Publications
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Design and Synthesis of New Dihydropyrimidine Derivatives with a Cytotoxic Effect as Dual EGFR/VEGFR-2 Inhibitors
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. ACS Omega, 9 (32), 34358–34369. doi:10.1021/acsomega.4c01361 -
New Diaryl-1,2,4-triazolo[3,4- a ]pyrimidine Hybrids as Selective COX-2/sEH Dual Inhibitors with Potent Analgesic/Anti-inflammatory and Cardioprotective Properties
Al-Wahaibi, L. H.; Abdel-Rahman, M. H.; El-Adl, K.; Youssif, B. G. M.; Bräse, S.; Abdel-Aziz, S. A.
2024. ACS Omega, 9 (31), 33494–33509. doi:10.1021/acsomega.4c00870 -
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/d4ob01032a -
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/D4RA02531H -
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-23-0354 -
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.2024.1419242 -
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/polym16111603 -
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, 27 (17), Art.-Nr.: e202400080. doi:10.1002/ejic.202400080 -
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/D3CC05783F -
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.e25248 -
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 -
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.3c05755 -
Synthesis of substituted triazole–pyrazole hybrids using triazenylpyrazole precursors
Gräßle, S.; Holzhauer, L.; Wippert, N.; Fuhr, O.; Nieger, M.; Jung, N.; Bräse, S.
2024. Beilstein Journal of Organic Chemistry, 20, 1396 – 1404. doi:10.3762/bjoc.20.121 -
(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-2024-1r9tb -
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.202404866 -
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 -
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.202403365 -
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.202402110 -
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/s41380-024-02614-5 -
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.2024.1387923 -
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/d4re00087k -
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/agt2.588 -
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/ijms25084462 -
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.202401956 -
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 -
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.202401938 -
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, 13 (8), e202400024. doi:10.1002/open.202400024 -
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:10.1080/14756366.2024.2305856 -
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.202313517 -
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/molecules29020446 -
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.202300222 -
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.202307318 -
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.202303615 -
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.202303929 -
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.202302630 -
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.202302157 -
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.202214932 -
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.202301093 -
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/d3ta05235d -
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/ijms241713300 -
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.3c00116 -
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/ph16071014 -
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-23-0111 -
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.adf4060 -
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 -
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:10.1002/2211-5463.13562 -
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.202200764 -
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 -
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.202200425 -
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 -
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/D3DD00143A -
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.202309226 -
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.202303613 -
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/ph16111522 -
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/molecules28207092 -
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/molecules28186586 -
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.202300540 -
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.202306155 -
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.16154 -
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 -
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.202300048 -
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.202218052 -
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 -
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.
2023. Molecules, 28 (4), Art.-Nr.: 1808. doi:10.3390/molecules28041808 -
Stacking Cyclophanes into Chiral Microvessels
Hassan, Z.; Bräse, S.
2023. Angewandte Chemie - International Edition, 62 (16), Art.-Nr.: e202214996. doi:10.1002/anie.202214996 -
F‐Tag Induced Acyl Shift in the Photochemical Cyclization of o ‐Alkynylated N ‐Alkyl‐ N ‐acylamides to Indoles
Simek Tosino, H.; Jung, A.; Fuhr, O.; Muhle-Goll, C.; Jung, N.; Bräse, S.
2023. European Journal of Organic Chemistry, 26 (11), Art.-Nr.: e202201132. doi:10.1002/ejoc.202201132 -
Stereoselective semisynthesis of uzarigenin and allo -uzarigenin
Al Muthafer, S.; Schissler, C.; Koch, V.; Kühner, H.; Nieger, M.; Bräse, S.
2023. Organic Chemistry Frontiers, 10, 1435–1440. doi:10.1039/D2QO01718K -
Emergence of Structural Phosphorescence in Free-Standing, Laterally Organized Polymer Nanofiber Membranes
Wawryszyn, M.; Wilhelm, R.; Kim, J.; Zhong, X.; Raymond, J. E.; Thelen, R.; Trouillet, V.; Schwotzer, M.; Bräse, S.; Kim, D. H.; Abbott, N. L.; Lahann, J.
2023. ACS Applied Polymer Materials, 5 (3), 1670–1680. doi:10.1021/acsapm.2c01477 -
Tris(4-azidophenyl)methanol – a novel and multifunctional thiol protecting group
Qiu, X.; Brückel, J.; Zippel, C.; Nieger, M.; Biedermann, F.; Bräse, S.
2023. RSC Advances, 13 (4), 2483–2486. doi:10.1039/D2RA05997E -
Twisting of Porphyrin by Assembly in a Metal‐Organic Framework yielding Chiral Photoconducting Films for Circularly‐Polarized‐Light Detection
Li, C.; Schopmans, H.; Langer, L.; Marschner, S.; Chandresh, A.; Bürck, J.; Tsuchiya, Y.; Chihaya, A.; Wenzel, W.; Bräse, S.; Kozlowska, M.; Heinke, L.
2023. Angewandte Chemie - International Edition, 62 (10), Art.-Nr.: e202217377. doi:10.1002/anie.202217377 -
A Novel P@SiO Nano-Composite as Effective Adsorbent to Remove Methylene Blue Dye from Aqueous Media
Nayl, A. A.; Abd-Elhamid, A. I.; Arafa, W. A. A.; Ahmed, I. M.; AbdEl-Rahman, A. M. E.; Soliman, H. M. A.; Abdelgawad, M. A.; Ali, H. M.; Aly, A. A.; Bräse, S.
2023. Materials, 16 (2), Art.-Nr.: 514. doi:10.3390/ma16020514 -
Minimum Information Standards in Chemistry: A Call for Better Research Data Management Practices
Herres-Pawlis, S.; Bach, F.; Bruno, I. J.; Chalk, S. J.; Jung, N.; Liermann, J. C.; McEwen, L. R.; Neumann, S.; Steinbeck, C.; Razum, M.; Koepler, O.
2022. Angewandte Chemie International Edition, 61 (51), e202203038. doi:10.1002/anie.202203038 -
Droplet Microarray as a Powerful Platform for Seeking New Antibiotics Against Multidrug‐Resistant Bacteria
Lei, W.; Deckers, A.; Luchena, C.; Popova, A.; Reischl, M.; Jung, N.; Bräse, S.; Schwartz, T.; Krimmelbein, I. K.; Tietze, L. F.; Levkin, P. A.
2022. Advanced Biology, 6 (12), Art.-Nr.: 2200166. doi:10.1002/adbi.202200166 -
Metal Complexes as Antifungals? From a Crowd-Sourced Compound Library to the First Experiments
Frei, A.; Elliott, A. G.; Kan, A.; Dinh, H.; Bräse, S.; Bruce, A. E.; Bruce, M. R.; Chen, F.; Humaidy, D.; Jung, N.; King, A. P.; Lye, P. G.; Maliszewska, H. K.; Mansour, A. M.; Matiadis, D.; Muñoz, M. P.; Pai, T.-Y.; Pokhrel, S.; Sadler, P. J.; Sagnou, M.; Taylor, M.; Wilson, J. J.; Woods, D.; Zuegg, J.; Zuegg, J.; Meyer, W.; Cain, A. K.; Cooper, M. A.
2022. Journal of the American Chemical Society, 2 (10), 2277–2294. doi:10.1021/jacsau.2c00308 -
Copper Complexes of 1,4-Naphthoquinone Containing Thiosemicarbazide and Triphenylphosphine Oxide Moieties; Synthesis and Identification by NMR, IR, Mass, UV Spectra, and DFT Calculations
Alshammari, M. B.; Aly, A. A.; Bräse, S.; Nieger, M.; Ibrahim, M. A. A.; Abd El-Haleem, L. E.
2022. ACS Omega, 7 (38), 34463–34475. doi:10.1021/acsomega.2c04113 -
Design Strategies for Structurally Controlled Polymer Surfaces via Cyclophane‐Based CVD Polymerization and Post‐CVD Fabrication
Hassan, Z.; Varadharajan, D.; Zippel, C.; Begum, S.; Lahann, J.; Bräse, S.
2022. Advanced Materials, 34 (37), Art.-Nr.: 2201761. doi:10.1002/adma.202201761 -
Scope of tetrazolo[1,5-a] quinoxalines in CuAAC reactions for the synthesis of triazoloquinoxalines, imidazoloquinoxalines, and rhenium complexes thereof
Holzhauer, L.; Liagre, C.; Fuhr, O.; Jung, N.; Bräse, S.
2022. Beilstein Journal of Organic Chemistry, 18, 1088–1099. doi:10.3762/bjoc.18.111 -
Solid and Hollow Poly(p-xylylene) Particles Synthesis via Metal–Organic Framework-Templated Chemical Vapor Polymerization
Begum, S.; Behboodi-Sadabad, F.; Pramudya, Y.; Dolle, C.; Kozlowska, M.; Hassan, Z.; Mattern, C.; Gorji, S.; Heißler, S.; Welle, A.; Koenig, M.; Wenzel, W.; Eggeler, Y. M.; Bräse, S.; Lahann, J.; Tsotsalas, M.
2022. Chemistry of Materials, 34 (14), 6268–6278. doi:10.1021/acs.chemmater.2c00111 -
A batch photoreactor for small-scale laboratory research - a technical note
Li, J.; Hodapp, P.; Ladewig, B. P.; Jung, N.; Dittmeyer, R.
2022. American Chemical Society (ACS). doi:10.26434/chemrxiv-2022-46w7s -
Data format standards in analytical chemistry
Rauh, D.; Blankenburg, C.; Fischer, T. G.; Jung, N.; Kuhn, S.; Schatzschneider, U.; Schulze, T.; Neumann, S.
2022. Pure and Applied Chemistry, 94 (6), 725–736. doi:10.1515/pac-2021-3101 -
Dynamic Surface Modification of Metal–Organic Framework Nanoparticles via Alkoxyamine Functional Groups
Spiegel, S.; Wagner, I.; Begum, S.; Schwotzer, M.; Wessely, I.; Bräse, S.; Tsotsalas, M.
2022. Langmuir : the ACS journal of surfaces and colloids, 38 (21), 6531–6538. doi:10.1021/acs.langmuir.2c00085 -
A chemical probe for BAG1 targets androgen receptor-positive prostate cancer through oxidative stress signaling pathway
Kuznik, N. C.; Solozobova, V.; Lee, I. I.; Jung, N.; Yang, L.; Nienhaus, K.; Ntim, E. A.; Rottenberg, J. T.; Muhle-Goll, C.; Kumar, A. R.; Peravali, R.; Gräßle, S.; Gourain, V.; Deville, C.; Cato, L.; Neeb, A.; Dilger, M.; Cramer von Clausbruch, C. A.; Weiss, C.; Kieffer, B.; Nienhaus, G. U.; Brown, M.; Bräse, S.; Cato, A. C. B.
2022. iScience, 25 (5), Art.Nr. 104175. doi:10.1016/j.isci.2022.104175 -
Poly(pentafluorobenzyl 2‐ylidene‐acetate): Polymerization and Postpolymerization Modification
Li, Z.; Zhang, H.; Theato, P.; Bräse, S.
2022. Macromolecular Chemistry and Physics, 223 (9), Art.-Nr.: 2100455. doi:10.1002/macp.202100455 -
Efficient Synthesis of Various Substituted (Thio)Ureas, Semicarbazides, Thiosemicarbazides, Thiazolidones, and Oxadiazole Derived from [2.2]Paracyclophane
Alshammari, M. B.; Aly, A. A.; Bräse, S.; Nieger, M.; Abd El-Haleem, L. E.
2022. ACS Omega, 7 (15), 12879–12890. doi:10.1021/acsomega.2c00141 -
Facile synthesis of new pyrano[3,2-c]quinolones via the reaction of quinolin-2-ones with ethene-1,2,3,4-tetracarbonitrile
Aly, A. A.; El-Naby, H. A. A.; Ahmed, E. K.; Shaker, R. M.; Gedamy, S. A.; Nieger, M.; Bräse, S.; El-Haleem, L. E. A.
2022. Monatshefte fur Chemie, 153, 277–284. doi:10.1007/s00706-022-02903-1 -
The jasmonate biosynthesis Gene OsOPR7 can mitigate salinity induced mitochondrial oxidative stress
Asfaw, K. G.; Liu, Q.; Eghbalian, R.; Purper, S.; Akaberi, S.; Dhakarey, R.; Münch, S. W.; Wehl, I.; Bräse, S.; Eiche, E.; Hause, B.; Bogeski, I.; Schepers, U.; Riemann, M.; Nick, P.
2022. Plant science, 316, Article no: 111156. doi:10.1016/j.plantsci.2021.111156 -
C–P bond formation of cyclophanyl-, and aryl halides a UV-induced photo Arbuzov reaction: a versatile portal to phosphonate-grafted scaffolds
Oßwald, S.; Zippel, C.; Hassan, Z.; Nieger, M.; Bräse, S.
2022. RSC Advances, 12 (6), 3309–3312. doi:10.1039/d2ra00094f -
Diversity-Oriented Synthesis of [2.2]Paracyclophane-derived Fused Imidazo[1,2-a]heterocycles by Groebke-Blackburn-Bienaymé Reaction: Accessing Cyclophanyl Imidazole Ligands Library
Stahlberger, M.; Schwarz, N.; Zippel, C.; Hohmann, J.; Nieger, M.; Hassan, Z.; Bräse, S.
2022. Chemistry - A European Journal, 28 (3), e202103511. doi:10.1002/chem.202103511 -
Design and synthesis of new thiazolidinone/uracil derivatives as antiproliferative agents targeting EGFR and/or BRAF
Alshammari, M. B.; Aly, A. A.; Youssif, B. G. M.; Bräse, S.; Ahmad, A.; Brown, A. B.; Ibrahim, M. A. A.; Mohamed, A. H.
2022. Frontiers in Chemistry, 10, Art.-Nr.: 1076383. doi:10.3389/fchem.2022.1076383 -
Design, Synthesis and Biological Evaluation of Syn and Anti-like Double Warhead Quinolinones Bearing Dihydroxy Naphthalene Moiety as Epidermal Growth Factor Receptor Inhibitors with Potential Apoptotic Antiproliferative Action
El-Sheref, E. M.; Ameen, M. A.; El-Shaieb, K. M.; Abdel-Latif, F. F.; Abdel-naser, A. I.; Brown, A. B.; Bräse, S.; Fathy, H. M.; Ahmad, I.; Patel, H.; Gomaa, H. A. M.; Youssif, B. G. M.; Mohamed, A. H.
2022. Molecules, 27 (24), Art.-Nr.: 8765. doi:10.3390/molecules27248765 -
Synthesis of novel amidines via one-pot three component reactions: Selective topoisomerase I inhibitors with antiproliferative properties
El-Sheref, E. M.; Tawfeek, H. N.; Hassan, A. A.; Bräse, S.; Elbastawesy, M. A. I.; Gomaa, H. A. M.; Mostafa, Y. A.; Youssif, B. G. M.
2022. Frontiers in Chemistry, 10, Art.-Nr.: 1039176. doi:10.3389/fchem.2022.1039176 -
Search for Alternative Two‐Step‐Absorption Photoinitiators for 3D Laser Nanoprinting
Bojanowski, N. M.; Vranic, A.; Hahn, V.; Rietz, P.; Messer, T.; Brückel, J.; Barner-Kowollik, C.; Blasco, E.; Bräse, S.; Wegener, M.
2022. Advanced Functional Materials, 33 (39), Art.-Nr.: 2212482. doi:10.1002/adfm.202212482 -
Metal complexes of new thiocarbohydrazones of Cu(I), Co(II), and Ni(II); identification by NMR, IR, mass, UV spectra, and DFT calculations
Aly, A. A.; Abdallah, E. M.; Ahmed, S. A.; Awad, M. K.; Rabee, M. M.; Mostafa, S. M.; Bräse, S.
2022. Journal of Sulfur Chemistry, 44 (3), 282–303. doi:10.1080/17415993.2022.2145846 -
Synthesis and Identification of New N,N-Disubstituted Thiourea, and Thiazolidinone Scaffolds Based on Quinolone Moiety as Urease Inhibitor
Elshaier, Y. A. M. M.; Aly, A. A.; Abdel-Aziz, M.; Fathy, H. M.; Brown, A. B.; Bräse, S.; Ramadan, M.
2022. Molecules, 27 (20), Art.-Nr.: 7126. doi:10.3390/molecules27207126 -
Design, synthesis, crystal structures and biological evaluation of some 1,3-thiazolidin-4-ones as dual CDK2/EGFR potent inhibitors with potential apoptotic antiproliferative effects
Tawfeek, H. N.; Hassan, A. A.; Bräse, S.; Nieger, M.; Mostafa, Y. A.; Gomaa, H. A. M.; Youssif, B. G. M.; El-Shreef, E. M.
2022. Arabian Journal of Chemistry, 15 (11), Art.-Nr.: 104280. doi:10.1016/j.arabjc.2022.104280 -
Functionalized C-Symmetric Building Blocks—The Chemistry of Triaminotrimesic Acid
Schmidt, L.; Wagner, D.; Nieger, M.; Bräse, S.
2022. Molecules, 27 (14), Art.-Nr.: 4369. doi:10.3390/molecules27144369 -
Azides in the Synthesis of Various Heterocycles
Nayl, A. A.; Aly, A. A.; Arafa, W. A. A.; Ahmed, I. M.; Abd-Elhamid, A. I.; El-Fakharany, E. M.; Abdelgawad, M. A.; Tawfeek, H. N.; Bräse, S.
2022. Molecules, 27 (12), Art.Nr. 3716. doi:10.3390/molecules27123716 -
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 -
Review of the Recent Advances in Electrospun Nanofibers Applications in Water Purification
Nayl, A. A.; Abd-Elhamid, A. I.; Awwad, N. S.; Abdelgawad, M. A.; Wu, J.; Mo, X.; Gomha, S. M.; Aly, A. A.; Bräse, S.
2022. Polymers, 14 (8), Art.-Nr.: 1594. doi:10.3390/polym14081594 -
Recent Progress and Potential Biomedical Applications of Electrospun Nanofibers in Regeneration of Tissues and Organs
Nayl, A. A.; Abd-Elhamid, A. I.; Awwad, N. S.; Abdelgawad, M. A.; Wu, J.; Mo, X.; Gomha, S. M.; Aly, A. A.; Bräse, S.
2022. Polymers, 14 (8), Art.-Nr.: 1508. doi:10.3390/polym14081508 -
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
Aly, A. A.; Nieger, M.; Bräse, S.; Bakheet, M. E. M.
2022. Journal of Chemical Crystallography, 53, 38–49. doi:10.1007/s10870-022-00939-z -
Autoxidation of 4-Hydrazinylquinolin-2(1H)-one; Synthesis of Pyridazino[4,3-c:5,6-c′ ]diquinoline-6,7(5H,8H)-diones
Mostafa, S. M.; Aly, A. A.; Hassan, A. A.; Osman, E. M.; Bräse, S.; Nieger, M.; Ibrahim, M. A. A.; Mohamed, A. H.
2022. Molecules, 27 (7), Art.-Nr.: 2125. doi:10.3390/molecules27072125 -
Synthesis, Characterization, and In Vivo Study of Some Novel 3,4,5-Trimethoxybenzylidene-hydrazinecarbothioamides and Thiadiazoles as Anti-Apoptotic Caspase-3 Inhibitors
Mostafa, S. M.; Aly, A. A.; Bräse, S.; Nieger, M.; Abdelhafez, S. M. N.; Abdelzaher, W. Y.; Abdelhafez, E.-S. M. N.
2022. Molecules, 27 (7), Art.Nr.: 2266. doi:10.3390/molecules27072266 -
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.
2022. Organic & Biomolecular Chemistry, 20 (17), 3598–3604. doi:10.1039/d2ob00372d -
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.
2022. Advanced Materials, 34 (9), Art.-Nr.: 2108386. doi:10.1002/adma.202108386 -
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.
2022. Journal of materials chemistry / C, 10 (12), 4757–4766. doi:10.1039/d1tc04918f -
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.
2022. International Journal of Molecular Sciences, 23 (2), 959. doi:10.3390/ijms23020959 -
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
Joseph, R.; Chauhan, A.; Eschke, C.; Ihsan A.; Jalali, M.; Jäntsch, U.; Jung, N.; Kumar, C. N. S.; Kübel, C.; Lucas, C.; Mail, M.; Mazilkin, A.; Neidiger, C.; Panighel, M.; Sandfeld, S.; Stotzka, R.; Thelen, R.; Aversa, R.
2021, November 4. Research Data Alliance Virtual Plenary 18 (2021), Online, October 27–November 11, 2021 -
Bio-instructive materials on-demand-combinatorial chemistry of peptoids, foldamers, and beyond
Herlan, C. N.; Feser, D.; Schepers, U.; Bräse, S.
2021. Chemical Communications, 57 (85), 11131–11152. doi:10.1039/d1cc04237h -
Metal‐to‐Metal Distance Modulation by Ligand Design: A Case Study of Structure‐Property Correlation in Planar Chiral Cyclophanyl Metal Complexes
Hassan, Z.; Bräse, S.
2021. Chemistry - a European journal, 27 (61), 15021–15027. doi:10.1002/chem.202102336 -
Novel Cofacial Porphyrin-Based Homo- and Heterotrimetallic Complexes of Transition Metals
Schissler, C.; Schneider, E. K.; Lebedkin, S.; Weis, P.; Niedner-Schatteburg, G.; Kappes, M. M.; Bräse, S.
2021. Chemistry - A European Journal, 27 (61), 15202–15208. doi:10.1002/chem.202102376 -
Targeting oxidative stress: Novel coumarin-based inverse agonists of GPR55
Apweiler, M.; Saliba, S. W.; Streyczek, J.; Hurrle, T.; Gräßle, S.; Bräse, S.; Fiebich, B. L.
2021. International Journal of Molecular Sciences, 22 (21), Art.Nr. 11665. doi:10.3390/ijms222111665 -
Platinum Cyclooctadiene Complexes with Activity against Gram-positive Bacteria
Frei, A.; Ramu, S.; Lowe, G. J.; Dinh, H.; Semenec, L.; Elliott, A. G.; Zuegg, J.; Deckers, A.; Jung, N.; Bräse, S.; Cain, A. K.; Blaskovich, M. A. T.
2021. ChemMedChem, 16 (20), 3165–3171. doi:10.1002/cmdc.202100157 -
Development of a Benzothiazole Scaffold-Based Androgen Receptor N-Terminal Inhibitor for Treating Androgen-Responsive Prostate Cancer
Kuznik, N. C.; Solozobova, V.; Jung, N.; Gräßle, S.; Lei, Q.; Lewandowski, E. M.; Munuganti, R.; Zoubeidi, A.; Chen, Y.; Bräse, S.; Cato, A. C. B.
2021. ACS Chemical Biology, 16 (11), 2103–2108. doi:10.1021/acschembio.1c00390 -
Molecular Design and Synthesis of Dicarbazolophane-Based Centrosymmetric Through-Space Donors for Solution-Processed Thermally Activated Delayed Fluorescence OLEDs
Zhang, Z.; Diesing, S.; Crovini, E.; Gupta, A. K.; Spuling, E.; Gan, X.; Fuhr, O.; Nieger, M.; Hassan, Z.; Samuel, I. D. W.; Bräse, S.; Zysman-Colman, E.
2021. Organic Letters, 23 (17), 6697–6702. doi:10.1021/acs.orglett.1c02273 -
In situ sensors for flow reactors – a review
Li, J.; Šimek, H.; Ilioae, D.; Jung, N.; Bräse, S.; Zappe, H.; Dittmeyer, R.; Ladewig, B. P.
2021. Reaction chemistry & engineering, 6 (9), 1497–1507. doi:10.1039/d1re00038a -
Direct Synthesis of ZIF-8 on Transmission Electron Microscopy Grids Allows Insights into the Growth Process
Hugenschmidt, M.; Kutonova, K.; Valadez Sánchez, E. P.; Moulai, S.; Gliemann, H.; Bräse, S.; Wöll, C.; Gerthsen, D.
2021, August 24. Microscopy Conference (MC 2021), Online, August 22–26, 2021 -
Synthesis and SAR evaluation of coumarin derivatives as potent cannabinoid receptor agonists
Mohr, F.; Hurrle, T.; Burggraaff, L.; Langer, L.; Bemelmans, M. P.; Knab, M.; Nieger, M.; Westen, G. J. P. van; Heitman, L. H.; Bräse, S.
2021. European Journal of Medicinal Chemistry, 220, Art. Nr. 113354. doi:10.1016/j.ejmech.2021.113354 -
Synthesis and post-polymerization modification of poly(propargyl 2-ylidene-acetate)
Li, Z.; Mutlu, H.; Theato, P.; Bräse, S.
2021. European polymer journal, 156, Art.-Nr.: 110564. doi:10.1016/j.eurpolymj.2021.110564 -
Substituted pyrazoles and their heteroannulated analogs—recent syntheses and biological activities
Ramadan, M.; Aly, A. A.; El-haleem, L. E. A.; Alshammari, M. B.; Bräse, S.
2021. Molecules, 26 (16), Art.-Nr.: 4995. doi:10.3390/molecules26164995 -
Macrocyclic tetramers—structural investigation of peptide-peptoid hybrids
Herlan, C. N.; Sonnefeld, A.; Gloge, T.; Brückel, J.; Schlee, L. C.; Muhle-Goll, C.; Nieger, M.; Bräse, S.
2021. Molecules, 26 (15), Art.Nr. 4548. doi:10.3390/molecules26154548 -
Cyclic Peptoid-Peptide Hybrids as Versatile Molecular Transporters
Herlan, C. N.; Meschkov, A.; Schepers, U.; Bräse, S.
2021. Frontiers in Chemistry, 9, Art. Nr.: 696957. doi:10.3389/fchem.2021.696957 -
Covalent triazine frameworks based on the first pseudo-octahedral hexanitrile monomer via nitrile trimerization: Synthesis, porosity, and CO gas sorption properties
Wessely, I. D.; Schade, A. M.; Dey, S.; Bhunia, A.; Nuhnen, A.; Janiak, C.; Bräse, S.
2021. Materials, 14 (12), 3214. doi:10.3390/ma14123214 -
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.
2021. Advanced synthesis & catalysis, 363 (11), 2861–2865. doi:10.1002/adsc.202001536 -
Investigation of Luminescent Triplet States in Tetranuclear Cu Complexes: Thermochromism and Structural Characterization
Boden, P.; Di Martino-Fumo, P.; Busch, J. M.; Rehak, F. R.; Steiger, S.; Fuhr, O.; Nieger, M.; Volz, D.; Klopper, W.; Bräse, S.; Gerhards, M.
2021. Chemistry - a European journal, 27 (17), 5439–5452. doi:10.1002/chem.202004539 -
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.
2021. CrystEngComm, 23 (24), 4247–4251. doi:10.1039/d1ce00494h -
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 -
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:10.1177/1747519820959737 -
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.202100035 -
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.
2021. Advanced materials, 33 (9), Art.-Nr.: 2005630. doi:10.1002/adma.202005630 -
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.
2021. International journal of molecular sciences, 22 (5), Art.-Nr. 2503. doi:10.3390/ijms22052503 -
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.
2021. Inorganic chemistry, 60 (4), 2315–2332. doi:10.1021/acs.inorgchem.0c03187 -
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/s13321-020-00481-0 -
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.
2021. Chemistry - a European journal, 27 (9), 3047–3054. doi:10.1002/chem.202002394 -
Id1 and Id3 Are Regulated Through Matrix‐Assisted Autocrine BMP Signaling and Represent Therapeutic Targets in Melanoma
Sedlmeier, G.; Al-Rawi, V.; Buchert, J.; Yserentant, K.; Rothley, M.; Steshina, A.; Gräßle, S.; Wu, R.-L.; Hurrle, T.; Richer, W.; Decraene, C.; Thiele, W.; Utikal, J.; Abuillan, W.; Tanaka, M.; Herten, D.-P.; Hill, C. S.; Garvalov, B. K.; Jung, N.; Bräse, S.; Sleeman, J. P.
2021. Advanced therapeutics, 4 (2), Art.-Nr.: 2000065. doi:10.1002/adtp.202000065 -
Regioselective and stereoselective synthesis of epithiomethanoiminoindeno[1,2-b]furan-3-carbonitrile: heterocyclic [3.3.3]propellanes
Hassan, A. A.; Mohamed, N. K.; Aly, A. A.; Tawfeek, H. N.; Bräse, S.; Nieger, M.
2021. Molecular diversity, 25 (1), 99–108. doi:10.1007/s11030-019-10027-8 -
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/s41598-021-99974-7 -
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.17.197 -
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 -
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 -
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.202000034 -
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 -
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.17.187 -
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.1c16173 -
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/molecules26226798 -
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 -
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 -
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.202101066 -
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/d1ra05265a -
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.202107490 -
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.202103287 -
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.2021.632639 -
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.
2021. Chemical science, 12 (27), 9420–9431. doi:10.1039/d1sc01411k -
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 -
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.202000343 -
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/d0dt03913f -
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 -
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.202001415 -
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/molecules26010150 -
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 -
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 -
Thiol-yne crosslinked triarylamine hole transport layers for solution-processable organic light-emitting diodes
Kutonova, K.; Ebenhoch, B.; Graf Von Reventlow, L.; Heißler, S.; Rothmann, L.; Bräse, S.; Colsmann, A.
2020. Journal of materials chemistry / C, 8 (46), 16498–16505. doi:10.1039/d0tc03514a -
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.202007702 -
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.202001354 -
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/molecules25235610 -
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/s41598-020-68491-4 -
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.202003709 -
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.200626 -
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.202000209 -
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 -
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.202000512 -
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 -
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.202000314 -
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 -
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 -
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.201907625 -
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.202000097 -
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.201901453 -
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.201904863 -
Modernes Forschungsdatenmanagement – ein Naturstoffprojekt als Fallstudie
Koch, V.; Bräse, S.
2020. Biospektrum, 26 (1), 107–109. doi:10.1007/s12268-020-1316-3 -
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.202014974 -
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/molecules25235569 -
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.2020.563411 -
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/molecules25215057 -
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.2020.00750 -
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/d0qo00269k -
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.0c01832 -
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 -
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/molecules25133089 -
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/molecules25133036 -
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/molecules25153315 -
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/s00706-020-02640-3 -
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/d0sc90075c -
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.9b00665 -
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/d0py90053b -
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/c9py01878f -
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.2020.00126 -
Reactive & Efficient: Organic Azides as Cross-Linkers in Material Sciences
Schock, M.; Bräse, S.
2020. Molecules, 25 (4), Art. Nr.: 1009. doi:10.3390/molecules25041009