Extraction of the intrinsic rate constant for a photocyclization reaction in capillary microreactors using a simplified reactor model
Li, J.; Šimek Tosino, H.; Ladewig, B. P.; Jung, N.; Bräse, S.; Dittmeyer, R.
2024. Reaction Chemistry & Engineering, 9 (8), 2149–2159. doi:10.1039/d4re00087k

Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
Neeb, A.; Figueiredo, I.; Bogdan, D.; Cato, L.; Stober, J.; Jiménez-Vacas, J. M.; Gourain, V.; Lee, I. I.; Seeger, R.; Muhle-Goll, C.; Gurel, B.; Welti, J.; Nava Rodrigues, D.; Rekowski, J.; Qiu, X.; Jiang, Y.; Di Micco, P.; Mateos, B.; Bielskutė, S.; Riisnaes, R.; Ferreira, A.; Miranda, S.; Crespo, M.; Buroni, L.; Ning, J.; Carreira, S.; Bräse, S.; Jung, N.; Gräßle, S.; Swain, A.; Salvatella, X.; Plymate, S. R.; Al-Lazikani, B.; Long, H. W.; Yuan, W.; Brown, M.; Cato, A. C. B.; de Bono, J. S.; Sharp, A.
2024. Molecular Cancer Therapeutics, 23 (6), 791–808. doi:10.1158/1535-7163.MCT-23-0354

Using the Chemotion repository to deposit and access FAIR research data for chemistry experiments
Huang, P.-C.; Lin, C.-L.; Tremouilhac, P.; Jung, N.; Bräse, S.
2024. Nature Protocols. doi:10.1038/s41596-024-01074-z

Synthesis of substituted triazole–pyrazole hybrids using triazenylpyrazole precursors
Gräßle, S.; Holzhauer, L.; Wippert, N.; Fuhr, O.; Nieger, M.; Jung, N.; Bräse, S.
2024. Beilstein Journal of Organic Chemistry, 20, 1396 – 1404. doi:10.3762/bjoc.20.121

Anti-Inflammatory Effects of GPR55 Agonists and Antagonists in LPS-Treated BV2 Microglial Cells
Sun, L.; Apweiler, M.; Normann, C.; Grathwol, C. W.; Hurrle, T.; Gräßle, S.; Jung, N.; Bräse, S.; Fiebich, B. L.
2024. Pharmaceuticals, 17 (6), Art.-Nr.: 674. doi:10.3390/ph17060674

Anti-Neuroinflammatory Effects of a Macrocyclic Peptide-Peptoid Hybrid in Lipopolysaccharide-Stimulated BV2 Microglial Cells
Sun, L.; Wilke Saliba, S.; Apweiler, M.; Akmermer, K.; Herlan, C.; Grathwol, C.; de Oliveira, A. C. P.; Normann, C.; Jung, N.; Bräse, S.; Fiebich, B. L.
2024. International Journal of Molecular Sciences, 25 (8), Artkl.Nr.:4462. doi:10.3390/ijms25084462

The Impact of Digitalized Data Management on Materials Systems Workflows
Tristram, F.; Jung, N.; Hodapp, P.; Schröder, R. R.; Wöll, C.; Bräse, S.
2024. Advanced Functional Materials, 34 (20), Art.-Nr.: 2303615. doi:10.1002/adfm.202303615

Functional Material Systems Enabled by Automated Data Extraction and Machine Learning
Kalhor, P.; Jung, N.; Bräse, S.; Wöll, C.; Tsotsalas, M.; Friederich, P.
2024. Advanced Functional Materials, 34 (20), Art.Nr.: 2302630. doi:10.1002/adfm.202302630

Identification of an imidazopyridine-based compound as an oral selective estrogen receptor degrader for breast cancer therapy
Pan, M.; Solozobova, V.; Kuznik, N. C.; Jung, N.; Graessle, S.; Gourain, V.; Heneka, Y. M.; Cramer von Clausbruch, C. A.; Fuhr, O.; Munuganti, R. S. N.; Maddalo, D.; Blattner, C.; Neeb, A.; Sharp, A.; Cato, L.; Weiss, C.; Jeselsohn, R. M.; Orian-Rousseau, V.; Bräse, S.; Cato, A. C. B.
2023. Cancer Research Communications, 3 (7), 1378–1396. doi:10.1158/2767-9764.CRC-23-0111

Controlled, Stepwise Syntheses of Oligomers with Modified Quinoxaline Backbones
Klein, J.; Jung, N.; Bräse, S.
2023. European Journal of Organic Chemistry, 26 (6), e202200764. doi:10.1002/ejoc.202200764

What is missing in autonomous discovery: open challenges for the community
Maffettone, P. M.; Friederich, P.; Baird, S. G.; Blaiszik, B.; Brown, K. A.; Campbell, S. I.; Cohen, O. A.; Davis, R. L.; Foster, I. T.; Haghmoradi, N.; Hereld, M.; Joress, H.; Jung, N.; Kwon, H.-K.; Pizzuto, G.; Rintamaki, J.; Steinmann, C.; Torresi, L.; Sun, S.
2023. Digital Discovery, 2 (6), 1644–1659. doi:10.1039/D3DD00143A

Pharmacological inhibition of TRPV2 attenuates phagocytosis and lipopolysaccharide‐induced migration of primary macrophages
Raudszus, R.; Paulig, A.; Urban, N.; Deckers, A.; Gräßle, S.; Vanderheiden, S.; Jung, N.; Bräse, S.; Schaefer, M.; Hill, K.
2023. British Journal of Pharmacology, 180 (21), 2736–2749. doi:10.1111/bph.16154

F‐Tag Induced Acyl Shift in the Photochemical Cyclization of o ‐Alkynylated N ‐Alkyl‐ N ‐acylamides to Indoles
Simek Tosino, H.; Jung, A.; Fuhr, O.; Muhle-Goll, C.; Jung, N.; Bräse, S.
2023. European Journal of Organic Chemistry, 26 (11), Art.-Nr.: e202201132. doi:10.1002/ejoc.202201132

Minimum Information Standards in Chemistry: A Call for Better Research Data Management Practices
Herres-Pawlis, S.; Bach, F.; Bruno, I. J.; Chalk, S. J.; Jung, N.; Liermann, J. C.; McEwen, L. R.; Neumann, S.; Steinbeck, C.; Razum, M.; Koepler, O.
2022. Angewandte Chemie International Edition, 61 (51), e202203038. doi:10.1002/anie.202203038

Droplet Microarray as a Powerful Platform for Seeking New Antibiotics Against Multidrug‐Resistant Bacteria
Lei, W.; Deckers, A.; Luchena, C.; Popova, A.; Reischl, M.; Jung, N.; Bräse, S.; Schwartz, T.; Krimmelbein, I. K.; Tietze, L. F.; Levkin, P. A.
2022. Advanced Biology, 6 (12), Art.-Nr.: 2200166. doi:10.1002/adbi.202200166

Metal Complexes as Antifungals? From a Crowd-Sourced Compound Library to the First Experiments
Frei, A.; Elliott, A. G.; Kan, A.; Dinh, H.; Bräse, S.; Bruce, A. E.; Bruce, M. R.; Chen, F.; Humaidy, D.; Jung, N.; King, A. P.; Lye, P. G.; Maliszewska, H. K.; Mansour, A. M.; Matiadis, D.; Muñoz, M. P.; Pai, T.-Y.; Pokhrel, S.; Sadler, P. J.; Sagnou, M.; Taylor, M.; Wilson, J. J.; Woods, D.; Zuegg, J.; Zuegg, J.; Meyer, W.; Cain, A. K.; Cooper, M. A.
2022. Journal of the American Chemical Society, 2 (10), 2277–2294. doi:10.1021/jacsau.2c00308

Sharing is Caring: Guidelines for Sharing in the Electronic Laboratory Notebook (ELN) Chemotion as applied by a Synthesis‐oriented Working Group
Fink, F.; Hüppe, H. M.; Jung, N.; Hoffmann, A.; Herres-Pawlis, S.
2022. Chemistry–Methods, 2 (10), Art.-Nr.: e202200026. doi:10.1002/cmtd.202200026

Scope of tetrazolo[1,5-a] quinoxalines in CuAAC reactions for the synthesis of triazoloquinoxalines, imidazoloquinoxalines, and rhenium complexes thereof
Holzhauer, L.; Liagre, C.; Fuhr, O.; Jung, N.; Bräse, S.
2022. Beilstein Journal of Organic Chemistry, 18, 1088–1099. doi:10.3762/bjoc.18.111

Data format standards in analytical chemistry
Rauh, D.; Blankenburg, C.; Fischer, T. G.; Jung, N.; Kuhn, S.; Schatzschneider, U.; Schulze, T.; Neumann, S.
2022. Pure and Applied Chemistry, 94 (6), 725–736. doi:10.1515/pac-2021-3101

A chemical probe for BAG1 targets androgen receptor-positive prostate cancer through oxidative stress signaling pathway
Kuznik, N. C.; Solozobova, V.; Lee, I. I.; Jung, N.; Yang, L.; Nienhaus, K.; Ntim, E. A.; Rottenberg, J. T.; Muhle-Goll, C.; Kumar, A. R.; Peravali, R.; Gräßle, S.; Gourain, V.; Deville, C.; Cato, L.; Neeb, A.; Dilger, M.; Cramer von Clausbruch, C. A.; Weiss, C.; Kieffer, B.; Nienhaus, G. U.; Brown, M.; Bräse, S.; Cato, A. C. B.
2022. iScience, 25 (5), Art.Nr. 104175. doi:10.1016/j.isci.2022.104175

Platinum Cyclooctadiene Complexes with Activity against Gram-positive Bacteria
Frei, A.; Ramu, S.; Lowe, G. J.; Dinh, H.; Semenec, L.; Elliott, A. G.; Zuegg, J.; Deckers, A.; Jung, N.; Bräse, S.; Cain, A. K.; Blaskovich, M. A. T.
2021. ChemMedChem, 16 (20), 3165–3171. doi:10.1002/cmdc.202100157

Development of a Benzothiazole Scaffold-Based Androgen Receptor N-Terminal Inhibitor for Treating Androgen-Responsive Prostate Cancer
Kuznik, N. C.; Solozobova, V.; Jung, N.; Gräßle, S.; Lei, Q.; Lewandowski, E. M.; Munuganti, R.; Zoubeidi, A.; Chen, Y.; Bräse, S.; Cato, A. C. B.
2021. ACS Chemical Biology, 16 (11), 2103–2108. doi:10.1021/acschembio.1c00390

In situ sensors for flow reactors – a review
Li, J.; Šimek, H.; Ilioae, D.; Jung, N.; Bräse, S.; Zappe, H.; Dittmeyer, R.; Ladewig, B. P.
2021. Reaction chemistry & engineering, 6 (9), 1497–1507. doi:10.1039/d1re00038a

ChemSpectra: a web-based spectra editor for analytical data
Huang, Y.-C.; Tremouilhac, P.; Nguyen, A.; Jung, N.; Bräse, S.
2021. Journal of Cheminformatics, 13 (1), Art.-Nr. 8. doi:10.1186/s13321-020-00481-0

Id1 and Id3 Are Regulated Through Matrix‐Assisted Autocrine BMP Signaling and Represent Therapeutic Targets in Melanoma
Sedlmeier, G.; Al-Rawi, V.; Buchert, J.; Yserentant, K.; Rothley, M.; Steshina, A.; Gräßle, S.; Wu, R.-L.; Hurrle, T.; Richer, W.; Decraene, C.; Thiele, W.; Utikal, J.; Abuillan, W.; Tanaka, M.; Herten, D.-P.; Hill, C. S.; Garvalov, B. K.; Jung, N.; Bräse, S.; Sleeman, J. P.
2021. Advanced therapeutics, 4 (2), Art.-Nr.: 2000065. doi:10.1002/adtp.202000065

A small molecule screen identifies novel inhibitors of mechanosensory nematocyst discharge in Hydra
Hofmann, D.; Garg, N.; Grässle, S.; Vanderheiden, S.; Bergheim, B. G.; Bräse, S.; Jung, N.; Özbek, S.
2021. Scientific reports, 11, Art.-Nr. 20627. doi:10.1038/s41598-021-99974-7

Chemotion Repository, a Curated Repository for Reaction Information and Analytical Data
Tremouilhac, P.; Huang, P.-C.; Lin, C.-L.; Huang, Y.-C.; Nguyen, A.; Jung, N.; Bach, F.; Bräse, S.
2021. Chemistry methods, 1 (1), 8–11. doi:10.1002/cmtd.202000034

NFDI4Chem – Infrastruktur für den digitalen Wandel in der Chemischen Forschung
Jung, N.; Neumann, S.; Koepler, O.; Bach, F.; Popp, C.; Herres-Pawlis, S.; Liermann, J.; Razum, M.; Steinbeck, C.
2021. Bunsen-Magazin, 23 (2), 100–103. doi:10.26125/r978-6f93

Synthesis of new pyrazolo[1,2,3]triazines by cyclative cleavage of pyrazolyltriazenes
Wippert, N.; Nieger, M.; Herlan, C.; Jung, N.; Bräse, S.
2021. Beilstein journal of organic chemistry, 17, 2773–2780. doi:10.3762/bjoc.17.187

The Repository Chemotion: Infrastructure for Sustainable Research in Chemistry
Tremouilhac, P.; Lin, C.-L.; Huang, P.-C.; Huang, Y.-C.; Nguyen, A.; Jung, N.; Bach, F.; Ulrich, R.; Neumair, B.; Streit, A.; Bräse, S.
2020. Angewandte Chemie / International edition, 59 (50), 22771–22778. doi:10.1002/anie.202007702

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

NFDI4Chem - Towards a National Research Data Infrastructure for Chemistry in Germany
Steinbeck, C.; Koepler, O.; Bach, F.; Herres-Pawlis, S.; Jung, N.; Liermann, J. C.; Neumann, S.; Razum, M.; Baldauf, C.; Biedermann, F.; Bocklitz, T. W.; Boehm, F.; Broda, F.; Czodrowski, P.; Engel, T.; Hicks, M. G.; Kast, S. M.; Kettner, C.; Koch, W.; Lanza, G.; Link, A.; Mata, R. A.; Nagel, W. E.; Porzel, A.; Schlörer, N.; Schulze, T.; Weinig, H.-G.; Wenzel, W.; Wessjohann, L. A.; Wulle, S.
2020. Research ideas and outcomes, (6), e55852, 1–100. doi:10.3897/rio.6.e55852

Correction: Metal complexes as a promising source for new antibiotics
Frei, A.; Zuegg, J.; Elliott, A. G.; Baker, M.; Braese, S.; Brown, C.; Chen, F.; Dowson, C. G.; Dujardin, G.; Jung, N.; King, A. P.; Mansour, A. M.; Massi, M.; Moat, J.; Mohamed, H. A.; Renfrew, A. K.; Rutledge, P. J.; Sadler, P. J.; Todd, M. H.; Willans, C. E.; Wilson, J. J.; Cooper, M. A.; Blaskovich, M. A. T.
2020. Chemical science, 11 (17), 4531. doi:10.1039/d0sc90075c

The Staudinger Ligation
Bednarek, C.; Wehl, I.; Jung, N.; Schepers, U.; Bräse, S.
2020. Chemical reviews, 120 (10), 4301–4354. doi:10.1021/acs.chemrev.9b00665

Metal complexes as a promising source for new antibiotics
Frei, A.; Zuegg, J.; Elliott, A. G.; Baker, M.; Braese, S.; Brown, C.; Chen, F.; Dowson, C. G.; Dujardin, G.; Jung, N.; King, A. P.; Mansour, A. M.; Massi, M.; Moat, J.; Mohamed, H. A.; Renfrew, A. K.; Rutledge, P. J.; Sadler, P. J.; Todd, M. H.; Willans, C. E.; Wilson, J. J.; Cooper, M. A.; Blaskovich, M. A. T.
2020. Chemical science, 11 (10), 2627–2639. doi:10.1039/c9sc06460e

A de novo strategy for predictive crystal engineering to tune excitonic coupling
Haldar, R.; Mazel, A.; Krstić, M.; Zhang, Q.; Jakoby, M.; Howard, I. A.; Richards, B. S.; Jung, N.; Jacquemin, D.; Diring, S.; Wenzel, W.; Odobel, F.; Wöll, C.
2019. Nature Communications, 10 (1), Art.Nr. 2048. doi:10.1038/s41467-019-10011-8

Miniaturized and Automated Synthesis of Biomolecules - Overview and Perspectives
Mattes, D. S.; Jung, N.; Weber, L. K.; Bräse, S.; Breitling, F.
2019. Advanced materials, 31 (26), Art.Nr. 1806656. doi:10.1002/adma.201806656

Toward Design of Novel Materials for Organic Electronics
Friederich, P.; Fediai, A.; Kaiser, S.; Konrad, M.; Jung, N.; Wenzel, W.
2019. Advanced materials, 31 (26), Art.Nr. 1808256. doi:10.1002/adma.201808256

Wie gelingt digitalisierte Forschung? Neues Open Source ELN für die Wissenschaft
Jung, N.; Tremouilhac, P.; Bach, F.; Kramer, C.; Bräse, S.; Ottleben, I.
2019. Labor-Praxis

ChemScanner: extraction and re-use(ability) of chemical information from common scientific documents containing ChemDraw files
Nguyen, A.; Huang, Y.-C.; Tremouilhac, P.; Jung, N.; Bräse, S.
2019. Journal of cheminformatics, 11 (1), Art. Nr.: 77. doi:10.1186/s13321-019-0400-5

Synthesis 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

Procedures for systematic capture and management of analytical data in academia
Potthoff, J.; Tremouilhac, P.; Hodapp, P.; Neumair, B.; Bräse, S.; Jung, N.
2019. Analytica Chimica Acta: X, 1, Article: 100007. doi:10.1016/j.acax.2019.100007

Chemotion-ELN part 2: adaption of an embedded Ketcher editor to advanced research applications
Kotov, S.; Tremouilhac, P.; Jung, N.; Bräse, S.
2018. Journal of cheminformatics, 10 (1), Art.Nr. 38. doi:10.1186/s13321-018-0292-9

Addition of dithi(ol)anylium tetrafluoroborates to α, β-unsaturated ketones
Huang, Y.-C.; Nguyen, A.; Gräßle, S.; Vanderheiden, S.; Jung, N.; Bräse, S.
2018. Beilstein journal of organic chemistry, 14, 515–522. doi:10.3762/bjoc.14.37

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

Chemotion ELN : an Open Source electronic lab notebook for chemists in academia
Tremouilhac, P.; Nguyen, A.; Huang, Y.-C.; Kotov, S.; Lütjohann, D. S.; Hübsch, F.; Jung, N.; Bräse, S.
2017. Journal of cheminformatics, 9 (1), Art.Nr. 54. doi:10.1186/s13321-017-0240-0

Ein Molekülarchiv als akademisch integrierte Service-Einrichtung
Jung, N.; Deckers, A.; Bräse, S.
2017. Biospektrum, 23 (2), 212–214

Development of Bag-1L as a therapeutic target in androgen receptor-dependent prostate cancer
Cato, L.; Neeb, A.; Sharp, A.; Buzón, V.; Ficarro, S. B.; Yang, L.; Muhle-Goll, C.; Kuznik, N. C.; Riisnaes, R.; Rodrigues, D. N.; Armant, O.; Gourain, V.; Adelmant, G.; Ntim, E. A.; Westerling, T.; Dolling, D.; Rescigno, P.; Figueiredo, I.; Fauser, F.; Wu, J.; Rottenberg, J. T.; Shatkina, L.; Ester, C.; Luy, B.; Puchta, H.; Troppmair, J.; Jung, N.; Bräse, S.; Strähle, U.; Marto, J. A.; Nienhaus, G. U.; Al-Lazikani, B.; Salvatella, X.; Bono, J. S. de; Cato, A. C. B.; Brown, M.
2017. eLife, 6, Art.Nr. e27159. doi:10.7554/eLife.27159

Synthesis and Investigation of S-Substituted 2-Mercaptobenzoimidazoles as Inhibitors of Hedgehog Signaling
Gräßle, S.; Susanto, S.; Sievers, S.; Tavsan, E.; Nieger, M.; Jung, N.; Stefan Bräse
2017. ACS medicinal chemistry letters, 8 (9), 931–935. doi:10.1021/acsmedchemlett.7b00100

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

Oxidation of diazenyl-protected N-heterocycles-a new entry to functionalized lactams
Petrović, M.; Scarpi, D.; Nieger, M.; Jung, N.; Occhiato, E. G.; Bräse, S.
2017. RSC Advances, 7 (16), 9461–9464. doi:10.1039/c6ra26546d

Synthesis of Diaziridines and Diazirines via Resin-Bound Sulfonyl Oximes
Protasova, I.; Bulat, B.; Jung, N.; Bräse, S.
2017. Organic letters, 19 (1), 34–37. doi:10.1021/acs.orglett.6b03252

Arenediazonium Tosylates (ADTs) as Efficient Reagents for Suzuki–Miyaura Cross-Coupling in Neat Water
Kutonova, K. V.; Jung, N.; Trusova, M. E.; Filimonov, V. D.; Postnikov, P. S.; Bräse, S.
2017. Synthesis, 49 (7), 1680–1688. doi:10.1055/s-0036-1588919

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

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

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

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

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

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

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

Reactions of resin-bound triazenes with dithianylium tetrafluoroborates: efficient synthesis of alpha-azo ketene dithioacetals and related hydrazones
Jung, N.; Stanek, B.; Gräßle, S.; Nieger, M.; Bräse, S.
2014. Organic letters, 16 (4), 1112–1115. doi:10.1021/ol4037133

Solid-Supported Odorless Reagents for the Dithioacetalization of Aldehydes and Ketones
Jung, N.; Grässle, S.; Lütjohann, D. S.; Bräse, S.
2014. Organic letters, 16 (4), 1036–1039. doi:10.1021/ol403313h

Das Internet der Dinge erobert das chemische Forschungslabor
Lütjohann, D.; Jung, N.; Tremouilhac, P.; Bräse, S.
2014. GIT Fachzeitschrift für das Laboratorium, (10), 22

Silver-mediated perfluoroalkylation reactions
Hafner, A.; Jung, N.; Bräse, S.
2014. Synthesis, 46, 1440–1447. doi:10.1055/s-0033-1341223

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

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

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

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

Neue Katalysatoren für Übergangsmetall-katalysierte Aziridin-Synthesen
Jung, N.; Bräse, S.
2012. Angewandte Chemie, 124 (23), 5632–5634. doi:10.1002/ange.201200966

Cell Penetrating Peptoids (CPPos): Synthesis of a Small Combinatorial Library by Using IRORI MiniKans
Kölmel, D. K.; Fürniss, D.; Susanto, S.; Lauer, A.; Grabher, C.; Bräse, S.; Schepers, U.
2012. Pharmaceuticals, 5 (12), 1265–1281. doi:10.3390/ph5121265

Synthesis of 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/bjoc.8.132

Continuously tunable solution-processed organic semiconductor DFB lasers pumped by laser diode
Klinkhammer, S.; Liu, X.; Huska, K.; Shen, Y.; Vanderheiden, S.; Valouch, S.; Vannahme, C.; Bräse, S.; Mappes, T.; Lemmer, U.
2012. Optics Express, 20 (6), 6357–6364. doi:10.1364/OE.20.006357

Vinyl- und Alkinyl-Azide: altbekannte Intermediate im Fokus moderner Synthesemethoden
Jung, N.; Bräse, S.
2012. Angewandte Chemie, 124, 12335–12337. doi:10.1002/ange.201206409

Synthesis of diverse indole libraries on polystyrene resin. Scope and limitations of an organometallic reaction on solid supports
Knepper, K.; Vanderheiden, S.; Bräse, S.
2012. Beilstein Journal of Organic Chemistry, 8, 1191–1199. doi:10.3762%2Fbjoc.8.132

New catalysts for the transition-metal-catalyzed synthesis of aziridines
Jung, N.; Bräse, S.
2012. Angewandte Chemie - International Edition, 51, 5538–5540. doi:10.1002/anie.201200966

Solid phase synthesis of selectively deuterated arenes
Vanderheiden, S.; Bulat, B.; Zevaco, T.; Jung, N.; Bräse, S.
2011. Chemical Communications, 47, 9063–9065. doi:10.1039/C1CC12950C

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

Synthese von Fluoraromaten in flüssiger und an fester Phase durch Verwendung fluorierter Lösungsmittel
Döbele, M.; Vanderheiden, S.; Jung, N.; Bräse, N.
2010. Angewandte Chemie, 122 (34), 6122–6125. doi:10.1002/ange.201001507

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

Synthesis of Natural Products on Solid Phases via Copper-Mediated Coupling: Synthesis of the Aristogin Family, Spiraformin A, and Hernandial
Jung, N.; Bräse, S.
2009. European Journal of Organic Chemistry, 2009 (26), 4494–4502. doi:10.1002/ejoc.200900632

Efficient synthesis of substituted 3-acyl-3,4-dihydrobenzo[d][1,2,3]triazines
Reingruber, R.; Vanderheiden, S.; Muller, T.; Nieger, M.; Es-Sayed, M.; Bräse, S.
2009. Tetrahedron Letters, 50 (26), 3439–3442. doi:10.1016/j.tetlet.2009.02.184

Functionalization of hexakis methanofullerene malonate crown-ethers: promising octahedral building blocks for molecular networks
Pierrat, P.; Vanderheiden, S.; Muller, T.; Bräse, S.
2009. Chemical Communications, (13), 1748–1750. doi:10.1039/B900367C

Diaryl Ether and Diaryl Thioether Syntheses on Solid Supports via Copper (I)-Mediated Coupling
Jung, N.; Bräse, S.
2009. Journal of Combinatorial Chemistry, 11 (1), 47–71. doi:10.1021/cc800032q

Automated solid-phase synthesis of heterocycle libraries
Jung, N.; Encinas, A.; Bräse, S.
2006. Current opinion in drug discovery & development, 9 (6), 713–728

An Interdisciplinary Approach to Manage Materials Data with Kadi4Mat and Chemotion
Altschuh, P.; Bräse, S.; Hartmann, T.; Jaeger, D.; Jung, N.; Koeppe, A.; Krauss, P.; Leister, C.; Nestler, B.; Schiefer, G.; Schreiber, C.; Selzer, M.; Starmann, M.; Tosato, G.
2023. E-Science-Tage 2023: Empower Your Research – Preserve Your Data. Ed.: Vincent Heuveline, Nina Bisheh, Philipp Kling, 264–269, heiBOOKS. doi:10.11588/heibooks.1288.c18086

Erfassung und Speicherung von Forschungsdaten im Fachbereich Chemie: Bereitstellung moderner Forschungs-infrastrukturen durch ein elektronisches Laborjournal mit Repositorium-Anbindung
Jung, N.; Tremouilhac, P.; Kramer, C.; Potthoff, J.
2017. E-Science-Tage 2017: Forschungsdaten managen. Hrsg.: J. Kratzke, 127–136, Heidelberger E-Books (heiBOOKS)

Cycloaddition Reactions with Azides: An Overview
Schilling, C.; Jung, N.; Bräse, S.
2009. Organic Azides: Syntheses and Applications. Ed.: S. Bräse, 269–284, John Wiley and Sons. doi:10.1002/9780470682517.ch9

Common Synthons for Click Chemistry in Biotechnology
Schilling, C.; Jung, N.; Bräse, S.
2009. Click Chemistry for Biotechnology and Materials Science. Ed.: J. Lahann, 9–28, John Wiley and Sons

Synthesis and Functionalization of Biomolecules via Click Chemistry
Schilling, C.; Jung, N.; Bräse, S.
2009. Click Chemistry for Biotechnology and Materials Science. Ed.: J. Lahann, 355–378, John Wiley and Sons. doi:10.1002/9780470748862.ch15

Tetrazenes
Jung, N.; Bräse, S.
2009. Science of Synthesis Houben-Weyl Methods of Molecular Transformations. Ed.: I. Shinkai, 641–650, Thieme Gruppe

Triazenes
Jung, N.; Bräse, S.
2009. Science of Synthesis Houben-Weyl Methods of Molecular Transformations. Ed.: I. Shinkai, 613–640, Thieme Gruppe

Safety-Catch and Traceless Linkers in Solid-Phase Organic Synthesis
Wiehn, M.; Jung, N.; Bräse, S.
2008. The Power of Functional Resins in Organic Synthesis. Ed.: F. Albercio, 437–465, Wiley-VCH Verlag

Multifunctional linkers for diversity-oriented solid phase syntheses
Jung, N.; Wiehn, M.; Bräse, S.
2007. Combinatorial Chemistry on Solid Supports, 1–88, Springer-Verlag

Synthese von Diazirinen über harzgebundene Sulfonyl-Oxime und in situ Raman-spektroskopische Untersuchungen von Festphasenreaktionen. Dissertation
Protasova, I.
2016. Logos Verlag Berlin

Neue Reaktionsmöglichkeiten von Dithianylium-Salzen. Dissertation
Stanek, B.
2015. Logos Verlag Berlin

Darstellung Diarylether-haltiger Naturstoffe an der festen Phase und Synthese neuartiger fluorierter Linker. Dissertation
Jung, N.
2008. Logos Verlag Berlin