Schölermann B, Zhang R, Bonowski J, Sievers S, Strohmann C, Ziegler S, Grigalunas M, Waldmann H. Synthetic Matching of Complex Monoterpene Indole Alkaloid Chemical Space. Angewandte Chemie (International Ed. in English). e202310222. PMID 37818743 DOI: 10.1002/anie.202310222 |
0.351 |
|
2023 |
Aoyama H, Davies C, Liu J, Pahl A, Kirchhoff JL, Scheel R, Sievers S, Strohmann C, Grigalunas M, Waldmann H. Collective Synthesis of Sarpagine and Macroline Alkaloid-Inspired Compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). e202303027. PMID 37755456 DOI: 10.1002/chem.202303027 |
0.385 |
|
2023 |
Liu J, Zhang R, Mallick S, Patil S, Wientjens C, Flegel J, Krupp A, Strohmann C, Grassin C, Merten C, Pahl A, Grigalunas M, Waldmann H. A highly enantioselective intramolecular 1,3-dipolar cycloaddition yields novel pseudo-natural product inhibitors of the Hedgehog signalling pathway. Chemical Science. 14: 7936-7943. PMID 37502335 DOI: 10.1039/d3sc01240a |
0.428 |
|
2023 |
Liu J, Mallick S, Xie Y, Grassin C, Lucas B, Schölermann B, Pahl A, Scheel R, Strohmann C, Protzel C, Berg T, Merten C, Ziegler S, Waldmann H. Morphological profiling identifies the motor protein Eg5 as cellular target of spirooxindoles. Angewandte Chemie (International Ed. in English). e202301955. PMID 36929571 DOI: 10.1002/anie.202301955 |
0.428 |
|
2022 |
Young RJ, Flitsch SL, Grigalunas M, Leeson PD, Quinn RJ, Turner NJ, Waldmann H. The Time and Place for Nature in Drug Discovery. Jacs Au. 2: 2400-2416. PMID 36465532 DOI: 10.1021/jacsau.2c00415 |
0.51 |
|
2022 |
Flegel J, Shaaban S, Jia ZJ, Schulte B, Lian Y, Krzyzanowski A, Metz M, Schneidewind T, Wesseler F, Flegel A, Reich A, Brause A, Xue G, Zhang M, Dötsch L, ... ... Waldmann H, et al. The Highly Potent AhR Agonist Picoberin Modulates Hh-Dependent Osteoblast Differentiation. Journal of Medicinal Chemistry. PMID 36459434 DOI: 10.1021/acs.jmedchem.2c00956 |
0.713 |
|
2022 |
Krzyzanowski A, Esser LM, Willaume A, Prudent R, Peter C, 't Hart P, Waldmann H. Development of Macrocyclic PRMT5-Adaptor Protein Interaction Inhibitors. Journal of Medicinal Chemistry. PMID 36378254 DOI: 10.1021/acs.jmedchem.2c01273 |
0.764 |
|
2022 |
Waldmann H, Akbarzadeh M, Flegel J, Patil S, Shang E, Narayan R, Buchholzer M, Jasemi NSK, Grigalunas M, Krzyzanowski A, Abegg D, Shuster A, Potowski M, Karatas H, Karageorgis G, et al. The Pseudo-Natural Product Rhonin Targets RHOGDI. Angewandte Chemie (International Ed. in English). PMID 35170181 DOI: 10.1002/anie.202115193 |
0.79 |
|
2022 |
Wesseler F, Riege D, Puthanveedu M, Halver J, Müller E, Bertrand J, Antonchick AP, Sievers S, Waldmann H, Schade D. Probing Embryonic Development Enables the Discovery of Unique Small-Molecule Bone Morphogenetic Protein Potentiators. Journal of Medicinal Chemistry. PMID 35108017 DOI: 10.1021/acs.jmedchem.1c01800 |
0.697 |
|
2021 |
Burhop A, Bag S, Grigalunas M, Woitalla S, Bodenbinder P, Brieger L, Strohmann C, Pahl A, Sievers S, Waldmann H. Synthesis of Indofulvin Pseudo-Natural Products Yields a New Autophagy Inhibitor Chemotype. Advanced Science (Weinheim, Baden-Wurttemberg, Germany). e2102042. PMID 34346568 DOI: 10.1002/advs.202102042 |
0.749 |
|
2021 |
Waldmann H, Liu J, Flegel J, Otte F, Pahl A, Sievers S, Strohmann C. Combination of pseudo-natural product design and formal natural product ring distortion yields stereochemically and biologically diverse pseudo-sesquiterpenoid alkaloids. Angewandte Chemie (International Ed. in English). PMID 34297473 DOI: 10.1002/anie.202106654 |
0.406 |
|
2021 |
Waldmann H, Yildirim O, Grigalunas M, Brieger L, Strohmann C, Antonchick AP. Dynamic Catalytic Highly Enantioselective 1,3-Dipolar Cycloadditions. Angewandte Chemie (International Ed. in English). PMID 34236754 DOI: 10.1002/anie.202108072 |
0.699 |
|
2021 |
Grigalunas M, Burhop A, Zinken S, Pahl A, Gally JM, Wild N, Mantel Y, Sievers S, Foley DJ, Scheel R, Strohmann C, Antonchick AP, Waldmann H. Natural product fragment combination to performance-diverse pseudo-natural products. Nature Communications. 12: 1883. PMID 33767198 DOI: 10.1038/s41467-021-22174-4 |
0.694 |
|
2020 |
Waldmann H, Liu J, Cremosnik GS, Otte F, Pahl A, Sievers S, Strohmann C. Design, synthesis and biological evaluation of chemically and biologically diverse pyrroquinoline pseudo natural products. Angewandte Chemie (International Ed. in English). PMID 33200868 DOI: 10.1002/anie.202013731 |
0.334 |
|
2020 |
Shaaban S, Li H, Otte F, Strohmann C, Antonchick AP, Waldmann H. Enantioselective Synthesis of Five-Membered-Ring Atropisomers with a Chiral Rh(III) Complex. Organic Letters. PMID 33186042 DOI: 10.1021/acs.orglett.0c03355 |
0.71 |
|
2020 |
Cremosnik GS, Liu J, Waldmann H. Guided by evolution: from biology oriented synthesis to pseudo natural products. Natural Product Reports. PMID 33020792 DOI: 10.1039/d0np00015a |
0.333 |
|
2020 |
Karatas H, Akbarzadeh M, Adihou H, Hahne G, Pobbati AV, Yihui Ng E, Guéret SM, Sievers S, Pahl A, Metz M, Zinken S, Dötsch L, Nowak C, Thavam S, Friese A, ... ... Waldmann H, et al. Discovery of Covalent Inhibitors Targeting the Transcriptional Enhanced Associate Domain (TEAD) Central Pocket. Journal of Medicinal Chemistry. PMID 32907324 DOI: 10.1021/Acs.Jmedchem.0C01275 |
0.33 |
|
2020 |
Kawamura T, Futamura Y, Shang E, Muroi M, Janning P, Ueno M, Wilke J, Takeda S, Kondoh Y, Ziegler S, Watanabe N, Waldmann H, Osada H. Discovery of small-molecule modulator of heterotrimeric G-protein by integrated phenotypic profiling and chemical proteomics. Bioscience, Biotechnology, and Biochemistry. 1-7. PMID 32867616 DOI: 10.1080/09168451.2020.1812375 |
0.334 |
|
2020 |
Waldmann H, Shaaban S, Davies C, Merten C, Flegel J, Otte F, Strohmann C. Rh(III)-catalyzed C-H Activation of Aryl-Hydroxamates for the Synthesis of Isoindolinones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32428319 DOI: 10.1002/Chem.202002384 |
0.367 |
|
2020 |
Waldmann H, Foley DJ, Zinken S, Corkery D, Laraia L, Pahl A, Wu Y. Phenotyping reveals the targets of a pseudo-natural product autophagy inhibitor. Angewandte Chemie (International Ed. in English). PMID 32108411 DOI: 10.1002/Anie.202000364 |
0.381 |
|
2020 |
Guéret SM, Thavam S, Carbajo RJ, Potowski M, Larsson N, Dahl G, Dells Eacute N A, Grossmann TN, Plowright AT, Valeur E, Lemurell M, Waldmann H. Macrocyclic Modalities Combining Peptide Epitopes and Natural Product Fragments. Journal of the American Chemical Society. PMID 32058716 DOI: 10.1021/Jacs.0C00269 |
0.348 |
|
2020 |
Karageorgis G, Foley DJ, Laraia L, Waldmann H. Principle and design of pseudo-natural products. Nature Chemistry. PMID 32015480 DOI: 10.1038/S41557-019-0411-X |
0.336 |
|
2019 |
Waldmann H, Winzker M, Friese A, Koch U, Janning P, Ziegler S. Development of a PDEδ targeting PROTAC that impairs lipid metabolism. Angewandte Chemie (International Ed. in English). PMID 31829492 DOI: 10.1002/Anie.201913904 |
0.346 |
|
2019 |
Waldmann H, Laraia L, Garivet G, Foley DJ, Kaiser N, Müller S, Zinken S, Pinkert T, Wilke J, Corkery D, Pahl A, Sievers S, Janning P, Arenz C, Wu Y, et al. Image-based morphological profiling identifies a lysosomotropic, iron-sequestering autophagy inhibitor. Angewandte Chemie (International Ed. in English). PMID 31769920 DOI: 10.1002/Anie.201913712 |
0.785 |
|
2019 |
Pobbati AV, Mejuch T, Chakraborty S, Karatas H, Bharath SR, Guéret SM, Goy PA, Hahne G, Pahl A, Sievers S, Guccione E, Song H, Waldmann H, Hong W. Identification of Quinolinols as Activators of TEAD-dependent Transcription. Acs Chemical Biology. PMID 31742995 DOI: 10.1021/Acschembio.9B00786 |
0.304 |
|
2019 |
Cromm PM, Adihou H, Kapoor S, Vazquez-Chantada M, Davey P, Longmire D, Hennes E, Hofer W, Küchler P, Chiarparin E, Waldmann H, Grossmann TN. Lipidated Stapled Peptides Targeting the Acyl Binding Protein UNC119. Chembiochem : a European Journal of Chemical Biology. PMID 31680402 DOI: 10.1002/Cbic.201900615 |
0.657 |
|
2019 |
Waldmann H, Ceballos J, Schwalfenberg M, Karageorgis G, Reckzeh ES, Sievers S, Ostermann C, Pahl A, Sellstedt M, Nowacki J, Carnero Corrales M, Wilke J, Laraia L, Tschapalda K, Metz M, et al. Synthesis of Indomorphan Pseudo Natural Product Inhibitors of Glucose Transporters GLUT-1 and -3. Angewandte Chemie (International Ed. in English). PMID 31469221 DOI: 10.1002/Anie.201909518 |
0.305 |
|
2019 |
Waldmann H, Kremer L, Hennes E, Brause A, Ursu A, Robke L, Matsubayashi HT, Nihongaki Y, Flegel J, Mejdrová I, Eickhoff J, Baumann M, Nencka R, Janning P, Kordes S, et al. Discovery of the Hedgehog Pathway Inhibitor Pipinib that Targets PI4KIIIß. Angewandte Chemie (International Ed. in English). PMID 31454140 DOI: 10.1002/Anie.201907632 |
0.312 |
|
2019 |
Furuta T, Mizukami Y, Asano L, Kotake K, Ziegler S, Yoshida H, Watanabe M, Sato SI, Waldmann H, Nishikawa M, Uesugi M. Nutrient-Based Chemical Library as a Source of Energy Metabolism Modulators. Acs Chemical Biology. PMID 31436407 DOI: 10.1021/Acschembio.9B00444 |
0.327 |
|
2019 |
Waldmann H, Christoforow A, Wilke J, Binici A, Pahl A, Ostermann C, Sievers S. Design, Synthesis and Phenotypic Profiling of Pyrano-Furo-Pyridone Pseudo Natural Products. Angewandte Chemie (International Ed. in English). PMID 31339620 DOI: 10.1002/Anie.201907853 |
0.302 |
|
2019 |
Laraia L, Friese A, Corkery DP, Konstantinidis G, Erwin N, Hofer W, Karatas H, Klewer L, Brockmeyer A, Metz M, Schölermann B, Dwivedi M, Li L, Rios-Munoz P, Köhn M, ... ... Waldmann H, et al. The cholesterol transfer protein GRAMD1A regulates autophagosome biogenesis. Nature Chemical Biology. PMID 31222192 DOI: 10.1038/S41589-019-0307-5 |
0.501 |
|
2019 |
Waldmann H, Friese A, Kapoor S, Schneidewind T, Vidadala SR, Sardana J, Brause A, Förster T, Bischoff M, Wagner J, Janning P, Ziegler S. Chemical genetics reveals a role of dCTP pyrophosphatase 1 in Wnt signaling. Angewandte Chemie (International Ed. in English). PMID 31173446 DOI: 10.1002/Anie.201905977 |
0.642 |
|
2019 |
Garivet G, Hofer W, Konitsiotis A, Klein C, Kaiser N, Mejuch T, Fansa E, Alsaabi R, Wittinghofer A, Bastiaens PIH, Waldmann H. Small-Molecule Inhibition of the UNC-Src Interaction Impairs Dynamic Src Localization in Cells. Cell Chemical Biology. PMID 30956149 DOI: 10.1016/J.Chembiol.2019.02.019 |
0.792 |
|
2019 |
Reckzeh ES, Brockmeyer A, Metz M, Waldmann H, Janning P. Target Engagement of Small Molecules: Thermal Profiling Approaches on Different Levels. Methods in Molecular Biology (Clifton, N.J.). 1888: 73-98. PMID 30519941 DOI: 10.1007/978-1-4939-8891-4_4 |
0.302 |
|
2019 |
‘T Hart P, Openy J, Krzyzanowski A, Adihou H, Waldmann H. Hot-spot guided design of macrocyclic inhibitors of the LSD1-CoREST1 interaction Tetrahedron. 75: 130685. DOI: 10.1016/J.Tet.2019.130685 |
0.327 |
|
2019 |
Cromm PM, Adihou H, Kapoor S, Vazquez‐Chantada M, Davey P, Longmire D, Hennes E, Hofer W, Küchler P, Chiarparin E, Waldmann H, Grossmann TN. Cover Feature: Lipidated Stapled Peptides Targeting the Acyl Binding Protein UNC119 (ChemBioChem 24/2019) Chembiochem. 20: 2971-2971. DOI: 10.1002/Cbic.201900704 |
0.647 |
|
2018 |
Schneidewind T, Kapoor S, Garivet G, Karageorgis G, Narayan R, Vendrell-Navarro G, Antonchick AP, Ziegler S, Waldmann H. The Pseudo Natural Product Myokinasib Is a Myosin Light Chain Kinase 1 Inhibitor with Unprecedented Chemotype. Cell Chemical Biology. PMID 30686759 DOI: 10.1016/J.Chembiol.2018.11.014 |
0.778 |
|
2018 |
Němec V, Hylsová M, Maier L, Flegel J, Sievers S, Ziegler S, Schroeder M, Berger BT, Chaikuad A, Valčíková B, Uldrijan S, Drápela S, Souček K, Waldmann H, Knapp S, et al. Furo[3,2-b]pyridine: A Privileged Scaffold for Highly Selective Kinase Inhibitors and Effective Modulators of the Hedgehog Pathway. Angewandte Chemie (International Ed. in English). PMID 30569600 DOI: 10.1002/anie.201810312 |
0.334 |
|
2018 |
Li H, Gontla R, Flegel J, Merten C, Ziegler S, Antonchick AP, Waldmann H. Enantioselective Formal C(sp )-H Bond Activation in the Synthesis of Bioactive Spiropyrazolone Derivatives. Angewandte Chemie (International Ed. in English). PMID 30511449 DOI: 10.1002/Anie.201811041 |
0.73 |
|
2018 |
Brand S, Roy S, Schröder P, Rathmer B, Roos J, Kapoor S, Patil S, Pommerenke C, Maier T, Janning P, Eberth S, Steinhilber D, Schade D, Schneider G, Kumar K, ... ... Waldmann H, et al. Combined Proteomic and In Silico Target Identification Reveal a Role for 5-Lipoxygenase in Developmental Signaling Pathways. Cell Chemical Biology. 25: 1095-1106.e23. PMID 30251630 DOI: 10.1016/J.Chembiol.2018.05.016 |
0.647 |
|
2018 |
Waldmann H, Shan G, Flegel J, Li H, Merten C, Ziegler S, Antonchick AP. C-H Bond Activation for the Synthesis of Heterocyclic Atropisomers Yields Hedgehog Pathway Inhibitors. Angewandte Chemie (International Ed. in English). PMID 30203905 DOI: 10.1002/Anie.201809680 |
0.735 |
|
2018 |
Karageorgis G, Reckzeh ES, Ceballos J, Schwalfenberg M, Sievers S, Ostermann C, Pahl A, Ziegler S, Waldmann H. Chromopynones are pseudo natural product glucose uptake inhibitors targeting glucose transporters GLUT-1 and -3. Nature Chemistry. PMID 30202104 DOI: 10.1038/S41557-018-0132-6 |
0.304 |
|
2018 |
Kaiser N, Mejuch T, Fedoryshchak R, Janning P, Tate EW, Waldmann H. Photoactivatable Myristic Acid Probes for UNC119-Cargo Interactions. Chembiochem : a European Journal of Chemical Biology. PMID 30129686 DOI: 10.1002/Cbic.201800406 |
0.348 |
|
2018 |
Winter RHA, Erwin N, Dwivedi M, Mejuch T, Waldmann H. UNC119A decreases the membrane-binding of myristoylated c-Src. Chembiochem : a European Journal of Chemical Biology. PMID 29700916 DOI: 10.1002/Cbic.201800158 |
0.503 |
|
2018 |
Jia ZJ, Takayama H, Futamura Y, Aono H, Bauer JO, Strohmann C, Antonchick AP, Osada H, Waldmann H. Catalytic Enantioselective Synthesis of a Pyrrolizidine-Alkaloid-Inspired Compound Collection with Antiplasmodial Activity. The Journal of Organic Chemistry. PMID 29460633 DOI: 10.1021/Acs.Joc.7B03202 |
0.734 |
|
2018 |
Waldmann H, Jia ZJ, Shan G, Daniliuc CG, Antonchick AP. Enantioselective Synthesis of the Spiro-Tropanyl Oxindole Scaffold Through Bimetallic Relay Catalysis. Angewandte Chemie (International Ed. in English). PMID 29419912 DOI: 10.1002/Anie.201712882 |
0.733 |
|
2018 |
Höing S, Yeh TY, Baumann M, Martinez NE, Habenberger P, Kremer L, Drexler HCA, Küchler P, Reinhardt P, Choidas A, Zischinsky ML, Zischinsky G, Nandini S, Ledray AP, Ketcham SA, ... ... Waldmann H, et al. Dynarrestin, a Novel Inhibitor of Cytoplasmic Dynein. Cell Chemical Biology. PMID 29396292 DOI: 10.1016/J.Chembiol.2017.12.014 |
0.314 |
|
2018 |
Karageorgis G, Waldmann H. Guided by Evolution: Biology-Oriented Synthesis of Bioactive Compound Classes Synthesis. 51: 55-66. DOI: 10.1055/S-0037-1610368 |
0.394 |
|
2018 |
Robke L, Rodrigues T, Schröder P, Foley DJ, Bernardes GJ, Laraia L, Waldmann H. Discovery of 2,4-dimethoxypyridines as novel autophagy inhibitors Tetrahedron. 74: 4531-4537. DOI: 10.1016/J.Tet.2018.07.021 |
0.338 |
|
2018 |
Laraia L, Robke L, Waldmann H. Bioactive Compound Collections: From Design to Target Identification Chem. 4: 705-730. DOI: 10.1016/J.Chempr.2018.01.012 |
0.332 |
|
2018 |
Lee Y, Knauer L, Louven K, Golz C, Strohmann C, Waldmann H, Kumar K. Gold(I)-Catalyzed and Nucleophile-Guided Ligand-Directed Divergent Synthesis European Journal of Organic Chemistry. 2018: 5688-5699. DOI: 10.1002/Ejoc.201801080 |
0.308 |
|
2017 |
Pries V, Nöcker C, Khan D, Johnen P, Hong Z, Tripathi A, Keller AL, Fitz M, Perruccio F, Filipuzzi I, Thavam S, Aust T, Riedl R, Ziegler S, Bono F, ... ... Waldmann H, et al. Target Identification and Mechanism of Action of Picolinamide and Benzamide Chemotypes with Antifungal Properties. Cell Chemical Biology. PMID 29307839 DOI: 10.1016/J.Chembiol.2017.12.007 |
0.333 |
|
2017 |
Muraki K, Ohnishi K, Takezawa A, Suzuki H, Hatano N, Muraki Y, Hamzah N, Foster R, Waldmann H, Nussbaumer P, Christmann M, Bon RS, Beech DJ. Na+ entry through heteromeric TRPC4/C1 channels mediates (-)Englerin A-induced cytotoxicity in synovial sarcoma cells. Scientific Reports. 7: 16988. PMID 29209034 DOI: 10.1038/S41598-017-17303-3 |
0.646 |
|
2017 |
Waldmann H, Lee YC, Kumar K. Ligand-directed Divergent Synthesis of Carbo- and Heterocyclic Ring Systems. Angewandte Chemie (International Ed. in English). PMID 29105306 DOI: 10.1002/Anie.201710247 |
0.357 |
|
2017 |
Pahl A, Waldmann H, Kumar K. Exploring Natural Product Fragments for Drug and Probe Discovery. Chimia. 71: 653-660. PMID 29070410 DOI: 10.2533/Chimia.2017.653 |
0.333 |
|
2017 |
Küchler P, Zimmermann G, Winzker M, Janning P, Waldmann H, Ziegler S. Identification of novel PDEδ interacting proteins. Bioorganic & Medicinal Chemistry. PMID 28935183 DOI: 10.1016/J.Bmc.2017.08.033 |
0.324 |
|
2017 |
Waldmann H, Kremer L, Schultz-Fademrecht C, Baumann M, Habenberger P, Choidas A, Klebl B, Kordes S, Schöler HJ, Sterneckert J, Ziegler S, Schneider G. Discovery of a Novel Hedgehog Signaling Pathway Inhibitor by Cell-based Compound Discovery and Target Prediction. Angewandte Chemie (International Ed. in English). PMID 28833911 DOI: 10.1002/Anie.201707394 |
0.337 |
|
2017 |
Waldmann H, Xu H, Laraia L, Schneider L, Louven K, Strohmann C, Antonchick AP. Highly Enantioselective Catalytic Vinylogous Propargylation of Coumarins Yields a Novel Autophagy Inhibitor Class. Angewandte Chemie (International Ed. in English). PMID 28696533 DOI: 10.1002/Anie.201706005 |
0.752 |
|
2017 |
Waldmann H, Sheremet M, Kapoor S, Schröder P, Kumar K, Ziegler S. Natural Product Withanolide-Inspired Small molecules as Potent Inhibitors of Wnt Signaling. Chembiochem : a European Journal of Chemical Biology. PMID 28678390 DOI: 10.1002/Cbic.201700260 |
0.66 |
|
2017 |
Winter RHA, Dwiwedi M, Mejuch T, Waldmann H. The Myristoyl Modification of c-Src Alters the Lateral Organization of Host Heterogenous Raft-like Membranes. Angewandte Chemie (International Ed. in English). PMID 28657213 DOI: 10.1002/Anie.201706233 |
0.479 |
|
2017 |
Laraia L, Waldmann H. Natural product inspired compound collections: evolutionary principle, chemical synthesis, phenotypic screening, and target identification. Drug Discovery Today. Technologies. 23: 75-82. PMID 28647090 DOI: 10.1016/J.Ddtec.2017.03.003 |
0.358 |
|
2017 |
Waldmann H, Robke L, Laraia L, Carnero Corrales MA, Konstantinidis G, Muroi M, Richters A, Winzker M, Engbring T, Tomassi S, Watanabe N, Osada H, Rauh D, Wu Y, Engel J. Phenotypic Identification of a Novel Autophagy Inhibitor Chemotype Targeting Lipid Kinase VPS34. Angewandte Chemie (International Ed. in English). PMID 28544137 DOI: 10.1002/Anie.201703738 |
0.319 |
|
2017 |
Mejuch T, Garivet G, Hofer W, Kaiser N, Fansa EK, Ehrt C, Koch O, Baumann M, Ziegler S, Wittinghofer A, Waldmann H. Small-Molecule Inhibition of the UNC119-Cargo Interaction. Angewandte Chemie (International Ed. in English). PMID 28471079 DOI: 10.1002/Anie.201701905 |
0.794 |
|
2017 |
Martín-Gago P, Fansa EK, Winzker M, Murarka S, Janning P, Schultz-Fademrecht C, Baumann M, Wittinghofer A, Waldmann H. Covalent Protein Labeling at Glutamic Acids. Cell Chemical Biology. PMID 28434875 DOI: 10.1016/J.Chembiol.2017.03.015 |
0.798 |
|
2017 |
Waldmann H, Förster T, Lopéz-Tosco S, Ziegler S, Antonchick AP. Enantioselective Organocatalytic Synthesis of a Secoyohimbane-Inspired Compound Collection with Neuritogenic Activity. Chembiochem : a European Journal of Chemical Biology. PMID 28421720 DOI: 10.1002/Cbic.201700015 |
0.74 |
|
2017 |
Rubaiy HN, Ludlow MJ, Henrot M, Gaunt HJ, Miteva K, Cheung SY, Tanahashi Y, Hamzah N, Musialowski KE, Blythe NM, Appleby HL, Bailey MA, McKeown L, Taylor R, Foster R, ... Waldmann H, et al. Picomolar, selective and subtype specific small-molecule inhibition of TRPC1/4/5 channels. The Journal of Biological Chemistry. PMID 28325835 DOI: 10.1074/Jbc.M116.773556 |
0.653 |
|
2017 |
Waldmann H, Martinez NE, Zimmermann TJ, Goosmann C, Alexander T, Hedberg C, Ziegler S, Zychlinsky A. Tetrahydroisoquinolines are Novel Inhibitors of Neutrophil Extracellular Trap (NET) Formation. Chembiochem : a European Journal of Chemical Biology. PMID 28240414 DOI: 10.1002/Cbic.201600650 |
0.325 |
|
2017 |
Lee YC, Patil S, Golz C, Strohmann C, Ziegler S, Kumar K, Waldmann H. A ligand-directed divergent catalytic approach to establish structural and functional scaffold diversity. Nature Communications. 8: 14043. PMID 28195128 DOI: 10.1038/Ncomms14043 |
0.345 |
|
2017 |
Waldmann H, Valeur E, Guéret SM, Adihou H, Gopalakrishnan R, Lemurell M, Grossmann TN, Plowright AT. New Modalities for Challenging Targets in Drug Discovery. Angewandte Chemie (International Ed. in English). PMID 28186380 DOI: 10.1002/Anie.201611914 |
0.355 |
|
2017 |
Jia ZJ, Merten C, Gontla R, Daniliuc CG, Antonchick AP, Waldmann H. General Enantioselective C-H Activation with Efficiently Tunable Cyclopentadienyl Ligands. Angewandte Chemie (International Ed. in English). PMID 28124831 DOI: 10.1002/Anie.201611981 |
0.709 |
|
2017 |
Martín-Gago P, Fansa EK, Klein CH, Murarka S, Janning P, Schürmann M, Metz M, Ismail S, Schultz-Fademrecht C, Baumann M, Bastiaens PI, Wittinghofer A, Waldmann H. A PDE6δ-KRas Inhibitor Chemotype with up to Seven H-Bonds and Picomolar Affinity that Prevents Efficient Inhibitor Release by Arl2. Angewandte Chemie (International Ed. in English). PMID 28106325 DOI: 10.1002/Anie.201610957 |
0.787 |
|
2017 |
Laraia L, Ohsawa K, Konstantinidis G, Robke L, Wu YW, Kumar K, Waldmann H. Discovery of Novel Cinchona-Alkaloid-Inspired Oxazatwistane Autophagy Inhibitors. Angewandte Chemie (International Ed. in English). PMID 28097798 DOI: 10.1002/Anie.201611670 |
0.39 |
|
2017 |
Jia Z, Merten C, Knauer L, Murarka S, Strohmann C, Waldmann H. Biology-Oriented Synthesis of Decahydro-4,8-epoxyazulene Scaffolds Synlett. 28: 2918-2922. DOI: 10.1055/S-0036-1588558 |
0.721 |
|
2016 |
Martín-Gago P, Fansa EK, Wittinghofer A, Waldmann H. Structure-based development of PDEδ inhibitors. Biological Chemistry. PMID 27935847 DOI: 10.1515/Hsz-2016-0272 |
0.777 |
|
2016 |
Murarka S, Martín-Gago P, Schultz-Fademrecht C, Al Saabi A, Baumann M, Fansa E, Ismail S, Nussbaumer P, Wittinghofer A, Waldmann H. Development of Pyridazinone Chemotypes Targeting the PDEδ Prenyl Binding Site. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27809361 DOI: 10.1002/Chem.201603222 |
0.782 |
|
2016 |
Jaiswal M, Fansa EK, Kösling SK, Mejuch T, Waldmann H, Wittinghofer A. Novel biochemical and structural insights into the interaction of myristoylated cargo with Unc119 and their release by Arl2/3. The Journal of Biological Chemistry. PMID 27481943 DOI: 10.1074/Jbc.M116.741827 |
0.319 |
|
2016 |
Mejuch T, Waldmann H. Synthesis of Lipidated Proteins. Bioconjugate Chemistry. PMID 27444727 DOI: 10.1021/Acs.Bioconjchem.6B00261 |
0.339 |
|
2016 |
Tschapalda K, Zhang YQ, Liu L, Golovnina K, Schlemper T, Eichmann TO, Lal-Nag M, Sreenivasan U, McLenithan J, Ziegler S, Sztalryd C, Lass A, Auld D, Oliver B, Waldmann H, et al. A Class of Diacylglycerol Acyltransferase 1 Inhibitors Identified by a Combination of Phenotypic High-throughput Screening, Genomics, and Genetics. Ebiomedicine. 8: 49-59. PMID 27428418 DOI: 10.1016/J.Ebiom.2016.04.014 |
0.321 |
|
2016 |
Sperlich B, Kapoor S, Waldmann H, Winter R, Weise K. Regulation of K-Ras4B Membrane Binding by Calmodulin. Biophysical Journal. 111: 113-22. PMID 27410739 DOI: 10.1016/J.Bpj.2016.05.042 |
0.685 |
|
2016 |
Schroeder P, Bauer JO, Strohmann C, Kumar K, Waldmann H. Synthesis of an Iridoid-Inspired Compound Collection and the Discovery of Autophagy Inhibitors. The Journal of Organic Chemistry. PMID 27352173 DOI: 10.1021/Acs.Joc.6B01185 |
0.386 |
|
2016 |
Cromm PM, Spiegel J, Kuechler P, Dietrich L, Kriegesmann J, Wendt M, Goody R, Waldmann H, Grossmann TN. Protease-resistant and cell-permeable double-stapled peptides targeting the Rab8a GTPase. Acs Chemical Biology. PMID 27336832 DOI: 10.1021/Acschembio.6B00386 |
0.355 |
|
2016 |
Kapoor S, Waldmann H, Ziegler S. Novel approaches to map small molecule-target interactions. Bioorganic & Medicinal Chemistry. PMID 27240466 DOI: 10.1016/J.Bmc.2016.05.020 |
0.659 |
|
2016 |
Kötzner L, Leutzsch M, Sievers S, Patil S, Waldmann H, Zheng Y, Thiel W, List B. The Organocatalytic Approach to Enantiopure 2H- and 3H-Pyrroles: Inhibitors of the Hedgehog Signaling Pathway. Angewandte Chemie (International Ed. in English). PMID 27239757 DOI: 10.1002/Anie.201602932 |
0.307 |
|
2016 |
Xu H, Golz C, Strohmann C, Antonchick AP, Waldmann H. Enantiodivergent Combination of Natural Product Scaffolds Enabled by Catalytic Enantioselective Cycloaddition. Angewandte Chemie (International Ed. in English). PMID 27193834 DOI: 10.1002/Anie.201602084 |
0.732 |
|
2016 |
Qian Y, Schürmann M, Janning P, Hedberg C, Waldmann H. Activity-Based Proteome Profiling Probes Based on Woodward's Reagent K with Distinct Target Selectivity. Angewandte Chemie (International Ed. in English). PMID 27159346 DOI: 10.1002/Anie.201602666 |
0.338 |
|
2016 |
Papke B, Murarka S, Vogel HA, Martín-Gago P, Kovacevic M, Truxius DC, Fansa EK, Ismail S, Zimmermann G, Heinelt K, Schultz-Fademrecht C, Al Saabi A, Baumann M, Nussbaumer P, Wittinghofer A, ... Waldmann H, et al. Identification of pyrazolopyridazinones as PDEδ inhibitors. Nature Communications. 7: 11360. PMID 27094677 DOI: 10.1038/Ncomms11360 |
0.794 |
|
2016 |
Cromm PM, Schaubach S, Spiegel J, Fürstner A, Grossmann TN, Waldmann H. Orthogonal ring-closing alkyne and olefin metathesis for the synthesis of small GTPase-targeting bicyclic peptides. Nature Communications. 7: 11300. PMID 27075966 DOI: 10.1038/Ncomms11300 |
0.527 |
|
2016 |
Erwin N, Sperlich B, Garivet G, Waldmann H, Weise K, Winter R. Lipoprotein insertion into membranes of various complexity: lipid sorting, interfacial adsorption and protein clustering. Physical Chemistry Chemical Physics : Pccp. PMID 26960984 DOI: 10.1039/C6Cp00563B |
0.784 |
|
2016 |
Kumar K, Dakas P, Waldmann H. Natural Product Inspired Enantioselective Synthesis of Hexahydro-aza-pentalenones Heterocycles. 93: 465. DOI: 10.3987/Com-15-S(T)61 |
0.334 |
|
2016 |
Baumann M, Höing S, Yeh T, Martinez N, Habenberger P, Kremer L, Drexler HC, Küchler P, Reinhardt P, Choidas A, Zischinsky M, Zischinsky G, Ketcham SA, Wagner L, Nussbaumer P, ... ... Waldmann H, et al. Abstract 2997: Dynarrestin, a novel dynein inhibitor that does not block ciliogenesis Cancer Research. 76: 2997-2997. DOI: 10.1158/1538-7445.Am2016-2997 |
0.34 |
|
2016 |
Antonchick A, Waldmann H, Murarka S, Golz C, Strohmann C. Biology-Oriented Synthesis of 3,3-Spiro(2-tetrahydrofuranyl)oxindoles Synthesis. 49: 87-95. DOI: 10.1055/S-0035-1561665 |
0.794 |
|
2016 |
Pérez-Galán P, Waldmann H, Kumar K. Building polycyclic indole scaffolds via gold(I)-catalyzed intra- and inter-molecular cyclization reactions of 1,6-enynes Tetrahedron. DOI: 10.1016/J.Tet.2016.03.020 |
0.326 |
|
2015 |
Sellstedt M, Schwalfenberg M, Ziegler S, Antonchick AP, Waldmann H. Trienamine catalyzed asymmetric synthesis and biological investigation of a cytochalasin B-inspired compound collection. Organic & Biomolecular Chemistry. PMID 26606903 DOI: 10.1039/C5Ob02272J |
0.709 |
|
2015 |
Pahl A, Lakemeyer M, Vielberg MT, Hackl MW, Vomacka J, Korotkov VS, Stein ML, Fetzer C, Lorenz-Baath K, Richter K, Waldmann H, Groll M, Sieber SA. Reversible Inhibitors Arrest ClpP in a Defined Conformational State that Can Be Revoked by ClpX Association. Angewandte Chemie (International Ed. in English). PMID 26566002 DOI: 10.1002/Anie.201507266 |
0.328 |
|
2015 |
Mejuch T, van Hattum H, Triola G, Jaiswal M, Waldmann H. Specificity of Lipoprotein Chaperones for the Characteristic Lipidated Structural Motifs of their Cognate Lipoproteins. Chembiochem : a European Journal of Chemical Biology. PMID 26503308 DOI: 10.1002/Cbic.201500355 |
0.304 |
|
2015 |
Cromm PM, Spiegel J, Grossmann TN, Waldmann H. Direct Modulation of Small GTPase Activity and Function. Angewandte Chemie (International Ed. in English). 54: 13516-37. PMID 26470842 DOI: 10.1002/Anie.201504357 |
0.348 |
|
2015 |
Meiß R, Kumar K, Waldmann H. Divergent Gold(I)-Catalyzed Skeletal Rearrangements of 1,7-Enynes. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 13526-30. PMID 26356499 DOI: 10.1002/Chem.201502843 |
0.327 |
|
2015 |
Ursu A, Waldmann H. Hide and seek: Identification and confirmation of small molecule protein targets. Bioorganic & Medicinal Chemistry Letters. PMID 26115575 DOI: 10.1016/J.Bmcl.2015.06.023 |
0.329 |
|
2015 |
Hackl MW, Lakemeyer M, Dahmen M, Glaser M, Pahl A, Lorenz-Baath K, Menzel T, Sievers S, Böttcher T, Antes I, Waldmann H, Sieber SA. Phenyl Esters Are Potent Inhibitors of Caseinolytic Protease P and Reveal a Stereogenic Switch for Deoligomerization. Journal of the American Chemical Society. PMID 26083639 DOI: 10.1021/Jacs.5B03084 |
0.368 |
|
2015 |
Vendrell-Navarro G, Rúa F, Bujons J, Brockmeyer A, Janning P, Ziegler S, Messeguer A, Waldmann H. Positional Scanning Synthesis of a Peptoid Library Yields New Inducers of Apoptosis that Target Karyopherins and Tubulin. Chembiochem : a European Journal of Chemical Biology. PMID 26010161 DOI: 10.1002/Cbic.201500169 |
0.351 |
|
2015 |
Murarka S, Jia ZJ, Merten C, Daniliuc CG, Antonchick AP, Waldmann H. Rhodium(II)-Catalyzed Enantioselective Synthesis of Troponoids. Angewandte Chemie (International Ed. in English). 54: 7653-6. PMID 25959033 DOI: 10.1002/Anie.201502233 |
0.794 |
|
2015 |
Schröder P, Förster T, Kleine S, Becker C, Richters A, Ziegler S, Rauh D, Kumar K, Waldmann H. Neuritogenic Militarinone-Inspired 4-Hydroxypyridones Target the Stress Pathway Kinase MAP4K4. Angewandte Chemie (International Ed. in English). PMID 25908259 DOI: 10.1002/Anie.201501515 |
0.326 |
|
2015 |
Danda A, Kumar K, Waldmann H. A general catalytic reaction sequence to access alkaloid-inspired indole polycycles. Chemical Communications (Cambridge, England). 51: 7536-9. PMID 25846800 DOI: 10.1039/C5Cc01555C |
0.314 |
|
2015 |
Potowski M, Golz C, Strohmann C, Antonchick AP, Waldmann H. Biology-oriented synthesis of benzopyrano[3,4-c]pyrrolidines. Bioorganic & Medicinal Chemistry. 23: 2895-903. PMID 25792140 DOI: 10.1016/J.Bmc.2015.02.044 |
0.737 |
|
2015 |
Švenda J, Sheremet M, Kremer L, Maier L, Bauer JO, Strohmann C, Ziegler S, Kumar K, Waldmann H. Biology-oriented synthesis of a withanolide-inspired compound collection reveals novel modulators of hedgehog signaling. Angewandte Chemie (International Ed. in English). 54: 5596-602. PMID 25736574 DOI: 10.1002/Anie.201500112 |
0.392 |
|
2015 |
Arndt HD, Rizzo S, Nöcker C, Wakchaure VN, Milroy LG, Bieker V, Calderon A, Tran TT, Brand S, Dehmelt L, Waldmann H. Divergent solid-phase synthesis of natural product-inspired bipartite cyclodepsipeptides: total synthesis of seragamide A. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 5311-6. PMID 25694199 DOI: 10.1002/Chem.201500368 |
0.359 |
|
2015 |
Potowski M, Merten C, Antonchick AP, Waldmann H. Catalytic aerobic oxidation and tandem enantioselective cycloaddition in cascade multicomponent synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 4913-7. PMID 25676025 DOI: 10.1002/Chem.201500125 |
0.726 |
|
2015 |
Sankar MG, Mantilli L, Bull J, Giordanetto F, Bauer JO, Strohmann C, Waldmann H, Kumar K. Stereoselective synthesis of a natural product inspired tetrahydroindolo[2,3-a]-quinolizine compound library. Bioorganic & Medicinal Chemistry. 23: 2614-20. PMID 25648684 DOI: 10.1016/J.Bmc.2015.01.019 |
0.392 |
|
2015 |
Vendrell-Navarro G, Brockmeyer A, Waldmann H, Janning P, Ziegler S. Identification of the targets of biologically active small molecules using quantitative proteomics. Methods in Molecular Biology (Clifton, N.J.). 1263: 263-86. PMID 25618352 DOI: 10.1007/978-1-4939-2269-7_21 |
0.341 |
|
2015 |
Jia ZJ, Daniliuc CG, Antonchick AP, Waldmann H. Phosphine-catalyzed dearomatizing [3+2] annulations of isoquinolinium methylides with allenes. Chemical Communications (Cambridge, England). 51: 1054-7. PMID 25434405 DOI: 10.1039/C4Cc08555H |
0.713 |
|
2015 |
Vidadala SR, Golz C, Strohmann C, Daniliuc CG, Waldmann H. Highly enantioselective intramolecular 1,3-dipolar cycloaddition: a route to piperidino-pyrrolizidines. Angewandte Chemie (International Ed. in English). 54: 651-5. PMID 25393926 DOI: 10.1002/Anie.201409942 |
0.36 |
|
2015 |
Vidadala SR, Waldmann H. One-pot synthesis of a natural product inspired pyrrolocoumarine compound collection by means of an intramolecular 1,3-dipolar cycloaddition as key step Tetrahedron Letters. 56: 3358-3360. DOI: 10.1016/J.Tetlet.2015.01.021 |
0.378 |
|
2014 |
Eschenbrenner-Lux V, Kumar K, Waldmann H. The asymmetric hetero-Diels-Alder reaction in the syntheses of biologically relevant compounds. Angewandte Chemie (International Ed. in English). 53: 11146-57. PMID 25220929 DOI: 10.1002/Anie.201404094 |
0.366 |
|
2014 |
van Hattum H, Waldmann H. Biology-oriented synthesis: harnessing the power of evolution. Journal of the American Chemical Society. 136: 11853-9. PMID 25074019 DOI: 10.1021/Ja505861D |
0.392 |
|
2014 |
Kolundži? F, Murali A, Pérez-Galán P, Bauer JO, Strohmann C, Kumar K, Waldmann H. A cyclization-rearrangement cascade for the synthesis of structurally complex chiral gold(I)-aminocarbene complexes. Angewandte Chemie (International Ed. in English). 53: 8122-6. PMID 25044294 DOI: 10.1002/Anie.201403651 |
0.343 |
|
2014 |
Basu S, Waldmann H. Polymer supported synthesis of a natural product-inspired oxepane library. Bioorganic & Medicinal Chemistry. 22: 4430-44. PMID 24947480 DOI: 10.1016/J.Bmc.2014.05.039 |
0.687 |
|
2014 |
Zimmermann G, Schultz-Fademrecht C, Küchler P, Murarka S, Ismail S, Triola G, Nussbaumer P, Wittinghofer A, Waldmann H. Structure guided design and kinetic analysis of highly potent benzimidazole inhibitors targeting the PDEδ prenyl binding site. Journal of Medicinal Chemistry. 57: 5435-48. PMID 24884780 DOI: 10.1021/Jm500632S |
0.697 |
|
2014 |
Narayan R, Potowski M, Jia ZJ, Antonchick AP, Waldmann H. Catalytic enantioselective 1,3-dipolar cycloadditions of azomethine ylides for biology-oriented synthesis. Accounts of Chemical Research. 47: 1296-310. PMID 24730692 DOI: 10.1021/Ar400286B |
0.808 |
|
2014 |
Bruss H, Schuster H, Martinez R, Kaiser M, Antonchick AP, Waldmann H. Synthesis of the B-seco limonoid core scaffold. Beilstein Journal of Organic Chemistry. 10: 194-208. PMID 24605139 DOI: 10.3762/Bjoc.10.15 |
0.711 |
|
2014 |
Rizzo S, Waldmann H. Development of a natural-product-derived chemical toolbox for modulation of protein function. Chemical Reviews. 114: 4621-39. PMID 24568160 DOI: 10.1021/Cr400442V |
0.329 |
|
2014 |
Tran TT, Gerding-Reimers C, Schölermann B, Stanitzki B, Henkel T, Waldmann H, Ziegler S. Podoverine A--a novel microtubule destabilizing natural product from the Podophyllum species. Bioorganic & Medicinal Chemistry. 22: 5110-6. PMID 24530033 DOI: 10.1016/J.Bmc.2014.01.039 |
0.339 |
|
2014 |
Vogel A, Nikolaus J, Weise K, Triola G, Waldmann H, Winter R, Herrmann A, Huster D. Interaction of the human N-Ras protein with lipid raft model membranes of varying degrees of complexity. Biological Chemistry. 395: 779-89. PMID 24526608 DOI: 10.1515/Hsz-2013-0294 |
0.49 |
|
2014 |
Spiegel J, Cromm PM, Itzen A, Goody RS, Grossmann TN, Waldmann H. Direct targeting of Rab-GTPase-effector interactions. Angewandte Chemie (International Ed. in English). 53: 2498-503. PMID 24481744 DOI: 10.1002/Anie.201308568 |
0.352 |
|
2014 |
Eschenbrenner-Lux V, Küchler P, Ziegler S, Kumar K, Waldmann H. An enantioselective inverse-electron-demand imino Diels-Alder reaction. Angewandte Chemie (International Ed. in English). 53: 2134-7. PMID 24470427 DOI: 10.1002/Anie.201309022 |
0.306 |
|
2014 |
Vartak N, Papke B, Grecco HE, Rossmannek L, Waldmann H, Hedberg C, Bastiaens PI. The autodepalmitoylating activity of APT maintains the spatial organization of palmitoylated membrane proteins. Biophysical Journal. 106: 93-105. PMID 24411241 DOI: 10.1016/J.Bpj.2013.11.024 |
0.324 |
|
2014 |
Weise K, Sperlich B, Kapoor S, Triola G, Waldmann H, Winter R. Regulation of K-RAS Membrane Association: Calmodulin Versus PDEδ Biophysical Journal. 106: 711a. DOI: 10.1016/J.Bpj.2013.11.3936 |
0.691 |
|
2013 |
Köhnke M, Delon C, Hastie ML, Nguyen UT, Wu YW, Waldmann H, Goody RS, Gorman JJ, Alexandrov K. Rab GTPase prenylation hierarchy and its potential role in choroideremia disease. Plos One. 8: e81758. PMID 24358126 DOI: 10.1371/Journal.Pone.0081758 |
0.305 |
|
2013 |
Narayan R, Bauer JO, Strohmann C, Antonchick AP, Waldmann H. Catalytic enantioselective synthesis of functionalized tropanes reveals novel inhibitors of hedgehog signaling. Angewandte Chemie (International Ed. in English). 52: 12892-6. PMID 24151037 DOI: 10.1002/Anie.201307392 |
0.796 |
|
2013 |
Werkmüller A, Triola G, Waldmann H, Winter R. Rotational and translational dynamics of ras proteins upon binding to model membrane systems. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. 14: 3698-705. PMID 24115726 DOI: 10.1002/Cphc.201300617 |
0.503 |
|
2013 |
Takayama H, Jia ZJ, Kremer L, Bauer JO, Strohmann C, Ziegler S, Antonchick AP, Waldmann H. Discovery of inhibitors of the Wnt and Hedgehog signaling pathways through the catalytic enantioselective synthesis of an iridoid-inspired compound collection. Angewandte Chemie (International Ed. in English). 52: 12404-8. PMID 24115579 DOI: 10.1002/Anie.201306948 |
0.727 |
|
2013 |
Potowski M, Antonchick AP, Waldmann H. Catalytic asymmetric exo-selective [6+3] cycloaddition of iminoesters with fulvenes. Chemical Communications (Cambridge, England). 49: 7800-2. PMID 23884088 DOI: 10.1039/C3Cc43824D |
0.735 |
|
2013 |
Weise K, Huster D, Kapoor S, Triola G, Waldmann H, Winter R. Gibbs energy determinants of lipoprotein insertion into lipid membranes: the case study of Ras proteins. Faraday Discussions. 161: 549-61; discussion 5. PMID 23805758 DOI: 10.1039/C2Fd20100C |
0.699 |
|
2013 |
Zimmermann G, Papke B, Ismail S, Vartak N, Chandra A, Hoffmann M, Hahn SA, Triola G, Wittinghofer A, Bastiaens PI, Waldmann H. Small molecule inhibition of the KRAS-PDEδ interaction impairs oncogenic KRAS signalling. Nature. 497: 638-42. PMID 23698361 DOI: 10.1038/Nature12205 |
0.337 |
|
2013 |
Antonchick AP, López-Tosco S, Parga J, Sievers S, Schürmann M, Preut H, Höing S, Schöler HR, Sterneckert J, Rauh D, Waldmann H. Highly enantioselective catalytic synthesis of neurite growth-promoting secoyohimbanes. Chemistry & Biology. 20: 500-9. PMID 23601639 DOI: 10.1016/J.Chembiol.2013.03.011 |
0.722 |
|
2013 |
Kapoor S, Werkmüller A, Goody RS, Waldmann H, Winter R. Pressure modulation of Ras-membrane interactions and intervesicle transfer. Journal of the American Chemical Society. 135: 6149-56. PMID 23560466 DOI: 10.1021/Ja312671J |
0.698 |
|
2013 |
Ziegler S, Pries V, Hedberg C, Waldmann H. Target identification for small bioactive molecules: finding the needle in the haystack. Angewandte Chemie (International Ed. in English). 52: 2744-92. PMID 23418026 DOI: 10.1002/Anie.201208749 |
0.326 |
|
2013 |
Zimmermann TJ, Roy S, Martinez NE, Ziegler S, Hedberg C, Waldmann H. Biology-oriented synthesis of a tetrahydroisoquinoline-based compound collection targeting microtubule polymerization. Chembiochem : a European Journal of Chemical Biology. 14: 295-300. PMID 23364933 DOI: 10.1002/Cbic.201200711 |
0.319 |
|
2013 |
Eschenbrenner-Lux V, Dückert H, Khedkar V, Bruss H, Waldmann H, Kumar K. Cascade syntheses routes to the centrocountins. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 2294-304. PMID 23319417 DOI: 10.1002/Chem.201203714 |
0.37 |
|
2013 |
Over B, Wetzel S, Grütter C, Nakai Y, Renner S, Rauh D, Waldmann H. Natural-product-derived fragments for fragment-based ligand discovery. Nature Chemistry. 5: 21-8. PMID 23247173 DOI: 10.1038/Nchem.1506 |
0.345 |
|
2013 |
Zimmermann TJ, Bürger M, Tashiro E, Kondoh Y, Martinez NE, Görmer K, Rosin-Steiner S, Shimizu T, Ozaki S, Mikoshiba K, Watanabe N, Hall D, Vetter IR, Osada H, Hedberg C, ... Waldmann H, et al. Boron-based inhibitors of acyl protein thioesterases 1 and 2. Chembiochem : a European Journal of Chemical Biology. 14: 115-22. PMID 23239555 DOI: 10.1002/Cbic.201200571 |
0.373 |
|
2013 |
Voigt T, Gerding-Reimers C, Ngoc Tran TT, Bergmann S, Lachance H, Schölermann B, Brockmeyer A, Janning P, Ziegler S, Waldmann H. A natural product inspired tetrahydropyran collection yields mitosis modulators that synergistically target CSE1L and tubulin. Angewandte Chemie (International Ed. in English). 52: 410-4. PMID 23080551 DOI: 10.1002/Anie.201205728 |
0.595 |
|
2013 |
Werkmüller A, Triola G, Waldmann H, Winter R. Inside Cover: Rotational and Translational Dynamics of Ras Proteins upon Binding to Model Membrane Systems (ChemPhysChem 16/2013) Chemphyschem. 14: 3634-3634. DOI: 10.1002/Cphc.201390077 |
0.486 |
|
2013 |
Potowski M, Bauer JO, Strohmann C, Antonchick AP, Waldmann H. Corrigendum: Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides Angewandte Chemie International Edition. 52: 7342-7342. DOI: 10.1002/Anie.201304263 |
0.71 |
|
2013 |
Potowski M, Bauer JO, Strohmann C, Antonchick AP, Waldmann H. Berichtigung: Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides Angewandte Chemie. 125: 7484-7484. DOI: 10.1002/Ange.201304263 |
0.71 |
|
2012 |
Matcha K, Madduri AV, Roy S, Ziegler S, Waldmann H, Hirsch AK, Minnaard AJ. Total synthesis of (-)-doliculide, structure-activity relationship studies and its binding to F-actin. Chembiochem : a European Journal of Chemical Biology. 13: 2537-48. PMID 23129522 DOI: 10.1002/Cbic.201200512 |
0.313 |
|
2012 |
Güldenhaupt J, Rudack T, Bachler P, Mann D, Triola G, Waldmann H, Kötting C, Gerwert K. N-Ras forms dimers at POPC membranes. Biophysical Journal. 103: 1585-93. PMID 23062351 DOI: 10.1016/J.Bpj.2012.08.043 |
0.304 |
|
2012 |
Sos ML, Dietlein F, Peifer M, Schöttle J, Balke-Want H, Müller C, Koker M, Richters A, Heynck S, Malchers F, Heuckmann JM, Seidel D, Eyers PA, Ullrich RT, Antonchick AP, ... ... Waldmann H, et al. A framework for identification of actionable cancer genome dependencies in small cell lung cancer. Proceedings of the National Academy of Sciences of the United States of America. 109: 17034-9. PMID 23035247 DOI: 10.1073/Pnas.1207310109 |
0.697 |
|
2012 |
Stigter EA, Guo Z, Bon RS, Wu YW, Choidas A, Wolf A, Menninger S, Waldmann H, Blankenfeldt W, Goody RS. Development of selective, potent RabGGTase inhibitors. Journal of Medicinal Chemistry. 55: 8330-40. PMID 22963166 DOI: 10.1021/Jm300624S |
0.689 |
|
2012 |
Potowski M, Bauer JO, Strohmann C, Antonchick AP, Waldmann H. Highly enantioselective catalytic [6+3] cycloadditions of azomethine ylides. Angewandte Chemie (International Ed. in English). 51: 9512-6. PMID 22893358 DOI: 10.1002/Anie.201204394 |
0.71 |
|
2012 |
Kapoor S, Weise K, Erlkamp M, Triola G, Waldmann H, Winter R. The role of G-domain orientation and nucleotide state on the Ras isoform-specific membrane interaction. European Biophysics Journal : Ebj. 41: 801-13. PMID 22851002 DOI: 10.1007/S00249-012-0841-5 |
0.697 |
|
2012 |
Weise K, Kapoor S, Werkmüller A, Möbitz S, Zimmermann G, Triola G, Waldmann H, Winter R. Dissociation of the K-Ras4B/PDEδ complex upon contact with lipid membranes: membrane delivery instead of extraction. Journal of the American Chemical Society. 134: 11503-10. PMID 22721555 DOI: 10.1021/Ja305518H |
0.687 |
|
2012 |
Tnimov Z, Guo Z, Gambin Y, Nguyen UT, Wu YW, Abankwa D, Stigter A, Collins BM, Waldmann H, Goody RS, Alexandrov K. Quantitative analysis of prenylated RhoA interaction with its chaperone, RhoGDI. The Journal of Biological Chemistry. 287: 26549-62. PMID 22628549 DOI: 10.1074/Jbc.M112.371294 |
0.309 |
|
2012 |
Lachance H, Wetzel S, Kumar K, Waldmann H. Charting, navigating, and populating natural product chemical space for drug discovery. Journal of Medicinal Chemistry. 55: 5989-6001. PMID 22537178 DOI: 10.1021/Jm300288G |
0.339 |
|
2012 |
Görmer K, Bürger M, Kruijtzer JA, Vetter I, Vartak N, Brunsveld L, Bastiaens PI, Liskamp RM, Triola G, Waldmann H. Chemical-biological exploration of the limits of the Ras de- and repalmitoylating machinery. Chembiochem : a European Journal of Chemical Biology. 13: 1017-23. PMID 22488913 DOI: 10.1002/Cbic.201200078 |
0.735 |
|
2012 |
Deraeve C, Guo Z, Bon RS, Blankenfeldt W, DiLucrezia R, Wolf A, Menninger S, Stigter EA, Wetzel S, Choidas A, Alexandrov K, Waldmann H, Goody RS, Wu YW. Psoromic acid is a selective and covalent Rab-prenylation inhibitor targeting autoinhibited RabGGTase. Journal of the American Chemical Society. 134: 7384-91. PMID 22480322 DOI: 10.1021/Ja211305J |
0.701 |
|
2012 |
Richter A, Rose R, Hedberg C, Waldmann H, Ottmann C. An optimised small-molecule stabiliser of the 14-3-3-PMA2 protein-protein interaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 6520-7. PMID 22467351 DOI: 10.1002/Chem.201103761 |
0.38 |
|
2012 |
Potowski M, Schürmann M, Preut H, Antonchick AP, Waldmann H. Programmable enantioselective one-pot synthesis of molecules with eight stereocenters. Nature Chemical Biology. 8: 428-30. PMID 22426113 DOI: 10.1038/Nchembio.901 |
0.722 |
|
2012 |
Das D, Tnimov Z, Nguyen UT, Thimmaiah G, Lo H, Abankwa D, Wu Y, Goody RS, Waldmann H, Alexandrov K. Flexible and general synthesis of functionalized phosphoisoprenoids for the study of prenylation in vivo and in vitro. Chembiochem : a European Journal of Chemical Biology. 13: 674-83. PMID 22351497 DOI: 10.1002/Cbic.201100733 |
0.381 |
|
2012 |
Samatov TR, Wolf A, Odenwälder P, Bessonov S, Deraeve C, Bon RS, Waldmann H, Lührmann R. Psoromic acid derivatives: a new family of small-molecule pre-mRNA splicing inhibitors discovered by a stage-specific high-throughput in vitro splicing assay. Chembiochem : a European Journal of Chemical Biology. 13: 640-4. PMID 22334518 DOI: 10.1002/Cbic.201100790 |
0.688 |
|
2012 |
Kapoor S, Triola G, Vetter IR, Erlkamp M, Waldmann H, Winter R. Revealing conformational substates of lipidated N-Ras protein by pressure modulation. Proceedings of the National Academy of Sciences of the United States of America. 109: 460-5. PMID 22203965 DOI: 10.1073/pnas.1110553109 |
0.709 |
|
2012 |
Dückert H, Pries V, Khedkar V, Menninger S, Bruss H, Bird AW, Maliga Z, Brockmeyer A, Janning P, Hyman A, Grimme S, Schürmann M, Preut H, Hübel K, Ziegler S, ... ... Waldmann H, et al. Natural product-inspired cascade synthesis yields modulators of centrosome integrity. Nature Chemical Biology. 8: 179-84. PMID 22198731 DOI: 10.1038/Nchembio.758 |
0.397 |
|
2012 |
Triola G, Waldmann H, Hedberg C. Chemical biology of lipidated proteins. Acs Chemical Biology. 7: 87-99. PMID 22148864 DOI: 10.1021/Cb200460U |
0.347 |
|
2012 |
Bürger M, Zimmermann TJ, Kondoh Y, Stege P, Watanabe N, Osada H, Waldmann H, Vetter IR. Crystal structure of the predicted phospholipase LYPLAL1 reveals unexpected functional plasticity despite close relationship to acyl protein thioesterases. Journal of Lipid Research. 53: 43-50. PMID 22052940 DOI: 10.1194/Jlr.M019851 |
0.332 |
|
2012 |
Werkmüller A, Denter C, Opitz N, Koch S, Zimmermann G, Triola G, Waldmann H, Winter R. Characterization of the Dynamical Properties of Ras Proteins upon Insertion into Model Biomembrane Systems Biophysical Journal. 102: 77a. DOI: 10.1016/J.Bpj.2011.11.448 |
0.503 |
|
2012 |
Weise K, Kapoor S, Koch S, Triola G, Waldmann H, Winter R. Ras Isoform-Specific Membrane Interactions: A Molecular Mechanism for Isoform-Specific Ras Signaling Biophysical Journal. 102: 18a. DOI: 10.1016/J.Bpj.2011.11.122 |
0.702 |
|
2011 |
Wetzel S, Bon RS, Kumar K, Waldmann H. Biology-oriented synthesis. Angewandte Chemie (International Ed. in English). 50: 10800-26. PMID 22038946 DOI: 10.1002/Anie.201007004 |
0.704 |
|
2011 |
Ismail SA, Chen YX, Rusinova A, Chandra A, Bierbaum M, Gremer L, Triola G, Waldmann H, Bastiaens PI, Wittinghofer A. Arl2-GTP and Arl3-GTP regulate a GDI-like transport system for farnesylated cargo. Nature Chemical Biology. 7: 942-9. PMID 22002721 DOI: 10.1038/Nchembio.686 |
0.337 |
|
2011 |
Rusch M, Zimmermann TJ, Bürger M, Dekker FJ, Görmer K, Triola G, Brockmeyer A, Janning P, Böttcher T, Sieber SA, Vetter IR, Hedberg C, Waldmann H. Identification of acyl protein thioesterases 1 and 2 as the cellular targets of the Ras-signaling modulators palmostatin B and M. Angewandte Chemie (International Ed. in English). 50: 9838-42. PMID 21905186 DOI: 10.1002/Anie.201102967 |
0.315 |
|
2011 |
Hedberg C, Dekker FJ, Rusch M, Renner S, Wetzel S, Vartak N, Gerding-Reimers C, Bon RS, Bastiaens PI, Waldmann H. Development of highly potent inhibitors of the Ras-targeting human acyl protein thioesterases based on substrate similarity design. Angewandte Chemie (International Ed. in English). 50: 9832-7. PMID 21905185 DOI: 10.1002/Anie.201102965 |
0.688 |
|
2011 |
Wittstein K, Kumar K, Waldmann H. Gold(I)-catalyzed synthesis of benzoxocines by an 8-endo-dig cyclization. Angewandte Chemie (International Ed. in English). 50: 9076-80. PMID 21866577 DOI: 10.1002/Anie.201103832 |
0.339 |
|
2011 |
Stöckigt J, Antonchick AP, Wu F, Waldmann H. The Pictet-Spengler reaction in nature and in organic chemistry. Angewandte Chemie (International Ed. in English). 50: 8538-64. PMID 21830283 DOI: 10.1002/Anie.201008071 |
0.73 |
|
2011 |
Eisenberg S, Beckett AJ, Prior IA, Dekker FJ, Hedberg C, Waldmann H, Ehrlich M, Henis YI. Raft protein clustering alters N-Ras membrane interactions and activation pattern. Molecular and Cellular Biology. 31: 3938-52. PMID 21807892 DOI: 10.1128/Mcb.05570-11 |
0.307 |
|
2011 |
Yi L, Sun H, Itzen A, Triola G, Waldmann H, Goody RS, Wu YW. One-pot dual-labeling of a protein by two chemoselective reactions. Angewandte Chemie (International Ed. in English). 50: 8287-90. PMID 21761514 DOI: 10.1002/Anie.201100840 |
0.509 |
|
2011 |
Richter A, Hedberg C, Waldmann H. Enantioselective synthesis of the C10-C20 fragment of fusicoccin A. The Journal of Organic Chemistry. 76: 6694-702. PMID 21755994 DOI: 10.1021/Jo201020V |
0.326 |
|
2011 |
Wagner BK, Gilbert TJ, Hanai J, Imamura S, Bodycombe NE, Bon RS, Waldmann H, Clemons PA, Sukhatme VP, Mootha VK. A small-molecule screening strategy to identify suppressors of statin myopathy. Acs Chemical Biology. 6: 900-4. PMID 21732624 DOI: 10.1021/Cb200206W |
0.649 |
|
2011 |
Chen YX, Triola G, Waldmann H. Bioorthogonal chemistry for site-specific labeling and surface immobilization of proteins. Accounts of Chemical Research. 44: 762-73. PMID 21648407 DOI: 10.1021/Ar200046H |
0.363 |
|
2011 |
Eberhardt L, Kumar K, Waldmann H. Exploring and exploiting biologically relevant chemical space. Current Drug Targets. 12: 1531-46. PMID 21561426 DOI: 10.2174/138945011798109482 |
0.391 |
|
2011 |
Schuster H, Martinez R, Bruss H, Antonchick AP, Kaiser M, Schürmann M, Waldmann H. Synthesis of the B-seco limonoid scaffold. Chemical Communications (Cambridge, England). 47: 6545-7. PMID 21552600 DOI: 10.1039/C1Cc11388G |
0.703 |
|
2011 |
He YP, Tan H, Arve L, Baumann S, Waldmann H, Arndt HD. Biphenomycin B and derivatives: total synthesis and translation inhibition. Chemistry, An Asian Journal. 6: 1546-56. PMID 21548101 DOI: 10.1002/Asia.201000908 |
0.615 |
|
2011 |
Bon RS, Guo Z, Stigter EA, Wetzel S, Menninger S, Wolf A, Choidas A, Alexandrov K, Blankenfeldt W, Goody RS, Waldmann H. Structure-guided development of selective RabGGTase inhibitors. Angewandte Chemie (International Ed. in English). 50: 4957-61. PMID 21520375 DOI: 10.1002/Anie.201101210 |
0.684 |
|
2011 |
Radtke L, Willot M, Sun H, Ziegler S, Sauerland S, Strohmann C, Fröhlich R, Habenberger P, Waldmann H, Christmann M. Total synthesis and biological evaluation of (-)-englerin A and B: synthesis of analogues with improved activity profile. Angewandte Chemie (International Ed. in English). 50: 3998-4002. PMID 21472928 DOI: 10.1002/Anie.201007790 |
0.504 |
|
2011 |
Dückert H, Khedkar V, Waldmann H, Kumar K. Lewis base catalyzed [4+2] annulation of electron-deficient chromone-derived heterodienes and acetylenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 5130-7. PMID 21432922 DOI: 10.1002/Chem.201003572 |
0.312 |
|
2011 |
Vintonyak VV, Waldmann H, Rauh D. Using small molecules to target protein phosphatases. Bioorganic & Medicinal Chemistry. 19: 2145-55. PMID 21420867 DOI: 10.1016/J.Bmc.2011.02.047 |
0.349 |
|
2011 |
Basu S, Ellinger B, Rizzo S, Deraeve C, Schürmann M, Preut H, Arndt HD, Waldmann H. Biology-oriented synthesis of a natural-product inspired oxepane collection yields a small-molecule activator of the Wnt-pathway. Proceedings of the National Academy of Sciences of the United States of America. 108: 6805-10. PMID 21415367 DOI: 10.1073/Pnas.1015269108 |
0.7 |
|
2011 |
Möcklinghoff S, van Otterlo WA, Rose R, Fuchs S, Zimmermann TJ, Dominguez Seoane M, Waldmann H, Ottmann C, Brunsveld L. Design and evaluation of fragment-like estrogen receptor tetrahydroisoquinoline ligands from a scaffold-detection approach. Journal of Medicinal Chemistry. 54: 2005-11. PMID 21381753 DOI: 10.1021/Jm1011116 |
0.72 |
|
2011 |
Hakki T, Hübel K, Waldmann H, Bernhardt R. The development of a whole-cell based medium throughput screening system for the discovery of human aldosterone synthase (CYP11B2) inhibitors: old drugs disclose new applications for the therapy of congestive heart failure, myocardial fibrosis and hypertension. The Journal of Steroid Biochemistry and Molecular Biology. 125: 120-8. PMID 21193036 DOI: 10.1016/J.Jsbmb.2010.12.011 |
0.317 |
|
2011 |
Weise K, Kapoor S, Denter C, Nikolaus J, Opitz N, Koch S, Triola G, Herrmann A, Waldmann H, Winter R. Membrane-mediated induction and sorting of K-Ras microdomain signaling platforms. Journal of the American Chemical Society. 133: 880-7. PMID 21141956 DOI: 10.1021/ja107532q |
0.704 |
|
2011 |
Frenzel LP, Feldhaus V, Rusch M, Brinker R, Claasen J, Pallasch CP, Waldmann H, Hallek M, Hedberg C, Wendtner C. Palmitoylation Controls Death Receptor Function in Chronic Lymphocytic Leukemia Blood. 118: 2829-2829. DOI: 10.1182/Blood.V118.21.2829.2829 |
0.316 |
|
2011 |
Waldmann H, Bruss H, Dückert H, Kumar K. Synthesis of novel electron-deficient chromone-fused dienes via phosphine catalyzed [4+2] annulation Tetrahedron Letters. 52: 2265-2267. DOI: 10.1016/J.Tetlet.2011.01.151 |
0.315 |
|
2011 |
Antonchick AP, Schuster H, Bruss H, Schürmann M, Preut H, Rauh D, Waldmann H. Enantioselective synthesis of the spirotryprostatin A scaffold Tetrahedron. 67: 10195-10202. DOI: 10.1016/J.Tet.2011.04.056 |
0.722 |
|
2011 |
Vintonyak VV, Warburg K, Over B, Hübel K, Rauh D, Waldmann H. Identification and further development of thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B Tetrahedron. 67: 6713-6729. DOI: 10.1016/J.Tet.2011.04.026 |
0.355 |
|
2011 |
Alexandrov K, Wu Y, Blankenfeldt W, Waldmann H, Goody RS. Organization and Function of the Rab Prenylation and Recycling Machinery Enzymes. 29: 147-162. DOI: 10.1016/B978-0-12-381339-8.00008-1 |
0.336 |
|
2011 |
Stöckigt J, Antonchick AP, Wu F, Waldmann H. Die Pictet-Spengler-Reaktion in der Natur und der organischen Chemie Angewandte Chemie. 123: 8692-8719. DOI: 10.1002/Ange.201008071 |
0.685 |
|
2011 |
Wetzel S, Bon RS, Kumar K, Waldmann H. Biologie-orientierte Synthese (BIOS) Angewandte Chemie. 123: 10990-11018. DOI: 10.1002/Ange.201007004 |
0.638 |
|
2010 |
Yi L, Sun H, Wu YW, Triola G, Waldmann H, Goody RS. A highly efficient strategy for modification of proteins at the C terminus. Angewandte Chemie (International Ed. in English). 49: 9417-21. PMID 21031382 DOI: 10.1002/Anie.201003834 |
0.513 |
|
2010 |
Antonchick AP, Gerding-Reimers C, Catarinella M, Schürmann M, Preut H, Ziegler S, Rauh D, Waldmann H. Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products. Nature Chemistry. 2: 735-40. PMID 20729892 DOI: 10.1038/Nchem.730 |
0.749 |
|
2010 |
Chen YX, Koch S, Uhlenbrock K, Weise K, Das D, Gremer L, Brunsveld L, Wittinghofer A, Winter R, Triola G, Waldmann H. Synthesis of the Rheb and K-Ras4B GTPases. Angewandte Chemie (International Ed. in English). 49: 6090-5. PMID 20652921 DOI: 10.1002/Anie.201001884 |
0.759 |
|
2010 |
Triola G, Gerauer M, Görmer K, Brunsveld L, Waldmann H. Solid-phase synthesis of lipidated Ras peptides employing the Ellman sulfonamide linker. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 9585-91. PMID 20648498 DOI: 10.1002/Chem.201001642 |
0.739 |
|
2010 |
Vintonyak VV, Warburg K, Kruse H, Grimme S, Hübel K, Rauh D, Waldmann H. Identification of thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase B. Angewandte Chemie (International Ed. in English). 49: 5902-5. PMID 20632348 DOI: 10.1002/Anie.201002138 |
0.306 |
|
2010 |
Wu YW, Oesterlin LK, Tan KT, Waldmann H, Alexandrov K, Goody RS. Membrane targeting mechanism of Rab GTPases elucidated by semisynthetic protein probes. Nature Chemical Biology. 6: 534-40. PMID 20512138 DOI: 10.1038/Nchembio.386 |
0.339 |
|
2010 |
Gohlke A, Triola G, Waldmann H, Winter R. Influence of the lipid anchor motif of N-ras on the interaction with lipid membranes: a surface plasmon resonance study. Biophysical Journal. 98: 2226-35. PMID 20483331 DOI: 10.1016/J.Bpj.2010.02.005 |
0.5 |
|
2010 |
Bon RS, Waldmann H. Bioactivity-guided navigation of chemical space. Accounts of Chemical Research. 43: 1103-14. PMID 20481515 DOI: 10.1021/Ar100014H |
0.719 |
|
2010 |
Rose R, Erdmann S, Bovens S, Wolf A, Rose M, Hennig S, Waldmann H, Ottmann C. Identification and structure of small-molecule stabilizers of 14-3-3 protein-protein interactions. Angewandte Chemie (International Ed. in English). 49: 4129-32. PMID 20437433 DOI: 10.1002/Anie.200907203 |
0.325 |
|
2010 |
Dekker FJ, Rocks O, Vartak N, Menninger S, Hedberg C, Balamurugan R, Wetzel S, Renner S, Gerauer M, Schölermann B, Rusch M, Kramer JW, Rauh D, Coates GW, Brunsveld L, ... ... Waldmann H, et al. Small-molecule inhibition of APT1 affects Ras localization and signaling. Nature Chemical Biology. 6: 449-56. PMID 20418879 DOI: 10.1038/Nchembio.362 |
0.801 |
|
2010 |
Rocks O, Gerauer M, Vartak N, Koch S, Huang ZP, Pechlivanis M, Kuhlmann J, Brunsveld L, Chandra A, Ellinger B, Waldmann H, Bastiaens PI. The palmitoylation machinery is a spatially organizing system for peripheral membrane proteins. Cell. 141: 458-71. PMID 20416930 DOI: 10.1016/J.Cell.2010.04.007 |
0.741 |
|
2010 |
Waldmann H, Eberhardt L, Wittstein K, Kumar K. Silver catalyzed cascade synthesis of alkaloid ring systems: Concise total synthesis of fascaplysin, homofascaplysin C and analogues Chemical Communications. 46: 4622-4624. PMID 20386812 DOI: 10.1039/C001350A |
0.353 |
|
2010 |
Tannert R, Milroy LG, Ellinger B, Hu TS, Arndt HD, Waldmann H. Synthesis and structure-activity correlation of natural-product inspired cyclodepsipeptides stabilizing F-actin. Journal of the American Chemical Society. 132: 3063-77. PMID 20148556 DOI: 10.1021/Ja9095126 |
0.385 |
|
2010 |
Görmer K, Waldmann H, Triola G. Efficient microwave-assisted synthesis of unsymmetrical disulfides. The Journal of Organic Chemistry. 75: 1811-3. PMID 20121046 DOI: 10.1021/Jo902695A |
0.329 |
|
2010 |
Weinrich D, Lin PC, Jonkheijm P, Nguyen UT, Schröder H, Niemeyer CM, Alexandrov K, Goody R, Waldmann H. Oriented immobilization of farnesylated proteins by the thiol-ene reaction. Angewandte Chemie (International Ed. in English). 49: 1252-7. PMID 20069617 DOI: 10.1002/Anie.200906190 |
0.321 |
|
2010 |
Weinrich D, Köhn M, Jonkheijm P, Westerlind U, Dehmelt L, Engelkamp H, Christianen PC, Kuhlmann J, Maan JC, Nüsse D, Schröder H, Wacker R, Voges E, Breinbauer R, Kunz H, ... ... Waldmann H, et al. Preparation of biomolecule microstructures and microarrays by thiol-ene photoimmobilization. Chembiochem : a European Journal of Chemical Biology. 11: 235-47. PMID 20043307 DOI: 10.1002/Cbic.200900559 |
0.456 |
|
2010 |
Wilk W, Zimmermann TJ, Kaiser M, Waldmann H. Principles, implementation, and application of biology-oriented synthesis (BIOS). Biological Chemistry. 391: 491-7. PMID 20030592 DOI: 10.1515/Bc.2010.013 |
0.349 |
|
2010 |
Weise K, Triola G, Janosch S, Waldmann H, Winter R. Visualizing association of lipidated signaling proteins in heterogeneous membranes--partitioning into subdomains, lipid sorting, interfacial adsorption, and protein association. Biochimica Et Biophysica Acta. 1798: 1409-17. PMID 20025847 DOI: 10.1016/J.Bbamem.2009.12.006 |
0.492 |
|
2010 |
Vogel A, Reuther G, Roark MB, Tan KT, Waldmann H, Feller SE, Huster D. Backbone conformational flexibility of the lipid modified membrane anchor of the human N-Ras protein investigated by solid-state NMR and molecular dynamics simulation. Biochimica Et Biophysica Acta. 1798: 275-85. PMID 19819220 DOI: 10.1016/J.Bbamem.2009.09.023 |
0.313 |
|
2010 |
Wilk W, Nören-Müller A, Kaiser M, Waldmann H. Biology-oriented combined solid- and solution-phase synthesis of a macroline-like compound collection. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 11976-84. PMID 19784970 DOI: 10.1002/Chem.200901797 |
0.344 |
|
2010 |
Waldmann H, Antonchick A, Gerding-Reimers C, Catarinella M, Schürmann M, Preut H, Ziegler S, Rauh D. Enantioselective Synthesis of Spirooxindoles Inspired by Natural Products Synfacts. 2010: 1379-1379. DOI: 10.1055/s-0030-1258906 |
0.701 |
|
2010 |
Weise K, Triola G, Koch S, Waldmann H, Winter R. Interactions of Lipidated Ras Proteins With Raft Membranes Studied By Time-Lapse Atomic Force Microscopy Biophysical Journal. 98: 19a-20a. DOI: 10.1016/J.Bpj.2009.12.119 |
0.506 |
|
2010 |
Lin P, Weinrich D, Waldmann H. Protein Biochips: Oriented Surface Immobilization of Proteins Macromolecular Chemistry and Physics. 211: 136-144. DOI: 10.1002/Macp.200900539 |
0.337 |
|
2010 |
Seitz O, Heinemann I, Mattes A, Waldmann H. ChemInform Abstract: Synthetic Peptide Conjugates - Tailor-Made Probes for the Biology of Protein Modification and Protein Processing Cheminform. 32: no-no. DOI: 10.1002/chin.200124237 |
0.484 |
|
2010 |
Pathak T, Waldmann H. ChemInform Abstract: Enzymic Protecting Group Techniques in Organic Synthesis Cheminform. 32: no-no. DOI: 10.1002/chin.200121247 |
0.531 |
|
2010 |
PATHAK T, WALDMANN H. ChemInform Abstract: Enzymes and Protecting Group Chemistry Cheminform. 29: no-no. DOI: 10.1002/chin.199835350 |
0.515 |
|
2010 |
KUNZ H, UNVERZAGT C, DOMBO B, KOSCH W, WALDMANN H. ChemInform Abstract: Synthesis of Glycopeptide Partial Structures of Virus Coat Glycoproteins Cheminform. 26: no-no. DOI: 10.1002/chin.199515318 |
0.37 |
|
2010 |
WALDMANN H, HEUSER A, BRAUN P, SCHULTZ M, KUNZ H. ChemInform Abstract: New Enzymic Methods for the Selective Functionalization of Carbohydrate Derivatives Cheminform. 24: no-no. DOI: 10.1002/chin.199333292 |
0.394 |
|
2010 |
WALDMANN H, HEUSER A, BRAUN P, KUNZ H. ChemInform Abstract: New Enzymatic Protecting Group Techniques for Peptide and Carbohydrate Chemistry. Cheminform. 24: no-no. DOI: 10.1002/chin.199313067 |
0.387 |
|
2010 |
BRAUN P, WALDMANN H, VOGT W, KUNZ H. ChemInform Abstract: Selective Enzymatic Removal of Protecting Groups: n-Heptyl Esters as Carboxy Protecting Functions in Peptide Synthesis. Cheminform. 22: no-no. DOI: 10.1002/chin.199117251 |
0.428 |
|
2010 |
SCHULTZ M, WALDMANN H, KUNZ H, VOGT W. ChemInform Abstract: Chemoenzymatic “Chiral-Pool” Synthesis of (+)-exo-Brevicomin from Carbohydrates Using Fructose 1,6-Diphosphate Aldolase. Cheminform. 22: no-no. DOI: 10.1002/chin.199102093 |
0.436 |
|
2009 |
Tan KT, Guiu-Rozas E, Bon RS, Guo Z, Delon C, Wetzel S, Arndt S, Alexandrov K, Waldmann H, Goody RS, Wu YW, Blankenfeldt W. Design, synthesis, and characterization of peptide-based rab geranylgeranyl transferase inhibitors. Journal of Medicinal Chemistry. 52: 8025-37. PMID 19894725 DOI: 10.1021/Jm901117D |
0.712 |
|
2009 |
Vogel A, Reuther G, Weise K, Triola G, Nikolaus J, Tan KT, Nowak C, Herrmann A, Waldmann H, Winter R, Huster D. The lipid modifications of Ras that sense membrane environments and induce local enrichment. Angewandte Chemie (International Ed. in English). 48: 8784-7. PMID 19830755 DOI: 10.1002/Anie.200903396 |
0.471 |
|
2009 |
Knoth T, Warburg K, Katzka C, Rai A, Wolf A, Brockmeyer A, Janning P, Reubold TF, Eschenburg S, Manstein DJ, Hübel K, Kaiser M, Waldmann H. The Ras pathway modulator melophlin A targets dynamins. Angewandte Chemie (International Ed. in English). 48: 7240-5. PMID 19722243 DOI: 10.1002/Anie.200902023 |
0.344 |
|
2009 |
Westerlind U, Schröder H, Hobel A, Gaidzik N, Kaiser A, Niemeyer CM, Schmitt E, Waldmann H, Kunz H. Tumor-associated MUC1 tandem-repeat glycopeptide microarrays to evaluate serum- and monoclonal-antibody specificity. Angewandte Chemie (International Ed. in English). 48: 8263-7. PMID 19718733 DOI: 10.1002/Anie.200902963 |
0.396 |
|
2009 |
Wetzel S, Klein K, Renner S, Rauh D, Oprea TI, Mutzel P, Waldmann H. Interactive exploration of chemical space with Scaffold Hunter. Nature Chemical Biology. 5: 581-3. PMID 19561620 DOI: 10.1038/Nchembio.187 |
0.31 |
|
2009 |
Renner S, Van Otterlo WAL, Dominguez Seoane M, Möcklinghoff S, Hofmann B, Wetzel S, Schuffenhauer A, Ertl P, Oprea TI, Steinhilber D, Brunsveld L, Rauh D, Waldmann H. Bioactivity-guided mapping and navigation of chemical space Nature Chemical Biology. 5: 585-592. PMID 19561619 DOI: 10.1038/Nchembio.188 |
0.734 |
|
2009 |
Vintonyak VV, Antonchick AP, Rauh D, Waldmann H. The therapeutic potential of phosphatase inhibitors Current Opinion in Chemical Biology. 13: 272-283. PMID 19410499 DOI: 10.1016/J.Cbpa.2009.03.021 |
0.714 |
|
2009 |
Walther T, Renner S, Waldmann H, Arndt HD. Synthesis and structure-activity correlation of brunsvicamide-inspired cyclopeptide collection Chembiochem. 10: 1153-1162. PMID 19360807 DOI: 10.1002/Cbic.200900035 |
0.334 |
|
2009 |
Kumar K, Waldmann H. Synthesis of natural product inspired compound collections Angewandte Chemie - International Edition. 48: 3224-3242. PMID 19267376 DOI: 10.1002/Anie.200803437 |
0.362 |
|
2009 |
Nguyen UT, Guo Z, Delon C, Wu Y, Deraeve C, Fränzel B, Bon RS, Blankenfeldt W, Goody RS, Waldmann H, Wolters D, Alexandrov K. Analysis of the eukaryotic prenylome by isoprenoid affinity tagging. Nature Chemical Biology. 5: 227-35. PMID 19219049 DOI: 10.1038/Nchembio.149 |
0.698 |
|
2009 |
Waldmann H. Killing 84 birds with one stone Nature Chemical Biology. 5: 76-77. PMID 19148173 DOI: 10.1038/Nchembio0209-76 |
0.339 |
|
2009 |
Weise K, Triola G, Brunsveld L, Waldmann H, Winter R. Influence of the lipidation motif on the partitioning and association of N-Ras in model membrane subdomains. Journal of the American Chemical Society. 131: 1557-64. PMID 19133719 DOI: 10.1016/J.Bpj.2008.12.3224 |
0.762 |
|
2009 |
Wilk W, Waldmann H, Kaiser M. γ-Pyrone natural products-A privileged compound class provided by nature Bioorganic and Medicinal Chemistry. 17: 2304-2309. PMID 19042133 DOI: 10.1016/J.Bmc.2008.11.001 |
0.347 |
|
2009 |
Alexander M, Gerauer M, Pechlivanis M, Popkirova B, Dvorsky R, Brunsveld L, Waldmann H, Kuhlmann J. Mapping the isoprenoid binding pocket of PDEdelta by a semisynthetic, photoactivatable N-Ras lipoprotein. Chembiochem : a European Journal of Chemical Biology. 10: 98-108. PMID 18846587 DOI: 10.1002/Cbic.200800275 |
0.742 |
|
2009 |
Brunsveld L, Waldmann H, Huster D. Membrane binding of lipidated Ras peptides and proteins - The structural point of view Biochimica Et Biophysica Acta - Biomembranes. 1788: 273-288. PMID 18771652 DOI: 10.1016/J.Bbamem.2008.08.006 |
0.748 |
|
2009 |
Triola G, Wetzel S, Ellinger B, Koch MA, Hübel K, Rauh D, Waldmann H. ATP competitive inhibitors of d-alanine-d-alanine ligase based on protein kinase inhibitor scaffolds Bioorganic and Medicinal Chemistry. 17: 1079-1087. PMID 18321716 DOI: 10.1016/J.Bmc.2008.02.046 |
0.312 |
|
2009 |
KUNZ H, WALDMANN H, UNVERZAGT C. Allyl ester as temporary protecting group for the β-carboxy function of aspartic acid International Journal of Peptide and Protein Research. 26: 493-497. DOI: 10.1111/J.1399-3011.1985.Tb01016.X |
0.505 |
|
2009 |
Ludolph B, Waldmann H. Solid-phase synthesis of benzodiazepinediones mimicking the C-terminus of the H-Ras protein Tetrahedron Letters. 50: 3148-3150. DOI: 10.1016/J.Tetlet.2009.01.016 |
0.331 |
|
2009 |
Gohlke A, Triola G, Waldmann H, Meister A, Blume A, Winter R. Influence of Lipid Modifications of NRas on the Interaction with different Model Biomembranes and their Orientation at the Lipid Interface Biophysical Journal. 96: 612a. DOI: 10.1016/J.Bpj.2008.12.3239 |
0.496 |
|
2009 |
Vogel A, Reuther G, Tan K, Waldmann H, Brown MF, Feller SE, Huster D. Backbone Conformation and Dynamics of the Lipid-Modified Membrane Anchor of Human N-Ras Investigated by Solid-State NMR and Molecular Dynamics Simulations Biophysical Journal. 96: 198a. DOI: 10.1016/J.Bpj.2008.12.1062 |
0.3 |
|
2009 |
Westerlind U, Schröder H, Hobel A, Gaidzik N, Kaiser A, Niemeyer C, Schmitt E, Waldmann H, Kunz H. Cover Picture: Tumor-Associated MUC1 Tandem-Repeat Glycopeptide Microarrays to Evaluate Serum- and Monoclonal-Antibody Specificity (Angew. Chem. Int. Ed. 44/2009) Angewandte Chemie International Edition. 48: 8151-8151. DOI: 10.1002/Anie.200904924 |
0.401 |
|
2009 |
Westerlind U, Schröder H, Hobel A, Gaidzik N, Kaiser A, Niemeyer C, Schmitt E, Waldmann H, Kunz H. Titelbild: Tumor-Associated MUC1 Tandem-Repeat Glycopeptide Microarrays to Evaluate Serum- and Monoclonal-Antibody Specificity (Angew. Chem. 44/2009) Angewandte Chemie. 121: 8297-8297. DOI: 10.1002/Ange.200904924 |
0.398 |
|
2009 |
Vogel A, Reuther G, Weise K, Triola G, Nikolaus J, Tan K, Nowak C, Herrmann A, Waldmann H, Winter R, Huster D. Die Lipidmodifikationen von Ras passen sich an die Membranumgebung an und beeinflussen die lokale Konzentration Angewandte Chemie. 121: 8942-8945. DOI: 10.1002/Ange.200903396 |
0.443 |
|
2008 |
Jonkheijm P, Weinrich D, Schröder H, Niemeyer CM, Waldmann H. Chemical strategies for generating protein biochips Angewandte Chemie - International Edition. 47: 9618-9647. PMID 19025742 DOI: 10.1002/Anie.200801711 |
0.313 |
|
2008 |
Güldenhaupt J, Adigüzel Y, Kuhlmann J, Waldmann H, Kötting C, Gerwert K. Secondary structure of lipidated Ras bound to a lipid bilayer. The Febs Journal. 275: 5910-8. PMID 19021766 DOI: 10.1111/J.1742-4658.2008.06720.X |
0.314 |
|
2008 |
Waldmann H, He YP, Tan H, Arve L, Arndt HD. Flexible total synthesis of biphenomycin B Chemical Communications. 5562-5564. PMID 18997952 DOI: 10.1039/B811583D |
0.626 |
|
2008 |
Bisek N, Wetzel S, Arndt HD, Waldmann H. Synthesis and conformational analysis of stevastelin C3 analogues and their activity against the dual-specific vaccina H1-related phosphatase Chemistry - a European Journal. 14: 8847-8860. PMID 18767075 DOI: 10.1002/Chem.200800692 |
0.349 |
|
2008 |
Guo Z, Wu YW, Das D, Delon C, Cramer J, Yu S, Thuns S, Lupilova N, Waldmann H, Brunsveld L, Goody RS, Alexandrov K, Blankenfeldt W. Structures of RabGGTase-substrate/product complexes provide insights into the evolution of protein prenylation. The Embo Journal. 27: 2444-56. PMID 18756270 DOI: 10.1038/Emboj.2008.164 |
0.749 |
|
2008 |
Wong E, Okhonin V, Berezovski MV, Nozaki T, Waldmann H, Alexandrov K, Krylov SN. "Inject-mix-react-separate-and-quantitate" (IMReSQ) method for screening enzyme inhibitors. Journal of the American Chemical Society. 130: 11862-3. PMID 18702487 DOI: 10.1021/Ja804544X |
0.308 |
|
2008 |
Govindaraju T, Jonkheijm P, Gogolin L, Schroeder H, Becker CF, Niemeyer CM, Waldmann H. Surface immobilization of biomolecules by click sulfonamide reaction. Chemical Communications (Cambridge, England). 3723-5. PMID 18685756 DOI: 10.1039/B806764C |
0.56 |
|
2008 |
Waldmann H, Khedkar V, Dückert H, Schürmann M, Oppel IM, Kumar K. Asymmetric synthesis of natural product inspired tricyclic benzopyrones by an organocatalyzed annulation reaction Angewandte Chemie - International Edition. 47: 6869-6872. PMID 18661463 DOI: 10.1002/Anie.200802413 |
0.34 |
|
2008 |
Wang Z, Gu C, Colby T, Shindo T, Balamurugan R, Waldmann H, Kaiser M, Van Der Hoorn RAL. β-Lactone probes identify a papain-like peptide ligase in Arabidopsis thaliana Nature Chemical Biology. 4: 557-563. PMID 18660805 DOI: 10.1038/Nchembio.104 |
0.677 |
|
2008 |
Nören-Müller A, Wilk W, Saxena K, Schwalbe H, Kaiser M, Waldmann H. Discovery of a new class of inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B by biology-oriented synthesis. Angewandte Chemie (International Ed. in English). 47: 5973-7. PMID 18604796 DOI: 10.1002/Anie.200801566 |
0.332 |
|
2008 |
Walther T, Arndt HD, Waldmann H. Solid-support based total synthesis and stereochemical correction of brunsvicamide A Organic Letters. 10: 3199-3202. PMID 18590275 DOI: 10.1021/Ol801064D |
0.341 |
|
2008 |
Hübel K, Leßmann T, Waldmann H. Chemical biology - Identification of small molecule modulators of cellular activity by natural product inspired synthesis Chemical Society Reviews. 37: 1361-1374. PMID 18568162 DOI: 10.1039/B704729K |
0.372 |
|
2008 |
Mishra R, Bulic B, Sellin D, Jha S, Waldmann H, Winter R. Small-molecule inhibitors of islet amyloid polypeptide fibril formation Angewandte Chemie - International Edition. 47: 4679-4682. PMID 18470855 DOI: 10.1002/Anie.200705372 |
0.461 |
|
2008 |
Waldmann H, Karunakar GV, Kumar K. Gold(III)-mediated aldol condensations provide efficient access to nitrogen heterocycles Organic Letters. 10: 2159-2162. PMID 18461950 DOI: 10.1021/Ol8005634 |
0.31 |
|
2008 |
Guo Z, Wu YW, Tan KT, Bon RS, Guiu-Rozas E, Delon C, Nguyen TU, Wetzel S, Arndt S, Goody RS, Blankenfeldt W, Alexandrov K, Waldmann H. Development of selective RabGGTase inhibitors and crystal structure of a RabGGTase-inhibitor complex. Angewandte Chemie (International Ed. in English). 47: 3747-50. PMID 18399557 DOI: 10.1002/Anie.200705795 |
0.67 |
|
2008 |
Triola G, Brunsveld L, Waldmann H. Racemization-free synthesis of S-alkylated cysteines via thiol-ene reaction Journal of Organic Chemistry. 73: 3646-3649. PMID 18376863 DOI: 10.1021/Jo800198S |
0.737 |
|
2008 |
Waldmann H, Kühn M, Liu W, Kumar K. Reagent-controlled domino synthesis of skeletally-diverse compound collections Chemical Communications. 1211-1213. PMID 18309420 DOI: 10.1039/B717635J |
0.357 |
|
2008 |
Kaiser M, Wetzel S, Kumar K, Waldmann H. Biology-inspired synthesis of compound libraries Cellular and Molecular Life Sciences. 65: 1186-1201. PMID 18193390 DOI: 10.1007/S00018-007-7492-1 |
0.36 |
|
2008 |
Wetzel S, Renner S, Nören-Müller A, Schuffenhauer A, Ertl P, Waldmann H. BIOS: Similarity-based design of natural product derived compound collections Chemistry Central Journal. 2. DOI: 10.1186/1752-153X-2-S1-P48 |
0.349 |
|
2008 |
Scheck M, Koch MA, Waldmann H. Synthesis of a dysidiolide-inspired compound library and discovery of acetylcholinesterase inhibitors based on protein structure similarity clustering (PSSC) Tetrahedron. 64: 4792-4802. DOI: 10.1016/J.Tet.2008.02.106 |
0.398 |
|
2008 |
Sommer S, Kühn M, Waldmann H. Solid-phase synthesis of [5.5]-spiroketals Advanced Synthesis and Catalysis. 350: 1736-1750. DOI: 10.1002/Adsc.200800154 |
0.347 |
|
2007 |
Broussy S, Waldmann H. Solid phase synthesis of highly substituted tetrahydropyrans by tandem ene-reaction/intramolecular sakurai cyclization Journal of Combinatorial Chemistry. 9: 1138-1143. PMID 17935301 DOI: 10.1021/Cc7001099 |
0.34 |
|
2007 |
Corrêa IR, Nören-Müller A, Ambrosi HD, Jakupovic S, Saxena K, Schwalbe H, Kaiser M, Waldmann H. Identification of inhibitors for mycobacterial protein tyrosine phosphatase B (MptpB) by biology-oriented synthesis (BIOS). Chemistry, An Asian Journal. 2: 1109-26. PMID 17685373 DOI: 10.1002/Asia.200700125 |
0.424 |
|
2007 |
Wu YW, Tan KT, Waldmann H, Goody RS, Alexandrov K. Interaction analysis of prenylated Rab GTPase with Rab escort protein and GDP dissociation inhibitor explains the need for both regulators. Proceedings of the National Academy of Sciences of the United States of America. 104: 12294-9. PMID 17640890 DOI: 10.1073/Pnas.0701817104 |
0.337 |
|
2007 |
Ulaczyk-Lesanko A, Pelletier E, Lee M, Prinz H, Waldmann H, Hall DG. Optimization of three- and four-component reactions for polysubstituted piperidines: application to the synthesis and preliminary biological screening of a prototype library. Journal of Combinatorial Chemistry. 9: 695-703. PMID 17521171 DOI: 10.1021/Cc0700344 |
0.339 |
|
2007 |
Lessmann T, Leuenberger MG, Menninger S, Lopez-Canet M, Müller O, Hümmer S, Bormann J, Korn K, Fava E, Zerial M, Mayer TU, Waldmann H. Natural product-derived modulators of cell cycle progression and viral entry by enantioselective oxa Diels-Alder reactions on the solid phase. Chemistry & Biology. 14: 443-51. PMID 17462579 DOI: 10.1016/J.Chembiol.2007.02.008 |
0.374 |
|
2007 |
Umarye JD, Leßmann T, García AB, Mamane V, Sommer S, Waldmann H. Biology-oriented synthesis of stereochemically diverse natural-product- derived compound collections by iterative allylations on a solid support Chemistry - a European Journal. 13: 3305-3319. PMID 17310497 DOI: 10.1002/Chem.200601698 |
0.363 |
|
2007 |
Nguyen UT, Cramer J, Gomis J, Reents R, Gutierrez-Rodriguez M, Goody RS, Alexandrov K, Waldmann H. Exploiting the substrate tolerance of farnesyltransferase for site-selective protein derivatization. Chembiochem : a European Journal of Chemical Biology. 8: 408-23. PMID 17279592 DOI: 10.1002/Cbic.200600440 |
0.359 |
|
2007 |
de Araújo AD, Palomo JM, Cramer J, Seitz O, Alexandrov K, Waldmann H. Diels-Alder ligation of peptides and proteins. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 6095-109. PMID 16807971 DOI: 10.1002/Chem.200600148 |
0.562 |
|
2007 |
Wetzel S, Schuffenhauer A, Roggo S, Ertl P, Waldmann H. Cheminformatic analysis of natural products and their chemical space Chimia. 61: 355-360. DOI: 10.2533/Chimia.2007.355 |
0.3 |
|
2007 |
Hu TS, Tannert R, Arndt HD, Waldmann H. Solid-phase based synthesis of jasplakinolide analogs by intramolecular azide-alkyne cycloadditions Chemical Communications. 3942-3944. DOI: 10.1039/B710650E |
0.335 |
|
2007 |
Mamane V, García AB, Umarye JD, Lessmann T, Sommer S, Waldmann H. Stereoselective allylation of aldehydes on solid support and its application in biology-oriented synthesis (BIOS) Tetrahedron. 63: 5754-5767. DOI: 10.1016/J.Tet.2007.01.041 |
0.354 |
|
2007 |
Umarye J, Leßmann T, García A, Mamane V, Sommer S, Waldmann H. Cover Picture: Biology-Oriented Synthesis of Stereochemically Diverse Natural-Product-Derived Compound Collections by Iterative Allylations on a Solid Support (Chem. Eur. J. 12/2007) Chemistry - a European Journal. 13: 3277-3277. DOI: 10.1002/Chem.200790036 |
0.351 |
|
2006 |
Garcia AB, Lessmann T, Umarye JD, Mamane V, Sommer S, Waldmann H. Stereocomplementary synthesis of a natural product-derived compound collection on a solid phase. Chemical Communications (Cambridge, England). 3868-70. PMID 17268653 DOI: 10.1039/B607816H |
0.319 |
|
2006 |
Reuther G, Tan KT, Vogel A, Nowak C, Arnold K, Kuhlmann J, Waldmann H, Huster D. The lipidated membrane anchor of full length N-Ras protein shows an extensive dynamics as revealed by solid-state NMR spectroscopy. Journal of the American Chemical Society. 128: 13840-6. PMID 17044712 DOI: 10.1021/Ja063635S |
0.338 |
|
2006 |
Brunsveld L, Kuhlmann J, Alexandrov K, Wittinghofer A, Goody RS, Waldmann H. Lipidated ras and rab peptides and proteins--synthesis, structure, and function. Angewandte Chemie (International Ed. in English). 45: 6622-46. PMID 17031879 DOI: 10.1002/Anie.200600855 |
0.763 |
|
2006 |
Brunsveld L, Kuhlmann J, Waldmann H. Synthesis of palmitoylated Ras-peptides and -proteins. Methods (San Diego, Calif.). 40: 151-65. PMID 17012027 DOI: 10.1016/J.Ymeth.2006.04.014 |
0.745 |
|
2006 |
Gelb MH, Brunsveld L, Hrycyna CA, Michaelis S, Tamanoi F, Van Voorhis WC, Waldmann H. Therapeutic intervention based on protein prenylation and associated modifications. Nature Chemical Biology. 2: 518-28. PMID 16983387 DOI: 10.1038/Nchembio818 |
0.74 |
|
2006 |
Lessmann T, Waldmann H. Enantioselective synthesis on the solid phase. Chemical Communications (Cambridge, England). 3380-9. PMID 16896470 DOI: 10.1039/B602822E |
0.349 |
|
2006 |
Müller D, Krick A, Kehraus S, Mehner C, Hart M, Küpper FC, Saxena K, Prinz H, Schwalbe H, Janning P, Waldmann H, König GM. Brunsvicamides A-C: sponge-related cyanobacterial peptides with Mycobacterium tuberculosis protein tyrosine phosphatase inhibitory activity. Journal of Medicinal Chemistry. 49: 4871-8. PMID 16884299 DOI: 10.1021/Jm060327W |
0.331 |
|
2006 |
Reuther G, Tan KT, Köhler J, Nowak C, Pampel A, Arnold K, Kuhlmann J, Waldmann H, Huster D. Structural model of the membrane-bound C terminus of lipid-modified human N-ras protein. Angewandte Chemie (International Ed. in English). 45: 5387-90. PMID 16847854 DOI: 10.1002/Anie.200504266 |
0.308 |
|
2006 |
Nören-Müller A, Reis-Corrêa I, Prinz H, Rosenbaum C, Saxena K, Schwalbe HJ, Vestweber D, Cagna G, Schunk S, Schwarz O, Schiewe H, Waldmann H. Discovery of protein phosphatase inhibitor classes by biology-oriented synthesis. Proceedings of the National Academy of Sciences of the United States of America. 103: 10606-11. PMID 16809424 DOI: 10.1073/Pnas.0601490103 |
0.81 |
|
2006 |
Meister A, Nicolini C, Waldmann H, Kuhlmann J, Kerth A, Winter R, Blume A. Insertion of lipidated Ras proteins into lipid monolayers studied by infrared reflection absorption spectroscopy (IRRAS). Biophysical Journal. 91: 1388-401. PMID 16731561 DOI: 10.1529/Biophysj.106.084624 |
0.515 |
|
2006 |
Seibert SF, Eguereva E, Krick A, Kehraus S, Voloshina E, Raabe G, Fleischhauer J, Leistner E, Wiese M, Prinz H, Alexandrov K, Janning P, Waldmann H, König GM. Polyketides from the marine-derived fungus Ascochyta salicorniae and their potential to inhibit protein phosphatases. Organic & Biomolecular Chemistry. 4: 2233-40. PMID 16729132 DOI: 10.1039/B601386D |
0.307 |
|
2006 |
Watzke A, Gutierrez-Rodriguez M, Köhn M, Wacker R, Schroeder H, Breinbauer R, Kuhlmann J, Alexandrov K, Niemeyer CM, Goody RS, Waldmann H. A generic building block for C- and N-terminal protein-labeling and protein-immobilization. Bioorganic & Medicinal Chemistry. 14: 6288-306. PMID 16725326 DOI: 10.1016/J.Bmc.2006.05.006 |
0.345 |
|
2006 |
Basu S, Waldmann H. Regioselectivity in the formation of small- and medium-sized cyclic ethers by diene-ene ring-closing metathesis. The Journal of Organic Chemistry. 71: 3977-9. PMID 16674078 DOI: 10.1021/Jo052367Y |
0.625 |
|
2006 |
Biel M, Deck P, Giannis A, Waldmann H. Synthesis and evaluation of acyl protein thioesterase 1 (APT1) inhibitors. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 4121-43. PMID 16528788 DOI: 10.1002/Chem.200501128 |
0.364 |
|
2006 |
Dursina B, Reents R, Delon C, Wu Y, Kulharia M, Thutewohl M, Veligodsky A, Kalinin A, Evstifeev V, Ciobanu D, Szedlacsek SE, Waldmann H, Goody RS, Alexandrov K. Identification and specificity profiling of protein prenyltransferase inhibitors using new fluorescent phosphoisoprenoids. Journal of the American Chemical Society. 128: 2822-35. PMID 16506760 DOI: 10.1021/Ja052196E |
0.365 |
|
2006 |
Goody RS, Durek T, Waldmann H, Brunsveld L, Alexandrov K. Application of protein semisynthesis for the construction of functionalized posttranslationally modified rab GTPases. Methods in Enzymology. 403: 29-42. PMID 16473575 DOI: 10.1016/S0076-6879(05)03004-1 |
0.762 |
|
2006 |
Pylypenko O, Rak A, Durek T, Kushnir S, Dursina BE, Thomae NH, Constantinescu AT, Brunsveld L, Watzke A, Waldmann H, Goody RS, Alexandrov K. Structure of doubly prenylated Ypt1:GDI complex and the mechanism of GDI-mediated Rab recycling. The Embo Journal. 25: 13-23. PMID 16395334 DOI: 10.1038/Sj.Emboj.7600921 |
0.741 |
|
2006 |
Gottlieb D, Grunwald C, Nowak C, Kuhlmann J, Waldmann H. Intein-mediated in vitro synthesis of lipidated Ras proteins. Chemical Communications (Cambridge, England). 260-2. PMID 16391727 DOI: 10.1039/B511736D |
0.339 |
|
2006 |
Nicolini C, Baranski J, Schlummer S, Palomo J, Lumbierres-Burgues M, Kahms M, Kuhlmann J, Sanchez S, Gratton E, Waldmann H, Winter R. Visualizing association of N-ras in lipid microdomains: influence of domain structure and interfacial adsorption. Journal of the American Chemical Society. 128: 192-201. PMID 16390147 DOI: 10.1021/Ja055779X |
0.471 |
|
2006 |
Lumbierres M, Palomo JM, Kragol G, Roehrs S, Müller O, Waldmann H. Solid-phase synthesis of lipidated peptides. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 7405-15. PMID 16193522 DOI: 10.1002/Chem.200500476 |
0.329 |
|
2006 |
Bialy L, Waldmann H. Inhibitors of protein tyrosine phosphatases: next-generation drugs? Angewandte Chemie (International Ed. in English). 44: 3814-39. PMID 15900534 DOI: 10.1002/Anie.200461517 |
0.338 |
|
2006 |
Brunsveld L, Watzke A, Durek T, Alexandrov K, Goody RS, Waldmann H. Synthesis of functionalized rab GTPases by a combination of solution- or solid-phase lipopeptide synthesis with expressed protein ligation. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 2756-72. PMID 15729676 DOI: 10.1002/Chem.200401041 |
0.752 |
|
2006 |
Lumbierres M, Palomo JM, Kragol G, Waldmann H. Solid-phase synthesis of palmitoylated and farnesylated lipopeptides employing the fluoride-labile PTMSEL linker Tetrahedron Letters. 47: 2671-2674. DOI: 10.1016/J.Tetlet.2006.02.109 |
0.3 |
|
2006 |
Arve L, Voigt T, Waldmann H. Charting Biological and Chemical Space: PSSC and SCONP as Guiding Principles for the Development of Compound Collections Based on Natural Product Scaffolds. Cheminform. 37. DOI: 10.1002/Qsar.200540213 |
0.599 |
|
2006 |
Arve L, Voigt T, Waldmann H. Charting biological and chemical space: PSSC and SCONP as guiding principles for the development of compound collections based on natural product scaffolds Qsar and Combinatorial Science. 25: 449-456. DOI: 10.1002/qsar.200540213 |
0.506 |
|
2006 |
Röttger S, Waldmann H. Solid-Phase Synthesis of Decalin Scaffolds by Robinson Annulation with Immobilised Nazarov Reagents European Journal of Organic Chemistry. 2006: 2093-2099. DOI: 10.1002/Ejoc.200500917 |
0.339 |
|
2006 |
Brunsveld L, Kuhlmann J, Alexandrov K, Wittinghofer A, Goody RS, Waldmann H. Lipidierte Ras- und Rab-Peptide und -Proteine: Synthese, Struktur und Funktion Angewandte Chemie. 118: 6774-6798. DOI: 10.1002/Ange.200600855 |
0.303 |
|
2006 |
Sanz MA, Voigt T, Waldmann H. Enantioselective catalysis on the solid phase: Synthesis of natural product-derived tetrahydropyrans employing the enantioselective oxa-Diels-Alder reaction Advanced Synthesis and Catalysis. 348: 1511-1515. DOI: 10.1002/Adsc.200606026 |
0.574 |
|
2005 |
Balamurugan R, Dekker FJ, Waldmann H. Design of compound libraries based on natural product scaffolds and protein structure similarity clustering (PSSC). Molecular Biosystems. 1: 36-45. PMID 16880961 DOI: 10.1039/B503623B |
0.705 |
|
2005 |
Koch MA, Schuffenhauer A, Scheck M, Wetzel S, Casaulta M, Odermatt A, Ertl P, Waldmann H. Charting biologically relevant chemical space: a structural classification of natural products (SCONP). Proceedings of the National Academy of Sciences of the United States of America. 102: 17272-7. PMID 16301544 DOI: 10.1073/Pnas.0503647102 |
0.347 |
|
2005 |
Sommer S, Waldmann H. Solid phase synthesis of a spiro[5.5]ketal library. Chemical Communications (Cambridge, England). 5684-6. PMID 16292390 DOI: 10.1039/B511177C |
0.368 |
|
2005 |
Weide T, Arve L, Prinz H, Waldmann H, Kessler H. 3-Substituted indolizine-1-carbonitrile derivatives as phosphatase inhibitors. Bioorganic & Medicinal Chemistry Letters. 16: 59-63. PMID 16236508 DOI: 10.1016/J.Bmcl.2005.09.051 |
0.348 |
|
2005 |
Manger M, Scheck M, Prinz H, von Kries JP, Langer T, Saxena K, Schwalbe H, Fürstner A, Rademann J, Waldmann H. Discovery of Mycobacterium tuberculosis protein tyrosine phosphatase A (MptpA) inhibitors based on natural products and a fragment-based approach. Chembiochem : a European Journal of Chemical Biology. 6: 1749-53. PMID 16196020 DOI: 10.1002/Cbic.200500171 |
0.353 |
|
2005 |
Vogel A, Katzka CP, Waldmann H, Arnold K, Brown MF, Huster D. Lipid modifications of a Ras peptide exhibit altered packing and mobility versus host membrane as detected by 2H solid-state NMR. Journal of the American Chemical Society. 127: 12263-72. PMID 16131204 DOI: 10.1021/Ja051856C |
0.321 |
|
2005 |
Deck P, Pendzialek D, Biel M, Wagner M, Popkirova B, Ludolph B, Kragol G, Kuhlmann J, Giannis A, Waldmann H. Development and biological evaluation of acyl protein thioesterase 1 (APT1) inhibitors. Angewandte Chemie (International Ed. in English). 44: 4975-80. PMID 16003812 DOI: 10.1002/Anie.200462625 |
0.34 |
|
2005 |
Dekker FJ, Koch MA, Waldmann H. Protein structure similarity clustering (PSSC) and natural product structure as inspiration sources for drug development and chemical genomics. Current Opinion in Chemical Biology. 9: 232-9. PMID 15939324 DOI: 10.1016/J.Cbpa.2005.03.003 |
0.375 |
|
2005 |
Koch MA, Waldmann H. Protein structure similarity clustering and natural product structure as guiding principles in drug discovery. Drug Discovery Today. 10: 471-83. PMID 15809193 DOI: 10.1016/S1359-6446(05)03419-7 |
0.353 |
|
2005 |
Watzke A, Brunsveld L, Durek T, Alexandrov K, Rak A, Goody RS, Waldmann H. Chemical biology of protein lipidation: semi-synthesis and structure elucidation of prenylated RabGTPases. Organic & Biomolecular Chemistry. 3: 1157-64. PMID 15785799 DOI: 10.1039/B417573E |
0.764 |
|
2005 |
Rosenbaum C, Röhrs S, Müller O, Waldmann H. Modulation of MRP-1-mediated multidrug resistance by indomethacin analogues. Journal of Medicinal Chemistry. 48: 1179-87. PMID 15715484 DOI: 10.1021/Jm0499099 |
0.315 |
|
2005 |
Reents R, Wagner M, Schlummer S, Kuhlmann J, Waldmann H. Synthesis and application of fluorescent ras proteins for live-cell imaging. Chembiochem : a European Journal of Chemical Biology. 6: 86-94. PMID 15637662 DOI: 10.1002/Cbic.200400233 |
0.341 |
|
2005 |
Durek T, Alexandrov K, Goody RS, Hildebrand A, Heinemann I, Waldmann H. Synthesis of fluorescently labeled mono- and diprenylated Rab7 GTPase. Journal of the American Chemical Society. 126: 16368-78. PMID 15600338 DOI: 10.1021/Ja046164N |
0.366 |
|
2005 |
Dursina BE, Reents R, Niculae A, Veligodsky A, Breitling R, Pyatkov K, Waldmann H, Goody RS, Alexandrov K. A genetically encodable microtag for chemo-enzymatic derivatization and purification of recombinant proteins. Protein Expression and Purification. 39: 71-81. PMID 15596362 DOI: 10.1016/J.Pep.2004.09.015 |
0.35 |
|
2005 |
Bialy L, Waldmann H. Total synthesis and biological evaluation of the protein phosphatase 2A inhibitor cytostatin and analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 2759-80. PMID 15195307 DOI: 10.1002/Chem.200305543 |
0.381 |
|
2005 |
Barun O, Kumar K, Sommer S, Langerak A, Mayer TU, Müller O, Waldmann H. Cover Picture: Natural Product-Guided Synthesis of a Spiroacetal Collection Reveals Modulators of Tubulin Cytoskeleton Integrity (Eur. J. Org. Chem. 22/2005) European Journal of Organic Chemistry. 2005: 4731-4731. DOI: 10.1002/Ejoc.200590044 |
0.363 |
|
2005 |
Barun O, Kumar K, Sommer S, Langerak A, Mayer TU, Müller O, Waldmann H. Natural Product-Guided Synthesis of a Spiroacetal Collection Reveals Modulators of Tubulin Cytoskeleton Integrity European Journal of Organic Chemistry. 2005: 4773-4788. DOI: 10.1002/Ejoc.200500605 |
0.394 |
|
2004 |
Koch MA, Wittenberg LO, Basu S, Jeyaraj DA, Gourzoulidou E, Reinecke K, Odermatt A, Waldmann H. Compound library development guided by protein structure similarity clustering and natural product structure. Proceedings of the National Academy of Sciences of the United States of America. 101: 16721-6. PMID 15548605 DOI: 10.1073/Pnas.0404719101 |
0.677 |
|
2004 |
Fürstner A, Reinecke K, Prinz H, Waldmann H. The core structures of roseophilin and the prodigiosin alkaloids define a new class of protein tyrosine phosphatase inhibitors Chembiochem. 5: 1575-1579. PMID 15515092 DOI: 10.1002/Cbic.200400135 |
0.517 |
|
2004 |
Soulère L, Aldrich C, Daumke O, Gail R, Kissau L, Wittinghofer A, Waldmann H. Synthesis of GTP-derived Ras ligands Chembiochem. 5: 1448-1453. PMID 15457534 DOI: 10.1002/Cbic.200400133 |
0.564 |
|
2004 |
Janosch S, Nicolini C, Ludolph B, Peters C, Völkert M, Hazlet TL, Gratton E, Waldmann H, Winter R. Partitioning of dual-lipidated peptides into membrane microdomains: lipid sorting vs peptide aggregation. Journal of the American Chemical Society. 126: 7496-503. PMID 15198596 DOI: 10.1021/Ja049922I |
0.481 |
|
2004 |
Peters C, Wolf A, Wagner M, Kuhlmann J, Waldmann H. The cholesterol membrane anchor of the Hedgehog protein confers stable membrane association to lipid-modified proteins. Proceedings of the National Academy of Sciences of the United States of America. 101: 8531-6. PMID 15163793 DOI: 10.1073/Pnas.0308449101 |
0.346 |
|
2004 |
Fürstner A, Ruiz-Caro J, Prinz H, Waldmann H. Structure Assignment, Total Synthesis, and Evaluation of the Phosphatase Modulating Activity of Glucolipsin A Journal of Organic Chemistry. 69: 459-467. PMID 14725460 DOI: 10.1021/Jo035079F |
0.523 |
|
2004 |
Rosenbaum C, Baumhof P, Mazitschek R, Müller O, Giannis A, Waldmann H. Synthesis and biological evaluation of an indomethacin library reveals a new class of angiogenesis-related kinase inhibitors. Angewandte Chemie (International Ed. in English). 43: 224-8. PMID 14695616 DOI: 10.1002/Anie.200352582 |
0.333 |
|
2004 |
Rosenbaum C, Katzka C, Marzinzik A, Waldmann H. Traceless Fischer indole synthesis on the solid phase. Chemical Communications (Cambridge, England). 1822-3. PMID 12931984 DOI: 10.1039/B305497G |
0.321 |
|
2004 |
Waldmann H. At the crossroads of chemistry and biology. Bioorganic & Medicinal Chemistry. 11: 3045-51. PMID 12818666 DOI: 10.1016/S0968-0896(03)00266-9 |
0.33 |
|
2004 |
Thutewohl M, Waldmann H. Solid-phase synthesis of a pepticinnamin E library. Bioorganic & Medicinal Chemistry. 11: 2591-615. PMID 12757726 DOI: 10.1016/S0968-0896(03)00159-7 |
0.353 |
|
2004 |
Fürstner A, Feyen F, Prinz H, Waldmann H. Synthesis and evaluation of the antitumor agent TMC-69-6H and a focused library of analogs Tetrahedron. 60: 9543-9558. DOI: 10.1016/J.Tet.2004.06.139 |
0.567 |
|
2004 |
Reents R, Wagner M, Kuhlmann J, Waldmann H. Synthese und Anwendung fluoreszenzmarkierter Ras-Proteine in der Bildgebung lebender Zellen Angewandte Chemie. 116: 2765-2768. DOI: 10.1002/Ange.200353265 |
0.303 |
|
2003 |
Fürstner A, Feyen F, Prinz H, Waldmann H. Total Synthesis and Reassessment of the Phosphatase-Inhibitory Activity of the Antitumor Agent TMC-69-6H Angewandte Chemie - International Edition. 42: 5361-5364. PMID 14613177 DOI: 10.1002/Anie.200352268 |
0.472 |
|
2003 |
Rak A, Pylypenko O, Durek T, Watzke A, Kushnir S, Brunsveld L, Waldmann H, Goody RS, Alexandrov K. Structure of Rab GDP-dissociation inhibitor in complex with prenylated YPT1 GTPase. Science (New York, N.Y.). 302: 646-50. PMID 14576435 DOI: 10.1126/Science.1087761 |
0.747 |
|
2003 |
Völkert M, Uwai K, Tebbe A, Popkirova B, Wagner M, Kuhlmann J, Waldmann H. Synthesis and biological activity of photoactivatable N-ras peptides and proteins. Journal of the American Chemical Society. 125: 12749-58. PMID 14558822 DOI: 10.1021/Ja036178D |
0.364 |
|
2003 |
Koch MA, Breinbauer R, Waldmann H. Protein structure similarity as guiding principle for combinatorial library design. Biological Chemistry. 384: 1265-72. PMID 14515987 DOI: 10.1515/Bc.2003.140 |
0.338 |
|
2003 |
Ludolph B, Waldmann H. The synthesis of acid- and base-labile lipopeptides on solid support. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 3683-91. PMID 12898695 DOI: 10.1002/Chem.200304822 |
0.339 |
|
2003 |
Stieber F, Grether U, Mazitschek R, Soric N, Giannis A, Waldmann H. Multistep solid-phase synthesis of an antibiotic and receptor tyrosine kinase inhibitors using the traceless phenylhydrazide linker. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 3282-91. PMID 12866072 DOI: 10.1002/Chem.200304821 |
0.319 |
|
2003 |
Stieber F, Grether U, Waldmann H. Development of the traceless phenylhydrazide linker for solid-phase synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 3270-81. PMID 12866071 DOI: 10.1002/Chem.200304820 |
0.347 |
|
2003 |
Kissau L, Stahl P, Mazitschek R, Giannis A, Waldmann H. Development of natural product-derived receptor tyrosine kinase inhibitors based on conservation of protein domain fold. Journal of Medicinal Chemistry. 46: 2917-31. PMID 12825933 DOI: 10.1021/Jm0307943 |
0.359 |
|
2003 |
Thutewohl M, Kissau L, Popkirova B, Karaguni IM, Nowak T, Bate M, Kuhlmann J, Müller O, Waldmann H. Identification of mono- and bisubstrate inhibitors of protein farnesyltransferase and inducers of apoptosis from a pepticinnamin E library. Bioorganic & Medicinal Chemistry. 11: 2617-26. PMID 12757727 DOI: 10.1016/S0968-0896(03)00160-3 |
0.358 |
|
2003 |
Huster D, Vogel A, Katzka C, Scheidt HA, Binder H, Dante S, Gutberlet T, Zschörnig O, Waldmann H, Arnold K. Membrane insertion of a lipidated ras peptide studied by FTIR, solid-state NMR, and neutron diffraction spectroscopy Journal of the American Chemical Society. 125: 4070-4079. PMID 12670227 DOI: 10.1021/Ja0289245 |
0.305 |
|
2003 |
Brohm D, Metzger S, Bhargava A, Müller O, Lieb F, Waldmann H. Natural products are biologically validated starting points in structural space for compound library development: solid-phase synthesis of dysidiolide-derived phosphatase inhibitors. Angewandte Chemie (International Ed. in English). 41: 307-11. PMID 12491416 DOI: 10.1002/1521-3773(20020118)41:2<307::Aid-Anie307>3.0.Co;2-1 |
0.356 |
|
2003 |
Reents R, Jeyaraj DA, Waldmann H. Enzymatically cleavable linker groups in polymer-supported synthesis. Drug Discovery Today. 7: 71-6. PMID 11790606 DOI: 10.1016/S1359-6446(01)02088-8 |
0.318 |
|
2003 |
Bialy L, Waldmann H. Synthesis and Biological Evaluation of Cytostatin Analogues. Cheminform. 34. DOI: 10.1039/B305308N |
0.334 |
|
2003 |
Waldmann H. Synthesis of Calicheamitin γ1I Organic Synthesis Set. 371-380. DOI: 10.1002/9783527620784.Ch39A |
0.331 |
|
2003 |
Waldmann H. Synthesis of Mitomycins Organic Synthesis Set. 309-314. DOI: 10.1002/9783527620784.Ch33A |
0.33 |
|
2003 |
Waldmann H. Synthesis of O‐Glycosides Organic Synthesis Set. 289-299. DOI: 10.1002/9783527620784.Ch31A |
0.331 |
|
2003 |
Waldmann H. Chapter 23. General Methods and Reagents for Organic Synthesis: Domino Reactions Organic Synthesis Set. 193-202. DOI: 10.1002/9783527620784.Ch23A |
0.303 |
|
2003 |
Waldmann H. Enzymatic Synthesis of O‐Glycosides Organic Synthesis Set. 157-166. DOI: 10.1002/9783527620784.Ch18A |
0.344 |
|
2002 |
Breinbauer R, Manger M, Scheck M, Waldmann H. Natural product guided compound library development. Current Medicinal Chemistry. 9: 2129-45. PMID 12470251 DOI: 10.2174/0929867023368773 |
0.339 |
|
2002 |
Peters C, Wagner M, Völkert M, Waldmann H. Bridging the gap between cell biology and organic chemistry: chemical synthesis and biological application of lipidated peptides and proteins. Die Naturwissenschaften. 89: 381-90. PMID 12435088 DOI: 10.1007/S00114-002-0354-7 |
0.394 |
|
2002 |
Brohm D, Philippe N, Metzger S, Bhargava A, Müller O, Lieb F, Waldmann H. Solid-phase synthesis of dysidiolide-derived protein phosphatase inhibitors. Journal of the American Chemical Society. 124: 13171-8. PMID 12405845 DOI: 10.1021/Ja027609F |
0.411 |
|
2002 |
Völkert M, Koul S, Müller GH, Lehnig M, Waldmann H. Phenylhydrazide as an enzyme-labile protecting group in peptide synthesis. The Journal of Organic Chemistry. 67: 6902-10. PMID 12353981 DOI: 10.1021/Jo0259966 |
0.686 |
|
2002 |
Kuhlmann J, Tebbe A, Völkert M, Wagner M, Uwai K, Waldmann H. Photoactivatable synthetic Ras proteins: "Baits" for the identification of plasma-membrane-bound binding partners of Ras Angewandte Chemie - International Edition. 41: 2546-2550. PMID 12203529 DOI: 10.1002/1521-3773(20020715)41:14<2546::Aid-Anie2546>3.0.Co;2-E |
0.335 |
|
2002 |
Breinbauer R, Vetter IR, Waldmann H. From protein domains to drug candidates-natural products as guiding principles in the design and synthesis of compound libraries. Angewandte Chemie (International Ed. in English). 41: 2879-90. PMID 12203413 DOI: 10.1002/1521-3773(20020816)41:16<2878::Aid-Anie2878>3.0.Co;2-B |
0.398 |
|
2002 |
Eisele F, Kuhlmann J, Waldmann H. Synthesis and membrane binding properties of a lipopeptide fragment from influenza virus A hemagglutinin Chemistry - a European Journal. 8: 3362-3376. PMID 12203317 DOI: 10.1002/1521-3765(20020802)8:15<3362::Aid-Chem3362>3.0.Co;2-0 |
0.314 |
|
2002 |
Ludolph B, Eisele F, Waldmann H. Solid-phase synthesis of lipidated peptides. Journal of the American Chemical Society. 124: 5954-5. PMID 12022824 DOI: 10.1021/Ja025768T |
0.332 |
|
2002 |
Alexandrov K, Heinemann I, Durek T, Sidorovitch V, Goody RS, Waldmann H. Intein-mediated synthesis of geranylgeranylated Rab7 protein in vitro. Journal of the American Chemical Society. 124: 5648-9. PMID 12010032 DOI: 10.1021/Ja017799E |
0.373 |
|
2002 |
Jeyaraj DA, Prinz H, Waldmann H. Synthesis of nucleopeptides by employing an enzyme-labile urethane protecting group. Chemistry: a European Journal. 8: 1879-1887. PMID 12007098 DOI: 10.1002/1521-3765(20020415)8:8<1879::Aid-Chem1879>3.0.Co;2-5 |
0.336 |
|
2002 |
Scheck M, Waldmann H. Chemo-enzymatic synthesis of the C15C23 unit of Leptomycin B Canadian Journal of Chemistry. 80: 571-576. DOI: 10.1139/V02-070 |
0.333 |
|
2002 |
Brohm D, Metzger S, Bhargava A, Müller O, Lieb F, Waldmann H. Naturstoffe sind biologisch validierte Startpunkte im Strukturraum zur Entwicklung von Substanzbibliotheken: Festphasensynthese von Analoga des Protein-Phosphatase-Inhibitors Dysidiolid Angewandte Chemie. 114: 319-323. DOI: 10.1002/1521-3757(20020118)114:2<319::Aid-Ange319>3.0.Co;2-E |
0.306 |
|
2001 |
Stahl P, Kissau L, Mazitschek R, Huwe A, Furet P, Giannis A, Waldmann H. Total synthesis and biological evaluation of the nakijiquinones. Journal of the American Chemical Society. 123: 11586-93. PMID 11716712 DOI: 10.1021/Ja011413I |
0.363 |
|
2001 |
Völkert M, Wagner M, Peters C, Waldmann H. The chemical biology of Ras lipidation. Biological Chemistry. 382: 1133-1145. PMID 11592394 DOI: 10.1515/Bc.2001.143 |
0.381 |
|
2001 |
Nazaré M, Waldmann H. Enantiospecific synthesis of the (9S,18R)-diastereomer of the leukocyte adhesion inhibitor cyclamenol A. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 3363-76. PMID 11531123 DOI: 10.1002/1521-3765(20010803)7:15<3363::Aid-Chem3363>3.0.Co;2-Y |
0.368 |
|
2001 |
Machauer R, Waldmann H. Synthesis of lipidated eNOS peptides by combining enzymatic, noble metal- and acid-mediated protecting group techniques with solid phase peptide synthesis and fragment condensation in solution. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 2940-56. PMID 11486971 DOI: 10.1002/1521-3765(20010702)7:13<2933::Aid-Chem2933>3.0.Co;2-E |
0.359 |
|
2001 |
Kuhn K, Owen DJ, Bader B, Wittinghofer A, Kuhlmann J, Waldmann H. Synthesis of functional ras lipoproteins and fluorescent derivatives Journal of the American Chemical Society. 123: 1023-1035. PMID 11456655 DOI: 10.1021/Ja002723O |
0.37 |
|
2001 |
Kadereit D, Deck P, Heinemann I, Waldmann H. Acid-labile protecting groups for the synthesis of lipidated peptides. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 1184-93. PMID 11322544 DOI: 10.1002/1521-3765(20010316)7:6<1184::Aid-Chem1184>3.0.Co;2-5 |
0.344 |
|
2001 |
Grether U, Waldmann H. An enzyme-labile safety catch linker for synthesis on a soluble polymeric support. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 959-71. PMID 11303876 DOI: 10.1002/1521-3765(20010302)7:5<959::Aid-Chem959>3.0.Co;2-K |
0.311 |
|
2001 |
Huttenloch O, Spieler J, Waldmann H. Chiral bicyclic phosphoramidites--a new class of ligands for asymmetric catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 671-5. PMID 11261665 DOI: 10.1002/1521-3765(20010202)7:3<671::Aid-Chem671>3.0.Co;2-M |
0.308 |
|
2001 |
Thomä NH, Iakovenko A, Kalinin A, Waldmann H, Goody RS, Alexandrov K. Allosteric regulation of substrate binding and product release in geranylgeranyltransferase type II. Biochemistry. 40: 268-74. PMID 11141079 DOI: 10.1021/Bi002034P |
0.311 |
|
2001 |
Meseguer B, Alonso-Díaz D, Griebenow N, Herget T, Waldmann H. Solid-phase synthesis and biological evaluation of a teleocidin library--discovery of a selective PKCdelta down regulator. Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 3943-57. PMID 11126955 DOI: 10.1002/1521-3765(20001103)6:21<3943::Aid-Chem3943>3.3.Co;2-K |
0.389 |
|
2001 |
Seitz O, Heinemann I, Mattes A, Waldmann H. Synthetic peptide conjugates - Tailor-made probes for the biology of protein modification and protein processing Tetrahedron. 57: 2247-2277. DOI: 10.1016/S0040-4020(00)01115-7 |
0.538 |
|
2001 |
Reents R, Jeyaraj D, Waldmann H. Biocatalysis in Polymer-Supported Synthesis: Enzyme-Labile Linker Groups Advanced Synthesis & Catalysis. 343: 501-513. DOI: 10.1002/1615-4169(200108)343:6/7<501::Aid-Adsc501>3.0.Co;2-D |
0.342 |
|
2000 |
Wittinghofer A, Waldmann H. Ras-A Molecular Switch Involved in Tumor Formation. Angewandte Chemie (International Ed. in English). 39: 4192-4214. PMID 29711921 DOI: 10.1002/1521-3773(20001201)39:23<4192::Aid-Anie4192>3.0.Co;2-Y |
0.301 |
|
2000 |
Kadereit D, Kuhlmann J, Waldmann H. Linking the fields--the interplay of organic synthesis, biophysical chemistry, and cell biology in the chemical biology of protein lipidation Chembiochem : a European Journal of Chemical Biology. 1: 144-169. PMID 11828408 DOI: 10.1002/1439-7633(20001002)1:3<144::Aid-Cbic144>3.0.Co;2-D |
0.386 |
|
2000 |
Gum AG, Kappes-Roth T, Waldmann H. Enzyme-labile protecting groups in peptide synthesis: development of glucose- and galactose-derived urethanes. Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 3714-21. PMID 11073241 DOI: 10.1002/1521-3765(20001016)6:20<3714::Aid-Chem3714>3.0.Co;2-Z |
0.324 |
|
2000 |
Kuder N, Zelinski T, Pathak T, Seitz O, Waldmann H. Synthesis of a triply phosphorylated pentapeptide from human tau-protein. Bioorganic & Medicinal Chemistry. 8: 2433-9. PMID 11058038 DOI: 10.1016/S0968-0896(00)00174-7 |
0.687 |
|
2000 |
Müller R, Röttele H, Henke H, Waldmann H. Asymmetric steering of the Mannich reaction with phthaloyl amino acids Chemistry: a European Journal. 6: 2032-2043. PMID 10894403 DOI: 10.1002/1521-3765(20000602)6:11<2032::Aid-Chem2032>3.0.Co;2-B |
0.344 |
|
2000 |
Sander J, Waldmann H. Enzymatic protecting group techniques for glyco- and phosphopeptide chemistry: synthesis of a glycophosphopeptide from human serum response factor. Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 1564-77. PMID 10839174 DOI: 10.1002/(Sici)1521-3765(20000502)6:9<1564::Aid-Chem1564>3.3.Co;2-H |
0.352 |
|
2000 |
Bader B, Kuhn K, Owen DJ, Waldmann H, Wittinghofer A, Kuhlmann J. Bioorganic synthesis of lipid-modified proteins for the study of signal transduction Nature. 403: 223-226. PMID 10646611 DOI: 10.1038/35003249 |
0.383 |
|
2000 |
Rubio I, Wittig U, Meyer C, Heinze R, Kadereit D, Waldmann H, Downward J, Wetzker R. Farnesylation of Ras is important for the interaction with phosphoinositide 3-kinase gamma. European Journal of Biochemistry. 266: 70-82. PMID 10542052 DOI: 10.1046/J.1432-1327.1999.00815.X |
0.31 |
|
2000 |
Nazaré M, Waldmann H. Synthesis of the (9S,18R)-seco acid of the leukocyte adhesion inhibitor cyclamenol A Tetrahedron Letters. 41: 625-628. DOI: 10.1016/S0040-4039(99)02135-8 |
0.313 |
|
2000 |
Kadereit D, Waldmann H. Invited Review Chemoenzymatic Synthesis of Lipidated Peptides Monatshefte Fuer Chemie/Chemical Monthly. 131: 571-584. DOI: 10.1007/S007060070087 |
0.349 |
|
2000 |
Spieler J, Huttenloch O, Waldmann H. Synthesis of Chiral Amino Alcohols Embodying the Bispidine Framework and Their Application as Ligands in Enantioselectively Catalyzed Additions to CO and CC Groups European Journal of Organic Chemistry. 2000: 391-399. DOI: 10.1002/(Sici)1099-0690(200002)2000:3<391::Aid-Ejoc391>3.0.Co;2-R |
0.3 |
|
1999 |
Owen DJ, Alexandrov K, Rostkova E, Scheidig AJ, Goody RS, Waldmann H. Chemo-Enzymatic Synthesis of Fluorescent Rab 7 Proteins: Tools to Study Vesicular Trafficking in Cells. Angewandte Chemie (International Ed. in English). 38: 509-512. PMID 29711783 DOI: 10.1002/(Sici)1521-3773(19990215)38:4<509::Aid-Anie509>3.3.Co;2-V |
0.317 |
|
1999 |
Meseguer B, Alonso-Díaz D, Griebenow N, Herget T, Waldmann H. Natural Product Synthesis on Polymeric Supports-Synthesis and Biological Evaluation of an Indolactam Library. Angewandte Chemie. 38: 2902-2906. PMID 10540387 DOI: 10.1002/(Sici)1521-3773(19991004)38:19<2902::Aid-Anie2902>3.0.Co;2-2 |
0.404 |
|
1999 |
Schmittberger T, Waldmann H. Synthesis of the palmitoylated and prenylated C-terminal lipopeptides of the human R- and N-Ras proteins. Bioorganic & Medicinal Chemistry. 7: 749-62. PMID 10400328 DOI: 10.1016/S0968-0896(98)00251-X |
0.36 |
|
1999 |
Eisele F, Owen DJ, Waldmann H. Peptide conjugates as tools for the study of biological signal transduction Bioorganic and Medicinal Chemistry. 7: 193-224. PMID 10218812 DOI: 10.1016/S0968-0896(98)00204-1 |
0.377 |
|
1999 |
Hinterding K, Knebel A, Herrlich P, Waldmann H. Synthesis and biological evaluation of aeroplysinin analogues: a new class of receptor tyrosine kinase inhibitors. Bioorganic & Medicinal Chemistry. 6: 1153-62. PMID 9784857 DOI: 10.1016/S0968-0896(98)00070-4 |
0.322 |
|
1999 |
Stahl P, Waldmann H. Asymmetric Synthesis of the Nakijiquinones-Selective Inhibitors of the Her-2/Neu Protooncogene. Angewandte Chemie. 38: 3710-3713. DOI: 10.1002/(Sici)1521-3773(19991216)38:24<3710::Aid-Anie3710>3.3.Co;2-8 |
0.336 |
|
1999 |
Schelhaas M, Nägele E, Kuder N, Bader B, Kuhlmann J, Wittinghofer A, Waldmann H. Chemoenzymatic Synthesis of Biotinylated Ras Peptides and Their Use in Membrane Binding Studies of Lipidated Model Proteins by Surface Plasmon Resonance Chemistry - a European Journal. 5: 1239-1252. DOI: 10.1002/(Sici)1521-3765(19990401)5:4<1239::Aid-Chem1239>3.0.Co;2-N |
0.368 |
|
1999 |
Cotté A, Bader B, Kuhlmann J, Waldmann H. Synthesis of the N‐Terminal Lipohexapeptide of Human GαO‐Protein and Fluorescent‐Labeled Analogues for Biological Studies Chemistry: a European Journal. 5: 922-936. DOI: 10.1002/(Sici)1521-3765(19990301)5:3<922::Aid-Chem922>3.0.Co;2-O |
0.317 |
|
1999 |
Flohr S, Jungmann V, Waldmann H. Chemoenzymatic Synthesis of Nucleopeptides Chemistry - a European Journal. 5: 669-681. DOI: 10.1002/(Sici)1521-3765(19990201)5:2<669::Aid-Chem669>3.0.Co;2-V |
0.311 |
|
1999 |
Bläser E, Kolar P, Fenske D, Goesmann H, Waldmann H. Asymmetric Steering of Oxa Diels–Alder Reactions with Silyloxydienes Employing Proline Esters as Chiral Auxiliary Groups European Journal of Organic Chemistry. 1999: 329-333. DOI: 10.1002/(Sici)1099-0690(199901)1999:1<329::Aid-Ejoc329>3.0.Co;2-Z |
0.31 |
|
1998 |
Hinterding K, Alonso-Díaz D, Waldmann H. Organic Synthesis and Biological Signal Transduction. Angewandte Chemie (International Ed. in English). 37: 688-749. PMID 29711371 DOI: 10.1002/(Sici)1521-3773(19980403)37:6<688::Aid-Anie688>3.0.Co;2-B |
0.337 |
|
1998 |
Hinterding K, Hagenbuch P, Rétey J, Waldmann H. Synthesis and In Vitro Evaluation of the Ras Farnesyltransferase Inhibitor Pepticinnamin E. Angewandte Chemie (International Ed. in English). 37: 1236-1239. PMID 29711232 DOI: 10.1002/(Sici)1521-3773(19980518)37:9<1236::Aid-Anie1236>3.0.Co;2-F |
0.338 |
|
1998 |
Pathak T, Waldmann H. Enzymes and protecting group chemistry. Current Opinion in Chemical Biology. 2: 112-20. PMID 9667905 DOI: 10.1016/S1367-5931(98)80042-2 |
0.578 |
|
1998 |
Schmittberger T, Cotte A, Waldmann H. Synthesis of characteristic lipopeptides of lipid modified proteins employing the allyl ester as protecting group Chemical Communications. 937-938. DOI: 10.1039/A708749G |
0.348 |
|
1998 |
Kirschbaum S, Waldmann H. Three-Step Access to the Tricyclic Benzo[a]quinolizine Ring System The Journal of Organic Chemistry. 63: 4936-4946. DOI: 10.1021/Jo972035W |
0.312 |
|
1998 |
Nägele E, Schelhaas M, Kuder N, Waldmann H. Chemoenzymatic Synthesis of N-RasLipopeptides Journal of the American Chemical Society. 120: 6889-6902. DOI: 10.1021/Ja9805627 |
0.376 |
|
1998 |
Brohm D, Waldmann H. Stereoselective synthesis of the core structure of the protein phosphatase inhibitor dysidiolide Tetrahedron Letters. 39: 3995-3998. DOI: 10.1016/S0040-4039(98)00702-3 |
0.369 |
|
1998 |
Schlede U, Nazaré M, Waldmann H. Efficient enantioselective synthesis of a β-hydroxyepoxide building block for the construction of macrocyclic natural products Tetrahedron Letters. 39: 1143-1144. DOI: 10.1016/S0040-4039(97)10874-7 |
0.312 |
|
1998 |
Jungmann V, Waldmann H. An enzymatic protecting group strategy for the synthesis of nucleopeptides Tetrahedron Letters. 39: 1139-1142. DOI: 10.1016/S0040-4039(97)10873-5 |
0.318 |
|
1998 |
Hinterding K, Hagenbuch P, Rétey J, Waldmann H. Synthesis and in vitro evaluation of the Ras farnesyltransferase inhibitor pepticinnamin E Angewandte Chemie - International Edition. 37: 1236-1239. DOI: 10.1002/(Sici)1521-3765(19990104)5:1<227::Aid-Chem227>3.0.Co;2-X |
0.318 |
|
1998 |
Hinterding K, Alonso-Díaz D, Waldmann H. Organische Synthese und biologische Signaltransduktion Angewandte Chemie. 110: 716-780. DOI: 10.1002/(Sici)1521-3757(19980316)110:6<716::Aid-Ange716>3.0.Co;2-8 |
0.304 |
|
1997 |
Schroeder H, Leventis R, Rex S, Schelhaas M, Nägele E, Waldmann H, Silvius JR. S-acylation and plasma membrane targeting of the farnesylated carboxyl- terminal peptide of N-ras in mammalian fibroblasts Biochemistry. 36: 13102-13109. PMID 9335573 DOI: 10.1021/Bi9709497 |
0.338 |
|
1997 |
Stöber P, Schelhaas M, Nägele E, Hagenbuch P, Rétey J, Waldmann H. Synthesis of characteristic lipopeptides of the human N-Ras protein and their evaluation as possible inhibitors of protein farnesyl transferase. Bioorganic & Medicinal Chemistry. 5: 75-83. PMID 9043659 DOI: 10.1016/S0968-0896(96)00213-1 |
0.369 |
|
1997 |
Sebastian D, Waldmann H. Chemoenzymatic synthesis of a characteristic phosphopeptide fragment of the Raf-1 kinase Tetrahedron Letters. 38: 2927-2930. DOI: 10.1016/S0040-4039(97)00514-5 |
0.323 |
|
1997 |
Kappes T, Waldmann H. The tetrabenzylglucosyloxycarbonyl(BGloc)-group-A carbohydrate-derived enzyme-labile urethane protecting group Carbohydrate Research. 305: 341-349. DOI: 10.1016/S0008-6215(97)00224-3 |
0.347 |
|
1997 |
Kappes T, Waldmann H. Enzymatic Synthesis of Peptide Conjugates: Tools for the Study of Biological Signal Transduction Liebigs Annalen. 1997: 803-813. DOI: 10.1007/Bfb0119220 |
0.373 |
|
1997 |
Lock R, Waldmann H. Enantioselective Construction of Highly Functionalized Indoloquinolizines—congeners to Polycyclic Indole Alkaloids Chemistry - a European Journal. 3: 143-151. DOI: 10.1002/Chem.19970030122 |
0.355 |
|
1997 |
Waldmann H, Schelhaas M, Nägele E, Kuhlmann J, Wittinghofer A, Schroeder H, Silvius JR. Chemoenzymatic Synthesis of Fluorescent N-Ras Lipopeptides and Their Use in Membrane Localization Studies in Vivo Angewandte Chemie International Edition in English. 36: 2238-2241. DOI: 10.1002/Anie.199722381 |
0.304 |
|
1996 |
Pohl T, Waldmann H. Enzymatic Synthesis of a Characteristic Phosphorylated and Glycosylated Peptide Fragment of the Large Subunit of Mammalian RNA Polymerase II Angewandte Chemie International Edition in English. 35: 1720-1723. DOI: 10.1021/Ja970709E |
0.334 |
|
1996 |
Lock R, Waldmann H. Asymmetric synthesis of highly functionalized tetracyclic indole bases embodying the basic skeleton of yohimbine- and reserpine type alkaloids Tetrahedron Letters. 37: 2753-2756. DOI: 10.1016/0040-4039(96)00388-7 |
0.343 |
|
1996 |
Schelhaas M, Glomsda S, Hänsler M, Jakubke H, Waldmann H. Enzymatic Synthesis of Peptides andRas Lipopeptides Employing Choline Ester as a Solubilizing, Protecting, and Activating Group Angewandte Chemie International Edition in English. 35: 106-109. DOI: 10.1002/Anie.199601061 |
0.314 |
|
1995 |
Waldmann H. Amino Acid Esters: Versatile Chiral Auxiliary Groups for the Asymmetric Synthesis of Nitrogen Heterocycles Synlett. 1995: 133-141. DOI: 10.1055/S-1995-4882 |
0.307 |
|
1995 |
Nettekoven M, Psiorz M, Waldmann H. Synthesis of enantiomerically pure 4-alkylsubstituted tryptophan derivatives by a combination of organometallic reactions with enantioselective enzymatic transformations Tetrahedron Letters. 36: 1428-1428. DOI: 10.1016/0040-4039(95)00001-S |
0.362 |
|
1995 |
Waldmann H, Bläser E, Jansen M, Letschert H. Asymmetric Control of 1,3-Dipolar Cycloaddition Reactions with Azomethine Ylides by Means of Proline Esters as Chiral Auxiliary Groups Chemistry - a European Journal. 1: 150-154. DOI: 10.1002/Chem.19950010209 |
0.314 |
|
1995 |
Waldmann H, Nägele E. Synthesis of the Palmitoylated and Farnesylated C-Terminal Lipohexapeptide of the Human N-Ras Protein by Employing an Enzymatically Removable Urethane Protecting Group Angewandte Chemie International Edition in English. 34: 2259-2262. DOI: 10.1002/Anie.199522591 |
0.33 |
|
1994 |
Waldmann H. Asymmetric Hetero Diels-Alder Reactions Synthesis. 1994: 535-551. DOI: 10.1055/S-1994-25519 |
0.321 |
|
1994 |
Pohl T, Nägele E, Waldmann H. Biocatalysts as chemo- and regioselecting tools in organic synthesis Catalysis Today. 22: 407-426. DOI: 10.1016/0920-5861(94)80115-0 |
0.328 |
|
1994 |
Waldmann H, Weigerding M, Dreisbach C, Wandrey C. C2-Symmetric Bicyclic Diols as Chiral Ligands in the titanate-catalyzed enantioselective addition of alkylzinc reagents to aldehydes Helvetica Chimica Acta. 77: 2111-2116. DOI: 10.1002/Hlca.19940770803 |
0.303 |
|
1994 |
Waldmann H, Bläser E, Jansen M, Letschert H. Asymmetric Synthesis of Highly Substituted Pyrrolidines by 1,3-Dipolar Cycloadditions of Azomethine Ylides withN-Acryloylproline Benzyl Ester Angewandte Chemie International Edition in English. 33: 683-685. DOI: 10.1002/Anie.199406831 |
0.358 |
|
1994 |
Waldmann H, Bläser E, Jansen M, Letschert H. Asymmetrische Synthese hochsubstituierter Pyrrolidine durch 1,3-Dipolare Cycloaddition von Azomethin-Yliden anN-Acryloylprolinbenzylester, Angewandte Chemie. 106: 717-719. DOI: 10.1002/Ange.19941060629 |
0.326 |
|
1993 |
Braun P, Waldmann H, Kunz H. Chemoenzymatic synthesis of O-glycopeptides carrying the tumor associated TN-antigen structure. Bioorganic & Medicinal Chemistry. 1: 197-207. PMID 8081853 DOI: 10.1016/S0968-0896(00)82122-7 |
0.452 |
|
1993 |
Waldmann H, Schmidt G, Jansen M, Geb J. Asymmetric Pictet-Spengler reactions employing amino acid esters as mediators of selectivity Tetrahedron Letters. 34: 5867-5870. DOI: 10.1016/S0040-4039(00)73800-7 |
0.304 |
|
1993 |
Waldmann H, Braun a, Weymann M, Gewehr M. Asymmetric synthesis of indolo[2,3-a]quinolizidin-2-ones - congeners to yohimbine-type alkaloids Tetrahedron. 49: 397-416. DOI: 10.1016/S0040-4020(01)80309-4 |
0.321 |
|
1993 |
Reidel A, Waldmann H. Enzymatic Protecting Group Techniques in bioorganic synthesis Journal F�R Praktische Chemie/Chemiker-Zeitung. 335: 109-127. DOI: 10.1002/Prac.19933350202 |
0.313 |
|
1992 |
Braun P, Waldmann H, Kunz H. Selective Enzymatic Removal of Protecting Functions: Heptyl Esters as Carboxy Protecting Groups in Glycopeptide Synthesis Synlett. 1992: 39-40. DOI: 10.1055/S-1992-21258 |
0.493 |
|
1992 |
Waldmann H, Braun M. Asymmetric tandem Mannich-Michael reactions of amino acid ester imines with Danishefsky's diene The Journal of Organic Chemistry. 57: 4444-4451. DOI: 10.1021/Jo00042A027 |
0.304 |
|
1991 |
Waldmann H, Braun P, Kunz H. New enzymatic protecting group techniques for the construction of peptides and glycopeptides. Biomedica Biochimica Acta. 50: S243-8. PMID 1820053 |
0.423 |
|
1991 |
Waldmann H, Braun M, Dräger M. Asymmetric aza Diels-Alder reactions of amino acid ester imines with Brassard's diene Tetrahedron: Asymmetry. 2: 1231-1246. DOI: 10.1016/S0957-4166(00)80023-3 |
0.322 |
|
1991 |
Braun P, Waldmann H, Vogt W, Kunz H. Selektive enzymatische Schutzgruppenabspaltungen: Der n-Heptylester als Carboxylschutzgruppe in der Peptidsynthese Liebigs Annalen Der Chemie. 1991: 165-170. DOI: 10.1002/Jlac.199119910130 |
0.49 |
|
1991 |
Waldmann H, Braun M. Asymmetric synthesis of bicyclic amino acid derivatives by Aza-Diels-Alder reactions in aqueous solution Liebigs Annalen Der Chemie. 1991: 1045-1048. DOI: 10.1002/Jlac.1991199101180 |
0.313 |
|
1990 |
Kunz H, Wernig P, Schilling M, März J, Unverzagt C, Birnbach S, Lang U, Waldmann H. Synthetic tumor-associated glycopeptide antigens. Environmental Health Perspectives. 88: 247-9. PMID 2272318 DOI: 10.2307/3431084 |
0.451 |
|
1990 |
Waldmann H, März J, Kunz H. Synthesis of 2-acetamido-2-deoxyglucosylasparagine glyco-tripeptides and -pentapeptides by selective C- and N-terminal elongation of the peptide chain. Carbohydrate Research. 196: 75-93. PMID 2161285 DOI: 10.1016/0008-6215(90)84107-6 |
0.53 |
|
1990 |
Braun P, Waldmann H, Vogt W, Kunz H. Selective Enzymatic Removal of Protecting Functions: Heptyl Esters as Carboxy Protecting Groups in Peptide Synthesis Synlett. 1990: 105-107. DOI: 10.1055/S-1990-21002 |
0.495 |
|
1990 |
Schultz M, Waldmann H, Vogt W, Kunz H. Stereospecific CC-bond formation with rabbit muscle aldolase - A chemoenzymatic synthesis of (+)-exo-brevicomin Tetrahedron Letters. 31: 867-868. DOI: 10.1016/S0040-4039(00)94649-5 |
0.473 |
|
1990 |
Schultz M, Waldmann H, Kunz H, Vogt W. Chemoenzymatische „Chiral-Pool”-Synthese von (+)-exo-Brevicomin aus Kohlenhydraten mit Fructose-1,6-diphosphat-Aldolase Liebigs Annalen Der Chemie. 1990: 1019-1024. DOI: 10.1002/Jlac.1990199001184 |
0.519 |
|
1990 |
Waldmann H. Aminosäureester als chirale Hilfsgruppen in Lewis-Säure-katalysierten Diels-Alder-Reaktionen Liebigs Annalen Der Chemie. 1990: 671-680. DOI: 10.1002/Jlac.1990199001127 |
0.321 |
|
1989 |
Friedrich-Bochnitschek S, Waldmann H, Kunz H. Allyl esters as carboxy protecting groups in the synthesis of O-glycopeptides The Journal of Organic Chemistry. 54: 751-756. DOI: 10.1021/Jo00265A007 |
0.466 |
|
1989 |
Bednarski MD, Simon ES, Bischofberger N, Fessner WD, Kim MJ, Lees W, Saito T, Waldmann H, Whitesides GM. Rabbit muscle aldolase as a catalyst in organic synthesis Journal of the American Chemical Society. 111: 627-635. DOI: 10.1021/Ja00184A034 |
0.608 |
|
1989 |
Waldmann H. Asymmetrische Hetero-Diels-Alder-Reaktionen in wäßriger Lösung unter Verwendung von Aminosäureestern als chiralen Auxiliaren Liebigs Annalen Der Chemie. 1989: 231-238. DOI: 10.1002/Jlac.198919890145 |
0.307 |
|
1989 |
Kunz H, Waldmann H, März J. Synthese vonN-Glycopeptid-Partialstrukturen der Verknüpfungsregion sowohl der Transmembran-Neuraminidase eines Influenza-Virus als auch des Faktors B des menschlichen Komplementsystems Liebigs Annalen Der Chemie. 1989: 45-49. DOI: 10.1002/Jlac.198919890110 |
0.427 |
|
1989 |
BEDNARSKI MD, SIMON ES, BISCHOFBERGER N, FESSNER W, KIM M, LEES W, SAITO T, WALDMANN H, WHITESIDES GM. ChemInform Abstract: Rabbit Muscle Aldolase as a Catalyst in Organic Synthesis. Cheminform. 20. DOI: 10.1002/chin.198919286 |
0.577 |
|
1989 |
BISCHOFBERGER N, WALDMANN H, SAITO T, SIMON ES, LEES W, BEDNARSKI MD, WHITESIDES GM. ChemInform Abstract: Synthesis of Analogues of 1,3-Dihydroxyacetone Phosphate and Glyceraldehyde 3-Phosphate for Use in Studies of Fructose-1,6-diphosphate Aldolase. Cheminform. 20. DOI: 10.1002/chin.198901205 |
0.565 |
|
1988 |
Waldmann H, Kunz H. 1,3-Dithian-2-ylmethyl esters as two-step carboxy-protecting groups in the synthesis of N-glycopeptides The Journal of Organic Chemistry. 53: 4172-4175. DOI: 10.1021/Jo00253A003 |
0.45 |
|
1988 |
Bischofberger N, Waldmann H, Saito T, Simon ES, Lees W, Bednarski MD, Whitesides GM. Synthesis of analogs of 1,3-dihydroxyacetone phosphate and glyceraldehyde 3-phosphate for use in studies of fructose-1,6-diphosphate aldolase The Journal of Organic Chemistry. 53: 3457-3465. DOI: 10.1021/Jo00250A010 |
0.767 |
|
1988 |
Waldmann H. The use of penicillin acylase for selective N-terminal deprotection in peptide synthesis Tetrahedron Letters. 29: 1131-1134. DOI: 10.1016/S0040-4039(00)86668-X |
0.314 |
|
1988 |
Waldmann H. Der Phenylacetyl-(PhAc-)Rest als enzymatisch ablösbare Schutzgruppe für Peptide und Kohlenhydrate: Selektive Schutzgruppenabspaltungen mit Penicillin-Acylase Liebigs Annalen Der Chemie. 1988: 1175-1180. DOI: 10.1002/Jlac.198819881212 |
0.302 |
|
1988 |
Kunz H, Waldmann H, Klinkhammer U. The Allyl Ester as Carboxy-Protecting Group in the Stereoselective Construction of Neuraminic-Acid Glycosides Helvetica Chimica Acta. 71: 1868-1874. DOI: 10.1002/Hlca.19880710804 |
0.455 |
|
1986 |
Waldmann H, Gygax D, Bednarski MD, Shangraw WR, Whitesides GM. The enzymic utilization of sucrose in the synthesis of amylose and derivatives of amylose, using phosphorylases. Carbohydrate Research. 157: c4-7. PMID 2949832 DOI: 10.1016/0008-6215(86)85078-9 |
0.761 |
|
1986 |
Bednarski MD, Waldmann HJ, Whitesides GM. Aldolase-catalyzed synthesis of complex C8 and C9 monosaccharides. Tetrahedron Letters. 27: 5807-5810. DOI: 10.1016/S0040-4039(00)85332-0 |
0.596 |
|
1986 |
KUNZ H, WALDMANN H. ChemInform Abstract: Construction of Disaccharidic N-Glycopeptides. Synthesis of the Transmembrane Neuraminidase Binding Site of Influenza Virus. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198603323 |
0.373 |
|
1985 |
Kunz H, Waldmann H. Directed Stereoselective Synthesis Of Alpha-N-Acetyl And Beta-N-Acetyl Neuraminic Acid Galactose Disaccharides Using 2-Chloro And 2-Fluoro Derivatives Of Neuraminic Acid Allyl Ester Journal of the Chemical Society, Chemical Communications. 638-640. DOI: 10.1039/C39850000638 |
0.475 |
|
1985 |
Kunz H, Waldmann H. Synthesis of the Glycopeptide Partial Sequence A80-A84 of Human Fibroblast Interferon Helvetica Chimica Acta. 68: 618-622. DOI: 10.1002/Chin.198535293 |
0.419 |
|
1985 |
Kunz H, Waldmann H. Construction of DisaccharideN-Glycopeptides?Synthesis of the Linkage Region of the Transmembrance-Neuraminidase of an Influenza Virus Angewandte Chemie International Edition in English. 24: 883-885. DOI: 10.1002/Anie.198508831 |
0.429 |
|
1985 |
Kunz H, Waldmann H. Aufbau disaccharidischerN-Glycopeptide – Synthese der Verknüpfungsregion der Transmembran-Neuraminidase eines Influenza-Virus Angewandte Chemie. 97: 885-887. DOI: 10.1002/Ange.19850971033 |
0.435 |
|
1984 |
KUNZ H, WALDMANN H. ChemInform Abstract: ALLYL GROUPS AS MILD AND SELECTIVE CLEAVABLE CARBOXY PROTECTIVE GROUPS FOR THE SYNTHESIS OF SENSITIVE O-GLYCOPEPTIDES Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198415343 |
0.392 |
|
1984 |
WALDMANN H, KUNZ H. ChemInform Abstract: ALLYL ESTERS AS SELECTIVELY REMOVABLE CARBOXY-PROTECTING FUNCTIONS IN PEPTIDE AND N-GLYCOPEPTIDE SYNTHESES Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198402318 |
0.487 |
|
1984 |
Kunz H, Waldmann H. The Allyl Group as Mildly and Selectively Removable Carboxy-Protecting Group for the Synthesis of LabileO-Glycopeptides Angewandte Chemie International Edition in English. 23: 71-72. DOI: 10.1002/Anie.198400711 |
0.472 |
|
1984 |
Kunz H, Waldmann H. Die Allylgruppe als mild und selektiv abspaltbare Carboxy-Schutzgruppe zur Synthese empfindlicherO-Glycopeptide Angewandte Chemie. 96: 49-50. DOI: 10.1002/Ange.19840960108 |
0.431 |
|
1983 |
Waldmann H, Kunz H. Allylester als selektiv abspaltbare Carboxyschutzgruppen in der Peptid- undN-Glycopeptidsynthese Liebigs Annalen Der Chemie. 1983: 1712-1725. DOI: 10.1002/Jlac.198319831007 |
0.484 |
|
1983 |
KUNZ H, WALDMANN H. ChemInform Abstract: 1,3-DITHIAN-2-YLMETHYL ESTER AS INTERMEDIATE PROTECTIVE GROUPS FOR CARBOXYL FUNCTION IN PEPTIDE SYNTHESIS Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198315335 |
0.426 |
|
1983 |
Kunz H, Waldmann H. 1,3-Dithian-2-yl Methyl Ester as Two-Step Protecting Group for the Carboxy Function in Peptide Synthesis Angewandte Chemie International Edition in English. 22: 62-62. DOI: 10.1002/Anie.198300621 |
0.489 |
|
1983 |
Kunz H, Waldmann H. 1,3‐Dithian‐2‐yl‐methylester als Zweistufen‐Schutzgruppe für die Carboxyfunktion bei der Peptidsynthese Angewandte Chemie. 95: 47-48. DOI: 10.1002/Ange.19830950108 |
0.4 |
|
Low-probability matches (unlikely to be authored by this person) |
1994 |
Waldmann H, Schmidt G, Jansen M, Geb J. Asymmetric steering of the Pictet-Spengler reaction by means of amino acid esters as chiral auxiliary groups Tetrahedron. 50: 11865-11884. DOI: 10.1016/S0040-4020(01)89301-7 |
0.3 |
|
1989 |
Waldmann H, Dräger M. On the enhancement of stereoselection by cooperation between chiral auxiliaries. Asymmetric diels-alder reactions with fumaric acid bis ((S)-proline benzyl ester) amide Tetrahedron Letters. 30: 4227-4230. DOI: 10.1016/S0040-4039(01)80696-1 |
0.3 |
|
2010 |
Rose R, Erdmann S, Bovens S, Wolf A, Rose M, Hennig S, Waldmann H, Ottmann C. Cover Picture: Identification and Structure of Small-Molecule Stabilizers of 14-3-3 Protein-Protein Interactions (Angew. Chem. Int. Ed. 24/2010) Angewandte Chemie International Edition. 49: 3991-3991. DOI: 10.1002/Anie.201002255 |
0.3 |
|
2007 |
Rauh D, Waldmann H. Linking chemistry and biology for the study of protein function Angewandte Chemie - International Edition. 46: 826-829. PMID 17195266 DOI: 10.1002/Anie.200602979 |
0.299 |
|
2010 |
Wu Y, Oesterlin LK, Tan K, Waldmann H, Alexandrov K, Goody RS. Erratum: Membrane targeting mechanism of Rab GTPases elucidated by semisynthetic protein probes Nature Chemical Biology. 6: 630-630. DOI: 10.1038/Nchembio0810-630B |
0.299 |
|
1998 |
Sauerbrei B, Jungmann V, Waldmann H. An Enzyme-Labile Linker Group for Organic Syntheses on Solid Supports. Angewandte Chemie (International Ed. in English). 37: 1143-1146. PMID 29711024 DOI: 10.1002/(Sici)1521-3773(19980504)37:8<1143::Aid-Anie1143>3.0.Co;2-E |
0.299 |
|
2001 |
Rak A, Reents R, Pylypenko O, Niculae A, Sidorovitch V, Thomä NH, Waldmann H, Schlichting I, Goody RS, Alexandrov K. Crystallization and preliminary X-ray diffraction analysis of the Rab escort protein-1 in complex with Rab geranylgeranyltransferase Journal of Structural Biology. 136: 158-161. PMID 11886217 DOI: 10.1006/Jsbi.2001.4433 |
0.299 |
|
2012 |
Xu J, Hedberg C, Dekker FJ, Li Q, Haigis KM, Hwang E, Waldmann H, Shannon K. Inhibiting the palmitoylation/depalmitoylation cycle selectively reduces the growth of hematopoietic cells expressing oncogenic Nras. Blood. 119: 1032-5. PMID 22144181 DOI: 10.1182/Blood-2011-06-358960 |
0.299 |
|
2016 |
Schürmann M, Janning P, Ziegler S, Waldmann H. Small-Molecule Target Engagement in Cells. Cell Chemical Biology. PMID 27049669 DOI: 10.1016/J.Chembiol.2016.03.008 |
0.299 |
|
1991 |
Waldmann H. Aminosäureester als chirale Hilfsgruppen bei Barbier-Reaktionen in wäßriger Lösung Liebigs Annalen Der Chemie. 1991: 1317-1322. DOI: 10.1002/Jlac.1991199101226 |
0.298 |
|
2013 |
Dakas PY, Parga JA, Höing S, Schöler HR, Sterneckert J, Kumar K, Waldmann H. Discovery of neuritogenic compound classes inspired by natural products. Angewandte Chemie (International Ed. in English). 52: 9576-81. PMID 23733315 DOI: 10.1002/Anie.201302045 |
0.297 |
|
1996 |
Waldmann H, Heuser A, Schulze S. Selective enzymatic removal of protecting groups: The phenylacetamide as amino protecting group in phosphopeptide synthesis Tetrahedron Letters. 37: 8725-8728. DOI: 10.1016/S0040-4039(96)02041-2 |
0.297 |
|
2007 |
Köhn M, Gutierrez-Rodriguez M, Jonkheijm P, Wetzel S, Wacker R, Schroeder H, Prinz H, Niemeyer C, Breinbauer R, Szedlacsek S, Waldmann H. Eine Mikroarray-Strategie zur Untersuchung der Substratspezifitäten von Protein-Tyrosin-Phosphatasen Angewandte Chemie. 119: 7844-7847. DOI: 10.1002/Ange.200701601 |
0.297 |
|
2008 |
Jonkheijm P, Weinrich D, Schröder H, Niemeyer C, Waldmann H. Cover Picture: Chemical Strategies for Generating Protein Biochips (Angew. Chem. Int. Ed. 50/2008) Angewandte Chemie International Edition. 47: 9575-9575. DOI: 10.1002/Anie.200890256 |
0.297 |
|
2004 |
Müller O, Gourzoulidou E, Carpintero M, Karaguni IM, Langerak A, Herrmann C, Möröy T, Klein-Hitpass L, Waldmann H. Identification of potent Ras signaling inhibitors by pathway-selective phenotype-based screening. Angewandte Chemie (International Ed. in English). 43: 450-4. PMID 14735532 DOI: 10.1002/Anie.200352587 |
0.296 |
|
2004 |
Huttenloch O, Laxman E, Waldmann H. Solid-phase development of chiral phosphoramidite ligands for enantioselective conjugate addition reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 4767-80. PMID 12561117 DOI: 10.1002/1521-3765(20021018)8:20<4767::Aid-Chem4767>3.0.Co;2-O |
0.296 |
|
2014 |
Stieber F, Grether U, Waldmann H. An oxidation-labile traceless linker for solid-phase synthesis. Angewandte Chemie (International Ed. in English). 38: 1073-7. PMID 25138498 DOI: 10.1002/(Sici)1521-3773(19990419)38:8<1073::Aid-Anie1073>3.0.Co;2-Y |
0.296 |
|
2020 |
Schneidewind T, Brause A, Pahl A, Burhop A, Mejuch T, Sievers S, Waldmann H, Ziegler S. Morphological profiling enables the identification of common mode of action for small molecules with different targets. Chembiochem : a European Journal of Chemical Biology. PMID 32618075 DOI: 10.1002/Cbic.202000381 |
0.296 |
|
2001 |
Jeyaraj DA, Waldmann H. Synthesis of nucleopeptides by an enzyme labile urethane protecting group Tetrahedron Letters. 42: 835-837. DOI: 10.1016/S0040-4039(00)02121-3 |
0.296 |
|
2005 |
Rocks O, Peyker A, Kahms M, Verveer PJ, Koerner C, Lumbierres M, Kuhlmann J, Waldmann H, Wittinghofer A, Bastiaens PI. An acylation cycle regulates localization and activity of palmitoylated Ras isoforms. Science (New York, N.Y.). 307: 1746-52. PMID 15705808 DOI: 10.1126/Science.1105654 |
0.296 |
|
2009 |
Tannert R, Hu TS, Arndt HD, Waldmann H. Solid-phase based total synthesis of Jasplakinolide by ring-closing metathesis Chemical Communications. 1493-1495. PMID 19277367 DOI: 10.1039/B900342H |
0.296 |
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2004 |
Heinemann I, Völkert M, Waldmann H. Synthesis of lipidated peptides. Methods in Molecular Biology (Clifton, N.J.). 283: 221-32. PMID 15197314 DOI: 10.1385/1-59259-813-7:221 |
0.296 |
|
2003 |
Huttenloch O, Laxman E, Waldmann H. Combinatorial development of chiral phosphoramidite-ligands for enantioselective conjugate addition reactions. Chemical Communications (Cambridge, England). 673-5. PMID 12119669 DOI: 10.1039/B200454B |
0.296 |
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2018 |
Lee Y, Kumar K, Waldmann H. Ligandengesteuerte divergente Synthese von carbo- und heterocyclischen Ringsystemen Angewandte Chemie. 130: 5308-5322. DOI: 10.1002/Ange.201710247 |
0.296 |
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1990 |
Waldmann H. Prolin-benzylester als chirale Hilfsgruppen in asymmetrischen 1,3-dipolaren Cycloadditionen mit Nitriloxiden Liebigs Annalen Der Chemie. 1990: 1013-1017. DOI: 10.1002/Jlac.1990199001183 |
0.295 |
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2010 |
Waldmann H. Protein Targeting with Small Molecules. Chemical Biology Techniques and Applications. Herausgegeben von Hiroyuki Osada. Angewandte Chemie. 122: 2522-2522. DOI: 10.1002/Ange.201000606 |
0.295 |
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