Publications


  1. The jasmonate biosynthesis Gene OsOPR7 can mitigate salinity induced mitochondrial oxidative stress.
    Asfaw, K. G.; Liu, Q.; Eghbalian, R.; Purper, S.; Akaberi, S.; Dhakarey, R.; Münch, S. W.; Wehl, I.; Bräse, S.; Eiche, E.; Hause, B.; Bogeski, I.; Schepers, U.; Riemann, M.; Nick, P.
    2021. Plant science, 316, 111156. doi:10.1016/j.plantsci.2021.111156
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. 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
  10. 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
  11. 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.; van Westen, G. J. P.; Heitman, L. H.; Bräse, S.
    2021. European Journal of Medicinal Chemistry, 220, Art. Nr. 113354. doi:10.1016/j.ejmech.2021.113354
  12. 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
  13. 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
  14. 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
  15. 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
  16. 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
  17. 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
  18. 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
  19. 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
  20. 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
  21. 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
  22. 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
  23. 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
  24. 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
  25. 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
  26. 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
  27. 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
  28. 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.; Hurrle, T.; Richer, W.; Decraene, C.; Thiele, W.; Utikal, J.; Abuillan, W.; Tanaka, M.; Herten, D.; 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
  29. 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
  30. 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
  31. 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
  32. 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
  33. 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
  34. 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
  35. 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. doi:10.1080/17415993.2021.2006659
  36. 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
  37. 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
  38. 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
  39. 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
  40. 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
  41. 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
  42. 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
  43. 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
  44. 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
  45. 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
  46. 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
  47. 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
  48. 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
  49. 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
  50. 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
  51. 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
  52. 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
  53. 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
  54. 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
  55. 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
  56. 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
  57. 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
  58. 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
  59. 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
  60. 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
  61. 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.; Lei, A.; Bräse, S.; Cossy, J.
    2020. Chemistry - a European journal, 26 (58), 13163–13169. doi:10.1002/chem.202001721
  62. 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
  63. 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
  64. 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
  65. 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
  66. 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
  67. 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
  68. 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
  69. 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
  70. 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
  71. 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
  72. 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
  73. 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
  74. 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
  75. 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
  76. 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
  77. 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
  78. 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
  79. Polymerization in MOF-Confined Nanospaces: Tailored Architectures, Functions, and Applications.
    Begum, S.; Hassan, Z.; Bräse, S.; Tsotsalas, M.
    2020. Langmuir, 36 (36), 10657–10673. doi:10.1021/acs.langmuir.0c01832
  80. 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
  81. 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
  82. 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
  83. 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
  84. 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
  85. 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
  86. The Staudinger Ligation.
    Bednarek, C.; Wehl, I.; Jung, N.; Schepers, U.; Bräse, S.
    2020. Chemical reviews, 120 (10), 4301–4354. doi:10.1021/acs.chemrev.9b00665
  87. 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
  88. 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
  89. 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
  90. 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
  91. 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
  92. 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
  93. 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
  94. 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
  95. 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
  96. 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
  97. 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
  98. 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
  99. 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
  100. 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
  101. 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
  102. 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
  103. 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
  104. 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
  105. 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
  106. 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
  107. 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
  108. 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
  109. 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
  110. 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
  111. 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
  112. 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
  113. 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
  114. 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
  115. 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
  116. 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
  117. 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
  118. 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
  119. 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
  120. 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
  121. 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
  122. 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
  123. 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
  124. 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
  125. 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
  126. 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
  127. 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
  128. 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
  129. 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
  130. 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
  131. 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
  132. 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
  133. 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
  134. 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
  135. 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
  136. 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
  137. 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
  138. 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
  139. 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
  140. 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
  141. 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
  142. 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
  143. 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
  144. 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
  145. 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
  146. 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
  147. 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
  148. 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
  149. 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
  150. (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
  151. 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
  152. 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
  153. 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
  154. 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
  155. 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
  156. 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
  157. 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
  158. 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
  159. 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
  160. 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
  161. 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
  162. 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
  163. 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
  164. 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, heiBOOKS Full textFull text of the publication as PDF document
  165. 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
  166. 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
  167. 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
  168. [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
  169. 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
  170. 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
  171. 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
  172. 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
  173. 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
  174. 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
  175. Ein Molekülarchiv als akademisch integrierte Service-Einrichtung.
    Jung, N.; Deckers, A.; Bräse, S.
    2017. Biospektrum, 23 (2), 212–214 
  176. 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
  177. 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
  178. 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
  179. 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
  180. 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
  181. 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
  182. 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
  183. 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
  184. 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
  185. 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
  186. 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
  187. 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
  188. 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
  189. 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
  190. 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
  191. 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
  192. 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
  193. 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
  194. 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
  195. 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, The Optical Society of America (OSA) 
  196. 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
  197. 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
  198. 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
  199. 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
  200. 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
  201. 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
  202. 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
  203. 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
  204. 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
  205. Towards Printed Organic Light-Emitting Devices: A Solution-Stable, Highly Soluble Cu-NHetPHOS.
    Wallesch, M.; Verma, A.; Fléchon, C.; Flügge, H.; Zink, D. M.; Seifermann, S. M.; Navarro, J. M.; Vitova, T.; Göttlicher, J.; Steininger, R.; Weinhardt, L.; Zimmer, M.; Gerhards, M.; Heske, C.; Bräse, S.; Baumann, T.; Volz, D.
    2016. Chemistry - a European journal, 22 (46), 16400–16405. doi:10.1002/chem.201603847
  206. 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
  207. 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
  208. 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
  209. 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
  210. 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
  211. 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
  212. 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
  213. 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
  214. 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
  215. 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
  216. 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
  217. 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
  218. 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
  219. 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
  220. 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
  221. 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
  222. 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
  223. 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
  224. 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
  225. 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 
  226. 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 
  227. 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
  228. 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
  229. 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
  230. 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
  231. 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
  232. 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
  233. 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
  234. 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
  235. 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
  236. 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
  237. 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
  238. 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
  239. 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
  240. 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
  241. 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
  242. 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
  243. 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
  244. 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
  245. 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
  246. 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
  247. 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
  248. 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
  249. 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
  250. 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
  251. 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
  252. 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
  253. 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
  254. 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
  255. 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
  256. 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
  257. 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
  258. 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
  259. 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
  260. 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
  261. 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
  262. 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
  263. 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
  264. 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
  265. 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
  266. 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
  267. 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
  268. 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
  269. 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
  270. 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
  271. 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
  272. 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
  273. 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
  274. 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
  275. 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
  276. 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
  277. 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
  278. Cross-coupling of organyl halides with alkenes The Heck reaction.
    Bräse, S.; de Meijere, A.
    2014. de Meijere, A. [Hrsg.] Metal-Catalyzed Cross-Coupling Reactions and More Weinheim : Wiley-VCH, 2014, 533–663 
  279. Metal-catalyzed cross-coupling reactions and more.
    de Meijere, A.; Bräse, S.; Oestreich, M.
    2014. Weinheim : Wiley-VCH, 2014 
  280. Das Internet der Dinge erobert das chemische Forschungslabor.
    Lütjohann, D.; Jung, N.; Tremouilhac, P.; Bräse, S.
    2014. GIT Fachzeitschrift für das Laboratorium, (10), 22 
  281. 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
  282. A mild method for eliminating alkyl ethers to alkenes.
    Lindner, S.; Bräse, S.
    2014. RSC Advances, 4 (56), 29439–29442. doi:10.1039/C4RA03785E
  283. 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
  284. 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
  285. Silver-mediated perfluoroalkylation reactions.
    Hafner, A.; Jung, N.; Bräse, S.
    2014. Synthesis, 46, 1440–1447. doi:10.1055/s-0033-1341223
  286. 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
  287. 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
  288. 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
  289. 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
  290. 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
  291. 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
  292. 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
  293. A new route to dithia- and thiaoxacyclooctynes via Nicholas reaction.
    Hagendorn, T.; Bräse, S.
    2014. RSC Advances, 4, 15493–15495. doi:10.1039/C4RA01345J
  294. Luminescent cell-penetrating pentadecanuclear lanthanide clusters.
    Thielemann, D. T.; Wagner, A. T.; Rösch, E.; Kölmel, D. K.; Heck, J. G.; Rudat, B.; Neumaier, M.; Feldmann, C.; Schepers, U.; Bräse, S.; Roesky, P. W.
    2013. Journal of the American Chemical Society, 135 (20), 7454–7457. doi:10.1021/ja403539t
  295. Deuterium and tritium labelling of N-acyl-L-homoserine lactones (AHLs) by catalytic reduction of a double bond in the layer-by-layer method.
    Jakubczyk, D.; Merle, C.; Brenner-Weiss, G.; Luy, B.; Bräse, S.
    2013. European Journal of Organic Chemistry, (24), 5323–5330. doi:10.1002/ejoc.201300084
  296. Alternating asymmetric self-induction in functionalized pyrrolidine oligomers.
    Kudryavtsev, K. V.; Ivantcova, P. M.; Churakov, A. V.; Wiedmann, S.; Luy, B.; Muhle-Goll, C.; Zefirov, N. S.; Bräse, S.
    2013. Angewandte Chemie - International Edition, 52 (48), 12736–12740. doi:10.1002/anie.201302862
  297. Synthetic approaches to polycyclic semiochemicals and their derivatives: Combinatorial methods towards phytochemicals.
    Jung, N.; Gläser, F.; Bräse, S.
    2013. Phytochemistry Reviews, 12 (4), 603–651. doi:10.1007/s11101-013-9298-0
  298. Ortho-perfluoroalkylation and ethoxycarbonyldifluoromethylation of aromatic triazenes.
    Hafner, A.; Bihlmeier, A.; Nieger, M.; Klopper, W.; Bräse, S.
    2013. The journal of organic chemistry, 78 (16), 7938–7948. doi:10.1021/jo401145g
  299. Single and multiple additions of dibenzoylmethane onto buckminsterfullerene.
    Giovannitti, A.; Seifermann, S. M.; Bihlmeier, A.; Muller, T.; Topic, F.; Rissanen, K.; Nieger, M.; Klopper, W.; Bräse, S.
    2013. European journal of organic chemistry, (35), 7907–7913. doi:10.1002/ejoc.201301146
  300. Tethering for selective synthesis of 2,2’-biphenols: The acetal method.
    Masters, K.-S.; Bihlmeier, A.; Klopper, W.; Bräse, S.
    2013. Chemistry - a European journal, 19 (52), 17827–17835. doi:10.1002/chem.201301969
  301. Roadmap towards N-Heterocyclic [2.2]Paracyclophanes and their application in asymmetric catalysis.
    Busch, M.; Cayir, M.; Nieger, M.; Thiel, W. R.; Bräse, S.
    2013. European Journal of Organic Chemistry, (27), 6108–6123. doi:10.1002/ejoc.201300508
  302. A stereoselective approach to functionalized cyclohexenones.
    Meister, A. C.; Sauter, P. F.; Bräse, S.
    2013. European Journal of Organic Chemistry, (31), 7110–7116. doi:10.1002/ejoc.201300752
  303. Trifluoromethylation of 1-aryl-3,3-diisopropyltriazenes.
    Hafner, A.; Bräse, S.
    2013. Advanced Synthesis and Catalysis, 355, 996–1000. doi:10.1002/adsc.201201040
  304. Molecular construction kit for tuning solubility, stability and luminescence properties: Heteroleptic MePyrPHOS-copper iodide-complexes and their application in organic light-emitting diodes.
    Volz, D.; Zink, D. M.; Bocksrocker, T.; Friedrichs, J.; Nieger, M.; Baumann, T.; Lemmer, U.; Bräse, S.
    2013. Chemistry of materials, 25 (17), 3414–3426. doi:10.1021/cm4010807
  305. Soccer goes BOXing: synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes.
    Seifermann, S. M.; Réthoré, C.; Muller, T.; Bräse, S.
    2013. Scientific reports, 3, 2817. doi:10.1038/srep02817Full textFull text of the publication as PDF document
  306. Amphiphilic peptoid transporters - synthesis and evaluation.
    Vollrath, S. B. L.; Fürniss, D.; Schepers, U.; Bräse, S.
    2013. Organic and Biomolecular Chemistry, 11, 8197–8201. doi:10.1039/C3OB41139G
  307. Chemie auf der Spitze des Eisbergs: Zu viele Forschungsdaten gehen bislang unter!.
    Jung, N.; Lütjohann, D.
    2013. Chemie in unserer Zeit, 47, 334–335. doi:10.1002/ciuz.201390062
  308. The chemistry of mycotoxins.
    Bräse, S.; Gläser, F.; Kramer, C. S.; Lindner, S.; Linsenmeier, A. M.; Masters, K. S.; Meister, A. C.; Ruff, B. M.; Zhong, S.
    2013. Wien [u.a.] : Springer, 2013 (Progress in the Chemistry of Organic and Natural Products ; 97) 
  309. Post-synthetic modification of metal-organic framework thin films using click chemistry: The importance of strained C-C triple bonds.
    Wang, Z.; Liu, J.; Arslan, H. K.; Grosjean, S.; Hagendorn, T.; Gliemann, H.; Bräse, S.; Wöll, C.
    2013. Langmuir, 29, 15958–15964. doi:10.1021/la403854w
  310. Delphinidin is a novel inhibitor of lymphangiogenesis but promotes mammary tumor growth and metastasis formation in syngeneic experimental rats.
    Thiele, W.; Rothley, M.; Teller, N.; Jung, N.; Bulat, B.; Plaumann, D.; Vanderheiden, S.; Schmaus, A.; Cremers, N.; Göppert, B.; Dimmler, A.; Eschbach, V.; Quagliata, L.; Thaler, S.; Marko, D.; Bräse, S.; Sleeman, J. P.
    2013. Carcinogenesis, 34, 2804–2813. doi:10.1093/carcin/bgt291
  311. Heteroleptic, dinuclear copper(I) complexes for application in organic light-emitting diodes.
    Zink, D. M.; Volz, D.; Baumann, T.; Mydlak, M.; Flügge, H.; Friedrichs, J.; Nieger, M.; Bräse, S.
    2013. Chemistry of Materials, 25, 4471–4486. doi:10.1021/cm4018375
  312. Copper(I) complexes based on five-membered (PN)-N-boolean AND heterocycles: Structural diversity linked to exciting luminescence properties.
    Zink, D. M.; Baumann, T.; Friedrichs, J.; Nieger, M.; Bräse, S.
    2013. Inorganic Chemistry, 52, 13509–13520. doi:10.1021/ic4019162
  313. BOX structures with additional coordination sites: potential ligands for bifunctional catalysis.
    Seifermann, S. M.; Muller, T.; Bräse, S.
    2013. European Journal of Organic Chemistry, (16), 3215–3218. doi:10.1002/ejoc.201300279
  314. Thiourea-catalyzed Diels-Alder reaction of a naphthoquinone monoketal dienophile.
    Kramer, C. S.; Bräse, S.
    2013. Beilstein Journal of Organic Chemistry, 9, 1414–1418. doi:10.3762/bjoc.9.158
  315. Synthesis of CF₃-substituted olefins by Julia-Kocienski olefination using 2-[(2,2,2-trifluoroethyl)sulfonyl]benzo[d]thiazole as trifluoromethylation agent.
    Hafner, A.; Fischer, T. S.; Bräse, S.
    2013. European Journal of Organic Chemistry, (35), 7996–8003. doi:10.1002/ejoc.201301070
  316. A radical access to highly functionalized tetrahydroxanthones.
    Meister, A. C.; Nieger, M.; Bräse, S.
    2013. Chemistry - A European Journal, 19, 10836–10839. doi:10.1002/chem.201301358
  317. Influence of Perfluorinated End Groups on the SFRD of [Pt(cod)Me(CnF2n+1)] onto Porous Al2O3 in CO2 under Reductive Conditions.
    Aggarwal, V.; Reichenbach, L. F.; Enders, M.; Muller, T.; Wolff, S.; Crone, M.; Türk, M.; Bräse, S.
    2013. Chemistry - a European journal, 19 (38), 12794–12799. doi:10.1002/chem.201301191
  318. Controlled microstructuring of Janus particles based on a multifunctional poly(ethylene glycol).
    Sokolovskaya, E.; Yoon, J.; Misra, A. C.; Bräse, S.; Lahann, J.
    2013. Macromolecular Rapid Communications, 34, 1554–1559. doi:10.1002/marc.201300427
  319. A chemical screening procedure for glucocorticoid signaling with a Zebrafish larva luciferase reporter system.
    Weger, B. D.; Weger, M.; Jung, N.; Lederer, C.; Bräse, S.; Dickmeis, T.
    2013. Journal of Visualized Experiments, 79, e50439/1–9. doi:10.3791/50439
  320. Peptoid-based rare-earth (group 3 and lanthanide) transporters.
    Kölmel, D. K.; Rudat, B.; Schepers, U.; Bräse, S.
    2013. European Journal of Organic Chemistry, (14), 2761–2765. doi:10.1002/ejoc.201300219
  321. Outstanding luminescence from neutral copper(I) complexes with pyridyl-tetrazolate and phosphine ligands.
    Bergmann, L.; Friedrichs, J.; Mydlak, M.; Baumann, T.; Nieger, M.; Bräse, S.
    2013. Chemical Communications, 49, 6501–6503. doi:10.1039/C3CC42280A
  322. Silver-mediated methoxycarbonyltetrafluoroethylation of arenes.
    Hafner, A.; Feuerstein, T. J.; Bräse, S.
    2013. Organic Letters, 15, 3468–3471. doi:10.1021/ol401558z
  323. Antagonists for the orphan G-protein-coupled receptor GPR55 based on a coumarin scaffold.
    Rempel, V.; Volz, N.; Gläser, F.; Nieger, M.; Bräse, S.; Müller, C. E.
    2013. Journal of Medicinal Chemistry, 56, 4798–4810. doi:10.1021/jm4005175
  324. Rhodamine F: a novel class of fluorous ponytailed dyes for bioconjugation.
    Kölmel, D. K.; Rudat, B.; Braun, D. M.; Bednarek, C.; Schepers, U.; Bräse, S.
    2013. Organic and Biomolecular Chemistry, 11, 3954–3962. doi:10.1039/C3OB40267C
  325. The acetal concept: regioselective access to ortho,ortho-diphenols via dibenzo-1,3,dioxepines.
    Masters, K. S.; Bräse, S.
    2013. Angewandte Chemie - International Edition, 52, 866–869. doi:10.1002/anie.201207485
  326. Peptoids and polyamines going sweet: Modular synthesis of glycosylated peotoids and polyamines using click chemistry.
    Fürniss, D.; Mack, T.; Hahn, F.; Vollrath, S. B. L.; Koroniak, K.; Schepers, U.; Bräse, S.
    2013. Beilstein Journal of Organic Chemistry, 9, 56–63. doi:10.3762/bjoc.9.7
  327. Structural Characterization of a Peptoid with Lysine-like Side Chains and Biological Activity using NMR and Computational Methods.
    Sternberg, U.; Birtalan, E.; Jakovkin, I.; Luy, B.; Schepers, U.; Bräse, S.; Muhle-Goll, C.
    2013. Organic and Biomolecular Chemistry, 11 (4), 640–647. doi:10.1039/c2ob27039k
  328. Neue Katalysatoren für Übergangsmetall-katalysierte Aziridin-Synthesen.
    Jung, N.; Bräse, S.
    2012. Angewandte Chemie, 124 (23), 5632–5634. doi:10.1002/ange.201200966
  329. Xanthones from Fungi, Lichens and Bacteria : The Natural Products and their Synthesis.
    Masters, K.-S.; Bräse, S.
    2012. Chemical reviews, 112 (7), 3717–3776. doi:10.1021/cr100446h
  330. Cell Penetrating Peptoids (CPPos): Synthesis of a Small Combinatorial Library by Using IRORI MiniKans.
    Kölmel, D. K.; Fürniss, D.; Susanto, S.; Lauer, A.; Grabher, C.; Bräse, S.; Schepers, U.
    2012. Pharmaceuticals, 5 (12), 1265–1281. doi:10.3390/ph5121265
  331. Synthesis of Functionalized Glutamine- and Asparagine-Type Peptoids : Scope and Limitations.
    Cardenal, C.; Vollrath, S. B. L.; Schepers, U.; Bräse, S.
    2012. Helvetica chimica acta, 95 (11), 2237–2248. doi:10.1002/hlca.201200451
  332. Killing double bonds softly: the reduction of polymer-bound alkenes.
    Fürniss, D.; Schepers, U.; Bräse, S.
    2012. RSC Advances, 2 (30), 11273–11278. doi:10.1039/c2ra22189f
  333. The plakotenins: biomimetic Diels-Alder reactions, total synthesis, structural investigations, and chemical biology.
    Bourcet, E.; Kaufmann, L.; Arzt, S.; Bihlmeier, A.; Klopper, W.; Schepers, U.; Bräse, S.
    2012. Chemistry - a European journal, 18 (47), 15004–15020. doi:10.1002/chem.201201585
  334. Highly enantioselective access to cannabinoid-type tricyles by organocatalytic Diels-Alder reactions.
    Bräse, S.; Volz, N.; Gläser, F.; Nieger, M.
    2012. Beilstein journal of organic chemistry, 8, 1385–1392. doi:10.3762/bjoc.8.160Full textFull text of the publication as PDF document
  335. Secretome Protein Enrichment with Click Sugars Identifies Physiological Substrates of the Alzheimer Protease BACE1 in Primary Neurons.
    Kuhn, P. H.; Koroniak, K.; Hogl, S.; Colombo, A.; Zeitschel, U.; Willem, M.; Volbracht, C.; Schepers, U.; Imhof, A.; Hoffmeister, A.; Haass, C.; Roßner, S.; Bräse, S.; Lichtenthaler, S. F.
    2012. The EMBO journal, 31 (14), 3157–3168. doi:10.1038/emboj.2012.173
  336. Photochemistry with laser radiation in condensed phase using miniaturized photoreactors.
    Bremus-Köbberling, E.; Gillner, A.; Avemaria, F.; Réthoré, C.; Bräse, S.
    2012. Beilstein journal of organic chemistry, 8, 1213–1218. doi:10.3762/bjoc.8.135Full textFull text of the publication as PDF document
  337. Interkingdom Signaling: Integration, Conformation, and Orientation of N-Acyl-L-Homoserine Lactones in Supported Lipid Bilayers.
    Barth, C.; Jakubczyk, D.; Kubas, A.; Anastassacos, F.; Brenner-Weiss, G.; Fink, K.; Schepers, U.; Bräse, S.; Koelsch, P.
    2012. Langmuir, 28 (22), 8456–8462. doi:10.1021/la301241s
  338. Deuterium labelled N-acyl-L-homoserine lactones (AHLs) - Inter-kingdom signalling molecules - synthesis, structural studies, interaction with model lipid membranes.
    Jakubczyk, D.; Barth, C.; Kubas, A.; Anastassacos, F.; Koelsch, P.; Fink, K.; Schepers, U.; Brenner-Weiß, G.; Bräse, S.
    2012. Analytical and bioanalytical chemistry, 403 (2), 473–482. doi:10.1007/s00216-012-5839-4
  339. Vinyl- und Alkinyl-Azide: altbekannte Intermediate im Fokus moderner Synthesemethoden.
    Jung, N.; Bräse, S.
    2012. Angewandte Chemie, 124, 12335–12337. doi:10.1002/ange.201206409
  340. Synthesis of diverse indole libraries on polystyrene resin. Scope and limitations of an organometallic reaction on solid supports.
    Knepper, K.; Vanderheiden, S.; Bräse, S.
    2012. Beilstein Journal of Organic Chemistry, 8, 1191–1199. doi:10.3762%2Fbjoc.8.132
  341. New catalysts for the transition-metal-catalyzed synthesis of aziridines.
    Jung, N.; Bräse, S.
    2012. Angewandte Chemie - International Edition, 51, 5538–5540. doi:10.1002/anie.201200966
  342. Photophysical properties of fluorescently-labeled peptoids.
    Rudat, B.; Birtalan, E.; Vollrath, S. B. L.; Fritz, D.; Kölmel, D. K.; Nieger, M.; Schepers, U.; Müllen, K.; Eisler, H.-J.; Lemmer, U.; Bräse, S.
    2011. European Journal of Medicinal Chemistry, 46 (9), 4457–4465. doi:10.1016/j.ejmech.2011.07.020
  343. Bioconjugation via azide-Staudinger ligation: an overview.
    Schilling, C. I.; Jung, N.; Biskup, M. B.; Schepers, U.; Bräse, S.
    2011. Chemical Society Reviews, 40 (9), 4840–4871. doi:10.1039/C0CS00123F
  344. Investigating rhodamine B-labelled peptoids: Scopes and Limitations of its applications.
    Birtalan, E.; Rudat, B.; Kölmel, D. K.; Fritz, D.; Vollrath, S. B. L.; Schepers, U.; Bräse, S.
    2011. Peptide science, 96 (5), 694–701. doi:10.1002/bip.21617
  345. Multi-Gram Synthesis of a Hyaluronic Acid Subunit and Synthesis of Fully Protected Oligomers.
    Virlouvet, M.; Gartner, M.; Koroniak, K.; Sleeman, J. P.; Bräse, S.
    2010. Advanced synthesis & catalysis, 352 (14-15), 2657–2662. doi:10.1002/adsc.201000008
  346. Synthesis of aryl fluorides on a solid support and in solution by utilizing a fluorinated solvent.
    Döbele, M.; Vanderheiden, S.; Jung, N.; Bräse, S.
    2010. Angewandte Chemie - International Edition, 49, 5986–88. doi:10.1002/anie.201001507