Publications

A. Papers in refereed journals (independent)

B. Papers in refereed journals (in press)

C. Book chapters and review articles

D. Book chapters and review articles (in press)

E. Papers in refereed journals (Doctorate and Postdoctorate)

F. Book chapters and review articles (Doctorate and Postdoctorate)

G. Articles in Proceedings (listed in Chemical Abstracts)

H. Other publications

I. Other publications (book reviews etc.)

J. Books

K. Patents

L. Series

Highlighted Papers

A Trifunctional Linker for Purified 3D Assembled Peptide Structure Arrays, https://www.advancedsciencenews.com/lets-play-proteins-microarrays-3d-assembled-peptide-structures/

ortho-Trofluoromethylation of Functionalized Triazenes, Synfacts 2012; 8: 0779-0779

Solid-Phase Synthesis of Trifluoromethyl-arenes, Synfacts 2012; 8: 0229-0229

Denitrogenative Deuteration of Solid-Supported Triazenes, Synfacts 2011; 2011: 1252-1252

Prepare hyper–cross-linked polymers by click polymerization

Synthesis of Diversonol, Synfacts 2006; 2006: 0639-0639

Pd(0)/JosiPhos-Catalyzed Desymmetrization, Synfacts 2006; 2006: 0793-0793

A. Papers in refereed journals (independent)

B. Papers in refereed journals (in press)

S. M. Marschner, R. Haldar, O. Fuhr, C. Wöll, S. Bräse, Chem. Eur. J. 2020, in press. Modular Synthesis of trans-A2B2-Porphyrins with Terminal Esters – Systematically Broadening the Scope of Linear Linkers for Porphyrin-Based MOFs 

https://doi.org/10.1002/chem.202003885

A. A. Aly, A. A. Hassan, N. K. Mohamed, M. Ramadan, A. S. Abd El-Aal, S. Bräse, M. Nieger, J. Chem. Res. 2020, in press. Quinones-based heterocycles of broad spectrum potent anticancer activity

https://doi.org/10.1177/1747519820959737

A. Aly, A. A. Hassan, A. Mahmoud, E. M. Osman, S. Bräse, M. Nieger, M. A. A. Ibrahim, S. M. Mostafa, Mol. Divers. 2020, in press. Synthesis of 3,3'-methylenebis(4-hydroxyquinolin-2(1H)-ones) of prospective anti-Covid-19 drugs

https://link.springer.com/article/10.1007%2Fs11030-020-10140-z

P. Tremouilhac, P.-C. Huang, C.-L. Lin, Y.-C. Huang, A. Nguyen, N. Jung, F. Bach, S. Bräse, Chem. Meth. 2020, in press. Chemotion repository, a curated repository for reaction information and analytical data

https://doi.org/10.1002/cmtd.202000034

Y. Matt, I. Wessely, L. Gramespacher, M. Tsotsalas, S. Bräse, Eur. J. Org. Chem. 2020, in press. Synthesis of Rigid Multidimensional Alkoxyamines: A Versatile Basis for Nitroxide Exchange Reaction and Nitroxide Mediated Polymerization

https://doi.org/10.1002/ejoc.202001415

P. Boden, P. Di Martino-Fumo, J. M. Busch, F. R. Rehak, S. Steiger, O. Fuhr, W. Klopper, S. Bräse, M. Gerhards, Chem. Eur. J. 2020, in press. Investigation of the Luminescence Pathways in Tetranuclear Cu(I) Complexes

chem.202004539

https://doi.org/10.1002/chem.202003885

C. Schissler, E. K. Schneider, B. Felker, P. Weis, M. Nieger, M. M. Kappes, S. Bräse, Chem Eur. J. 2020, in press. A new synthetic strategy for cofacial porphyrin-based homo and heterobimetallic complexes

chem.202002394R3

A. A. Aly, A. A. Hassan, M. Ramadan, M., M. Makhlouf, S. Mohammed Naguib Abdel Hafez, M. M.M. Refaie, S. Bräse, M. Nieger, Archiv Pharm. 2020, in press. Design, Synthesis of New hydrazinecarbothioamide sulfones as potential Antidiabetic agents

ardp.202000336

P. Puthanveetil, X. Kong, S. Bräse, G. Voros. W. A. Peer, Eur. J. Pharmcol. 2020, in press. Transcriptome analysis following treatment of two structurally related flavonoids, Apigenin and Chrysin revealed their hypocholesterolemic and ketogenic property in vitro

Y.-C. Huang, P. Tremouilhac, A. Nguyen, N. Jung, S. Bräse, J. Cheminform. 2020, in press. ChemSpectra: A web-based spectra editor for spectroscopic data

J. M. Busch, D. S. Koshelev, A. A. Vashchenko, O. Fuhr, M. Nieger, V. V. Utochnikova, S. Bräse, Inorg. Chem. 2020, in press. Unlimited Structural Design: para-substituted Diphenyl­phos­phino­pyridine Bridged Cu(I) Complexes in Organic Light Emitting Diodes

C. Book chapters and review articles

A. de Meijere, S. Bräse, J. Organomet. Chem. 1999, 576, 88-110. [CA 130:352294] Palladium in Action: Domino and Cascade Coupling Reactions for the Efficient Construction of Complex Organic Molecules.

A. de Meijere, S. Bräse in Perspectives in Organopalladium Chemistry for the 21st Century, Elsevier-Publications, Ed.: J. Tsuji, 1999. Palladium in Action: Domino and Cascade Coupling Reactions for the Efficient Construction of Complex Organic Molecules

S. Bräse, S. Dahmen, Chem. Eur. J. 2000, 6, 1899-1905. [AN 2000:771973] Traceless Linkers - Only Disappearing Links in Solid-Phase Organic Synthesis?

S. Bräse, Chim. Oggi 2000, 18 (9), 14-19. New linkers for solid phase organic chemistry. Multidirectional (multifunctional), backbone amide, and traceless linker

S. Bräse, Nachr. Tech. Lab. 2001, 311-315. Trendberichte „Kombinatorische Chemie“

S. Dahmen, S. Bräse, Synthesis 2001, 1431-1149. Combinatorial Methods for the Discovery and Optimisation of Homogeneous Catalysts.

J. H. Kirchhoff, M. E. P. Lormann, S. Bräse, Chimica Oggi 2001, 10/11, 28-33. Polymer-bound Auxiliaries for Asymmetric Synthesis on Solid Support: New Approaches to Chiral, Non-racemic Drugs?

S. Bräse, A. de Meijere, in Handbook of Organo-Palladium Chemistry, Ed.: E.-i. Negishi. Wiley. New York. 2002. 1123-1132. IV.1. Background

S. Bräse, A. de Meijere, in Handbook of Organo-Palladium Chemistry, Ed.: E.-i. Negishi. Wiley. New York. 2002. 1179-1208. IV.2.1.2. Double and Multiple Heck Reaction

S. Bräse, A. de Meijere, in Handbook of Organo-Palladium Chemistry, Ed.: E.-i. Negishi. Wiley. New York. 2002. 1223-1254. IV.2.2. Synthesis of Carbocycles

S. Bräse, A. de Meijere, in Handbook of Organo-Palladium Chemistry, Ed.: E.-i. Negishi. Wiley. New York. 2002. 1369-1405. IV.3.1. Palladium-Catalyzed Tandem and Cascade Carbopalladation - Termination with Alkenes, Arenes and Related p-Compounds

S. Bräse, A. de Meijere, in Handbook of Organo-Palladium Chemistry, Ed.: E.-i. Negishi. Wiley. New York. 2002. 1405-1430. IV.3.2. Palladium-Catalyzed Tandem and Cascade Carbopalladation - Termination by Nucleophilic Reagents

S. Bräse, J. Köbberling N. Griebenow, in Handbook of Organo-Palladium Chemistry, Ed.: E.-i. Negishi. Wiley. New York. 2002. 3031-3128. X.3. Organopalladium Reactions in Combinatorial Chemistry

S. Bräse, S. Dahmen, in Combinatorial Chemistry (Ed.: K. C. Nicolaou, R. Hanko, W. Hartwig), VCH, Weinheim 2002, Chapter 4. Linker for Solid-Phase Synthesis

S. Bräse, C. Gil, K. Knepper, Bioorg. Med. Chem. 2002, 10, 2415-2437. The recent impact of solid-phase synthesis on medicinally relevant benzoannelated nitrogen heterocycles

S. Bräse, Nachr. Tech. Lab. 2003, 50, 289. Trendberichte „Festphasensynthese“

S. Bräse, J. Köbberling J. Kirchhoff, Tetrahedron 2003, 59, 885-939. Palladium-catalysed reactions in solid phase organic syntheses.

C. Gil, K. Knepper, S. Bräse, in Polymeric Materials in Organic Synthesis and Catalysis. Ed. M. R. Buchmeiser, Wiley-VCH, Weinheim, 2003, 137-199. Organic Synthesis on Polymeric Supports.

K. Knepper, R. E. Ziegert, S. Bräse, PharmaChem 2003, 6, 8-11. Solid-phase indole synthesis.

S. Bräse, F. Lauterwasser, R. Ziegert, Adv. Synth. Catal. 2003, 345, 869-929. Recent advances in asymmetric C-C and C-heteroatom forming reactions using polymer-bound catalysts.

K. Knepper, C. Gil, S. Bräse, Comb. Chem. High T. Scr. 2003, 6, 673-679. Natural product-like and other biologically active heterocyclic libraries in the post-genomic era using solid-phase techniques.

S. Bräse, S. Dahmen, M. Lormann, in Methods in Enzymology, 369, (Eds.: G. Morales, B. Bunin), Academic Press 2003, 127-150. Multifunctional Linker as an Efficient Tool for the Synthesis of Diverse Small Molecule Libraries: The Triazene Linkers

K. Knepper, C. Gil, S. Bräse, in Highlights in Bioorganic Chemistry.C. Schmuck, H. Wennemers, Eds., Wiley-VCH, 2004. 449-484. Linkers for Solid Phase Synthesis.

S. Bräse, Nachr. Chemie 2004, 52, 270-271. Trendberichte „Festphasensynthese“.

C. Gil, S. Bräse, Curr. Opin. Chem. Biol. 2004, 8, 230-237. Traceless and multifunctional linkers for the generation of small molecules on solid supports.

S. Bräse, Acc. Chem. Res. 2004, 37, 805-815. The Virtue of the Multifunctional Triazene Linkers in the Efficient Solid-Phase Synthesis of Heterocycle Libraries.

S. Bräse, A. de Meijere in Metal-catalyzed Cross-Coupling Reactions II, Eds.: A. de Meijere, F. Diederich, VCH-Wiley, Weinheim, 2004, 217–315. The Alkenylation and Arylation of Olefins: The Heck-Reaction.

S. Bräse, S. Dahmen, S. Höfener, F. Lauterwasser, M. Kreis, R. E. Ziegert, Synlett 2004, 2647-2669. Planar and Central Chiral [2.2]Paracyclophanes as Powerful Catalysts for Asymmetric 1,2-Addition Reactions.

S. Bräse et al., Nachr. Chemie 2005, 53, 252-273. Trendberichte „Festphasensynthese“.

R. E. Ziegert, J. Toräng, K. Knepper, S. Bräse, J. Comb. Chem. 2005, 7, 147-169. The recent impact of solid-phase synthesis on medicinally relevant benzoannelated oxygen heterocycles

A. de Meijere, P. von Zezschwitz, S. Bräse, Acc. Chem. Res. 2005, 38, 413-422. The Virtue of Palladium-Catalyzed Domino Reactions – Diverse Oligocyclizations of Acyclic 2-Bromoenynes and 2-Bromoenediynes

S. Bräse, C. Gil, K. Knepper, V. Zimmermann, Angew. Chem. 2005, 117, 5320–5374, DOI: 10.1002/angew.200400657; Angew. Chem. Int. Ed. 2005, 44, 5188–5240. DOI: 10.1002/anie.200400657. Organic Azides: An Exploding Diversity of a Unique Class of Compounds [Organische Azide: explodierende Vielfalt bei einer einzigartigen Substanzklasse].

R. E. Ziegert, K. Knepper, S. Bräse, in Targets in Heterocyclic Systems – Chemistry and Properties (Vol. 9), Ed. O. A. Attanasi and D. Spinelli, 2005, 230-253. Italian Chemical Society, Rome Targets. Solid Phase Indol Synthesis

S. Bräse, F. Würthner, C. Tschierske, A. Krüger, K. Ditrich, R. Pfau, H. Priepke, R. Breinbauer, H. Wagenknecht, G. Draeger, A. Kirschning, N. Sewald, U. Beifuss, M. O. Senge, T. J. J. Müller, R. Gschwind, B. F. Straub, K. Muniz, M. Oestreich, J. Pietruszka, T. Lindel, R. Süssmuth, P. Bisel, M. Müller, E. Weinhold, A. Jäschke, M. Albrecht, T. Bach, G. Bucher, H. Heydt, J. Hartung, Nachr. Chemie 2006, 54, 241-264. Organic Chemistry 2005.

S. Bräse in Asymmetric Synthesis – The Essentials, M. Christmann, S. Bräse, Eds., Wiley-VCH, Weinheim, 2006. Planar Chiral Ligands based on [2.2]Paracyclophanes.

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

H. Vogt, S. Bräse, Org. Biomol. Chem. 2007, 5, 406–430. Recent approaches towards the asymmetric synthesis of a,a-disubstituted amino acids.

S. Bräse, T. Baumann, S. Dahmen, H. Vogt, Chem. Commun. 2007, 1881-1890 (Feature article). Enantioselective catalytic syntheses of a-branched chiral amines.

S. Bräse, in Asymmetric Synthesis with Chemical and Biological Methods, D. Enders, Ed., Wiley-VCH, Weinheim, 2007. Asymmetric 1,2-Addition Reactions by Planar and Central Chiral [2.2]Paracyclophanes.

S. Bräse, F. Würthner, C. Tschierske, A. Krüger, K. Ditrich, R. Pfau, H. Priepke, R. Breinbauer, H. Wagenknecht, G. Draeger, A. Kirschning, N. Sewald, U. Beifuss, M. O. Senge, T. J. J. Müller, R. Gschwind, B. F. Straub, K. Muniz, M. Oestreich, J. Pietruszka, T. Lindel, R. Süssmuth, P. Bisel, M. Müller, E. Weinhold, A. Jäschke, M. Albrecht, T. Bach, G. Bucher, H. Heydt, J. Hartung, Nachr. Chemie 2007, 55, 252-275. Organic Chemistry 2006.

S. Bräse, D. Keck, Science of Synthesis, Thieme, 2007. Chapter 31.42. Aryl azides

S. Bräse, T. Muller, Science of Synthesis, Thieme, 2007. Chapter 31.43. Aryltriazenes, Aryltetrazenes and Related Compounds

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

S. Bräse, F. Würthner, C. Tschierske, A. Krüger, K. Ditrich, R. Pfau, H. Priepke, R. Breinbauer, H. Wagenknecht, G. Draeger, A. Kirschning, N. Sewald, U. Beifuss, M. O. Senge, T. J. J. Müller, R. Gschwind, B. F. Straub, K. Muniz, M. Oestreich, J. Pietruszka, T. Lindel, R. Süssmuth, P. Bisel, M. Müller, E. Weinhold, A. Jäschke, M. Albrecht, T. Bach, G. Bucher, H. Heydt, J. Hartung, Nachr. Chemie 2008, 269. Organic Chemistry 2007.

C. F. Nising, S. Bräse, Chem. Soc. Rev. 2008, 37, 1218-1228. The Oxa-Michael-Reaction: From Recent Developments to Applications in Natural Product Synthesis

S. Bräse, A. Friedrich, M. Gartner, T. Grab, T. Schröder, Topics in Heterocycl. 2008, 12, 45-116. Cycloaddition Reactions of Azides, Springer.

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

C. F. Nising, S. Bräse, Angew. Chem. 2008, 120, 9529-9531; Angew. Chem. Int. Ed. 2008, 47, 9389-9391. Neue Highlights der Steroidchemie: Chemische Totalsynthese versus Semisynthese (Highlights in Steroid Chemistry: Total Synthesis versus Semisynthesis)

C. Gil, S. Bräse, J. Comb. Chem. 2009, 11, 175-197. Solid-Phase Synthesis of Biologically Active Benzoannelated Nitrogen Heterocycles – An Update

T. Muller, S. Bräse, in Mizoroki-Heck Reaction, M. Oestreich (Ed), Wiley, Chichester, 2009, 215-258. Formation of Heterocycles.

T. Muller, S. Bräse, in Mizoroki-Heck Reaction, M. Oestreich (Ed), Wiley, Chichester, 2009, 485-493. Combinatorial and solid-phase syntheses.

S. Bräse, F. Würthner, C. Tschierske, A. Krüger, K. Ditrich, R. Pfau, H. Priepke, R. Breinbauer, H. Wagenknecht, G. Draeger, A. Kirschning, N. Sewald, U. Beifuss, M. O. Senge, T. J. J. Müller, R. Gschwind, B. F. Straub, K. Muniz, M. Oestreich, J. Pietruszka, T. Lindel, R. Süssmuth, P. Bisel, M. Müller, E. Weinhold, A. Jäschke, M. Albrecht, T. Bach, G. Bucher, H. Heydt, J. Hartung, Nachr. Chemie 2009, 252-277. Organic Chemistry 2008.

S. Bräse, A. Encinas, J. Keck, C. F. Nising, Chem. Rev. 2009,
109, 3903-3990. The Chemistry and Biology of Mycotoxins and Related Fungal Metabolites.

V. Zimmermann, B. Lesch, S. Bräse, Science of Synthesis, Thieme, 2009. Volume 41. Azidoalkanes

N. Jung, S. Bräse, Science of Synthesis, Thieme, 2009. Volume 41. Triazenes

N. Jung, S. Bräse, Science of Synthesis, Thieme, 2009. Volume 41. Tetrazenes

C. Schilling, N. Jung, S. Bräse, in Click Chemistry for Biotechnology and Materials Science, J. Lahann (Ed.), Chapter 15, Wiley 2009, 355-378. Synthesis and Functionalization of Biomolecules via Click Chemistry

C. Schilling, N. Jung, S. Bräse, in Click Chemistry for Biotechnology and Materials Science, J. Lahann (Ed.), Chapter 2, Wiley 2009, 9-28. Common Synthons for Click Chemistry in Biotechnology

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

N. Volz, M. C. Bröhmer, J. Toräng, M. Nieger, S. Bräse, Ind. J. Chem. 2009, 1699. Adventures in Heterocycle Chemistry: The Oxa-Michael Cascade for the Synthesis of Complex Natural Products and Highly Functionalized Bioactive Compounds

S. Bräse, F. Würthner, C. Tschierske, A. Krüger, K. Ditrich, R. Pfau, H. Priepke, R. Breinbauer, H. Wagenknecht, G. Draeger, A. Kirschning, N. Sewald, U. Beifuss, M. O. Senge, T. J. J. Müller, R. Gschwind, B. F. Straub, K. Muniz, M. Oestreich, J. Pietruszka, T. Lindel, R. Süssmuth, P. Bisel, M. Müller, E. Weinhold, A. Jäschke, M. Albrecht, T. Bach, G. Bucher, H. Heydt, J. Hartung, Nachr. Chemie 2010, 269-299. Organische Chemie 2009

K. Eggenberger, N. Frey, B. Zienicke, J. Siebenbrock, T. Schunck, R. Fischer, S. Bräse, E. Birtalan, T. Nann, P. Nick, Adv. Biomat. 2010. Use of nanoparticles to study and manipulate plant cells

S. Bräse, F. Würthner, C. Tschierske, A. Krüger, K. Ditrich, R. Pfau, H. Priepke, R. Breinbauer, H. Wagenknecht, G. Draeger, A. Kirschning, N. Sewald, U. Beifuss, M. O. Senge, T. J. J. Müller, R. Gschwind, B. F. Straub, K. Muniz, M. Oestreich, J. Pietruszka, T. Lindel, R. Süssmuth, P. Bisel, M. Müller, E. Weinhold, A. Jäschke, M. Albrecht, T. Bach, G. Bucher, H. Heydt, J. Hartung, Nachr. Chemie 2011, 59, 254-283. Organische Cheme 2010

C. I. Schilling, N. Jung, M. B. Biskup, U. Schepers, S. Bräse, Chem. Soc. Rev. 2011, 40, 4840 – 4871. Bioconjugation via Azide-Staudinger Ligation - An Overview

C. F. Nising, S. Bräse, Chem. Soc. Rev. 2012, 41, 988 – 999. Recent developments in the field of oxa-Michael-Reactions

K.-S. Masters, S. Bräse, Chem. Rev. 2012, 112, 3717–3776. Xanthones from Fungi, Lichens and Bacteria: The Natural Products and their Synthesis

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 synthesis of aziridines

S. Bräse, F. Beuerle, Krüger, M. Lehmann, T. Bach, U. Beifuss, T. J. J. Müller, M. O. Senge, R. Giernoth, K. Ditrich, J. Paradies, K. Muniz, B. F. Straub, P. R. Schreiner, D. Schroeder, T. Lindel, J. Pietruszka, C.Soeffing, R. Pfau, R, Breinbauer, N. Sewald, E. Weinhold, M. B. Biskup, G. Dräger, C.Arenz, J. Andexer, M. Müller, W. von Deyn, T. Newton, J. Rheinheimer, C. Muhle-Goll, B. Luy, Nachr. Chem. 2012, 60(3), 265-299.

T. Muller, S. Bräse, Azides, in Kirk-Othmer, Kirk-Othmer Encyclopedia of Chemical Technology, 1–21.

A. J. Rüger, J. Kramer, S. Seifermann, M. Busch, T. Muller, S. Bräse, Chemie in unserer Zeit 2012, 46, 294–301. Händigkeit – Leben in einer chiralen Welt (Handedness - life in a chiral world: mirror images in everyday life)

N. Jung, S. Bräse, Angew. Chem. Int. Ed. 2012, 51, 12169-12171. Vinyl- und Alkinyl-Azide: altbekannte Intermediate im Fokus moderner Synthesemethoden

D. C. Kapeller, S. Bräse, Towards tomorrow's drugs: The synthesis of compound libraries by solid-phase chemistry in New Strategies in Chemical Synthesis and Catalysis, Ed. B. Pignataro, Wiley-VCH, Chapter 15, 2012, 343–375.

S. Vanderheiden, N. Jung, S. Bräse, (2012) Heck Cleavage of Resin-Bound Triazenes, in Solid-Phase Organic Syntheses, Volume 2 (ed P. J. H. Scott), John Wiley & Sons, Inc., Hoboken, NJ, USA, p. 129-137.

S. Bräse, F. Gläser, C. S. Kramer, S. Lindner, A. M. Linsenmeier, K.-S. Masters, A. C. Meister, B. M. Ruff, S. Zhong Progress in the chemistry of organic natural products (2013), 97, v-xv, 1-300. Progress in the chemistry of organic natural products. The chemistry of mycotoxins

S. Bräse, H. Vogt, T. Baumann, in Comprehensive Chirality 2013, 6, 374–398, (Eds.: E. M. Carreira, H. Yamamoto), C-N bond formation: a-amination and a-hydrazination of carbonyl compounds with DEAD and related compounds

S. Bräse, F. Beuerle, Krüger, M. Lehmann, T. Bach, U. Beifuss, T. J. J. Müller, M. O. Senge, R. Giernoth, K. Ditrich, J. Paradies, K. Muniz, B. F. Straub, P. R. Schreiner, D. Schroeder, T. Lindel, J. Pietruszka, C. Soeffing, R. Pfau, R, Breinbauer, N. Sewald, E. Weinhold, M. B. Biskup, G. Dräger, C. Arenz, J. Andexer, M. Müller, W. von Deyn, T. Newton, J. Rheinheimer, C. Muhle-Goll, B. Luy, Nachr. Chem. 2013, 61, 265–297.

C. Kramer, S. Bräse, Nucleophile Addition to C=X Bonds - Hydrocyanation and Strecker Reactions in Comprehensive Enantioselective Organocatalysis (Ed. P. Dalko), Wiley-VCH, 2013 (ISBN: 978-3-527-33236-6).

N. Jung, F. Gläser, S. Bräse, Phyth. Rev. 2013. Synthetic approaches to polycyclic semiochemicals and their derivatives – combinatorial methods towards phytochemicals

S. Bräse, Organopalladium chemistry, in Organometallics in Synthesis, Ed.: M. Schlosser, 2013, Wiley, Pages 777-1000. 

S. B. L. Vollrath, S. Bräse, Lab & More 2013, 6/2013. Synthese von Peptoiden in der Mikrowelle.

N. Jung, S. Bräse, Kirk-Othmer 2013. Click reactions: the Azide-Alkyne Cycloaddition

D. Lütjohann, N. Jung, S. Bräse, LaborPraxis 2013, November, 40. LIMS für Jedermann

T. Muller, S. Bräse, RSC Advances 2014, 4, 6886-6907. Tetraedral organic molecules as monomers for porous supramolecular networks.

D. K. Kölmel, N. Jung, S. Bräse, Austr. J. Chem. 2014, 67, 328-336. Azides – Diazonium ions – Triazenes: Versatile nitrogen-rich functional groups


S. Bräse, F. Beuerle, A. Krüger, M. Lehmann, T. Bach, U. Beifuss, T. J. J. Müller, M. O. Senge, R. Giernoth, K. Ditrich, J. Paradies, K. Muniz, B. F. Straub, P. R. Schreiner, T. Lindel, J. Pietruszka, C. Soeffing, R. Pfau, R. Breinbauer, N. Sewald, E. Weinhold, M. B. Biskup, G. Dräger, C. Arenz, J. Andexer, M. Müller, W. von Deyn, T. Newton, J. Rheinheimer, C. Muhle-Goll, B. Luy, Nachr. Chem. 2014, 62, 264.

T. Wezeman, K. Masters, S. Bräse, Angew. Chem. Int. Ed. 2014, 53, 4524-4526. Double Trouble - The Art of Synthesis of Chiral Dimeric Natural Products

M. Wallesch, D. Volz, D. Zink, U. Schepers, M. Nieger, T. Baumann, S. Bräse, Chem. Eur. J. 2014, 20, 6578-6590. Bright coppertunities: Multinuclear copper complexes from N,P-ligands and their applications 

A. Hafner, N. Jung, S. Bräse, Synthesis 2014, 46, 1440-1447. Silver-Mediated Perfluoroalkylation Reactions

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

T. Wezeman, K. Masters, S. Bräse, Nat. Prod. Rep. 2015, 8-28. Xanthone dimers - A Rare Case of Being Common and Privileged

W. Yan, S. Seifermann, P. Pierrat, S. Bräse, Org. Biomol. Chem. 2015, 13, 25-54. Synthesis of highly functionalized C60 fullerene derivatives and their applications in material and life sciences

D. Volz, M. Wallesch, C. Fléchon, M. Danz, A. Verma, J. M. Navarro, S. Bräse, T. Baumann, Green Chemistry 2015, 1988 – 2011. From iridium and platinum to copper and carbon: new avenues for more sustainability in organic light-emitting diodes

DOI: 10.1039/C4OB01663G

J. F. Schneider, C. L. Ladd, S. Bräse, Proline as an asymmetric organocatalyst; RSC book: Sustainable Catalysis, Ed. M. North, 2015, RSC Green Chemistry Series (2016), 40(Sustainable Catalysis, Part 1), 79-119.

Print ISBN: 978-1-78262-058-7

S. Bräse, M. Mende, H. H. Jobelius, H.-D. Scharff, Hydrazoic Acid and Azides, Ullmann, 2015.

DOI: 10.1002/14356007.a13_193.pub2

L. Bergmann, M. Wallesch, D. M. Zink, S. Bräse, T. Baumann, D. Volz, Topics Curr. Chem. 2016, 373, 1-39. Metal-organic and Organic TADF-Materials: Status, Challenges and Characterization

DOI: 10.1007/s41061-016-0022-6

S. Bräse, S. Lindner, eEROS, 2016, 1-3 Methyl Trifluoroacrylate.

DOI: 10.1002/047084289X.rn01937

M. Mende, C. Bednarek, M. Wawryszyn, P. Sauter, M. B. Biskup, U. Schepers, S. Bräse, Chem. Rev. 2016, 116, 8193-8255. Chemical synthesis of glycosaminoglycans

DOI: 10.1021/acs.chemrev.6b00010

D. Volz, S. Bräse, GIT Laborjounal 2016, Issue 10, 60-63. Organische Leuchtdioden - Der Stand der Technik

http://www.git-labor.de/forschung/materialien/organische-leuchtdioden

A. M. Dilmaç, E. Spuling, A. de Meijere, S. Bräse, Angew. Chem. Int. Ed. 2017, 5684–5718. Propellanes– From a Chemical Curiosity to "Explosive" Materials and Natural Products

10.1002/anie.201603951

N. Jung, A. Deckers, S. Bräse, Biospektrum 2017, Issue 2, 212-214. Ein Molekülarchiv als akademisch integrierte Service-Einrichtung

C. Bizzarri, F. Hundemer, J. Busch, S. Bräse Polyhedron, 2018, 140, 51-66. Triplet Emitters vs TADF Emitters in OLEDs: a comparative study

J. Arras, S. Bräse, ChemPhotoChem 2018, 2, 54-66. The World Needs New Colors: Cutting Edge Mobility Focusing on Long Persistent Luminescence Materials

DOI:10.1002/cptc.201700215

C. Bizzarri, E. Spuling, D. M. Knoll, D. Volz, S. Bräse, Coord. Chem. Rev. 2018, 373, 49-82. Sustainable Metal Complexes for Organic Light Emitting Diodes (OLEDs)

DOI: 10.1016/j.ccr.2017.09.011

Z. Hassan, E. Spuling, D. Knoll, J. Lahann, S. Bräse, Chem. Soc. Rev. 2018, 47, 6947-6963. Planar Chiral [2.2]Paracyclophanes: From Synthetic Curiosity to Applications in Asymmetric Synthesis and Materials

DOI: 10.1039/c7cs00803a

A. A. Aly, M. A.-M. Gomaa, S. Bräse, ARKIVOC 2018, (6), 85-138. Amidines: their synthesis, reactivity, and applications in heterocyclic synthesis

DOI: 10.24820/ark.5550190.p010.607

C. M. Niemeyer, M. Bastmeyer, S. Bräse, J. Lahann, C. Wöll, Preprints 2018, 2018120329 White Paper on the Biologization of Materials Research

DOI: 10.20944/preprints201812.0329.v1

V. Koch, A. Hafner, S. Bräse, Wiley-VCH 2019. ISBN: 978-3-527-34281-5, Silver-Mediated Fluorination, Perfluoroalkylation and Trifluoromethylthiolation Reactions

D. S. Mattes, N. Jung, L. Weber, S. Bräse, F. Breitling, Adv. Mat. 2019, e1806656. Miniaturized and automated organic synthesis – Overview and perspectives

DOI:10.1002/adma.201806656

S. Begum, Z. Hassan, S. Bräse, C. Wöll, M. Tsotsalas, Acc. Chem. Res. 2019, 52, 1598-1610. Metal-Organic Framework Templated Biomaterials: Recent Progress in Synthesis, Functionalization and Applications

DOI:10.1021/acs.accounts.9b00039

C. Zippel, N. Rosenbaum, S. Bräse, Science China Chemistry 2019, 62(8), 923-924. Alkaline generation and reactions of CF3CHN2

DOI:10.1007/s11426-019-9479-2

J. M. Busch, D. M. Knoll, C. Zippel, S. Bräse, C. Bizzarri, Dalton Trans. 2019, 48, 15338-15357. Metal-supported and –assisted stereoselective cooperative photocatalysis

DOI:10.1039/c9dt02094b

S. Grosjean, M. Wawryszyn, H. Mutlu, S. Bräse, J. Lahann, P. Theato, Adv. Mat. 2019, 31, 1806334. Soft Matter Technology at KIT: Chemical Perspective from Nanoarchitectures to Microstructures

DOI:10.1002/adma.201806334

S. Bräse, B. Nestler, Laborpraxis 2019. Einheitliche digitale Plattform für Chemie und Materialwissenschaft

https://www.laborpraxis.vogel.de/einheitliche-digitale-plattform-fuer-chemie-und-materialwissenschaft-a-822428/

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

https://www.laborpraxis.vogel.de/wie-gelingt-digitalisierte-forschung-a-829394/

A. A. Aly, E. M. El-Sheref, A.-F.. E. Mourad, M E. M. Bakheet, S. Bräse, Mol. Divers. 2019, https://doi.org/10.1007/s11030-019-09952-5. 4-Hydroxy-2-quinolones - syntheses, reactions and fused heterocycles

DOI:10.1007/s11030-019-09952-5

Z. Hassan, Y. Matt, S. Begum, M. Tsotsalas, S. Bräse, Adv. Funct. Mat. 2020, 1907625. Metal-supported and –assisted stereoselective cooperative photocatalysis Assembly of Molecular Building Blocks into Integrated Complex Functional Molecular Systems: Structuring Matter Made-to-Order

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adfm.201907625

Z. Hassan, E. Spuling, D. M. Knoll, S. Bräse, Angew. Chem. Int. Ed. 2020, 2156-2170. Application-based Regioselective Functionalization of [2.2]Paracyclophanes: Recent Synthetic Progress and Perspectives

https://onlinelibrary.wiley.com/doi/10.1002/anie.201904863

V. Koch, S. Bräse, Biospektrum 2020, 1, 107. Modernes Forschungsdatenmanagement – ein Naturstoffprojekt als Case Study

Doi: 10.1007/s12268-020-1316-3

R. Bär, A. Dilmac, T. Wezeman, S. Bräse, Nat. Prod. Rep. 2020, 37, 224-245. Occurrence, Synthesis and Applications of Natural and Designed [3.3.3]Propellanes

DOI:10.1039/c8np00086g

C. Herlan, S. Bräse, Dalton Trans. 2020, 49, 2397-2402. Lanthanide-conjugates as versatile instruments for therapy and diagnostics

DOI:10.1039/c9dt04851k

M. Schock, S. Bräse, Molecules 2020, 25(4), 1009. Reactive & Efficient: Organic Azides as Cross-Linkers in Material Sciences

10.3390/molecules25041009

C. Bednarek, I. Wehl, N. Jung, U. Schepers, S. Bräse, Chem. Rev. 2020, 120, 4301-4354. The Staudinger Ligation

10.1021: acs.chemrev.9b00665

D. Book chapters and review articles (in press)

A. Aly, A. A. Hassan, M. M. Makhlouf, S. Bräse, Molecules 2020, in press. Chemistry and biological activities of 1,2,4-triazolthiones - antiviral and anti-infective drugs

molecules-844229

E. Papers in refereed journals (Doctorate and Postdoctorate)

P. K. Baker, T. Birkbeck, S. Bräse, A. Bury, H. M. Naylor, Transition Met. Chem. 1992, 17, 401-403. [CA 118:93155] Synthesis and Reactions with Donor Ligands of the Mixed Halide Seven-Coordinate Molybdenum(II) Complex [µoMoClI(CO)3(NCMe)2]

G. McGaffin, S. Michalski, A. Stolle, S. Bräse, J. Salaün, A. de Meijere, Synlett 1992, 558-560. [CA 117:212035] Pd(0)-Catalyzed SN2'-Displacement on 1-Chloro-1-ethenylcyclopropanes: A Versatile Preparation of Substituted Methylenecyclopropanes

H.-C. Militzer, S. Schömenauer, C. Otte, C. Puls, J. Hain, S. Bräse, A. de Meijere, Synthesis 1993, 998-1012. [CA 121:108015] Versatile Synthesis of Alkynyl- and Substituted Alkynylcyclopropanes: 2-Alkoxyethynylcyclopropanes for the Anellation of Bicyclo[3.3.0]octane Fragments

S. Bräse, A. de Meijere, Angew. Chem. 1995, 107, 2741-2743; Angew. Chem. Int. Ed. Engl. 1995, 34, 2545-2547. [CA 124:175430] Unprecedented Intra- and Intermolecular Palladium-Catalyzed Coupling Reactions with Methylenecyclopropane Type Tetrasubstituted Alkenes

S. Bräse, S. Schömenauer, G. McGaffin, A. Stolle, A. de Meijere, Chem. Eur. J. 1996, 2, 545-555. [CA 125:86223] Versatile Synthesis of Enantiomerically Pure 2-Alkoxy-1-ethynylcyclopropanes and their Application in the EPC-Synthesis of Bicyclo[3.3.0]oct-1-en-3-ones

K. H. Ang, S. Bräse, A. G. Steinig, A. Llebaria, F. E. Meyer, K. Voigt, A. de Meijere, Tetrahedron 1996, 52, 11503-11528. [CA 125:300495] Versatile Synthesis of Bicyclo[4.3.0]nonenes and Bicyclo[4.4.0]decenes by a Domino Heck-Diels-Alder Reaction

K. C. Nicolaou, C. N. C. Boddy, S. Natarajan, T.-Y. Yue, H. Li, S. Bräse, J. M. Ramanjulu, J. Am. Chem. Soc. 1997, 119, 3421-3422. [CA 126:277757] New Synthetic Technology for the Construction of the Aryl Ethers: Construction of C-O-D and D-O-E Ring Model Systems of Vancomycin

K. C. Nicolaou, X.-J. Chu, J. M. Ramanjulu, S. Natarajan, S. Bräse, C. N. C. Boddy, Angew. Chem. 1997, 109, 1551-1552; Angew. Chem. Int. Ed. Engl. 1997, 36, 1539-1540. [CA 127:220974] New Synthetic Technology for the Construction of the Vancomycin Biaryl Ring Systems

K. C. Nicolaou, J. M. Ramanjulu, S. Natarajan, S. Bräse, H. Li, C. N. C. Boddy, F. Rübsam, Chem. Commun. 1997, 1899-1900. [CA 127:331735] A Macrolactamization-Suzuki coupling approach to the AB-COD bicyclic system of Vancomycin

M. Brandl, S. I. Kozhushkov, S. Bräse, A. de Meijere, Eur. J. Org. Chem. 1998, 1, 453-457. [CA 128:270395] Ring Opening of Methylenecyclopropane Moieties in the Palladium-Catalyzed Cross-Coupling of Methylenecyclopropyl Bromides with Metallated CH-Acidic Compounds

S. Bräse, B. Waegell, A. de Meijere, Synthesis 1998, 148-152. [CA 128:243775] Palladium-Catalyzed Coupling Reactions of 1-Bromoadamantane with Styrenes and Arenes

S. Bräse, J. Rümper, K. Voigt, S. Albecq, G. Thurau, R. Villard, B. Waegell, A. de Meijere, Eur. J. Org. Chem. 1998, 1, 671-678. [CA 129:15951] Synthesis of o-Dialkenylbenzenes and Indenes Using Heck and Oxypallation Reaction

S. Bräse, P. Klæboe, K.-M. Marstokk, A. de Meijere, H. Møllendahl, C. J. Nielsen, Acc. Chem. Scand. 1998, 52, 1122-1136. [CA 129:275514] Conformational Properties of 2-Cyclopropylidenethanol as studied by Microwave, Infrared and Raman Spectroscopy and by ab Initio Computations

K. C. Nicolaou, H. Li, C. N. C. Boddy, J. M. Ramanjulu, T.-Y. Yue, S. Natarajan, X.-J. Chu, S. Bräse, F. Rübsam, Chem. Eur. J. 1999, 5, 2584-2601. [CA 131:351647] Total Synthesis of Vancomycin - Part 1: Design and Development of Methodology

K. C. Nicolaou, C. N. C. Boddy, H. Li, A. E. Koumbis, R. Hughes, S. Natarajan, N. F. Jain, J. M. Ramanjulu, S. Bräse, M. E. Solomon, Chem. Eur. J. 1999, 5, 2602-2621. [CA 131:351648] Total Synthesis of Vancomycin - Part 2: Retrosynthetic Analysis, Synthesis of Amino Acid Building Blocks and Strategy Evaluations

H. Nüske, S. Bräse, A. de Meijere, Synlett 2000, 1467-1469. Catalyzed Nucleophilic Substitution on Cyclopropenylmethyl Esters - Reactions via a 1,2-Methano-p-allylpalladium Intermediate
H. Nüske, S. Bräse, S. I. Kozhushkov, M. Noltemeyer, M. Es-Sayed, A. de Meijere, Chem. Eur. J. 2002, 8, 2350-2369. A New Highly Efficient Three-Component Domino Heck-Diels-Alder Reaction with Bicyclopropylidene: Rapid Access to Spiro[2.5]oct-4-ene Derivatives

F. Book chapters and review articles (Doctorate and Postdoctorate)

K. C. Nicolaou, S. Bräse, J. Pastor, F. R. Sarabia, R. M. Rodriguez in Proceedings of the 26th Reunion Bienal De La Real Sociedad Española De Quimica, Servicio de Publicaciones de la Universidad de Cádiz, 1997. Total Synthesis of Naturally Occurring Substances

S. Bräse, A. de Meijere in Metal-catalyzed Cross-Coupling Reactions, Ed.: F. Diederich, P. J. Stang, VCH-Wiley, Weinheim 1998, 99-166. [CA 128:166974] The Alkenylation and Arylation of Olefins: The Heck-Reaction

A. de Meijere, S. Bräse in Chemistry for the 21st Century: Transition Metal-catalysed Reactions: Ed.: S. Murahashi, S. G. Davies, Blackwell Sciences, 1999, S. 99-131. Palladium-Catalyzed Cross-Coupling Reactions - A Personalized Account

K. C. Nicolaou, C. N. C. Boddy, S. Bräse, N. Winssinger, Angew. Chem. 1999, 111, 2230-2287; Angew. Chem. Int. Ed. 1999, 38, 2097-2152. [CA 131:272142] Chemistry, Biology and Medicine of Glycopeptide Antibiotics

G. Articles in Proceedings (listed in Chemical Abstracts)

S. Bräse, M. Lormann, H. Vogt, Proceedings of ECSOC-4, The Fourth International Electronic Conference on Synthetic Organic Chemistry, http://www.mdpi.org/ecsoc-4.htm, September 1?30, 2000, B-16. Eds. T. Wirth, C. O. Kappe, E. Felder, U. Diederichsen and S.-K. Lin, CD-ROM edition ISBN 3-906980-05-7, Published in 2000 by MDPI, Basel, Switzerland Nitrogen-Based Linker, Part 10. Scope and Limitation of a Tin Promoted Amidation on Solid Phase: A New Monitoring for the T1 Triazene Linker.

S. Bräse, S. Dahmen, M. Lormann, Proceedings of ECSOC-3, The Third International Electronic Conference on Synthetic Organic Chemistry, http://www.mdpi.org/ecsoc-3.htm, September 1-30, 1999, Eds. E. Pombo-Villar, R. Neier and S. K. Lin, CD-ROM edition ISBN 3-906980-04-9, Published in 1999 by MDPI, Basel, Switzerland. Nitrogen-Based Linker, Part 2. The T1 Linker: Multidirectional Cleavage for Solid Phase Organic Synthesis.

A. de Meijere, S. Bräse. Semin. Org. Synth., Summer Sch. "A. Corbella", 24th 1999, 7-50. (AN 2000:842636). Palladium-catalyzed sequential reactions for the efficient construction of complex organic molecules - a personal update.

J. H. Kirchhoff, M. E. P. Lormann, S. Bräse, Proceedings of ECSOC-5, The Fifth International Electronic Conference on Synthetic Organic Chemistry, http://www.mdpi.org/ecsoc-5.htm, Polymer-bound Auxiliaries for Asymmetric Synthesis on Solid Support: New Approaches to Chiral, Non-racemic Drugs?, 2001, 741-754.

M. Es-Sayed, M. Beck, S. Bräse, A. de Meijere, C. Funke, K. Kather, M. Limbach, M. Lormann, C. Paulitz, C. Schulze, H. Wroblowsky, V. Zimmermann, Proceedings of the 3rd Pacific Conference on Pesticide Science, Hawaii 2003. ACS Symposium Series (2005), 892 (New Discoveries in Agrochemicals), 74-86. J. M. Clark, H. Ohkawa, Eds. Combichem at Bayer CropScience – What we have Learned, Exemplified by Recent Chemistry.

S. Bräse, M. Schroen, eEROS, 2005. The Triazene Linkers. DOI: 10.1002/047084289X.rn00557.

T. Schröder, A. Quintilla, J. Setzler, E. Birtalan, W. Wenzel, S. Bräse, WSEAS Trans. Biol. Biomed. 2007, 4 (9), 120. Joint experimental and theoretical investigation of the propensity of peptoids as drug carriers

K. Eggenberger, T. Schröder, E. Birtalan, A. Merkoulov, M. Darbandi, T. Nann, S. Bräse, P. Nick, Eur. J. Cell. Biol. 2008, 87, 62, Suppl. 58. The use of nanoparticles to study and manipulate the polarity of plant cells

M. S. Wiehn, N. Jung, S. Bräse, Abstracts of Papers, 236th ACS National Meeting, Philadelphia, PA, United States, August 17-21, 2008 (2008), FLUO-008. Fluorine-containing linkers for quantitative analysis of resin-bound molecules.

N. Allendorfer, S. Bräse, Abstracts of Papers, 236th ACS National Meeting, Philadelphia, PA, United States, August 17-21, 2008 (2008), FLUO-009. Fluorolefins as peptidomimetics

M. S. Wiehn, S. Bräse, Abstracts of Papers, 236th ACS National Meeting, Philadelphia, PA, United States, August 17-21, 2008 (2008), FLUO-010. Fluorous cleavage: New multifunctional cleavage for solid-phase syntheses

T. Baumann, S. Bräse, S. Dahmen, T. Grab, Chemie Ingenieur Technik 2008, 80, 1267. P1.24. (Metallkomplexe - Katalysatoren in der organischen Synthese - und Grundstein für optische Materialien der Zukunft?) Metal complexes, catalysts in organic synthesis, and basis for optical materials of the future?

H. Blank, R. Schneider, P. Brenner, D. Gerthsen, M. Esselen, D. Marko, M. Crone, M. Türk, T. Muller, S. Bräse, EMC 2008 14th European Microscopy Congress 1–5 September 2008, Aachen, Germany, Study of the cellular uptake of Pt nanoparticles in human colon carcinoma cells

J. P. Sleeman, W. Thiele, A. Schmid, M. Rothley, N. Grau, M. Gartner, N. Teller, D. Marko, A. Giannis, S. Bräse, 21. Clin. Exp. Metastasis 2009, 26, 923-923. The relationship between tumors and the lymphatics: implications for metastasis

M. S. Wiehn, S. Bräse, Abstracts of Papers, 239th ACS National Meeting, San Francisco, CA, United States, March 21-25, 2010 (2010), FLUO-023. Combinatorial solid-phase synthesis of gem-difluoro compound libraries

M. S. Wiehn, S. Bräse, Abstracts of Papers, 239th ACS National Meeting, San Francisco, CA, United States, March 21-25, 2010 (2010), FLUO-022. Solid-phase synthesis of functionalized fluoroarenes and trifluoromethylarenes 

B. Rudat, S. Vollrath, E. Birtalan, H.-J. Eisler U. Lemmer, S. Bräse, Conference Information: Conference on the NATO Advanced Study Institute on Bio-Photonics: Spectroscopy, Imaging, Sensing, and Manipulation, JUL 02-17, 2009 Erice, ITALY, BIOPHOTONICS: SPECTROSCOPY, IMAGING, SENSING, AND MANIPULATION Book Series: NATO Science for Peace and Security Series B-Physics and Biophysics Pages: 373-373 2011.ON THE WAY TO STUDY THE UPTAKE MECHANISMS OF CELL PENETRATING PEPTOIDS BY SINGLE-MOLECULE METHODS,

I. Meliciani, N. Volz, V. Rempel, S. Hinz, T. Karcz, C. E. Müller, S. Bräse, W. Wenzel, FEBS J. 2011, 278, SI, 1, 118-118. A combined experimental and simulation approach to develop selective high-affinity small-molecule inhibitors of cannabinoid receptors Cb1/Cb2

I. Meliciani, N. Volz, V. Rempel, S. Hinz, T. Karcz, C. E. Müller, S. Bräse, W. Wenzel, Biophys. J. 2011, 100, SI, 1, 548-549. A combined experimental and simulation approach to develop selective high-affinity small-molecule inhibitors of cannabinoid receptors Cb1/Cb2

E. Sokolovskaya, S. Bräse, J. Lahann, PMSE Preprints 2012, PPMRA9. Synthesis and purification of homomultifunctional polyethers and their block copolymers

E. Sokolovskaya, S. Bräse, J. Lahann, Abstracts of Papers, 244th ACS National Meeting & Exposition, Philadelphia, PA, United States, August 19-23, 2012, PMSE-155. Synthesis and purification of homomultifunctional polyethers and their block copolymers 

M. Busch, F. Bally, A. Kubas, J. Lahann, K. Fink, S. Bräse, Abstracts of Papers, 38th Northeast Regional Meeting of the American Chemical Society, Rochester, NY, United States, Sept. 30-Oct. 3
NERM-27, 2012. Spectrum of [2.2]Paracyclophane Chemistry

D. Volz, L. Bergmann, D. M. Zink, T. Baumann, S. Bräse. Are copper(I) complexes tough enough to be processed from solution? 29 August 2013, SPIE Newsroom.

D. M. Zink, D. Volz, L. Bergmann, M. Nieger, S. Bräse, H. Yersin, T. Baumann. Novel oligonuclear copper complexes featuring exciting luminescent characteristics ", Proc. SPIE 8829, Organic Light Emitting Materials and Devices XVII, 882907.

http://dx.doi.org/10.1117/12.2028619

D. Volz, M. Wallesch, T. Baumann, S. Bräse. Late bloomers: copper complexes in organic LEDs. 29 September 2014, SPIE Newsroom. DOI: 10.1117/2.1201409.005617

A. Kalyakina, V. Utochnikova, A. Trigub, Y. Zubavichus, N. Kuzmina, S. Bräse, Journal of Physics Conference Series 712(1):012137 · May 2016. EXAFS characterisation of metal bonding in highly luminescent, UV stable, water-soluble and biocompatible lanthanide complexes

http://iopscience.iop.org/1742-6596/712/1/012137

doi:10.1088/1742-6596/712/1/012137

K. Cheng, C. Hussal, E. Spuling, S. Bräse, J. Lahann, Directed assembly of twisted polymeric nanofibers via chemical vapor deposition in liquid crystals, Abstracts of Papers, 254th ACS National Meeting & Exposition, Washington, DC, USA, August 20-24, 2017 (2017), PMSE-26

C. Koehler, P. Sauter, M. Wawryszyn, G. Estrada Girona, M. H. Fritz, M. Biskup, H. Besir, I. Berger, V. Benes, Jan Korbel, S. Braese, E. A. Lemke, Biophys. J. 2016, A New Tool for Custom Protein Design and Engineering - DH10 Bac-TAG

Jung, Nicole; Tremouilhac, Pierre; Braese, Stefan Scope of ELNs and repositories to improve scientific documentation and reporting: Examples taken from the Chemotion-​ELN and Chemotion-​Repository, Abstracts of Papers, 256th ACS National Meeting & Exposition, Boston, MA, United States, August 19-23, 2018 (2018), CINF-29

H. Other publications

S. Bräse, Diplomarbeit Universität Göttingen 1992. Palladium-katalysierte allylische Substitution an 2-substituierten 1-Ethenylcyclopropylestern - Eine Route zu diastereomeren- und enantiomerenreinen Spirobicyclo[3.3.0]octenonen

S. Bräse, Dissertation Universität Göttingen 1995. Neue intra- und intermolekulare Reaktionen von Methylencyclopropanderivaten - Palladium katalysierte und Cobalt-vermittelte Transformationen

S. Bräse, Habilitationsarbeit RWTH Aachen 2001. Multifunktionelle Ankergruppen für die organische Festphasensynthese.

S. Bräse, innovations 2/99 [Flyer], Calbiochem-Novabiochem AG, http://www.nova.ch, 1999 (http://www.nova.ch/newsletters/inn2_99/2_99inn.htm). Triazene-based resins for the traceless synthesis of arenes.

S. Bräse, M. Lormann, book review, Angew. Chem. 2000, 112, 995-96; Angew. Chem. Int. Ed. 2000, 39, 4165-4166. Solid-Supported Combinatorial and Parallel Synthesis of Small-Molecular-Weight Compound Libraries, D. Obrecht, J. M. Villalgordo, Pergamon Press, Oxford 1998.

S. Dahmen, S. Bräse, book review, Angew. Chem. 2000, 112, 995; Angew. Chem. Int. Ed. 2000, 39, 4165. Solid-Phase Organic Synthesis. K. Burgess (Ed.). John Wiley & Sons, Inc., New York, 2000.

S. Dahmen, S. Bräse, book review, Nachr. Lab. Tech. 2000. Organic Synthesis on Solid Phase – Supports, Linkers, Reactions. F. Zaragoza Dörwald, Wiley-VCH, Weinheim, 2000.

M. Lormann, S. Bräse, book review, Angew. Chem. Int. Ed. 2001, 40, 256. Organic Synthesis on Solid Phase – Supports, Linkers, Reactions. F. Zaragoza Dörwald, Wiley-VCH, Weinheim, 2000.

S. Dahmen, M. Lormann, S. Bräse, book review, Angew. Chem. Int. Ed. 2001, 40, 257. Combinatorial Chemistry – A Practical Approach. W. Bannwarth, E. Felder (Ed.), Wiley-VCH, Weinheim, 2000.

S. Dahmen, S. Bräse, book review, Angew. Chem. 2001, 40, 256-257. Solid-Phase Synthesis and Combinatorial Technologies. P. Seneci, Wiley-Interscience, New York, 2000.

F. Avemaria, S. Bräse, book review, Angew. Chem. Int. Ed. 2001, 40, 2551-2552. Solid-Phase Synthesis and Combinatorial Technologies. H. Fenniri, Wiley-Interscience, New York, 2000.

S. Bräse, B. Neuss, Angew. Chem. 2002, 114, 893-906. Glossar von Begriffen der Kombinatorischen Chemie.

K. Knepper, S. Bräse, book review, Angew. Chem. 2003, 115, 2313. Combinatorial Library Methods and Protocols, Ed. L. B. English.

K. Knepper, S. Bräse, book review, Kombinatorische Chemie – Konzepte und Strategien, J. Eichler, Nachrichten aus der Chemie 2003, 51, 1287.

S. Bräse, book review, Amino Group Chemistry: From Synthesis to the Life Sciences, A. Ricci, Ed., ChemBioChem 2008, 9, 1509.

S. Bräse, W. Runge, Nachr. Chemie 2008, 56, 845-847. Unternehmerisch denken und handeln lernen (Learn business to think and act)

S. Bräse, E. Birtalan, S. Vollrath, U. Schepers in NANO! –Nutzen und Visionen einer neuen Technologie, Technoseum, Mannheim, 2010. Ohne Barrieren geht es nicht: Abtauchen in die Welt des biologischen Nanokosmos

B. Rudat, S. B. L. Vollrath, E. Birtalan, H.-J. Eisler, U. Lemmer, T. S. Balaban, S. Bräse, Eur. Cells Mater. 2010, 20, Suppl. 2, 218. Photophysics of peptoid transporters – From the ensemble down to the single-molecule level

B. Rudat, S. B. L. Vollrath, E. Birtalan, H.-J. Eisler, U. Lemmer, S. Bräse, Bio-Photonics: Spectroscopy, Imaging, Sensing, and Manipulation, B. Di Bartolo and J. Collins (Herausgeber), Springer NATO Science Series, Dordrecht, 2011, S. 373. On the way to study the uptake mechanisms of cell penetrating peptoids by single-molecule methods

I. Other publications (book reviews etc.)

S. Bräse, innovations 2/99 [Flyer], Calbiochem-Novabiochem AG, http://www.nova.ch, 1999 (http://www.nova.ch/newsletters/inn2_99/2_99inn.htm). Triazene-based resins for the traceless synthesis of arenes.

S. Bräse, M. Lormann, book review, Angew. Chem. 2000, 112, 995-96; Angew. Chem., Int. Ed. 2000, 39, 4165-4166. Solid-Supported Combinatorial and Parallel Synthesis of Small-Molecular-Weight Compound Libraries, D. Obrecht, J. M. Villalgordo, Pergamon Press, Oxford 1998.

S. Dahmen, S. Bräse, book review, Angew. Chem. 2000, 112, 995; Angew. Chem., Int. Ed. 2000, 39, 4165. Solid-Phase Organic Synthesis. K. Burgess (Ed.). John Wiley & Sons, Inc., New York, 2000.

S. Dahmen, S. Bräse, book review, Nachr. Lab. Tech. 2000. Organic Synthesis on Solid Phase – Supports, Linkers, Reactions. F. Zaragoza Dörwald, Wiley-VCH, Weinheim, 2000.

M. Lormann, S. Bräse, book review, Angew. Chem. Int. Ed. 2001, 40, 256. Organic Synthesis on Solid Phase – Supports, Linkers, Reactions. F. Zaragoza Dörwald, Wiley-VCH, Weinheim, 2000.

S. Dahmen, M. Lormann, S. Bräse, book review, Angew. Chem. Int. Ed. 2001, 40, 257. Combinatorial Chemistry – A Practical Approach. W. Bannwarth, E. Felder (Ed.), Wiley-VCH, Weinheim, 2000.

S. Dahmen, S. Bräse, book review, Angew. Chem. 2001, 40, 256-257. Solid-Phase Synthesis and Combinatorial Technologies. P. Seneci, Wiley-Interscience, New York, 2000.

F. Avemaria, S. Bräse, book review, Angew. Chem. Int. Ed. 2001, 40, 2551-2552. Solid-Phase Synthesis and Combinatorial Technologies. H. Fenniri, Wiley-Interscience, New York, 2000.

S. Bräse, B. Neuss, Angew. Chem. 2002, 114, 893-906. Glossar von Begriffen der Kombinatorischen Chemie.

K. Knepper, S. Bräse, book review, Angew. Chem. 2003, 115, 2313. Combinatorial Library Methods and Protocols, Ed. L. B. English.

K. Knepper, S. Bräse, Kombinatorische Chemie – Konzepte und Strategien, J. Eichler, Nachrichten aus der Chemie 2003, 51, 1287.

S. Bräse, book review, Amino Group Chemistry: From Synthesis to the Life Sciences, A. Ricci, Ed., ChemBioChem 2008, 9, 1509.

S. Bräse, W. Runge, Nachr. Chemie 2008, 56, 845-847. Unternehmerisch denken und handeln lernen (Learn business to think and act)

S. Bräse, E. Birtalan, S. Vollrath, U. Schepers in NANO! –Nutzen und Visionen einer neuen Technologie, Technoseum, Mannheim, 2010. Ohne Barrieren geht es nicht: Abtauchen in die Welt des biologischen Nanokosmos

J. Books

M. Christmann, S. Bräse, Eds., Asymmetric Synthesis – The Essentials, Wiley-VCH, Weinheim, 2006; 2nd editition, 2007.

S. Bräse, Guest editor, Top. Curr. Chem., Springer, 2007, Combinatorial Chemistry on Solid Supports

S. Bräse, J. Bülle, A. Hüttermann, Basiswissen der Organischen Chemie, Wiley-VCH, Weinheim, 2008

S. Bräse, K. Banert, Eds., Organic Azides – Syntheses and Applications, Wiley, Chichester, 2009. 978-0-470-51998-1

M. Christmann, S. Bräse, Eds., Asymmetric Synthesis II – More methods and applications, Wiley-VCH, Weinheim, 2012.

A. de Meijere, S. Bräse, M. Oestreich, Eds., Metal-Catalyzed Cross-Coupling Reactions and More, Wiley-VCh, Weinheim, 2014. 978-3-527-33154-3

S. Bräse (ed.), in press. RSC publisher, 2015. Privileged Scaffolds in Medicinal Chemistry: Design, Synthesis and Evaluation. Print ISBN: 978-1-78262-030-3

K. Patents

S. Bräse, Deutsche Patentanmeldung 198 47 230.7-43, Ger. Off. 198 47 230.7 A1, 20.4.2000. [CA 132:293571, AN 2000:254082] Harz mit Triazenlinker zur "Traceless"-Synthese von Aromaten

S. Bräse, J. Köbberling, D. Enders, Deutsche Patentanmeldung 198 47 231.5-47. Harz mit Triazenlinker zur Synthese von Aminen

S. Bräse, S. Dahmen, Deutsche Patentanmeldung 199 31 727.5. Ger. Offen. (2001), DE 19931727 A1 26.4.2001 [AN: 2001:297427] Festphasen-gebundene, stabile Diazoniumionen

A. Gillner, E. Bremus, J. Köbberling, S. Bräse, Deutsches Patent 199 17 433, PCT-Application PCT/EP00/03360 [AN 2000:756607]. Mikroreaktormatrix zum Erzeugen und Testen von Substanzen und Wirkstoffen

J. H. Kirchhoff, J. Köbberling, D. Enders, S. Bräse, Deutsche Patentanmeldung 100 07 704.8. Ger. Offen. (2001), DE 10007704 A1 6.9.2001. Festphasengebundene Hydrazinverbindungen als Linker und Scavenger für Carbonylverbindungen

N. Herrmanns, S. Dahmen, C. Bolm, S. Bräse, Deutsche Patentanmeldung 102 40 935 A1. Ger. Offen. (2004), DE 102 40 935 A1 18.3.2004. Verfahren zur Herstellung von optische aktiven Diarylmethanen durch Arylübertragung auf Imine

S. Bräse, T. Grab, T. Muller, C. Schilling, Deutsche Patentanmeldung 10 2007 047 569.3.

Stabile starre tetraedrische Polyazide und ihre Anwendung in thermischen und katalytischen Cycloadditionen.

R. Engel, W. Gerlinger, S. Bräse, T. Muller, C. Belenki, H. Schuchmann, M. Gedrat, PCT Int. Appl. (2011), WO 2011110990 A1 20110915. Method for producing nanoparticle suspensions

   Also: US 9296685 B2 20160329

R. Engel, W. Gerlinger, S. Bräse, T. Muller, C. Belenki, H. Schuchmann, M. Gedrat, EP 2544811. VERFAHREN ZUR HERSTELLUNG VON NANOPARTIKELSUSPENSIONEN

M. Enders, M. Seipenbusch, W. Gerlinger, S. Bräse, T. Muller, Europäische Patentanmeldung PF 73976 SE/DRO. Precursors for the metal organic vapor deposition process (MOCVD), and their use; U.S. Pat. Appl. Publ. (2014), US 20140065060 A1 20140306

Polymer-​fixed derivatives of dithiolane or dithiane, Jung, N.; Grässle, S.; Bräse, S., PCT Int. Appl. (2015), WO 2015044108 A1 20150402; Ger. Offen. (2015), DE 102013110740 A1 20150402

Process for the marking of a cell, Volz, D.; Wallesch, M.; Seltenreich, J.; Schepers, U.; Bräse, S., Ger. Offen. (2015), DE 102015100171 A1 20150903; A two-​stage process for labeling of cells with reporter moieties using Click chemistry, Volz, D.; Wallesch, M.; Seltenreich, J.; Schepers, U.; Bräse, S. DE 102015100171 A1 20150903

N. Griebenow, S. Bräse, A. Dilmac, Method for targeted conjugation of peptides and proteins by paired c2 bridging of cysteine amino acids Nov 12, 2015, WO 2015169784 A1; EP 2014-167772

F. Franzreb, P. Lindemann, M. Tsotsalas, C. Wöll, S. Bräse, Process for the production of micro-​porous organic membranes, micro-​porous organic membranes and their use: Ger. Offen. (2016), DE 102014112088 A1 20160225.

V. V. Utochnikova, A. S. Kalyakina, V. Y. Khudoleeva, S. Bräse, N. P. Kuzmina, From Russ. (2016), RU 2605746 C1 20161227. Fluoro-​substituted benzoates of lanthanides, exhibit luminescent properties in visible and infrared range

A. Hörner, S. Bräse, Appl. (2017), WO 2017081283 A1 20170518. Luminescent dyes as emitter dyes having at least 3 emission bands

A. Hörner, S. Bräse, Ger. Offen. (2017), DE 102015119569 A1 20170518. Lumineszenz-Farbstoffe mit mindestens 3 Emissionsbanden als Emitterfarbstoffe

J. Caro, A. Knebel, L. Heinke, S. Grosjean, C. Wöll, Z. Wang, S. Bräse, Eur. Pat. Appl. (2018), EP 3305392 A1 20180411. Photo-​switching and tuning of gas transport through metal- organic framework membranes

STEFAN BRASE [RU]; VASHCHENKO ANDREJ ALEKSANDROVICH [RU]; KALYAKINA ALENA SERGEEVNA [RU]; SOLODUKHIN NIKOLAJ NIKOLAEVICH [RU]; ASLANDUKOV ANDREJ NIKOLAEVICH [UA]; SHTEFAN BREZE [DE]; KUZMINA NATALIYA PETROVNA [RU] Different-​ligand fluoro-​substituted aromatic lantanide carboxylates, luminescent properties, and organic led based diodes, RU 2657496

Heteroleptic fluoro-​substituted aromatic lanthanide carboxylates, luminescent properties, and organic LED- based diodes Stefan, B. B.; Vashchenko, A. A.; Kalyakina, A. S.; Solodukhin, N. N.; Aslandukov, A. N.; Braese, Stefan; Kuzmina, N. P. Russ. (2018), RU 2657496 C1 20180614.

U. Schepers, S. Bräse, B. Olshausen, Fluorescent compounds for the detection of malignant melanoma. Eur. Pat. Appl. (2018), EP 3373009 A1 20180912

S. M. Aslan, A. Gall, P. Lieber, U. Lemmer, S. Bräse, Siebdrucktinte und Verfahren zu deren Herstellung. Eur. Pat. Appl. (2018), EP 18190210.7 – 1102 – EPA 18179061 EPA 18179067

S. M. Aslan, A. Gall, U. Lemmer, S. Bräse, Siebdruckfähiges Titansulfid für die Anwendung in einem thermoelektrischen Generator. Eur. Pat. Appl. (2018), EP 18190209.9 – 1102 – EPA 18179061 EPA 18179067

J. Arras, S. Bräse, R. Reimert, Surface-​functionalized luminophore, composition and cured composition comprising same and use of same, and method for producing a luminescence-​marked article From PCT Int. Appl. (2019), WO 2019016274 A1 20190124

S. M. Aslan, A. Gall, P. Lieber, U. Lemmer, S. Bräse, Siebdrucktinte und Verfahren zu deren Herstellung. Eur. Pat. Appl. (2020), EP 3587507 A1 20200101.

L. Series

 

Beiträge zur organischen Synthese, Logos-Verlag, ISSN: 1862-5681, Editor: S. Bräse

Bd. 1: Ulrike Ohnemüller, Effiziente Synthese hochsubstituierter enantiomerenreiner Cyclohexenone und Tetrahydroxanthenone

Bd. 2: Carl Friedrich Nising, Die Totalsynthese des Pilzmetaboliten Diversonol und analoger Verbindungen mit Tetrahydroxanthenon-Gerüst

Bd. 3: Maarten Schroen, Synthese, Zersetzungskinetik und basische Abspaltung von festphasengebundenen Triazenen, Diazoniumionen und Sulfonamiden

Bd. 4: Daniel Keck, Virantmycin und Spiculoinsäure A - die intramolekulare Diels-Alder-Reaktionin in der Synthese komplexer Naturstoffe

Bd. 5: Julia Gall, Stereoselektive Synthese von Mycotoxinen mit Macrolactongrundgerüst

Bd. 6: Thomas Baumann, Organokatalytische Synthesestrategien zur Darstellung a,a-disubstituierter Aminosäurederivate

Bd. 7: Tina Schröder, Synthese und Anwendung neuer funktionalisierter Peptoide als zellgängige (Antitumor-) Wirkstofftransporter

Bd. 8: Anne Friedrich, Chemische und biochemische Methoden zum Aufbau bioaktiver Stickstoff-Heterozyklen

Bd. 9: Nicole Jung, Darstellung Diarylether-haltiger Naturstoffe an der festen Phase und Synthese neuartiger fluorierter Linker

Bd. 10: Sefer Ay, Synthese und Anwendung von[2.2]Paracyclophanliganden in der asymmetrischen konjugaten Addition

Bd. 11: Emilie Gérard, Total Synthesis of Blennolide C and related C4a-functionalized Tetrahydroxanthenones

Bd. 12: Rüdiger Reingruber: Darstellung chiraler Amine und Aldehyde durch metall- und organokatalysierte Methoden sowie deren Anwendung in der Natur- und Wirkstoffsynthese

Bd. 13: Manuel Jainta: Die Rostratine - Intramolekulare Diels-Alder-Reaktion, Aufbau von Diketopiperazinen und thiogene Funktionalisierung

Bd. 14: Daniel Fritz: Peptoide als Peptidomimetica: Synthese, Struktur- und Aktivitätsuntersuchung

Bd. 15: Caroline Hartmann: Anwendung organokatalytischer Strategien zur Synthese biologisch-aktiver Strukturen und Untersuchung NHC-Palladium-katalysierter Prozesse

Bd. 16: Hülya Sahin: Synthese von Ergochromen und deren Dimerisierung zum Aufbau von Secalonsäuren

Bd. 17: Esther Birtalan: Chemische Biologie von Molekularen Transportern auf Peptoid-Basis

Bd. 18: Christian Friedmann, Synthese und Anwendung chiraler [2.2]Paracyclophan- und BINOL-Derivate

Bd. 19: Matthias Wiehn, Darstellung funktionalisierter Organofluorverbindungen durch die Entwicklung fluorierend spaltbarer Linker für die Festphasensynthese und durch aromatische Substitution

Bd. 20: Nicole Volz, Sauerstoff-Heterocyclen als neue, selektive Liganden für die Cannabinoid-Rezeptoren

Bd. 21: Patrick Groß, Die Totalsynthese von (+)-Fumimycin

Bd. 22: Ulrike Groß, Entwicklung einer flexiblen stereoselektiven Synthesestrategie zur Darstellung der Thiodiketopiperazin-Naturstoffe Aranotin, Gliotoxin, Epicoccin A-H, Epicorazin A-C, Exserohilon und Rostratin A

Bd. 23: Christine Schilling, Synthese symmetrischer Tetraphenyaldamantane und deren Anwendung zur Darstellung molekularer organischer Nanostrukturen

Bd. 24: Stephanie Arzt, Asymmetrische Totalsynthese von Plakotenin-Estern und analogen Verbindungen

Bd. 25: Oliver Plietzsch, Modulare Synthesen funktionalisierter Tetraphenylmethanderivate als Bausteine für supramolekulare Netzwerke 

Bd. 27: Nadine Allendörfer, Entwicklung neuer Methoden zur Synthese von Organofluorverbindungen und deren Anwendungen in der Wirkstoff-Optimierung 

Bd. 28: Birgit Rudat, Photophysikalische Eigenschaften fluorophormarkierter Peptoide. - vom Ensemble zu Einzelmolekülmessungen

Bd. 30: Manuel C. Bröhmer, Die Domino-oxa-Michael-Aldol-Reaktion in der Naturstoffsynthese: Asymmetrische Totalsynthesen von (-)-Diversonol, (+)-Lachnon C und Tetrahydrocannabinol-Analoga

Bd. 31: Bettina Ruff, Chemische und biochemische Methoden zur stereoselektiven Synthese von komplexen Naturstoffen

Bd. 32: Sebastian Schaarschmidt, Synthese von geminal difluorierten Glycosphingolipiden

Bd. 33: Anna M. Linsenmeier, Parnafungine und Phenanthridine -Leitstrukturen für die Wirkstoffsynthese

Bd. 34: Sidonie B. L. Vollrath, Synthese Funktioneller Peptoide und Peptoid-Macrocyclen

Bd. 35: Marion Döbele, Entwicklung neuer Linker und fluorierender Spaltungsmethoden zur diversitätsorientierten Darstellung von Organofluorverbindungen

Bd. 36: Daniel Fürniß, Neue molekulare Transporter auf Polyamin- und Peptoidbasis

Bd. 37: Dominik K. Kölmel, Chemische Biologie von neuen zellgängigen Peptoiden und Synthese fluoriger Farbstoffe

Bd. 38: Ekaterina Sokolovskaya, Synthesis and Biomedical Applications of Multifunctional Poly(ethylene glycol) Derivatives

Bd. 39: Anne Claire Meister, Flexible Synthesestrategie zur Darstellung von Tetrahydroxanthenon-Naturstoffen

Bd. 40: Daniel M. Zink, Entwicklung neuartiger oligonuklearer Kupferkomplexe als Emittermaterialien für organische Leuchtdioden

Bd. 41: Stefan Michael Seifermann, Mono- und Hexakis-Funktionalisierung von Buckminster-Fulleren C60 mit Methylen-Bisoxazolinen

Bd. 42: Tobias Hagendorn, Neue Wege zu (Hetero-)Cyclooctinen

Bd. 43: Andreas Hafner, Entwicklung neuer Perfluoralkylierungsmethoden zur Darstellung von fluorierten aromatischen und olefinischen Bausteinen

Bd. 44: Carsten S. Kramer, Synthetische Zugänge zum A,B,C-Ringsystem des Naturstoffes Beticolin 0 durch regioselektive Naphthochinon-Diels-Alder-Reaktionen

Bd. 45: Joshua Kramer, Neue Funktionalisierungs- und Anwendungsmöglichkeiten von [2.2]Paracyclophanen und [2](1,4)Benzo[2](2,5)pyridinophanen

Bd. 46: Mark Busch, Synthese und Funktionalisierung von stickstoffhaltigen Heterozyklen und deren Anwendung

Bd. 47: Carmen Cardenal, Design, Synthesis and Evaluation of Highly Functionalized Peptoids as Antitumor Peptidomimetics

Bd. 48: Franziska Gläser, Neuartige Cannabinoide - Synthese und biologische Evaluierung

Bd. 49: Daniel Volz, Zweikernige Kupfer(I)-Komplexe als OLED-Leuchtstoffe. Synthese, Eigenschaften und neue Konzepte

Bd. 50: Stephanie Lindner, Methoden zur chemischen Synthese sowie zur mechanistischen Untersuchung der Biosynthese von polycyclischen Naturstoffen

Bd. 51: Mirja Enders, Neue Materialien für die heterogene und homogene Katalyse: Synthesen und Anwendungen von Platin-Cyclooctadien-Komplexen und [2.2]Paracyclophan-Derivaten

Bd. 52: Dominic Lütjohann, Das Digitale Labor: Erfassen, Finden und Veröffentlichen von Daten am Beispiel der Chemie

Bd. 53: Sabilla Zhong, Stereoselektive Synthese von Hydroindolen, Bisindolen und Thiodiketopiperazinen als Bausteine für Rostratin C sowie als neuartige Leitstrukturen für die Wirkstoffentwicklung

Bd. 54: Bettina Stanek, Neue Reaktionsmöglichkeiten von Dithianylium-Salzen

Bd. 55: Alexandra Maria Schade, Synthese pseudo-oktaedrischer Hexaphenyl-p-xylol-Derivate als rigide Bausteine zur Darstellung supramolekularer Netzwerke sowie deren potentielle Anwendung als selektive Gasspeicher

Bd. 56: Christina Belenki, Synthese von photoschaltbaren Emulgatoren und Modellsystemen großtechnisch relevanter Polymere sowie Untersuchung deren Eigenschaften

Bd. 57: Larissa Bergmann, New Emitters for OLEDs: The Coordination- and Photo-Chemistry of Mononuclear Neutral Copper(I) Complexes

Bd. 58: Manuela Wallesch, Synthesis and Characterization of Luminescent Cu(I) Complexes, Reihe: Beiträge zur organischen Synthese

Bd. 59: Anna Hörner, Mikroskopische und spektroskopische Untersuchungen von Fluoreszenzfarbstoffen und fluoreszenzmarkierten Glykostrukturen

Bd. 60: Katharina Stefanie Peschko, Synthese cyclischer Peptoide und Anwendung der kupferkatalysierten 1,3-dipolaren Cycloaddition zur Herstellung neuartiger Sekundärstrukturen

Bd. 61: Irina Protasova, Synthese von Diazirinen über harzgebundene Sulfonyl-Oxime und in situ Raman-spektroskopische Untersuchungen von Festphasenreaktionen

Bd. 62: Tim Wezeman, Sulfonyl Ynamides as Useful Tools for N-Heterocyclic Chemistry

Bd. 63: Paul Felix Sauter, Synthese von N-Glykanen zur chemischen Glykomodifikation von Proteinen

Bd. 64: Carolin Braun, Synthese und Anwendung planar-chiraler [2.2]Paracyclophanliganden mit N-Donorfunktionen und deren Übergangsmetallkomplexe zur Synthese substituierter Amine

Bd. 65: Marco Mende, Chemische Synthese von bioisosteren Hyaluronsäure-Oligomeren und anderen Saccharid-Derivaten

Bd. 66: Isabelle D. Wessel, Synthese organischer Bausteine für kovalent gebundene, poröse Netzwerke über Nitroxid-Austausch-Reaktion

Bd. 68: Angela Wandler, Entwicklung neuartiger Platin(II)-Komplexe mit 1,5-Cyclooctadienliganden: Ligandendesign, Charakterisierung und biologische Evaluation

Bd. 69: Steven Susanto, Methodenentwicklung an der festen Phase: Etablierung neuer Dithian-Linker zur Synthese flexibler Bausteine am Beispiel von neuen fluorierten Verbindungen. Studien zur Synthese von Sibiromycin-Analoga

Bd. 70: Mirella Wawryszyn, Glycokonjugate - Strategien und Möglichkeiten

Bd. 71: Mathias Lang, Darstellung poröser organischer Netzwerke via Thiol-Click-Reaktionen sowie die festphasenbasierte Synthese von para-Oligo(phenylenethinyl)-Derivaten

Bd. 72: Suparna Tambe, Structure Performance Relationships of the Novel MALDI-MS Matrices

Bd. 73: Thomas Hurrle, Synthesis of Cannabinoid Ligands. Novel Compound Classes, Routes and Perspectives

Bd. 74: Stephan W. Münch, Festphasensynthese neuartiger molekularer Transporter und funktioneller Peptoide

Bd. 75: Vanessa Koch, Entwicklung neuer Synthesemethoden zur Darstellung von Calotropin und verwandten Cardenoliden als Leitstrukturen für potentielle Anti-Tumor-Wirkstoffe

Bd. 76: Alena Kalyakina, Novel Lanthanide-Based Luminescent Probes for Biological and Lighting Applications

Bd. 77: Christina Retich, Stereoselektive Synthese von N-haltigen Heterocyclen und thio-modifizierten Apicidin-Derivaten als neuartige Leitstrukturen für die Wirkstoffentwicklung

Bd. 78: Anne Christine Schneider, Lineare und zyklische Peptoide. Funktionelles Design und Anwendung als potentielle Pharmazeutika

Bd. 79: Yuling Hu, Metal-Catalyzed N–H and O–H Insertion from α-Diazocarbonyl Compounds

Bd. 80: Alexander Braun, Synthese neuer Fluorophore für biologische Bildgebungsverfahren und Imagingexperimente

Bd. 81: Patrick Hodapp, Methodenentwicklung an der festen Phase: Kombinatorische Abspaltung immobilisierter pseudo-Oxazolone als biologisch relevante Leitstrukturen

Bd. 82: Eduard Spuling, Synthesis of New [2.2]Paracyclophane Derivatives for Application in Material Sciences

Bd. 83: Yu-Chieh Huang. Methods for adapting virtual environments to the challenges of efficient digitization strategies in synthetic chemistry