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81.
Carsten Schultz 《Israel Journal of Mathematics》2009,170(1):125-134
We show that the n-th power of the first Stiefel-Whitney class of the ℤ2-action on the graph complex Hom(C
2r+1, K
n+2) is zero, confirming a conjecture by Babson and Kozlov. This yields a considerably simplified proof of their graph colouring
theorem, which is also known as the Lovsz conjecture.
This research was supported by the Deutsche Forschungsgemeinschaft within the European graduate program “ Combinatorics, Geometry,
and Computation” (No. GRK 588/2) 相似文献
82.
Radical S‐Adenosyl Methionine Epimerases: Regioselective Introduction of Diverse D‐Amino Acid Patterns into Peptide Natural Products 下载免费PDF全文
Dr. Brandon I. Morinaka Dr. Anna L. Vagstad Maximilian J. Helf Dr. Muriel Gugger Dr. Carsten Kegler Dr. Michael F. Freeman Prof. Dr. Helge B. Bode Prof. Dr. Jörn Piel 《Angewandte Chemie (International ed. in English)》2014,53(32):8503-8507
PoyD is a radical S‐adenosyl methionine epimerase that introduces multiple D ‐configured amino acids at alternating positions into the highly complex marine peptides polytheonamide A and B. This novel post‐translational modification contributes to the ability of the polytheonamides to form unimolecular minimalistic ion channels and its cytotoxic activity at picomolar levels. Using a genome mining approach we have identified additional PoyD homologues in various bacteria. Three enzymes were expressed in E. coli with their cognate as well as engineered peptide precursors and shown to introduce diverse D ‐amino acid patterns into all‐L peptides. The data reveal a family of architecturally and functionally distinct enzymes that exhibit high regioselectivity, substrate promiscuity, and irreversible action and thus provide attractive opportunities for peptide engineering. 相似文献
83.
Development of Polar Order in the Liquid Crystal Phases of a 4‐Cyanoresorcinol‐Based Bent‐Core Mesogen with Fluorinated Azobenzene Wings 下载免费PDF全文
Dr. Mohamed Alaasar Dr. Marko Prehm Dr. Maria‐Gabriela Tamba Dr. Nerea Sebastián Dr. Alexey Eremin Prof. Dr. Carsten Tschierske 《Chemphyschem》2016,17(2):278-287
A bent‐core mesogen consisting of a 4‐cyanoresorcinol unit as the central core and laterally fluorinated azobenzene wings forms four different smectic LC phase structures in the sequence SmA–SmCs–SmCsPAR–M, all involving polar SmCsPS domains with growing coherence length of tilt and polar order on decreasing temperature. The SmA phase is a cluster‐type de Vries phase with randomized tilt and polar direction; in the paraelectric SmCs phase the tilt becomes uniform, although polar order is still short‐range. Increasing polar correlation leads to a new tilted and randomized polar smectic phase with antipolar correlation between the domains (SmCsPAR) which then transforms into a viscous polar mesophase M. As another interesting feature, spontaneous symmetry breaking by formation of a conglomerate of chiral domains is observed in the non‐polar paraelectric SmCs phase. 相似文献
84.
Guyon F Hameau A Khatyr A Knorr M Amrouche H Fortin D Harvey PD Strohmann C Ndiaye AL Huch V Veith M Avarvari N 《Inorganic chemistry》2008,47(17):7483-7492
The dinuclear gold complexes [{Au(PPh 3)} 2(mu- dmid)] ( 1) ( dmid = 1,3-dithiole-2-one-4,5-dithiolate) and [{Au(PPh 3)} 2(mu- dddt)] ( 2) ( dddt = 5,6-dihydro-1,4-dithiine-2,3-dithiolate) were synthesized and characterized by X-ray crystallography. Both complexes exhibit intramolecular aurophilic interactions with Au...Au distances of 3.1984(10) A for 1 and 3.1295(11) A for 2. A self-assembly reaction between 4,5-bis(2-hydroxyethylthio)-1,3-dithiole-2-thione ( (HOCH 2 CH 2 ) 2 dmit) and [AuCl(tht)] affords the complex [AuCl{ (HOCH 2 CH 2 ) 2 dmit}] 2 ( 4), which possesses an antiparallel dimeric arrangement resulting from a short aurophilic contact of 3.078(6) A. This motif is extended into two dimensions due to intra- and intermolecular hydrogen bonds via the hydroxyethyl groups, giving rise to a supramolecular network. Three compounds were investigated for their rich photophysical properties at 298 and 77 K in 2-MeTHF and in the solid state; [Au 2(mu- dmid)(PPh 3) 2] ( 1), [Au 2(mu- dddt)(PPh 3) 2] ( 2), and [AuCl{( HOCH 2 CH 2 ) 2 dmit}] ( 4). 1 exhibits relatively long-lived LMCT (ligand-to-metal charge transfer) emissions at 298 K in solution (370 nm; tau e approximately 17 ns, where M is a single gold not interacting with the other gold atom; i.e., the fluxional C-SAuPPh 3 units are away from each other) and in the solid state (410 nm; tau e approximately 70 mus). At 77 K, a new emission band is observed at 685 nm (tau e = 132 mus) and assigned to a LMCT emission where M is representative for two gold atoms interacting together consistent with the presence of Au...Au contacts as found in the crystal structure. In solution at 77 K, the LMCT emission is also red-shifted to 550 nm (tau e approximately 139 mus). It is believed to be associated to a given rotamer. 2 also exhibits LMCT emissions at 380 nm at 298 K in solution and at 470 nm in the solid state. 4 exhibits X/MLCT emission (halide/metal to ligand charge transfer) where M is a dimer in the solid state with obvious Au...Au interactions, resulting in red-shifted emission band, and is a monomer in solution in the 10 (-5) M concentration (i.e., no Au...Au interactions) resulting in blue-shifted luminescence. Both fluorescence and phosphorescence are observed for 4. 相似文献
85.
Carsten von Hänisch PD Dr. 《无机化学与普通化学杂志》2008,634(4):701-703
Synthesis and Metalation of the Diaminosiloxane O(SiiPr2NH2)2 The 1,3‐diaminoldisiloxane O(SiiPr2NH2)2 ( 1 ) was obtained from the reaction of O(SiiPr2Cl)2 with NH3. The reactions of 1 with AlEt3 or GaEt3 produced the compounds [O{SiiPr2N(H)MEt2}{SiiPr2NMEt}]2 ( 2 : M = Al; 3 : M = Ga). The crystal structures of 2 and 3 were determined by single crystal X‐ray diffraction, showing a polycyclic M4N4Si4O2 core structure of these molecules. 相似文献
86.
Amy M. Zimmermann-Klemd Jakob K. Reinhardt Moritz Winker Carsten Gründemann 《Molecules (Basel, Switzerland)》2022,27(10)
Modern phytotherapy is part of today’s conventional evidence-based medicine and the use of phytopharmaceuticals in integrative oncology is becoming increasingly popular. Approximately 40% of users of such phytopharmaceuticals are tumour patients. The present review provides an overview of the most important plants and nature-based compounds used in integrative oncology and illustrates their pharmacological potential in preclinical and clinical settings. A selection of promising anti-tumour plants and ingredients was made on the basis of scientific evidence and therapeutic practical relevance and included Boswellia, gingko, ginseng, ginger, and curcumin. In addition to these nominees, there is a large number of other interesting plants and plant ingredients that can be considered for the treatment of cancer diseases or for the treatment of tumour or tumour therapy-associated symptoms. Side effects and interactions are included in the discussion. However, with the regular and intended use of phytopharmaceuticals, the occurrence of adverse side effects is rather rare. Overall, the use of defined phytopharmaceuticals is recommended in the context of a rational integrative oncology approach. 相似文献
87.
Alfred Baszczyk Matthias Fischer Carsten vonHnisch Marcel Mayor 《Helvetica chimica acta》2006,89(9):1986-2005
The synthesis, characterization, and optical properties of a series of new 2,6‐disubstituted naphthalene‐bisimide dyes as molecular rods comprising terminal AcS groups is reported. The first series of dyes ( 1 – 3 ), comprising phenylhetero (Ph‐X) core substituents, cover a broad range of the VIS spectrum, ranging from yellow ( 2 ) over red ( 3 ) to blue ( 1 ). The second series of dyes contains benzylhetero (Bn‐X) core substituents ( 4 – 7 ). For the same heteroatom connecting the substituent to the naphthalene core, both series were found to display comparable colors. For the second series, the colors were blue ( 4 ), red ( 5 ), and violet ( 6, 7 ). The Ph‐X‐substituted dyes 1 – 3 are nonfluorescent, in contrast to the Bn‐X‐substituted compounds 4 – 7 . This rich variety of optical features that can be adjusted by rather small alterations of the core substituents makes these structurally very comparable molecular rods ideal candidates for optically triggered molecular‐transport investigations. Also, thanks to the terminal AcS groups, these compounds can be placed between nobel‐metal electrodes for optically triggered transport experiments. 相似文献
88.
α,β-Unsaturated nitriles can be hydrogenated with enantioselectivities up to 88% ee using chiral ruthenium-diphenylphosphino bisaryl and bisheteroaryl complexes such as ruthenium(II)-BINAP and ruthenium(II)-BINP. Mechanistic investigations indicate that conversion is accelerated by electron-rich ligands and that an additional coordinative group needs be present in order to promote conversion. The chiral products are useful building blocks for the synthesis of histamine H2 agonists of the arpromidine type. 相似文献
89.
Arráez-Román D Zurek G Bässmann C Segura-Carretero A Fernández-Gutiérrez A 《Electrophoresis》2008,29(10):2112-2116
This short communication describes the characterization of seven tropane alkaloid compounds in Atropa belladonna L. Thus a rapid and easy CE-electrospray interface (ESI)-TOF-MS procedure is developed to analyze these compounds in a pharmaceutical preparations of A. belladonna L. leaf extract. Optimum electrophoretic separation is obtained using an alkaline solution of 60 mM ammonium acetate at pH 8.5 containing 5% isopropanol. Under the optimum CE-ESI-TOF-MS conditions several important compounds such as tropine, belladonnine, norhyoscyamine, apoatropine, hyoscyamine, 6beta-hydroxyhyoscyamine, and scopolamine have been simultaneously identified from A. belladonna L. CE-ESI-IT-MS has been used to discriminate the putative presence of littorine. The sensitivity, together with mass accuracy and true isotopic pattern of the TOF-MS, allowed the identification of a broad series of tropane alkaloid compounds present in pharmaceutical preparations of A. belladonna L. leaf extract. 相似文献
90.