Publikationsliste

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. PhD dissertation
Protasova, I.
2016. Logos Verlag Berlin

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

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

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

MoMaF Science Data Center für Molekulare Materialforschung
Altschuh, P.; Bach, F.; Bräse, S.; Hartmann, T.; Jung, N.; Krauß, P.; Nestler, B.; Schiefer, G.; Schreiber, C.; Selzer, M.; Terzijska, D.
2021. E-Science-Tage 2021: Share Your Research Data, Heidelberg, 04.03. - 05.03.2021. doi:10.11588/heidok.00029699

Synthesis of Substituted Triazole-Pyrazole Hybrids using Triazenopyrazoles Precursors
Graessle, S.; Holzhauer, L.; Wippert, N.; Fuhr, olaf; Nieger, M.; Jung, N.; Bräse, S.
2024. American Chemical Society (ACS). doi:10.26434/chemrxiv-2024-4j0rx

(Semi-) Automatic Review Process for Common Compound Characterization Data in Organic Synthesis
Huang, Y.-C.; Tremouilhac, P.; Kuhn, S.; Huang, P.-C.; Lin, C.-L.; Schlörer, N.; Taubert, O.; Götz, M.; Jung, N.; Bräse, S.
2024. ChemRxiv. doi:10.26434/chemrxiv-2024-1r9tb

A batch photoreactor for small-scale laboratory research - a technical note
Li, J.; Hodapp, P.; Ladewig, B. P.; Jung, N.; Dittmeyer, R.
2022. American Chemical Society (ACS). doi:10.26434/chemrxiv-2022-46w7s

NFDI4Chem – Fachkonsortium für die Chemie - Bausteine Forschungsdatenmanagement Empfehlungen und Erfahrungsberichte für die Praxis von Forschungsdatenmanagerinnen und -managern
Ortmeyer, J.; Schön, F.; Herres-Pawlis, S.; Jung, N.; Bach, F.; Liermann, J.; Neumann, S.; Popp, C.; Razum, M.; Koepler, O.; Steinbeck, C.
2021. doi:10.17192/bfdm.2021.2.8340