Publications
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Synthesis, Antioxidant and Antiproliferative Actions of 4-(1,2,3-Triazol-1-yl)quinolin-2(1H)-ones as Multi-Target Inhibitors
El-Sheref, E. M.; Bräse, S.; Tawfeek, H. N.; Alasmary, F. A.; Youssif, B. G. M.
2023. International Journal of Molecular Sciences, 24 (17), Art.-Nr.: 13300. doi:10.3390/ijms241713300 -
Marriage of an N-Fused and a Regular Porphyrin in a Cofacial Ligand System
Schissler, C.; Schneider, E. K.; Rotter, M.; Notter, S.; Geier, C.; Weis, P.; Kappes, M. M.; Bräse, S.
2023. Organometallics, 42 (15), 1882 – 1889. doi:10.1021/acs.organomet.3c00116 -
Synthesis and Structure Determination of Substituted Thiazole Derivatives as EGFR/BRAF Dual Inhibitors Endowed with Antiproliferative Activity
Al-Wahaibi, L. H.; El-Sheref, E. M.; Hassan, A. A.; Bräse, S.; Nieger, M.; Youssif, B. G. M.; Ibrahim, M. A. A.; Tawfeek, H. N.
2023. Pharmaceuticals, 16 (7), Art.-Nr.: 1014. doi:10.3390/ph16071014 -
Identification of an imidazopyridine-based compound as an oral selective estrogen receptor degrader for breast cancer therapy
Pan, M.; Solozobova, V.; Kuznik, N. C.; Jung, N.; Graessle, S.; Gourain, V.; Heneka, Y. M.; Cramer von Clausbruch, C. A.; Fuhr, O.; Munuganti, R. S. N.; Maddalo, D.; Blattner, C.; Neeb, A.; Sharp, A.; Cato, L.; Weiss, C.; Jeselsohn, R. M.; Orian-Rousseau, V.; Bräse, S.; Cato, A. C. B.
2023. Cancer Research Communications, 3 (7). 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 -
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 -
The Impact of Digitalized Data Management on Materials Systems Workflows
Tristram, F.; Jung, N.; Hodapp, P.; Schröder, R. R.; Wöll, C.; Bräse, S.
2023. Advanced Functional Materials, 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.
2023. Advanced Functional Materials, Art.-Nr.: 2303929. doi:10.1002/adfm.202303929 -
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, 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, 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. doi:10.1111/bph.16154 -
Functional Material Systems Enabled by Automated Data Extraction and Machine Learning
Kalhor, P.; Jung, N.; Bräse, S.; Wöll, C.; Tsotsalas, M.; Friederich, P.
2023. Advanced Functional Materials, Art.Nr. 2302630. doi:10.1002/adfm.202302630 -
Synthesis of bis-thiohydantoin derivatives as an antiproliferative agents targeting EGFR inhibitory pathway
Hassan, A. A.; Aly, A. A.; Ramadan, M.; Mohamed, N. K.; Youssif, B. G. M.; Gomaa, H. A. M.; Bräse, S.; Nieger, M.; El-Aal, A. S. A.
2023. Molecular Diversity. doi:10.1007/s11030-023-10653-3 -
Recent Advances of Transition Metal Complexes for Photopolymerization and 3D Printing under Visible Light
Ferraro, V.; Adam, C. R.; Vranic, A.; Bräse, S.
2023. Advanced Functional Materials, Art.-Nr.: 2302157. doi:10.1002/adfm.202302157 -
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, 2300048. doi:10.1002/mame.202300048 -
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.
2023. Advanced Functional Materials, 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.
2023. Advanced Functional Materials. doi:10.1002/adfm.202301093 -
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, 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, 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. 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. 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 -
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 -
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 -
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.
2022. Angewandte Chemie - International Edition, 62 (10), Art.-Nr.: e202217377. doi:10.1002/anie.202217377 -
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, 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