Veröffentlichungen 2018
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Chemotion-ELN part 2: adaption of an embedded Ketcher editor to advanced research applications
Kotov, S.; Tremouilhac, P.; Jung, N.; Bräse, S.
2018. Journal of cheminformatics, 10 (1), Art.Nr. 38. doi:10.1186/s13321-018-0292-9 -
Superoleophobic Slippery Lubricant-Infused Surfaces: Combining Two Extremes in the Same Surface
Dong, Z.; Schumann, M. F.; Hokkanen, M. J.; Chang, B.; Welle, A.; Zhou, Q.; Ras, R. H. A.; Xu, Z.; Wegener, M.; Levkin, P. A.
2018. Advanced materials, 30 (45), Art.-Nr.: 1803890. doi:10.1002/adma.201803890 -
Surface Functionalization and Patterning by Multifunctional Resorcinarenes
Behboodi-Sadabad, F.; Trouillet, V.; Welle, A.; Messersmith, P. B.; Levkin, P. A.
2018. ACS applied materials & interfaces, 10 (45), 39268–39278. doi:10.1021/acsami.8b14771 -
Sustainable metal complexes for organic light-emitting diodes (OLEDs)
Bizzarri, C.; Spuling, E.; Knoll, D. M.; Volz, D.; Bräse, S.
2018. Coordination chemistry reviews, 373, 49–82. doi:10.1016/j.ccr.2017.09.011 -
Reparable Superhydrophobic Surface with Hidden Reactivity, Its Photofunctionalization and Photopatterning
Du, X.; Wang, M.; Welle, A.; Behboodi-Sadabad, F.; Wang, Y.; Levkin, P. A.; Gu, Z.
2018. Advanced functional materials, 28 (41), Art.-Nr.: 1803765. doi:10.1002/adfm.201803765 -
Lanthanide pyrazolecarboxylates for OLEDs and bioimaging
Utochnikova, V. V.; Latipov, E. V.; Dalinger, A. I.; Nelyubina, Y. V.; Vashchenko, A. A.; Hoffmann, M.; Kalyakina, A. S.; Vatsadze, S. Z.; Schepers, U.; Bräse, S.; Kuzmina, N. P.
2018. Journal of luminescence, 202, 38–46. doi:10.1016/j.jlumin.2018.05.022 -
Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates with Pyridyl and Pyrimidyl Building Blocks
Knoll, D. M.; Bräse, S.
2018. ACS omega, 3 (9), 12158–12162. doi:10.1021/acsomega.8b01774 -
Formation of Liquid-Liquid Micropatterns through Guided Liquid Displacement on Liquid-Infused Surfaces
Paulssen, D.; Feng, W.; Pini, I.; Levkin, P. A.
2018. Advanced materials interfaces, 5 (18), 1800852. doi:10.1002/admi.201800852 -
Series of Photoswitchable Azobenzene-Containing Metal–Organic Frameworks with Variable Adsorption Switching Effect
Wang, Z.; Müller, K.; Valášek, M.; Grosjean, S.; Bräse, S.; Wöll, C.; Mayor, M.; Heinke, L.
2018. The journal of physical chemistry <Washington, DC> / C, 122 (33), 19044–19050. doi:10.1021/acs.jpcc.8b05843 -
Surface Functionalization of Silicon, HOPG, and Graphite Electrodes: Toward an Artificial Solid Electrolyte Interface
Moock, D. S.; Steinmüller, S. O.; Wessely, I. D.; Llevot, A.; Bitterer, B.; Meier, M. A. R.; Bräse, S.; Ehrenberg, H.; Scheiba, F.
2018. ACS applied materials & interfaces, 10 (28), 24172–24180. doi:10.1021/acsami.8b04877 -
One-Pot Parallel Synthesis of Lipid Library via Thiolactone Ring Opening and Screening for Gene Delivery
Molla, M. R.; Böser, A.; Rana, A.; Schwarz, K.; Levkin, P. A.
2018. Bioconjugate chemistry, 29 (4), 992–999. doi:10.1021/acs.bioconjchem.8b00007 -
Regulation of Staphylococcus aureus Infection of Macrophages by CD44, Reactive Oxygen Species, and Acid Sphingomyelinase
Li, C.; Wu, Y.; Riehle, A.; Orian-Rousseau, V.; Zhang, Y.; Gulbins, E.; Grassmé, H.
2018. Antioxidants & redox signaling, 28 (10), 916–934. doi:10.1089/ars.2017.6994 -
Bioinspired Strategy for Controlled Polymerization and Photopatterning of Plant Polyphenols
Behboodi-Sadabad, F.; Zhang, H.; Trouillet, V.; Welle, A.; Plumeré, N.; Levkin, P. A.
2018. Chemistry of materials, 30 (6), 1937–1946. doi:10.1021/acs.chemmater.7b04914 -
Triplet emitters versus TADF emitters in OLEDs : A comparative study
Bizzarri, C.; Hundemer, F.; Busch, J.; Bräse, S.
2018. Polyhedron, 140, 51–66. doi:10.1016/j.poly.2017.11.032 -
TGFβ counteracts LYVE-1-mediated induction of lymphangiogenesis by small hyaluronan oligosaccharides
Bauer, J.; Rothley, M.; Schmaus, A.; Quagliata, L.; Ehret, M.; Biskup, M.; Orian-Rousseau, V.; Jackson, D. G.; Pettis, R. J.; Harvey, A.; Bräse, S.; Thiele, W.; Sleeman, J. P.
2018. Journal of molecular medicine, 96 (2), 199–209. doi:10.1007/s00109-017-1615-4 -
Collision Induced Dissociation of Benzylpyridinium-Substituted Porphyrins : Towards a Thermometer Scale for Multiply Charged Ions?
Brendle, K.; Kordel, M.; Schneider, E.; Wagner, D.; Bräse, S.; Weis, P.; Kappes, M. M.
2018. Journal of the American Society for Mass Spectrometry, 29 (2), 382–392. doi:10.1007/s13361-017-1835-4 -
Differential recruitment of CD44 isoforms by ErbB ligands reveals an involvement of CD44 in breast cancer
Morath, I.; Jung, C.; Lévêque, R.; Linfeng, C.; Toillon, R.-A.; Warth, A.; Orian-Rousseau, V.
2018. Oncogene, 37, 1472–1484. doi:10.1038/s41388-017-0030-1 -
Asymmetric Organocatalytic Synthesis of Bisindoles - Scope and Derivatizations
Retich, C.; Bräse, S.
2018. European journal of organic chemistry, 2018 (1), 60–77. doi:10.1002/ejoc.201701502 -
Combinatorial Synthesis of Peptoid Arrays via Laser-Based Stacking of Multiple Polymer Nanolayers
Mattes, D. S.; Streit, B.; Bhandari, D. R.; Greifenstein, J.; Foertsch, T. C.; Münch, S. W.; Ridder, B.; v. Bojničić-Kninski, C.; Nesterov-Mueller, A.; Spengler, B.; Schepers, U.; Bräse, S.; Loeffler, F. F.; Breitling, F.
2018. Macromolecular rapid communications, 40 (6), Art.Nr.: 1800533. doi:10.1002/marc.201800533 -
Anti-neuroinflammatory effects of GPR55 antagonists in LPS-activated primary microglial cells
Saliba, S. W.; Jauch, H.; Gargouri, B.; Keil, A.; Hurrle, T.; Volz, N.; Mohr, F.; Stelt, M. van der; Bräse, S.; Fiebich, B. L.
2018. Journal of neuroinflammation, 15 (1), Art. Nr.: 322. doi:10.1186/s12974-018-1362-7 -
Amidines: Their synthesis, reactivity, and applications in heterocycle synthesis
Aly, A. A.; Bräse, S.; Gomaa, M. A.-M.
2018. Arkivoc, 2018 (6), 85–138. doi:10.24820/ark.5550190.p010.607 -
Synthesis of novel 1,2-bis-quinolinyl-1,4-naphthoquinones: ERK2 inhibition, cytotoxicity and molecular docking studies
Aly, A. A.; El-Sheref, E. M.; Bakheet, M. E. M.; Mourad, M. A. E.; Brown, A. B.; Bräse, S.; Nieger, M.; Ibrahim, M. A. A.
2018. Bioorganic chemistry, 81, 700–712. doi:10.1016/j.bioorg.2018.09.017 -
Homonuclear decoupling by projection reconstruction
Görling, B.; Bermel, W.; Bräse, S.; Luy, B.
2018. Magnetic resonance in chemistry, 56 (10), 1006–1020. doi:10.1002/mrc.4784 -
Synthesis of Azido-Glycans for Chemical Glycomodification of Proteins
Wawryszyn, M.; Sauter, P. F.; Nieger, M.; Koos, M. R. M.; Koehler, C.; Luy, B.; Lemke, E. A.; Bräse, S.
2018. European journal of organic chemistry, 2018 (31), 4296–4305. doi:10.1002/ejoc.201800602 -
Nanoliter deposition on star-shaped hydrophilic-superhydrophobic patterned surfaces
Chang, B.; Kivinen, O.; Pini, I.; Levkin, P. A.; Ras, R. H. A.; Zhou, Q.
2018. Soft matter, 14 (36), 7500–7506. doi:10.1039/c8sm01288a -
Planar chiral [2.2]paracyclophanes: From synthetic curiosity to applications in asymmetric synthesis and materials
Hassan, Z.; Spuling, E.; Knoll, D. M.; Lahann, J.; Bräse, S.
2018. Chemical Society reviews, 47 (18), 6947–6963. doi:10.1039/c7cs00803a -
(Deep) blue through-space conjugated TADF emitters based on [2.2]paracyclophanes
Spuling, E.; Sharma, N.; Samuel, I. D. W.; Zysman-Colman, E.; Bräse, S.
2018. Chemical communications, 54 (67), 9278–9281. doi:10.1039/c8cc04594a -
Droplet microarray: Miniaturized platform for rapid formation and high-throughput screening of embryoid bodies
Tronser, T.; Demir, K.; Reischl, M.; Bastmeyer, M.; Levkin, P. A.
2018. Lab on a chip, 18 (15), 2257–2269. doi:10.1039/c8lc00450a -
Improved Extraction Repeatability and Spectral Reproducibility for Liquid Extraction Surface Analysis-Mass Spectrometry Using Superhydrophobic-Superhydrophilic Patterning
Meurs, J.; Alexander, M. R.; Levkin, P. A.; Widmaier, S.; Bunch, J.; Barrett, D. A.; Kim, D.-H.
2018. Analytical chemistry, 90 (10), 6001–6005. doi:10.1021/acs.analchem.8b00973 -
Click chemistry-mediated biotinylation reveals a function for the protease BACE1 in modulating the neuronal surface glycoproteome
Herber, J.; Njavro, J.; Feederle, R.; Schepers, U.; Müller, U.; Bräse, S.; Müller, S.; Lichtenthaler, S. F.
2018. Molecular & cellular proteomics, 17 (8), 1487–1501. doi:10.1074/mcp.RA118.000608 -
Remarkable high efficiency of red emitters using Eu(III) ternary complexes
Kalyakina, A. S.; Utochnikova, V. V.; Zimmer, M.; Dietrich, F.; Kaczmarek, A. M.; Van Deun, R.; Vashchenko, A. A.; Goloveshkin, A. S.; Nieger, M.; Gerhards, M.; Schepers, U.; Bräse, S.
2018. Chemical communications, 54 (41), 5221–5224. doi:10.1039/C8CC02930J -
Micro-patterns on nanocellulose films and paper by photo-induced thiol–yne click coupling: a facile method toward wetting with spatial resolution
Guo, J.; Filpponen, I.; Johansson, L.-S.; Heiβler S.; Li, L.; Levkin, P.; Rojas, O. J.
2018. Cellulose, 25 (1), 367–375. doi:10.1007/s10570-017-1593-2 -
Patterned superhydrophobic surfaces to process and characterize biomaterials and 3D cell culture
Neto, A. I.; Levkin, P. A.; Mano, J. F.
2018. Materials Horizons, 5 (3), 379–393. doi:10.1039/C7MH00877E -
Free-standing three-dimensional hollow bacterial cellulose structures with controlled geometry via patterned superhydrophobic-hydrophilic surfaces
Laromaine, A.; Tronser, T.; Pini, I.; Parets, S.; Levkin, P. A.; Roig, A.
2018. Soft matter, 14 (19), 3955–3962. doi:10.1039/C8SM00112J -
Droplet Microarrays: From Surface Patterning to High-Throughput Applications
Feng, W.; Ueda, E.; Levkin, P. A.
2018. Advanced materials, 30 (20), 1706111. doi:10.1002/adma.201706111 -
Bacterial cellulose promotes long-term stemness of mESC
Tronser, T.; Laromaine, A.; Roig, A.; Levkin, P. A.
2018. ACS applied materials & interfaces, 10 (19), 16260–16269. doi:10.1021/acsami.8b01992 -
1,5-Cyclooctadienyl alcohols and ketones generate a new class of COD Pt complexes
Wandler, A. E. E.; Koos, M. R. M.; Nieger, M.; Luy, B.; Bräse, S.
2018. Dalton transactions, 47 (11), 3689–3692. doi:10.1039/C8DT00075A -
Alkyl and Aryl Thiol Addition to [1.1.1]Propellane: Scope and Limitations of a Fast Conjugation Reaction
Bär, R. M.; Kirschner, S.; Nieger, M.; Bräse, S.
2018. Chemistry - a European journal, 24 (6), 1373–1382. doi:10.1002/chem.201704105 -
Theoretical and NMR Conformational Studies of β-Proline Oligopeptides With Alternating Chirality of Pyrrolidine Units
Mantsyzov, A. B.; Savelyev, O. Y.; Ivantcova, P. M.; Bräse, S.; Kudryavtsev, K. V.; Polshakov, V. I.
2018. Frontiers in Chemistry, 6, Art.Nr. 91. doi:10.3389/fchem.2018.00091 -
Addition of dithi(ol)anylium tetrafluoroborates to α, β-unsaturated ketones
Huang, Y.-C.; Nguyen, A.; Gräßle, S.; Vanderheiden, S.; Jung, N.; Bräse, S.
2018. Beilstein journal of organic chemistry, 14, 515–522. doi:10.3762/bjoc.14.37 -
Relative Reactivity of Benzothiophene-Fused Enediynes in the Bergman Cyclization
Lyapunova, A. G.; Danilkina, N. A.; Rumyantsev, A. M.; Khlebnikov, A. F.; Chislov, M. V.; Starova, G. L.; Sambuk, E. V.; Govdi, A. I.; Bräse, S.; Balova, I. A.
2018. The journal of organic chemistry, 83 (5), 2788–2801. doi:10.1021/acs.joc.7b03258 -
Thermal cis-to-trans Isomerization of Azobenzene Side Groups in Metal-Organic Frameworks investigated by Localized Surface Plasmon Resonance Spectroscopy
Zhou, W.; Grosjean, S.; Bräse, S.; Heinke, L.
2018. Zeitschrift für physikalische Chemie, 233 (SI, 1), 15–22. doi:10.1515/zpch-2017-1081 -
Fish-Microarray: A Miniaturized Platform for Single-Embryo High-Throughput Screenings
Popova, A. A.; Marcato, D.; Peravali, R.; Wehl, I.; Schepers, U.; Levkin, P. A.
2018. Advanced functional materials, 28 (3), 1703486. doi:10.1002/adfm.201703486 -
Microenvironment-induced CD44v6 promotes early disease progression in chronic lymphocytic leukemia
Gutjahr, J. C.; Szenes, E.; Tschech, L.; Asslaber, D.; Schlederer, M.; Roos, S.; Yu, X.; Girbl, T.; Sternberg, C.; Egle, A.; Aberger, F.; Alon, R.; Kenner, L.; Greil, R.; Orian-Rousseau, V.; Hartmann, T. N.
2018. Blood, 131 (12), 1337–1349. doi:10.1182/blood-2017-08-802462 -
The coordination- and photochemistry of copper(I) complexes: variation of N^N ligands from imidazole to tetrazole
Bergmann, L.; Braun, C.; Nieger, M.; Bräse, S.
2018. Dalton transactions, 47 (2), 608–621. doi:10.1039/C7DT03682E -
Ultra-fast Suzuki and Heck reactions for the synthesis of styrenes and stilbenes using arenediazonium salts as super-electrophiles
Trusova, M. E.; Rodriguez-Zubiri, M.; Kutonova, K. V.; Jung, N.; Bräse, S.; Felpin, F.-X.; Postnikov, P. S.
2018. Organic chemistry frontiers, 5 (1), 41–45. doi:10.1039/C7QO00750G