Publications


  1. 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
  2. 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.2c00141Full textFull text of the publication as PDF document
  3. 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
  4. 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, 104175. doi:10.1016/j.isci.2022.104175
  5. 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
  6. 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/polym14081594Full textFull text of the publication as PDF document
  7. 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/polym14081508Full textFull text of the publication as PDF document
  8. 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. doi:10.1007/s10870-022-00939-z
  9. Poly(pentafluorobenzyl 2‐ylidene‐acetate): Polymerization and Postpolymerization Modification
    Li, Z.; Zhang, H.; Theato, P.; Bräse, S.
    2022. Macromolecular Chemistry and Physics, Art.-Nr.: 2100455. doi:10.1002/macp.202100455Full textFull text of the publication as PDF document
  10. 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/molecules27072125Full textFull text of the publication as PDF document
  11. 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/molecules27072266Full textFull text of the publication as PDF document
  12. 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. doi:10.1039/d2ob00372dFull textFull text of the publication as PDF document
  13. 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
  14. 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. doi:10.1039/d1tc04918fFull textFull text of the publication as PDF document
  15. 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/ijms23020959Full textFull text of the publication as PDF document
  16. 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.
    2021. Plant science, 316, 111156. doi:10.1016/j.plantsci.2021.111156
  17. 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 Full textFull text of the publication as PDF document
  18. 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/d1cc04237hFull textFull text of the publication as PDF document
  19. 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.202102336Full textFull text of the publication as PDF document
  20. 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.202102376Full textFull text of the publication as PDF document
  21. 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/ijms222111665Full textFull text of the publication as PDF document
  22. 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.202100157Full textFull text of the publication as PDF document
  23. 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
  24. 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
  25. 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/d1re00038aFull textFull text of the publication as PDF document
  26. 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 Full textFull text of the publication as PDF document
  27. 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
  28. 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
  29. 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/molecules26164995Full textFull text of the publication as PDF document
  30. 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/molecules26154548Full textFull text of the publication as PDF document
  31. 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.2021.696957Full textFull text of the publication as PDF document
  32. 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/ma14123214Full textFull text of the publication as PDF document
  33. 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.202001536Full textFull text of the publication as PDF document
  34. 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.202004539Full textFull text of the publication as PDF document
  35. 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/d1ce00494hFull textFull text of the publication as PDF document
  36. 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
  37. Synthesis of quinone-based heterocycles of broad-spectrum anticancer activity
    Aly, A. A.; Hassan, A. A.; Mohamed, N. K.; Ramadan, M.; Abd El-Aal, A. S.; Bräse, S.; Nieger, M.
    2021. Journal of chemical research, 45 (5-6), 562–571. doi:10.1177/1747519820959737Full textFull text of the publication as PDF document
  38. Formal Semisynthesis of Demethylgorgosterol Utilizing a Stereoselective Intermolecular Cyclopropanation Reaction
    Rosenbaum, N.; Schmidt, L.; Mohr, F.; Fuhr, O.; Nieger, M.; Bräse, S.
    2021. European journal of organic chemistry, 2021 (10), 1568–1574. doi:10.1002/ejoc.202100035Full textFull text of the publication as PDF document
  39. 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.202005630Full textFull text of the publication as PDF document
  40. 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/ijms22052503Full textFull text of the publication as PDF document
  41. 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
  42. ChemSpectra: a web-based spectra editor for analytical data
    Huang, Y.-C.; Tremouilhac, P.; Nguyen, A.; Jung, N.; Bräse, S.
    2021. Journal of Cheminformatics, 13 (1), Art.-Nr. 8. doi:10.1186/s13321-020-00481-0Full textFull text of the publication as PDF document
  43. 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.202002394Full textFull text of the publication as PDF document
  44. 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.202000065Full textFull text of the publication as PDF document
  45. 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
  46. A small molecule screen identifies novel inhibitors of mechanosensory nematocyst discharge in Hydra
    Hofmann, D.; Garg, N.; Grässle, S.; Vanderheiden, S.; Bergheim, B. G.; Bräse, S.; Jung, N.; Özbek, S.
    2021. Scientific reports, 11, Art.-Nr. 20627. doi:10.1038/s41598-021-99974-7Full textFull text of the publication as PDF document
  47. Effect of a twin-emitter design strategy on a previously reported thermally activated delayed fluorescence organic light-emitting diode
    Crovini, E.; Zhang, Z.; Kusakabe, Y.; Ren, Y.; Wada, Y.; Naqvi, B. A.; Sahay, P.; Matulaitis, T.; Diesing, S.; Samuel, I. D. W.; Brütting, W.; Suzuki, K.; Kaji, H.; Bräse, S.; Zysman-Colman, E.
    2021. Beilstein Journal of Organic Chemistry, 17, 2894–2905. doi:10.3762/bjoc.17.197Full textFull text of the publication as PDF document
  48. 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
  49. Metadata schema to support FAIR data in scanning electron microscopy
    Joseph, R.; Chauhan, A.; Eschke, C.; Ihsan, A. Z.; Jalali, M.; Jäntsch, U.; Jung, N.; Shyam Kumar, C. N.; Kübel, C.; Lucas, C.; Mail, M.; Mazilkin, A.; Neidiger, C.; Panighel, M.; Sandfeld, S.; Stotzka, R.; Thelen, R.; Aversa, R.
    2021. Supplementary Proceedings of the XXIII International Conference on Data Analytics and Management in Data Intensive Domains (DAMDID/RCDL 2021): Moscow, Russia, October 26-29, 2021. Ed.: A. Pozanenko, 265–277, CEUR-WS.org Full textFull text of the publication as PDF document
  50. 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.
    2021. Chemistry - A European Journal. doi:10.1002/chem.202103511Full textFull text of the publication as PDF document
  51. Chemotion Repository, a Curated Repository for Reaction Information and Analytical Data
    Tremouilhac, P.; Huang, P.-C.; Lin, C.-L.; Huang, Y.-C.; Nguyen, A.; Jung, N.; Bach, F.; Bräse, S.
    2021. Chemistry methods, 1 (1), 8–11. doi:10.1002/cmtd.202000034Full textFull text of the publication as PDF document
  52. 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
  53. Synthesis of new pyrazolo[1,2,3]triazines by cyclative cleavage of pyrazolyltriazenes
    Wippert, N.; Nieger, M.; Herlan, C.; Jung, N.; Bräse, S.
    2021. Beilstein journal of organic chemistry, 17, 2773–2780. doi:10.3762/bjoc.17.187Full textFull text of the publication as PDF document
  54. 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
  55. Design and synthesis of (2-oxo-1,2-dihydroquinolin-4-yl)-1,2,3-triazole derivatives via click reaction: Potential apoptotic antiproliferative agents
    El-Sheref, E. M.; Elbastawesy, M. A. I.; Brown, A. B.; Shawky, A. M.; Gomaa, H. A. M.; Bräse, S.; Youssif, B. G. M.
    2021. Molecules, 26 (22), 6798. doi:10.3390/molecules26226798Full textFull text of the publication as PDF document
  56. 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
  57. 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
  58. Regioselective ortho-Palladation of [2.2]Paracyclophane Scaffolds: Accessing Planar and Central Chiral N,C-Palladacycles
    Zippel, C.; Bartholomeyzik, T.; Friedmann, C.; Nieger, M.; Hassan, Z.; Bräse, S.
    2021. European Journal of Organic Chemistry, 2021 (36), 5090–5093. doi:10.1002/ejoc.202101066Full textFull text of the publication as PDF document
  59. Dynamic porous organic polymers with tuneable crosslinking degree and porosity
    Wessely, I. D.; Matt, Y.; An, Q.; Bräse, S.; Tsotsalas, M.
    2021. RSC Advances, 11 (44), 27714–27719. doi:10.1039/d1ra05265aFull textFull text of the publication as PDF document
  60. Skeletal Editing—Nitrogen Deletion of Secondary Amines by Anomeric Amide Reagents
    Zippel, C.; Seibert, J.; Bräse, S.
    2021. Angewandte Chemie / International edition, 60 (36), 19522–19524. doi:10.1002/anie.202107490Full textFull text of the publication as PDF document
  61. 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, Art.-Nr. 2103287. doi:10.1002/adma.202103287Full textFull text of the publication as PDF document
  62. Corrigendum: What Controls the Orientation of TADF Emitters?
    Naqvi, B. A.; Schmid, M.; Crovini, E.; Sahay, P.; Naujoks, T.; Rodella, F.; Zhang, Z.; Strohriegl, P.; Bräse, S.; Zysman-Colman, E.; Brütting, W.
    2021. Frontiers in Chemistry, 9, Art.Nr. 632639. doi:10.3389/fchem.2021.632639Full textFull text of the publication as PDF document
  63. 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/d1sc01411kFull textFull text of the publication as PDF document
  64. 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
  65. The Diels-Alder Approach towards Cannabinoid Derivatives and Formal Synthesis of Tetrahydrocannabinol (THC)
    Hurrle, T.; Gläser, F.; Bröhmer, M. C.; Nieger, M.; Bräse, S.
    2021. ChemistryOpen, 10 (5), 587–592. doi:10.1002/open.202000343Full textFull text of the publication as PDF document
  66. 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
  67. 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
  68. Rigid Multidimensional Alkoxyamines: A Versatile Building Block Library
    Matt, Y.; Wessely, I.; Gramespacher, L.; Tsotsalas, M.; Bräse, S.
    2021. European journal of organic chemistry, 2021 (2), 239–245. doi:10.1002/ejoc.202001415Full textFull text of the publication as PDF document
  69. Structural Diversity of Peptoids: Tube-Like Structures of Macrocycles
    Herlan, C. N.; Sommer, K.; Weis, P.; Nieger, M.; Bräse, S.
    2021. Molecules, 26 (1), Art.-Nr.: 150. doi:10.3390/molecules26010150Full textFull text of the publication as PDF document
  70. 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
  71. 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
  72. 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/d0tc03514aFull textFull text of the publication as PDF document
  73. The Repository Chemotion: Infrastructure for Sustainable Research in Chemistry
    Tremouilhac, P.; Lin, C.-L.; Huang, P.-C.; Huang, Y.-C.; Nguyen, A.; Jung, N.; Bach, F.; Ulrich, R.; Neumair, B.; Streit, A.; Bräse, S.
    2020. Angewandte Chemie / International edition, 59 (50), 22771–22778. doi:10.1002/anie.202007702Full textFull text of the publication as PDF document
  74. Efficient Sky-Blue Organic Light-Emitting Diodes Using a Highly Horizontally Oriented Thermally Activated Delayed Fluorescence Emitter
    Zhang, Z.; Crovini, E.; Santos, P. L. dos; Naqvi, B. A.; Cordes, D. B.; Slawin, A. M. Z.; Sahay, P.; Brütting, W.; Samuel, I. D. W.; Bräse, S.; Zysman-Colman, E.
    2020. Advanced optical materials, 8 (23), Art. Nr.: 2001354. doi:10.1002/adom.202001354Full textFull text of the publication as PDF document
  75. Chemistry of Substituted Thiazinanes and Their Derivatives
    Hassan, A. A.; Bräse, S.; Aly, A. A.; Tawfeek, H. N.
    2020. Molecules, 25 (23), Art.-Nr.: 5610. doi:10.3390/molecules25235610Full textFull text of the publication as PDF document
  76. A mitochondria-targeted coenzyme Q peptoid induces superoxide dismutase and alleviates salinity stress in plant cells
    Asfaw, K. G.; Liu, Q.; Xu, X.; Manz, C.; Purper, S.; Eghbalian, R.; Münch, S. W.; Wehl, I.; Bräse, S.; Eiche, E.; Hause, B.; Bogeski, I.; Schepers, U.; Riemann, M.; Nick, P.
    2020. Scientific reports, 10, Article number:11563. doi:10.1038/s41598-020-68491-4Full textFull text of the publication as PDF document
  77. Controlling Regioselectivity in Palladium‐Catalyzed C−H Activation/Aryl–Aryl Coupling of 4‐Phenylamino[2.2]paracyclophane
    Zippel, C.; Spuling, E.; Hassan, Z.; Polamo, M.; Nieger, M.; Bräse, S.
    2020. Chemistry - a European journal, 26 (61), 13771–13775. doi:10.1002/chem.202003709Full textFull text of the publication as PDF document
  78. A versatile Diels–Alder approach to functionalized hydroanthraquinones
    Beck, J.; Fuhr, O.; Nieger, M.; Bräse, S.
    2020. Royal Society Open Science, 7 (11), Article: 200626. doi:10.1098/rsos.200626Full textFull text of the publication as PDF document
  79. Direct Synthesis of ZIF-8 on Transmission Electron Microscopy Grids Allows Structure Analysis and 3D Reconstruction
    Hugenschmidt, M.; Kutonova, K.; Valadez Sánchez, E. P.; Moulai, S.; Gliemann, H.; Bräse, S.; Wöll, C.; Gerthsen, D.
    2020. AgBioForum, 37 (11), Art.-Nr.: 2000209. doi:10.1002/ppsc.202000209Full textFull text of the publication as PDF document
  80. 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
  81. Design and Synthesis of a [2.2]Paracyclophane‐based Planar Chiral Dirhodium Catalyst and its Applications in Cyclopropanation Reaction of Vinylarenes with α‐Methyl‐α‐Diazo Esters
    Zippel, C.; Hassan, Z.; Nieger, M.; Bräse, S.
    2020. Advanced synthesis & catalysis, 362 (16), 3431–3436. doi:10.1002/adsc.202000512Full textFull text of the publication as PDF document
  82. 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
  83. On Demand Light‐Degradable Polymers Based on 9,10‐Dialkoxyanthracenes
    Becker, F.; Klaiber, M.; Franzreb, M.; Bräse, S.; Lahann, J.
    2020. Macromolecular rapid communications, 41 (15), Art. Nr.: 2000314. doi:10.1002/marc.202000314Full textFull text of the publication as PDF document
  84. 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
  85. 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
  86. Assembly of Molecular Building Blocks into Integrated Complex Functional Molecular Systems: Structuring Matter Made to Order
    Hassan, Z.; Matt, Y.; Begum, S.; Tsotsalas, M.; Bräse, S.
    2020. Advanced functional materials, 30 (26), Art.Nr. 1907625. doi:10.1002/adfm.201907625Full textFull text of the publication as PDF document
  87. Sodium Bicyclo[1.1.1]pentanesulfinate: A Bench‐Stable Precursor for Bicyclo[1.1.1]pentylsulfones and Bicyclo‐ [1.1.1]pentanesulfonamides
    Bär, R. M.; Gross, P. J.; Nieger, M.; Bräse, S.
    2020. Chemistry - a European journal, 26 (19), 4242–4245. doi:10.1002/chem.202000097Full textFull text of the publication as PDF document
  88. Bicyclo[1.1.1]pentyl Sulfoximines: Synthesis and Functionalizations
    Bär, R. M.; Langer, L.; Nieger, M.; Bräse, S.
    2020. Advanced synthesis & catalysis, 362 (6), 1356–1361. doi:10.1002/adsc.201901453Full textFull text of the publication as PDF document
  89. Regioselective Functionalization of [2.2]Paracyclophanes: Recent Synthetic Progress and Perspectives
    Hassan, Z.; Spuling, E.; Knoll, D. M.; Bräse, S.
    2020. Angewandte Chemie / International edition, 59 (6), 2156–2170. doi:10.1002/anie.201904863Full textFull text of the publication as PDF document
  90. Modernes Forschungsdatenmanagement – ein Naturstoffprojekt als Fallstudie
    Koch, V.; Bräse, S.
    2020. Biospektrum, 26 (1), 107–109. doi:10.1007/s12268-020-1316-3Full textFull text of the publication as PDF document
  91. Criegee Intermediates Beyond Ozonolysis: Synthetic and Mechanistic Insights
    Hassan, Z.; Stahlberger, M.; Rosenbaum, N.; Bräse, S.
    2020. Angewandte Chemie - International Edition, 60 (28), 15138–15152. doi:10.1002/anie.202014974Full textFull text of the publication as PDF document
  92. Design, Synthesis, and Molecular Docking of Paracyclophanyl-Thiazole Hybrids as Novel CDK1 Inhibitors and Apoptosis Inducing Anti-Melanoma Agents
    Aly, A. A.; Bräse, S.; Hassan, A. A.; Mohamed, N. K.; El-Haleem, L. E. A.; Nieger, M.; Morsy, N. M.; Alshammari, M. B.; Ibrahim, M. A. A.; Abdelhafez, E. M. N.
    2020. Molecules, 25 (23), Art.-Nr.: 5569. doi:10.3390/molecules25235569Full textFull text of the publication as PDF document
  93. OBO-Fused Benzo[fg]tetracene as Acceptor With Potential for Thermally Activated Delayed Fluorescence Emitters
    Zhang, Z.; Kumar, S.; Bagnich, S.; Spuling, E.; Hundemer, F.; Nieger, M.; Hassan, Z.; Köhler, A.; Zysman-Colman, E.; Bräse, S.
    2020. Frontiers in Chemistry, 8, Art. Nr.: 563411. doi:10.3389/fchem.2020.563411Full textFull text of the publication as PDF document
  94. Design, Synthesis, Molecular Docking, Antiapoptotic and Caspase-3 Inhibition of New 1,2,3-Triazole/Bis-2(1H)-Quinolinone Hybrids
    El-Sheref, E. M.; Aly, A. A.; Alshammari, M. B.; Brown, A. B.; Abdel-Hafez, S. M. N.; Abdelzaher, W. Y.; Bräse, S.; Abdelhafez, E. M. N.
    2020. Molecules, 25 (21), Art. Nr.: 5057. doi:10.3390/molecules25215057Full textFull text of the publication as PDF document
  95. What Controls the Orientation of TADF Emitters?
    Naqvi, B. A.; Schmid, M.; Crovini, E.; Sahay, P.; Naujoks, T.; Rodella, F.; Zhang, Z.; Strohriegl, P.; Bräse, S.; Zysman-Colman, E.; Brütting, W.
    2020. Frontiers in Chemistry, 8, Art. Nr.: 750. doi:10.3389/fchem.2020.00750Full textFull text of the publication as PDF document
  96. Towards the synthesis of calotropin and related cardenolides from 3-epiandrosterone: A-ring related modifications
    Koch, V.; Nieger, M.; Bräse, S.
    2020. Organic chemistry frontiers, 7 (18), 2670–2681. doi:10.1039/d0qo00269kFull textFull text of the publication as PDF document
  97. Polymerization in MOF-Confined Nanospaces: Tailored Architectures, Functions, and Applications
    Begum, S.; Hassan, Z.; Bräse, S.; Tsotsalas, M.
    2020. Langmuir, 36 (36), 10657–10673. doi:10.1021/acs.langmuir.0c01832Full textFull text of the publication as PDF document
  98. 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
  99. New Paracyclophanylthiazoles with Anti-Leukemia Activity: Design, Synthesis, Molecular Docking, and Mechanistic Studies
    Aly, A. A.; Bräse, S.; Hassan, A. A.; Mohamed, N. K.; Abd El-Haleem, L. E.; Nieger, M.; Morsy, N. M.; Abdelhafez, E. M. N.
    2020. Molecules, 25 (13), Art.Nr. 3089. doi:10.3390/molecules25133089Full textFull text of the publication as PDF document
  100. Chemistry and Biological Activities of 1,2,4-Triazolethiones—Antiviral and Anti-Infective Drugs
    Aly, A. A.; A. Hassan, A.; Makhlouf, M. M.; Bräse, S.
    2020. Molecules, 25 (13), Article: 3036. doi:10.3390/molecules25133036Full textFull text of the publication as PDF document
  101. Synthesis of New Planar-Chiral Linked [2.2]Paracyclophanes-N-([2.2]-Paracyclophanylcarbamoyl)-4-([2.2]Paracyclophanylcarboxamide, [2.2]Paracyclophanyl-Substituted Triazolthiones and -Substituted Oxadiazoles
    Aly, A. A.; Bräse, S.; Hassan, A. A.; Mohamed, N. K.; El-Haleem, L. E. A.; Nieger, M.
    2020. Molecules, 25 (15), Article: 3315. doi:10.3390/molecules25153315Full textFull text of the publication as PDF document
  102. Synthesis and structure confirmation of 2,4-disubstituted thiazole and 2,3,4-trisubstituted thiazole as thiazolium bromide salts
    Hassan, A. A.; Mohamed, N. K.; Aly, A. A.; Tawfeek, H. N.; Bräse, S.; Nieger, M.
    2020. Monatshefte für Chemie, 151, 1143–1152. doi:10.1007/s00706-020-02640-3Full textFull text of the publication as PDF document
  103. Correction: Metal complexes as a promising source for new antibiotics
    Frei, A.; Zuegg, J.; Elliott, A. G.; Baker, M.; Braese, S.; Brown, C.; Chen, F.; Dowson, C. G.; Dujardin, G.; Jung, N.; King, A. P.; Mansour, A. M.; Massi, M.; Moat, J.; Mohamed, H. A.; Renfrew, A. K.; Rutledge, P. J.; Sadler, P. J.; Todd, M. H.; Willans, C. E.; Wilson, J. J.; Cooper, M. A.; Blaskovich, M. A. T.
    2020. Chemical science, 11 (17), 4531. doi:10.1039/d0sc90075cFull textFull text of the publication as PDF document
  104. The Staudinger Ligation
    Bednarek, C.; Wehl, I.; Jung, N.; Schepers, U.; Bräse, S.
    2020. Chemical reviews, 120 (10), 4301–4354. doi:10.1021/acs.chemrev.9b00665Full textFull text of the publication as PDF document
  105. Correction: Dynamic covalent polymer networks combined nitroxide exchange reaction and nitroxide mediated polymerization
    Jia, Y.; Matt, Y.; An, Q.; Wessely, I.; Mutlu, H.; Theato, P.; Bräse, S.; Llevot, A.; Tsotsalas, M.
    2020. Polymer chemistry, 11 (15), 2761. doi:10.1039/d0py90053bFull textFull text of the publication as PDF document
  106. Dynamic covalent polymer networks via combined nitroxide exchange reaction and nitroxide mediated polymerization
    Jia, Y.; Matt, Y.; An, Q.; Wessely, I.; Mutlu, H.; Theato, P.; Bräse, S.; Llevot, A.; Tsotsalas, M.
    2020. Polymer chemistry, 11 (14), 2502–2510. doi:10.1039/c9py01878fFull textFull text of the publication as PDF document
  107. Sensitizing TADF Absorption Using Variable Length Oligo(phenylene ethynylene) Antennae
    Franco, O.; Jakoby, M.; Schneider, R. V.; Hundemer, F.; Hahn, D.; Richards, B. S.; Bräse, S.; Meier, M. A. R.; Lemmer, U.; Howard, I. A.
    2020. Frontiers in Chemistry, 8, Art.-Nr.: 126. doi:10.3389/fchem.2020.00126Full textFull text of the publication as PDF document
  108. Reactive & Efficient: Organic Azides as Cross-Linkers in Material Sciences
    Schock, M.; Bräse, S.
    2020. Molecules, 25 (4), Art. Nr.: 1009. doi:10.3390/molecules25041009Full textFull text of the publication as PDF document
  109. Metal complexes as a promising source for new antibiotics
    Frei, A.; Zuegg, J.; Elliott, A. G.; Baker, M.; Braese, S.; Brown, C.; Chen, F.; Dowson, C. G.; Dujardin, G.; Jung, N.; King, A. P.; Mansour, A. M.; Massi, M.; Moat, J.; Mohamed, H. A.; Renfrew, A. K.; Rutledge, P. J.; Sadler, P. J.; Todd, M. H.; Willans, C. E.; Wilson, J. J.; Cooper, M. A.; Blaskovich, M. A. T.
    2020. Chemical science, 11 (10), 2627–2639. doi:10.1039/c9sc06460eFull textFull text of the publication as PDF document
  110. Proton-conduction photomodulation in spiropyran-functionalized MOFs with large on–off ratio
    Kanj, A. B.; Chandresh, A.; Gerwien, A.; Grosjean, S.; Bräse, S.; Wang, Y.; Dube, H.; Heinke, L.
    2020. Chemical science, 11 (5), 1404–1410. doi:10.1039/c9sc04926fFull textFull text of the publication as PDF document
  111. Lanthanide conjugates as versatile instruments for therapy and diagnostics
    Herlan, C.; Bräse, S.
    2020. Dalton transactions, 49 (8), 2397–2402. doi:10.1039/C9DT04851KFull textFull text of the publication as PDF document
  112. Post-synthetic Modification of DUT-5-based Metal Organic Frameworks for the Generation of Single-site Catalysts and their Application in Selective Epoxidation Reactions
    Yildiz, C.; Kutonova, K.; Oßwald, S.; Titze-Alonso, A.; Bitzer, J.; Bräse, S.; Kleist, W.
    2020. ChemCatChem, 12 (4), 1134–1142. doi:10.1002/cctc.201901434Full textFull text of the publication as PDF document
  113. Acceptor Derivatization of the 4CzIPN TADF System: Color Tuning and Introduction of Functional Groups
    Hundemer, F.; Reventlow, L. G. von; Leonhardt, C.; Polamo, M.; Nieger, M.; Seifermann, S. M.; Colsmann, A.; Bräse, S.
    2019. ChemistryOpen, 8 (12), 1413–1420. doi:10.1002/open.201900141Full textFull text of the publication as PDF document
  114. Author Correction: A Peptoid Delivers CoQ-derivative to Plant Mitochondria via Endocytosis
    Asfaw, K. G.; Liu, Q.; Maisch, J.; Münch, S. W.; Wehl, I.; Bräse, S.; Bogeski, I.; Schepers, U.; Nick, P.
    2019. Scientific reports, 9 (1), Art.Nr.: 18832. doi:10.1038/s41598-019-54996-0Full textFull text of the publication as PDF document
  115. A Peptoid Delivers CoQ-derivative to Plant Mitochondria via Endocytosis
    Asfaw, K. G.; Liu, Q.; Maisch, J.; Münch, S. W.; Wehl, I.; Bräse, S.; Bogeski, I.; Schepers, U.; Nick, P.
    2019. Scientific reports, 9 (1), Art.Nr.: 9839. doi:10.1038/s41598-019-46182-zFull textFull text of the publication as PDF document
  116. Preparation and Synthetic Applications of [2.2]Paracyclophane Trifluoroborates: An Efficient and Convenient Route to Nucleophilic [2.2]Paracyclophane Cross‐Coupling Building Blocks
    Knoll, D. M.; Šimek, H.; Hassan, Z.; Bräse, S.
    2019. European journal of organic chemistry, 2019 (36), 6198–6202. doi:10.1002/ejoc.201901171Full textFull text of the publication as PDF document
  117. 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
  118. 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
  119. 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
  120. 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
  121. ChemScanner: extraction and re-use(ability) of chemical information from common scientific documents containing ChemDraw files
    Nguyen, A.; Huang, Y.-C.; Tremouilhac, P.; Jung, N.; Bräse, S.
    2019. Journal of cheminformatics, 11 (1), Art. Nr.: 77. doi:10.1186/s13321-019-0400-5Full textFull text of the publication as PDF document
  122. 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
  123. Planar chiral [2.2]paracyclophane-based bisoxazoline ligands and their applications in Cu-Mediated N-H insertion reaction
    Knoll, D. M.; Hu, Y.; Hassan, Z.; Nieger, M.; Bräse, S.
    2019. Molecules, 24 (22), Art.-Nr.: 4122. doi:10.3390/molecules24224122Full textFull text of the publication as PDF document
  124. 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
  125. Highly soluble fluorine containing Cu(i) AlkylPyrPhos TADF complexes
    Busch, J. M.; Zink, D. M.; Di Martino-Fumo, P.; Rehak, F. R.; Boden, P.; Steiger, S.; Fuhr, O.; Nieger, M.; Klopper, W.; Gerhards, M.; Bräse, S.
    2019. Dalton transactions, 48 (41), 15687–15698. doi:10.1039/c9dt02447fFull textFull text of the publication as PDF document
  126. Metal-supported and -assisted stereoselective cooperative photoredox catalysis
    Busch, J.; Knoll, D. M.; Zippel, C.; Bräse, S.; Bizzarri, C.
    2019. Dalton transactions, 48 (41), 15338–15357. doi:10.1039/c9dt02094bFull textFull text of the publication as PDF document
  127. Synthesis of New Fused Heterocyclic 2-Quinolones and 3-Alkanonyl-4-Hydroxy-2-Quinolones
    Aly, A. A.; Hassan, A. A.; Mohamed, N. K.; El-Haleem, L. E. A.; Bräse, S.; Polamo, M.; Nieger, M.; Brown, A. B.
    2019. Molecules, 24 (20), 3782. doi:10.3390/molecules24203782Full textFull text of the publication as PDF document
  128. 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
  129. Functionalized 1,3-Thiazolidin-4-Ones from 2-Oxo-Acenaphthoquinylidene- and [2.2]Paracyclophanylidene-Thiosemicarbazones
    Aly, A. A.; Mohamed, N. K.; Hassan, A. A.; El-Shaieb, K. M.; Makhlouf, M. M.; Bräse, S.; Nieger, M.; Brown, A. B.
    2019. Molecules, 24 (17), Article: 3069. doi:10.3390/molecules24173069Full textFull text of the publication as PDF document
  130. Synthesis and characterization of rigid [2.2]paracyclophane–porphyrin conjugates as scaffolds for fixed-distance bimetallic complexes
    Knoll, D. M.; Wiesner, T. B.; Marschner, S. M.; Hassan, Z.; Weis, P.; Kappes, M.; Nieger, M.; Bräse, S.
    2019. RSC Advances, 9 (52), 30541–30544. doi:10.1039/c9ra07055aFull textFull text of the publication as PDF document
  131. Synthesis, Transfer, and Gas Separation Characteristics of MOF-Templated Polymer Membranes
    Schmitt, S.; Shishatskiy, S.; Krolla, P.; An, Q.; Begum, S.; Welle, A.; Hashem, T.; Grosjean, S.; Abetz, V.; Bräse, S.; Wöll, C.; Tsotsalas, M.
    2019. Membranes, 9 (10), Art. Nr.: 124. doi:10.3390/membranes9100124Full textFull text of the publication as PDF document
  132. 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
  133. 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
  134. 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
  135. Switching the enantioselectivity of nanoporous host materials by light
    Kanj, A. B.; Bürck, J.; Grosjean, S.; Bräse, S.; Heinke, L.
    2019. Chemical communications, 55 (60), 8776–8779. doi:10.1039/c9cc02849hFull textFull text of the publication as PDF document
  136. Turn on of sky-blue thermally activated delayed fluorescence and circularly polarized luminescence (CPL): Via increased torsion by a bulky carbazolophane donor
    Sharma, N.; Spuling, E.; Mattern, C. M.; Li, W.; Fuhr, O.; Tsuchiya, Y.; Adachi, C.; Bräse, S.; Samuel, I. D. W.; Zysman-Colman, E.
    2019. Chemical science, 10 (27), 6689–6696. doi:10.1039/c9sc01821bFull textFull text of the publication as PDF document
  137. Rational design and implementation of a cucurbit[8]uril-based indicator-displacement assay for application in blood serum
    Sinn, S.; Spuling, E.; Bräse, S.; Biedermann, F.
    2019. Chemical science, 10 (27), 6584–6593. doi:10.1039/c9sc00705aFull textFull text of the publication as PDF document
  138. 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
  139. Insertion of [1.1.1]propellane into aromatic disulfides
    Bär, R. M.; Heinrich, G.; Nieger, M.; Fuhr, O.; Bräse, S.
    2019. Beilstein journal of organic chemistry, 15, 1172–1180. doi:10.3762/bjoc.15.114Full textFull text of the publication as PDF document
  140. 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
  141. 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
  142. 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
  143. 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
  144. Procedures for systematic capture and management of analytical data in academia
    Potthoff, J.; Tremouilhac, P.; Hodapp, P.; Neumair, B.; Bräse, S.; Jung, N.
    2019. Analytica Chimica Acta: X, 1, Article: 100007. doi:10.1016/j.acax.2019.100007Full textFull text of the publication as PDF document
  145. Soft Matter Technology at KIT: Chemical Perspective from Nanoarchitectures to Microstructures
    Grosjean, S.; Wawryszyn, M.; Mutlu, H.; Bräse, S.; Lahann, J.; Theato, P.
    2019. Advanced materials, 31 (26), Art.-Nr.: 1806334. doi:10.1002/adma.201806334Full textFull text of the publication as PDF document
  146. 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
  147. 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
  148. 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
  149. 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
  150. Chemotion-ELN part 2: adaption of an embedded Ketcher editor to advanced research applications
    Kotov, S.; Tremouilhac, P.; Jung, N.; Bräse, S.
    2018. Journal of cheminformatics, 10 (1), Art.Nr. 38. doi:10.1186/s13321-018-0292-9Full textFull text of the publication as PDF document
  151. 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
  152. 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
  153. 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
  154. 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
  155. 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
  156. 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
  157. 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
  158. 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
  159. 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
  160. Combinatorial Synthesis of Peptoid Arrays via Laser-Based Stacking of Multiple Polymer Nanolayers
    Mattes, D. S.; Streit, B.; Bhandari, D. R.; Greifenstein, J.; Foertsch, T. C.; Münch, S. W.; Ridder, B.; v. Bojničić-Kninski, C.; Nesterov-Mueller, A.; Spengler, B.; Schepers, U.; Bräse, S.; Loeffler, F. F.; Breitling, F.
    2018. Macromolecular rapid communications, 40 (6), Art.Nr.: 1800533. doi:10.1002/marc.201800533Full textFull text of the publication as PDF document
  161. Anti-neuroinflammatory effects of GPR55 antagonists in LPS-activated primary microglial cells
    Saliba, S. W.; Jauch, H.; Gargouri, B.; Keil, A.; Hurrle, T.; Volz, N.; Mohr, F.; Stelt, M. van der; Bräse, S.; Fiebich, B. L.
    2018. Journal of neuroinflammation, 15 (1), Art. Nr.: 322. doi:10.1186/s12974-018-1362-7Full textFull text of the publication as PDF document
  162. 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
  163. 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
  164. 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
  165. 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
  166. 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
  167. (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
  168. 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
  169. 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
  170. 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
  171. 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
  172. Theoretical and NMR Conformational Studies of β-Proline Oligopeptides With Alternating Chirality of Pyrrolidine Units
    Mantsyzov, A. B.; Savelyev, O. Y.; Ivantcova, P. M.; Bräse, S.; Kudryavtsev, K. V.; Polshakov, V. I.
    2018. Frontiers in Chemistry, 6, Art.Nr. 91. doi:10.3389/fchem.2018.00091Full textFull text of the publication as PDF document
  173. Addition of dithi(ol)anylium tetrafluoroborates to α, β-unsaturated ketones
    Huang, Y.-C.; Nguyen, A.; Gräßle, S.; Vanderheiden, S.; Jung, N.; Bräse, S.
    2018. Beilstein journal of organic chemistry, 14, 515–522. doi:10.3762/bjoc.14.37Full textFull text of the publication as PDF document
  174. 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
  175. 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
  176. 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
  177. 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
  178. 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
  179. 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
  180. 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
  181. 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
  182. Erfassung und Speicherung von Forschungsdaten im Fachbereich Chemie: Bereitstellung moderner Forschungs-infrastrukturen durch ein elektronisches Laborjournal mit Repositorium-Anbindung
    Jung, N.; Tremouilhac, P.; Kramer, C.; Potthoff, J.
    2017. E-Science-Tage 2017: Forschungsdaten managen. Hrsg.: J. Kratzke, 127–136, Heidelberger E-Books (heiBOOKS) Full textFull text of the publication as PDF document
  183. 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
  184. 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
  185. 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
  186. [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
  187. 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
  188. Chemotion ELN : an Open Source electronic lab notebook for chemists in academia
    Tremouilhac, P.; Nguyen, A.; Huang, Y.-C.; Kotov, S.; Lütjohann, D. S.; Hübsch, F.; Jung, N.; Bräse, S.
    2017. Journal of cheminformatics, 9 (1), Art.Nr. 54. doi:10.1186/s13321-017-0240-0Full textFull text of the publication as PDF document
  189. 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
  190. 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
  191. 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
  192. 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
  193. Ein Molekülarchiv als akademisch integrierte Service-Einrichtung
    Jung, N.; Deckers, A.; Bräse, S.
    2017. Biospektrum, 23 (2), 212–214 
  194. Development of Bag-1L as a therapeutic target in androgen receptor-dependent prostate cancer
    Cato, L.; Neeb, A.; Sharp, A.; Buzón, V.; Ficarro, S. B.; Yang, L.; Muhle-Goll, C.; Kuznik, N. C.; Riisnaes, R.; Rodrigues, D. N.; Armant, O.; Gourain, V.; Adelmant, G.; Ntim, E. A.; Westerling, T.; Dolling, D.; Rescigno, P.; Figueiredo, I.; Fauser, F.; Wu, J.; Rottenberg, J. T.; Shatkina, L.; Ester, C.; Luy, B.; Puchta, H.; Troppmair, J.; Jung, N.; Bräse, S.; Strähle, U.; Marto, J. A.; Nienhaus, G. U.; Al-Lazikani, B.; Salvatella, X.; Bono, J. S. de; Cato, A. C. B.; Brown, M.
    2017. eLife, 6, Art.Nr. e27159. doi:10.7554/eLife.27159Full textFull text of the publication as PDF document
  195. 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
  196. 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
  197. 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
  198. 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
  199. 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
  200. 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
  201. 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
  202. 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
  203. 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
  204. Fast and efficient synthesis of microporous polymer nanomembranes via light-induced click reaction
    An, Q.; Hassan, Y.; Yan, X.; Krolla-Sidenstein, P.; Mohammed, T.; Lang, M.; Bräse, S.; Tsotsalas, M.
    2017. Beilstein journal of organic chemistry, 13, 558–563. doi:10.3762/bjoc.13.54Full textFull text of the publication as PDF document
  205. 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
  206. Oxidation of diazenyl-protected N-heterocycles-a new entry to functionalized lactams
    Petrović, M.; Scarpi, D.; Nieger, M.; Jung, N.; Occhiato, E. G.; Bräse, S.
    2017. RSC Advances, 7 (16), 9461–9464. doi:10.1039/c6ra26546dFull textFull text of the publication as PDF document
  207. 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
  208. 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
  209. 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
  210. 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
  211. 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
  212. 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
  213. 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) 
  214. Tunable molecular separation by nanoporous membranes
    Wang, Z.; Knebel, A.; Grosjean, S.; Wagner, D.; Bräse, S.; Wöll, C.; Caro, J.; Heinke, L.
    2016. Nature Communications, 7, 13872. doi:10.1038/ncomms13872Full textFull text of the publication as PDF document
  215. EXAFS characterisation of metal bonding in highly luminescent, UV stable, water-soluble and biocompatible lanthanide complexes
    Kalyakina, A.; Utochnikova, V.; Trigub, A.; Zubavichus, Y.; Kuzmina, N.; Bräse, S.
    2016. Journal of physics / Conference Series, 712, 012137. doi:10.1088/1742-6596/712/1/012137Full textFull text of the publication as PDF document
  216. 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
  217. 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
  218. Synthesis of three-dimensional porous hyper-crosslinked polymers via thiol-yne reaction
    Lang, M.; Schade, A.; Bräse, S.
    2016. Beilstein journal of organic chemistry, 12, 2570–2576. doi:10.3762/bjoc.12.252Full textFull text of the publication as PDF document
  219. 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
  220. Direct observation of intersystem crossing in a thermally activated delayed fluorescence copper complex in the solid state
    Bergmann, L.; Hedley, G. J.; Baumann, T.; Bräse, S.; Samuel, I. D. W.
    2016. Science advances, 2 (1), e1500889. doi:10.1126/sciadv.1500889Full textFull text of the publication as PDF document
  221. 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
  222. 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
  223. Towards Printed Organic Light-Emitting Devices: A Solution-Stable, Highly Soluble Cu-NHetPHOS
    Wallesch, M.; Verma, A.; Fléchon, C.; Flügge, H.; Zink, D. M.; Seifermann, S. M.; Navarro, J. M.; Vitova, T.; Göttlicher, J.; Steininger, R.; Weinhardt, L.; Zimmer, M.; Gerhards, M.; Heske, C.; Bräse, S.; Baumann, T.; Volz, D.
    2016. Chemistry - a European journal, 22 (46), 16400–16405. doi:10.1002/chem.201603847Full textFull text of the publication as PDF document
  224. 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
  225. 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
  226. 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
  227. 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
  228. NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents
    Görling, B.; Bräse, S.; Luy, B.
    2016. Metabolites, 6 (3), 27. doi:10.3390/metabo6030027Full textFull text of the publication as PDF document
  229. 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
  230. 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
  231. Radical exchange reaction of multi-spin isoindoline nitroxides followed by EPR spectroscopy
    Wessely, I.; Mugnaini, V.; Bihlmeier, A.; Jeschke, G.; Bräse, S.; Tsotsalas, M.
    2016. RSC Advances, 6 (61), 55715–55719. doi:10.1039/c6ra06510dFull textFull text of the publication as PDF document
  232. 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
  233. 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
  234. High-flexibility combinatorial peptide synthesis with laser-based transfer of monomers in solid matrix material
    Loeffler, F. F.; Foertsch, T. C.; Popov, R.; Mattes, D. S.; Schlageter, M.; Sedlmayr, M.; Ridder, B.; Dang, F.-X.; Bojnicic-Kninski, C. von; Weber, L. K.; Fischer, A.; Greifenstein, J.; Bykovskaya, V.; Buliev, I.; Bischoff, F. R.; Hahn, L.; Meier, M. A. R.; Bräse, S.; Powell, A. K.; Balaban, T. S.; Breitling, F.; Nesterov-Mueller, A.
    2016. Nature Communications, 7, Article number 11844. doi:10.1038/ncomms11844Full textFull text of the publication as PDF document
  235. 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
  236. 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
  237. 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
  238. 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
  239. 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
  240. 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
  241. 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
  242. Synthesis and post-synthetic modification of amine-, alkyne-, azide- and nitro-functionalized metal-organic frameworks based on DUT-5
    Gotthardt, M. A.; Grosjean, S.; Brunner, T. S.; Kotzel, J.; Gänzler, A. M.; Wolf, S.; Bräse, S.; Kleist, W.
    2015. Dalton transactions, 44 (38), 16802–16809. doi:10.1039/c5dt02276bFull textFull text of the publication as PDF document
  243. 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 
  244. 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 
  245. 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
  246. Chemical synthesis and enzymatic, stereoselective hydrolysis of a functionalized dihydropyrimidine for the synthesis of β-amino acids
    Slomka, C.; Zhong, S.; Fellinger, A.; Engel, U.; Syldatk, C.; Bräse, S.; Rudat, J.
    2015. AMB Express, 5 (1), 85. doi:10.1186/s13568-015-0174-8Full textFull text of the publication as PDF document
  247. 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
  248. 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
  249. 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
  250. 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
  251. 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
  252. 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
  253. 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
  254. 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
  255. 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
  256. Ruthenium-catalyzed C-H activation of thioxanthones
    Wagner, D.; Bräse, S.
    2015. Beilstein journal of organic chemistry, 11, 431–435. doi:10.3762/bjoc.11.49Full textFull text of the publication as PDF document
  257. 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
  258. 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
  259. 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
  260. 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
  261. 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
  262. 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
  263. 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
  264. 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
  265. 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
  266. Photoswitching in nanoporous, crystalline solids: An experimental and theoretical study for azobenzene linkers incorporated in MOFs
    Wang, Z.; Heinke, L.; Jelic, J.; Cakici, M.; Dommaschk, M.; Maurer, R. J.; Oberhofer, H.; Grosjean, S.; Herges, R.; Bräse, S.; Reuter, K.; Wöll, C.
    2015. Physical chemistry, chemical physics, 17 (22), 14582–14587. doi:10.1039/c5cp01372kFull textFull text of the publication as PDF document
  267. 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
  268. 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
  269. 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
  270. 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
  271. 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
  272. 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
  273. 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
  274. 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
  275. Synthesis of highly functionalized C₆₀ fullerene derivatives and their applications in material and life sciences
    Yan, W.; Seifermann, S. M.; Pierrat, P.; Bräse, S.
    2015. Organic and Biomolecular Chemistry, 13 (1), 25–54. doi:10.1039/C4OB01663GFull textFull text of the publication as PDF document
  276. Xanthone dimers: a compound family which is both common and privileged
    Wezeman, T.; Bräse, S.; Masters, K.-S.
    2015. Natural Product Reports, 32 (1), 6–28. doi:10.1039/C4NP00050AFull textFull text of the publication as PDF document
  277. 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
  278. 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
  279. 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
  280. 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
  281. 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
  282. 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
  283. 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
  284. 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
  285. 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
  286. Azaporphine guest-host complexes in solution and gas-phase: evidence for partially filled nanoprisms and exchange reactions
    Weis, P.; Schwarz, U.; Hennrich, F.; Wagner, D.; Bräse, S.; Kappes, M.
    2014. Physical Chemistry Chemical Physics, 16 (13), 6225–6232. doi:10.1039/C3CP55486DFull textFull text of the publication as PDF document
  287. Asymmetric organocatalytic synthesis of 4,6-bis(1H-indole-3-yl)-piperidine-2 carboxylates
    Zhong, S.; Nieger, M.; Bihlmeier, A.; Shi, M.; Bräse, S.
    2014. Organic & biomolecular chemistry, 12 (20), 3265–3270. doi:10.1039/C4OB00234BFull textFull text of the publication as PDF document
  288. Switchable fluorescence by click reaction of a novel azidocarbazole dye
    Hörner, A.; Volz, D.; Hagendorn, T.; Furniss, D.; Greb, L.; Ronicke, F.; Nieger, M.; Schepers, U.; Bräse, S.
    2014. RSC Advances, 4 (23), 11528–11534. doi:10.1039/C3RA47964AFull textFull text of the publication as PDF document
  289. 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
  290. 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
  291. 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
  292. 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
  293. 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
  294. 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
  295. 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
  296. 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 
  297. Metal-catalyzed cross-coupling reactions and more
    Meijere, A. de; Bräse, S.; Oestreich, M.
    2014. Weinheim : Wiley-VCH, 2014 
  298. Das Internet der Dinge erobert das chemische Forschungslabor
    Lütjohann, D.; Jung, N.; Tremouilhac, P.; Bräse, S.
    2014. GIT Fachzeitschrift für das Laboratorium, (10), 22 
  299. 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
  300. A mild method for eliminating alkyl ethers to alkenes
    Lindner, S.; Bräse, S.
    2014. RSC Advances, 4 (56), 29439–29442. doi:10.1039/C4RA03785E
  301. 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
  302. 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
  303. Silver-mediated perfluoroalkylation reactions
    Hafner, A.; Jung, N.; Bräse, S.
    2014. Synthesis, 46, 1440–1447. doi:10.1055/s-0033-1341223
  304. 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
  305. 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
  306. 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
  307. 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
  308. 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
  309. 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
  310. 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