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Kooperationen seit 2014

Alabugin FSU

P. Poonpatana, G. dos Passos Gomes, T. Hurrle, K. Chardon, S. Bräse, K.-S. Masters, I. Alabugin, Chem. Eur. J. 2017, 23, 9091-9097. 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

Aly El Minia

A. A Aly, T. El Malah, E. A. Ishak, S. Bräse, J. Sulfur Chem. 2016, 37, 141-147. Reaction of dithiocarbamates with malononitrile dimer; simple synthesis of new 1,4-dihydropyridine-2-thiols

DOI: 10.1080/17415993.2015.1102911

T. El Malah, A. A. Aly, S. Bräse, N. A. A. Elkanzi, A. B. Brown, J. Sulfur Chem. 2016, 37, 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. Aly, M. Ramadan, M. Abd Al-Aziz, H. M. Fathy, S. Bräse, A. B. Brown, M. Nieger, J. Chem. Res. 2016, 637-639. Reaction of amidrazones with 2,3-diphenylcyclopropenone - Synthesis of 3-(aryl)-2,5,6-triphenylpyrimidin-4(3H)-ones

JCR1604173

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

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

A. A Aly, M. Ramadan, M. Abd Al-Aziz, Hazem M. Fathy, S. Bräse, A. B. Brown, M. Nieger, Chem. Pap. 2017, 71, 1409-1417. 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

A. Aly, E. El-Sheref, A.-F. Mourad, A. Brown, S- Bräse, M. El-Sayed, Chem. Pap. 2018, 181-190. Synthesis of pyrano[3,2-c]quinoline-4-carboxylates and 2-(4-oxo-1,4-dihydroquinolin-3-yl)fumarates

DOI: 10.1007/s11696-017-0269-6

A. A. Aly, E. M. El-Sheref, A.-F. E. Mourad, A. B. Brown, S. Bräse, M. E. M. Bakheet, M. Nieger, Monatshefte Chemie - Chemical Monthly 2018, in press. Synthesis of Spiro[indoline-3,4'-pyrano[3,2-c]quinoline]-3'-carbonitrile

DOI: 10.1007/s00706-017-2078-6

Arras KIT

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

DOI: 10.1002/cptc.201700215

Belova/Danilkina St. Petersburg

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

http://pubs.acs.org/doi/abs/10.1021/jo501396s

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. G. Lyapunova, N. A. Danilkina, A. F. Khlebnikov, B. Köberle, S. Bräse, I. A. Balova, Eur. J. Org. Chem. 2016, 4842-4851. Oxaenediynes through the Nicholas Type Macrocyclization Approach

http://dx.doi.org/10.1002/ejoc.201600767

A. Lyapunova, N. Danilkina, A. Rumyantsev, A. Khlebnikov, M. Chislov, G. Starova, E. Sambuk, A. Govdi, S. Bräse, I. Balova, J. Org. Chem. 2018, in press. The Relative Reactivity of Benzothiophene-fused Enediynes in the Bergman Cyclization

DOI: 10.1021/acs.joc.7b03258

Barner-Kowolik KIT/Brisbane D. Volz, A. F. Hirschbiel, D. M. Zink, J. Friedrichs, M. Nieger, T. Baumann, S. Bräse, C. Barner-Kowollik, J. Mat. Chem. C (Materials for Optical and Electronic Devices) 20142, 1457-1462. Highly Efficient Photoluminescent Cu(I)-PyrPHOS-Metallopolymers
Baumann Cynora

D. Volz, M. Wallesch, S. Grage, J. Göttlicher, R. Steininger, D. Batchelor, D. Vitova, 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?"

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

DOI: 10.1002/adma.201405897

L. Bergmann G. Hedley T. Baumann S. Bräse I. Samuel, Science Adv. 2016, 2(1), e1500889. Direct Observation of Intersystem Crossing in A Thermally Activated Delayed Florescence Copper Complex in the Solid State

http://advances.sciencemag.org/content/2/1/e1500889.full-text.pdf+html

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. , 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

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

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

DOI: 10.1039/C4OB01663G

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

DOI: 10.1007/s41061-016-0022-6

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

DOI: 10.1117/2.1201409.005617

Bihlmeier KIT

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

DOI: 10.1039/C4OB00234B

M. Enders, C. J. Friedmann, P. Plessow, A. Bihlmeier, M. Nieger, W. Klopper, S. Bräse, Chem. Commun. 201551, 4793 - 4795. Unprecedented pseudo-ortho and ortho metalation of [2.2]paracyclophanes – a methyl group matters

DOI: 10.1039/C5CC00492F

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

DOI: 10.1021/acs.jpcc.6b00096

L. Barros, T. Cardoso, A. Bihlmeier, D. Kölmel, A. Hörner, D. Wagner, S. Bräse, C. Brito Cruz, L. Padilha, PCCP 2017, 19, 21683-21690. Two-Photon Absorption in a Series of 2,6-Disubstituted BODIPY Dyes

DOI: 10.1039/c6cp07849d

Biskup KIT

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

DOI: 10.1021/acs.chemrev.6b00010

Bizzarri KIT

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

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

DOI: 10.1016/j.ccr.2017.09.011

Blackwell Madison

A. Schneider, D. Fritz, J. Vasquez, S. Vollrath, H. Blackwell, S. Bräse, ACS Comb. Sci. 2017, 19, 715-737. Microwave-Facilitated SPOT-Synthesis of Antibacterial Dipeptoids.

DOI: 10.1021/acscombsci.7b00096

Breher KIT 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.
Breitling/Nesterov-Müller KIT

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

DOI: 10.1038/ncomms11844

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

D. S. Mattes, S. Rentschler, T. C. Foertsch, S. Münch, F. F. Loeffler, A. Nesterov-Müller, S. Bräse, F. Breitling, Small Methods 2018, in press. A Trifunctional Linker for Purified Three Dimensional Protein-Like Structure Arrays

DOI: 10.1002/smtd.201700205

Brenner-Weiß KIT

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

W. Yan, C. Réthoré, S. Menning, G. Brenner-Weiβ, T. Muller, P. Pierrat, S. Bräse, Chem. Eur. J. 2016, 22, 11522-11526. Hexakis terpyridine fullerene ligand and six-fold ruthenium, iridium and iron complexes. Synthesis and electrochemical properties

DOI: 10.1002/chem.201600796

Caro Hannover

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

Cato KIT

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

DOI: 10.1074/jbc.M113.534859

L. Cato et al, eLife 2017, 6:e27159 Development of Bag-1L as a Therapeutic Target in Androgen Receptor-Dependent Prostate Cancer

doi: 10.7554/eLife.27159

De Meijere Göttingen

S. Bräse, A. de Meijere Metal-Catalyzed Cross-Coupling Reactions and More, A. de Meijere, S. Bräse, M. Oestreich, Eds, Wiley-VCh, Weinheim, 2014. 533-664. Palladium-catalyzed coupling of organyl halides to alkenes - the Heck reaction

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

DOI: 10.1002/anie.201603951

Frimmel KIT

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

A. Kondrakov, A. N. Ignatev, V. V. Lunin, F. H. Frimmel, S. Bräse, H. Horn, Appl. Catal. B: Environ. 2016, 182, 424-430. Do free OH radicals in TiO2 photocatalysis come from H2O or dissolved O2? An isotope labeling study

Gerhards Kaiserslautern

M. Zimmer, F. Dietrich, D. Volz, S. Bräse, M. Gerhards, ChemPhysChem 2017, 18, 3023-3029. Solid State Step-Scan FTIR Spectroscopy of Binuclear Copper(I) Complexes

DOI: 10.1002/cphc.201700753

F. Bäppler, M. Zimmer, F. Dietrich, M. Grupe, M. Wallesch, D. Volz, S. Bräse, M. Gerhards, R. Diller, PCCP 2017, 19, 29438-29448. Photophysical Dynamics of a Binuclear Cu(I)-Emitter on the fs to µs Timescale, in Solid Phase and in Solution

DOI: 10.1039/c7cp05791a

Gil Madrid

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

Griebenow Bayer

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.

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

Harrity Sheffield

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

DOI: 10.1002/chem.201600796

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

Hassan El Minia

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

http://dx.doi.org/10.1016/j.tetlet.2014.02.107

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

DOI: 10.1002/jhet.1642

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

DOI: 10.1055/s-0034-1378551

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

DOI: 10.1515/chempap-2015-0092

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

DOI: 10.1515/znb-2014-0226

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. 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

DOI: 10.1016/j.cclet.2015.05.034

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

DOI: 10.1002/jhet.2240

A. A. Hassan, N. K. Mohamed, K. M. A. El-Shaieb, H. N. Tawfeek, S. Bräse, M. Nieger, J. Heterocyclic Chem. 2016, 53, 46-50. The Reactivity of Dimethyl Acetylenedicarboxylate and Heterocyclization of Hydrazinecarbothioamides to 1,​3-​Thiazolidin-​4-​ones

DOI: 10.1002/jhet.2392

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

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

DOI: 10.1002/jhet.2336

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

DOI: 10.1002/jhet.2350

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

DOI: 10.1002/cjoc.2011xxxxx.

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

SS-2016-01-0044-OP.R1

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

A. A. Hassan, N. K. Mohamed, K. M. A. El-Shaieb, H. N. Tawfeek, S. Bräse, M. Nieger, ARKIVOC 2016, (vi), 163-171. Reactivity of 2-Substituted Hydrazinecarbothioamides Towards Tetracyanoethylene and Convenient Synthesis of (5-Amino-2-diazenylthiazolylmethylene)malononitrile Derivatives

http://www.arkat-usa.org/get-file/59370/

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. 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. 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

A. A. Hassan, N. K. Mohamed, K. M. A. El-Shaieb, H. N. Tawfeek, S. Bräse, M. Nieger, Synthesis 2017, 3720-3725. Eschenmoser Coupling Reaction and Reactivity of Hydrazinecarbothio-amides in the Synthesis of Benzindazole and Naphthothiazole derivatives

SS-2017-03-0149-OP.R1

A Aly, A. Hassan, E.-S. Abd El-Latif, S. Bräse, M. Mahmoud, M. Nieger, Arkivoc 2018, part iii, 102-111. Reaction of N,N’-disubstituted hydrazinecarbothioamides with 2-bromo-2-substituted acetophenones

17-10385XP

http://www.arkat-usa.org/get-file/62040/

A. A. Hassan, K. M. El-Shaieb, N. K. Mohamed, H. N. Tawfeek, S. Bräse, M. Nieger, Arab. J. Chem. 2018, 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. Hassan, F. F. Abdel-Latif, M. Abdel-Aziz, S. M. Mostafa, S. Bräse, M. Nieger, J. Heterocyclic Chem. 2018, in press. Reactivity of 2-(Hydrazinecarbothionyl)-N-substituted hydrazinecarbo-thioamides Towards Dimethyl acetylenedicarboxylate

Heinke KIT

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

DOI: 10.1039/C5CC00694E

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

DOI: 10.1002/cphc.201500829

W. Zhou, S. Grosjean, S. Bräse, L. Heinke, Z. Phys. Chem. 2018, in press. Thermal cis-to-trans Isomerization of Azobenzene Side Groups in Metal-Organic Frameworks investigated by Localized Surface Plasmon Resonance Spectroscopy

DOI: 10.1515/zpch-2017-1081
 
Heine Leipzig

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. Soc2014136, 8-11. Fabrication of highly uniform gel-coatings by conversion of surface-anchored metal-organic framework

DOI: 10.1021/ja409205s

Herges Kiel

L. Heinke, M. Cakici, M. Dommaschk, S. Grosjean, R. Herges, S. Bräse, C. Wöll, ACS Nano 20148, 1463-1467. Photoswitching in two-component SURMOFs: Optically triggered release from a molecular container

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 201517, 14582-14587. Photoswitching in nanoporous, crystalline solids: An experimental and theoretical study for azobenzene linkers incorporated in metal-organic frameworks

Heissler KIT

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

I. Protasova, S. Heissler, N. Jung, S. Bräse, Chem. Eur. J. 2017, 23, 8703-8711. Monitoring of Reactions on Solid Phases via Raman Spectroscopy

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

10.1002/chem.201700907

Junker/Hopf Aalen/Mannheim

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

DOI: 10.1007/s00216-016-0096-6

Kappes KIT

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 

DOI: 10.1039/C3CP55486D

K. Brendle, M. Kordel, E. Schneider, D. Wagner, S. Bräse, P. Weis, M. M. Kappes, J. Am. Soc. Mass. Spec. 2018, 29, 382-392. Collision Induced Dissociation of Benzylpyridinium-Substituted Porphyrins: Towards a Thermometer Scale for Multiply Charged Ions?

DOI: 10.1007/s13361-017-1835-4

Kleist KIT/RUB

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

Klopper KIT

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

DOI: 10.1039/C5CC00492F

Kudryatsew Moscow

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

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

K. V. Kudryavtsev, A. B. Mantsyzov, P. M. Ivantcova, M. N. Sokolov, A. V. Churakov, S. Bräse, N. S. Zefirov, V. I. Polshakov, Org. Lett. 2016, 18, 4698–4701. Control of Azomethine Cycloaddition Stereochemistry by CF3-Group: Structural Diversity of Fluorinated β-Proline Dimers

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, 8:96668-96683. 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

DOI: 10.18632/oncotarget.18040
Kuzmina Moscow

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. 2016, 4, 9848-9855. Lanthanide anthracene-9-carboxylates – emitters for efficient NIR-emitting OLEDs 

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, 143, 348-355. Surface modified EuxLa1-xF3 nanoparticles as luminescent biomarkers: still plenty of room at the bottom

DT-ART-12-2016-004920

A. Kalyakina, V. Utochnikova, I. Bushmarinov, I. Le-Deygen, D. Volz, P. Weis, U. Schepers, N. Kuzmina, S. Bräse, Chem. Eur. J. 2017, 14944-14953. Lanthanide fluorobenzoates as bio-probes: a quest for the optimal ligand fluorination degree

DOI: 10.1002/chem.201703543

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

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

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

Lahann KIT/Michigan

E. Sokolovskaya, L. Barner, S. Bräse, J. Lahann, Macromol. Rapid Commun. 2014, 35, 780-786. Synthesis and On-Demand Gelation of Multifunctional Poly(ethylene glycol) Derivatives 

DOI: 10.1002/marc.201300909

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

DOI: 10.1002/ejoc.201402734

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

F. Bally-Le Gall, C. Hussal, J. J. P. Kramer, K. Cheng, R. Kumar, T. Eyster, V. Trouillet, M. Nieger, S. Bräse, J. Lahann, Chem. Eur. J. 2017, 13342–13350. Polylutidines: Multifunctional surfaces via vapour-based polymerization of substituted pyridinophanes

DOI: 10.1002/chem.201700901

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

Lemke EMBL

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. Lemke, Nature Methods 2016, 13, 997-1000. Genetic code expansion for multiprotein complex engineering

DOI: 10.1038/nmeth.4032

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

Lemmer KIT 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
Lichtenthaler LMU

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

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

Luy KIT

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 

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

A. E. E. Wandler, M. Koos, M. Nieger, B. Luy, S. Bräse, Dalton 2018, in press. 1,5-Cyclooctadienyl alcohols and ketones generate a new class of COD Pt complexes

DOI: 10.1039/C8DT00075A 

Meier KIT

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

DOI: 10.1038/ncomms11844

A. Llevot, S. O. Steinmüller, B. Bitterer, B. Ridder, J. Berson, S. Walheim, T. Schimmel, S. Bräse, F. Scheiba, M. A. R. Meier, Polymer Chem. 2017, 8, 5824-5828. Sequence-controlled molecular layers on surfaces by thiol-ene chemistry: synthesis and multitechnique characterization

DOI: 10.1039/C7PY01515A

Majewsky KIT

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

DOI: 10.1021/tx500267x

Masters Brisbane

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

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

DOI: 10.1016/j.jfluchem.2015.06.010

T. Wezeman, K. Masters, S. Bräse, Nat. Prod. Rep. 2015, 8-28. Xanthone dimers: a compound family which is both common and privileged

DOI: 10.1039/C4NP00050A

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

DOI: 10.1071/CH15465

P. Poonpatana, G. dos Passos Gomes, T. Hurrle, K. Chardon, S. Bräse, K.-S. Masters, I. AlabuginChem. Eur. J201723, 9091-9097. 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

Nieger Helsinki

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

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

J. Kramer, C. Yildiz, M. Nieger, S. Bräse, 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

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

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

DOI: 10.1002/ejoc.201402083

S. Zhong, A. Hafner, C. Hussal, M. Nieger, S. Bräse, RSC Advances 2015, 5, 6255-6258. Metal-Free Radical Perfluoroalkylation of (Hetero)Arenes

DOI: 10.1039/C4RA13430C

F. Gläser, M. Bröhmer, M. Nieger, T. Hurrle, S. Bräse, Eur. J. Org. Chem. 2015, 1516-1524. The Diels-Alder Approach towards Tetrahydrocannabinol Derivatives

DOI: 10.1002/ejoc.201403379

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

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

S. Lindner, M. Nieger, S. Bräse, Adv. Synth. Catal. 2015, 357, 3303-3308. Stannylation and Stille Coupling of Base-Sensitive Tetrahydroxanthones to Heteromeric Biaryls

DOI: 10.1002/adsc.201500524

T. Wezeman S. Zhong, M. Nieger, S. Bräse, Angew. Chem. Int. Ed. 2016, 55, 3823-3827. Synthesis of highly functionalized 4-aminoquinolines

DOI: 10.1002/anie.201511385

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

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

DOI: 10.1021/acs.orglett.6b01609

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

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

DOI: 10.1002/slct.201700667

L. Geiger, M. Nieger, S. Bräse, Adv. Synth. Catal. 2017, 359, 3421-3427. Suzuki-Miyaura Cross-Coupling Reactions of Tetrahydroxanthones and 4-Chromanone Lactones to Heteromeric Biaryls

DOI: 10.1002/adsc.201700497

S. Gräßle, S. Susanto, S. Sievers, E. Tavsan, M. Nieger, N. Jung, S. Bräse, ACS Med. Chem. Lett. 2017, 8, 931-935. Synthesis and Investigation of S-substituted 2‑Mercaptobenzoimidazoles as Inhibitors of Hedgehog Signaling

DOI: 10.1021/acsmedchemlett.7b00100

M. Mende, M. Nieger, S. Bräse, Chem. Eur. J. 2017, 23, 12283–12296.

Chemical Synthesis of Modified Hyaluronic Acid Disaccharides

DOI: 10.1002/chem.201701238

M. Wallesch, M. Nieger, D. Volz, S. Bräse, Inorg. Chem. Commun. 2017, 86, 232-240. Copper(I) Complexes of 8-(Diphenylphosphanyl-oxy)-quinoline: Photophysics, Structures and Reactivity

DOI: 10.1016/j.inoche.2017.10.012

C. Braun, M. Nieger, S. Bräse, Chem. Eur. J. 2017, 23, 16452-16455. Unprecedented one-pot reaction to chiral, non-racemic copper(I) complexes of [2.2]paracyclophane-based P,N-ligands

DOI: 10.1002/chem.201704115

L. Bergmann, C. Braun, M. Nieger, S. Bräse, Dalton 2018, 47, 608-621. The Coordination- and Photochemistry of Copper(I) Complexes: Variation of N^N Ligands from Imidazole to Tetrazole

DOI: 10.1039/C7DT03682E

R. Bär, M. Nieger, S. Bräse, Chem. Eur. J. 2018, 24, 1373-1382. Alkyl and aryl thiol addition to [1.1.1]propellane - scope and limitations of a fast conjugation reaction

DOI: 10.1002/chem.201704105
Occhiato Florence 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
O'Connor Norwich

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

DOI: 10.1016/j.chembiol.2014.09.010

Padilha Campina

D. K. Kölmel, A. Hörner, J. A. Castañeda, J. A. P. Ferencz, A. Bihlmeier, M. Nieger, S. Bräse, L. Padilha, J. Phys. Chem. 2016, 120, 4538-4545. Linear and Nonlinear Optical Spectroscopy of Fluoroalkylated BODIPY Dyes

DOI: 10.1021/acs.jpcc.6b00096

L. Barros, T. Cardoso, A. Bihlmeier, D. Kölmel, A. Hörner, D. Wagner, S. Bräse, C. Brito Cruz, L. Padilha, PCCP 2017, 19, 21683-21690. Two-Photon Absorption in a Series of 2,6-Disubstituted BODIPY Dyes

DOI: 10.1039/c6cp07849d

Postnikov/Filimonov Tomsk

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

M. E. Trusova, M. Rodríguez-Zubiri, K. V. Kutonova, N. Jung, S. Bräse, F.-X. Felpin, P. S. Postnikov, Org. Chem. Frontiers 2018, 5, 41-45. Ultra-Fast Suzuki and Heck Reactions for the Synthesis of Styrenes and Stilbenes Using Arenediazonium Salts as Super-Electrophiles

DOI: 10.1039/C7QO00750G

Powell KIT

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

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. RoeskyChem. Eur. J2015, 2813-2820. Peptoid Ligated Pentadecanuclear Yttrium and Dysprosium Hydroxy Clusters

DOI: 10.1002/chem.201406230

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

DOI: 10.1038/ncomms11844

Rizzacasa Melbourne 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.
Roesky KIT

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. J. 2015, 2813-2820. Peptoid Ligated Pentadecanuclear Yttrium and Dysprosium Hydroxy Clusters

DOI: 10.1002/chem.201406230

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, 23, 6315-6322. Double-strand DNA breaks induced by Paracyclophane Gold(I) Complexes

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

DOI: 10.1016/j.dyepig.2017.04.058 

Rudat/Syldatk KIT 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
Schafer Vancouver

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

DOI: 10.1002/ejoc.201700101

Schepers KIT

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

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

DOI: 10.1016/j.ejmech.2014.03.078

M. Enders, B. Görling, A. B. Braun, J. Seltenreich, L. Reichenbach, M. Nieger, K. Rissanen, B. Luy, U. Schepers, S. Bräse, Organometallics 2014, 33, 4027-4034. Cytotoxicity and NMR Studies of Platinum Complexes with Cyclooctadiene Ligands

DOI: 10.1021/om500540x

M. Wallesch, D. Volz, D. Zink, U. Schepers, M. Nieger, T. Baumann, S. Bräse, Chem. Eur. J. 201420, 6578-6590. Bright coppertunities: Multinuclear copper complexes from N,P-ligands and their applications

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. 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

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

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

DOI: 10.1002/ejoc.201500900

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

DOI: 10.1002/chem.201501816

I. M. Deygen, C. Seidl, D. K. Kölmel, C. Bednarek, S. Heissler, E. V. Kudryashova, S. Bräse, U. Schepers, Langmuir 2016, 32, 10861-10869. Novel form of doxorubicin modified by stearoylspermine encapsulated into PEGchitosan stabilized liposomes.

DOI: 10.1021/acs.langmuir.6b01023

M. Mende, C. Bednarek, M. Wawryszyn, P. Sauter, M. B. Biskup, U. Schepers, S. Bräse, Chem. Rev2016116, 8193-8255. Chemical synthesis of glycosaminoglycans

DOI: 10.1021/acs.chemrev.6b00010

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. HarrityChem. Eur. J. 201622, 12430-12438. A Modular Class of Fluorescent Difluoroboranes: Synthesis, Structure, Optical Properties, Theoretical Calculations and Applications for Biological Imaging

DOI: 10.1002/chem.201600796

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. LichtenthalerELife 2016, 5. Systematic substrate identification reveals a central role for the metalloprotease ADAM10 in axon and synapse function

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

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 2017143, 348-355. Surface modified EuxLa1-xF3 nanoparticles as luminescent biomarkers: still plenty of room at the bottom

DT-ART-12-2016-004920

A. Kalyakina, V. Utochnikova, I. Bushmarinov, I. Le-Deygen, D. Volz, P. Weis, U. Schepers, N. Kuzmina, S. Bräse, Chem. Eur. J. 2017, 14944-14953. Lanthanide fluorobenzoates as bio-probes: a quest for the optimal ligand fluorination degree

DOI: 10.1002/chem.201703543

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. J201723, 6315-6322. Double-strand DNA breaks induced by Paracyclophane Gold(I) Complexes

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

DOI: 10.1016/j.dyepig.2017.04.058 

V.V. Utochnikova, D. S. Koshelev, A. Medvedko, A. S. Kalyakina, I. S. Bushmarinov, A. Y. Grishko, U. Schepers, S. Bräse, S. Z. Vatsadze, Optical Materials 2017, 74, 191–196. Europium 2-benzofuranoate: synthesis and use for bioimaging

DOI:10.1016/j.optmat.2017.05.038

Seipenbusch Stuttgart

M. Faust, M. Dinkel, M. Bruns, S. Bräse, M. Seipenbusch, Ind. & Eng. Chem. Res201756, 3194-3203. Support Effect on the Water Gas Shift Activity of Chemical Vapor Deposition-Tailored-Pt/TiO2 Catalysts

DOI: 10.1021/acs.iecr.6b04512

Sleeman/Orian-Roisseau KIT

J. P. Sleeman, J. Bauer, A. Schmaus, M. Rothley, L. Quagliata, M. Ehret, M. Biskup, V. Orian-Rousseau, D. Jackson, R. Pettis, A. Harvey, S. Bräse, W. Thiele, J. Mol. Med. 2018, 96, 199-209. TGFβ counteracts LYVE-1-mediated induction of lymphangiogenesis by small hyaluronan oligosaccharides

DOI: 10.1007/s00109-017-1615-4

Thiel Kaiserslautern

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

C. Braun, M. Nieger, W. R. THIEL , S. Bräse, Chem. Eur. J. 2017, 23, 15474-15483. [2.2]Paracyclophanes with N-Heterocycles as Ligands for Mono- and Dinuclear Ruthenium(II) Complexe

DOI: 10.1002/chem.201703291

F. Schön, M. Leist, A. Neuba J. Lang, C. Braun, Y. Sun, G. Niedner-Schatteburg, S. Bräse, W. R. THIEL , Chem. Commun. 2017, 53, 12016-12019. A direct access to heterobimetallic complexes by roll-over cyclometallation

DOI: 10.1039/c7cc07119a

Thompson USC

B. K. T. Batagoda, P. I. Djurovich, S. Bräse, M. E. Thompson, Polyhedron 2016116, 182-188. Synthesis and characterization of phosphorescent cyclometalated Ir and Pt heteroleptic complexes using cyclophane-based chelates

DOI: 10.1016/j.poly.2016.04.039

Tsotsalas KIT

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

http://pubs.rsc.org/en/content/articlepdf/2016/ra/c6ra06510d

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

Türk KIT 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
Utochnikova Moscow

V.V. Utochnikova, D. S. Koshelev, A. Medvedko, A. S. Kalyakina, I. S. Bushmarinov, A. Y. Grishko, U. Schepers, S. Bräse, S. Z. Vatsadze, Optical Materials 2017, 74, 191–196. Europium 2-benzofuranoate: synthesis and use for bioimaging

DOI:10.1016/j.optmat.2017.05.038

Wöll KIT

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

DOI: 10.1021/ja409205s

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

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

DOI: 10.1039/C4CC03521F, Communication

P. Lindemann, M. Tsotsalas, S. Shishatskiy, V. Abetz, P. Krolla-Sidenstein, C. Azucena, L. Monnereau, A. Beyer, A. Gölzhäuser, H. Gliemann, S. Bräse, C. Wöll, Chem. Mater. 2014, 26, 7189-7193. Preparation of Freestanding Conjugated Microporous Polymer Nanomembranes for Gas Separation

DOI: 10.1021/cm503924h

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

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

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

Z. Wang, J. Liu, S. Grosjean, D. Wagner, W. Guo, G. Gu, L. , H. Gliemann, S. Bräse, C. Wöll, ChemNanoMat 2015, 1, 338-345. Monolithic, Crystalline MOF Coating: An Excellent Patterning and Photoresist Material (Cover picture)

DOI: 10.1002/cnma.201500031

P. Lindemann, A. Schade, L. Monnereau, W. Feng, K. Batra, H. Gliemann, P. A. Levkin, S. Bräse, C. Wöll, M. Tsotsalas, Chem. Materials A 2016, 4, 6815-6818. Surface Functionalization of Microporous Polymer Thin Films and Nanomembranes using Orthogonal Chemistries

DOI: 10.1039/C5TA09429A

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

Z. Wang, A. Knebel, S. Grosjean, D. Wagner, S. Bräse, C. Wöll, J. Caro, L. Heinke, Nature Comms. 2016, 7, 13872. Tunable Molecular Separation by Nanoporous Membranes

DOI: 10.1038/ncomms13872

W. Zhou, S. Begum, Z. Wang P. Krolla D. Wagner, S. Bräse, C. Wöll, M. Tsotsalas, ACS Appl. Mater. Interfaces 2018, 10, 1528-1533.

High Antimicrobial Activity of MOF-​Templated Porphyrin Polymer Thin Films

DOI: 10.1021/acsami.7b14866

Z. Wang, C. Liang, H. Tang, S. Grosjean, A. Shahnas, J. Lahann, S. Bräse, C. Wöll, Macromol. Chem. Rapid Commun. 2018, in press. Water-​Stable Nanoporous Polymer Films with Excellent Proton Conductivity

DOI: 10.1002/marc.201700676

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