Publications


  1. Key role of cycloalkyne nature in alkyne-dye reagents for enhanced specificity of intracellular imaging by bioorthogonal bioconjugation
    Vidyakina, A. A.; Silonov, S. A.; Govdi, A. I.; Ivanov, A. Y.; Podolskaya, E. P.; Balova, I. A.; Bräse, S.; Danilkina, N. A.
    2024. Organic & Biomolecular Chemistry. doi:10.1039/d4ob01032aFull textFull text of the publication as PDF document
  2. Convenient synthesis and X-ray determination of 2-amino-6 H -1,3,4-thiadiazin-3-ium bromides endowed with antiproliferative activity
    Tawfeek, H. N.; Abdelmoez, A.; Dahlous, K. A.; Youssif, B. G. M.; Bräse, S.; Rissanen, K.; Nieger, M.; El-Sheref, E. M.
    2024. RSC Advances, 14 (25), 17866 – 17876. doi:10.1039/D4RA02531HFull textFull text of the publication as PDF document
  3. Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
    Neeb, A.; Figueiredo, I.; Bogdan, D.; Cato, L.; Stober, J.; Jiménez-Vacas, J. M.; Gourain, V.; Lee, I. I.; Seeger, R.; Muhle-Goll, C.; Gurel, B.; Welti, J.; Nava Rodrigues, D.; Rekowski, J.; Qiu, X.; Jiang, Y.; Di Micco, P.; Mateos, B.; Bielskutė, S.; Riisnaes, R.; Ferreira, A.; Miranda, S.; Crespo, M.; Buroni, L.; Ning, J.; Carreira, S.; Bräse, S.; Jung, N.; Gräßle, S.; Swain, A.; Salvatella, X.; Plymate, S. R.; Al-Lazikani, B.; Long, H. W.; Yuan, W.; Brown, M.; Cato, A. C. B.; de Bono, J. S.; Sharp, A.
    2024. Molecular Cancer Therapeutics, 23 (6), 791–808. doi:10.1158/1535-7163.MCT-23-0354Full textFull text of the publication as PDF document
  4. Discovery of new Schiff bases of the disalicylic acid scaffold as DNA gyrase and topoisomerase IV inhibitors endowed with antibacterial properties
    Al-Wahaibi, L. H.; Mahmoud, M. A.; Alzahrani, H. A.; Abou-Zied, H. A.; Gomaa, H. A. M.; Youssif, B. G. M.; Bräse, S.; Rabea, S. M.
    2024. Frontiers in Chemistry, 12, Art.-Nr.: 1419242. doi:10.3389/fchem.2024.1419242Full textFull text of the publication as PDF document
  5. A New Class of Chiral Polyethers and Polyesters Based on the [2.2]Paracyclophane Scaffold
    Kern, P.; Tappert, H.; Bräse, S.
    2024. Polymers, 16 (11), Art.-Nr.: 1603. doi:10.3390/polym16111603Full textFull text of the publication as PDF document
  6. Substituted Pyrrole‐based Schiff Bases: Effect On The Luminescence Of Neutral Heteroleptic Cu(I) Complexes
    Ferraro, V.; Fuhr, O.; Bizzarri, C.; Bräse, S.
    2024. European Journal of Inorganic Chemistry, Art.-Nr.: e202400080. doi:10.1002/ejic.202400080Full textFull text of the publication as PDF document
  7. Reversing the stereoselectivity of intramolecular [2+2] photocycloaddition utilizing cucurbit[8]uril as a molecular flask
    Qiu, X.; Seibert, J.; Fuhr, O.; Biedermann, F.; Bräse, S.
    2024. Chemical Communications, 60 (24), 3267–3270. doi:10.1039/D3CC05783FFull textFull text of the publication as PDF document
  8. Stereoselective synthesis and X-ray structure determination of novel 1,2-dihydroquinolinehydrazonopropanoate derivatives
    Tawfeek, H. N.; Tawfeek, A. M.; Bräse, S.; Nieger, M.; El-Sheref, E. M.
    2024. Heliyon, 10 (4), Art.-Nr.: e25248. doi:10.1016/j.heliyon.2024.e25248Full textFull text of the publication as PDF document
  9. Optimized Detection of Volatile Organic Compounds Utilizing Durable and Selective Arrays of Tailored UiO-66-X SURMOF Sensors
    Okur, S.; Hashem, T.; Bogdanova, E.; Hodapp, P.; Heinke, L.; Bräse, S.; Wöll, C.
    2024. ACS Sensors, 9 (2), 622–630. doi:10.1021/acssensors.3c01575
  10. From Mono- to Polynuclear 2-(Diphenylphosphino)pyridine-Based Cu(I) and Ag(I) Complexes: Synthesis, Structural Characterization, and DFT Calculations
    Busch, J. M.; Rehak, F. R.; Ferraro, V.; Nieger, M.; Kemell, M.; Fuhr, O.; Klopper, W.; Bräse, S.
    2024. ACS Omega, 9 (2), 2220–2233. doi:10.1021/acsomega.3c05755Full textFull text of the publication as PDF document
  11. (Semi-) Automatic Review Process for Common Compound Characterization Data in Organic Synthesis
    Huang, Y.-C.; Tremouilhac, P.; Kuhn, S.; Huang, P.-C.; Lin, C.-L.; Schlörer, N.; Taubert, O.; Götz, M.; Jung, N.; Bräse, S.
    2024. ChemRxiv. doi:10.26434/chemrxiv-2024-1r9tbFull textFull text of the publication as PDF document
  12. Thermally Activated Delayed Fluorescence (TADF) Materials Based on Earth‐Abundant Transition Metal Complexes: Synthesis, Design and Applications
    Ferraro, V.; Bizzarri, C.; Bräse, S.
    2024. Advanced Science, 2404866. doi:10.1002/advs.202404866Full textFull text of the publication as PDF document
  13. Effect of tert-butyl substitution on controlling the orientation of TADF emitters in guest–host systems
    Sahay, P.; Crovini, E.; Stavrou, K.; Zhang, Z.; Nguyên, B. M.; Wagner, D.; Strohriegl, P.; Bräse, S.; Monkman, A.; Zysman-Colman, E.; Brütting, W.
    2024. Journal of Materials Chemistry C. doi:10.1039/D4TC01195C
  14. From Molecules to Materials: Collaborative Research at the Chemistry—Materials Science Interface and Lessons Learned in Cyclophane Chemistry
    Hassan, Z.; Zysman-Colman, E.; Lahann, J.; Bräse, S.
    2024. Advanced Functional Materials, Art.-Nr.: 202403365. doi:10.1002/adfm.202403365Full textFull text of the publication as PDF document
  15. Doping Strategies for Tetrasubstituted Paracyclophane Hole Transport Layers in Perovskite Solar Cells
    Schulz, A. D.; Otterbach, S. A.; Tappert, H.; Elsing, D.; Wenzel, W.; Kozlowska, M.; Bräse, S.; Colsmann, A.; Röhm, H.
    2024. Advanced Functional Materials, Art.-Nr.: 2402110. doi:10.1002/adfm.202402110Full textFull text of the publication as PDF document
  16. Modulation of neuroinflammation and oxidative stress by targeting GPR55 – new approaches in the treatment of psychiatric disorders
    Apweiler, M.; Saliba, S. W.; Sun, L.; Streyczek, J.; Normann, C.; Hellwig, S.; Bräse, S.; Fiebich, B. L.
    2024. Molecular Psychiatry. doi:10.1038/s41380-024-02614-5Full textFull text of the publication as PDF document
  17. Design and synthesis of new dihydropyrimidine/sulphonamide hybrids as promising anti-inflammatory agents via dual mPGES-1/5-LOX inhibition
    Al-Wahaibi, L. H.; Elshamsy, A. M.; Ali, T. F. S.; Youssif, B. G. M.; Bräse, S.; Abdel-Aziz, M.; El-Koussi, N. A.
    2024. Frontiers in Chemistry, 12, Art.-Nr.: 1387923. doi:10.3389/fchem.2024.1387923Full textFull text of the publication as PDF document
  18. Extraction of the intrinsic rate constant for a photocyclization reaction in capillary microreactors using a simplified reactor model
    Li, J.; Šimek Tosino, H.; Ladewig, B. P.; Jung, N.; Bräse, S.; Dittmeyer, R.
    2024. Reaction Chemistry & Engineering. doi:10.1039/d4re00087kFull textFull text of the publication as PDF document
  19. Linker aggregation engineering of TADF materials to tune carrier balance for highly efficient organic LEDs with long operational lifetime
    Zhang, Z.; Xia, R.; Wang, K.; Wu, Y.; Zang, P.; Gan, X.; Liao, Z.; Wei, B.; Wu, P.; Bräse, S.; Wang, Z.
    2024. Aggregate, Art.-Nr.: e588. doi:10.1002/agt2.588Full textFull text of the publication as PDF document
  20. Anti-Neuroinflammatory Effects of a Macrocyclic Peptide-Peptoid Hybrid in Lipopolysaccharide-Stimulated BV2 Microglial Cells
    Sun, L.; Wilke Saliba, S.; Apweiler, M.; Akmermer, K.; Herlan, C.; Grathwol, C.; de Oliveira, A. C. P.; Normann, C.; Jung, N.; Bräse, S.; Fiebich, B. L.
    2024. International Journal of Molecular Sciences, 25 (8), Artkl.Nr.:4462. doi:10.3390/ijms25084462Full textFull text of the publication as PDF document
  21. A Novel Carbazolophane: A Comparison of the Performance of Two Planar Chiral CP‐TADF Emitters
    Seibert, J.; Xu, Y.; Hafeez, H.; Podlech, J.; Favereau, L.; Spuling, E.; Waldhelm, C.; Nieger, M.; Fuhr, O.; Hassan, Z.; Crassous, J.; Samuel, I. D. W.; Zysman-Colman, E.; Bräse, S.
    2024. Advanced Functional Materials, Art.-Nr.: 2401956. doi:10.1002/adfm.202401956Full textFull text of the publication as PDF document
  22. Synthetic methodology of pyrimido[4,5‐ b ]quinoline derivatives
    Tawfeek, H. N.; Hasanin, T. H. A.; Bräse, S.
    2024. Journal of Heterocyclic Chemistry, 61 (6), 971–1008. doi:10.1002/jhet.4815
  23. Modulating and Accelerating Photolysis of Photoactivatable [2.2]Paracyclophane Aryl Azide in Supramolecular Host for Bioimaging
    Qiu, X.; Pohl, E.; Cai, Q.; Seibert, J.; Li, Y.; Leopold, S.; Fuhr, O.; Meier, M. A. R.; Schepers, U.; Bräse, S.
    2024. Advanced Functional Materials, Art.-Nr.: 2401938. doi:10.1002/adfm.202401938Full textFull text of the publication as PDF document
  24. Synthesis of Mono‐, Di‐, Tri‐, and Tetra‐cationic Pyridinium and Vinylpyridinium Modified [2.2]Paracyclophanes: Modular Receptors for Supramolecular Systems
    Wang, Y.; Li, Y.; Fuhr, O.; Nieger, M.; Hassan, Z.; Bräse, S.
    2024. ChemistryOpen. doi:10.1002/open.202400024Full textFull text of the publication as PDF document
  25. Design, synthesis, and apoptotic antiproliferative action of new 1,2,3-triazole/1,2,4-oxadiazole hybrids as dual EGFR/VEGFR-2 inhibitors
    Mahmoud, M. A.; Mohammed, A. F.; Salem, O. I. A.; Almutairi, T. M.; Bräse, S.; Youssif, B. G. M.
    2024. Journal of Enzyme Inhibition and Medicinal Chemistry, 39 (1), Art.-Nr.: 2305856. doi:10.1080/14756366.2024.2305856Full textFull text of the publication as PDF document
  26. Constructing [2.2]Paracyclophane‐Based Ultrasensitive Optical Fluorescent‐Phosphorescent Thermometer with Cucurbit[8]uril Supramolecular Assembly
    Qiu, X.; Zheng, T.; Runowski, M.; Woźny, P.; Martín, I. R.; Soler-Carracedo, K.; Piñero, C. E.; Lebedkin, S.; Fuhr, O.; Bräse, S.
    2024. Advanced Functional Materials, Art.-Nr.: 2313517. doi:10.1002/adfm.202313517Full textFull text of the publication as PDF document
  27. Benzimidazole-Based Derivatives as Apoptotic Antiproliferative Agents: Design, Synthesis, Docking, and Mechanistic Studies
    Youssif, B. G. M.; Morcoss, M. M.; Bräse, S.; Abdel-Aziz, M.; Abdel-Rahman, H. M.; Abou El-Ella, D. A.; Abdelhafez, E. S. M. N.
    2024. Molecules, 29 (2), Art.-Nr.: 446. doi:10.3390/molecules29020446Full textFull text of the publication as PDF document
  28. Azide Thermolysis Frameworks: Self‐inflating, Porous, and Lightweight Materials
    Brückel, J.; Matt, Y.; Schmidt, L.; Mattern, C. M.; Schepers, U.; Leopold, S.; Calkovsky, M.; Gerthsen, D.; Bräse, S.
    2024. ChemNanoMat, 10 (2), Art.-Nr.: e202300222. doi:10.1002/cnma.202300222Full textFull text of the publication as PDF document
  29. Modulating Aryl Azide Photolysis: Synthesis of a Room‐Temperature Phosphorescent Carboline in Cucurbit[7]uril Host
    Qiu, X.; Wang, Y.; Leopold, S.; Lebedkin, S.; Schepers, U.; Kappes, M. M.; Biedermann, F.; Bräse, S.
    2024. Small, 20 (16), Art.Nr.: 2307318. doi:10.1002/smll.202307318Full textFull text of the publication as PDF document
  30. The Impact of Digitalized Data Management on Materials Systems Workflows
    Tristram, F.; Jung, N.; Hodapp, P.; Schröder, R. R.; Wöll, C.; Bräse, S.
    2024. Advanced Functional Materials, 34 (20), Art.-Nr.: 2303615. doi:10.1002/adfm.202303615Full textFull text of the publication as PDF document
  31. Disulfide‐Bridged Dynamic Covalent Triazine Polymer Thin Films by Interface Polymerization: High Refractive Index with Excellent Optical Transparency
    Begum, S.; Kutonova, K.; Mauri, A.; Koenig, M.; Chan, K. C.; Sprau, C.; Dolle, C.; Trouillet, V.; Hassan, Z.; Leonhard, T.; Heißler, S.; Eggeler, Y. M.; Wenzel, W.; Kozlowska, M.; Bräse, S.
    2024. Advanced Functional Materials, 34 (20), Art.-Nr.: 2303929. doi:10.1002/adfm.202303929Full textFull text of the publication as PDF document
  32. Functional Material Systems Enabled by Automated Data Extraction and Machine Learning
    Kalhor, P.; Jung, N.; Bräse, S.; Wöll, C.; Tsotsalas, M.; Friederich, P.
    2024. Advanced Functional Materials, 34 (20), Art.Nr.: 2302630. doi:10.1002/adfm.202302630Full textFull text of the publication as PDF document
  33. Recent Advances of Transition Metal Complexes for Photopolymerization and 3D Printing under Visible Light
    Ferraro, V.; Adam, C. R.; Vranic, A.; Bräse, S.
    2024. Advanced Functional Materials, 34 (20), Art.-Nr.: 2302157. doi:10.1002/adfm.202302157Full textFull text of the publication as PDF document
  34. Selective Peptide Binders to the Perfluorinated Sulfonic Acid Ionomer Nafion
    Schmidt, D.; Gartner, P.; Berezkin, I.; Rudat, J.; Bilger, M.; Grünert, T.; Zimmerer, N.; Quarz, P.; Scharfer, P.; Brückel, J.; Jung, A. P.; Singh, P.; Pooja, P.; Meier, B.; Stahlberger, M.; Schabel, W.; Bräse, S.; Lanza, G.; Nesterov-Mueller, A.
    2024. Advanced Functional Materials, 34 (20), Article no: 2214932. doi:10.1002/adfm.202214932Full textFull text of the publication as PDF document
  35. Exploring Functional Photonic Devices made from a Chiral Metal–Organic Framework Material by a Multiscale Computational Method
    Zerulla, B.; Li, C.; Beutel, D.; Oßwald, S.; Holzer, C.; Bürck, J.; Bräse, S.; Wöll, C.; Fernandez-Corbaton, I.; Heinke, L.; Rockstuhl, C.; Krstić, M.
    2024. Advanced Functional Materials, 34 (20), Art.-Nr.: 2301093. doi:10.1002/adfm.202301093Full textFull text of the publication as PDF document
  36. Utilizing machine learning to optimize metal–organic framework-derived polymer membranes for gas separation
    Pilz, L.; Natzeck, C.; Wohlgemuth, J.; Scheuermann, N.; Spiegel, S.; Oßwald, S.; Knebel, A.; Bräse, S.; Wöll, C.; Tsotsalas, M.; Prasetya, N.
    2023. Journal of Materials Chemistry A, 11 (45), 24724–24737. doi:10.1039/d3ta05235dFull textFull text of the publication as PDF document
  37. Synthesis, Antioxidant and Antiproliferative Actions of 4-(1,2,3-Triazol-1-yl)quinolin-2(1H)-ones as Multi-Target Inhibitors
    El-Sheref, E. M.; Bräse, S.; Tawfeek, H. N.; Alasmary, F. A.; Youssif, B. G. M.
    2023. International Journal of Molecular Sciences, 24 (17), Art.-Nr.: 13300. doi:10.3390/ijms241713300Full textFull text of the publication as PDF document
  38. Marriage of an N-Fused and a Regular Porphyrin in a Cofacial Ligand System
    Schissler, C.; Schneider, E. K.; Rotter, M.; Notter, S.; Geier, C.; Weis, P.; Kappes, M. M.; Bräse, S.
    2023. Organometallics, 42 (15), 1882 – 1889. doi:10.1021/acs.organomet.3c00116Full textFull text of the publication as PDF document
  39. Synthesis and Structure Determination of Substituted Thiazole Derivatives as EGFR/BRAF Dual Inhibitors Endowed with Antiproliferative Activity
    Al-Wahaibi, L. H.; El-Sheref, E. M.; Hassan, A. A.; Bräse, S.; Nieger, M.; Youssif, B. G. M.; Ibrahim, M. A. A.; Tawfeek, H. N.
    2023. Pharmaceuticals, 16 (7), Art.-Nr.: 1014. doi:10.3390/ph16071014Full textFull text of the publication as PDF document
  40. Identification of an imidazopyridine-based compound as an oral selective estrogen receptor degrader for breast cancer therapy
    Pan, M.; Solozobova, V.; Kuznik, N. C.; Jung, N.; Graessle, S.; Gourain, V.; Heneka, Y. M.; Cramer von Clausbruch, C. A.; Fuhr, O.; Munuganti, R. S. N.; Maddalo, D.; Blattner, C.; Neeb, A.; Sharp, A.; Cato, L.; Weiss, C.; Jeselsohn, R. M.; Orian-Rousseau, V.; Bräse, S.; Cato, A. C. B.
    2023. Cancer Research Communications, 3 (7), 1378–1396. doi:10.1158/2767-9764.CRC-23-0111Full textFull text of the publication as PDF document
  41. Efficient deep-blue luminescence based on dual-channel intra/intermolecular exciplexes
    Zhang, Z.; Dou, D.; Xia, R.; Wu, P.; Spuling, E.; Wang, K.; Cao, J.; Wei, B.; Li, X.; Zhang, J.; Bräse, S.; Wang, Z.
    2023. Science Advances, 9 (20), Art.-Nr.: eadf4060. doi:10.1126/sciadv.adf4060Full textFull text of the publication as PDF document
  42. Practical synthesis and biological screening of sulfonyl hydrazides
    Macara, J.; Caldeira, C.; Cunha, J.; Coelho, J. A. S.; Silva, M. J. S. A.; Krämer, K.; Grathwol, C. W.; Bräse, S.; Marques, M. M. B.
    2023. Organic & Biomolecular Chemistry, 21 (10), 2118–2126. doi:10.1039/D2OB02160A
  43. Membrane‐acting biomimetic peptoids against visceral leishmaniasis
    Kumar, V.; Lin, J. S.; Molchanova, N.; Fortkort, J. A.; Reckmann, C.; Bräse, S.; Jenssen, H.; Barron, A. E.; Chugh, A.
    2023. FEBS Open Bio, 13 (3), 519–531. doi:10.1002/2211-5463.13562Full textFull text of the publication as PDF document
  44. Controlled, Stepwise Syntheses of Oligomers with Modified Quinoxaline Backbones
    Klein, J.; Jung, N.; Bräse, S.
    2023. European Journal of Organic Chemistry, 26 (6), e202200764. doi:10.1002/ejoc.202200764Full textFull text of the publication as PDF document
  45. Challenges and Opportunities in 3D Laser Printing Based on (1 + 1)-Photon Absorption
    Hahn, V.; Bojanowski, N. M.; Rietz, P.; Feist, F.; Kozlowska, M.; Wenzel, W.; Blasco, E.; Bräse, S.; Barner-Kowollik, C.; Wegener, M.
    2023. ACS Photonics, 10 (1), 24–33. doi:10.1021/acsphotonics.2c01632
  46. Synthesis of Non‐centrosymmetric Dipolar 4,4′‐Bipyridines: Potential Molecular Tectons for Programmed Assembly of Supramolecular Systems
    Kühner, H.; Leyen, L.; Hassan, Z.; Wöll, C.; Bräse, S.
    2023. ChemPlusChem, 88 (1), Art.-Nr.: e202200425. doi:10.1002/cplu.202200425Full textFull text of the publication as PDF document
  47. A Novel Route towards Bicyclo[1.1.1]pentane Sulfoxides from a Bench-Stable Starting Material
    Langer, L. S.; Stahlberger, M.; Bär, R. M.; Bräse, S.
    2023. Synlett, 34, A-E. doi:10.1055/a-2210-0893
  48. What is missing in autonomous discovery: open challenges for the community
    Maffettone, P. M.; Friederich, P.; Baird, S. G.; Blaiszik, B.; Brown, K. A.; Campbell, S. I.; Cohen, O. A.; Davis, R. L.; Foster, I. T.; Haghmoradi, N.; Hereld, M.; Joress, H.; Jung, N.; Kwon, H.-K.; Pizzuto, G.; Rintamaki, J.; Steinmann, C.; Torresi, L.; Sun, S.
    2023. Digital Discovery, 2 (6), 1644–1659. doi:10.1039/D3DD00143AFull textFull text of the publication as PDF document
  49. Pseudo‐ Para ‐Substituted [2.2]Paracyclophanes for Hole Transport in Perovskite Solar Cells
    Otterbach, S. A.; Elsing, D.; Schulz, A. D.; Tappert, H.; Wenzel, W.; Kozlowska, M.; Röhm, H.; Bräse, S.
    2023. Advanced Functional Materials. doi:10.1002/adfm.202309226Full textFull text of the publication as PDF document
  50. Bioconjugation in Materials Science
    Bednarek, C.; Schepers, U.; Thomas, F.; Bräse, S.
    2023. Advanced Functional Materials, 34 (20), Art.-Nr.: 2303613. doi:10.1002/adfm.202303613Full textFull text of the publication as PDF document
  51. Quinazolin-4-one/3-cyanopyridin-2-one Hybrids as Dual Inhibitors of EGFR and BRAF: Design, Synthesis, and Antiproliferative Activity
    Al-Wahaibi, L. H.; Hisham, M.; Abou-Zied, H. A.; Hassan, H. A.; Youssif, B. G. M.; Bräse, S.; Hayallah, A. M.; Abdel-Aziz, M.
    2023. Pharmaceuticals, 16 (11), Art.-Nr.: 1522. doi:10.3390/ph16111522Full textFull text of the publication as PDF document
  52. New 1,2,3-Triazole/1,2,4-triazole Hybrids as Aromatase Inhibitors: Design, Synthesis, and Apoptotic Antiproliferative Activity
    Maghraby, M. T.-E.; Mazyad Almutairi, T.; Bräse, S.; Salem, O. I. A.; Youssif, B. G. M.; Sheha, M. M.
    2023. Molecules, 28 (20), Art.-Nr.: 7092. doi:10.3390/molecules28207092Full textFull text of the publication as PDF document
  53. Design, Synthesis, and Biological Evaluation of Novel 3-Cyanopyridone/Pyrazoline Hybrids as Potential Apoptotic Antiproliferative Agents Targeting EGFR/BRAF Inhibitory Pathways
    Al-Wahaibi, L. H.; Abou-Zied, H. A.; Hisham, M.; Beshr, E. A. M.; Youssif, B. G. M.; Bräse, S.; Hayallah, A. M.; Abdel-Aziz, M.
    2023. Molecules, 28 (18), Art.-Nr.: 6586. doi:10.3390/molecules28186586Full textFull text of the publication as PDF document
  54. Development of Fluorescent Isocoumarin‐Fused Oxacyclononyne – 1,2,3‐Triazole Pairs
    Vidyakina, A. A.; Shtyrov, A. A.; Ryazantsev, M. N.; Khlebnikov, A. F.; Kolesnikov, I. E.; Sharoyko, V. V.; Spiridonova, D. V.; Balova, I. A.; Bräse, S.; Danilkina, N. A.
    2023. Chemistry – A European Journal, 29 (47), Art.-Nr.: e202300540. doi:10.1002/chem.202300540Full textFull text of the publication as PDF document
  55. Metal‐Organic Framework Thin Films as Ideal Matrices for Azide Photolysis in Vacuum
    Song, J.; Yu, X.; Nefedov, A.; Weidler, P. G.; Grosjean, S.; Bräse, S.; Wang, Y.; Wöll, C.
    2023. Angewandte Chemie - International Edition, 62 (34), Art.-Nr.: e202306155. doi:10.1002/anie.202306155Full textFull text of the publication as PDF document
  56. Pharmacological inhibition of TRPV2 attenuates phagocytosis and lipopolysaccharide‐induced migration of primary macrophages
    Raudszus, R.; Paulig, A.; Urban, N.; Deckers, A.; Gräßle, S.; Vanderheiden, S.; Jung, N.; Bräse, S.; Schaefer, M.; Hill, K.
    2023. British Journal of Pharmacology, 180 (21), 2736–2749. doi:10.1111/bph.16154Full textFull text of the publication as PDF document
  57. Synthesis of bis-thiohydantoin derivatives as an antiproliferative agents targeting EGFR inhibitory pathway
    Hassan, A. A.; Aly, A. A.; Ramadan, M.; Mohamed, N. K.; Youssif, B. G. M.; Gomaa, H. A. M.; Bräse, S.; Nieger, M.; El-Aal, A. S. A.
    2023. Molecular Diversity. doi:10.1007/s11030-023-10653-3
  58. Biofunctionalization of Metal–Organic Framework Nanoparticles via Combined Nitroxide‐Mediated Polymerization and Nitroxide Exchange Reaction
    Wagner, I.; Spiegel, S.; Brückel, J.; Schwotzer, M.; Welle, A.; Stenzel, M. H. H.; Bräse, S.; Begum, S.; Tsotsalas, M.
    2023. Macromolecular Materials and Engineering, 308 (9), Art.-Nr.: 2300048. doi:10.1002/mame.202300048Full textFull text of the publication as PDF document
  59. Substrate‐Bound Diarylethene‐Based Anisotropic Metal–Organic Framework Films as Photoactuators with a Directed Response
    Jiang, Y.; Liu, Y.; Grosjean, S.; Bon, V.; Hodapp, P.; Kanj, A. B.; Kaskel, S.; Bräse, S.; Wöll, C.; Heinke, L.
    2023. Angewandte Chemie - International Edition, 62 (20), Art.-Nr.: e202218052. doi:10.1002/anie.202218052Full textFull text of the publication as PDF document
  60. Manipulation of Pt···Pt Interaction in Platinum Complex by Methyl Group to Achieve Single-Doped White OLEDs: An Approach to Simulation of Daylight from Dawn until Dusk
    Zhang, Z.; Wu, P.; Wang, K.; Lin, H.; Spuling, E.; Xia, R.; Wu, Y.; Cao, J.; Zhang, J.; Wei, B.; Bräse, S.; Wang, Z.
    2023. ACS Materials Letters, 5, 920–927. doi:10.1021/acsmaterialslett.2c01191
  61. Transition Metal Complexes of Thiosemicarbazides, Thiocarbohydrazides, and Their Corresponding Carbazones with Cu(I), Cu(II), Co(II), Ni(II), Pd(II), and Ag(I)—A Review
    Aly, A. A.; Abdallah, E. M.; Ahmed, S. A.; Rabee, M. M.; Bräse, S.
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  62. Stacking Cyclophanes into Chiral Microvessels
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  63. F‐Tag Induced Acyl Shift in the Photochemical Cyclization of o ‐Alkynylated N ‐Alkyl‐ N ‐acylamides to Indoles
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  64. Stereoselective semisynthesis of uzarigenin and allo -uzarigenin
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  65. Emergence of Structural Phosphorescence in Free-Standing, Laterally Organized Polymer Nanofiber Membranes
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    2023. ACS Applied Polymer Materials, 5 (3), 1670–1680. doi:10.1021/acsapm.2c01477
  66. Tris(4-azidophenyl)methanol – a novel and multifunctional thiol protecting group
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  67. Twisting of Porphyrin by Assembly in a Metal‐Organic Framework yielding Chiral Photoconducting Films for Circularly‐Polarized‐Light Detection
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    2023. Angewandte Chemie - International Edition, 62 (10), Art.-Nr.: e202217377. doi:10.1002/anie.202217377Full textFull text of the publication as PDF document
  68. A Novel P@SiO Nano-Composite as Effective Adsorbent to Remove Methylene Blue Dye from Aqueous Media
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  69. Minimum Information Standards in Chemistry: A Call for Better Research Data Management Practices
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  70. Droplet Microarray as a Powerful Platform for Seeking New Antibiotics Against Multidrug‐Resistant Bacteria
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  71. Metal Complexes as Antifungals? From a Crowd-Sourced Compound Library to the First Experiments
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  72. Copper Complexes of 1,4-Naphthoquinone Containing Thiosemicarbazide and Triphenylphosphine Oxide Moieties; Synthesis and Identification by NMR, IR, Mass, UV Spectra, and DFT Calculations
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  74. Scope of tetrazolo[1,5-a] quinoxalines in CuAAC reactions for the synthesis of triazoloquinoxalines, imidazoloquinoxalines, and rhenium complexes thereof
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  75. Solid and Hollow Poly(p-xylylene) Particles Synthesis via Metal–Organic Framework-Templated Chemical Vapor Polymerization
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  76. A batch photoreactor for small-scale laboratory research - a technical note
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  78. Dynamic Surface Modification of Metal–Organic Framework Nanoparticles via Alkoxyamine Functional Groups
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  80. Poly(pentafluorobenzyl 2‐ylidene‐acetate): Polymerization and Postpolymerization Modification
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  81. Efficient Synthesis of Various Substituted (Thio)Ureas, Semicarbazides, Thiosemicarbazides, Thiazolidones, and Oxadiazole Derived from [2.2]Paracyclophane
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  83. The jasmonate biosynthesis Gene OsOPR7 can mitigate salinity induced mitochondrial oxidative stress
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  85. Diversity-Oriented Synthesis of [2.2]Paracyclophane-derived Fused Imidazo[1,2-a]heterocycles by Groebke-Blackburn-Bienaymé Reaction: Accessing Cyclophanyl Imidazole Ligands Library
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  86. Design and synthesis of new thiazolidinone/uracil derivatives as antiproliferative agents targeting EGFR and/or BRAF
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  88. Synthesis of novel amidines via one-pot three component reactions: Selective topoisomerase I inhibitors with antiproliferative properties
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  89. Search for Alternative Two‐Step‐Absorption Photoinitiators for 3D Laser Nanoprinting
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  90. Metal complexes of new thiocarbohydrazones of Cu(I), Co(II), and Ni(II); identification by NMR, IR, mass, UV spectra, and DFT calculations
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    2022. Journal of Sulfur Chemistry, 44 (3), 282–303. doi:10.1080/17415993.2022.2145846
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  93. Functionalized C-Symmetric Building Blocks—The Chemistry of Triaminotrimesic Acid
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  94. Azides in the Synthesis of Various Heterocycles
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  95. Facile synthesis of hydrazono bis-4-oxothiazolidines
    Mostafa, S. M.; Aly, A. A.; Bräse, S.; Nieger, M.; Mohamed, A. H.
    2022. Journal of Sulfur Chemistry, 43 (6), 606–619. doi:10.1080/17415993.2022.2083454
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  97. Recent Progress and Potential Biomedical Applications of Electrospun Nanofibers in Regeneration of Tissues and Organs
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  98. X-ray Structure Analyses of 4-Hydroxy-1-Methylquinolin-2(1H)-One, 6-Ethyl-4-Hydroxy-2 H-Pyrano[3,2-c]Quinoline-2,5(6H)-Dione, (E)-4-(2-Benzylidene-Hydrazineyl)Quinolin-2(1H)-One and Diethyl (E)-2-(2-(1-Methyl-2-Oxo-1,2-Dihydro-Quinolin-4-yl)Hydrazineylidene)Succinate
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    2022. Journal of Chemical Crystallography, 53, 38–49. doi:10.1007/s10870-022-00939-z
  99. Autoxidation of 4-Hydrazinylquinolin-2(1H)-one; Synthesis of Pyridazino[4,3-c:5,6-c′ ]diquinoline-6,7(5H,8H)-diones
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  100. Synthesis, Characterization, and In Vivo Study of Some Novel 3,4,5-Trimethoxybenzylidene-hydrazinecarbothioamides and Thiadiazoles as Anti-Apoptotic Caspase-3 Inhibitors
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  101. Fluorescent annulated imidazo[4,5- c ]isoquinolines via a GBB-3CR/imidoylation sequence – DNA-interactions in pUC-19 gel electrophoresis mobility shift assay
    Stahlberger, M.; Steinlein, O.; Adam, C. R.; Rotter, M.; Hohmann, J.; Nieger, M.; Köberle, B.; Bräse, S.
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  102. Surfaces Decorated with Enantiomorphically Pure Polymer Nanohelices via Hierarchical Chirality Transfer across Multiple Length Scales
    Varadharajan, D.; Nayani, K.; Zippel, C.; Spuling, E.; Cheng, K. C.; Sarangarajan, S.; Roh, S.; Kim, J.; Trouillet, V.; Bräse, S.; Abbott, N. L.; Lahann, J.
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  103. Fluorinated dibenzo[a,c]-phenazine-based green to red thermally activated delayed fluorescent OLED emitters
    Hong, G.; Si, C.; Gupta, A. K.; Bizzarri, C.; Nieger, M.; Samuel, I. D. W.; Zysman-Colman, E.; Bräse, S.
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  104. Functional Selectivity of Coumarin Derivates Acting via GPR55 in Neuroinflammation
    Apweiler, M.; Streyczek, J.; Saliba, S. W.; Collado, J. A.; Hurrle, T.; Gräßle, S.; Muñoz, E.; Normann, C.; Hellwig, S.; Bräse, S.; Fiebich, B. L.
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  105. Metadata Schemas for FAIR* Data in Materials Science: Scanning Electron Microscopy (SEM) Use Case : A detailed and practical schema developed in cooperation with materials scientists
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  106. Bio-instructive materials on-demand-combinatorial chemistry of peptoids, foldamers, and beyond
    Herlan, C. N.; Feser, D.; Schepers, U.; Bräse, S.
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  107. Metal‐to‐Metal Distance Modulation by Ligand Design: A Case Study of Structure‐Property Correlation in Planar Chiral Cyclophanyl Metal Complexes
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  108. Novel Cofacial Porphyrin-Based Homo- and Heterotrimetallic Complexes of Transition Metals
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  110. Platinum Cyclooctadiene Complexes with Activity against Gram-positive Bacteria
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  111. Development of a Benzothiazole Scaffold-Based Androgen Receptor N-Terminal Inhibitor for Treating Androgen-Responsive Prostate Cancer
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  112. Molecular Design and Synthesis of Dicarbazolophane-Based Centrosymmetric Through-Space Donors for Solution-Processed Thermally Activated Delayed Fluorescence OLEDs
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  113. In situ sensors for flow reactors – a review
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  119. Cyclic Peptoid-Peptide Hybrids as Versatile Molecular Transporters
    Herlan, C. N.; Meschkov, A.; Schepers, U.; Bräse, S.
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  121. Multigram‐Scale Kinetic Resolution of 4‐Acetyl[2.2]Paracyclophane Ru‐Catalyzed Enantioselective Hydrogenation: Accessing [2.2]Paracyclophanes with Planar and Central Chirality
    Zippel, C.; Hassan, Z.; Parsa, A. Q.; Hohmann, J.; Bräse, S.
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  122. Investigation of Luminescent Triplet States in Tetranuclear Cu Complexes: Thermochromism and Structural Characterization
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  123. Halogen-bonded one-dimensional chains of functionalized ditopic bipyridines co-crystallized with mono-, di-, and triiodofluorobenzenes
    Vulpe, E.; Grosjean, S.; Hassan, Z.; Bulach, V.; Hosseini, M. W.; Bräse, S.
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  124. Design and synthesis of hydrazinecarbothioamide sulfones as potential antihyperglycemic agents
    Aly, A. A.; Hassan, A. A.; Makhlouf, M. M.; Alshammari, M. B.; Mohamed Naguib Abdel Hafez, S.; Refaie, M. M. M.; Bräse, S.; Nieger, M.; Ramadan, M.
    2021. Archiv der Pharmazie, 354 (5), Art.Nr. 2000336. doi:10.1002/ardp.202000336
  125. Synthesis of quinone-based heterocycles of broad-spectrum anticancer activity
    Aly, A. A.; Hassan, A. A.; Mohamed, N. K.; Ramadan, M.; Abd El-Aal, A. S.; Bräse, S.; Nieger, M.
    2021. Journal of chemical research, 45 (5-6), 562–571. doi:10.1177/1747519820959737Full textFull text of the publication as PDF document
  126. Formal Semisynthesis of Demethylgorgosterol Utilizing a Stereoselective Intermolecular Cyclopropanation Reaction
    Rosenbaum, N.; Schmidt, L.; Mohr, F.; Fuhr, O.; Nieger, M.; Bräse, S.
    2021. European journal of organic chemistry, 2021 (10), 1568–1574. doi:10.1002/ejoc.202100035Full textFull text of the publication as PDF document
  127. A Brief History of OLEDs—Emitter Development and Industry Milestones
    Hong, G.; Gan, X.; Leonhardt, C.; Zhang, Z.; Seibert, J.; Busch, J. M.; Bräse, S.
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  128. Effects of a Novel GPR55 Antagonist on the Arachidonic Acid Cascade in LPS-Activated Primary Microglial Cells
    Saliba, S. W.; Gläser, F.; Deckers, A.; Keil, A.; Hurrle, T.; Apweiler, M.; Ferver, F.; Volz, N.; Endres, D.; Bräse, S.; Fiebich, B. L.
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  129. Various Structural Design Modifications: para-Substituted Diphenylphosphinopyridine Bridged Cu(I) Complexes in Organic Light-Emitting Diodes
    Busch, J. M.; Koshelev, D. S.; Vashchenko, A. A.; Fuhr, O.; Nieger, M.; Utochnikova, V. V.; Bräse, S.
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  130. ChemSpectra: a web-based spectra editor for analytical data
    Huang, Y.-C.; Tremouilhac, P.; Nguyen, A.; Jung, N.; Bräse, S.
    2021. Journal of Cheminformatics, 13 (1), Art.-Nr. 8. doi:10.1186/s13321-020-00481-0Full textFull text of the publication as PDF document
  131. A Synthetic Strategy for Cofacial Porphyrin-Based Homo- and Heterobimetallic Complexes
    Schissler, C.; Schneider, E. K.; Felker, B.; Weis, P.; Nieger, M.; Kappes, M. M.; Bräse, S.
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  132. Id1 and Id3 Are Regulated Through Matrix‐Assisted Autocrine BMP Signaling and Represent Therapeutic Targets in Melanoma
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    2021. Advanced therapeutics, 4 (2), Art.-Nr.: 2000065. doi:10.1002/adtp.202000065Full textFull text of the publication as PDF document
  133. Regioselective and stereoselective synthesis of epithiomethanoiminoindeno[1,2-b]furan-3-carbonitrile: heterocyclic [3.3.3]propellanes
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    2021. Molecular diversity, 25 (1), 99–108. doi:10.1007/s11030-019-10027-8
  134. A small molecule screen identifies novel inhibitors of mechanosensory nematocyst discharge in Hydra
    Hofmann, D.; Garg, N.; Grässle, S.; Vanderheiden, S.; Bergheim, B. G.; Bräse, S.; Jung, N.; Özbek, S.
    2021. Scientific reports, 11, Art.-Nr. 20627. doi:10.1038/s41598-021-99974-7Full textFull text of the publication as PDF document
  135. Effect of a twin-emitter design strategy on a previously reported thermally activated delayed fluorescence organic light-emitting diode
    Crovini, E.; Zhang, Z.; Kusakabe, Y.; Ren, Y.; Wada, Y.; Naqvi, B. A.; Sahay, P.; Matulaitis, T.; Diesing, S.; Samuel, I. D. W.; Brütting, W.; Suzuki, K.; Kaji, H.; Bräse, S.; Zysman-Colman, E.
    2021. Beilstein Journal of Organic Chemistry, 17, 2894–2905. doi:10.3762/bjoc.17.197Full textFull text of the publication as PDF document
  136. An efficient approach for the synthesis of novel series of 1,3-dihydrospiro[indene-2,6ʹ-[1,3]thiazine] derivatives
    Mostafa, S. M.; Aly, A. A.; Bräse, S.; Mohamed, A. H.
    2021. Monatshefte fur Chemie, 153, 87–94. doi:10.1007/s00706-021-02878-5
  137. Metadata schema to support FAIR data in scanning electron microscopy
    Joseph, R.; Chauhan, A.; Eschke, C.; Ihsan, A. Z.; Jalali, M.; Jäntsch, U.; Jung, N.; Shyam Kumar, C. N.; Kübel, C.; Lucas, C.; Mail, M.; Mazilkin, A.; Neidiger, C.; Panighel, M.; Sandfeld, S.; Stotzka, R.; Thelen, R.; Aversa, R.
    2021. Supplementary Proceedings of the XXIII International Conference on Data Analytics and Management in Data Intensive Domains (DAMDID/RCDL 2021): Moscow, Russia, October 26-29, 2021. Ed.: A. Pozanenko, 265–277, CEUR-WS.org Full textFull text of the publication as PDF document
  138. Chemotion Repository, a Curated Repository for Reaction Information and Analytical Data
    Tremouilhac, P.; Huang, P.-C.; Lin, C.-L.; Huang, Y.-C.; Nguyen, A.; Jung, N.; Bach, F.; Bräse, S.
    2021. Chemistry methods, 1 (1), 8–11. doi:10.1002/cmtd.202000034Full textFull text of the publication as PDF document
  139. Regioselective formation of new 3-S-alkylated-1,2,4-triazole-quinolones
    Aly, A. A.; Abd El-Aziz, M.; Elshaier, Y. A. M. M.; Brown, A. B.; Fathy, H. M.; Bräse, S.; Nieger, M.; Ramadan, M.
    2021. Journal of Sulfur Chemistry, 43 (2), 215–231. doi:10.1080/17415993.2021.2006659
  140. Synthesis of new pyrazolo[1,2,3]triazines by cyclative cleavage of pyrazolyltriazenes
    Wippert, N.; Nieger, M.; Herlan, C.; Jung, N.; Bräse, S.
    2021. Beilstein journal of organic chemistry, 17, 2773–2780. doi:10.3762/bjoc.17.187Full textFull text of the publication as PDF document
  141. Photoinduced Delamination of Metal-Organic Framework Thin Films by Spatioselective Generation of Reactive Oxygen Species
    Liu, X.; Mazel, A.; Marschner, S.; Fu, Z.; Muth, M.; Kirschhöfer, F.; Brenner-Weiss, G.; Bräse, S.; Diring, S.; Odobel, F.; Haldar, R.; Wöll, C.
    2021. ACS Applied Materials and Interfaces, 13 (48), 57768–57773. doi:10.1021/acsami.1c16173Full textFull text of the publication as PDF document
  142. Design and synthesis of (2-oxo-1,2-dihydroquinolin-4-yl)-1,2,3-triazole derivatives via click reaction: Potential apoptotic antiproliferative agents
    El-Sheref, E. M.; Elbastawesy, M. A. I.; Brown, A. B.; Shawky, A. M.; Gomaa, H. A. M.; Bräse, S.; Youssif, B. G. M.
    2021. Molecules, 26 (22), 6798. doi:10.3390/molecules26226798Full textFull text of the publication as PDF document
  143. Heterocycloalkynes Fused to a Heterocyclic Core: Searching for an Island with Optimal Stability-Reactivity Balance
    Danilkina, N. A.; Govdi, A. I.; Khlebnikov, A. F.; Tikhomirov, A. O.; Sharoyko, V. V.; Shtyrov, A. A.; Ryazantsev, M. N.; Bräse, S.; Balova, I. A.
    2021. Journal of the American Chemical Society, 143 (40), 16519–16537. doi:10.1021/jacs.1c06041
  144. Stereoselective synthesis of homochiral paracyclophanylindenofuranylimidazo[3.3.3]propellanes
    Hassan, A. A.; Bräse, S.; Aly, A. A.; Mohamed, N. K.; El-Haleem, L. E. A.; Nieger, M.
    2021. Monatshefte fur Chemie, 152, 1571–1579. doi:10.1007/s00706-021-02853-0
  145. Regioselective ortho-Palladation of [2.2]Paracyclophane Scaffolds: Accessing Planar and Central Chiral N,C-Palladacycles
    Zippel, C.; Bartholomeyzik, T.; Friedmann, C.; Nieger, M.; Hassan, Z.; Bräse, S.
    2021. European Journal of Organic Chemistry, 2021 (36), 5090–5093. doi:10.1002/ejoc.202101066Full textFull text of the publication as PDF document
  146. Dynamic porous organic polymers with tuneable crosslinking degree and porosity
    Wessely, I. D.; Matt, Y.; An, Q.; Bräse, S.; Tsotsalas, M.
    2021. RSC Advances, 11 (44), 27714–27719. doi:10.1039/d1ra05265aFull textFull text of the publication as PDF document
  147. Skeletal Editing—Nitrogen Deletion of Secondary Amines by Anomeric Amide Reagents
    Zippel, C.; Seibert, J.; Bräse, S.
    2021. Angewandte Chemie / International edition, 60 (36), 19522–19524. doi:10.1002/anie.202107490Full textFull text of the publication as PDF document
  148. Avoiding the Center-Symmetry Trap: Programmed Assembly of Dipolar Precursors into Porous, Crystalline Molecular Thin Films
    Nefedov, A.; Haldar, R.; Xu, Z.; Kühner, H.; Hofmann, D.; Goll, D.; Sapotta, B.; Hecht, S.; Krstić, M.; Rockstuhl, C.; Wenzel, W.; Bräse, S.; Tegeder, P.; Zojer, E.; Wöll, C.
    2021. Advanced Materials, 33 (35), Art.-Nr. 2103287. doi:10.1002/adma.202103287Full textFull text of the publication as PDF document
  149. Corrigendum: What Controls the Orientation of TADF Emitters?
    Naqvi, B. A.; Schmid, M.; Crovini, E.; Sahay, P.; Naujoks, T.; Rodella, F.; Zhang, Z.; Strohriegl, P.; Bräse, S.; Zysman-Colman, E.; Brütting, W.
    2021. Frontiers in Chemistry, 9, Art.Nr. 632639. doi:10.3389/fchem.2021.632639Full textFull text of the publication as PDF document
  150. Fluorescence detected circular dichroism (FDCD) for supramolecular host–guest complexes
    Prabodh, A.; Wang, Y.; Sinn, S.; Albertini, P.; Spies, C.; Spuling, E.; Yang, L.-P.; Jiang, W.; Bräse, S.; Biedermann, F.
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  151. Quinolones as prospective drugs: Their syntheses and biological applications
    Aly, A. A.; Ramadan, M.; Abuo-Rahma, G. E.-D. A.; Elshaier, Y. A. M. M.; Elbastawesy, M. A. I.; Brown, A. B.; Bräse, S.
    2021. Advances in Heterocyclic Chemistry. Vol. 135. Ed.: Eric F. V. Scriven, 147–196, Elsevier. doi:10.1016/bs.aihch.2020.08.001
  152. The Diels-Alder Approach towards Cannabinoid Derivatives and Formal Synthesis of Tetrahydrocannabinol (THC)
    Hurrle, T.; Gläser, F.; Bröhmer, M. C.; Nieger, M.; Bräse, S.
    2021. ChemistryOpen, 10 (5), 587–592. doi:10.1002/open.202000343Full textFull text of the publication as PDF document
  153. Highly NIR-emitting ytterbium complexes containing 2-(tosylaminobenzylidene)-N-benzoylhydrazone anions: structure in solution and use for bioimaging
    Kovalenko, A. D.; Pavlov, A. A.; Ustinovich, I. D.; Kalyakina, A. S.; Goloveshkin, A. S.; Marciniak, Ł.; Lepnev, L. S.; Burlov, A. S.; Schepers, U.; Bräse, S.; Utochnikova, V. V.
    2021. Dalton Transactions, 50 (11), 3786–3791. doi:10.1039/d0dt03913fFull textFull text of the publication as PDF document
  154. Expanded Cyclotetrabenzoins
    Eisterhold, A. M.; Puangsamlee, T.; Otterbach, S.; Bräse, S.; Weis, P.; Wang, X.; Kutonova, K. V.; Miljanić, O. Š.
    2021. Organic letters, 23 (3), 781–785. doi:10.1021/acs.orglett.0c04014
  155. Rigid Multidimensional Alkoxyamines: A Versatile Building Block Library
    Matt, Y.; Wessely, I.; Gramespacher, L.; Tsotsalas, M.; Bräse, S.
    2021. European journal of organic chemistry, 2021 (2), 239–245. doi:10.1002/ejoc.202001415Full textFull text of the publication as PDF document
  156. Structural Diversity of Peptoids: Tube-Like Structures of Macrocycles
    Herlan, C. N.; Sommer, K.; Weis, P.; Nieger, M.; Bräse, S.
    2021. Molecules, 26 (1), Art.-Nr.: 150. doi:10.3390/molecules26010150Full textFull text of the publication as PDF document
  157. Transcriptome analysis of two structurally related flavonoids; Apigenin and Chrysin revealed hypocholesterolemic and ketogenic effects in mouse embryonic fibroblasts
    Puthanveetil, P.; Kong, X.; Bräse, S.; Voros, G.; Peer, W. A.
    2021. European journal of pharmacology, 893, Art.-Nr.: 173804. doi:10.1016/j.ejphar.2020.173804
  158. Synthesis of 3,3′-methylenebis(4-hydroxyquinolin-2(1H)-ones) of prospective anti-COVID-19 drugs
    Aly, A. A.; Hassan, A. A.; Mohamed, A. H.; Osman, E. M.; Bräse, S.; Nieger, M.; Ibrahim, M. A. A.; Mostafa, S. M.
    2021. Molecular diversity, 25, 461–471. doi:10.1007/s11030-020-10140-z
  159. Thiol-yne crosslinked triarylamine hole transport layers for solution-processable organic light-emitting diodes
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    2020. Journal of materials chemistry / C, 8 (46), 16498–16505. doi:10.1039/d0tc03514aFull textFull text of the publication as PDF document
  160. The Repository Chemotion: Infrastructure for Sustainable Research in Chemistry
    Tremouilhac, P.; Lin, C.-L.; Huang, P.-C.; Huang, Y.-C.; Nguyen, A.; Jung, N.; Bach, F.; Ulrich, R.; Neumair, B.; Streit, A.; Bräse, S.
    2020. Angewandte Chemie / International edition, 59 (50), 22771–22778. doi:10.1002/anie.202007702Full textFull text of the publication as PDF document
  161. Efficient Sky-Blue Organic Light-Emitting Diodes Using a Highly Horizontally Oriented Thermally Activated Delayed Fluorescence Emitter
    Zhang, Z.; Crovini, E.; Santos, P. L. dos; Naqvi, B. A.; Cordes, D. B.; Slawin, A. M. Z.; Sahay, P.; Brütting, W.; Samuel, I. D. W.; Bräse, S.; Zysman-Colman, E.
    2020. Advanced optical materials, 8 (23), Art. Nr.: 2001354. doi:10.1002/adom.202001354Full textFull text of the publication as PDF document
  162. Chemistry of Substituted Thiazinanes and Their Derivatives
    Hassan, A. A.; Bräse, S.; Aly, A. A.; Tawfeek, H. N.
    2020. Molecules, 25 (23), Art.-Nr.: 5610. doi:10.3390/molecules25235610Full textFull text of the publication as PDF document
  163. A mitochondria-targeted coenzyme Q peptoid induces superoxide dismutase and alleviates salinity stress in plant cells
    Asfaw, K. G.; Liu, Q.; Xu, X.; Manz, C.; Purper, S.; Eghbalian, R.; Münch, S. W.; Wehl, I.; Bräse, S.; Eiche, E.; Hause, B.; Bogeski, I.; Schepers, U.; Riemann, M.; Nick, P.
    2020. Scientific reports, 10, Article number:11563. doi:10.1038/s41598-020-68491-4Full textFull text of the publication as PDF document
  164. Controlling Regioselectivity in Palladium‐Catalyzed C−H Activation/Aryl–Aryl Coupling of 4‐Phenylamino[2.2]paracyclophane
    Zippel, C.; Spuling, E.; Hassan, Z.; Polamo, M.; Nieger, M.; Bräse, S.
    2020. Chemistry - a European journal, 26 (61), 13771–13775. doi:10.1002/chem.202003709Full textFull text of the publication as PDF document
  165. A versatile Diels–Alder approach to functionalized hydroanthraquinones
    Beck, J.; Fuhr, O.; Nieger, M.; Bräse, S.
    2020. Royal Society Open Science, 7 (11), Article: 200626. doi:10.1098/rsos.200626Full textFull text of the publication as PDF document
  166. Direct Synthesis of ZIF-8 on Transmission Electron Microscopy Grids Allows Structure Analysis and 3D Reconstruction
    Hugenschmidt, M.; Kutonova, K.; Valadez Sánchez, E. P.; Moulai, S.; Gliemann, H.; Bräse, S.; Wöll, C.; Gerthsen, D.
    2020. AgBioForum, 37 (11), Art.-Nr.: 2000209. doi:10.1002/ppsc.202000209Full textFull text of the publication as PDF document
  167. Cobalt‐Catalyzed α‐Arylation of Substituted α‐Bromo α‐Fluoro β‐Lactams with Diaryl Zinc Reagents: Generalization to Functionalized Bromo Derivatives
    Lorion, M. M.; Koch, V.; Nieger, M.; Chen, H.-Y.; Lei, A.; Bräse, S.; Cossy, J.
    2020. Chemistry - a European journal, 26 (58), 13163–13169. doi:10.1002/chem.202001721
  168. Design and Synthesis of a [2.2]Paracyclophane‐based Planar Chiral Dirhodium Catalyst and its Applications in Cyclopropanation Reaction of Vinylarenes with α‐Methyl‐α‐Diazo Esters
    Zippel, C.; Hassan, Z.; Nieger, M.; Bräse, S.
    2020. Advanced synthesis & catalysis, 362 (16), 3431–3436. doi:10.1002/adsc.202000512Full textFull text of the publication as PDF document
  169. Increasing the Functional Group Diversity in Helical β-Peptoids: Achievement of Solvent- and pH-Dependent Folding
    Wellhöfer, I.; Beck, J.; Frydenvang, K.; Bräse, S.; Olsen, C. A.
    2020. The journal of organic chemistry, 85 (16), 10466–10478. doi:10.1021/acs.joc.0c00780
  170. On Demand Light‐Degradable Polymers Based on 9,10‐Dialkoxyanthracenes
    Becker, F.; Klaiber, M.; Franzreb, M.; Bräse, S.; Lahann, J.
    2020. Macromolecular rapid communications, 41 (15), Art. Nr.: 2000314. doi:10.1002/marc.202000314Full textFull text of the publication as PDF document
  171. Naturally Occurring Cardenolides Affecting Schistosoma mansoni
    Keiser, J.; Koch, V.; Deckers, A.; Cheung, H. T. A.; Jung, N.; Bräse, S.
    2020. ACS infectious diseases, 6 (7), 1922–1927. doi:10.1021/acsinfecdis.0c00175
  172. Regioselective synthesis of new 7,8-dichlorobenzofuro[3,2-c]quinoline-6,9,10(5H)-triones from reactions of 4-hydroxy-2-quinolones with 3,4,5,6-tetrachloro-1,2-benzoquinone
    Aly, A. A.; Hassan, A. A.; Mohamed, N. K.; Abd El-Haleem, L. E.; Bräse, S.
    2020. Journal of chemical research, 44 (7-8), 388–392. doi:10.1177/1747519820902669
  173. Assembly of Molecular Building Blocks into Integrated Complex Functional Molecular Systems: Structuring Matter Made to Order
    Hassan, Z.; Matt, Y.; Begum, S.; Tsotsalas, M.; Bräse, S.
    2020. Advanced functional materials, 30 (26), Art.Nr. 1907625. doi:10.1002/adfm.201907625Full textFull text of the publication as PDF document
  174. Sodium Bicyclo[1.1.1]pentanesulfinate: A Bench‐Stable Precursor for Bicyclo[1.1.1]pentylsulfones and Bicyclo‐ [1.1.1]pentanesulfonamides
    Bär, R. M.; Gross, P. J.; Nieger, M.; Bräse, S.
    2020. Chemistry - a European journal, 26 (19), 4242–4245. doi:10.1002/chem.202000097Full textFull text of the publication as PDF document
  175. Bicyclo[1.1.1]pentyl Sulfoximines: Synthesis and Functionalizations
    Bär, R. M.; Langer, L.; Nieger, M.; Bräse, S.
    2020. Advanced synthesis & catalysis, 362 (6), 1356–1361. doi:10.1002/adsc.201901453Full textFull text of the publication as PDF document
  176. Regioselective Functionalization of [2.2]Paracyclophanes: Recent Synthetic Progress and Perspectives
    Hassan, Z.; Spuling, E.; Knoll, D. M.; Bräse, S.
    2020. Angewandte Chemie / International edition, 59 (6), 2156–2170. doi:10.1002/anie.201904863Full textFull text of the publication as PDF document
  177. Modernes Forschungsdatenmanagement – ein Naturstoffprojekt als Fallstudie
    Koch, V.; Bräse, S.
    2020. Biospektrum, 26 (1), 107–109. doi:10.1007/s12268-020-1316-3Full textFull text of the publication as PDF document
  178. Criegee Intermediates Beyond Ozonolysis: Synthetic and Mechanistic Insights
    Hassan, Z.; Stahlberger, M.; Rosenbaum, N.; Bräse, S.
    2020. Angewandte Chemie - International Edition, 60 (28), 15138–15152. doi:10.1002/anie.202014974Full textFull text of the publication as PDF document
  179. Design, Synthesis, and Molecular Docking of Paracyclophanyl-Thiazole Hybrids as Novel CDK1 Inhibitors and Apoptosis Inducing Anti-Melanoma Agents
    Aly, A. A.; Bräse, S.; Hassan, A. A.; Mohamed, N. K.; El-Haleem, L. E. A.; Nieger, M.; Morsy, N. M.; Alshammari, M. B.; Ibrahim, M. A. A.; Abdelhafez, E. M. N.
    2020. Molecules, 25 (23), Art.-Nr.: 5569. doi:10.3390/molecules25235569Full textFull text of the publication as PDF document
  180. OBO-Fused Benzo[fg]tetracene as Acceptor With Potential for Thermally Activated Delayed Fluorescence Emitters
    Zhang, Z.; Kumar, S.; Bagnich, S.; Spuling, E.; Hundemer, F.; Nieger, M.; Hassan, Z.; Köhler, A.; Zysman-Colman, E.; Bräse, S.
    2020. Frontiers in Chemistry, 8, Art. Nr.: 563411. doi:10.3389/fchem.2020.563411Full textFull text of the publication as PDF document
  181. Design, Synthesis, Molecular Docking, Antiapoptotic and Caspase-3 Inhibition of New 1,2,3-Triazole/Bis-2(1H)-Quinolinone Hybrids
    El-Sheref, E. M.; Aly, A. A.; Alshammari, M. B.; Brown, A. B.; Abdel-Hafez, S. M. N.; Abdelzaher, W. Y.; Bräse, S.; Abdelhafez, E. M. N.
    2020. Molecules, 25 (21), Art. Nr.: 5057. doi:10.3390/molecules25215057Full textFull text of the publication as PDF document
  182. What Controls the Orientation of TADF Emitters?
    Naqvi, B. A.; Schmid, M.; Crovini, E.; Sahay, P.; Naujoks, T.; Rodella, F.; Zhang, Z.; Strohriegl, P.; Bräse, S.; Zysman-Colman, E.; Brütting, W.
    2020. Frontiers in Chemistry, 8, Art. Nr.: 750. doi:10.3389/fchem.2020.00750Full textFull text of the publication as PDF document
  183. Towards the synthesis of calotropin and related cardenolides from 3-epiandrosterone: A-ring related modifications
    Koch, V.; Nieger, M.; Bräse, S.
    2020. Organic chemistry frontiers, 7 (18), 2670–2681. doi:10.1039/d0qo00269kFull textFull text of the publication as PDF document
  184. Polymerization in MOF-Confined Nanospaces: Tailored Architectures, Functions, and Applications
    Begum, S.; Hassan, Z.; Bräse, S.; Tsotsalas, M.
    2020. Langmuir, 36 (36), 10657–10673. doi:10.1021/acs.langmuir.0c01832Full textFull text of the publication as PDF document
  185. Real-time observation of molecular flattening and intersystem crossing in [(DPEPhos)Cu()(PyrTet)] via ultrafast UV/Vis- and mid-IR spectroscopy on solution and solid samples
    Grupe, M.; Bäppler, F.; Theiß, M.; Busch, J. M.; Dietrich, F.; Volz, D.; Gerhards, M.; Bräse, S.; Diller, R.
    2020. Physical chemistry, chemical physics, 22 (25), 14187–14200. doi:10.1039/c9cp05749h
  186. New Paracyclophanylthiazoles with Anti-Leukemia Activity: Design, Synthesis, Molecular Docking, and Mechanistic Studies
    Aly, A. A.; Bräse, S.; Hassan, A. A.; Mohamed, N. K.; Abd El-Haleem, L. E.; Nieger, M.; Morsy, N. M.; Abdelhafez, E. M. N.
    2020. Molecules, 25 (13), Art.Nr. 3089. doi:10.3390/molecules25133089Full textFull text of the publication as PDF document
  187. Chemistry and Biological Activities of 1,2,4-Triazolethiones—Antiviral and Anti-Infective Drugs
    Aly, A. A.; A. Hassan, A.; Makhlouf, M. M.; Bräse, S.
    2020. Molecules, 25 (13), Article: 3036. doi:10.3390/molecules25133036Full textFull text of the publication as PDF document
  188. Synthesis of New Planar-Chiral Linked [2.2]Paracyclophanes-N-([2.2]-Paracyclophanylcarbamoyl)-4-([2.2]Paracyclophanylcarboxamide, [2.2]Paracyclophanyl-Substituted Triazolthiones and -Substituted Oxadiazoles
    Aly, A. A.; Bräse, S.; Hassan, A. A.; Mohamed, N. K.; El-Haleem, L. E. A.; Nieger, M.
    2020. Molecules, 25 (15), Article: 3315. doi:10.3390/molecules25153315Full textFull text of the publication as PDF document
  189. Synthesis and structure confirmation of 2,4-disubstituted thiazole and 2,3,4-trisubstituted thiazole as thiazolium bromide salts
    Hassan, A. A.; Mohamed, N. K.; Aly, A. A.; Tawfeek, H. N.; Bräse, S.; Nieger, M.
    2020. Monatshefte für Chemie, 151, 1143–1152. doi:10.1007/s00706-020-02640-3Full textFull text of the publication as PDF document
  190. Correction: Metal complexes as a promising source for new antibiotics
    Frei, A.; Zuegg, J.; Elliott, A. G.; Baker, M.; Braese, S.; Brown, C.; Chen, F.; Dowson, C. G.; Dujardin, G.; Jung, N.; King, A. P.; Mansour, A. M.; Massi, M.; Moat, J.; Mohamed, H. A.; Renfrew, A. K.; Rutledge, P. J.; Sadler, P. J.; Todd, M. H.; Willans, C. E.; Wilson, J. J.; Cooper, M. A.; Blaskovich, M. A. T.
    2020. Chemical science, 11 (17), 4531. doi:10.1039/d0sc90075cFull textFull text of the publication as PDF document
  191. The Staudinger Ligation
    Bednarek, C.; Wehl, I.; Jung, N.; Schepers, U.; Bräse, S.
    2020. Chemical reviews, 120 (10), 4301–4354. doi:10.1021/acs.chemrev.9b00665Full textFull text of the publication as PDF document
  192. Correction: Dynamic covalent polymer networks combined nitroxide exchange reaction and nitroxide mediated polymerization
    Jia, Y.; Matt, Y.; An, Q.; Wessely, I.; Mutlu, H.; Theato, P.; Bräse, S.; Llevot, A.; Tsotsalas, M.
    2020. Polymer chemistry, 11 (15), 2761. doi:10.1039/d0py90053bFull textFull text of the publication as PDF document
  193. Dynamic covalent polymer networks via combined nitroxide exchange reaction and nitroxide mediated polymerization
    Jia, Y.; Matt, Y.; An, Q.; Wessely, I.; Mutlu, H.; Theato, P.; Bräse, S.; Llevot, A.; Tsotsalas, M.
    2020. Polymer chemistry, 11 (14), 2502–2510. doi:10.1039/c9py01878fFull textFull text of the publication as PDF document
  194. Sensitizing TADF Absorption Using Variable Length Oligo(phenylene ethynylene) Antennae
    Franco, O.; Jakoby, M.; Schneider, R. V.; Hundemer, F.; Hahn, D.; Richards, B. S.; Bräse, S.; Meier, M. A. R.; Lemmer, U.; Howard, I. A.
    2020. Frontiers in Chemistry, 8, Art.-Nr.: 126. doi:10.3389/fchem.2020.00126Full textFull text of the publication as PDF document
  195. Reactive & Efficient: Organic Azides as Cross-Linkers in Material Sciences
    Schock, M.; Bräse, S.
    2020. Molecules, 25 (4), Art. Nr.: 1009. doi:10.3390/molecules25041009Full textFull text of the publication as PDF document
  196. Metal complexes as a promising source for new antibiotics
    Frei, A.; Zuegg, J.; Elliott, A. G.; Baker, M.; Braese, S.; Brown, C.; Chen, F.; Dowson, C. G.; Dujardin, G.; Jung, N.; King, A. P.; Mansour, A. M.; Massi, M.; Moat, J.; Mohamed, H. A.; Renfrew, A. K.; Rutledge, P. J.; Sadler, P. J.; Todd, M. H.; Willans, C. E.; Wilson, J. J.; Cooper, M. A.; Blaskovich, M. A. T.
    2020. Chemical science, 11 (10), 2627–2639. doi:10.1039/c9sc06460eFull textFull text of the publication as PDF document
  197. Proton-conduction photomodulation in spiropyran-functionalized MOFs with large on–off ratio
    Kanj, A. B.; Chandresh, A.; Gerwien, A.; Grosjean, S.; Bräse, S.; Wang, Y.; Dube, H.; Heinke, L.
    2020. Chemical science, 11 (5), 1404–1410. doi:10.1039/c9sc04926fFull textFull text of the publication as PDF document
  198. Lanthanide conjugates as versatile instruments for therapy and diagnostics
    Herlan, C.; Bräse, S.
    2020. Dalton transactions, 49 (8), 2397–2402. doi:10.1039/C9DT04851KFull textFull text of the publication as PDF document
  199. Post-synthetic Modification of DUT-5-based Metal Organic Frameworks for the Generation of Single-site Catalysts and their Application in Selective Epoxidation Reactions
    Yildiz, C.; Kutonova, K.; Oßwald, S.; Titze-Alonso, A.; Bitzer, J.; Bräse, S.; Kleist, W.
    2020. ChemCatChem, 12 (4), 1134–1142. doi:10.1002/cctc.201901434Full textFull text of the publication as PDF document
  200. Acceptor Derivatization of the 4CzIPN TADF System: Color Tuning and Introduction of Functional Groups
    Hundemer, F.; Reventlow, L. G. von; Leonhardt, C.; Polamo, M.; Nieger, M.; Seifermann, S. M.; Colsmann, A.; Bräse, S.
    2019. ChemistryOpen, 8 (12), 1413–1420. doi:10.1002/open.201900141Full textFull text of the publication as PDF document
  201. Author Correction: A Peptoid Delivers CoQ-derivative to Plant Mitochondria via Endocytosis
    Asfaw, K. G.; Liu, Q.; Maisch, J.; Münch, S. W.; Wehl, I.; Bräse, S.; Bogeski, I.; Schepers, U.; Nick, P.
    2019. Scientific reports, 9 (1), Art.Nr.: 18832. doi:10.1038/s41598-019-54996-0Full textFull text of the publication as PDF document
  202. A Peptoid Delivers CoQ-derivative to Plant Mitochondria via Endocytosis
    Asfaw, K. G.; Liu, Q.; Maisch, J.; Münch, S. W.; Wehl, I.; Bräse, S.; Bogeski, I.; Schepers, U.; Nick, P.
    2019. Scientific reports, 9 (1), Art.Nr.: 9839. doi:10.1038/s41598-019-46182-zFull textFull text of the publication as PDF document
  203. Preparation and Synthetic Applications of [2.2]Paracyclophane Trifluoroborates: An Efficient and Convenient Route to Nucleophilic [2.2]Paracyclophane Cross‐Coupling Building Blocks
    Knoll, D. M.; Šimek, H.; Hassan, Z.; Bräse, S.
    2019. European journal of organic chemistry, 2019 (36), 6198–6202. doi:10.1002/ejoc.201901171Full textFull text of the publication as PDF document
  204. Alkaline generation and reactions of CF3CHN2
    Rosenbaum, N.; Zippel, C.; Bräse, S.
    2019. Science China / Chemistry, 62 (8), 923–924. doi:10.1007/s11426-019-9479-2
  205. Cobalt-Catalyzed α-Arylation of Substituted α-Halogeno β-Lactams
    Koch, V.; Lorion, M. M.; Barde, E.; Bräse, S.; Cossy, J.
    2019. Organic letters, 21 (16), 6241–6244. doi:10.1021/acs.orglett.9b02122
  206. Photoconductivity in Metal–Organic Framework (MOF) Thin Films
    Liu, X.; Kozlowska, M.; Okkali, T.; Wagner, D.; Higashino, T.; Brenner-Weiß, G.; Marschner, S. M.; Fu, Z.; Zhang, Q.; Imahori, H.; Bräse, S.; Wenzel, W.; Wöll, C.; Heinke, L.
    2019. Angewandte Chemie / International edition, 58 (28), 9590–9595. doi:10.1002/anie.201904475Full textFull text of the publication as PDF document
  207. Design, synthesis, and DNA interaction studies of furo-imidazo[3.3.3]propellane derivatives: Potential anticancer agents
    Hassan, A. A.; Aly, A. A.; Mohamed, N. K.; El Shaieb, K. M.; Makhlouf, M. M.; Abdelhafez, E.-S. M. N.; Bräse, S.; Nieger, M.; Dalby, K. N.; Kaoud, T. S.
    2019. Bioorganic chemistry, 85, 585–599. doi:10.1016/j.bioorg.2019.02.027
  208. ChemScanner: extraction and re-use(ability) of chemical information from common scientific documents containing ChemDraw files
    Nguyen, A.; Huang, Y.-C.; Tremouilhac, P.; Jung, N.; Bräse, S.
    2019. Journal of cheminformatics, 11 (1), Art. Nr.: 77. doi:10.1186/s13321-019-0400-5Full textFull text of the publication as PDF document
  209. Synthesis, Characterization, and Biological Properties of Steroidal Ruthenium(II) and Iridium(III) Complexes Based on the Androst-16-en-3-ol Framework
    Koch, V.; Meschkov, A.; Feuerstein, W.; Pfeifer, J.; Fuhr, O.; Nieger, M.; Schepers, U.; Bräse, S.
    2019. Inorganic chemistry, 58 (23), 15917–15926. doi:10.1021/acs.inorgchem.9b02402Full textFull text of the publication as PDF document
  210. Planar chiral [2.2]paracyclophane-based bisoxazoline ligands and their applications in Cu-Mediated N-H insertion reaction
    Knoll, D. M.; Hu, Y.; Hassan, Z.; Nieger, M.; Bräse, S.
    2019. Molecules, 24 (22), Art.-Nr.: 4122. doi:10.3390/molecules24224122Full textFull text of the publication as PDF document
  211. New quinoline-2-one/pyrazole derivatives; design, synthesis, molecular docking, anti-apoptotic evaluation, and caspase-3 inhibition assay
    Aly, A. A.; Sayed, S. M.; Abdelhafez, E.-S. M. N.; Abdelhafez, S. M. N.; Abdelzaher, W. Y.; Raslan, M. A.; Ahmed, A. E.; Thabet, K.; El-Reedy, A. A. M.; Brown, A. B.; Bräse, S.
    2019. Bioorganic chemistry, 94, Article No.103348. doi:10.1016/j.bioorg.2019.103348
  212. Highly soluble fluorine containing Cu(i) AlkylPyrPhos TADF complexes
    Busch, J. M.; Zink, D. M.; Di Martino-Fumo, P.; Rehak, F. R.; Boden, P.; Steiger, S.; Fuhr, O.; Nieger, M.; Klopper, W.; Gerhards, M.; Bräse, S.
    2019. Dalton transactions, 48 (41), 15687–15698. doi:10.1039/c9dt02447fFull textFull text of the publication as PDF document
  213. Metal-supported and -assisted stereoselective cooperative photoredox catalysis
    Busch, J.; Knoll, D. M.; Zippel, C.; Bräse, S.; Bizzarri, C.
    2019. Dalton transactions, 48 (41), 15338–15357. doi:10.1039/c9dt02094bFull textFull text of the publication as PDF document
  214. Synthesis of New Fused Heterocyclic 2-Quinolones and 3-Alkanonyl-4-Hydroxy-2-Quinolones
    Aly, A. A.; Hassan, A. A.; Mohamed, N. K.; El-Haleem, L. E. A.; Bräse, S.; Polamo, M.; Nieger, M.; Brown, A. B.
    2019. Molecules, 24 (20), 3782. doi:10.3390/molecules24203782Full textFull text of the publication as PDF document
  215. Chemoenzymatic Synthesis of O-Containing Heterocycles from α-Diazo Esters
    Mittmann, E.; Hu, Y.; Peschke, T.; Rabe, K. S.; Niemeyer, C. M.; Bräse, S.
    2019. ChemCatChem, 11 (22), 5519–5523. doi:10.1002/cctc.201901602Full textFull text of the publication as PDF document
  216. Functionalized 1,3-Thiazolidin-4-Ones from 2-Oxo-Acenaphthoquinylidene- and [2.2]Paracyclophanylidene-Thiosemicarbazones
    Aly, A. A.; Mohamed, N. K.; Hassan, A. A.; El-Shaieb, K. M.; Makhlouf, M. M.; Bräse, S.; Nieger, M.; Brown, A. B.
    2019. Molecules, 24 (17), Article: 3069. doi:10.3390/molecules24173069Full textFull text of the publication as PDF document
  217. Synthesis and characterization of rigid [2.2]paracyclophane–porphyrin conjugates as scaffolds for fixed-distance bimetallic complexes
    Knoll, D. M.; Wiesner, T. B.; Marschner, S. M.; Hassan, Z.; Weis, P.; Kappes, M.; Nieger, M.; Bräse, S.
    2019. RSC Advances, 9 (52), 30541–30544. doi:10.1039/c9ra07055aFull textFull text of the publication as PDF document
  218. Synthesis, Transfer, and Gas Separation Characteristics of MOF-Templated Polymer Membranes
    Schmitt, S.; Shishatskiy, S.; Krolla, P.; An, Q.; Begum, S.; Welle, A.; Hashem, T.; Grosjean, S.; Abetz, V.; Bräse, S.; Wöll, C.; Tsotsalas, M.
    2019. Membranes, 9 (10), Art. Nr.: 124. doi:10.3390/membranes9100124Full textFull text of the publication as PDF document
  219. When Does a Supramolecular Synthon Fail? Comparison of Bridgehead-Functionalized Adamantanes: The Tri: The Tetra-amides and Amine Hydrochlorides
    Boldog, I.; Reiss, G. J.; Domasevitch, K. V.; Baše, T.; Bräse, S.
    2019. Crystal growth & design, 19 (9), 5218–5227. doi:10.1021/acs.cgd.9b00594
  220. Synthesis of Arylamides via Ritter-Type Cleavage of Solid-Supported Aryltriazenes
    Wippert, N. A.; Jung, N.; Bräse, S.
    2019. ACS combinatorial science, 21 (8), 568–572. doi:10.1021/acscombsci.9b00096
  221. Star-shaped triarylamines – One-step metal-free synthesis and optoelectronic properties
    Meli, A.; Ebenhoch, B.; Kutonova, K.; Bihlmeier, A.; Feyrer, A.; Deck, E.; Breher, F.; Nieger, M.; Colsmann, A.; Bräse, S.
    2019. Synthetic metals, 256, 116138. doi:10.1016/j.synthmet.2019.116138
  222. Switching the enantioselectivity of nanoporous host materials by light
    Kanj, A. B.; Bürck, J.; Grosjean, S.; Bräse, S.; Heinke, L.
    2019. Chemical communications, 55 (60), 8776–8779. doi:10.1039/c9cc02849hFull textFull text of the publication as PDF document
  223. Turn on of sky-blue thermally activated delayed fluorescence and circularly polarized luminescence (CPL): Via increased torsion by a bulky carbazolophane donor
    Sharma, N.; Spuling, E.; Mattern, C. M.; Li, W.; Fuhr, O.; Tsuchiya, Y.; Adachi, C.; Bräse, S.; Samuel, I. D. W.; Zysman-Colman, E.
    2019. Chemical science, 10 (27), 6689–6696. doi:10.1039/c9sc01821bFull textFull text of the publication as PDF document
  224. Rational design and implementation of a cucurbit[8]uril-based indicator-displacement assay for application in blood serum
    Sinn, S.; Spuling, E.; Bräse, S.; Biedermann, F.
    2019. Chemical science, 10 (27), 6584–6593. doi:10.1039/c9sc00705aFull textFull text of the publication as PDF document
  225. Synthesis of Functionalized Azobiphenyl- and Azoterphenyl- Ditopic Linkers: Modular Building Blocks for Photoresponsive Smart Materials
    Grosjean, S.; Hodapp, P.; Hassan, Z.; Wöll, C.; Nieger, M.; Bräse, S.
    2019. ChemistryOpen, 8 (6), 743–759. doi:10.1002/open.201900031
  226. Insertion of [1.1.1]propellane into aromatic disulfides
    Bär, R. M.; Heinrich, G.; Nieger, M.; Fuhr, O.; Bräse, S.
    2019. Beilstein journal of organic chemistry, 15, 1172–1180. doi:10.3762/bjoc.15.114Full textFull text of the publication as PDF document
  227. New Polyfluorinated Cyanine Dyes for Selective NIR Staining of Mitochondria
    Braun, A. B.; Wehl, I.; Kölmel, D. K.; Schepers, U.; Bräse, S.
    2019. Chemistry - a European journal, 25 (34), 7998–8002. doi:10.1002/chem.201900412
  228. Planar-chiral [2.2]Paracyclophane-based Pyridonates as Ligands for Tantalum-catalyzed Hydroaminoalkylation
    Braun, C.; Nieger, M.; Bräse, S.; Schafer, L. L.
    2019. ChemCatChem, 11 (21), 5264–5268. doi:10.1002/cctc.201900416
  229. Bridging the Green Gap: Metal–Organic Framework Heteromultilayers Assembled from Porphyrinic Linkers Identified by Using Computational Screening
    Haldar, R.; Batra, K.; Marschner, S. M.; Kuc, A. B.; Zahn, S.; Fischer, R. A.; Bräse, S.; Heine, T.; Wöll, C.
    2019. Chemistry - a European journal, 25 (33), 7847–7851. doi:10.1002/chem.201901585
  230. Metal-Organic Framework-Templated Biomaterials: Recent Progress in Synthesis, Functionalization, and Applications
    Begum, S.; Hassan, Z.; Bräse, S.; Wöll, C.; Tsotsalas, M.
    2019. Accounts of chemical research, 52 (6), 1598–1610. doi:10.1021/acs.accounts.9b00039
  231. Procedures for systematic capture and management of analytical data in academia
    Potthoff, J.; Tremouilhac, P.; Hodapp, P.; Neumair, B.; Bräse, S.; Jung, N.
    2019. Analytica Chimica Acta: X, 1, Article: 100007. doi:10.1016/j.acax.2019.100007Full textFull text of the publication as PDF document
  232. Soft Matter Technology at KIT: Chemical Perspective from Nanoarchitectures to Microstructures
    Grosjean, S.; Wawryszyn, M.; Mutlu, H.; Bräse, S.; Lahann, J.; Theato, P.
    2019. Advanced materials, 31 (26), Art.-Nr.: 1806334. doi:10.1002/adma.201806334Full textFull text of the publication as PDF document
  233. Investigations on the Staudinger explosion and its prevention
    Schaberg, A.; Goertz, R.; Bräse, S.
    2019. Journal of hazardous materials, 367, 375–380. doi:10.1016/j.jhazmat.2018.12.097
  234. Diverse Multi-Functionalized Oligoarenes and Heteroarenes for Porous Crystalline Materials
    Grosjean, S.; Hassan, Z.; Wöll, C.; Bräse, S.
    2019. European journal of organic chemistry, (7), 1446–1460. doi:10.1002/ejoc.201801232
  235. Design, synthesis and biological evaluation of fused naphthofuro[3,2-c] quinoline-6,7,12-triones and pyrano[3,2-c]quinoline-6,7,8,13-tetraones derivatives as ERK inhibitors with efficacy in BRAF-mutant melanoma
    Aly, A. A.; El-Sheref, E. M.; Bakheet, M. E. M.; Mourad, M. A. E.; Bräse, S.; Ibrahim, M. A. A.; Nieger, M.; Garvalov, B. K.; Dalby, K. N.; Kaoud, T. S.
    2019. Bioorganic chemistry, 82, 290–305. doi:10.1016/j.bioorg.2018.10.044
  236. Brightly luminescent lanthanide pyrazolecarboxylates: Synthesis, luminescent properties and influence of ligand isomerism
    Utochnikova, V. V.; Abramovich, M. S.; Latipov, E. V.; Dalinger, A. I.; Goloveshkin, A. S.; Vashchenko, A. A.; Kalyakina, A. S.; Vatsadze, S. Z.; Schepers, U.; Bräse, S.; Kuzmina, N. P.
    2019. Journal of luminescence, 205, 429–439. doi:10.1016/j.jlumin.2018.09.027
  237. 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/s13321-018-0292-9Full textFull text of the publication as PDF document
  238. 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
  239. 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
  240. 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
  241. 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
  242. 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
  243. 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
  244. 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
  245. 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
  246. 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
  247. 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.201800533Full textFull text of the publication as PDF document
  248. 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/s12974-018-1362-7Full textFull text of the publication as PDF document
  249. 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
  250. 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
  251. 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
  252. 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
  253. 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
  254. (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
  255. 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
  256. 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
  257. 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
  258. 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
  259. 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.2018.00091Full textFull text of the publication as PDF document
  260. 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.14.37Full textFull text of the publication as PDF document
  261. 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
  262. 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
  263. 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
  264. 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
  265. 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
  266. 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
  267. 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
  268. 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
  269. Erfassung und Speicherung von Forschungsdaten im Fachbereich Chemie: Bereitstellung moderner Forschungs-infrastrukturen durch ein elektronisches Laborjournal mit Repositorium-Anbindung
    Jung, N.; Tremouilhac, P.; Kramer, C.; Potthoff, J.
    2017. E-Science-Tage 2017: Forschungsdaten managen. Hrsg.: J. Kratzke, 127–136, Heidelberger E-Books (heiBOOKS) Full textFull text of the publication as PDF document
  270. 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
  271. 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
  272. 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
  273. [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
  274. 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
  275. 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/s13321-017-0240-0Full textFull text of the publication as PDF document
  276. 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
  277. 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
  278. 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
  279. 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
  280. Ein Molekülarchiv als akademisch integrierte Service-Einrichtung
    Jung, N.; Deckers, A.; Bräse, S.
    2017. Biospektrum, 23 (2), 212–214 
  281. 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.27159Full textFull text of the publication as PDF document
  282. Synthesis and Investigation of S-Substituted 2-Mercaptobenzoimidazoles as Inhibitors of Hedgehog Signaling
    Gräßle, S.; Susanto, S.; Sievers, S.; Tavsan, E.; Nieger, M.; Jung, N.; Stefan Bräse
    2017. ACS medicinal chemistry letters, 8 (9), 931–935. doi:10.1021/acsmedchemlett.7b00100
  283. 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
  284. 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
  285. 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
  286. 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
  287. 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
  288. 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
  289. 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
  290. 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
  291. 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.13.54Full textFull text of the publication as PDF document
  292. 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
  293. 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/c6ra26546dFull textFull text of the publication as PDF document
  294. 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
  295. 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
  296. 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
  297. 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
  298. 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
  299. 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
  300. Enhancement of Two-Photon Absorption in Highly Emissive BODIPY Dyes
    Barros, L. W.; Castaneda, J. A.; Cardoso, T. A.; Kölmel, D. K.; Hörner, A.; Bihlmeier, A.; Nieger, M.; Bräse, S.; Cruz, C. H. B.; Padilha, L. A.
    2016. Conference on Lasers and Electro-Optics (CLEO 2016), San Jose, CA, June 5-10, 2016. OSA Technical Digest, Paper JW2A.62, Optica Publishing Group (OSA) 
  301. Tunable molecular separation by nanoporous membranes
    Wang, Z.; Knebel, A.; Grosjean, S.; Wagner, D.; Bräse, S.; Wöll, C.; Caro, J.; Heinke, L.
    2016. Nature Communications, 7, 13872. doi:10.1038/ncomms13872Full textFull text of the publication as PDF document
  302. EXAFS characterisation of metal bonding in highly luminescent, UV stable, water-soluble and biocompatible lanthanide complexes
    Kalyakina, A.; Utochnikova, V.; Trigub, A.; Zubavichus, Y.; Kuzmina, N.; Bräse, S.
    2016. Journal of physics / Conference Series, 712, 012137. doi:10.1088/1742-6596/712/1/012137Full textFull text of the publication as PDF document
  303. Structure-performance relationships of phenyl cinnamic acid derivatives as MALDI-MS matrices for sulfatide detection
    Tambe, S.; Blott, H.; Fülöp, A.; Spang, N.; Flottmann, D.; Bräse, S.; Hopf, C.; Junker, H.-D.
    2016. Analytical and bioanalytical chemistry, 409 (6), 1569–1580. doi:10.1007/s00216-016-0096-6
  304. Expeditious Synthesis of Functionalized 1-Arylcyclooctadienes via Palladium-Catalyzed Lithium Cross-Coupling
    Wandler, A. E. E.; Bräse, S.
    2016. Advanced synthesis & catalysis, 358 (24), 4125–4128. doi:10.1002/adsc.201600887
  305. Synthesis of three-dimensional porous hyper-crosslinked polymers via thiol-yne reaction
    Lang, M.; Schade, A.; Bräse, S.
    2016. Beilstein journal of organic chemistry, 12, 2570–2576. doi:10.3762/bjoc.12.252Full textFull text of the publication as PDF document
  306. Lanthanide 9-anthracenate: solution processable emitters for efficient purely NIR emitting host-free OLEDs
    Utochnikova, V. V.; Kalyakina, A. S.; Bushmarinov, I. S.; Vashchenko, A. A.; Marciniak, L.; Kaczmarek, A. M.; Van Deun, R.; Bräse, S.; Kuzmina, N. P.
    2016. Journal of materials chemistry / C, 4 (41), 9848–9855. doi:10.1039/C6TC03586H
  307. Direct observation of intersystem crossing in a thermally activated delayed fluorescence copper complex in the solid state
    Bergmann, L.; Hedley, G. J.; Baumann, T.; Bräse, S.; Samuel, I. D. W.
    2016. Science advances, 2 (1), e1500889. doi:10.1126/sciadv.1500889Full textFull text of the publication as PDF document
  308. Novel Prodrug of Doxorubicin Modified by Stearoylspermine Encapsulated into PEG-Chitosan-Stabilized Liposomes
    Deygen, I. M.; Seidl, C.; Kölmel, D. K.; Bednarek, C.; Heissler, S.; Kudryashova, E. V.; Bräse, S.; Schepers, U.
    2016. Langmuir, 32 (42), 10861–10869. doi:10.1021/acs.langmuir.6b01023
  309. Tuning the Cell Adhesion on Biofunctionalized Nanoporous Organic Frameworks
    Schmitt, S.; Hümmer, J.; Kraus, S.; Welle, A.; Grosjean, S.; Hanke-Roos, M.; Rosenhahn, A.; Bräse, S.; Wöll, C.; Lee-Thedieck, C.; Tsotsalas, M.
    2016. Advanced functional materials, 26 (46), 8455–8462. doi:10.1002/adfm.201603054
  310. Towards Printed Organic Light-Emitting Devices: A Solution-Stable, Highly Soluble Cu-NHetPHOS
    Wallesch, M.; Verma, A.; Fléchon, C.; Flügge, H.; Zink, D. M.; Seifermann, S. M.; Navarro, J. M.; Vitova, T.; Göttlicher, J.; Steininger, R.; Weinhardt, L.; Zimmer, M.; Gerhards, M.; Heske, C.; Bräse, S.; Baumann, T.; Volz, D.
    2016. Chemistry - a European journal, 22 (46), 16400–16405. doi:10.1002/chem.201603847Full textFull text of the publication as PDF document
  311. Oxaenediynes through the Nicholas-Type Macrocyclization Approach
    Lyapunova, A. G.; Danilkina, N. A.; Khlebnikov, A. F.; Köberle, B.; Bräse, S.; Balova, I. A.
    2016. European journal of organic chemistry, 2016 (28), 4842–4851. doi:10.1002/ejoc.201600767
  312. Control of Azomethine Cycloaddition Stereochemistry by CF3 Group: Structural Diversity of Fluorinated β-Proline Dimers
    Kudryavtsev, K. V.; Mantsyzov, A. B.; Ivantcova, P. M.; Sokolov, M. N.; Churakov, A. V.; Bräse, S.; Zefirov, N. S.; Polshakov, V. I.
    2016. Organic letters, 18 (18), 4698–4701. doi:10.1021/acs.orglett.6b02327
  313. Solid Phase Synthesis of (Benzannelated) Six-Membered Heterocycles via Cyclative Cleavage of Resin-Bound Pseudo-Oxazolones
    Gräßle, S.; Vanderheiden, S.; Hodapp, P.; Bulat, B.; Nieger, M.; Jung, N.; Bräse, S.
    2016. Organic letters, 18 (15), 3598–3601. doi:10.1021/acs.orglett.6b01609
  314. Replication of Polymer-Based Peptide Microarrays by Multi-Step Transfer
    Striffler, J.; Mattes, D. S.; Schillo, S.; Münster, B.; Palermo, A.; Ridder, B.; Welle, A.; Trouillet, V.; Stadler, V.; Markovic, G.; Proll, G.; Bräse, S.; Loeffler, F. F.; Nesterov-Müller, A.; Breitling, F.
    2016. ChemNanoMat, 2 (9), 897–903. doi:10.1002/cnma.201600194
  315. NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents
    Görling, B.; Bräse, S.; Luy, B.
    2016. Metabolites, 6 (3), 27. doi:10.3390/metabo6030027Full textFull text of the publication as PDF document
  316. A Modular Class of Fluorescent Difluoroboranes: Synthesis, Structure, Optical Properties, Theoretical Calculations and Applications for Biological Imaging
    Bachollet, S. P. J. T.; Volz, D.; Fiser, B.; Münch, S.; Rönicke, F.; Carrillo, J.; Adams, H.; Schepers, U.; Gómez-Bengoa, E.; Bräse, S.; Harrity, J. P. A.
    2016. Chemistry - a European journal, 22 (35), 12430–12438. doi:10.1002/chem.201601915
  317. Chemical Synthesis of Glycosaminoglycans
    Mende, M.; Bednarek, C.; Wawryszyn, M.; Sauter, P.; Biskup, M. B.; Schepers, U.; Bräse, S.
    2016. Chemical reviews, 116 (14), 8193–8255. doi:10.1021/acs.chemrev.6b00010
  318. Radical exchange reaction of multi-spin isoindoline nitroxides followed by EPR spectroscopy
    Wessely, I.; Mugnaini, V.; Bihlmeier, A.; Jeschke, G.; Bräse, S.; Tsotsalas, M.
    2016. RSC Advances, 6 (61), 55715–55719. doi:10.1039/c6ra06510dFull textFull text of the publication as PDF document
  319. Solid phase syntheses of: S, N -substituted 2-mercaptobenzoimidazoles
    Susanto, S.; Jung, N.; Bräse, S.
    2016. RSC Advances, 6 (46), 39573–39576. doi:10.1039/c6ra05702k
  320. Metal-Organic and Organic TADF-Materials: Status, Challenges and Characterization
    Bergmann, L.; Zink, D. M.; Bräse, S.; Baumann, T.; Volz, D.
    2016. Topics in current chemistry, 374 (3), Article nr. 22. doi:10.1007/s41061-016-0022-6
  321. High-flexibility combinatorial peptide synthesis with laser-based transfer of monomers in solid matrix material
    Loeffler, F. F.; Foertsch, T. C.; Popov, R.; Mattes, D. S.; Schlageter, M.; Sedlmayr, M.; Ridder, B.; Dang, F.-X.; Bojnicic-Kninski, C. von; Weber, L. K.; Fischer, A.; Greifenstein, J.; Bykovskaya, V.; Buliev, I.; Bischoff, F. R.; Hahn, L.; Meier, M. A. R.; Bräse, S.; Powell, A. K.; Balaban, T. S.; Breitling, F.; Nesterov-Mueller, A.
    2016. Nature Communications, 7, Article number 11844. doi:10.1038/ncomms11844Full textFull text of the publication as PDF document
  322. Site-Specific Conjugation of Peptides and Proteins via Rebridging of Disulfide Bonds Using the Thiol-Yne Coupling Reaction
    Griebenow, N.; Dilmaç, A. M.; Greven, S.; Bräse, S.
    2016. Bioconjugate Chemistry, 27 (4), 911–917. doi:10.1021/acs.bioconjchem.5b00682
  323. Surface functionalization of conjugated microporous polymer thin films and nanomembranes using orthogonal chemistries
    Lindemann, P.; Schade, A.; Monnereau, L.; Feng, W.; Batra, K.; Gliemann, H.; Levkin, P.; Bräse, S.; Wöll, C.; Tsotsalas, M.
    2016. Journal of Materials Chemistry A, 4, 6815–6818. doi:10.1039/C5TA09429A
  324. Synthesis of Highly Functionalized 4-Aminoquinolines
    Wezeman, T.; Zhong, S.; Nieger, M.; Bräse, S.
    2016. Angewandte Chemie - International Edition, 55 (11), 3823–3827. doi:10.1002/anie.201511385
  325. Tunable porosity of 3D-networks with germanium nodes
    Monnereau, L.; Muller, T.; Lang, M.; Bräse, S.
    2016. Chemical Communications, 52 (3), 571–574. doi:10.1039/c5cc06790a
  326. Linear and Nonlinear Optical Spectroscopy of Fluoroalkylated BODIPY Dyes
    Kölmel, D. K.; Hörner, A.; Castaneda, J. A.; Ferencz, J. A. P.; Bihlmeier, A.; Nieger, M.; Bräse, S.; Padilha, L. A.
    2016. Journal of Physical Chemistry C, 120 (8), 4538–4545. doi:10.1021/acs.jpcc.6b00096
  327. Hydrazoic acid and azides
    Bräse, S.; Mende, M.; Jobelius, H. H.; Scharf, H.-D.
    2015. Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH Verlag. doi:10.1002/14356007.a13_193.pub2
  328. Menthols as Chiral Auxiliaries for Asymmetric Cycloadditive Oligomerization: Syntheses and Studies of β-Proline Hexamers
    Kudryavtsev, K.; Ivantcova, P. M.; Muhle-Goll, C.; Churakov, A. V.; Sokolov, M. N.; Dyuba, A. V.; Arutyunyan, A. M.; Howard, J. A. K.; Yu, C.-C.; Guh, J.-H.; Zefirov, N. S.; Bräse, S.
    2015. Organic Letters, 17 (24), 6178–6181. doi:10.1021/acs.orglett.5b03154
  329. Synthesis and post-synthetic modification of amine-, alkyne-, azide- and nitro-functionalized metal-organic frameworks based on DUT-5
    Gotthardt, M. A.; Grosjean, S.; Brunner, T. S.; Kotzel, J.; Gänzler, A. M.; Wolf, S.; Bräse, S.; Kleist, W.
    2015. Dalton transactions, 44 (38), 16802–16809. doi:10.1039/c5dt02276bFull textFull text of the publication as PDF document
  330. Cu K XANES and EXAFS spectroscopy on Cu(I)-emitters
    Wallesch, M.; Volz, D.; Batchelor, D.; Vitova, T.; Steininger, R.; Göttlicher, J.; Bräse, S.; Heske, C.; Weinhardt, L.
    2015. 16th International Conference on X-Ray Absorption Fine Structure (XAFS16), Karlsruhe, August 23-28, 2015 Book of Abstracts 
  331. Using X-ray absorption to probe the structural integrity of photoluminescent Cu(I)-complexes upon processing
    Wallesch, M.; Volz, D.; Vitova, T.; Göttlicher, J.; Steininger, R.; Bräse, S.; Heske, C.; Weinhardt, L.
    2015. 21st International Symposium on the Photochemistry nd Photophysics of Coordination Compounds (ISPPCC 2015), Krakow, PL, July 5-9, 2015 
  332. Enantioselective adsorption in homochiral metal-organic frameworks: The pore size influence
    Gu, Z. G.; Grosjean, S.; Bräse, S.; Wöll, C.; Heinke, L.
    2015. Chemical communications, 51 (43), 8998–9001. doi:10.1039/C5CC02706C
  333. Chemical synthesis and enzymatic, stereoselective hydrolysis of a functionalized dihydropyrimidine for the synthesis of β-amino acids
    Slomka, C.; Zhong, S.; Fellinger, A.; Engel, U.; Syldatk, C.; Bräse, S.; Rudat, J.
    2015. AMB Express, 5 (1), 85. doi:10.1186/s13568-015-0174-8Full textFull text of the publication as PDF document
  334. Monolithic crystalline MOF coating: An excellent patterning and photoresist material
    Wang, Z.; Liu, J.; Grosjean, S.; Wagner, D.; Guo, W.; Gu, Z.; Heinke, L.; Gliemann, H.; Bräse, S.; Wöll, C.
    2015. ChemNanoMat, 1, 338–345. doi:10.1002/cnma.201500031
  335. Cis-to-trans isomerization of azobenzene investigated by using thin films of metal-organic frameworks
    Yu, X.; Wang, Z.; Buchholz, M.; Füllgrabe, N.; Grosjean, S.; Bebensee, F.; Bräse, S.; Wöll, C.; Heinke, L.
    2015. Physical chemistry, chemical physics, 17, 22721–22725. doi:10.1039/C5CP03091A
  336. Photoswitchable adsorption in metal-organic frameworks based on polar guest-host interactions
    Wang, Z.; Grosjean, S.; Bräse, S.; Heinke, L.
    2015. ChemPhysChem, 16, 3779–3783. doi:10.1002/cphc.201500829
  337. Simple and expedient metal-free C-H-functionalization of fluoro-arenes by the BHAS method - Scope and limitations
    Lindner, S.; Bräse, S.; Masters, K. S.
    2015. Journal of fluorine chemistry, 179, 102–105. doi:10.1016/j.jfluchem.2015.06.010
  338. Highly luminescent, water-soluble lanthanide fluorobenzonates : Syntheses, structures and photophysics, Part I : Lanthanide pentafluorobenzoates
    Kalyakina, A. S.; Utochnikova, V. V.; Bushmarinov, I. S.; Ananyev, I. V.; Eremenko, I. L.; Volz, D.; Rönicke, F.; Schepers, U.; Van Deun, R.; Trigub, A. L.; Zubavichus, Y. V.; Kuzmina, N. P.; Bräse, S.
    2015. Chemistry - a European journal, 21 (49), 17921–17932. doi:10.1002/chem.201501816
  339. Synthesis of new diketopiperazines, thiolation to thiodiketopiperazines, and examination of ateir ROS-generating properties
    Zhong, S.; Wandler, A. E. E.; Schepers, U.; Nieger, M.; Bräse, S.
    2015. European Journal of Organic Chemistry, (31), 6858–6871. doi:10.1002/ejoc.201500900
  340. Stereoselective synthesis of highly functionalized hydroindoles as building blocks for rostratins B-D and synthesis of the pentacyclic core of rostratin C
    Zhong, S.; Sauter, P. F.; Nieger, M.; Bräse, S.
    2015. Chemistry - a European journal, 21, 11219–11225. doi:10.1002/chem.201501199
  341. Secretome analysis identifies novel signal peptide peptidase-like 3 (Sppl3) substrates and reveals a role of Sppl3 in multiple golgi glycosylation pathways
    Kuhn, P. H.; Voss, M.; Haug-Kröper, M.; Schröder, B.; Schepers, U.; Bräse, S.; Haass, C.; Lichtenthaler, S. F.; Fluhrer, R.
    2015. Molecular & cellular proteomics, 14 (6), 1584–1598. doi:10.1074/mcp.M115.048298
  342. Photophysical properties and synthesis of new dye-cyclooctyne conjugates for multicolor and advanced microscopy
    Hörner, A.; Hagendorn, T.; Schepers, U.; Bräse, S.
    2015. Bioconjugate chemistry, 26 (4), 718–724. doi:10.1021/acs.bioconjchem.5b00059
  343. Ruthenium-catalyzed C-H activation of thioxanthones
    Wagner, D.; Bräse, S.
    2015. Beilstein journal of organic chemistry, 11, 431–435. doi:10.3762/bjoc.11.49Full textFull text of the publication as PDF document
  344. Open source life science automation: Design of experiments and data acquisition via ’dial-a-device’
    Lütjohann, D. S.; Jung, N.; Bräse, S.
    2015. Chemometrics and intelligent laboratory systems, 144, 100–107. doi:10.1016/j.chemolab.2015.04.002
  345. Structural studies and anticancer activity of a novel class of β-peptides
    Kudryavtsev, K. V.; Yu, C. C.; Ivantcova, P. M.; Polshakov, V. I.; Churakov, A. V.; Bräse, S.; Zefirov, N. S.; Guh, J. H.
    2015. Chemistry, 10 (2), 383–389. doi:10.1002/asia.201403171
  346. Solid phase synthesis of functionalized indazoles using triazenes-scope and limitations
    Garcia, A. M.; Jung, N.; Gil, C.; Nieger, M.; Bräse, S.
    2015. RSC Advances, 5 (80), 65540–65545. doi:10.1039/C5RA09705C
  347. From iridium and platinum to copper and carbon: New avenues for more sustainability in organic light-emitting diodes
    Volz, D.; Wallesch, M.; Flechon, C.; Danz, M.; Verma, A.; Navarro, J. M.; Zink, D. M.; Bräse, S.; Baumann, T.
    2015. Green chemistry, 17, 1988–2011. doi:10.1039/C4GC02195A
  348. Functionalized triazolopeptoids-a novel class for mitochondrial targeted delivery
    Althuon, D.; Rönicke, F.; Fürniss, D.; Quan, J.; Wellhöfer, I.; Jung, N.; Schepers, U.; Bräse, S.
    2015. Organic & biomolecular chemistry, 13, 4226–4230. doi:10.1039/C5OB00250H
  349. Application of a novel small scale UV LED photochemical batch reactor for the thiol-yne reaction
    Griebenow, N.; Bräse, S.; Dilmac, A. M.
    2015. RSC Advances, 5 (67), 54301–54303. doi:10.1039/C5RA08787B
  350. Metal-free radical perfluoroalkylation of (hetero)arenes
    Zhong, S.; Hafner, A.; Hussal, C.; Nieger, M.; Bräse, S.
    2015. RSC Advances, 5, 6255–6258. doi:10.1039/C4RA13430C
  351. Ring-closing metathesis of Co₂(CO)₆-alkyne complexes for the synthesis of 11-membered dienediynes: Overcoming thermodynamic barriers
    Danilkina, N. A.; Lyapunova, A. G.; Khlebnikov, A. F.; Starova, G. L.; Bräse, S.; Balova, I. A.
    2015. The journal of organic chemistry, 80 (11), 5546–5555. doi:10.1021/acs.joc.5b00409
  352. Highly efficient synthesis of polyfluorinated dendrons suitable for click chemistry
    Kölmel, D. K.; Nieger, M.; Bräse, S.
    2015. RSC Advances, 5 (46), 36762–36765. doi:10.1039/C5RA02804C
  353. Photoswitching in nanoporous, crystalline solids: An experimental and theoretical study for azobenzene linkers incorporated in MOFs
    Wang, Z.; Heinke, L.; Jelic, J.; Cakici, M.; Dommaschk, M.; Maurer, R. J.; Oberhofer, H.; Grosjean, S.; Herges, R.; Bräse, S.; Reuter, K.; Wöll, C.
    2015. Physical chemistry, chemical physics, 17 (22), 14582–14587. doi:10.1039/c5cp01372kFull textFull text of the publication as PDF document
  354. Hierarchically functionalized magnetic core/multishell particles and their postsynthetic conversion to polymer capsules
    Schmitt, S.; Silvestre, M.; Tsotsalas, M.; Winkler, A. L.; Shahnas, A.; Grosjean, S.; Laye, F.; Gliemann, H.; Lahann, J.; Bräse, S.; Franzreb, M.; Wöll, C.
    2015. ACS nano, 9, 4219–4226. doi:10.1021/acsnano.5b00483
  355. Degradation mechanisms of polyfluorene-based organic semiconductor lasers under ambient and oxygen-free conditions
    Brenner, P.; Fleig, L. M.; Liu, X.; Welle, A.; Bräse, S.; Lemmer, U.
    2015. Journal of polymer science / B, 53, 1029–1034. doi:10.1002/polb.23733
  356. Dual-stimuli-responsive microparticles
    Sokolovskaya, E.; Rahmani, S.; Misra, A. C.; Bräse, S.; Lahann, J.
    2015. ACS applied materials & interfaces, 7, 9744–9751. doi:10.1021/acsami.5b01592
  357. The Diels-Alder approach to Δ⁹-tetrahydrocannabinol derivatives
    Gläser, F.; Bröhmer, M. C.; Hurrle, T.; Nieger, M.; Bräse, S.
    2015. European Journal of Organic Chemistry, 2015 (7), 1516–1524. doi:10.1002/ejoc.201403379
  358. Planar-chiral building blocks for metal-organic frameworks
    Cakici, M.; Gu, Z. G.; Nieger, M.; Bürck, J.; Heinke, L.; Bräse, S.
    2015. Chemical communications, 51 (23), 4796–4798. doi:10.1039/C5CC00694E
  359. Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes - A methyl group matters
    Enders, M.; Friedmann, C. J.; Plessow, P. N.; Bihlmeier, A.; Nieger, M.; Klopper, W.; Bräse, S.
    2015. Chemical communications, 51 (23), 4793–4795. doi:10.1039/C5CC00492F
  360. Bridging the efficiency gap: Fully bridged dinuclear Cu(I)-complexes for singlet harvesting in high-efficiency OLEDs
    Volz, D.; Chen, Y.; Wallesch, M.; Liu, R.; Flechon, C.; Zink, D. M.; Friedrichs, J.; Flügge, H.; Steininger, R.; Göttlicher, J.; Heske, C.; Weinhardt, L.; Bräse, S.; So, F.; Baumann, T.
    2015. Advanced materials, 27, 2538–2543. doi:10.1002/adma.201405897
  361. Sulfur-based hyper cross-linked polymers
    Monnereau, L.; Grandclaudon, C.; Muller, T.; Bräse, S.
    2015. RSC Advances, 5 (30), 23152–23159. doi:10.1039/C5RA01463H
  362. Synthesis of highly functionalized C₆₀ fullerene derivatives and their applications in material and life sciences
    Yan, W.; Seifermann, S. M.; Pierrat, P.; Bräse, S.
    2015. Organic and Biomolecular Chemistry, 13 (1), 25–54. doi:10.1039/C4OB01663GFull textFull text of the publication as PDF document
  363. Xanthone dimers: a compound family which is both common and privileged
    Wezeman, T.; Bräse, S.; Masters, K.-S.
    2015. Natural Product Reports, 32 (1), 6–28. doi:10.1039/C4NP00050AFull textFull text of the publication as PDF document
  364. A convenient and efficient synthesis of thiazolidin-4-ones via cyclization of substituted hydrazinecarbothioamides
    Hassan, A. A.; Mohamed, N. K.; El-Shaieb, K. M. A.; Tawfeek, H. N.; Bräse, S.; Nieger, M.
    2014. Arabian journal of chemistry. doi:10.1016/j.arabjc.2014.10.035
  365. Bright coppertunities: efficient OLED devices with copper(I)iodide-NHetPHOS-emitters
    Wallesch, M.; Volz, D.; Fléchon, C.; Zink, D. M.; Bräse, S.; Baumann, T.
    2014. Organic Light Emitting Materials and Devices XVIII, San Diego, California, United States, 17 - 20 August 2014. Ed.: F. So, 918309, Society of Photo-optical Instrumentation Engineers (SPIE). doi:10.1117/12.2060499
  366. Bright Coppertunities: Multinuclear CuI Complexes with N-P Ligands and Their Applications
    Wallesch, M.; Volz, D.; Zink, D. M.; Schepers, U.; Nieger, M.; Baumann, T.; Bräse, S.
    2014. Chemistry - a European journal, 20 (22), 6578–6590. doi:10.1002/chem.201402060
  367. Double trouble - the art of synthesis of chiral dimeric natural products
    Wezeman, T.; Masters, K.-S.; Bräse, S.
    2014. Angewandte Chemie - International edition, 53 (18), 4524–4526. doi:10.1002/anie.201402384
  368. Azides - Diazonium Ions - Triazenes: Versatile Nitrogen-rich Functional Groups
    Kölmel, D. K.; Jung, N.; Bräse, S.
    2014. Australian journal of chemistry, 67 (3), 328–336. doi:10.1071/CH13533
  369. Tetrahedral organic molecules as components in supramolecular architectures and in covalent assemblies, networks and polymers
    Muller, T.; Bräse, S.
    2014. RSC ADVANCES, 4 (14), 6886–6907. doi:10.1039/C3RA46951D
  370. Coregulator Control of Androgen Receptor Action by a Novel Nuclear Receptor-Binding Motif
    Jehle, K.; Cato, L.; Neeb, A.; Muhle-Goll, C.; Jung, N.; Smith, E. W.; Buzon, V.; Carbo, L. R.; Estebanez-Perpina, E.; Schmitz, K.; Fruk, L.; Luy, B.; Chen, Y.; Cox, M. B.; Bräse, S.; Brown, M.; Cato, A. C. B.
    2014. Journal of biological chemistry, 289 (13), 8839–8851. doi:10.1074/jbc.M113.534859
  371. Synthesis and On-Demand Gelation of Multifunctional Poly(ethylene glycol)-Based Polymers
    Sokolovskaya, E.; Barner, L.; Bräse, S.; Lahann, J.
    2014. Macromolecular rapid communications, 35 (8), 780–786. doi:10.1002/marc.201300909
  372. Naphthoquinone Diels-Alder Reactions: Approaches to the ABC Ring System of Beticolin
    Kramer, C. S.; Nieger, M.; Bräse, S.
    2014. European journal of organic chemistry, 2014 (10), 2150–2159. doi:10.1002/ejoc.201301763
  373. Azaporphine guest-host complexes in solution and gas-phase: evidence for partially filled nanoprisms and exchange reactions
    Weis, P.; Schwarz, U.; Hennrich, F.; Wagner, D.; Bräse, S.; Kappes, M.
    2014. Physical Chemistry Chemical Physics, 16 (13), 6225–6232. doi:10.1039/C3CP55486DFull textFull text of the publication as PDF document
  374. Asymmetric organocatalytic synthesis of 4,6-bis(1H-indole-3-yl)-piperidine-2 carboxylates
    Zhong, S.; Nieger, M.; Bihlmeier, A.; Shi, M.; Bräse, S.
    2014. Organic & biomolecular chemistry, 12 (20), 3265–3270. doi:10.1039/C4OB00234BFull textFull text of the publication as PDF document
  375. Switchable fluorescence by click reaction of a novel azidocarbazole dye
    Hörner, A.; Volz, D.; Hagendorn, T.; Furniss, D.; Greb, L.; Ronicke, F.; Nieger, M.; Schepers, U.; Bräse, S.
    2014. RSC Advances, 4 (23), 11528–11534. doi:10.1039/C3RA47964AFull textFull text of the publication as PDF document
  376. A Route to Cyclooct-2-ynol and Its Functionalization by Mitsunobu Chemistry
    Hagendorn, T.; Bräse, S.
    2014. European journal of organic chemistry, (6), 1280–1286. doi:10.1002/ejoc.201301375
  377. Reactions of resin-bound triazenes with dithianylium tetrafluoroborates: efficient synthesis of alpha-azo ketene dithioacetals and related hydrazones
    Jung, N.; Stanek, B.; Gräßle, S.; Nieger, M.; Bräse, S.
    2014. Organic letters, 16 (4), 1112–1115. doi:10.1021/ol4037133
  378. Solid-Supported Odorless Reagents for the Dithioacetalization of Aldehydes and Ketones
    Jung, N.; Grässle, S.; Lütjohann, D. S.; Bräse, S.
    2014. Organic letters, 16 (4), 1036–1039. doi:10.1021/ol403313h
  379. Tetrakis-(4-thiyphenyl)methane: Origin of a Reversible 3D-Homopolymer
    Monnereau, L.; Nieger, M.; Muller, T.; Bräse, S.
    2014. Advanced functional materials, 24 (8), 1054–1058. doi:10.1002/adfm.201302483
  380. Synthesis of Tritium Labelled and Photoactivatable N‐Acyl‐L‐homoserine Lactones : Inter‐Kingdom Signalling Molecules
    Jakubczyk, D.; Brenner-Weiss, G.; Bräse, S.
    2014. European journal of organic chemistry, 2014 (3), 592–597. doi:10.1002/ejoc.201300800
  381. Highly efficient photoluminescent Cu(I)-PyrPHOS-metallopolymers
    Volz, D.; Hirschbiel, A. F.; Zink, D. M.; Friedrichs, J.; Nieger, M.; Baumann, T.; Bräse, S.; Barner-Kowollik, C.
    2014. Journal of materials chemistry / C, 2 (8), 1457–1462. doi:10.1039/C3TC32347A
  382. Fabrication of Highly Uniform Gel Coatings by the Conversion of Surface-Anchored Metal–Organic Frameworks
    Tsotsalas, M.; Liu, J.; Tettmann, B.; Grosjean, S.; Shahnas, A.; Wang, Z.; Azucena, C.; Addicoat, M.; Heine, T.; Lahann, J.; Overhage, J.; Bräse, S.; Gliemann, H.; Wöll, C.
    2014. Journal of the American Chemical Society, 136 (1), 8–11. doi:10.1021/ja409205s
  383. Cross-coupling of organyl halides with alkenes The Heck reaction
    Bräse, S.; Meijere, A. de
    2014. de Meijere, A. [Hrsg.] Metal-Catalyzed Cross-Coupling Reactions and More Weinheim : Wiley-VCH, 2014, 533–663 
  384. Metal-catalyzed cross-coupling reactions and more
    Meijere, A. de; Bräse, S.; Oestreich, M.
    2014. Weinheim : Wiley-VCH, 2014 
  385. Das Internet der Dinge erobert das chemische Forschungslabor
    Lütjohann, D.; Jung, N.; Tremouilhac, P.; Bräse, S.
    2014. GIT Fachzeitschrift für das Laboratorium, (10), 22 
  386. Labile or stable: Can homoleptic and heteroleptic pyrphos-copper complexes be processed from solution?
    Volz, D.; Wallesch, M.; Grage, S. L.; Göttlicher, J.; Steininger, R.; Batchelor, D.; Vitova, T.; Ulrich, A. S.; Heske, C.; Weinhardt, L.; Baumann, T.; Bräse, S.
    2014. Inorganic chemistry frontiers, 53, 7837–7847. doi:10.1021/ic500135mFull textFull text of the publication as PDF document
  387. A mild method for eliminating alkyl ethers to alkenes
    Lindner, S.; Bräse, S.
    2014. RSC Advances, 4 (56), 29439–29442. doi:10.1039/C4RA03785E
  388. Total synthesis of blennolide mycotoxins: design, synthetic routes and completion
    Meister, A. C.; Encinas, A.; Sahin, H.; Singer, E. M. C.; Nising, C. F.; Nieger, M.; Bräse, S.
    2014. European Journal of Organic Chemistry, (22), 4861–4875. doi:10.1002/ejoc.201402083
  389. Electrophilic cyclization of aryldiacetylenes in the synthesis of functionalized enediynes fused to a heterocyclic core
    Danilkina, N. A.; Kulyashova, A. E.; Khlebnikov, A. F.; Bräse, S.; Balova, I. A.
    2014. The journal of organic chemistry, 79, 9018–9045. doi:10.1021/jo501396s
  390. Silver-mediated perfluoroalkylation reactions
    Hafner, A.; Jung, N.; Bräse, S.
    2014. Synthesis, 46, 1440–1447. doi:10.1055/s-0033-1341223
  391. Preparation of aromatic triazenes and their application in silver-mediated perfluoroalkylation reactions
    Hafner, A.; Hussal, C.; Bräse, S.
    2014. Synthesis, 46, 1448–1454. doi:10.1055/s-0033-1341249
  392. Hexaphenyl-p-xylene: A rigid pseudo-octahedral core at the service of three-dimensional porous frameworks
    Schade, A.; Monnereau, L.; Muller, T.; Bräse, S.
    2014. ChemPlusChem, 79, 1176–1182. doi:10.1002/cplu.201402093
  393. Dendrimer-type peptoid-decorated hexaphenylxylenes and tetraphenylmethanes: Synthesis and structure in solution and in the gas phase
    Peschko, K.; Schade, A.; Vollrath, S. B. L.; Schwarz, U.; Luy, B.; Muhle-Goll, C.; Weis, P.; Bräse, S.
    2014. Chemistry - a European journal, 20, 16273–16278. doi:10.1002/chem.201404024
  394. Conversion of substrate analogs suggests a Michael cyclization in iridoid biosynthesis
    Lindner, S.; Geu-Flores, F.; Bräse, S.; Sherden, N. H.; O’Connor, S. E.
    2014. Chemistry & biology, 21, 1452–1456. doi:10.1016/j.chembiol.2014.09.010
  395. Cytotoxicity and NMR studies of platinum complexes with cyclooctadiene ligands
    Enders, M.; Görling, B.; Braun, A. B.; Seltenreich, J. E.; Reichenbach, L. F.; Rissanen, K.; Nieger, M.; Luy, B.; Schepers, U.; Bräse, S.
    2014. Organometallics, 33, 4027–4034. doi:10.1021/om500540x
  396. Electrochemical investigation of covalently post-synthetic modified SURGEL coatings
    Mugnaini, V.; Tsotsalas, M.; Bebensee, F.; Grosjean, S.; Shahnas, A.; Bräse, S.; Lahann, J.; Buck, M.; Wöll, C.
    2014. Chemical communications, 50, 11129–11131. doi:10.1039/C4CC03521F
  397. Cell-penetrating peptoids: introduction of novel cationic side chains
    Kölmel, D. K.; Hörner, A.; Rönicke, F.; Nieger, M.; Schepers, U.; Bräse, S.
    2014. European journal of medicinal chemistry, 79, 231–243. doi:10.1016/j.ejmech.2014.03.078
  398. A new route to dithia- and thiaoxacyclooctynes via Nicholas reaction
    Hagendorn, T.; Bräse, S.
    2014. RSC Advances, 4, 15493–15495. doi:10.1039/C4RA01345J
  399. Luminescent cell-penetrating pentadecanuclear lanthanide clusters
    Thielemann, D. T.; Wagner, A. T.; Rösch, E.; Kölmel, D. K.; Heck, J. G.; Rudat, B.; Neumaier, M.; Feldmann, C.; Schepers, U.; Bräse, S.; Roesky, P. W.
    2013. Journal of the American Chemical Society, 135 (20), 7454–7457. doi:10.1021/ja403539t
  400. Deuterium and tritium labelling of N-acyl-L-homoserine lactones (AHLs) by catalytic reduction of a double bond in the layer-by-layer method
    Jakubczyk, D.; Merle, C.; Brenner-Weiss, G.; Luy, B.; Bräse, S.
    2013. European Journal of Organic Chemistry, (24), 5323–5330. doi:10.1002/ejoc.201300084
  401. Alternating asymmetric self-induction in functionalized pyrrolidine oligomers
    Kudryavtsev, K. V.; Ivantcova, P. M.; Churakov, A. V.; Wiedmann, S.; Luy, B.; Muhle-Goll, C.; Zefirov, N. S.; Bräse, S.
    2013. Angewandte Chemie - International Edition, 52 (48), 12736–12740. doi:10.1002/anie.201302862
  402. Synthetic approaches to polycyclic semiochemicals and their derivatives: Combinatorial methods towards phytochemicals
    Jung, N.; Gläser, F.; Bräse, S.
    2013. Phytochemistry Reviews, 12 (4), 603–651. doi:10.1007/s11101-013-9298-0
  403. Ortho-perfluoroalkylation and ethoxycarbonyldifluoromethylation of aromatic triazenes
    Hafner, A.; Bihlmeier, A.; Nieger, M.; Klopper, W.; Bräse, S.
    2013. The journal of organic chemistry, 78 (16), 7938–7948. doi:10.1021/jo401145g
  404. Single and multiple additions of dibenzoylmethane onto buckminsterfullerene
    Giovannitti, A.; Seifermann, S. M.; Bihlmeier, A.; Muller, T.; Topic, F.; Rissanen, K.; Nieger, M.; Klopper, W.; Bräse, S.
    2013. European journal of organic chemistry, (35), 7907–7913. doi:10.1002/ejoc.201301146
  405. Tethering for selective synthesis of 2,2’-biphenols: The acetal method
    Masters, K.-S.; Bihlmeier, A.; Klopper, W.; Bräse, S.
    2013. Chemistry - a European journal, 19 (52), 17827–17835. doi:10.1002/chem.201301969
  406. Roadmap towards N-Heterocyclic [2.2]Paracyclophanes and their application in asymmetric catalysis
    Busch, M.; Cayir, M.; Nieger, M.; Thiel, W. R.; Bräse, S.
    2013. European Journal of Organic Chemistry, (27), 6108–6123. doi:10.1002/ejoc.201300508
  407. A stereoselective approach to functionalized cyclohexenones
    Meister, A. C.; Sauter, P. F.; Bräse, S.
    2013. European Journal of Organic Chemistry, (31), 7110–7116. doi:10.1002/ejoc.201300752
  408. Trifluoromethylation of 1-aryl-3,3-diisopropyltriazenes
    Hafner, A.; Bräse, S.
    2013. Advanced Synthesis and Catalysis, 355, 996–1000. doi:10.1002/adsc.201201040
  409. Molecular construction kit for tuning solubility, stability and luminescence properties: Heteroleptic MePyrPHOS-copper iodide-complexes and their application in organic light-emitting diodes
    Volz, D.; Zink, D. M.; Bocksrocker, T.; Friedrichs, J.; Nieger, M.; Baumann, T.; Lemmer, U.; Bräse, S.
    2013. Chemistry of materials, 25 (17), 3414–3426. doi:10.1021/cm4010807
  410. Soccer goes BOXing: synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes
    Seifermann, S. M.; Réthoré, C.; Muller, T.; Bräse, S.
    2013. Scientific reports, 3, 2817. doi:10.1038/srep02817Full textFull text of the publication as PDF document
  411. Amphiphilic peptoid transporters - synthesis and evaluation
    Vollrath, S. B. L.; Fürniss, D.; Schepers, U.; Bräse, S.
    2013. Organic and Biomolecular Chemistry, 11, 8197–8201. doi:10.1039/C3OB41139G
  412. Chemie auf der Spitze des Eisbergs: Zu viele Forschungsdaten gehen bislang unter!
    Jung, N.; Lütjohann, D.
    2013. Chemie in unserer Zeit, 47, 334–335. doi:10.1002/ciuz.201390062
  413. The chemistry of mycotoxins
    Bräse, S.; Gläser, F.; Kramer, C. S.; Lindner, S.; Linsenmeier, A. M.; Masters, K. S.; Meister, A. C.; Ruff, B. M.; Zhong, S.
    2013. Wien [u.a.] : Springer, 2013 (Progress in the Chemistry of Organic and Natural Products ; 97) 
  414. Post-synthetic modification of metal-organic framework thin films using click chemistry: The importance of strained C-C triple bonds
    Wang, Z.; Liu, J.; Arslan, H. K.; Grosjean, S.; Hagendorn, T.; Gliemann, H.; Bräse, S.; Wöll, C.
    2013. Langmuir, 29, 15958–15964. doi:10.1021/la403854w
  415. Delphinidin is a novel inhibitor of lymphangiogenesis but promotes mammary tumor growth and metastasis formation in syngeneic experimental rats
    Thiele, W.; Rothley, M.; Teller, N.; Jung, N.; Bulat, B.; Plaumann, D.; Vanderheiden, S.; Schmaus, A.; Cremers, N.; Göppert, B.; Dimmler, A.; Eschbach, V.; Quagliata, L.; Thaler, S.; Marko, D.; Bräse, S.; Sleeman, J. P.
    2013. Carcinogenesis, 34, 2804–2813. doi:10.1093/carcin/bgt291
  416. Heteroleptic, dinuclear copper(I) complexes for application in organic light-emitting diodes
    Zink, D. M.; Volz, D.; Baumann, T.; Mydlak, M.; Flügge, H.; Friedrichs, J.; Nieger, M.; Bräse, S.
    2013. Chemistry of Materials, 25, 4471–4486. doi:10.1021/cm4018375
  417. Copper(I) complexes based on five-membered (PN)-N-boolean AND heterocycles: Structural diversity linked to exciting luminescence properties
    Zink, D. M.; Baumann, T.; Friedrichs, J.; Nieger, M.; Bräse, S.
    2013. Inorganic Chemistry, 52, 13509–13520. doi:10.1021/ic4019162
  418. BOX structures with additional coordination sites: potential ligands for bifunctional catalysis
    Seifermann, S. M.; Muller, T.; Bräse, S.
    2013. European Journal of Organic Chemistry, (16), 3215–3218. doi:10.1002/ejoc.201300279
  419. Thiourea-catalyzed Diels-Alder reaction of a naphthoquinone monoketal dienophile
    Kramer, C. S.; Bräse, S.
    2013. Beilstein Journal of Organic Chemistry, 9, 1414–1418. doi:10.3762/bjoc.9.158
  420. Synthesis of CF₃-substituted olefins by Julia-Kocienski olefination using 2-[(2,2,2-trifluoroethyl)sulfonyl]benzo[d]thiazole as trifluoromethylation agent
    Hafner, A.; Fischer, T. S.; Bräse, S.
    2013. European Journal of Organic Chemistry, (35), 7996–8003. doi:10.1002/ejoc.201301070
  421. A radical access to highly functionalized tetrahydroxanthones
    Meister, A. C.; Nieger, M.; Bräse, S.
    2013. Chemistry - A European Journal, 19, 10836–10839. doi:10.1002/chem.201301358
  422. Influence of Perfluorinated End Groups on the SFRD of [Pt(cod)Me(CnF2n+1)] onto Porous Al2O3 in CO2 under Reductive Conditions
    Aggarwal, V.; Reichenbach, L. F.; Enders, M.; Muller, T.; Wolff, S.; Crone, M.; Türk, M.; Bräse, S.
    2013. Chemistry - a European journal, 19 (38), 12794–12799. doi:10.1002/chem.201301191
  423. Controlled microstructuring of Janus particles based on a multifunctional poly(ethylene glycol)
    Sokolovskaya, E.; Yoon, J.; Misra, A. C.; Bräse, S.; Lahann, J.
    2013. Macromolecular Rapid Communications, 34, 1554–1559. doi:10.1002/marc.201300427
  424. A chemical screening procedure for glucocorticoid signaling with a Zebrafish larva luciferase reporter system
    Weger, B. D.; Weger, M.; Jung, N.; Lederer, C.; Bräse, S.; Dickmeis, T.
    2013. Journal of Visualized Experiments, 79, e50439/1–9. doi:10.3791/50439
  425. Peptoid-based rare-earth (group 3 and lanthanide) transporters
    Kölmel, D. K.; Rudat, B.; Schepers, U.; Bräse, S.
    2013. European Journal of Organic Chemistry, (14), 2761–2765. doi:10.1002/ejoc.201300219
  426. Outstanding luminescence from neutral copper(I) complexes with pyridyl-tetrazolate and phosphine ligands
    Bergmann, L.; Friedrichs, J.; Mydlak, M.; Baumann, T.; Nieger, M.; Bräse, S.
    2013. Chemical Communications, 49, 6501–6503. doi:10.1039/C3CC42280A
  427. Silver-mediated methoxycarbonyltetrafluoroethylation of arenes
    Hafner, A.; Feuerstein, T. J.; Bräse, S.
    2013. Organic Letters, 15, 3468–3471. doi:10.1021/ol401558z
  428. Antagonists for the orphan G-protein-coupled receptor GPR55 based on a coumarin scaffold
    Rempel, V.; Volz, N.; Gläser, F.; Nieger, M.; Bräse, S.; Müller, C. E.
    2013. Journal of Medicinal Chemistry, 56, 4798–4810. doi:10.1021/jm4005175
  429. Rhodamine F: a novel class of fluorous ponytailed dyes for bioconjugation
    Kölmel, D. K.; Rudat, B.; Braun, D. M.; Bednarek, C.; Schepers, U.; Bräse, S.
    2013. Organic and Biomolecular Chemistry, 11, 3954–3962. doi:10.1039/C3OB40267C
  430. The acetal concept: regioselective access to ortho,ortho-diphenols via dibenzo-1,3,dioxepines
    Masters, K. S.; Bräse, S.
    2013. Angewandte Chemie - International Edition, 52, 866–869. doi:10.1002/anie.201207485
  431. Peptoids and polyamines going sweet: Modular synthesis of glycosylated peotoids and polyamines using click chemistry
    Fürniss, D.; Mack, T.; Hahn, F.; Vollrath, S. B. L.; Koroniak, K.; Schepers, U.; Bräse, S.
    2013. Beilstein Journal of Organic Chemistry, 9, 56–63. doi:10.3762/bjoc.9.7
  432. Structural Characterization of a Peptoid with Lysine-like Side Chains and Biological Activity using NMR and Computational Methods
    Sternberg, U.; Birtalan, E.; Jakovkin, I.; Luy, B.; Schepers, U.; Bräse, S.; Muhle-Goll, C.
    2013. Organic and Biomolecular Chemistry, 11 (4), 640–647. doi:10.1039/c2ob27039k
  433. Neue Katalysatoren für Übergangsmetall-katalysierte Aziridin-Synthesen
    Jung, N.; Bräse, S.
    2012. Angewandte Chemie, 124 (23), 5632–5634. doi:10.1002/ange.201200966
  434. Xanthones from Fungi, Lichens and Bacteria : The Natural Products and their Synthesis
    Masters, K.-S.; Bräse, S.
    2012. Chemical reviews, 112 (7), 3717–3776. doi:10.1021/cr100446h
  435. Cell Penetrating Peptoids (CPPos): Synthesis of a Small Combinatorial Library by Using IRORI MiniKans
    Kölmel, D. K.; Fürniss, D.; Susanto, S.; Lauer, A.; Grabher, C.; Bräse, S.; Schepers, U.
    2012. Pharmaceuticals, 5 (12), 1265–1281. doi:10.3390/ph5121265
  436. Synthesis of Functionalized Glutamine- and Asparagine-Type Peptoids : Scope and Limitations
    Cardenal, C.; Vollrath, S. B. L.; Schepers, U.; Bräse, S.
    2012. Helvetica chimica acta, 95 (11), 2237–2248. doi:10.1002/hlca.201200451
  437. Killing double bonds softly: the reduction of polymer-bound alkenes
    Fürniss, D.; Schepers, U.; Bräse, S.
    2012. RSC Advances, 2 (30), 11273–11278. doi:10.1039/c2ra22189f
  438. The plakotenins: biomimetic Diels-Alder reactions, total synthesis, structural investigations, and chemical biology
    Bourcet, E.; Kaufmann, L.; Arzt, S.; Bihlmeier, A.; Klopper, W.; Schepers, U.; Bräse, S.
    2012. Chemistry - a European journal, 18 (47), 15004–15020. doi:10.1002/chem.201201585
  439. Highly enantioselective access to cannabinoid-type tricyles by organocatalytic Diels-Alder reactions
    Bräse, S.; Volz, N.; Gläser, F.; Nieger, M.
    2012. Beilstein journal of organic chemistry, 8, 1385–1392. doi:10.3762/bjoc.8.160Full textFull text of the publication as PDF document
  440. Secretome Protein Enrichment with Click Sugars Identifies Physiological Substrates of the Alzheimer Protease BACE1 in Primary Neurons
    Kuhn, P. H.; Koroniak, K.; Hogl, S.; Colombo, A.; Zeitschel, U.; Willem, M.; Volbracht, C.; Schepers, U.; Imhof, A.; Hoffmeister, A.; Haass, C.; Roßner, S.; Bräse, S.; Lichtenthaler, S. F.
    2012. The EMBO journal, 31 (14), 3157–3168. doi:10.1038/emboj.2012.173
  441. Photochemistry with laser radiation in condensed phase using miniaturized photoreactors
    Bremus-Köbberling, E.; Gillner, A.; Avemaria, F.; Réthoré, C.; Bräse, S.
    2012. Beilstein journal of organic chemistry, 8, 1213–1218. doi:10.3762/bjoc.8.135Full textFull text of the publication as PDF document
  442. Interkingdom Signaling: Integration, Conformation, and Orientation of N-Acyl-L-Homoserine Lactones in Supported Lipid Bilayers
    Barth, C.; Jakubczyk, D.; Kubas, A.; Anastassacos, F.; Brenner-Weiss, G.; Fink, K.; Schepers, U.; Bräse, S.; Koelsch, P.
    2012. Langmuir, 28 (22), 8456–8462. doi:10.1021/la301241s
  443. Deuterium labelled N-acyl-L-homoserine lactones (AHLs) - Inter-kingdom signalling molecules - synthesis, structural studies, interaction with model lipid membranes
    Jakubczyk, D.; Barth, C.; Kubas, A.; Anastassacos, F.; Koelsch, P.; Fink, K.; Schepers, U.; Brenner-Weiß, G.; Bräse, S.
    2012. Analytical and bioanalytical chemistry, 403 (2), 473–482. doi:10.1007/s00216-012-5839-4
  444. Vinyl- und Alkinyl-Azide: altbekannte Intermediate im Fokus moderner Synthesemethoden
    Jung, N.; Bräse, S.
    2012. Angewandte Chemie, 124, 12335–12337. doi:10.1002/ange.201206409
  445. Synthesis of diverse indole libraries on polystyrene resin. Scope and limitations of an organometallic reaction on solid supports
    Knepper, K.; Vanderheiden, S.; Bräse, S.
    2012. Beilstein Journal of Organic Chemistry, 8, 1191–1199. doi:10.3762%2Fbjoc.8.132
  446. New catalysts for the transition-metal-catalyzed synthesis of aziridines
    Jung, N.; Bräse, S.
    2012. Angewandte Chemie - International Edition, 51, 5538–5540. doi:10.1002/anie.201200966
  447. Photophysical properties of fluorescently-labeled peptoids
    Rudat, B.; Birtalan, E.; Vollrath, S. B. L.; Fritz, D.; Kölmel, D. K.; Nieger, M.; Schepers, U.; Müllen, K.; Eisler, H.-J.; Lemmer, U.; Bräse, S.
    2011. European Journal of Medicinal Chemistry, 46 (9), 4457–4465. doi:10.1016/j.ejmech.2011.07.020
  448. Bioconjugation via azide-Staudinger ligation: an overview
    Schilling, C. I.; Jung, N.; Biskup, M. B.; Schepers, U.; Bräse, S.
    2011. Chemical Society Reviews, 40 (9), 4840–4871. doi:10.1039/C0CS00123F
  449. Investigating rhodamine B-labelled peptoids: Scopes and Limitations of its applications
    Birtalan, E.; Rudat, B.; Kölmel, D. K.; Fritz, D.; Vollrath, S. B. L.; Schepers, U.; Bräse, S.
    2011. Peptide science, 96 (5), 694–701. doi:10.1002/bip.21617
  450. Multi-Gram Synthesis of a Hyaluronic Acid Subunit and Synthesis of Fully Protected Oligomers
    Virlouvet, M.; Gartner, M.; Koroniak, K.; Sleeman, J. P.; Bräse, S.
    2010. Advanced synthesis & catalysis, 352 (14-15), 2657–2662. doi:10.1002/adsc.201000008
  451. Synthesis of aryl fluorides on a solid support and in solution by utilizing a fluorinated solvent
    Döbele, M.; Vanderheiden, S.; Jung, N.; Bräse, S.
    2010. Angewandte Chemie - International Edition, 49, 5986–88. doi:10.1002/anie.201001507
  452. Peptoidic amino- and guanidinium-carrier systems: targeted drug delivery into the cell cytosol or the nucleus
    Schröder, T.; Niemeier, N.; Afonin, S.; Ulrich, A. S.; Krug, H. F.; Bräse, S.
    2008. Journal of Medicinal Chemistry, 51, 376–79. doi:10.1021/jm070603m
  453. A new azide staining reagent based on "click chemistry"
    Schröder, T.; Gartner, M.; Grab, T.; Bräse, S.
    2007. Organic and Biomolecular Chemistry, 5, 2767–69. doi:10.1039/b706719b