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

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

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

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

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

Prepare hyper–cross-linked polymers by click polymerization

A. Eigenständige Zeitschriftenartikel

2017

V. Koch, S. Bräse, Org. Biomol. Chem. 2017, 15, 92-95. Pd-mediated cross-coupling of C-17 lithiated androst-16-en-3-kol – An access to functionalized arylated steroid derivatives

DOI: 10.1039/C6OB02496C

I. Protasova, B. Bulat, N. Jung, S. Bräse, Org. Lett. 2017, 19, 34-37. Synthesis of Diaziridines and Diazirines via Resin-bound Sulfonyl Oximes

DOI:10.1021/acs.orglett.6b03252

A. A Aly, A. A. Hassan, S. Bräse, M. A. A. Ibrahim, El-Shimaa S. M. AbdAl-Latifa, E. Spuling, M. Nieger, J. Sulf. Chem. 2017, 38, 69-73. 1,3,4-Thiadiazoles and 1,3-thiazoles from one-pot reaction of bisthioureas with 2-(bis(methylthio)methylene)malononitrile and ethyl 2-cyano-3,3-bis(methylthio)acrylate

DOI:10.1080/17415993.2016.1237637

A. A Aly, A. A. Hassan, S. Bräse, M. A.-M. Gomaa, F. M. Nemr, J. Heterocyclic Chem. 2017, 54, 480-483. Reaction of amidrazones with diaminomaleonitrile - Synthesis of 4-amino-5-iminopyrazoles

DOI:10.1002/jhet.2607

A. A. Aly, A. A. Hassan, M. Gomaa, S. Bräse, F. M. Nemr, J. Heterocyclic Chem2017, 54, 775-779. Reaction of Amidrazones with Phthaloyl Chloride-Synthesis of 1,2,4-Triazolium Salts (Part I)

DOI:10.1002/jhet.2643

A. A. Aly, A. A. Hassan, M. Gomaa, S. Bräse, F. M. Nemr, J. Heterocyclic Chem2017, 54, 775-779. Reaction of Amidrazones with Phthaloyl Chloride-Synthesis of 1,2,4-Triazolium Salts (Part I)

DOI:10.1002/jhet.2643

S. Tambe, H. Blott, A. Fülöp, N. Spang, D. Flottmann, S. Bräse, C. Hopf, H.-D. Junker, Anal. Bioanal. Chem. 2017, 409(6), 1569-1580. Structure Performance Relationships of Phenyl Cinnamic Acid Derivatives as MALDI-MS Matrices for Sulfatide Detection

DOI:10.1007/s00216-016-0096-6

M. Petrović, D. Scarpi, M. Nieger, N. Jung, E. G. Occhiato, S. Bräse, RSC Advances 2017, 7, 9461-9464. Oxidation of Diazenyl-protected N-Heterocycles - A new Entry to Functionalized Lactams

T. Wezeman, J. Comas-Barceló, M. Nieger, J. P. A. Harrity, S. Bräse, Org. Biomol. Chem.. 2017, 15, 1575-1579. Synthesis of aminopyrazoles from sydnones and ynamides

V. Koch, M. Nieger, S. Bräse, Adv. Synth. Catal. 2017, 359, 832-840. Stille and Suzuki Cross-Coupling Reactions as Versatile Tool for Modifications at C-17 of Steroidal Skeletons – A Comprehensive Study

K. V. Kutonova, N. Jung, P. S. Postnikov, M. E. Trusova, V. D. Filimonov, S. Bräse, Synthesis 2017, 49, 1680-1688. Arenediazonium tosylates (ADTs) as efficient reagents for Suzuki-Miyaura cross-coupling in neat water

DOI: 10.1055/s-0036-1588919

A. Serdaroglu, S. A. Müller, U. Schepers, S. Bräse, S. F. Lichtenthaler, P.-H. Kuhn, Proteomics 2017, 17(5). 1600423. An optimized version of the Secretome Protein Enrichment with Click Sugars (1 SPECS) method leads to enhanced coverage of the secretome

DOI: 10.1002/pmic.201600423

Q. An, Y. Hassan, X. Yan, P. Krolla-Sidenstein, T. Mohammed, M. Lang, S. Bräse, M. Tsotsalas, Beilstein J. Org. Chem. 2017, 13, 558–563. Fast and efficient synthesis of microporous polymer nanomembranes via light induced click reaction

M. Faust, M. Dinkel, M. Bruns, S. Bräse, M. Seipenbusch, Ind. & Eng. Chem. Res. 2017, 56, 3194-3203. Correlations between the structure and the water-gas shift activity of highly defined CVD generated Pt/TiO2 nanoparticles

Doi:10.1021/acs.iecr.6b04512

A. A. Hassan, S. K. Mohamed, F. F. Abdel-Latif, S. M. Mostafa, M. Abdel-Aziz, J. T. Mague, M. Akkurt, S. Bräse, M. Nieger, J. Heterocyclic Chem. 2017, 54(2), 959-964. (Substituted Ylidene)​Amino-​2-​Oxo-​Indolylidene Thioureas and Bis(2-​Oxo-​Indolylidene)​Urea from (Ylidene)​Thiocarbonohydrazides and Isatylidene Malononitrile

DOI: 10.1002/jhet.2660

C. Braun, S. Bräse, L. L. Schafer, Eur. J. Org. Chem. 2017, 1760–1764. Planar-chiral [2.2]Paracyclophane-based Amides as Proligands for Titanium and Zirconium Catalyzed Hydroamination

http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201700101/abstract

 L. Geiger, M. Nieger, S. Bräse, ChemistrySelect 2017, 3268-3275. Scope and Limitations of the Domino Vinylogous Aldol-oxa-Michael Reaction

 https://doi.org/10.1002/slct.201700667

A. Aly, S. Bräse, J. Sulf. Chem. 2017, 38, 291-302. Oxidation-reduction and heterocyclization of the reactions of alkanedithiols with π-deficient compounds

https://www.tandfonline.com/doi/full/10.1080/17415993.2017.1278762

2016

A. Kondrakov, A. N. Ignatev, V. V. Lunin, F. H. Frimmel, S. Bräse, H. Horn, Appl. Catal. B: Environ. 2016182, 424-430. Do free OH radicals in TiO2 photocatalysis come from H2O or dissolved O2? An isotope labeling study
 
L. Monnereau, T. Muller, M. Lang, S. Bräse, Chem. Commun. 201652, 571–574. Tunable porosity of 3D-networks with germanium nodes
    DOI: 10.1039/C5CC06790A
 
A. A. Hassan, N. K. Mohamed, K. M. A. El-Shaieb, H. N. Tawfeek, S. Bräse, M. Nieger, J. Heterocyclic Chem. 201653, 46-50. The Reactivity of Dimethyl Acetylenedicarboxylate and Heterocyclization of Hydrazinecarbothioamides to 1,3-Thiazolidin-4-ones
 
L. Bergmann G. Hedley T. Baumann S. Bräse I. Samuel, Science Adv. 20162(1), e1500889. Direct Observation of Intersystem Crossing in A Thermally Activated Delayed Florescence Copper Complex in the Solid State
 
P.-H. Kuhn, A. Colombo, B. Schusser, D. Dreymueller, J. Prox, U. Schepers, J. Herber, A. Ludwig, E. Kremmer, D. Montag, P. Saftig, S. Bräse, S. F. Lichtenthaler, ELife 2016, 5. Systematic substrate identification reveals a central role for the metalloprotease ADAM10 in axon and synapse function
 
D. K. Kölmel, A. Hörner, J. A. Castañeda, J. A. P. Ferencz, A. Bihlmeier, M. Nieger, S. Bräse, L. Padilha J. Phys. Chem2016120, 4538-4545. Linear and Nonlinear Optical Spectroscopy of Fluoroalkylated BODIPY Dyes
 
T. Wezeman S. Zhong, M. Nieger, S. Bräse, Angew. Chem. Int. Ed. 201655, 3823-3827. Synthesis of highly functionalized 4-aminoquinolines
 
A. A Aly, T. El Malah, E. A. Ishak, S. Bräse, J. Sulfur Chem. 201637, 141-147. Reaction of dithiocarbamates with malononitrile dimer; simple synthesis of new 1,4-dihydropyridine-2-thiols 
 
T. El Malah, A. A. Aly, S. Bräse, N. A. A. Elkanzi, A. B. Brown, J. Sulfur Chem. 201637, 222-228. Reaction of dithiocarbamates with 2-[bis(methylthio)-methylene]malononitrile. Unexpected formation of 4-imino-6-(methylthio)-3-substituted-3,4-dihydro-2H-1,3-thiazine-2-thiones 
 
A. A. Hassan, N. K. Mohamed, L. E. Abd El-Haleem, S. Bräse, M. Nieger, Curr. Org. Synth. 2016, 426-431. Synthesis of New Furo-imidazo[3.3.3]propellanes
 
N. Griebenow, A. Dilmaç, S. Greven, S. Bräse, Bioconj. Chem. 2016, 27, 911-917. Site-specific conjugation of peptides and proteins via re-bridging of disulfide bonds using the thiol-yne coupling reaction. 
 
S. Susanto, N. Jung, S. Bräse, RSC Advances 2016, 6, 39573-39576 Solid Phase Syntheses of S,N-substituted 2-Mercaptobenzoimidazoles
 
A. A. Hassan, F. F. Abdel-latif, M. Abdel Aziz, S. M. Mostafa, S. Bräse, M. Nieger,, J. Heterocyclic Chem. 2016, 633–636. Efficient and farcile synthesis of substituted aminothiadiazolylhydrazonoindolin-2-ones
 
A. A. Hassan, Y. R. Ibrahima, E. M. El-Sheref, S. Bräse, J. Heterocyclic Chem. 2016, 53, 876-881. Novel Synthesis of 1,3-Thiazine and Pyrimidinethione Derivatives from (1-Arylethylidene)hydrazinecarbothioamides and Tetracyanoethylene 
 
C. Braun, E. Spuling, N. Heine, M. Cakici, M. Nieger, S. Bräse, Adv. Synth. Catal. 2016, 1664-1670. Efficient and Modular Synthesis of Isomeric Mono- and Bis-pyridylparacyclophanes by Cross-Coupling Reactions
 
I. Wessely, V. Mugnaini, G. Jeschke, S. Bräse M. Tsotsalas, RSC Advances 2016, 6, 55715–55719. Radical exchange reaction of multi-spin isoindoline nitroxides followed by EPR spectroscopy
 
F. F. Loeffler, T. C. Foertsch, R. Popov, M. Schlageter, M. Sedlmayr, B. Mattes, D. Althuon, C. von Bojničić-Kninski, L. K. Weber, A. Fischer, V. Bykovskaya, I. Buliev, L. Hahn, M. A. R. Meier, S. Bräse, A. K. Powell, S. Balaban, F. Breitling, A. Nesterov-Müller, Nature Communs 2016, 7, 11844. High-flexibility combinatorial peptide synthesis with laser-based transfer of monomers in solid matrix material
D. Loits, S. Bräse, P. Donnelly, J. M. White, M. A. Rizzacasa, Eur. J. Inorg. Chem. 2016, 3541-3544. Synthesis of Homochiral CoIII and MnIV [2.2]Paracyclophane SALPN Complexes with Highly Selective Predetermined Chirality at the Metal Centre.
 
S. Grässle, S. Vanderheiden, P. Hodapp, B. Bulat, M. Nieger, N. Jung, S. Bräse, Org. Lett. 2016, 18, 3598-3601. Solid Phase Synthesis of (Benzannelated) Six-Membered Heterocycles via Cleavage of Resin-Bound Pseudo-Oxazolones 
 
S. P. J. T. Bachollet, D. Volz, B. Fiser, S. Münch, F. Rönicke, J. Carrillo, H. Adams, U. Schepers, E. Gómez-Bengoa, S. Bräse, J. P. A. Harrity, Chem. Eur. J. 2016, 22, 12430-12438. A Modular Class of Fluorescent Difluoroboranes: Synthesis, Structure, Optical Properties, Theoretical Calculations and Applications for Biological Imaging 
 
A. A. Hassan, N. K. Mohamed, L. E. Abd El-Haleem, S. Bräse, M. Nieger,, Chin. J. Org. Chem. 2016, 34, 814-822. Facile Synthesis of Naphtho[2,3-d]thiazoles, Naphtho[2,3-e]-[1,3,4]thiadiazines and Bis(naphtho[2,3-d]thiazole)copper(II) Derivatives from Heteroylthiosemicarbazides
 
 
A. A. Hassan, N. K. Mohamed, M. M. Makhlouf, S. Bräse, M. Nieger, H. Hopf, Synthesis 2016, 3134-3140. (Hex-2-en-ylidene)-N-Substituted hydrazinecarbothioamides and 2,3-Dichloro-1,4-naphthoquinone: Synthesis of Naphtho[2,3-f][1,3,4]thiadia-zepines and Naphtho[2,3-d]thiazoles
 
B. K. T. Batagoda, P. I. Djurovich, S. Bräse, M. E. Thompson, Polyhedron 2016, 116, 182-188. Synthesis and characterization of phosphorescent cyclometalated Ir and Pt heteroleptic complexes using cyclophane-based chelates
 
J. Striffler, D. Mattes, S. Schillo, B. Muenster, A. Fischer, B. Ridder, A. Welle, V. Trouillet, V. Stadler, G. Markovic, G. Proll, S. Bräse, F. F. Loeffler, A. Nesterov-Mueller, F. Breitling, ChemNanoMat 2016, 2, 897-903. Replication of Polymer Based Peptide Microarrays by Multi Step Transfer
 
DOI: 10.1002/cnma.201600194
 
K. V. Kudryavtsev, A. B. Mantsyzov, P. M. Ivantcova, M. N. Sokolov, A. V. Churakov, S. Bräse, N. S. Zefirov, V. I. Polshakov, Org. Lett2016, 18, 4698–4701. Control of Azomethine Cycloaddition Stereochemistry by CF3-Group: Structural Diversity of Fluorinated β-Proline Dimers
 
A. A. Aly, M. Ramadan, M. Abd Al-Aziz, H. M. Fathy, S. Bräse, A. B. Brown, M. Nieger, J. Chem. Res2016, 637-639. Reaction of amidrazones with 2,3-diphenylcyclopropenone - Synthesis of 3-(aryl)-2,5,6-triphenylpyrimidin-4(3H)-ones
 
 JCR1604173
 
P. Lindemann, A. Schade, L. Monnereau, W. Feng, K. Batra, H. Gliemann, P. A. Levkin, S. Bräse, C. Wöll, M. Tsotsalas, Chem. Materials A 20164, 6815-6818. Surface Functionalization of Microporous Polymer Thin Films and Nanomembranes using Orthogonal Chemistries
 
DOI: 10.1039/C5TA09429A
 
I. M. Deygen, C. Seidl, D. K. Kölmel, C. Bednarek, S. Heissler, E. V. Kudryashova, S. Bräse, U. Schepers, Langmuir 201632, 10861-10869. Novel form of doxorubicin modified by stearoylspermine encapsulated into PEGchitosan stabilized liposomes.
 
DOI: 10.1021/acs.langmuir.6b01023
 
V. V. Utochnikova, A. S. Kalyakina, I. S. Bushmarinov, A. A. Vashchenko, L. Marciniak, A. Kaczmarek, R. van Deun, S. Bräse, N. P. Kuzmina, J. Mat Chem. C. 20164, 9848-9855. Lanthanide anthracene-9-carboxylates – emitters for efficient NIR-emitting OLEDs
 
A. G. Lyapunova, N. A. Danilkina, A. F. Khlebnikov, B. Köberle, S. Bräse, I. A. Balova, Eur. J. Org. Chem2016, 4842-4851. Oxaenediynes through the Nicholas Type Macrocyclization Approach
 
 
W. Yan, C. Réthoré, S. Menning, G. Brenner-Weiβ, T. Muller, P. Pierrat, S. Bräse, Chem. Eur. J201622, 11522-11526. Hexakis terpyridine fullerene ligand and six-fold ruthenium, iridium and iron complexes. Synthesis and electrochemical properties
 
 doi:10.1002/chem.201600796
 
M. Wallesch, A. Verma, C. Fléchon, H. Flügge, D. M. Zink, S. Seifermann, J. M. Navarro,T. Vitova, J. Göttlicher, R. Steininger, L. Weinhardt, M. Zimmer, M. Gerhards, C. Heske, S. Bräse, T. Baumann, D. Volz, Chem. Eur. J. 2016, 16400-16405. Towards Printed Organic Light-emitting Devices: A solution-stable, highly soluble Cu(I)-NHetPHOS-complex for inkjet processing
 
A. A. Hassan, K. M. A. El-Shaieb, A. S. Abd El-Aal, S. Bräse, M. Nieger, J. Heterocyclic Chem. 2016, 2025–2029. Reactivity of N, N"-1,w-Alkanediyl-bis-[N'-organylthiourea] Derivatives Towards Isatylidene malononitrile
 
             DOI:10.1002/jhet.2524
 
B. Görling, S. Bräse, B. Luy, Metabolites 2016, 6(3), 27. NMR Chemical Shift Range of Urine in Various Organics Solvents
 
             doi: 10.3390/metabo6030027
 
M. Lang, A. M. SchadeS. Bräse, Beilstein J. Org. Chem. 2016, 2570-2576. Synthesis of Three-Dimensional Porous Hyper-crosslinked Polymers via Thiol-Yne Reaction
 
C. Koehler, P. Sauter, M. Wawryszyn, G. Estrada Girona, K. Gupta, M. H. Fritz, J.-E. Hofmann, A. Gyenesei, B. Galik, S. Junttila, P. Stolt-Bergner, C. Schultz, M. Biskup, H. Besir, V. Benes, J. Korbel, I. Berger, S. Bräse, E. A. LemkeNature Methods 201613, 997-1000. Genetic code expansion for multiprotein complex engineering
 
             doi:10.1038/nmeth.4032
 
S. Schmitt, J. Hümmer, S. Kraus, A. Welle, S. Grosjean, M. Hanke-Roos, A. Rosenhahn, S. Bräse, C. Wöll, C. Lee-Thedieck, M. Tsotsalas, Adv. Funct. Mat. 2016, 26, 8455-8462. Tuning the Cell Adhesion on Biofunctionalized Nanoporous Organic Frameworks
 
             DOI: 10.1002/adfm.201603054
 
A. A. Hassan, K. M. A. El-Shaieb, A. S. Abd El-Aal, S. Bräse, M. Nieger, ARKIVOC 2016, 406-415. Synthesis of Bis-oxathiaaza[3.3.3]propellanes via Nucleophilic Addition of (1,ω-Alkanediyl)bis(N'-organylthiourea) on Dicyanomethylene-1,3-indanedione
 
A. A. Aly, A. B. Brown, M. Ramadan, M. Abd El-Aziz, S. Bräse, H. M. Fathy, ARKIVOC 2016, 461-471. Selectivity of amidrazones towards activated nitriles. –Synthesis of new pyrazoles and NMR investigation
 
V. Koch, S. Bräse, Org. BiomolChem201715, 92-95. Pd-mediated cross-coupling of C-17 lithiated androst-16-en-3-kol – An access to functionalized arylated steroid derivatives
 
            DOI: 10.1039/C6OB02496C
 
I. Protasova, B. Bulat, N. Jung, S. Bräse, Org. Lett. 201719, 34-37. Synthesis of Diaziridines and Diazirines via Resin-bound Sulfonyl Oximes
 
             DOI:10.1021/acs.orglett.6b03252
 
A. Wandler, S. Bräse, Adv. Syn. Catal2016, 358, 4125-4128. Expeditious Synthesis of Functionalized 1-Arylcyclooctadienes via Palladium-Catalyzed Lithium Cross-Coupling Reactions
 
             DOI: 10.1002/adsc.201600887
 
Z. Wang, A. Knebel, S. Grosjean, D. Wagner, S. Bräse, C. Wöll, J. Caro, L. Heinke, Nature Comms2016, 7, 13872. Tunable Molecular Separation by Nanoporous Membranes

             DOI:10.1038/ncomms13872

2015

S. Zhong, A. Hafner, C. Hussal, M. Nieger, S. Bräse, RSC Advances 20155, 6255-6258. Metal-Free Radical Perfluoroalkylation of (Hetero)Arenes 

K. V. Kudryavtsev, C. Yu, P. M. Ivantcova, V. I. Polshakov, A. V. Churakov, S. Bräse, N. S. Zefirov, J.-H. Guh, Chemistry – Asian J. 2015, 383-389. Structural studies and anticancer activity of a novel class of beta-peptides

D. T. Thielemann, A. T. Wagner, Y. Lan, P. Oña-Burgos, I. Fernández, E. Rösch, D. K. Kölmel, A. K. Powell, S. Bräse, P. W. Roesky, Chem. Eur. J2015, 2813-2820. Peptoid Ligated Pentadecanuclear Yttrium and Dysprosium Hydroxy Clusters see paper here

F. Gläser, M. Bröhmer, M. Nieger, T. Hurrle, S. Bräse, Eur. J. Org. Chem2015, 1516-1524. The Diels-Alder Approach towards Tetrahydrocannabinol Derivatives see paper here

L. Monnereau, C. Grandclaudon, T. Muller, S. Bräse, RSC Advances. 2015, 23152-23159. Sulfur-based hyper cross-linked polymers DOI: 10.1039/C5RA01463H

M. Enders, C. J. Friedmann, P. Plessow, A. Bihlmeier, M. Nieger, W. Klopper, S. Bräse, Chem. Comm. 2015, 51, 4793 - 4795. Unprecedented pseudo-ortho and ortho metalation of [2.2]paracyclophanes – a methyl group matters

M. Cakici, Z.-G. Gu, M. Nieger, J. Bürck, L. Heinke, S. Bräse, Chem. Comm. 2015, 51, 4796-4798. Planar-chiral building blocks for metal-organic frameworks

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

A. Baniodeh, N. Magnani, S. Bräse, C. E. Anson, A. K. Powell, Dalton Trans. 2015, 6343-6347. Ligand field variations: Tuning the toroidal moment of Dy6 rings

F. A. A. Hassan, F. F. Abdel-Latif, M. Abdel Aziz, S. M. Mostafa, S. Bräse, M. Nieger, Chem. Pap. 2015, 69, 973-982. Heterocyclization of substituted ylidenethiocarbonohydrazides using dimethyl acetylenedicarboxylate     Article ID: 0595-14.

A. A. Hassan, K. M. A. EL-Shaieb, A. S. Abd El-Aal, S. Bräse, M. Nieger, Z. Naturf. 2015, 243-248. Novel Synthesis of Bis-thiazolidin-4-ones from N,N’’-1,ω-Alkanediyl-bis[Ǹ̀-organylthiourea]Derivatives

D. Volz, Y. Chen, M. Wallesch, R. Liu, C. Fléchon, D. M. Zink, H. Flügge, J. Friedrichs, R. Steininger, J. Göttlicher, C. Heske, L. Weinhardt, S. Bräse, F. So, T. Baumann, Adv. Mater. 2015, 27, 2538-2543. Bridging the Efficiency Gap: Fully Bridged Dinuclear Cu(I)-complexes for Singlet Harvesting in High-Efficiency OLEDs

 A. Hörner, T. Hagendorn, U. Schepers, S. Bräse, Bioconjugate Chemistry 2015, 26, 718-724. Photophysical properties and synthesis of new dye-cyclooctyne conjugates for multicolor and advanced microscopy

 D. Wagner, S. Bräse, Beilstein J. Org. Chem. 2015, 431-436. Selective Ruthenium-Catalyzed CH-Activation of Thioxanthones

D. K. Kölmel, M. Nieger, S. Bräse, RSC Advances 2015, 36762 - 36765. Highly Efficient Synthesis of Polyfluorinated Dendrons Suitable for Click Chemistry

D. Lütjohann, N. Jung, S. Bäse, Chemomet. Intel. Lab. Syst. 2015, 144, 100-107. Open Source Life Science Automation, Part 1: Design of experiments and data acquisition via “dial-a-device 
 

Z. Gu, S. Grosjean, S. Bräse, C. Wöll, L. Heinke, Chem. Commun. 2015, 51, 8998-9001. Enantioselective Adsorption in Homochiral Metal-Organic Frameworks: The Pore Size Influence

E. Sokolovskaya, S. Rahmani, A. Misra, S. Bräse, J. Lahann, ACS Applied Materials & Interfaces 2015, 7, 9744-9751. Dual-Stimuli Responsive Microparticles

Z. Wang, L. Heinke, J. Jelic, M. Cakici, M. Dommaschk, R. J. Maurer, H. Oberhofer, S. Grosjean, R. Herges, S. Bräse, K. Reuter, C. Wöll, PCCP 2015, 17, 14582-14587. Photoswitching in nanoporous, crystalline solids: An experimental and theoretical study for azobenzene linkers incorporated in metal-organic frameworks

P.-H. Kuhn, M. Voss, M. Haug-Kröper, B. Schröder, U. Schepers, S. Bräse, C. Haass, S. F. Lichtenthaler, R. Fluhrer, Mol. Cell. Prot. 2015, 14, 1584-1598. Secretome analysis identifies novel signal peptide peptidase-like 3 (SPPL3) substrates and reveals a role of SPPL3 in multiple Golgi glycosylation pathways

N. Danilkina, A. Lyapunova, A. Khlebnikov, G. Starova, S. Bräse, I. Balova, J. Org. Chem. 2015, 80, 5546-5555. Ring closing metathesis of Co2(CO)6-alkyne complexes for the synthesis of 11-membered dienediynes: how to overcome thermodynamical barriers

A. Dilmac, N. Griebenow, S. Bräse, RSC Advances 2015, 5, 54301-54303. Application of a novel small scale UV LED photochemical batch reactor for the thiol-yne reaction

P. Brenner, L.-M. Fleig, A. Welle, X. Liu, S. Bräse, U. Lemmer, J. Polymer Science: Polymer Physics 2015, 53, 1029-1034. Degradation mechanisms of polyfluorene-based organic semiconductor lasers under ambient and oxygen-free conditions.

S. Zhong, P. F. Sauter, M. Nieger, S. Bräse, Chem. Eur. J. 2015, 21, 11219-11225. Stereoselective Synthesis of Highly Functionalized Hydroindoles as Building Blocks for Rostratins B-D and Synthesis of the Pentacyclic Core of Rostratin C
DOI: 10.1002/chem.201501199

A. A. Hassan, Y. R. Ibrahim, E. M. El-Sheref, Mahmoud, A. A. Ibrahim, S. Bräse, J. Heterocyclic Chem. 2015, 52, 1201-1207. A Facile Synthesis of Oxoindenothiazine and Dioxospiro(indene-2,4'-thiazine) Derivatives from (Substituted ethylidene)hydrazinecarbothioamides 
DOI: 10.1002/jhet.2234

A. Garcia, C. Gil, N. Jung, S. Bräse, RSC Advances 2015, 65540-65545. Solid Phase Synthesis of Functionalized Indazoles using Triazenes – Scope and Limitations
DOI: 10.1039/C5RA09705C

S. Schmitt, M. Silvestre, M. Tsotsalas, A. Winkler, A. Shahnas, S. Grosjean, H. Gliemann, J. Lahann, S. Bräse, M. Franzreb, C. Wöll, ACS Nano 2015, 4219–4226. Hierarchically functionalized magnetic core/multi-shell particles and their post-synthetic conversion to polymer capsules
DOI:10.1021/acsnano.5b00483

X. Yu, Z. Wang, M. Buchholz, N. Füllgrabe, S. Grosjean, F. Bebensee, S. Bräse, C. Wöll, L. Heinke, PCCP 2015, 17, 22721-22725. Cis-to-Trans Isomerization of Azobenzene Investigated by Using Thin Films of Metal-Organic Frameworks
 
A. A. Hassan, F. F. Abdel-Latif, M. Abdel Aziz, S. M. Mostafa, S. Bräse M. Nieger, Chin. Chem. Lett. 2015, 1183-1186. Heterocyclization of Thiocarbonohydrazides: Facile Synthesis of 5-Unsubstituted-1,3,4-Thiadiazoles
 
M. A. Gotthardt, S. Grosjean, Tobias S. Brunner, S. Wolf, S. Bräse, W. Kleist, Dalton 2015, 16802-16809. Synthesis and post synthetic modification of amine , alkyne , azide  and nitro functionalized metal organic frameworks based on DUT 5
    DOI: 10.1039/C5DT02276B
 
A. A. Hassan, N. K. Mohamed, M. M. Makhlouf, S. Bräse, M. Nieger, Synthesis 2015, 3036-3042. Synthesis of Oxa-aza- and Bis-oxathiaaza[3.3.3]propellanes from Dicyanomethylene-1,3-indanedione and 2,5-Dithioureas 
DOI:10.1055/s-0034-1380447
 
A. A. Hassan, N. K. Mohamed, L. E. Abd El-Haleem, S. Bräse, M. Nieger, J. Heterocyclic Chem. 2015, 52, 1368-1372. Synthesis of some New Heteroylhydrazono-1,3-thiazolidin-4-ones
 
S. Lindner, M. Nieger, S. Bräse, Adv. Synth. Catal. 2015, 357, 3303-3308. Stannylation and Stille Coupling of Base-Sensitive Tetrahydroxanthones to Heteromeric Biaryls
 
S. Zhong, A. E. E. Wandler, U. Schepers, M. Nieger, S. Bräse, Eur. J. Org. Chem. 2015, 6858-6871. Synthesis of New Diketopiperazines, Thiolation to Thiodiketopiperazines, and Examination of Their ROS-Generating Properties
 
S. Lindner, K. Masters, S. Bräse, J. Fluorine Chem. 2015, 179, 102-105. Metal-free Synthesis of (Poly)fluorobiaryls from (Poly)fluorobenzenes and Arylhalides – Scope and Limitations
 
A. S. Kalyakina, V. V. Utochnikova, I. S. Bushmarinov, I. V. Ananyev, I. L. Eremenko, D. Volz, F. Rönicke, U. Schepers, R. Van Deun, A. L. Trigub, Y. V. Zubavichus, N. P. Kuzmina, S. Bräse, Chem. Eur. J. 2015, 21, 17921-17932. Highly Luminescent, Water-soluble Lanthanide Pentafluorobenzoates: Syntheses, Structures and Photophysics 
 
Z. Wang, J. Liu, S. Grosjean, D. Wagner, W. Guo, G. Gu, L. Heinke, H. Gliemann, S. Bräse, C. Wöll, ChemNanoMat 2015, 1, 338-345. Monolithic, Crystalline MOF Coating: An Excellent Patterning and Photoresist Material (Cover picture)
 
T. Wezeman, Y. Hu, J. McMurtrie, S. Bräse, K.-S. Masters, Austr. J. Chem. 2015, 68, 1859-1865. Synthesis of Non-Symmetrical & Axially-Chiral Dibenzo[1,3]diazepines: Pd/CPhos-Catalysed Direct Arylation of 1-(ortho-haloaryl)-3-aryl-aminals
 
K. Kudryavtsev, P. Ivantcova, C. Yu, C. Muhle-Goll, A. Churakov, M. Sokolov, A. Dyuba, A. Arutyunyan, J. Howard, N. Zefirov, S. Bräse, J.-H. Guh, Org. Lett. 2015, 17, 6178-6181. Menthols as Chiral Auxiliaries for Asymmetric Cycloadditive Oligomerization: Syntheses and Studies of β-Proline Hexamers
 
N. Griebenow, S. Greven, M. Lobell, A. M. Dilmaç, S. Bräse, RSC Advances 2015, 5, 103506-103511. A study on the trastuzumab conjugation at tyrosine using diazonium salts
    DOI: 10.1039/C5RA18271A
 
Z. Wang, S. Grosjean, S. Bräse, L. Heinke, ChemPhysChem 2015, 16, 3779-3783.,Photoswitchable Adsorption in Metal-Organic Framework based on Polar Guest-Host Interaction 
 
C. Slomka, S. Zhong, A. Fellinger, U. Engel, C. Syldatk, S. Bräse, J. Rudat, AMB Express, 2015, 5, 85. Chemical synthesis and enzymatic, stereoselective hydrolysis of a functionalized dihydropyrimidine for the synthesis of β-amino acids
 
 

 

 

2014

M. Tsotsalas, J. Liu, B. Tettmann, S. Bräse, S. Grosjean, A. Shahnas, Z. Wang, C. Azucena, M. Addicoat, T. Heine, J. Lahann, J. Overhage, H. Gliemann, C. Wöll, J. Am. Chem. Soc. 2014, 136, 8-11. Fabrication of highly uniform gel-coatings by conversion of surface-anchored metal-organic Framework

D. Volz, A. F. Hirschbiel, D. M. Zink, J. Friedrichs, M. Nieger, T. Baumann, S. Bräse, C. Barner-Kowollik, J. Mat. Chem. C 2014, 2, 1457-1462. Highly Efficient Photoluminescent Cu(I)-PyrPHOS-Metallopolymers 

D. Jakubczyk, G. Brenner-Weiss, S. Bräse, Eur. J. Org. Chem. 2014, 592-597. Synthesis of tritium labelled and photoactivatable N-acyl-L-homoserine lactones - inter kingdom signalling molecules 

L. Monnereau, M. Nieger, T. Muller, S. Bräse, Adv. Funct. Mat. 2014, 24, 1054-1058. Tetrakis(4-thiylphenyl)methane: Origin of a Reversible 3D-Polymer

L. Heinke, M. Cakici, M. Dommaschk, S. Grosjean, R. Herges, S. Bräse, C. Wöll, ACS Nano 2014, 8, 1463-1467. Photoswitching in two-component SURMOFs: Optically triggered release from a molecular container

S. González-Gallardo, I. Kuzu, P. Oña-Burgos, T. Wolfer, C. Wang, K. Klinkhammer, W. Klopper, S. Bräse, F. Breher, Organometallics 2014, 33, 941-951. Coinage Metal Complexes of a Tris(pyrazolyl)methanide-based Redox-Active Metalloligand.

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

N. Jung, B. Stanek, S. Grässle, M. Nieger, S. Bräse, Org. Lett. 2014, 16, 1112-1115. Reactions of resin-bound triazenes with dithianylium tetrafluoroborates: efficient synthesis of α-azo ketene dithioacetals and related hydrazones

T. Hagendorn, S. Bräse, Eur. J. Org. Chem. 2014, 1280–1286. A New Route to Cyclooct-2-ynol and its Functionalization by Mitsunobu Chemistry

J. Kramer, C. Yildiz, M. Nieger, Eur. J. Org. Chem. 2014, 1287–1295. Direct Access to 4,5-Disubstituted [2.2]Paracyclophanes by Selective ortho-Halogenation with Pd-Catalyzed C-H Activation 

A. Hörner, D. Volz, T. Hagendorn, D. Fürniss, L. Greb, F. Rönicke, M. Nieger, U. Schepers, S. Bräse, RSC Advances 2014, 4, 11528-11534. Switchable Fluorescence by Click Reaction of Azidocarbazole Dye

P. Weis, U. Schwarz, F. Hennrich, D. Wagner, S. Bräse, M. Kappes, PCCP 2014, 6225-6332. Azaporphine guest-host complexes in solution and gas-phase: evidence for partially filled nanoprisms and exchange reactions

T. Hagendorn, S. Bräse, RSC Advances 2014, 15493-15495. A new route to dithia- and thiaoxacyclooctynes via Nicholas reaction

C. S. Kramer, M. Nieger, S. Bräse, Eur. J. Org. Chem. 2014, 2150–2159. Regioselective Naphthoquinone Diels–Alder-Reactions – Towards the ABC Ring System of Beticolin 0 

K. Jehle, L. Cato, A. Neeb, C. Muhle-Goll, N. Jung, E. W. Smith, V. Buzon, L. R. Carbó, E. Estébanez-Perpiñá, K. Schmitz, L. Fruk, B. Luy, Yu Chen, M. B. Cox, S. Bräse, M. Brown, A. C. B. Cato, J. Biol. Chem. 2014, 8839-8851. Coregulator control of androgen receptor action by a novel nuclear receptor-binding motif

A. A. Hassan, K. El-Shaieb, N. K. Mohamed, H. N. Tawfeek, S. Bräse, M. Nieger, Tetrahedron Lett. 2014, 55, 2385-2388. A novel and facile synthesis of mesoionic 1,2,4-triazolium-3-thiolate derivatives

E. Sokolovskaya, L. Barner, S. Bräse, J. Lahann, Macromol. Rapid Commun2014, 35, 780-786.  Synthesis and On-Demand Gelation of Multifunctional Poly(ethylene glycol) Derivatives 

D. K. Kölmel, A. Hörner, F. Rönicke, M. Nieger, U. Schepers, S. Bräse, Eur. J. Med. Chem. 2014, 79C, 231-243. Cell-penetrating peptoids: Introduction of novel cationic side chains

S. Zhong, M. Nieger, A. Bihlmeier, M. Shi, S. Bräse, Org. Biomol. Chem. 2014, 3265-3270. Asymmetric Organocatalytic Synthesis of 4,6-Bis(1H-indole-3-yl)-piperidine-2 carboxylates

A. A. Hassan, A. A. Aly, Kamal M. A. El-Shaieb, T. M. I. Bedair, S. Bräse, J. Heterocyclic Chem. 2014, 51, 674-682. Synthesis of 1,3-thiazine-4-ones from substituted (ylidene)hydrazinecarbothioamides and dimethyl acetylenedicarboxylate

M. Cayir, L. Taghizadeh Goochany, A. Walli, M. Busch, Y. Sun, F. Meyer, S. Bräse, W. R. Thiel, Eur. J. Inorg. Chem. 2014, 2618-2624. C-H Activation at a Bidentate Ligand coordinated to Palladium(II): an Electrophilic Attack Supported by an External Base

A. Hafner, C. Hussal, S. Bräse, Synthesis 2014, 1448-1454. Preparation of Aromatic Triazenes and their application in Silver-mediated Perfluoroalkylation Reactions

S. Lindner, S. Bräse, RSC Advances 2014, 4, 29439-29442. A mild method for eliminating alkyl ethers to alkenes

A. C. Meister, A. Encinas, H. Sahin, E. M. C. Singer, C. F. Nising, M. Nieger, S. Bräse, Eur. J. Org. Chem. 2014, 4861-4875. Total Synthesis of Blennolide mycotoxins - Design, Synthetic Routes and Completion

A. O. Kondrakov, A. N. Ignatev, F. H. Frimmel, S. Bräse, H. Horn, I. A. Revelsky, Appl. Catal. B 2014, 160-161, 106-114. Formation of genotoxic quinones during bisphenol A degradation by TiO2 photocatalysis and UV photolysis: A comparative study

M. Enders, B. Görling, A. B. Braun, J. Seltenreich, L. Reichenbach, M. Nieger, K. Rissanen, B. Luy, U. Schepers, S. Bräse, Organometallics 2014, 33, 4027-4043. Cytotoxicity and NMR Studies of Platinum Complexes with Cyclooctadiene Ligands

D. Volz, M. Wallesch, S. Grage, J. Göttlicher, R. Steininger, D. Batchelor, A. S. Ulrich, C. Heske, L. Weinhardt, T. Baumann, S. Bräse, Inorg. Chem. 2014, 53, 7837-7847. Labile or stable: Can homoleptic and heteroleptic PyrPHOS-copper complexes be processed from solution?

A. Schade, L. Monnereau, T. Muller, S. Bräse, ChemPlusChem 2014, 1176-1182. Hexaphenyl-p-xylene, a rigid pseudo-octahedral core for 3D porous frameworks

V. Mugnaini, M. Tsotsalas, F. Bebensee, S. Grosjean, A. Shahnas, S. Bräse, J. Lahann, M. Buck, C. Wöll, Chem. Commun. 2014, 11129-11131. Electrochemical investigation of covalently post-synthetic modified SURGEL coatings

N. A. Danilkina, A. E. Kulyashova, A. F. Khlebnikov, S. Bräse, I. A. Balova, J. Org. Chem. 2014, 9018-9045. Electrophilic Cyclization of Aryldiacetylenes in the Synthesis of Functionalized Enediynes Fused to a Heterocyclic Core

M. Majewsky, R. Peschke, D. Wagner, M. Delay, S. Bräse, V. Yargeau, H. Horn, Chem. Res. Toxicol. 2014, 27, 1821-1828. Antibacterial activity of sulfamethoxazole transformation products (TPs): General relevance for sulfonamide TPs modified at the para-position

A. Hassan, N. K. Mohamed, M. M. Makhlouf, S. Bräse, M. Nieger, Synthesis 2014, 3097-3102. Reaction of Dimethyl Acetylenedicarboxylate with Dithiobiurea Derivatives 

K. Peschko, A. Schade, S. B. L. Vollrath, U. Schwarz, B. Luy, C. Muhle-Goll, P. Weis, S. Bräse, Chem. Eur. J. 2014, 16273-16278. Dendrimer-Type Peptoid-decorated Hexaphenylxylenes or Tetraphenylmethane – Synthesis and Structure in Solution & Gas Phase 

S. Lindner, F. Geu-Flores, S. Bräse, N. H. Sherden, S. E. O'Connor, Chemistry & Biology 2014, 21, 1452–1456. Conversion of substrate analogues suggests a Michael cyclization in iridoid biosynthesis  

D. Kratzer, L. Barner, C. Friedmann, S. Bräse, J. Lahann, Eur. J. Org. Chem. 2014, 8064–8071. A Novel Synthetic Route to Sulfobetaine Methacrylates with Variable Charge Distance

S. Wolff, M. Crone, T. Muller, M. Enders, S. Bräse, M. Türk, J. Supercrit. Fluids 2014, 95, 588-596. Preparation of supported Pt nanoparticles by Supercritical Fluid Reactive Deposition: Influence of precursor, substrate and pressure on product properties

 

 

2013

 

U. Sternberg, E. Birtalan, I. Jakovkin, B. Luy, U. Schepers, S. Bräse, C. Muhle-Goll, Org. Biomol. Chem. 2013, 640–647. Structural Characterization of a Peptoid with Lysine-like Side Chains and Biological Activity using NMR and Computational Methods.

C. Belenki, M. Winkelmann, M. Nieger; W. Gerlinger; B. Sachweh, H. P. Schuchmann, T. Muller, S. Bräse, J. Coll. Int. 2013, 393, 203–209. Cleavable surfactants to tune the stability of W/O miniemulsions.

J. J. P. Kramer, M. Nieger, S. Bräse,. Eur. J. Org. Chem. 2013, 541–549. Synthesis of Novel Planar Chiral N-Heterocyclic Substituted Pyridinophanes.

K.-S. Masters, S. Bräse, Angew Chem. 2013, 125, 899–903; Angew Chem. Int. Chem. 2013, 52, 866–869. The Acetal Concept: Regioselective Access to ortho,ortho- Biphenols via Dibenzo-[1,3]-dioxepines.

O. Plietzsch, A. Schade, A. Hafner, J. Huuskonen, K. Rissanen, M. Nieger, T. Muller, S. Bräse, Eur. J. Org. Chem. 2013, 283–299. Synthesis and topological determination of novel hexakis-substituted 1,4 bistritylbenzene and nonakis-substituted 1,3,5 tristritylbenzene derivatives: Building blocks for higher supramolecular assemblies.

D. Zink, M. Bächle, T. Baumann, M. Nieger, M. Kühn, C. Wang, W. Klopper, U. Monkowius, T. Hofbeck, H. Yersin, S. Bräse, Inorg. Chem. 2013, 52, 2292–2305. Synthesis, structure, and characterization of dinuclear copper(I) halide complexes with N^P ligands featuring exciting photoluminescence properties.

D. Fürniss, T. Mack, S. B. L. Vollrath, K. Koroniak, F. Hahn, U. Schepers, S. Bräse, Beilstein J. Org. Chem. 2013, 9, 56–63. Peptoids and Polyamines going Sweet: Part 1. Modular synthesis of Glycosylated Peptoids and Polyamines using Click Chemistry.

S. Vollrath, C. Hu, S. Bräse, K. Kirshenbaum, Chem. Commun. 2013, 49, 2317-2319. Peptoid Nanotubes: An Oligomer Macrocycle that Reversibly Sequesters Water via Single-Crystal-To-Single-Crystal Transformations

S. Halbedl, M.-C. Kratzer, K. Rahm, N. Crosta, K.-S.Masters, S. Bräse, D. Gradl, FEBS Letters 2013, 587, 522–527. Synthesis of novel inhibitors blocking Wnt signaling downstream of beta-Catenin

M. Austeri, M. Enders, M. Nieger, S. Bräse, Eur. J. Org. Chem. 2013, 1667-1670. [2.2]Paracyclophane-triazolyl Monophosphine Ligands: Synthesis and their Copper and Palladium Complexes 

D. Volz, M. Nieger, J. Friedrichs, T. Baumann, S. Bräse, Langmuir 2013, 3034-3044. How the Quantum-efficiency of a Highly Emissive Binuclear Copper Complex is Enhanced by Changing the Processing Solvent

A. Hafner, S. Bräse, Adv. Synth. Catal. 2013, 355, 996-1000. Trifluoromethylation and further Transformations of 1-Aryl-3,3-diisopropyltriazenes

A. A. Hassan, S. M. Mostafa, S. Bräse, M. Nieger, Tetrahedron Lett. 2013, 2690-2692. A simple and efficient synthesis of 3-amino-5-benzyl-6-phenylpyridazine-4-carbonitrile

N. Crosta, S. Müller, D. Gradl, K.-S.Masters, S. Bräse, D. Gradl, Synlett 2013, 951-954. Rediscovering the Double Friedel-Crafts Acylation: An Expedient Entry to Phenanthrene-9,10-diones

D. T. Thielemann, A. T. Wagner, E. Birtalan, D. Kölmel, J. Heck, B. Rudat, M. Neumaier, C. Feldmann, U. Schepers, S. Bräse, P. W. Roesky, J. Am. Chem. Soc. 2013, 135, 7454-7457. Luminescent Cell-Penetrating Pentadecanuclear Rare-Earth Metal Clusters

D. Kölmel, B. Rudat, U. Schepers, S. Bräse, Eur. J. Org. Chem. 2013, 2761–2765. Peptoid-based Rare Earth (Group 3 and Lanthanide) Transporters

S. Seifermann, T. Muller, S. Bräse, Eur. J. Org. Chem. 2013, 3215-3218. Novel BOX structures with additional coordination sites: Potential ligands for bifunctional catalysis

D. K. Kölmel, B. Rudat, D. M. Braun, C. Bednarek, U. Schepers, S. Bräse, Org. Biomol. Chem. 2013, 11, 3954-3962. Rhodamine F: A Novel Class of Fluorous Ponytailed Dyes 

V. Rempel, N. Volz, F. Gläser, M. Nieger, S. Bräse, C. E. Müller, J. Med. Chem. 2013, 4798-4810. Antagonists for the orphan G protein-coupled receptor GPR55 based on a coumarin scaffold

A. Linsenmeier, C. M. Williams, S. Bräse, Eur. J. Org. Chem. 2013, 4798-4810. Photochemical Synthesis of Phenanthridines: Scope and Limitations 

L. Bergmann, J. Friedrichs, M. Mydlak, T. Baumann, S. Bräse, Chem. Comm. 2013, 49, 6501-6503. Outstanding luminescence from neutral copper(I) complexes with pyridyl-tetrazolate and phosphine ligands

A. A. Hassan, Y. R. Ibrahim, E. M. El-Sheref, M. Abdel-Aziz, S. Bräse, M. Nieger, Arch. Pharm. 2013, 346, 562-570. Synthesis and Antibacterial Activity of 4-Aryl-2-(1-substituted ethylidene)thiazoles

A. Hafner, T. J. Feuerstein, S. Bräse, Org. Lett. 2013, 15, 3468-3471. Silver-Mediated Methoxycarbonyltetrafluoropropylation of Arenes

M. Faust, M. Enders, M. Bruns, S. Bräse, K. Gao, M. Seipenbusch, Surface & Coatings Technology 2013, 230, 284-289. Synthesis of nanostructured Pt/oxide catalyst particles by MOCVD process at ambient pressure

A. C. Meister, M. Lang, M. Nieger, S. Bräse, Acta Cryst E. 2013, 69, o1303-o1304. 4-(2-Hydroxyethoxy)phenol

A. C. Meister, M. Nieger, S. Bräse, Chem. Eur. J. 2013, 19, 10836-10839. A Radical Access to Highly Functionalized Tetrahydroxanthones 

C. S. Kramer, S. Bräse, Beilstein J. Org. Chem. 2013, 9, 1414–1418. Thiourea-catalyzed Diels–Alder-reaction of a Naphthoquinone Monoketal Dienophile

D. Jakubczyk, C. Merle, G. Brenner-Weiss, B. Luy, S. Bräse, Eur. J. Org. Chem. 2013, 5323-5330. Deuterium and Tritium Labelling of N-Acyl- -homoserine Lactones (AHLs) by Catalytic Reduction of a Double Bond in the Layer-by-Layer Method

A. Hafner, A. Bihlmeier, W. Klopper, M. Nieger, S. Bräse, J. Org. Chem. 2013, 78, 7938-7948. Ortho-Perfluoroalkylation and Ethoxycarbonyldifluorination of Aromatic Triazenes 

M. Busch, M. Cayir, M. Nieger, W. R. Thiel, S. Bräse, Eur. J. Org. Chem. 2013, 6108-6123. Roadmap towards novel N-heterocyclic [2.2]paracyclophanes

V. Aggarwal, L. Reichenbach, M. Enders, T. Muller, S.Wolff, M. Crone, M. Türk, S. Bräse, Chem. Eur. J. 2013, 19, 12794-12799. Influence of the perfluorinated end groups in Supercritical Fluid Reactive Deposition of [Pt(cod)Me(CnF2n+1)] on porous Al2O3 in CO2 under reductive conditions

D. Volz, D. M. Zink, T. Bocksrocker, J. Friedrichs, M. Nieger, T. Baumann, U. Lemmer, S. Bräse, Chem. Mater. 2013, 25, 3414-3426. A Molecular LEGO-Kit for Tuning Solubility, Stability and Luminescence-Properties: Heteroleptic MePyrPHOS-Copperiodide-Complexes and their Application in Organic Light-emitting Diodes

M. Faust, M. Enders, K. Gao, L. F. Reichenbach, T. Muller, W. Gerlinger, B. Sachweh, G. Kasper, H.-M. Bruns, S. Bräse, M. Seipenbusch, Chem. Vapour Dep. 2013, 230, 284-289. Production of Pt/SiO2 catalyst nanoparticles from a continuous aerosol process using newly synthesized cyclooctadienylplatinum precursors

B. D. Weger, M. Weger, N. Jung, S. Bräse, T. Dickmeis, JOVE 2013, (73). A chemical screening procedure for glucocorticoid signaling with a zebrafish larva luciferase reporter system

E. Sokolovskaya, J. Yoon, A. C. Misra, S. Bräse, J. Lahann, Macromol. Rapid Commun. 2013, 34, 1554-1559. Controlled Microstructuring of Janus Particles Based on Multifunctional Poly(ethylene glycol)s.

F. Rajabi, J. Trampert, Y. Yu, M. Busch, S. Bräse, W. R. Thiel, J. Organomet. Chem. 2013, 744, 101-107. Synthesis and Characterization of a 4-Nitrophenyl Functionalized NHC Ligand and its Palladium(II) Complex

A. C. Meister, P. F. Sauter, S. Bräse, Eur. J. Org. Chem. 2013, 7110-7116. A Stereoselective Access to Functionalized Cyclohexenones

S. B. L. Vollrath, D. Fürniss, U. Schepers, S. Bräse, Org. Biomol. Chem. 2013, 11, 8197-8201. Amphiphilic Peptoid Transporters - Synthesis and Evaluation

K. V. Kudryavtsev, P. M. Ivantcova, A. V. Churakov, S. Wiedmann, B. Luy, C. Muhle-Goll, N. S. Zefirov, S. Bräse Angew. Chem. 2013, 125, 12736-12740. Alternating Asymmetric Self-Induction in Functionalized Pyrrolidine Oligomers

D. M. Zink, D. Volz, T. Baumann, M. Mydlak, H. Flügge, J. Friedrichs, M. Nieger, S. Bräse, Chem. Mater. 2013, 25, 4471-4486. Heteroleptic, dinuclear copper(I) complexes for application in organic light-emitting diodes.

D. Volz, M. Nieger, J. Friedrichs, T. Baumann, S. Bräse, Inorg. Chem. Comm. 2013, 106-109. Small Change, Big Red Shift: Syntheses, Structure and Photoluminescence of Cu2Br2(Ph3P)2py2 (py = pyridine, 4-vinylpyridine)

D. M. Zink, J. Friedrichs, T. Baumann, M. Nieger, S. Bräse, Inorg. Chem. 2013, 52, 13509-13520. Copper(I) complexes based on five-membered P^N heterocycles: structural diversity linked to exciting luminescence properties

W. Thiele, M. Rothley, N. Teller, N. Jung, B. Bulat, D. Plaumann, S. Vanderheiden, A. Schmaus, N. Cremers, B. Göppert, V. Eschbach, L. Quagliata, S. Thaler, D. Marko, S. Bräse, J. P. Sleeman, Carcinogenesis 2013, 34, 2804-
2813. Delphinidin is a novel inhibitor of lymphangiogenesis, but promotes mammary tumor growth and metastasis formation in syngeneic experimental rats

A. Giovannitti, S. M. Seifermann, A. Bihlmeier, T. Muller, F. Topic, K. Rissanen, M. Nieger, W. Klopper, S. Bräse, Eur. J. Org. Chem. 2013, 7907-7913. Mono and Multiple Additions of Dibenzoylmethane onto Buckminster-Fullerene

K. S. M. Salih, S. Bergner, H. Kelm, Y. Sun, A. Grün, Y. Schmitt, R. Schoch, M. Busch, N. Deibel, S. Bräse, B. Sarkar, M. Bauer, M. Gerhards, W R. Thiel, Eur. J. Inorg. Chem. 2013, 6049-6059. Trinuclear diamagnetic nickel(II) complexes bridged by 3-arylpyrazolato ligands

A. Hafner, T. S. Fischer, S. Bräse, Eur. J. Org. Chem. 2013, 7996-8003. Synthesis of CF3-substituted Olefins via Julia-Kocienski-Olefination using 2-((2,2,2-Trifluoroethyl)sulfonyl)benzo[d]thiazole as Trifluoromethylation Agent

S. Seifermann, C. Rethore, T. Muller, S. Bräse, Sci. Rep. 2013, onl3, 2817. Soccer goes BOXing: Synthetic access to novel [6:0] hexakis[(bisoxazolinyl)methano]fullerenes

Z. Wang, H. K. Arslan, J. Liu, S. Grosjean, T. Hagendorn, H. Gliemann, S. Bräse, C. Wöll, Langmuir 2013, 15958-15964. Post-synthetic modification of molecular frameworks using click chemistry: the importance of strained C-C triple bonds

K.-S. Masters, A. Bihlmeier, W. Klopper, S. Bräse, Chem. Eur. J. 2013, 17827-17835. Tethering for Selective Synthesis of 2,2’-Biphenols: The Acetal Method

2012

B. M. Ruff, S. Zhong, M. Nieger, S. Bräse, Org. Biomol. Chem. 2012, 935 - 940. Thiolation of Symmetrical and Unsymmetrical Diketopiperazines

B. M. Ruff, S. Bräse, S. E. O’Connor, Tetrahedron Lett. 2012, 53, 1071-1074. Biocatalytic Production of Tetrahydroisoquinolines

N. Allendörfer, M. Es-Sayed, M. Nieger, S. Bräse, Tetrahedron Lett. 2012, 388-391. Nucleophilic Ring-Opening Reaction of Benzoxazinones – access to o-Amino-2,2,2-trifluoroacetophenones

A. Bihlmeier, E. Bourcet, S. Arzt, T. Muller, S. Bräse, W. Klopper, J. Am. Chem. Soc. 2012, 2154-2160. Structure Revision of Plakotenin based on the Computational Investigation of Transition States and Spectroscopic Properties

D. Frank, C. Friedmann, M. Nieger, J. Lahann, S. Bräse, Isr. J. Chem. 2012, 52, 143-148. Functional Paracyclophanes: Synthesis of [2.2]paracyclophanemethyldithiocarbonates using thione-thiol-rearrangement of S,O-dithiocarbonates (benzyl Schönberg rearrangement) at mild conditions

S. Dahmen, S. Bräse, Isr. J. Chem. 2012, 52, 52, 139–142. Paracyclophanes in Action: Asymmetric catalytic dibutylzinc addition to imines using [2.2]paracyclophane based N,O-ligands as catalysts

D. Jakubczyk, C. Barth, A. Kubas, F. Anastassacos, P. Koelsch, K. Fink, Karin, U. Schepers, G. Brenner-Weiß, S. Bräse, Anal. Bioanal. Chem. 2012, 403, 473-482. Deuterium labelled N-acyl-L-homoserine lactones (AHLs) - Inter-kingdom signalling molecules – synthesis, structural studies, interaction with model lipid membranes

A. Singh, M. Tolev, C. Schilling, S. Bräse, H. Griesser, C. Richert, J. Org. Chem. 2012, 2703–2717. Convenient Solution-Phase Synthesis of Branched DNA Hybrids via H-Phosphonate Dimers

A. A. Hassan, A. M. N. El-Din, F. F. Abdel-Latif, S. M. Mostafa, S. Bräse, Chemical Papers 2012, 66, 295-303. Formation of dioxospiroindene[1,3]thiazine and thioxoindeno[2,1-d]imidazolone derivatives from alkenylidene-hydrazinecarbothioamides

A. Hafner, S. Bräse, Angew. Chem. Int. Ed. 2012, 51, 3713-3715; Angew. Chem. 2012, 124, 3773–3775. Ortho-Trifluormethylierung funktionalisierter aromatischer Triazene

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

O. Altintas, T. Muller, E. Lejeune, O. Plietzsch, S. Bräse, C. Barner-Kowollik, Macromol. Rapid Commun. 2012, 33, 977–983. Combining Modular Ligation and Supramolecular Self-Assembly for the Construction of Star-Shaped Macromolecules

A. Kubas, S. Bräse, K. Fink, Chem. Eur. J. 2012, 18, 8377-8385. Theoretical Approach Towards Understanding of Asymmetric Additions of Dialkylzinc to Enals and Iminals Catalysed by [2.2]Paracyclophane-Based N,O-Ligands.

C. Barth, D. Jakubczyk, A. Kubas, F. Anastassacos, G. Brenner-Weiss, K. Fink, U. Schepers, S. Bräse, P. Koelsch, Langmuir 2012, 28, 8456–8462. Inter-kingdom Signaling: Integration, Conformation and Orientation of N-Acyl-L-Homoserine Lactones in Supported Lipid Bilayers

E. Bremus-Köbberling, A. Gillner, F. Avemaria, C. Réthoré, S. Bräse, Beilstein J. Org. Chem. 20128, 1213–1218. Photochemistry with laser radiation in condensed phase using miniaturized photoreactors

K. Knepper, S. Vanderheiden, S. Bräse, Beilstein J. Org. Chem. 2012, 8, 1191–1199. Synthesis of diverse indole libraries on polystyrene resin – Scope and limitations of an organometallic reaction on solid supports.

D. Volz, M. Nieger, S. Bräse, Acta Cryst. 2012, E68, 466-467. Di-μ-iodido-bis{[(R)-(+)-2,2'-bis(diphenylphosphanyl)-1,1'-binaphthyl-κ2P,P']copper(I)} 0.67-hydrate.

S. B. Vollrath, S. Bräse, K. Kirshenbaum, Chem. Sci. 2012, 3, 2726-2731. Twice Tied Tight: Enforcing Conformational Order in Bicyclic Peptoid Oligomers

A. A. Hassan, A. M. Nour El. Din, F. F. Abdel Latif, S. M. Mostafa, M. Nieger, S. Bräse, Tetrahedron 2012, 68, 8487-8492. Synthesis of (E)-2,5-Disubstituted 1,3,4-Thiadiazolyl-2,3-diphenylpropenones from Alkenylidene-hydrazinecarbothioamides.

A. C. Meister, M. Nieger, S. Bräse, Eur. J. Org. Chem. 2012, 5373-5380. Synthesis of 4-Hydroxy-5-methyl- and 4-Hydroxy-6-methylcyclohexenones via Pd(II) Catalyzed Oxidation and Lipase Catalyzed Hydrolysis.

P.-H. Kuhn, K. Koroniak, S. Hogl, A. Colombo, U. Zeitschel, M. Willem, U. Schepers, A. Imhof, A. Hoffmeister, C. Haass, S. Roßner, S. Bräse, S. F. Lichtenthaler, EMBO J. 2012, 31, 3157-3168. Secretome Protein Enrichment with Click Sugars Identifies Physiological Substrates of the Alzheimer Protease BACE1 in Primary Neurons.

N. Volz, F. Gläser, M. Nieger, S. Bräse, Beilstein J. Org. Chem. 2012, 8, 1385-1392. Highly Enantioselective Access to Cannabinoid-type Tricyles by Organocatalytic Diels-Alder Reactions.

A. J. Rüger, M. Nieger, S. Bräse, Tetrahedron 2012, 68, 8823-8829. Synthesis of tetra-substituted pyrazoles.

N. A. Danilkina, M. Nieger,S. Selivanov, S. Bräse, I. A. Balova, Eur. J. Org. Chem. 2012,
5660–5664. Electrophilic Cyclization and Ring Closing Metathesis as Key Steps in the Synthesis of a 12-Membered Cyclic Enediyne.
 

D. Volz, T. Baumann, H. Flügge, M. Mydlak, T. Grab, M. Bächle, C. Barner-Kowollik, S. Bräse, J. Mater. Chem. 2012, 22, 20786-20790. Auto-catalysed crosslinking for next-generation OLED design.

V. Rempel, N. Volz, S. Hinz, T. Karcz, I. Meliciani, M. Nieger, W. Wenzel, S. Bräse, C. E. Müller, J. Med. Chem. 2012, 55, 7967-7977. Alkyl-3-benzylcoumarins: a versatile scaffold for the development of potent and selective cannabinoid receptor agonists and antagonists.

E. Bourcet, L. Kaufmann, S. Arzt, A. Bihlmeier, W. Klopper, U. Schepers, S. Bräse, Chem. Eur. J. 2012, online. The Plakotenins: Biomimetic Diels-Alder Reactions, Total Synthesis, Structural Investigations, and Chemical Biology.

A. Linsenmeier, S. Bräse, Eur. J. Org. Chem. 2012, online. Lewis-Acid Promoted Double Bond Isomerization of Tetrahydroxanthones.

D. Fürniss, U. Schepers, S. Bräse, RSC Advances 2012, 2, 11273-11278. Killing double bonds softly: The reduction of polymer-bound alkenes.

D. Zink, M. Bächle, T. Baumann, M. Nieger, M. Kühn, C. Wang, W. Klopper, U. Monkowius, T. Hofbeck, H. Yersin, S. Bräse, Inorg. Chem. 2012, online. Synthesis, structure, and characterization of dinuclear copper(I) halide complexes with N^P ligands featuring exciting photoluminescence properties.

C. Cardenal, S. B. L. Vollrath, U. Schepers, S. Bräse, Helv. Chim. Acta 2012, 2237-2248. Synthesis of Functionalized Glutamine- and Asparagine-Type Peptoids – Scope and Limitations.

D. K. Kölmel, D. Fürniss, S. Susanto, A. Lauer, C. Grabher, S. Bräse, U. Schepers, Pharmaceuticals 2012, 5, 1265-1281. Synthesis of a small combinatorial Peptoid Library by using IRORI MiniKans.

A. A. Hassan, Y. R. Ibrahim, E. M. El-Sheref, A. A. Aly, S. Bräse, A. Brown, J. Het. Chem. 2012, 49, 1380-1385. Novel Synthesis of Pyrazolyloxothiazolidine Derivatives.

M. Cakici, S. Bräse, Eur. J. Org. Chem. 2012, 6132–6135. Modular Synthesis of Planar-chiral para-substituted Paracyclophanes by Double Suzuki Coupling.

J. Liu, B. Lukose, O. Shekhah, H. K. Arslan, P. Weidler, H. Gliemann, S. Bräse, S. Grosjean, A. Godt, X. Feng, K. Müllen, I.-B. Magdau, T. Heine, C. Wöll, Sci. Rep. 2012, 2, 921. A novel series of isoreticular metal organic frameworks: realizing metastable structures by liquid phase epitaxy.

B. Görling, S. Bräse, B. Luy, Mag. Res. Chem. 2012, 50, S58–S62. HR-HSBC: Measuring heteronuclear one-bond couplings with enhanced resolution.

U. Sternberg, E. Birtalan, I. Jakovkin, B. Luy, U. Schepers, S. Bräse, C. Muhle-Goll, Org. Biomol. Chem. 2013, 640–647. Structural Characterization of a Peptoid with Lysine-like Side Chains and Biological Activity using NMR and Computational Methods.

2011

D. Kapeller, S. Bräse, Synlett 2011, 161-164. Towards a Library of Chromene Cannabinoids: A Combinatorial Approach on Solid Supports

K.-S. Masters, M. Nieger, S. Bräse, Synlett 2011, 399-401. Solid-State Structure of some Substituted Hexahydro-1,4:5,8-diepoxynaphthalenes

H. Gehrke, J. Pelka, C. G. Hartinger, H. Blank, F. Bleimund, R. Schneider, D. Gerthsen, S. Bräse, M. Crone, M. Türk, D. Marko, Archiv Toxikol. 2011. Platinum nanoparticles and their cellular uptake and DNA platination at non-cytotoxic concentrations

N. A. Danilkina,S. Bräse, I. A. Balova, Synlett 2011, 517-520. Electrophilic Cyclization of Buta-1,3-diynylarenes: Synthesis of Precursors of (Z)-3-Ene-1,5-diyne Systems Fused to Heterocycles

C. I. Schilling,O. Plietzsch,T. Muller,S. Bräse, Eur. J. Org. Chem. 2011, 1743-1754.Fourfold Suzuki-Miyaura and Sonogashira cross-coupling reactions on tetrahedral methane and adamantane derivatives

D. Zink, T. Baumann, M. Nieger, S. Bräse, Eur. J. Org. Chem. 2011, 1432-1437.Improved One-Pot Synthesis of C3-Symmetric ClickPhos and Related Ligands: Structures of Unique Triazole-Zinc Complexes

A. Singh, M. Tolev, M. Meng, K. Klenin, O. Plietzsch, C. I. Schilling, T. Muller, M. Nieger, S. Bräse, W. Wenzel, C. Richert, Angew. Chem. 2011, 123, 3285-3289; Angew. Chem. Int. Ed. 2011, 50, 3227–3231. Branched DNA that Forms a Solid at 95 °C

E. Bourcet, M. C. Bröhmer, M. Nieger, S. Bräse, Org. Biomol. Chem. 2011, 9, 3136-3168. Synthetic Studies towards Marmycins A and B: Development of the vinylogous Aldol – aza-Michael Domino Reaction

U. Gross, P. J. Gross, M. Shi, S. Bräse, Synlett 2011, 635-638. Catalytic Synthesis of Coumarins via Direct Annulations of alpha,beta-Unsaturated Aldehydes and Salicylaldehydes

M. Klipfel, C. Réthoré, T. Muller, S. Bräse, W. Klopper, Compu. Theoret. Chem. 2011, 966, 186-193. Genetic algorithm density functional theory study of crown ether{dibenzylammonium [2]pseudorotaxanes

F. Lauterwasser, P. G. Hayes, W. E. Piers, L. L. Schafer, S. Bräse, Adv. Synth. Catal. 2011, 353, 1384-1391. Highly Active and Diastereoselective N,O- and N,N-Yttrium Complexes for Intramolecular Hydroamination

D. M. Zink, T. Grab, T. Baumann, M. Nieger, E. C. Barnes, W. Klopper, S. Bräse, Organometallics 2011, 3275–3283. An experimental and theoretical study of novel luminescent di-, tri- and tetranuclear copper triazole complexes

E. Birtalan, B. Rudat, D. Kölmel, D. Fritz, S. Vollrath, U. Schepers, S. Bräse, Biopolym. Pept. Sci. 2011. Investigating rhodamine B-labelled peptoids: Scopes and Limitations of its applications

M. C. Bröhmer, S. Mundinger, S. Bräse, W. Bannwarth, Angew. Chem. 2011, 123, 6299–6301; Angew. Chem. Int. Ed. 2011, 50, 6175–6177 Chelatbildende Carbonsäureamide als stabile Relay-Schutzgruppen für Carbonsäuren und ihre Spaltung unter milden Bedingungen (Chelating carboxylic acid amides as new and robust relay protection of carboxylic acids to be activated for mild cleavage (deprotection) by unusual complexation of the amide nitrogen)

O. Plietzsch, C. I. Schilling, T. Grab, S. L. Grage, A. S. Ulrich, A. Comotti, P. Sozzani, T. Muller, New J. Chem. 2011, 15, 1577-1581. Click Chemistry Produces Hyper-Cross-linked Polymers with Tetrahedral Cores

A. A. Hassan, F. F. Abdel-Latif, A. M. Nour El-Din, M. Abdel-Aziz, S. M. Mostafa, S. Bräse, J. Heterocyclic Chem. 2011, 48, 1050–1055. Synthesis of novel spiro(indolone-3,2′-[1,3,4]thiadiazol)-2-ones and evaluation of their antidepressant and anticonvulsant activities

B. Rudat, E. Birtalan, S. B. L. Vollrath, D. Fritz, D. K. Kölmel, M. Nieger, U. Schepers, K. Müllen, H.-J. Eisler, U. Lemmer, S. Bräse, Eur. J. Med. Chem. 2011, 46, 4457–4465. Photophysical properties of fluorescently-labeled peptoids

K. S. Masters, M. Wallesch, S. Bräse, J. Org. Chem. 2011, 76, 9060-9067. ortho-Bromo-(propa-1,2-dien-1-yl)arenes as Versatile Substrates in Pd-Catalysed Domino Reactions

A. Linsenmeier, S. Bräse, C. M. Williams, J. Org. Chem. 2011, 76, 9127-9132. Synthesis of Phenanthridine Derivatives via Photolysis

B. M. Ruff, S. Zhong, M. Nieger, M. Sickert, C. Schneider, S. Bräse, Eur. J. Org. Chem. 2011 6558–6566. A Combined Vinylogous Mannich/Diels-Alder Approach for the Stereoselective Synthesis of Highly Functionalized Hexahydroindoles

M. Döbele, M. S. Wiehn, S. Bräse, Angew. Chem. 2011, 123, 11737–11739. Angew. Chem. Int. Ed. 2011, 50, 11533–11535 Traceless solid-phase synthesis of trifluoromethylarenes (Festphasensynthese trifluormethylierter Arene)

M. Bröhmer, E. Bourcet, M. Nieger, S. Bräse, Chem-Eur. J. 2011, 17, 13706–13711 A unified strategy for the asymmetric synthesis of diversonol and lachnone C

A. Hafner, S. Bräse, Adv. Synth. Catal. 2011, 353, 3044-3048. Efficient trifluoromethylation of activated and non-activated alkenyl halides by using (trifluoromethyl)trimethylsilane

2010

A. J. Inglis, P. Pierrat, T. Muller, S. Bräse, C. Barner-Kowollik, Soft Matter 2010, 6, 82-84. Well-Defined Star Shaped Polymer-Fullerene Hybrids via Click Chemistry

P. J. Gross, C. E. Hartmann, M. Nieger, S. Bräse, J. Org. Chem. 2010, 75, 229-232. Synthesis of Methoxyfumimycin with 1,2-Addition to Ketimines

S. Ay, E. M. C. Gérard, M. Shi, S. Bräse, Synlett 2010, 128-130. The Domino Oxa-Michael-Aldol-Reaction Reinvestigated: A New P-Based Organocatalyst for Xanthenone Scaffolds

C. J. Friedmann, S. Bräse, Synlett 2010, 774-776.Synthesis of Paracyclophane Thiols via an Unprecedented Reduction/Deprotection Sequence: Direct Conversion of t-Butylsulfoxides into Thiols with Boron Tribromide

D. Fritz, S. Bräse, Synlett, 1544-1548. Solid-phase synthesis of w-aminoalkylpeptoids using azide chemistry

C. J. Friedmann, S. Ay, S. Bräse, J. Org. Chem. 2010, 75, 4612-4614. Improved Synthesis and Resolution of enantiopure 4-Hydroxy-[2.2]paracyclophane

S. Arzt, E. Bourcet, T. Muller, S. Bräse, Org. Biomol. Chem. 2010, 8, 3300-3306. Enantioselective total synthesis of Plakotenin, a cytotoxic metabolite from Plakortis sp.

A. J. Rüger, M. Nieger, M. Es-Sayed, S. Bräse, Eur. J. Org. Chem. 2010, 3837-3846. Novel 2,5-disubstituted-1,3-dioxanes and oxazolidines as potential chemoprevention agents and building blocks for organic synthesis

C. E. Hartmann, T. Baumann, M. Bächle, S. Bräse, Tetrahedron Asymmetry 2010, 21, 1341-1349. Efficient Synthesis of Deuterated and Fluorinated Aromatic α,α-disubstituted Amino Acid Derivatives

O. Plietzsch, C. I. Schilling, M. Nieger, T. Muller, S. Bräse, Tetrahedron Asymmetry 2010, 21, 1474-1479. Asymmetric synthesis of chiral tectons with tetrapodal symmetry: Fourfold asymmetric reactions

M. Döbele, S. Vanderheiden, N. Jung, S. Bräse, Angew. Chem. 2010, 49, 5986-5988. Synthese von Fluoraromaten in flüssiger und an fester Phase durch Verwendung fluorierter Lösungsmittel Synthesis of fluoroarenes in liquid phase and on solid suppports by using fluorinated solvents

S. Ay, R. E. Ziegert, H. Zhang, M. Nieger, K. Rissanen, R. M. Gschwind, S. Bräse, J. Am. Chem. Soc.2010, 132, 12899-12905. NMR-Spectroscopic and Solid-State Investigations of the Co-Metal Free Asymmetric Conjugate Addition: The First Paracyclophaneimine-Zinc-Methyl Complex

U. Gross, M. Nieger, S. Bräse, Chem. Eur. J. 2010, 16, 11624 – 11631.A Unified Strategy towards the Thiodiketopiperazine Mycotoxins Exserohilone, Gliotoxin, Epicoccins, Epicorazines, Rostratin A and Aranotin

P. J. Gross, S. Bräse, Chem. Eur. J. 2010, 16, 12660-12667. Totalsynthesis of (±)-Fumimycin

N. Allendörfer, M. Es-Sayed, M. Nieger, S. Bräse, Synthesis 2010, 3439-3448. Heterocyclic Fluoroolefins as peptide bond mimics via Fluoro-Julia-Kocienski Olefination

B. Rudat, E. Birtalan, I. Thomé, D. Kölmel, V. L. Horhoiu, M. D. Wissert, U. Lemmer, H.-J. Eisler, T. S. Balaban, S. Bräse, J. Chem. Phys. 2010, 114, 13473–13480. Novel pyridinium dyes that enable investigations of peptoids at the single-molecule level

W. Lu, D. Yuan, D. Zhao, C. I. Schilling, O. Plietzsch, T. Muller, S. Bräse, J. Guenther, J. Blümel, R. Krishna, Z. Li, H.-C. Zhou, Chem. Mater. 2010, 22, 5964–5972.Porous Organic Frameworks: Porosity and Clean Energy Applications

M. Virlouvet, M. Gartner, K. Koroniak, J. Sleeman, S. Bräse, Adv. Synth. Catal. 2010, 352, 3657-3662. Multi grams Synthesis of Hyaluronic Acid Subunit and Synthesis of their Fully Protected Oligomers

N. Allendörfer, A. Sudau, S. Bräse, Adv. Syth. Catal. 2010, 352, 2815-2824. Expedient Trimethylaluminium-Promoted One-Pot Synthesis of Functional Heteroaromatic and Carbocyclic Trifluoroethylamines

P. Gross, M. Nieger, F. Furche, S. Bräse, Chem. Commun. 2010, 9215-9217. Asymmetric Total Synthesis of (+)-Fumimycin via 1,2-Addition to Ketimines

A. A. Hassan, A. M. Nour El. Din, F. F. Abdel Latif, S. M. Mostafa, S. Bräse, J. Chem. Res. 2010, 493-497. Synthesis of spiro(indenepyrazole) and indenotriazinone derivatives from 4-substituted thiosemicarbazides and (1,3-dioxo-2,3-dihydro-1H-inden-2-ylidene)-propanedinitrile

2009

A. Friedrich, S. Bräse, S. E. O’Connor, Tetrahedron Lett. 2009, 50, 75-76. Synthesis of 4-, 5-, 6-, and 7-azidotryptamines

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

K. C. Nicolaou, R. Reingruber, D. Sarlah, S. Bräse, J. Am. Chem. Soc. 2009, 131, 2086-2087. Enantioselective Intramolecular Friedel-Crafts type α-Arylation of Aldehydes
Highlighted in: Synfacts 2009, 0449

M. Jainta, M. Nieger, S. Bräse, J. Mol. Struct. 2009, 921, 85-88. Facile synthesis and spectroscopic elucidation of 4,11-Bis(dehydroxy)-bipolaroamide

N. Volz, M. C. Bröhmer, S. Bräse, Synlett 2009, 550-553. An Organocatalytic Sequence towards 4a-Methyl Tetrahydroxanthones: Formal Synthesis of 4-Dehydroxydiversonol

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

A. Behrenswerth, N. Volz, J. Toräng, S. Hinz, S. Bräse, C. E. Müller, Bioorg. Med. Chem. 2009, 17, 2842–2851. Synthesis and Pharmacological Evaluation of Coumarine Derivatives as Cannabinoid Receptor Antagonists and Inverse Agonists

J. Pelka, H. Gehrke, M. Esselen, M. Türk, M. Crone, S. Bräse, T. Muller, W. Send, V. Zibat, P. Brenner, R. Schneider, D. Gerthsen, D. Marko, Chem. Res. Toxicol. 2009, 22, 649-659. Cellular uptake of platinum nanoparticles in human colon carcinoma cells and their impact on cellular redox systems and DNA integrity

R. Reingruber, T. Baumann, S. Dahmen, S. Bräse, Adv. Synth. Catal. 2009, 351, 1019-1024. Use of the Chiral Pool – Practical Asymmetric Organocatalytic Strecker Reaction with Quinine 

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

M. C. Bröhmer, N. Volz, S. Bräse, Synlett 2009, 1383. Rhodium-catalyzed decarbonylation of functionalized 3-formylchromenes: An (asymmetric) sequence for functionalized chromenes like deoxycordiachromene.

I. Warnke, S. Ay, S. Bräse, F. Furche, J. Chem. Phys. A 2009, 113, 6987-6993. Chiral Cooperativity and Solvent-Induced Tautomerism Effects in Electronic Circular Dichroism Spectra of [2.2]Paracyclophane Ketimines.

M. Meng, C. Ahlborn, M. Bauer, O. Plietzsch, S. A. Soomro, A. Singh, T. Muller, W. Wenzel, S. Bräse, C. Richert, ChemBioChem 2009, 10, 1335-1339. Two Base Pair Duplexes Suffice to Build a Novel Material

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.

K. Eggenberger, E. Birtalan, T. Schröder, S. Bräse, P. Nick, ChemBioChem 2009, 10, 2504-2512. Passage of Trojan Peptoids into Plant Cells
U. Gross, M. Nieger, S. Bräse, Org. Lett. 2009, 11, 4740-4742. Stereoselective Synthesis of the Epicoccin Core.

M. S. Wiehn, S. D. Lindell, S. Bräse, J. Comb. Chem. 2009, 11, 960-981. Solid-Phase Organic Synthesis of Difluoroalkyl Entities by a Novel Fluorinating Cleavage Strategy Part 1. Linker development: scope and limitations.

M. S. Wiehn, D. Fürniß, S. Bräse, J. Comb. Chem. 2009, 982-1006. Solid-Phase Organic Synthesis of Difluoroalkyl Entities by a Novel Fluorinating Cleavage Strategy Part 2. Library development.

H. Sahin, M. Nieger, C. F. Nising, S. Bräse, Synlett 2009, 3187-3191. Functionalization of Highly Oxygenated Xanthones: Unexpected Stereochemistry and Rearrangements

C. E. Hartmann, P. J. Gross, M. Nieger, S. Bräse, Org. Biomol. Chem. 2009, 7, 5059-5062. Towards an asymmetric synthesis of the bacterial peptide deformylase (PDF) inhibitor Fumimycin

O. Plietzsch, C. I. Schilling, M. Tolev, M. Nieger, C. Richert, T. Muller, S. Bräse, Org. Biomol. Chem. 2009, 4734-4743. Four-Fold Click Reactions: Generation of Tetrahedral Methane- and Adamantane-Based Building Blocks for High-Order Molecular Assemblies

P. Pierrat, C. Réthoré, T. Muller, S. Bräse, Chem.—Eur. J. 2009, 15, 11458-11460. Di- and Dodeca-Mitsunobu Reactions on C60 Derivatives: Post-Functionalization of Fullerene Mono- and Hexakis-Adducts

H. Sahin, M. Nieger S. Bräse, Eur. J. Org. Chem. 2009, 5576-5586. Probing the Oxidation of Functionalized (Hexahydro)xanthenols

2008

R. Reingruber, S. Bräse, Chem. Commun. 2008, 105-107. 1,2-Addition of Trialkylaluminium Reagents on N-Diphenylphosphinoyl-ketimines in the Absence of Any Additional Reagents 

V. Zimmermann, R. Müller, S. Bräse, Synlett 2008, 278-280. Synthesis of 1H-Benzotriazoles via Reductive Amination on Solid Supports.

A. Castro, A. Encinas, C. Gil, S. Bräse, C. Pérez, F. J. Moreno, A. Martínez, Bioorg. Med. Chem. Lett. 2008, 16, 495-510. Non ATP-Competitive Glycogen Synthase Kinase ß (GSK-3ß) Inhibitors: Study of Structural Requirements for Thiadiazolidinone Derivatives.

T. Schröder, N. Niemeier, H. F. Krug, S.Afonin, A. Ulrich, S. Bräse, J. Med. Chem. 2008, 51, 376-379. Peptoidic carrier systems: Studies of toxicity and cell penetrating effects of guanidinyl versus amino side chains

A. Friedrich, M. Jainta, C. F. Nising, S. Bräse, Synlett 2008, 589-591. Synthesis of Hexahydroindole Carboxylic Acids by Intramolecular Diels-Alder Reaction

T. Baumann, M. Bächle, C. Hartmann, S. Bräse, Eur. J. Org. Chem. 2008, 2207. Thermal Effects in the organocatalytic asymmetric a-amination of disubstituted aldehydes with azodicarboxylates: a high-temperature organo-catalysis (Cover picture)

P. Pierrat, C. Réthoré, T. Muller, S. Bräse, Synlett 2008, 1706. Design and Efficient Synthesis of Fullerene Bismalonates as Building Blocks for Metal Organic Frameworks

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

F. Hahn, K. Schmitz, T. S. Balaban, S. Bräse, U. Schepers, ChemMedChem 2008, 3, 1185-1188. Conjugation of Spermine Facilitates Cellular Uptake and Enhances Antitumor and Antibiotic Properties of Highly Lipophilic Porphyrins

E. M. C. Gérard, S. Bräse, Chem. Eur. J. 2008, 14, 8086-8089. Modular syntheses of diversonol-type tetrahydroxanthone mycotoxins: blennolide C (epi-hemirugulotrosin A) and analogs.

E. M. C. Gérard, H. Sahin, A. Encinas, S. Bräse, Synlett 2008, 2702-2704. Systematic Study of a Solvent- Free Mechanochemically Induced Domino. Oxa-Michael–Aldol Reaction in a Ball Mill

M. S. Wiehn, S. Lindell, S. Bräse, Angew. Chem. 2008, 120, 8240-8242; Angew. Chem. Int. Ed. 2008, 47, 8120-8122. Fluorinating Cleavage of Solid Phase Linkers for Combinatorial Synthesis (Ein fluorierend spaltbarer Linker für die kombinatorische Festphasensynthese)

C. Sauter, H. P. Schuchmann, S. Bräse, Chemie Ingenieur Technik 2008, 80, 1539-1543. Einschluss von Cyclodextrin durch kombinierte Dispergierung und Reagglomeration nanoskaliger Partikel (Operation of Cyclodextrin through combined defloccualtion and reagglomeration of nano type particles).

M. Jainta, M. Nieger, S. Bräse, Eur. J. Org. Chem. 2008, 5418-5424. Microwave-assisted stereoselective one-pot synthesis of symmetrical and unsymmetrical 2,5-diketopiperazines from unprotected amino acids.

S. Ay, M. Nieger, S. Bräse, Chem. Eur. J. 2008, 14, 11539-11556. Co-Metal-Free Enantioselective Conjugate Addition Reactions of Zinc Reagents

2007

T. Baumann, H. Vogt, S. Bräse, Eur. J. Org. Chem. 2007, 266–282. The proline-catalyzed asymmetric amination of branched aldehydes.

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

T. Schröder, K. Schmitz, N. Niemeier, T. S. Balaban, H. F. Krug, U. Schepers, S. Bräse, Bioconjugates 2007, 18, 342-354. Solid-Phase Synthesis, Bioconjugation, and Toxicology of Novel Cationic Oligopeptoids for Cellular Drug Delivery

V. Zimmermann, F. Avemaria, S. Bräse, J. Comb. Chem. 2007, 9, 200-203. Chemo-selective reduction of nitroarenes in the presence of acid-sensitive functional groups: Solid-phase syntheses of amino aryl azides and benzotriazoles

A. Friedrich, M. Jainta, M. Nieger, S. Bräse, Synlett 2007, 2127-2129. One-Pot Synthesis of Symmetrical and Unsymmetrical Diketopiperazines from Unprotected Amino Acids

U. K. Ohnemüller, C. F. Nising, A. Encinas, S. Bräse, Synthesis 2007, 2175-2185. A versatile access to enantiomerically pure 5-substituted 4-hydroxy-2-cyclohexenones. An advanced hemisecalonic acid A model.

T. Schröder, M. Gartner, T. Grab, S. Bräse, Org. Biomol. Chem. 2007, 5, 2767-2769. A new azide staining reagent based on “click chemistry”

V. Zimmermann, S. Bräse, J. Comb. Chem. 2007, 9, 1114-1137. The Hartwig-Buchwald Amination on Solid Supports: A Novel Access to 1H-Benzotriazoles

C. I. Schilling, S. Bräse, Org. Biomol. Chem. 2007, 5, 3586-3588. Stable organic azides based on rigid tetrahedral methane and adamantane structures as high energetic materials

C. F. Nising, A. Friedrich, S. Bräse, Synlett 2007, 2987-2990. The double oxa-Michael-aldol condensation: straightforward access to dimeric tetrahydroxanthenones

2006

C. F. Nising, U. K. Ohnemüller, S. Bräse, Angew. Chem. Int. Ed. 2006, 45, 307-309; Angew. Chem. 2006, 118, 313-315. The Total Synthesis of the Fungal Metabolite Diversonol (Die Totalsynthese des Pilzmetaboliten Diversonol)

U. K. Ohnemüller, C. F. Nising, M. Nieger, S. Bräse, Eur. J. Org. Chem. 2006, 1535-1546. The domino oxa-Michael-addition aldol reaction – an access to variably substituted tetrahydroxanthenones.

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

C. F. Nising, U. K. Ohnemüller (née Schmid), A. Friedrich, B. Lesch, J. Steiner, H. Schnöckel, M. Nieger, S. Bräse, Chem. Eur. J. 2006, 12, 3647-3654. The diastereoselective synthesis of highly functionalized tetrahydroxanthenols - an unprecedented access to privileged structural motives.

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.

M. E. P. Lormann, M. Nieger, S. Bräse, J. Organomet. Chem. 2006, 691, 2159-2161. Desymmetrisation of a Bicyclo[4.4.0]decadiene: The Influence of Ligand Structures in an Asymmetric Heck Reaction.

M. Kreis, M. Nieger, S. Bräse, J. Organomet. Chem. 2006, 691, 2171-2181. Synthesis of novel planar-chiral [2.2]paracyclophane derivatives as potential ligands for asymmetric catalysis.

C. F. Nising, U. K. Ohnemüller, S. Bräse, Synthesis 2006, 2643-2645. A short and practical access to both enantiomers of 4-hydroxy-cyclohexenone based on a desymmetrizing CBS reduction.

R. E. Ziegert, S. Bräse, Synlett 2006, 2119-2123. Enantiotopic Desymmetrization of a Cyclic Endoperoxide by Asymmetric Dialkylzinc Addition.

T. Baumann, M. Bächle, S. Bräse, Org Lett. 2006, 8, 3797-3800. Thermal Sulfamidation of 2-arylaldehydes and ketones with chloramine-T

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.

D. Keck, S. Bräse, Org. Biomol. Chem. 2006, 4, 3574-3575. Synthesis of a versatile multifunctional building block for the construction of polyketide natural products

F. Lauterwasser, J. Gall, S. Höfener, S. Bräse, Adv. Synth. Catal. 2006, 348, 2068-2074. Second-Generation N,O-[2.2]Paracyclophane Ketimine Ligands for the Alkenylzinc Addition to Aliphatic and Aromatic Aldehydes: Scope and Limitations.

H. Vogt, T. Baumann, M. Nieger, S. Bräse, Eur. J. Org. Chem. 2006, 5815-5838. Direct Asymmetric a-Sulfamidation of a-Branched Aldehydes:A Novel Approach to Enamine Catalysis

D. Keck, T. Muller, S. Bräse, Synlett 2006, 3457-3460. A Stereoselective Suzuki Cross-coupling Strategy for the Synthesis of Ethyl Substituted Conjugated Dienoic Esters and Conjugated Dienones

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

2005

N. Vorontsova, E. Vorontsov, D. Antonov, Z. A. Starikova, K. Butin, S. Höfener, S. Bräse, V. Rozenberg, Adv. Synth. Catal. 2005, 347, 129-135. Highly Stereoselective Synthesis of Novel Multistereogenic bis-Bifunctional Ligands Based on [2.2]Paracyclophane-4,7-quinone, their Structure Elucidation and Application in Asymmetric Catalysis.

M. Kreis, S. Bräse, Adv. Synth. Catal. 2005, 347, 313-320. A General and Efficient Method for the Synthesis of Silyl-protected Aryl Mercaptanes from Aryl Halides or Triflates.

C. Gil, S. Bräse, Chem. Eur. J. 2005, 11, 2680-2688. Efficient solid-phase synthesis of highly functionalized 1,4-benzodiazepin-5-one derivatives and related compounds by intramolecular aza-Wittig reactions.

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

M. Kreis, C. F. Nising, M. Schroen, K. Knepper, S. Bräse, Org. Biomol. Chem. 2005, 3, 1835-1837. Efficient solid phase synthesis of benzo[1,2,3]thiadiazoles and related structures.

B. Lesch, J. Toräng, M. Nieger, S. Bräse, Synthesis 2005, 1888-1900. The Diels-Alder Approach towards Cannabinoids.

F. Lauterwasser, M. Nieger, H. Mansikkamäki, K. Nättinen, S. Bräse, Chem. Eur. J. 2005, 11, 4509-4522. Structurally Diverse Second-Generation Planar- and Central-Chiral [2.2]Paracyclophane Ketimines: Syntheses, Structural Determination, and Evaluation for Asymmetric Catalysis.

T. Grab, S. Bräse, Adv. Synth. Catal. 2005, 347, 1765-1768. Efficient Synthesis of Lactate-containing Depsipeptides by the Mitsunobu Reaction of Lactates.

S. Bräse, H. Wertal (nee Nüske), D. Frank, D. Vidović, A. de Meijere, Eur. J. Org. Chem. 2005, 4167-4178. Intramolecular Heck Couplings and Cycloisomerization Reactions of Bromodienes and Enynes with Tetrasubstituted Methylenecyclopropane Terminators: Efficient Syntheses of [3]Dendralenes.

K. Knepper, A. Themann, S. Bräse, J. Comb. Chem. 2005, 7, 799 - 801. Syntheses of 5-oxa-10,11-diaza-dibenzo[a,d]cycloheptenes on solid supports.

M. Schroen, S. Bräse, Tetrahedron 2005, 61, 12186-12192. Polymer-bound Diazonium Salts for the Synthesis of Diazoacetic Esters.

M. Kreis, C. J. Friedmann, S. Bräse, Chem. Eur. J. 2005, 11, 7387-7394. Diastereoselective Hartwig-Buchwald reaction of chiral amines with racemic [2.2]paracyclophane derivatives.

S. Bräse, S. Höfener, Angew. Chem. 2005, 117, 8091-8093; Angew. Chem. Int. Ed. 2005, 44, 7879-7881. Asymmetric conjugate addition of organozinc compounds to a,b-unsaturated aldehydes and ketones with [2.2]paracyclophaneketimine ligands without added copper salts (Die Kupfer-freie asymmetrische konjugate Addition von Zinkorganylen an cyclische und acyclische a,b-ungesättigte Aldehyde durch monomere Ligandstrukturen)

2004

C. Gil, A. Schwögler, S. Bräse, J. Comb. Chem. 2004, 6, 38-42. The Synthesis of 3-substituted 6-Aryl-3 H-benzo[a][1,2,3]triazinones using Polymer-bound Triazenes.

B. Lesch, S. Bräse, Angew. Chem. 2004, 116, 118-120. Angew. Chem. Int. Ed. 2004, 42, 115-118. A Short, Atom-Economical Entry to Tetrahydroxanthenones.

T. I. Danilova, V. I. Rozenberg, Z. A. Starikova, S. Bräse, Tetrahedron: Asymmetry 2004, 15, 223-229. Planar-Chiral Salen and Hemisalen Type Ligands of [2.2]Paracyclophane Series for Asymmetric Diethylzinc Addition to Aldehydes.

O. Kivrakidou, S. Bräse, F. Hülshorst, N. Griebenow, Org. Lett. 2004, 6, 1143-1146. Solid-Phase Synthesis of 5-Biphenyl-2-yl-1H-tetrazoles.

F. Avemaria, V. Zimmermann, S. Bräse, Synlett 2004, 1163-1165. Synthesis of Aryl Azides via Post-Cleavage Modification of Polymer-bound Triazenes.

F. Lauterwasser, P. G. Hayes, S. Bräse, W. E. Piers, L. L. Schafer, Organometallics 2004, 23, 2234-2237. Scandium Catalyzed Intramolecular Hydroamination. The Development of a Highly Active Cationic Catalyst.

K. Knepper, M. E. P. Lormann, S. Bräse, J. Comb. Chem. 2004, 6, 460-463. Efficient Synthesis of Highly Substituted Diaryl Ethers on Solid Supports using Ullmann Reactions.

S. Höfener, F. Lauterwasser, S. Bräse, Adv. Synth. Catal. 2004, 346 755-759. Second-generation paracyclophane imine ligands for the dialkyl zinc addition to aldehydes. Optimization of the branched side chain leads to improvement for aliphatic aldehydes.

K. Knepper, R. E. Ziegert, S. Bräse, Tetrahedron 2004, 60, 8591-8603. Solid-phase Synthesis of Isoindolinones and Naturally-occurring Benzobutyrolactones (Phthalides) using a Cyclative-Cleavage Approach.

C. F. Nising, U. Schmid, M. Nieger, S. Bräse, J. Org. Chem. 2004, 69, 6830-6833. A new protocol for the one-pot synthesis of symmetrical biaryls.

S. Bräse, S. Dahmen, C. Popescu, M. Schroen, F.-J. Wortmann, Chem. Eur. J. 2004, 10, 5285-5296. The Structural Influence in the Stability of Polymer-bound Diazonium Salts.

2003

N. Vignola, S. Dahmen, D. Enders, S. Bräse, J. Comb. Chem. 2003, 5, 138-144. Efficient Synthesis of Sulfonic, Phosphoric and Phosphinic Esters Employing Alkylating Polymer-Bound Reagents.

T. I. Danilova, V. I. Rozenberg, E. V. Sergeeva, Z. A. Starikova, S. Bräse, Tetrahedron: Asymmetry 2003, 14, 2013-2019. A Novel Chiral Tridentate Schiff base ligands of [2.2]Paracyclophane Series: synthesis and application

K. Knepper, S. Bräse, Org. Lett. 2003, 5, 2829-2832. The Bartoli Indole Synthesis on Solid Support.

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.

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.

2002

S. Dahmen, S. Bräse, Chem. Commun. 2002, 26-27. Planar and central chiral [2.2]paracyclophane-based N,O-ligands as highly active catalysts in the diethylzinc addition to aldehydes.

S. Bräse, S. Dahmen, C. Popescu, M. Schroen, F.-J. Wortmann, Polym. Degr. Stab. 2002, 75, 325-335. Investigations on the Thermal Stability of a Diazonium Ion on Solid Support.

S. Dahmen, S. Bräse, J. Am. Chem. Soc. 2002, 124, 5940-5941. The Asymmetric Dialkylzinc Addition to Imines Catalyzed by [2.2]Paracyclophane-based N,O-Ligands.

S. Bräse, S. Dahmen, F. Lauterwasser, N. E. Leadbeater, E. L. Sharp, Bioorg. Med. Chem. Lett. 2002, 12, 1845-1848. Polymer-bound 1-Aryl-3-alkyltriazenes as Modular Ligands for Catalysis: Part 1. Synthesis and Metal Coordination.

S. Bräse, S. Dahmen, F. Lauterwasser, N. E. Leadbeater, E. L. Sharp, Bioorg. Med. Chem. Lett. 2002, 12, 1849-1851. Polymer-bound 1-Aryl-3-alkyltriazenes as Modular Ligands for Catalysis: Part 2. Screening Metal-Bound Complexes for Catalytic Activity.

M. E. P. Lormann, C. H. Walker, M Es-Sayed, S. Bräse, Chem. Commun. 2002, 1296-1297. Solid supported fluoronitroaryl triazenes as immobilized and convertible Sanger reagents - synthesis and SNAr reactions towards a novel preparation of 1-alkyl benzotriazoles.

M. Lormann, S. Dahmen, F. Avemaria, F. Lauterwasser, S. Bräse, Synlett 2002, 915-918. Base-induced Fragmentation of N,N-Dibenzyl-N'-aryltriazenes.

N. Hermanns, S. Dahmen, C. Bolm, S. Bräse, Angew. Chem. 2002, 114, 3844-3846. Asymmetric, Catalytic Phenyl Transfer to Imines: Highly Enantioselective Synthesis of Diarylmethylamines. Angew. Chem. Int. Ed. 2002, 41, 3692-3694. Asymmetric, Catalytic Phenyl Transfer to Imines: Highly Enantioselective Synthesis of Diarylmethylamines.

2001

J. H. Kirchhoff, S. Bräse, D. Enders, J. Comb. Chem. 2001, 3, 71-77. [AN 2000:749599] A Novel Hydrazine Linker Resin and its Application For the Solid-phase Synthesis of a-branched Primary Amines

R. Lazny, M. Sienkiewicz, S. Bräse, Tetrahedron 2001, 57, 5825-5832. Application of Triazenes for protection of secondary amines.

N. Vignola, S. Dahmen, D. Enders, S. Bräse, Tetrahedron Lett. 2001, 42, 7833-7836. Synthesis of alkyl sulfonates from sulfonic acids or sodium sulfonates using solid-phase bound reagents

S. Dahmen, S. Bräse, Org. Lett. 2001, 3, 4119-4122. [2,2]Paracyclophane-based N,O-Ligands in Alkenylzinc Additions to Aldehydes

S. Dahmen, S. Bräse, Tetrahedron Asymm. 2001, 12, 2845-2850. Preparation of planar chiral amino alcohols based on the [2.2]paracyclophane backbone

C. Pilot, S. Dahmen, F. Lauterwasser, S. Bräse, Tetrahedron Lett. 2001, 42, 9179-9181. Cleavage of Immobilised Disubstituted Triazenes with Electrophiles: Synthesis of Alkyl Halides and Esters with Polymer-bound Reagents.

2000

M. Lormann, S. Dahmen, S. Bräse, Tetrahedron Lett. 2000, 41, 3813-3815. Nitrogen-Based Linker, Part 7. [CAN 133:150295; AN 2000:393216] Hydro-dediazoniation of Diazonium Salts using Trichlorosilane: New Cleavage Conditions for the T1 Traceless Linker

S. Dahmen, S. Bräse, Angew. Chem. 2000, 112, 3827-3830; Angew. Chem. Int. Ed. 2000, 39, 3681-3683. Nitrogen-Based Linker, Part 8. [AN 2000:755914] Das erste stabile Diazoniumion an der festen Phase – Untersuchungen zur Stabilität und Verwendung als Linker und Scavenger in der Festphasenchemie (The First Stable Diazonium Ion on Solid Support - Investigations on Stability and Usage as Linker and Scavenger in Solid-Phase Organic Synthesis)

S. Dahmen, S. Bräse, Org. Lett. 2000, 2, 3563-3565. [AN 2000:755635] A Novel Solid Phase Synthesis of Highly Diverse Guanidines: Reactions of Primary Amines Attached to the T2 Linker

S. Bräse, S. Dahmen, M. Pfefferkorn, J. Comb. Chem. 2000, 2, 710-715. Nitrogen-Based Linker, Part 9. [AN 2000:745386] Solid-Phase Synthesis of Urea and Amide Libraries Using the T2 Triazene Linker

1999

S. Bräse, D. Enders, J. Köbberling, F. Avemaria, Angew. Chem. 1999, 110, 3614-3616; Angew. Chem. Int. Ed. Engl. 1999, 37, 3413-3415. [CA 130:196356] Nitrogen-Based Linker, Part 1. Entwicklung eines regenerierbaren "traceless linker"-Systems für Reaktionen an fester Phase – ein überraschender Festphasen-Effekt (A surprising solid-phase effect: Development of a recyclable "traceless" linker system for reactions on solid support)

S. Bräse, J. Köbberling, D. Enders, M. Wang, R. Lazny, S. Brandtner, Tetrahedron Lett. 1999, 40, 2105-2108. Nitrogen-Based Linker, Part 3. [CA 130:296215] Triazenes as Robust and Simple Linker for Amines in Solid-Phase Organic Synthesis

S. Bräse, M. Schroen, Angew. Chem. 1999, 111, 1139-1142; Angew. Chem. Int. Ed. 1999, 38, 1071-1073. Nitrogen-Based Linker, Part 5. [CA 131:31780] Eine neue effiziente Abspaltungs-Kreuzkupplungs-Strategie für Festphasenreaktionen – Ein Baukastensystem für die Kombinatorische Chemie (Efficient cleavage - Cross-coupling strategy for solid-phase synthesis - A modular building system for combinatorial chemistry)

S. Bräse, J. Heuts, S. Dahmen, Tetrahedron Lett. 1999, 40, 6201-6203. Nitrogen-Based Linker, Part 4. [CA 131:286471] Solid-phase Synthesis of Substituted Cinnolines by a Richter Type Cleavage Protocol

S. Bräse, Tetrahedron Lett. 1999, 40, 6757-6759. [CA 131:322509] Intramolecular Transition-Metal Catalyzed Cyclizations of Electron Rich Chloroarenes

R. Lazny, J. Poplawski, J. Köbberling, D. Enders, S. Bräse, Synlett 1999, 1304-1306. Triazenes: A Useful Protecting Strategy for Sensitive Secondary Amines

S. Bräse, Synlett 1999, 1654-1656. Synthesis of Bis(enolnonaflates) and their 4-exo-trig-Cyclizations by Intramolecular Heck Reactions

A. de Meijere, H. Nüske, M. Es-Sayed, T. Labahn, M. Schroen, S. Bräse, Angew. Chem. 1999, 111, 3881-3884; Angew. Chem. Int. Ed. 1999, 38, 3669-3672. Nitrogen-Based Linker, Part 6. Neue effiziente Mehrkomponenten-Reaktionen unter C-C-Knüpfung zur kombinatorischen Anwendung in flüssiger und an fester Phase (New efficient multicomponent reactions with C-C coupling for combinatorial application in liquid and on solid phase)

B. Eigenständige Zeitschriftenartikel (im Druck)

 

A. A. Hassan, K. M. El-Shaieb, N. K. Mohamed, H. N. Tawfeek, S. Bräse, M. Nieger, Arab. J. Chem. 2017, in press. A Convenient and Efficient Synthesis of Thiazolidin-4-ones via Cyclization of Substituted Hydrazinecarbothioamides

             doi:10.1016/j.arabjc.2014.10.035

A. A Aly, M. Ramadan, M. Abd Al-Aziz, Hazem M. Fathy, S. Bräse, A. B. Brown, M. Nieger, Chem. Papers 2017, in press. Synthesis of new 5-aminopyrazoles from reactions of amidrazones with activated nitriles. NMR investigation and X-ray structural analysis.

             DOI 10.1007/s11696-017-0131-x

S. Bestgen, C. Seidl, T. Wiesner, A. Zimmer, M. Falk, B. Köberle, M. Austeri, J. Paradies, S. Bräse, U. Schepers, P. W. Roesky, Chem. Eur. J. 2017, in press. Double-strand DNA breaks induced by Paracyclophane Gold(I) Complexes

        http://onlinelibrary.wiley.com/doi/10.1002/chem.201700517/full

A. A. Hassan, N. K. Mohamed, K. M. A. El-Shaieb, H. N. Tawfeek, S. Bräse, M. Nieger, ARKIVOC 2017, in press. Reactivity of 2-Substituted Hydrazinecarbothioamides Towards Tetracyanoethylene and Convenient Synthesis of (5-Amino-2-diazenylthiazolylmethylene)malononitrile Derivatives

I. Protasova, S. Heissler, N. Jung, S. Bräse, Chem. Eur. J. 2017, in press. Monitoring of Reactions on Solid Phases via Raman Spectroscopy

             http://onlinelibrary.wiley.com/doi/10.1002/chem.201700907/full

             10.1002/chem.201700907

 P. Poonpatana, G. dos Passos Gomes, T. Hurrle, K. Chardon, S. Bräse, K.-S. Masters, I. Alabugin, Chem. Eur. J. 2017, in press. Formaldehyde-Extruding Homolytic Aromatic Substitution via C→O Transposition: Evolution of a Contaminating Side-Reaction to ‘Traceless-Linker’ access to Congested Biaryl Bonds.

             DOI: 10.1002/chem.201700085

A. A. Hassan, N. K. Mohamed, K. M. A. El-Shaieb, H. N. Tawfeek, S. Bräse, M. Nieger, Synthesis 2017, in press. Eschenmoser Coupling Reaction and Reactivity of Hydrazinecarbothio-amides in the Synthesis of Benzindazole and Naphthothiazole derivatives

             SS-2017-03-0149-OP.R1

V. Khudoleeva, V. Utochnikova, A. Kalyakina, I. Deygen, A. Shiryaev, L. Marciniak, V. Lebedev, I. Roslyakov, A.Garshev, L. Lepnev, U. Schepers, S. Bräse, N. Kuzmina, Dyes Pigment 2017, in press. Surface modified EuxLa1-xF3 nanoparticles as luminescent biomarkers: still plenty of room at the bottom

             DT-ART-12-2016-004920

          DOI: 10.1016/j.dyepig.2017.04.058

M.-L. Chan, C.-C. Yu, J.-L. Hsu, W.-J. Leu, S. H. Chan, L.-C. Hsu, S.-P. Liu, P. M. Ivantcova, Ö. Dogan, S. Bräse, K. V. Kudryavtsev, J.-H. Guh, Oncotarget 2017, in press. Enantiomerically pure β-dipeptide derivative suppresses cell proliferation and induces both apoptosis and autophagy through inhibition of multiple oncogenic pathways in human hormone-refractory prostate cancer

 

 

C. Eigenständige Buchkapitel und Übersichtsartikel

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

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

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

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. Eigenständige Buchkapitel und Übersichtsartikel (im Druck)

U. Schepers, C. Bednarek, K. Schmitz, S. Bräse, Angew. Chem. 2014, in revision (27.12.2013) (Review article). Smart vehicles for drug delivery: Transporters and Trojan peptides for fast delivery.

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

E. Zeitschriftenartikel (Studium, Doktorat und Postdoktorat)

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. Buchkapitel und Übersichtsartikel (Studium, Postdoktorat)

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. Artikel in Proceedings (in Chemical Abstracts gelisted)

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.

H. Sonstige Publikationen

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.

I. Sonstige Veröffentlichungen (Buchrezensionen 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

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, 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

J. Bücher

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.

K. Patente

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

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

L. Serien

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