Publications
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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, 29 (12), 3779–3788. doi:10.1038/s41380-024-02614-5 -
Synthesis and Antimicrobial Evaluation of New 1,2,4-Triazolo[1,5- a ]pyrimidine-Based Derivatives as Dual Inhibitors of Bacterial DNA Gyrase and DHFR
Al-Wahaibi, L. H.; Rabea, S. M.; Mahmoud, M. A.; Youssif, B. G. M.; Bräse, S.; Abdel-Aziz, S. A.
2024. ACS Omega, 9 (47), 47261–47273. doi:10.1021/acsomega.4c08365 -
Cyclophanes as Emerging Materials — From Synthesis To Functions
Hassan, Z.; Lahann, J.; Bräse, S.
2024. Advanced Functional Materials, 34 (47), Art.-Nr.: 2410027. doi:10.1002/adfm.202410027 -
Photo‐Arbuzov Reactions as a Broadly Applicable Surface Modification Strategy
Plank, M.; Berardi, A.; Welle, A.; Sauter, E.; Krolla, P.; Haret, C.; Koenig, M.; Stahlberger, M.; Hassan, Z.; Oßwald, S.; Bräse, S.; Lahann, J.
2024. Advanced Functional Materials, 34 (47), Art.-Nr. 2403408. doi:10.1002/adfm.202403408 -
Modulating the photolysis of aryl azides in a supramolecular host to develop photoactivatable fluorophores
Qiu, X.; Pohl, E.; Jung, A.; Cai, Q.; Su, H.; Fuhr, O.; Schepers, U.; Bräse, S.
2024. Chemical Communications, 60 (88), 12856–12859. doi:10.1039/d4cc03907f -
A simple method to modulate the selectivity of aryl azide photolysis using cucurbit[8]uril
Qiu, X.; Cai, Q.; Pohl, E.; Jung, A.; Su, H.; Fuhr, O.; Schepers, U.; Bräse, S.
2024. Chemical Communications, 60 (88), 12852–12855. doi:10.1039/d4cc04209c -
[2.2]Paracyclophane‐Substituted Chiral Multiresonant Thermally Activated Delayed Fluorescence Emitters for Efficient Organic Light‐Emitting Diodes
Xu, Y.; Hafeez, H.; Seibert, J.; Wu, S.; Ortiz, J. S. O.; Crassous, J.; Bräse, S.; Samuel, I. D. W.; Zysman-Colman, E.
2024. Advanced Functional Materials, 34 (47), Art.-Nr.: 2402036. doi:10.1002/adfm.202402036 -
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, 34 (47), 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, 34 (47), Art.-Nr.: 2402110. doi:10.1002/adfm.202402110 -
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, 34 (47), Art.-Nr.: 2401956. doi:10.1002/adfm.202401956 -
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, 34 (47), Art.-Nr.: 2313517. doi:10.1002/adfm.202313517 -
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.
2024. Advanced Functional Materials, 34 (47). doi:10.1002/adfm.202309226 -
Tetrazole and Oxadiazole Derivatives as Thermally Activated Delayed Fluorescence Emitters
Leonhardt, C.; Mauri, A.; Garin, I.; Rosemann, N. W.; Wenzel, W.; Lemmer, U.; Kozlowska, M.; Bräse, S.
2024. Chemistry – A European Journal, 30 (57), Art.-Nr.: e202401682. doi:10.1002/chem.202401682 -
Digital chemistry: navigating the confluence of computation and experimentation – definition, status quo, and future perspective
Bräse, S.
2024. Digital Discovery, 3 (10), 1923–1932. doi:10.1039/D4DD00130C -
Design, synthesis, and biological evaluation of novel quinoline-based EGFR/HER-2 dual-target inhibitors as potential anti-tumor agents
Al-Wahaibi, L. H.; El-Sheref, E. M.; Tawfeek, H. N.; Abou-Zied, H. A.; Rabea, S. M.; Bräse, S.; Youssif, B. G. M.
2024. RSC Advances, 14 (45), 32978 – 32991. doi:10.1039/D4RA06394E -
Indole Derivatives: A Versatile Scaffold in Modern Drug Discovery—An Updated Review on Their Multifaceted Therapeutic Applications (2020–2024)
Mo, X.; Rao, D. P.; Kaur, K.; Hassan, R.; Abdel-Samea, A. S.; Farhan, S. M.; Bräse, S.; Hashem, H.
2024. Molecules, 29 (19), 4770. doi:10.3390/molecules29194770 -
New Pyrazole/Pyrimidine-Based Scaffolds as Inhibitors of Heat Shock Protein 90 Endowed with Apoptotic Anti-Breast Cancer Activity
Al-Wahaibi, L. H.; Elbastawesy, M. A. I.; Abodya, N. E.; Youssif, B. G. M.; Bräse, S.; Shabaan, S. N.; Sayed, G. H.; Anwer, K. E.
2024. Pharmaceuticals, 17 (10), 1284. doi:10.3390/ph17101284 -
Author Correction: Peptide-mimetic treatment of Pseudomonas aeruginosa in a mouse model of respiratory infection
Moule, M. G.; Benjamin, A. B.; Burger, M. L.; Herlan, C.; Lebedev, M.; Lin, J. S.; Koster, K. J.; Wavare, N.; Adams, L. G.; Bräse, S.; Munoz-Medina, R.; Cannon, C. L.; Barron, A. E.; Cirillo, J. D.
2024. Communications Biology, 7 (1), Art.-Nr.: 1137. doi:10.1038/s42003-024-06863-6 -
Design and synthesis new indole-based aromatase/iNOS inhibitors with apoptotic antiproliferative activity
Al-Wahaibi, L. H.; Abou-Zied, H. A.; Abdelrahman, M. H.; Morcoss, M. M.; Trembleau, L.; Youssif, B. G. M.; Bräse, S.
2024. Frontiers in Chemistry, 12, Art.-Nr.: 1432920. doi:10.3389/fchem.2024.1432920 -
Synthesis of New Thiazole-Privileged Chalcones as Tubulin Polymerization Inhibitors with Potential Anticancer Activities
Hashem, H.; Hassan, A.; Abdelmagid, W. M.; Habib, A. G. K.; Abdel-Aal, M. A. A.; Elshamsy, A. M.; El Zawily, A.; Radwan, I. T.; Bräse, S.; Abdel-Samea, A. S.; Rabea, S. M.
2024. Pharmaceuticals, 17 (9), 1154. doi:10.3390/ph17091154 -
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 -
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, 12 (29), 11041–11050. doi:10.1039/D4TC01195C -
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, 9 (8), 2149–2159. doi:10.1039/d4re00087k -
2,1,3-Benzoselenadiazole as Mono- and Bidentate N-Donor for Heteroleptic Cu(I) Complexes: Synthesis, Characterization and Photophysical Properties
Ferraro, V.; Hoffmann, F.; Fuhr, O.; Luy, B.; Bräse, S.
2024. Inorganics, 12 (8), Art.-Nr.: 201. doi:10.3390/inorganics12080201 -
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 -
Design of Imidazo[1,2-a]pyridine-Based Donor–Acceptor Chromophores through a Multicomponent Approach
Stahlberger, M.; Mergel, M.; Santos, J. M. dos; Matulaitis, T.; Nieger, M.; Zysman-Colman, E.; Bräse, S.
2024. Synlett, 35 (09), 1033–1041. doi:10.1055/a-2236-8949 -
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 -
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.
2024. Molecular Diversity, 28 (3), 1249–1260. doi:10.1007/s11030-023-10653-3 -
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 -
New series of 4,6-diaryl pyrimidines: facile synthesis and antiproliferative activity as dual EGFR/VEGFR-2 inhibitors
Mostafa, Y. A.; Assoud, J. A.; Desoky, A. Y.; Mohamady, S.; Mohamed, N. M.; Salem, O. I. A.; Almarhoon, Z. M.; Bräse, S.; Youssif, B. G. M.
2024. Frontiers in Chemistry, 12, Art.-Nr.: 1498104. doi:10.3389/fchem.2024.1498104 -
Using the Chemotion repository to deposit and access FAIR research data for chemistry experiments
Huang, P.-C.; Lin, C.-L.; Tremouilhac, P.; Jung, N.; Bräse, S.
2024. Nature Protocols. doi:10.1038/s41596-024-01074-z -
Zinc Phthalocyanine Core‐First Star Polymers Through Nitroxide Mediated Polymerization and Nitroxide Exchange Reaction
Ahmetali, E.; Kocaarslan, A.; Bräse, S.; Théato, P.; Kasım Şener, M.
2024. Macromolecular Rapid Communications, 2400601. doi:10.1002/marc.202400601 -
Peptide-mimetic treatment of Pseudomonas aeruginosa in a mouse model of respiratory infection
Moule, M. G.; Benjamin, A. B.; Buger, M. L.; Herlan, C.; Lebedev, M.; Lin, J. S.; Koster, K. J.; Wavare, N.; Adams, L. G.; Bräse, S.; Munoz-Medina, R.; Cannon, C. L.; Barron, A. E.; Cirillo, J. D.
2024. Communications Biology, 7 (1), Art.-Nr.: 1033. doi:10.1038/s42003-024-06725-1 -
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 -
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 -
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, 5 (5), 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 -
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 -
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 -
Dünne Schichten metallorganischer Gerüstverbindungen als ideale Matrizes für die Azid‐Photolyse im Vakuum
Song, J.; Yu, X.; Nefedov, A.; Weidler, P. G.; Grosjean, S.; Bräse, S.; Wang, Y.; Wöll, C.
2023. Angewandte Chemie, 135 (34), e202306155. doi:10.1002/ange.202306155 -
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 -
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 -
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 -
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/c9sc06460e -
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/c9sc04926f -
Lanthanide conjugates as versatile instruments for therapy and diagnostics
Herlan, C.; Bräse, S.
2020. Dalton transactions, 49 (8), 2397–2402. doi:10.1039/C9DT04851K -
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.201901434 -
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.201900141 -
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/s41598-019-54996-0 -
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-z -
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.201901171 -
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 -
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 -
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.201904475 -
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 -
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/s13321-019-0400-5 -
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.9b02402 -
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/molecules24224122 -
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 -
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/c9dt02447f -
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/c9dt02094b -
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/molecules24203782 -
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.201901602 -
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/molecules24173069 -
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/c9ra07055a -
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/membranes9100124 -
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 -
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 -
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 -
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/c9cc02849h -
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/c9sc01821b -
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/c9sc00705a -
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 -
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.15.114 -
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 -
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 -
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 -
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 -
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.2019.100007 -
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.201806334 -
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 -
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 -
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 -
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 -
Chemotion-ELN part 2: adaption of an embedded Ketcher editor to advanced research applications
Kotov, S.; Tremouilhac, P.; Jung, N.; Bräse, S.
2018. Journal of cheminformatics, 10 (1), Art.Nr. 38. doi:10.1186/s13321-018-0292-9 -
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 -
Lanthanide pyrazolecarboxylates for OLEDs and bioimaging
Utochnikova, V. V.; Latipov, E. V.; Dalinger, A. I.; Nelyubina, Y. V.; Vashchenko, A. A.; Hoffmann, M.; Kalyakina, A. S.; Vatsadze, S. Z.; Schepers, U.; Bräse, S.; Kuzmina, N. P.
2018. Journal of luminescence, 202, 38–46. doi:10.1016/j.jlumin.2018.05.022 -
Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates with Pyridyl and Pyrimidyl Building Blocks
Knoll, D. M.; Bräse, S.
2018. ACS omega, 3 (9), 12158–12162. doi:10.1021/acsomega.8b01774 -
Series of Photoswitchable Azobenzene-Containing Metal–Organic Frameworks with Variable Adsorption Switching Effect
Wang, Z.; Müller, K.; Valášek, M.; Grosjean, S.; Bräse, S.; Wöll, C.; Mayor, M.; Heinke, L.
2018. The journal of physical chemistry <Washington, DC> / C, 122 (33), 19044–19050. doi:10.1021/acs.jpcc.8b05843 -
Surface Functionalization of Silicon, HOPG, and Graphite Electrodes: Toward an Artificial Solid Electrolyte Interface
Moock, D. S.; Steinmüller, S. O.; Wessely, I. D.; Llevot, A.; Bitterer, B.; Meier, M. A. R.; Bräse, S.; Ehrenberg, H.; Scheiba, F.
2018. ACS applied materials & interfaces, 10 (28), 24172–24180. doi:10.1021/acsami.8b04877 -
Triplet emitters versus TADF emitters in OLEDs : A comparative study
Bizzarri, C.; Hundemer, F.; Busch, J.; Bräse, S.
2018. Polyhedron, 140, 51–66. doi:10.1016/j.poly.2017.11.032 -
TGFβ counteracts LYVE-1-mediated induction of lymphangiogenesis by small hyaluronan oligosaccharides
Bauer, J.; Rothley, M.; Schmaus, A.; Quagliata, L.; Ehret, M.; Biskup, M.; Orian-Rousseau, V.; Jackson, D. G.; Pettis, R. J.; Harvey, A.; Bräse, S.; Thiele, W.; Sleeman, J. P.
2018. Journal of molecular medicine, 96 (2), 199–209. doi:10.1007/s00109-017-1615-4 -
Collision Induced Dissociation of Benzylpyridinium-Substituted Porphyrins : Towards a Thermometer Scale for Multiply Charged Ions?
Brendle, K.; Kordel, M.; Schneider, E.; Wagner, D.; Bräse, S.; Weis, P.; Kappes, M. M.
2018. Journal of the American Society for Mass Spectrometry, 29 (2), 382–392. doi:10.1007/s13361-017-1835-4 -
Asymmetric Organocatalytic Synthesis of Bisindoles - Scope and Derivatizations
Retich, C.; Bräse, S.
2018. European journal of organic chemistry, 2018 (1), 60–77. doi:10.1002/ejoc.201701502 -
Combinatorial Synthesis of Peptoid Arrays via Laser-Based Stacking of Multiple Polymer Nanolayers
Mattes, D. S.; Streit, B.; Bhandari, D. R.; Greifenstein, J.; Foertsch, T. C.; Münch, S. W.; Ridder, B.; v. Bojničić-Kninski, C.; Nesterov-Mueller, A.; Spengler, B.; Schepers, U.; Bräse, S.; Loeffler, F. F.; Breitling, F.
2018. Macromolecular rapid communications, 40 (6), Art.Nr.: 1800533. doi:10.1002/marc.201800533 -
Anti-neuroinflammatory effects of GPR55 antagonists in LPS-activated primary microglial cells
Saliba, S. W.; Jauch, H.; Gargouri, B.; Keil, A.; Hurrle, T.; Volz, N.; Mohr, F.; Stelt, M. van der; Bräse, S.; Fiebich, B. L.
2018. Journal of neuroinflammation, 15 (1), Art. Nr.: 322. doi:10.1186/s12974-018-1362-7 -
Amidines: Their synthesis, reactivity, and applications in heterocycle synthesis
Aly, A. A.; Bräse, S.; Gomaa, M. A.-M.
2018. Arkivoc, 2018 (6), 85–138. doi:10.24820/ark.5550190.p010.607 -
Synthesis of novel 1,2-bis-quinolinyl-1,4-naphthoquinones: ERK2 inhibition, cytotoxicity and molecular docking studies
Aly, A. A.; El-Sheref, E. M.; Bakheet, M. E. M.; Mourad, M. A. E.; Brown, A. B.; Bräse, S.; Nieger, M.; Ibrahim, M. A. A.
2018. Bioorganic chemistry, 81, 700–712. doi:10.1016/j.bioorg.2018.09.017 -
Homonuclear decoupling by projection reconstruction
Görling, B.; Bermel, W.; Bräse, S.; Luy, B.
2018. Magnetic resonance in chemistry, 56 (10), 1006–1020. doi:10.1002/mrc.4784 -
Synthesis of Azido-Glycans for Chemical Glycomodification of Proteins
Wawryszyn, M.; Sauter, P. F.; Nieger, M.; Koos, M. R. M.; Koehler, C.; Luy, B.; Lemke, E. A.; Bräse, S.
2018. European journal of organic chemistry, 2018 (31), 4296–4305. doi:10.1002/ejoc.201800602 -
Planar chiral [2.2]paracyclophanes: From synthetic curiosity to applications in asymmetric synthesis and materials
Hassan, Z.; Spuling, E.; Knoll, D. M.; Lahann, J.; Bräse, S.
2018. Chemical Society reviews, 47 (18), 6947–6963. doi:10.1039/c7cs00803a -
(Deep) blue through-space conjugated TADF emitters based on [2.2]paracyclophanes
Spuling, E.; Sharma, N.; Samuel, I. D. W.; Zysman-Colman, E.; Bräse, S.
2018. Chemical communications, 54 (67), 9278–9281. doi:10.1039/c8cc04594a -
Click chemistry-mediated biotinylation reveals a function for the protease BACE1 in modulating the neuronal surface glycoproteome
Herber, J.; Njavro, J.; Feederle, R.; Schepers, U.; Müller, U.; Bräse, S.; Müller, S.; Lichtenthaler, S. F.
2018. Molecular & cellular proteomics, 17 (8), 1487–1501. doi:10.1074/mcp.RA118.000608 -
Remarkable high efficiency of red emitters using Eu(III) ternary complexes
Kalyakina, A. S.; Utochnikova, V. V.; Zimmer, M.; Dietrich, F.; Kaczmarek, A. M.; Van Deun, R.; Vashchenko, A. A.; Goloveshkin, A. S.; Nieger, M.; Gerhards, M.; Schepers, U.; Bräse, S.
2018. Chemical communications, 54 (41), 5221–5224. doi:10.1039/C8CC02930J -
1,5-Cyclooctadienyl alcohols and ketones generate a new class of COD Pt complexes
Wandler, A. E. E.; Koos, M. R. M.; Nieger, M.; Luy, B.; Bräse, S.
2018. Dalton transactions, 47 (11), 3689–3692. doi:10.1039/C8DT00075A -
Alkyl and Aryl Thiol Addition to [1.1.1]Propellane: Scope and Limitations of a Fast Conjugation Reaction
Bär, R. M.; Kirschner, S.; Nieger, M.; Bräse, S.
2018. Chemistry - a European journal, 24 (6), 1373–1382. doi:10.1002/chem.201704105 -
Theoretical and NMR Conformational Studies of β-Proline Oligopeptides With Alternating Chirality of Pyrrolidine Units
Mantsyzov, A. B.; Savelyev, O. Y.; Ivantcova, P. M.; Bräse, S.; Kudryavtsev, K. V.; Polshakov, V. I.
2018. Frontiers in Chemistry, 6, Art.Nr. 91. doi:10.3389/fchem.2018.00091 -
Addition of dithi(ol)anylium tetrafluoroborates to α, β-unsaturated ketones
Huang, Y.-C.; Nguyen, A.; Gräßle, S.; Vanderheiden, S.; Jung, N.; Bräse, S.
2018. Beilstein journal of organic chemistry, 14, 515–522. doi:10.3762/bjoc.14.37 -
Relative Reactivity of Benzothiophene-Fused Enediynes in the Bergman Cyclization
Lyapunova, A. G.; Danilkina, N. A.; Rumyantsev, A. M.; Khlebnikov, A. F.; Chislov, M. V.; Starova, G. L.; Sambuk, E. V.; Govdi, A. I.; Bräse, S.; Balova, I. A.
2018. The journal of organic chemistry, 83 (5), 2788–2801. doi:10.1021/acs.joc.7b03258 -
Thermal cis-to-trans Isomerization of Azobenzene Side Groups in Metal-Organic Frameworks investigated by Localized Surface Plasmon Resonance Spectroscopy
Zhou, W.; Grosjean, S.; Bräse, S.; Heinke, L.
2018. Zeitschrift für physikalische Chemie, 233 (SI, 1), 15–22. doi:10.1515/zpch-2017-1081 -
The coordination- and photochemistry of copper(I) complexes: variation of N^N ligands from imidazole to tetrazole
Bergmann, L.; Braun, C.; Nieger, M.; Bräse, S.
2018. Dalton transactions, 47 (2), 608–621. doi:10.1039/C7DT03682E -
Ultra-fast Suzuki and Heck reactions for the synthesis of styrenes and stilbenes using arenediazonium salts as super-electrophiles
Trusova, M. E.; Rodriguez-Zubiri, M.; Kutonova, K. V.; Jung, N.; Bräse, S.; Felpin, F.-X.; Postnikov, P. S.
2018. Organic chemistry frontiers, 5 (1), 41–45. doi:10.1039/C7QO00750G -
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 -
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 -
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 -
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 -
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) -
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 -
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 -
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 -
[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 -
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 -
Chemotion ELN : an Open Source electronic lab notebook for chemists in academia
Tremouilhac, P.; Nguyen, A.; Huang, Y.-C.; Kotov, S.; Lütjohann, D. S.; Hübsch, F.; Jung, N.; Bräse, S.
2017. Journal of cheminformatics, 9 (1), Art.Nr. 54. doi:10.1186/s13321-017-0240-0 -
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 -
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 -
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 -
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 -
Ein Molekülarchiv als akademisch integrierte Service-Einrichtung
Jung, N.; Deckers, A.; Bräse, S.
2017. Biospektrum, 23 (2), 212–214 -
Development of Bag-1L as a therapeutic target in androgen receptor-dependent prostate cancer
Cato, L.; Neeb, A.; Sharp, A.; Buzón, V.; Ficarro, S. B.; Yang, L.; Muhle-Goll, C.; Kuznik, N. C.; Riisnaes, R.; Rodrigues, D. N.; Armant, O.; Gourain, V.; Adelmant, G.; Ntim, E. A.; Westerling, T.; Dolling, D.; Rescigno, P.; Figueiredo, I.; Fauser, F.; Wu, J.; Rottenberg, J. T.; Shatkina, L.; Ester, C.; Luy, B.; Puchta, H.; Troppmair, J.; Jung, N.; Bräse, S.; Strähle, U.; Marto, J. A.; Nienhaus, G. U.; Al-Lazikani, B.; Salvatella, X.; Bono, J. S. de; Cato, A. C. B.; Brown, M.
2017. eLife, 6, Art.Nr. e27159. doi:10.7554/eLife.27159 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
Fast and efficient synthesis of microporous polymer nanomembranes via light-induced click reaction
An, Q.; Hassan, Y.; Yan, X.; Krolla-Sidenstein, P.; Mohammed, T.; Lang, M.; Bräse, S.; Tsotsalas, M.
2017. Beilstein journal of organic chemistry, 13, 558–563. doi:10.3762/bjoc.13.54 -
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 -
Oxidation of diazenyl-protected N-heterocycles-a new entry to functionalized lactams
Petrović, M.; Scarpi, D.; Nieger, M.; Jung, N.; Occhiato, E. G.; Bräse, S.
2017. RSC Advances, 7 (16), 9461–9464. doi:10.1039/c6ra26546d -
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 -
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 -
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 -
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 -
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 -
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 -
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) -
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/ncomms13872 -
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:10.1088/1742-6596/712/1/012137 -
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 -
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 -
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.12.252 -
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 -
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.1500889 -
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 -
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 -
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.201603847 -
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 -
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 -
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 -
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 -
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/metabo6030027 -
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 -
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 -
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/c6ra06510d -
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 -
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 -
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/ncomms11844 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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/c5dt02276b -
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 -
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 -
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 -
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/s13568-015-0174-8 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
Ruthenium-catalyzed C-H activation of thioxanthones
Wagner, D.; Bräse, S.
2015. Beilstein journal of organic chemistry, 11, 431–435. doi:10.3762/bjoc.11.49 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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/c5cp01372k -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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/C4OB01663G -
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/C4NP00050A -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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/C3CP55486D -
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/C4OB00234B -
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/C3RA47964A -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
Metal-catalyzed cross-coupling reactions and more
Meijere, A. de; Bräse, S.; Oestreich, M.
2014. Weinheim : Wiley-VCH, 2014 -
Das Internet der Dinge erobert das chemische Forschungslabor
Lütjohann, D.; Jung, N.; Tremouilhac, P.; Bräse, S.
2014. GIT Fachzeitschrift für das Laboratorium, (10), 22 -
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/ic500135m -
A mild method for eliminating alkyl ethers to alkenes
Lindner, S.; Bräse, S.
2014. RSC Advances, 4 (56), 29439–29442. doi:10.1039/C4RA03785E -
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 -
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 -
Silver-mediated perfluoroalkylation reactions
Hafner, A.; Jung, N.; Bräse, S.
2014. Synthesis, 46, 1440–1447. doi:10.1055/s-0033-1341223 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
A new route to dithia- and thiaoxacyclooctynes via Nicholas reaction
Hagendorn, T.; Bräse, S.
2014. RSC Advances, 4, 15493–15495. doi:10.1039/C4RA01345J -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
Trifluoromethylation of 1-aryl-3,3-diisopropyltriazenes
Hafner, A.; Bräse, S.
2013. Advanced Synthesis and Catalysis, 355, 996–1000. doi:10.1002/adsc.201201040 -
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 -
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/srep02817 -
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 -
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 -
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) -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
Silver-mediated methoxycarbonyltetrafluoroethylation of arenes
Hafner, A.; Feuerstein, T. J.; Bräse, S.
2013. Organic Letters, 15, 3468–3471. doi:10.1021/ol401558z -
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 -
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 -
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 -
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 -
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 -
Neue Katalysatoren für Übergangsmetall-katalysierte Aziridin-Synthesen
Jung, N.; Bräse, S.
2012. Angewandte Chemie, 124 (23), 5632–5634. doi:10.1002/ange.201200966 -
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 -
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 -
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 -
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 -
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 -
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.8.160 -
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 -
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.8.135 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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 -
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