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Publications

 

D. Lütjohann, N. Jung, S. Bäse, Chemometrics and Intelligent Laboratory Systems, 2015, 144, 100-107, Open source life science automation: Design of experiments and data acquisition via "dial-a-device".

D. Althuon, F. Rönicke, D. Fürniss, J. Quan, I. Wellhöfer, N. Jung, U. Schepers, S. Bräse, Org. Biomol. Chem. 2015, 13, 4226-4230. Functionalized Triazolopeptoids – a class for mitochondrial targeted delivery.

 

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., JBC 2014; 289(13); 8839–51, “Coregulator Control of Androgen Receptor Action by a Novel Nuclear Receptor-Binding Motif”.

Jung, N.; Stanek, B.; Grässle, S.; Nieger, M.; Bräse, S., Org. Lett. 2014; 1112–1115, “Reactions of Resin-Bound Triazenes with Dithianylium Tetrafluoroborates: Efficient Synthesis of α-Azo Ketene Dithioacetals and Related Hydrazones”.

Jung, N.; Grässle, S.; Lütjohann, D. S.; Bräse, S., Org. Lett. 2014; 1036–1039. „Solid-Supported Odorless Reagents for the Dithioacetalization of Aldehydes and Ketones”.

 

Dominik K. Kölmel, Nicole Jung, Stefan Bräse, Aust. J. Chem. 2013,  “Azides – Diazonium ions – Triazenes: Versatile nitrogen-rich functional groups.” http://dx.doi.org/10.1071/CH13533

Jung, N., et al., Phytochem. Rev.  2013, Volume 12, Issue 4, pp 603-651, "Synthetic approaches to polycyclic semiochemicals and their derivatives: combinatorial methods towards phytochemicals."

Jung, N.; Lütjohann, D. S., Chemie in unserer Zeit 2013; 47(6), „Chemie auf der Spitze des Eisbergs: Zu viele Forschungsdaten gehen bislang unter!“.

Weger, B. D., et al. (2013). "A chemical screening procedure for glucocorticoid signaling with a zebrafish larva luciferase reporter system." J Vis Exp (79).

Jung, N. and S. Bräse (2013). Click Reactions: Azide-Alkyne Cycloaddition. Kirk-Othmer Encyclopedia of Chemical Technology, John Wiley & Sons, Inc.

Thiele, W., et al. (2013). "Delphinidin is a novel inhibitor of lymphangiogenesis but promotes mammary tumor growth and metastasis formation in syngeneic experimental rats." Carcinogenesis 2013, 34(12):2804–13.

 

 

 

 

·         K. Knepper, S. Vanderheiden, S. Braese, Beilstein Journal of Organic Chemistry, 2012, 8, 1191-1199, No. 132, Synthesis of diverse indole libraries on polystyrene resin - scope and limitations of an organometallic reaction on solid supports. 

 

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

 

 

 

N.     N. Jung, S. Bräse, Angew. Chem. 2012, 124, 5632–5634; Angew. Chem. Int. Ed. 2012, 51, 5538-5540. Neue Katalysatoren für übergangsmetallkatalysierte Aziridin-Synthesen. New catalysts for the transition-metal-catalyzed snthesis of aziridines.  

 

 

N.     N. Jung, S. Bräse, Angew. Chem. 2012, 49, 12335-12337. Vinyl- und Alkinyl-Azide: altbekannte Intermediate im Fokus moderner Synthesemethoden.

 

 

 

      Schilling, Christine I.; Jung, Nicole; Biskup, Moritz; Schepers, Ute; Braese, Stefan, Chemical Society Reviews 2011, 40(9), 4840-4871, Bioconjugation via azide-Staudinger ligation: an overview.

 

 

S. Vanderheiden, B. Bulat, T. Zevaco, N. Jung and S. Bräse, Chem. Commun., 2011,47, 9063-9065, Solid phase synthesis of selectively deuterated arenes.

 

M.Döbele, S. Vanderheiden, N.Jung, S. Bräse, Angew. Chem. 2010, 122, 6122-6125, Synthese von Fluorarenen in flüssiger und an fester Phase unter Verwendung eines fluorierten Lösungsmittels, Angew. Chem. Int. Ed. 2010, 49, 5986-5988, Synthesis of Aryl Fluorides on a Solid Support and in Solution by Utilizing a Fluorinated Solvent.

 

N. Jung, S. Bräse, Eur. J. Org. Chem. 2009, 4494-4502. Synthesis of Natural Products on Solid Phases via Copper-Mediated Coupling: Synthesis of the Aristogin-Family, Spiraformin A and Hernandial

 

P. Pierrat, S. Vanderheiden, T. Muller, S. Bräse, Chem. Commun. 2009, 1748-1750. Functionalization of Hexakis Methanofullerene Malonate Crown-Ethers: Promising Octahedral Building Blocks for Molecular Networks.
Highlighted in: Synfacts 2009, 0613

 

R. Reingruber, S. Vanderheiden, T. Muller, M. Nieger, M. Es-Sayed, S. Bräse, Tetrahedron Lett. 2009, 50, 3439–3442, (invited for spezial issue: 50 years of Tetrahedron publications). Efficient synthesis of substituted 3-acyl-3,4-dihydrobenzo[d][1,2,3]triazines.

 

N. Jung, S. Bräse, J. Comb. Chem. 2009, 11, 47-71. Formation of Diaryl-Ethers on Solid Supports via Copper (I) Mediated Coupling.

 

R. Reingruber, S. Vanderheiden, A. Wagner, M. Nieger, T. Muller, M. Es-Sayed, S. Bräse, Eur. J. Org. Chem. 2008, 3314-3327. 1-Aryl-3,3-diisopropyltriazenes: An Easily Accessible and Particularly Stable Class of Triazenes Towards Strong Basic and Lewis Acid Conditions.

 

J. Toräng, S. Vanderheiden, M. Nieger, S. Bräse, Eur. J. Org. Chem. 2007, 943-952. Synthesis of 3-Alkylcoumarins from Salicylaldehydes and a,b-unsaturated Aldehydes utilizing Nucleophilic Carbenes: A New Umpoled Domino Reaction.

 

K.-H. Merz, T. Muller, S. Vanderheiden, G. Eisenbrand, D. Marko, S. Bräse, Synlett 2006, 3461-3463. An efficient Synthesis of a Lycobetaine-Tortuosine Analogue – A Potent Topoisomerase Inhibitor.

 

D. Keck, S. Vanderheiden, S. Bräse, Eur. J. Org. Chem. 2006, 4916-4923. A Formal Total Synthesis of Virantmycin: A Modular Approach towards Tetrahydroquinoline Natural Products.

 

K. Knepper, S. Vanderheiden, S. Bräse, Eur. J. Org. Chem. 2006, 1886-1898. Nitrogen Functionalities in Palladium-catalyzed Reactions on Solid Supports: A Case Study.

 

F. Lauterwasser, S. Vanderheiden, S. Bräse, Adv. Synth. Catal. 2006, 348, 443-448. Planar- and Central-Chiral N,O-[2.2]paracyclophane Ligands: Non-Linear Effects and Activity.

 

B. Lesch, J. Toräng, S. Vanderheiden, S. Bräse, Adv. Synth. Catal. 2005, 347, 555-562. Base-catalyzed condensation of 2-hydroxybenzaldehydes with a b -unsaturated aldehydes - scope and limitations.

 

H. Vogt, S. Vanderheiden, S. Bräse, Chem. Commun. 2003, 2448-2449. The proline-catalysed asymmetric amination of a,a-disubstituted aldehydes - Synthesis of configurationally stable enantioenriched a-aminoaldehyes.

 

F. Avemaria, S. Vanderheiden, S. Bräse, Tetrahedron 2003, 59, 6785-6796. The aza-xylylene Diels-Alder approach for the synthesis of naturally occurring 2-alkyl tetrahydroquinolines.

 

 

 

Buchartikel

 

 

S. Vanderheiden, N. Jung, S. Bräsein Solid-Phase Organic Syntheses, Volume 2, 2012, Heck Cleavage of Resin-Bound Triazenes.

 

N. Jung, S. Bräse, in Science of Synthesis, 2010, Volume Date2009, 41, 641-649, Product class 10: alkyltetrazenes.

 

 

·     N. Jung, S. Bräse, in Science of Synthesis, 2010, Volume Date2009, 41, 613-640, Product class 9: alkyltriazenes.

 

 

C. Schilling, N. Jung, S. Bräse, in Organic Azides – Syntheses and Applications, S. Bräse, K. Banert (Ed.), Wiley, 2009, 269-284. Cycloaddition Reactions with Azides: An Overview.

 

C. Schilling, N. Jung, S. Bräse, in Click Chemistry for Biotechnology and Materials Science, J. Lahann (Ed.), Chapter 2, Wiley 2009, xxxx. Common Synthons for Click Chemistry in Biotechnology.

 

C. Schilling, N. Jung, S. Bräse, in Click Chemistry for Biotechnology and Materials Science, J. Lahann (Ed.), Chapter 15, Wiley 2009, xxxx. Synthesis and Functionalization of Biomolecules via Click Chemistry.

 

N. Jung, S. Bräse, Science of Synthesis, Thieme, xxxx. Volume 41. Tetrazenes.

 

N. Jung, S. Bräse, Science of Synthesis, Thieme, xxxx. Volume 41. Triazenes.

 

M. Wiehn, N. Jung, S. Bräse, in The Power of Functional Resins in Organic Synthesis, F. Albercio, J. Tulla (Eds.), Wiley-VCH 2008, 437-465. Safety-Catch and Traceless Linkers in Solid-Phase Organic Synthesis.

 

 

N. Jung, M. Wiehn, S. Bräse, Top. Curr. Chem. 2007, Springer, Heidelberg. Multifunctional linkers for diversity-oriented solid phase syntheses.

 

N. Jung, A. Encinas, S. Bräse, Curr. Opin. Drug Disc. Develop. 2006, 9, 713-719. Automated solid-phase synthesis of heterocycle libraries.