Veröffentlichungen 2017


  1. Microwave-Facilitated SPOT-Synthesis of Antibacterial Dipeptoids
    Schneider, A. C.; Fritz, D.; Vasquez, J. K.; Vollrath, S. B. L.; Blackwell, H. E.; Bräse, S.
    2017. ACS combinatorial science, 19 (12), 715–737. doi:10.1021/acscombsci.7b00096 
  2. A Trifunctional Linker for Purified 3D Assembled Peptide Structure Arrays
    Mattes, D. S.; Rentschler, S.; Foertsch, T. C.; Münch, S. W.; Loeffler, F. F.; Nesterov-Mueller, A.; Bräse, S.; Breitling, F.
    2017. Small methods, 1700205. doi:10.1002/smtd.201700205 
  3. Droplet Microarray Based on Patterned Superhydrophobic Surfaces Prevents Stem Cell Differentiation and Enables High-Throughput Stem Cell Screening
    Tronser, T.; Popova, A. A.; Jaggy, M.; Bastmeyer, M.; Levkin, P. A.
    2017. Advanced healthcare materials, 6 (23), Art.Nr. 1700622. doi:10.1002/adhm.201700622 
  4. Miniaturized platform for high-throughput screening of stem cells
    Tronser, T.; Popova, A. A.; Levkin, P. A.
    2017. Current opinion in biotechnology, 46, 141–149. doi:10.1016/j.copbio.2017.03.005 
  5. An optimized version of the Secretome Protein Enrichment with Click Sugars (SPECS) method leads to enhanced coverage of the secretome
    Serdaroglu, A.; Müller, S. A.; Schepers, U.; Bräse, S.; Weichert, W.; Lichtenthaler, S. F.; Kuhn, P.-H.
    2017. Proteomics, 17 (5), Art.Nr. 1600423. doi:10.1002/pmic.201600423 
  6. A direct access to heterobimetallic complexes by roll-over cyclometallation
    Schön, F.; Leist, M.; Neuba, A.; Lang, J.; Braun, C.; Sun, Y.; Niedner-Schatteburg, G.; Bräse, S.; Thiel, W. R.
    2017. Chemical communications, 53 (88), 12016–12019. doi:10.1039/C7CC07119A 
  7. Photophysical dynamics of a binuclear Cu(I)-emitter on the fs to μs timescale, in solid phase and in solution
    Bäppler, F.; Zimmer, M.; Dietrich, F.; Grupe, M.; Wallesch, M.; Volz, D.; Bräse, S.; Gerhards, M.; Diller, R.
    2017. Physical chemistry, chemical physics, 19 (43), 29438–29448. doi:10.1039/c7cp05791a 
  8. Sequence-controlled molecular layers on surfaces by thiol–ene chemistry: synthesis and multitechnique characterization
    Llevot, A.; Steinmüller, S. O.; Bitterer, B.; Ridder, B.; Berson, J.; Walheim, S.; Schimmel, T.; Bräse, S.; Scheiba, F.; Meier, M. A. R.
    2017. Polymer chemistry, 8 (38), 5824–5828. doi:10.1039/C7PY01515A 
  9. Lanthanide Fluorobenzoates as Bio-Probes : a Quest for the Optimal Ligand Fluorination Degree
    Kalyakina, A. S.; Utochnikova, V. V.; Bushmarinov, I. S.; Le-Deygen, I. M.; Volz, D.; Weis, P.; Schepers, U.; Kuzmina, N. P.; Bräse, S.
    2017. Chemistry - a European journal, 23 (59), 14944–14953. doi:10.1002/chem.201703543 
  10. [2.2]Paracyclophanes with N-Heterocycles as Ligands for Mono- and Dinuclear Ruthenium(II) Complexes
    Braun, C.; Nieger, M.; Thiel, W. R.; Bräse, S.
    2017. Chemistry - a European journal, 23 (61), 15474–15483. doi:10.1002/chem.201703291 
  11. Unprecedented one-pot reaction to chiral, non-racemic copper(I) complexes of [2.2]paracyclophane-based P,N-ligands
    Braun, C.; Nieger, M.; Bräse, S.
    2017. Chemistry - a European journal, 23 (65), 16452–16455. doi:10.1002/chem.201704115 
  12. Chemotion ELN : an Open Source electronic lab notebook for chemists in academia
    Tremouilhac, P.; Nguyen, A.; Huang, Y.-C.; Kotov, S.; Lütjohann, D. S.; Hübsch, F.; Jung, N.; Bräse, S.
    2017. Journal of cheminformatics, 9 (1), Art.Nr. 54. doi:10.1186/s13321-017-0240-0 VolltextVolltext der Publikation als PDF-Dokument 
  13. Polylutidines : Multifunctional Surfaces through Vapor-Based Polymerization of Substituted Pyridinophanes
    Bally-Le Gall, F.; Hussal, C.; Kramer, J.; Cheng, K.; Kumar, R.; Eyster, T.; Baek, A.; Trouillet, V.; Nieger, M.; Bräse, S.; Lahann, J.
    2017. Chemistry - a European journal, 23 (54), 13342–13350. doi:10.1002/chem.201700901 
  14. Suzuki-Miyaura Cross-Coupling Reactions of Tetrahydroxanthones and 4-Chromanone Lactones to Heteromeric Biaryls
    Geiger, L.; Nieger, M.; Bräse, S.
    2017. Advanced synthesis & catalysis, 359 (19), 3421–3427. doi:10.1002/adsc.201700497 
  15. Two-photon absorption in a series of 2,6-disubstituted BODIPY dyes
    Barros, L. W. T.; Cardoso, T. A. S.; Bihlmeier, A.; Wagner, D.; Kölmel, D. K.; Hörner, A.; Bräse, S.; Brito Cruz, C. H.; Padilha, L. A.
    2017. Physical chemistry, chemical physics, 19 (32), 21683–21690. doi:10.1039/C6CP07849D 
  16. Solid State Step-Scan FTIR Spectroscopy of Binuclear Copper(I) Complexes
    Zimmer, M.; Dietrich, F.; Volz, D.; Bräse, S.; Gerhards, M.
    2017. ChemPhysChem, 18 (21), 3023–3029. doi:10.1002/cphc.201700753 
  17. Ein Molekülarchiv als akademisch integrierte Service-Einrichtung
    Jung, N.; Deckers, A.; Bräse, S.
    2017. Biospektrum, 23 (2), 212–214 
  18. Development of Bag-1L as a therapeutic target in androgen receptor-dependent prostate cancer
    Cato, L.; Neeb, A.; Sharp, A.; Buzón, V.; Ficarro, S. B.; Yang, L.; Muhle-Goll, C.; Kuznik, N. C.; Riisnaes, R.; Rodrigues, D. N.; Armant, O.; Gourain, V.; Adelmant, G.; Ntim, E. A.; Westerling, T.; Dolling, D.; Rescigno, P.; Figueiredo, I.; Fauser, F.; Wu, J.; Rottenberg, J. T.; Shatkina, L.; Ester, C.; Luy, B.; Puchta, H.; Troppmair, J.; Jung, N.; Bräse, S.; Strähle, U.; Marto, J. A.; Nienhaus, G. U.; Al-Lazikani, B.; Salvatella, X.; Bono, J. S. de; Cato, A. C. B.; Brown, M.
    2017. eLife, 6, Art.Nr. e27159. doi:10.7554/eLife.27159 VolltextVolltext der Publikation als PDF-Dokument 
  19. Enantiomerically pure β-dipeptide derivative induces anticancer activity against human hormone-refractory prostate cancer through both PI3K/Akt-dependent and -independent pathways
    Chan, M.-L.; Yu, C.-C.; Hsu, J.-L.; Leu, W.-J.; Chan, S.-H.; Hsu, L.-C.; Liu, S.-P.; Ivantcova, P. M.; Dogan, Ö.; Bräse, S.; Kudryavtsev, K. V.; Guh, J.-H.
    2017. OncoTarget, 8 (57), 96668–96683. doi:10.18632/oncotarget.18040 
  20. High-Density Droplet Microarray of Individually Addressable Electrochemical Cells
    Zhang, H.; Oellers, T.; Feng, W.; Abdulazim, T.; Saw, E. N.; Ludwig, A.; Levkin, P. A.; Plumeré, N.
    2017. Analytical chemistry, 89 (11), 5832–5839. doi:10.1021/acs.analchem.7b00008 
  21. Formaldehyde-Extruding Homolytic Aromatic Substitution via C→O Transposition: Selective ’Traceless-Linker’ access to Congested Biaryl Bonds
    Poonpatana, P.; Passos Gomes, G. dos; Hurrle, T.; Chardon, K.; Bräse, S.; Masters, K.-S.; Alabugin, I.
    2017. Chemistry - a European journal, 23 (38), 9091–9097. doi:10.1002/chem.201700085 
  22. Europium 2-benzofuranoate : Synthesis and use for bioimaging
    Utochnikova, V. V.; Koshelev, D. S.; Medvedko, A. V.; Kalyakina, A. S. ..; Bushmarinov, I. S.; Grishko, A. Y.; Schepers, U.; Bräse, S.; Vatsadze, S. Z.
    2017. Optical materials, 74, 191–196. doi:10.1016/j.optmat.2017.05.038 
  23. Chemical Synthesis of Modified Hyaluronic Acid Disaccharides
    Mende, M.; Nieger, M.; Bräse, S.
    2017. Chemistry - a European journal, 23 (50), 12283–12296. doi:10.1002/chem.201701238 
  24. Scope and Limitations of the Domino Vinylogous Aldol/oxa-Michael Reaction
    Geiger, L.; Nieger, M.; Bräse, S.
    2017. ChemistrySelect, 2 (11), 3268–3275. doi:10.1002/slct.201700667 
  25. Surface modified EuₓLa₁₋ₓF₃ nanoparticles as luminescent biomarkers : Still plenty of room at the bottom
    Khudoleeva, V.; Utochnikova, V. V.; Kalyakina, A. S.; Deygen, I. M.; Shiryaev, A. A.; Marciniak, Ł.; Lebedev, V. A.; Roslyakov, I. V.; Garshev, A. V.; Lepnev, L. S.; Schepers, U.; Bräse, S.; Kuzmina, N. P.
    2017. Dyes and pigments, 143, 348–355. doi:10.1016/j.dyepig.2017.04.058 
  26. UV-Triggered Polymerization, Deposition, and Patterning of Plant Phenolic Compounds
    Behboodi-Sadabad, F.; Zhang, H.; Trouillet, V.; Welle, A.; Plumeré, N.; Levkin, P. A.
    2017. Advanced functional materials, 27 (22), Art. Nr. 1700127. doi:10.1002/adfm.201700127 VolltextVolltext der Publikation als PDF-Dokument 
  27. Monitoring of Reactions on Solid Phases via Raman Spectroscopy
    Protasova, I.; Heissler, S.; Jung, N.; Bräse, S.
    2017. Chemistry - a European journal, 23 (36), 8703–8711. doi:10.1002/chem.201700907 
  28. Functional Genomic mRNA Profiling of Colorectal Adenomas : Identification and Validation of CD44 and Splice Variant CD44v6 as Molecular Imaging Targets
    Hartmans, E.; Orian-Rousseau, V.; Matzke-Ogi, A.; Karrenbeld, A.; Groot, D. J. A. de; Jong, S. de; Dam, G. M. van; Fehrmann, R. S. N.; Nagengast, W. B.
    2017. Theranostics, 7 (2), 482–492. doi:10.7150/thno.16816 VolltextVolltext der Publikation als PDF-Dokument 
  29. Bio-inspired strategy for controlled dopamine polymerization in basic solutions
    Du, X.; Li, L.; Behboodi-Sadabad, F.; Welle, A.; Li, J.; Heissler, S.; Zhang, H.; Plumeré, N.; Levkin, P. A.
    2017. Polymer chemistry, 8 (14), 2145–2151. doi:10.1039/C7PY00051K VolltextVolltext der Publikation als PDF-Dokument 
  30. Planar-Chiral [2.2]Paracyclophane-Based Amides as Proligands for Titanium- and Zirconium-Catalyzed Hydroamination
    Braun, C.; Bräse, S.; Schafer, L. L.
    2017. European journal of organic chemistry, 13 (3), 1760–1764. doi:10.1002/ejoc.201700101 
  31. Fast and efficient synthesis of microporous polymer nanomembranes via light-induced click reaction
    An, Q.; Hassan, Y.; Yan, X.; Krolla-Sidenstein, P.; Mohammed, T.; Lang, M.; Bräse, S.; Tsotsalas, M.
    2017. Beilstein journal of organic chemistry, 13, 558–563. doi:10.3762/bjoc.13.54 VolltextVolltext der Publikation als PDF-Dokument 
  32. Double-Strand DNA Breaks Induced by Paracyclophane Gold(I) Complexes
    Bestgen, S.; Seidl, C.; Wiesner, T.; Zimmer, A.; Falk, M.; Köberle, B.; Austeri, M.; Paradies, J.; Bräse, S.; Schepers, U.; Roesky, P. W.
    2017. Chemistry - a European journal, 23 (26), 6315–6322. doi:10.1002/chem.201605237 
  33. Oxidation of diazenyl-protected N-heterocycles-a new entry to functionalized lactams
    Petrović, M.; Scarpi, D.; Nieger, M.; Jung, N.; Occhiato, E. G.; Bräse, S.
    2017. RSC Advances, 7 (16), 9461–9464. doi:10.1039/c6ra26546d VolltextVolltext der Publikation als PDF-Dokument 
  34. Phospholipid arrays on porous polymer coatings generated by micro-contact spotting
    Sekula-Neuner, S.; Freitas, M. de; Tröster, L.-M.; Jochum, T.; Levkin, P. A.; Hirtz, M.; Fuchs, H.
    2017. Beilstein journal of nanotechnology, 8, 715–722. doi:10.3762/bjnano.8.75 VolltextVolltext der Publikation als PDF-Dokument 
  35. Synthesis of aminopyrazoles from sydnones and ynamides
    Wezeman, T.; Comas-Barceló, J.; Nieger, M.; Harrity, J. P. A.; Bräse, S.
    2017. Organic & biomolecular chemistry, 15 (7), 1575–1579. doi:10.1039/c6ob02518h 
  36. Stille and Suzuki Cross-Coupling Reactions as Versatile Tools for Modifications at C-17 of Steroidal Skeletons - A Comprehensive Study
    Koch, V.; Nieger, M.; Bräse, S.
    2017. Advanced synthesis & catalysis, 359 (5), 832–840. doi:10.1002/adsc.201601289 
  37. Synthesis of Diaziridines and Diazirines via Resin-Bound Sulfonyl Oximes
    Protasova, I.; Bulat, B.; Jung, N.; Bräse, S.
    2017. Organic letters, 19 (1), 34–37. doi:10.1021/acs.orglett.6b03252 
  38. A novel ZEB1/HAS2 positive feedback loop promotes EMT in breast cancer
    Preca, B.-T.; Bajdak, K.; Mock, K.; Lehmann, W.; Sundararajan, V.; Bronsert, P.; Matzge-Ogi, A.; Orian-Rousseau, V.; Brabletz, S.; Brabletz, T.; Maurer, J.; Stemmler, M. P.
    2017. OncoTarget, 8 (7), 11530–11543. doi:10.18632/oncotarget.14563 VolltextVolltext der Publikation als PDF-Dokument 
  39. CHAPTER 7: Patterned Superhydrophobic Surfaces
    Ueda, E.; Levkin, P. A.
    2017. Non-wettable surfaces : theory, preparation and applications. Ed. : A. Marmur, 182–222, Royal Society of Chemistry (RSC). doi:10.1039/9781782623953-00182 
  40. Evaluation of the Droplet-Microarray Platform for High-Throughput Screening of Suspension Cells
    Popova, A. A.; Depew, C.; Permana, K. M.; Trubitsyn, A.; Peravali, R.; Ordiano, J. Á. G.; Reischl, M.; Levkin, P. A.
    2017. Journal of laboratory automation, 22 (2), 163–175. doi:10.1177/2211068216677204 
  41. CD44v6-Peptide Functionalized Nanoparticles Selectively Bind to Metastatic Cancer Cells
    Li, L.; Schmitt, M.; Matzke-Ogi, A.; Wadhwani, P.; Orian-Rousseau, V.; Levkin, P. A.
    2017. Advanced science, 4 (1), Art.Nr. 1600202. doi:10.1002/advs.201600202 VolltextVolltext der Publikation als PDF-Dokument 
  42. Arenediazonium Tosylates (ADTs) as Efficient Reagents for Suzuki–Miyaura Cross-Coupling in Neat Water
    Kutonova, K. V.; Jung, N.; Trusova, M. E.; Filimonov, V. D.; Postnikov, P. S.; Bräse, S.
    2017. Synthesis, 49 (7), 1680–1688. doi:10.1055/s-0036-1588919 
  43. Propellanes : From a Chemical Curiosity to “Explosive” Materials and Natural Products
    Dilmac, A. M.; Spuling, E.; Meijere, A. de; Bräse, S.
    2017. Angewandte Chemie / International edition, 56 (21), 5684–5718. doi:10.1002/anie.201603951 
  44. Pd-mediated cross-coupling of C-17 lithiated androst-16-en-3-ol – access to functionalized arylated steroid derivatives
    Koch, V.; Bräse, S.
    2017. Organic & biomolecular chemistry, 15 (1), 92–95. doi:10.1039/C6OB02496C