Solution Structures of β Peptides from Raman Optical Activity (English)
- New search for: Kapitán, Josef
- New search for: Zhu, Fujiang
- New search for: Hecht, Lutz
- New search for: Gardiner, James
- New search for: Seebach, Dieter
- New search for: Barron, Laurence D.
- New search for: Kapitán, Josef
- New search for: Zhu, Fujiang
- New search for: Hecht, Lutz
- New search for: Gardiner, James
- New search for: Seebach, Dieter
- New search for: Barron, Laurence D.
In:
Angewandte Chemie
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120
, 34
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6492-6494
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2008
- Article (Journal) / Electronic Resource
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Title:Solution Structures of β Peptides from Raman Optical Activity
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Contributors:Kapitán, Josef ( author ) / Zhu, Fujiang ( author ) / Hecht, Lutz ( author ) / Gardiner, James ( author ) / Seebach, Dieter ( author ) / Barron, Laurence D. ( author )
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Published in:Angewandte Chemie ; 120, 34 ; 6492-6494
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Publisher:
- New search for: WILEY‐VCH Verlag
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Publication date:2008-08-11
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Size:3 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:
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Source:
Table of contents – Volume 120, Issue 34
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 6397
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Titelbild: Selenirenium‐ und Tellurireniumionen (Angew. Chem. 34/2008)Poleschner, Helmut / Seppelt, Konrad et al. | 2008
- 6398
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Innentitelbild: Echtzeitnachweis von Änderungen im Protein‐Wassernetzwerk während der Proteinfaltung mit Terahertz‐Absorptionsspektroskopie (Angew. Chem. 34/2008)Kim, Seung Joong / Born, Benjamin / Havenith, Martina / Gruebele, Martin et al. | 2008
- 6398
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Innentitelbild: Echtzeitnachweis von Anderungen im Protein-Wassernetzwerk wahrend der Proteinfaltung mit Terahertz-Absorptionsspektroskopie (Angew. Chem. 34/2008)Kim, S. J. / Born, B. / Havenith, M. / Gruebele, M. et al. | 2008
- 6401
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Graphisches Inhaltsverzeichnis: Angew. Chem. 34/2008| 2008
- 6414
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Top-Beitrage aus unseren Schwesterzeitschiften: Angew. Chem. 34/2008| 2008
- 6414
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Top‐Beiträge aus unseren Schwesterzeitschiften: Angew. Chem. 34/2008| 2008
- 6416
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Struktur und Reaktivität der Biomoleküle. Eine Einführung in die Organische Chemie. Von Albert Gossauer.Schmuck, Carsten et al. | 2008
- 6416
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Struktur und Reaktivitat der Biomolekule. Eine Einfuhrung in die Organische Chemie. Von Albert Gossauer.Schmuck, C. et al. | 2008
- 6417
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Supramolecular Catalysis. Herausgegeben von Piet W. N. M. van Leeuwen.Lützen, Arne et al. | 2008
- 6420
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Chemische Selektivität durch Kontrolle der Dynamik angeregter Zustände F.S. dankt A. Lami (IPCF-CNR), C. Petrongolo (Universität Siena) und L. Vaccaro (Universität Perugia) für hilfreiche Diskussionen.Olivucci, Massimo et al. | 2008
- 6420
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Chemische Selektivitat durch Kontrolle der Dynamik angeregter ZustandeOlivucci, M. / Santoro, F. et al. | 2008
- 6420
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Chemische Selektivität durch Kontrolle der Dynamik angeregter ZuständeOlivucci, Massimo / Santoro, Fabrizio et al. | 2008
- 6425
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GaI als Ligand in Übergangsmetallkomplexen – eine Alternative zu CO oder N2?Himmel, Hans‐Jörg / Linti, Gerald et al. | 2008
- 6425
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GaI als Ligand in Ubergangsmetallkomplexen - eine Alternative zu CO oder N2?Himmel, H. J. / Linti, G. et al. | 2008
- 6428
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Rolling-Circle-Amplifikation: Anwendungen in der Nanotechnologie und in der Biodetektion mit funktionellen NucleinsaurenZhao, W. / Ali, M. M. / Brook, M. A. / Li, Y. et al. | 2008
- 6428
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Rolling‐Circle‐Amplifikation: Anwendungen in der Nanotechnologie und in der Biodetektion mit funktionellen NucleinsäurenZhao, Weian / Ali, M. Monsur / Brook, Michael A. / Li, Yingfu et al. | 2008
- 6428
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Rolling-Circle-Amplifikation: Anwendungen in der Nanotechnologie und in der Biodetektion mit funktionellen Nucleinsäuren Hintergrundinformationen zu diesem Beitrag sind im WWW unter http: www.angewandte.de zu finden oder können beim Autor angefordert werden.Zhao, Weian et al. | 2008
- 6438
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Biarylphosphanliganden in der palladiumkatalysierten AminierungSurry, David S. / Buchwald, Stephen L. et al. | 2008
- 6462
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Loading Molecular Hydrogen Cargo within Viruslike NanocontainersSwaminathan Iyer, K. / Norret, Marck / Dalgarno, Scott J. / Atwood, Jerry L. / Raston, Colin L. et al. | 2008
- 6462
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Loading Molecular Hydrogen Cargo within Viruslike Nanocontainers We graciously acknowledge support of this work by the Australian Research Council (ARC) and the National Science Foundation (NSF). The authors thank Cameron Evans for assistance with the frontispiece.Swaminathan Iyer, K. et al. | 2008
- 6467
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Palladium‐Catalyzed Enantioselective Oxidation of Chiral Secondary Alcohols: Access to Both Enantiomeric SeriesEbner, David C. / Trend, Raissa M. / Genet, Cédric / McGrath, Matthew J. / O'Brien, Peter / Stoltz, Brian M. et al. | 2008
- 6467
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Palladium-Catalyzed Enantioselective Oxidation of Chiral Secondary Alcohols: Access to Both Enantiomeric Series We are grateful to the NIH-NIGMS (R01 GM65961-01), NSF (predoctoral fellowship to D.C.E.), NDSEG (predoctoral fellowship to D.C.E.), Bristol-Myers Squibb and the American Chemical Society (predoctoral fellowship to R.M.T.), EPSRC, and EU.Ebner, David C et al. | 2008
- 6471
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Concomitant and Controllable Chiral/Racemic Polymorphs: From Achirality to Isotactic, Syndiotactic, and Heterotactic ChiralityLi, Xin‐Zhi / Li, Mian / Li, Zhen / Hou, Jin‐Zhang / Huang, Xiao‐Chun / Li, Dan et al. | 2008
- 6471
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Concomitant and Controllable Chiral-Racemic Polymorphs: From Achirality to Isotactic, Syndiotactic, and Heterotactic Chirality This work was financially supported by the National Natural Science Foundation of China (Grant nos. 20571050 and 20771072). We thank Xin-Hui Zhou and Prof. Dr. Jing-Lin Zuo at Nanjing University for the CD spectroscopy measurement and explanation.Li, Xin-Zhi et al. | 2008
- 6475
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Lateral Association of Cylindrical Nanofibers into Flat Ribbons Triggered by “Molecular Glue”Lee, Eunji / Kim, Jung‐Keun / Lee, Myongsoo et al. | 2008
- 6475
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Lateral Association of Cylindrical Nanofibers into Flat Ribbons Triggered by "Molecular Glue" This work was supported by the National Creative Research Initiative Program of the Korean Ministry of Science and Technology. E.L. and J.-K.K acknowledge fellowships from the BK21 program of the Ministry of Education and Human Resources Development.Lee, Eunji et al. | 2008
- 6479
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Pronounced Steric Effects of Substituents in the Nazarov Cyclization of Aryl Dienyl Ketones A.P.M., A.S.L., and R.S. are grateful to UC Berkeley, the National Science Foundation (CAREER: CHE-0643264), GlaxoSmithKline, and Boehringer Ingelheim for generous financial support, and to Dr. Kathleen Durkin (NSF CHE-0233882) for help with molecular modeling, and Eric Bunnelle and Dr. William Bunnelle for helpful discussions. R.L.D. and D.J.T. gratefully acknowledge support from UC Davis and the National Science Foundation (CAREER: CHE-0449845 and computer time from the Pittsburgh Supercomputer Center).Marcus, Andrew P et al. | 2008
- 6479
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Pronounced Steric Effects of Substituents in the Nazarov Cyclization of Aryl Dienyl KetonesMarcus, Andrew P. / Lee, Amy S. / Davis, Rebecca L. / Tantillo, Dean J. / Sarpong, Richmond et al. | 2008
- 6484
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An Electron-Transfer Series of High-Valent Chromium Complexes with Redox Non-Innocent, Non-Heme Ligands C.C.L. thanks the Alexander von Humboldt Foundation for a postdoctoral fellowship. SSRL operations are funded by the DOE and BES. The SMB program is supported by the NIH, NCRR, BTP, and by the DOE, BER. This publication was made possible by grant number 5 P41 RR001209 from the NCRR, a component of the NIH. Its contents are the responsibility of the authors and do not represent the official view of the NCRR or NIH.Lu, Connie C et al. | 2008
- 6484
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An Electron‐Transfer Series of High‐Valent Chromium Complexes with Redox Non‐Innocent, Non‐Heme LigandsLu, Connie C. / DeBeer George, Serena / Weyhermüller, Thomas / Bill, Eckhard / Bothe, Eberhard / Wieghardt, Karl et al. | 2008
- 6488
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Microfluidic Self-Patterning of Large-Scale Crystalline Nanoarrays for High-Throughput Continuous DNA Fractionation This work was supported by the Natural Sciences and Engineering Research Council of Canada (NSERC). Microfabrication in this work was done at Nanofab, University of Alberta.Zeng, Yong et al. | 2008
- 6488
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Microfluidic Self‐Patterning of Large‐Scale Crystalline Nanoarrays for High‐Throughput Continuous DNA FractionationZeng, Yong / He, Mei / Harrison, D. Jed et al. | 2008
- 6492
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Solution Structures of b Peptides from Raman Optical ActivityKapitan, J. / Zhu, F. / Hecht, L. / Gardiner, J. / Seebach, D. / Barron, L. D. et al. | 2008
- 6492
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Solution Structures of β Peptides from Raman Optical Activity L.H. and L.D.B. thank the EPSRC for a research grant (EP-F029713-1). J.G. was a Postdoctoral Fellow at ETH, 2004-2007, funded by the New Zealand Foundation for Research, Science and Technology (SWSS0401).Kapitán, Josef et al. | 2008
- 6492
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Solution Structures of β Peptides from Raman Optical ActivityKapitán, Josef / Zhu, Fujiang / Hecht, Lutz / Gardiner, James / Seebach, Dieter / Barron, Laurence D. et al. | 2008
- 6495
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Synthesis of QS‐21‐Xylose: Establishment of the Immunopotentiating Activity of Synthetic QS‐21 Adjuvant with a Melanoma VaccineDeng, Kai / Adams, Michelle M. / Damani, Payal / Livingston, Philip O. / Ragupathi, Govind / Gin, David Y. et al. | 2008
- 6495
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Synthesis of QS-21-Xylose: Establishment of the Immunopotentiating Activity of Synthetic QS-21 Adjuvant with a Melanoma Vaccine This research was supported by the NIH (GM58833), William H. Goodwin & Alice Goodwin & The Commonwealth Foundation for Cancer Research, and the Experimental Therapeutics Center of MSKCC.Deng, Kai et al. | 2008
- 6499
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Site‐Specific Incorporation of Methyl‐ and Acetyl‐Lysine Analogues into Recombinant ProteinsGuo, Jiantao / Wang, Jiangyun / Lee, Jong Seok / Schultz, Peter G. et al. | 2008
- 6499
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Site-Specific Incorporation of Methyl- and Acetyl-Lysine Analogues into Recombinant Proteins We thank Bill Webb for help in protein mass spectrometry, and we are grateful to the DOE (ER46051) and the Skaggs Institute for Chemical Biology for support.Guo, Jiantao et al. | 2008
- 6502
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Palladium-Catalyzed Amination of Aryl Mesylates We thank the Research Grants Council of Hong Kong (Project No. CERG: PolyU5008-06P) and University Grants Committee Areas of Excellence Scheme (Project No. AoE-P-10-01) for financial support.So, Chau Ming et al. | 2008
- 6502
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Palladium‐Catalyzed Amination of Aryl MesylatesSo, Chau Ming / Zhou, Zhongyuan / Lau, Chak Po / Kwong, Fuk Yee et al. | 2008
- 6507
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Asymmetric Catalysis: Resin‐Bound Hydroxyprolylthreonine Derivatives in Enamine‐Mediated ReactionsCarpenter, Richard D. / Fettinger, James C. / Lam, Kit S. / Kurth, Mark J. et al. | 2008
- 6507
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Asymmetric Catalysis: Resin-Bound Hydroxyprolylthreonine Derivatives in Enamine-Mediated Reactions This work was supported by the National Science Foundation (NSF; CHE-0614756) and the National Institute for General Medical Sciences (GM076151). NMR spectrometers used in this work were funded in part by the NSF (CHE-0443516 and CHE-9808183). RDC thanks the American Chemical Society's Division of Medicinal Chemistry for Predoctoral Fellowship support (sponsored by Sanofi-Aventis), the Howard Hughes Medical Institute for their Med into Grad Fellowship, and UC Davis for their R. Bryan Miller Graduate Fellowship.Carpenter, Richard D et al. | 2008
- 6511
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Synthesis of 2-Arylbenzoxazoles by Copper-Catalyzed Intramolecular Oxidative C&bond;O Coupling of Benzanilides This work was supported in part by a Grant from The Saijiro Endo Memorial Foundation for Science & Technology and a Grant-in-Aid for Young Scientists (Start-up) (19890179) from Japan Society for the Promotion of Science (JSPS). We thank Dr. K. L. Kirk (NIDDK, NIH) for helpful suggestions.Ueda, Satoshi et al. | 2008
- 6511
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Synthesis of 2‐Arylbenzoxazoles by Copper‐Catalyzed Intramolecular Oxidative CO Coupling of BenzanilidesUeda, Satoshi / Nagasawa, Hideko et al. | 2008
- 6514
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Aryl Halide Tolerated Electrophilic Amination of Arylboronic Acids with N‐Chloroamides Catalyzed by CuCl at Room TemperatureHe, Chuan / Chen, Chong / Cheng, Jin / Liu, Chao / Liu, Wei / Li, Qiang / Lei, Aiwen et al. | 2008
- 6514
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Aryl Halide Tolerated Electrophilic Amination of Arylboronic Acids with N-Chloroamides Catalyzed by CuCl at Room Temperature This work was supported by the National Natural Science Foundation of China (20772093, 20502020), the Excellent Youth Foundation of Hubei Scientific Committee, and the startup fund from Wuhan University.He, Chuan et al. | 2008
- 6518
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Poly(Biradicals): Oligomers of 1,3‐Diphosphacyclobutane‐2,4‐diyl UnitsIto, Shigekazu / Miura, Joji / Morita, Noboru / Yoshifuji, Masaaki / Arduengo, Anthony J. III et al. | 2008
- 6518
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Poly(Biradicals): Oligomers of 1,3-Diphosphacyclobutane-2,4-diyl Units This work was supported in part by Grants-in-Aid for Scientific Research (Nos. 13304049 and 140440120) from the Ministry of Education, Culture, Sports, Science and Technology (Japan), the Program Research, Center for Interdisciplinary Research, Tohoku University, and the Support for Young Researchers, Graduate School of Science, Tohoku University The authors thank Dr. Chizuko Kabuto, Tohoku University, for obtaining the X-ray data.Ito, Shigekazu et al. | 2008
- 6522
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Homodinuclear Ruthenium Catalysts for Dimer Ring‐Closing MetathesisTzur, Eyal / Ben‐Asuly, Amos / Diesendruck, Charles E. / Goldberg, Israel / Lemcoff, N. Gabriel et al. | 2008
- 6522
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Homodinuclear Ruthenium Catalysts for Dimer Ring-Closing Metathesis This research was supported by a Young Scientist Grant from the German-Israeli Foundation for Scientific Research and Development (GIF).Tzur, Eyal et al. | 2008
- 6526
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Phosphorus‐Containing Ligands for Iron(III)‐Catalyzed Atom Transfer Radical PolymerizationXue, Zhigang / Linh, Nguyen Thuy Ba / Noh, Seok Kyun / Lyoo, Won Seok et al. | 2008
- 6526
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Phosphorus-Containing Ligands for Iron(III)-Catalyzed Atom Transfer Radical Polymerization We are grateful for the support of the Korean Ministry of Commerce, Industry, and Energy (Grant No.RTI04-01-04, Regional Technology Innovation Program).Xue, Zhigang et al. | 2008
- 6530
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Hybrid αγ Polypeptides: Structural Characterization of a C12-C10 Helix with Alternating Hydrogen-Bond Polarity We thank Dr. K. Nagarajan, Hikal R&D Centre, Bangalore, for gifts of 1-(aminomethyl)cyclohexaneacetic acid (Gpn) and for his continued interest. P.G.V. and S.C. thank the Council of Scientific and Industrial Research (CSIR), India, for the award of Senior Research Fellowships. Research grant support was from the CSIR, India, and from the Department of Biotechnology, India. The CCD facility is funded under the IRHPA program of the Department of Science and Technology, India.Vasudev, Prema G et al. | 2008
- 6530
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Hybrid αγ Polypeptides: Structural Characterization of a C12/C10 Helix with Alternating Hydrogen‐Bond PolarityVasudev, Prema G. / Chatterjee, Sunanda / Ananda, Kuppanna / Shamala, Narayanaswamy / Balaram, Padmanabhan et al. | 2008
- 6530
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Hybrid ag Polypeptides: Structural Characterization of a C12/C10 Helix with Alternating Hydrogen-Bond PolarityVasudev, P. G. / Chatterjee, S. / Ananda, K. / Shamala, N. / Balaram, P. et al. | 2008
- 6533
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Spin-Crossover Nanocrystals with Magnetic, Optical, and Structural Bistability Near Room Temperature Financial support from the Spanish Ministerio de Educación y Ciencia (MEC) (CTQ 2007-64727-FEDER), the Generalitat Valenciana (ACOMP07-110), and the European Network of excellence MAGMANET (contract: NMP3-CT-2005-515767-2) is acknowledged. A.B.G. thanks the Spanish MEC for a research contract (Programa Ramón y Cajal).Boldog, Ishtvan et al. | 2008
- 6533
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Spin‐Crossover Nanocrystals with Magnetic, Optical, and Structural Bistability Near Room TemperatureBoldog, Ishtvan / Gaspar, Ana B. / Martínez, Víctor / Pardo‐Ibañez, Pablo / Ksenofontov, Vadim / Bhattacharjee, Ashis / Gütlich, Philipp / Real, José A. et al. | 2008
- 6538
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Extreme Rate Acceleration by Axial Thiolate Coordination on the Isomerization of Endoperoxide Catalyzed by Iron PorphyrinYamane, Takehiro / Makino, Kohei / Umezawa, Naoki / Kato, Nobuki / Higuchi, Tsunehiko et al. | 2008
- 6538
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Extreme Rate Acceleration by Axial Thiolate Coordination on the Isomerization of Endoperoxide Catalyzed by Iron Porphyrin This work was supported in part by Grants-in-Aid for Scientific Research (Nos. 18390039 and 19028054) from the Ministry of Education, Science, Sports, and Culture (Japan). We are grateful to Dr. Hidehiko Nakagawa for his help with ESR measurements.Yamane, Takehiro et al. | 2008
- 6541
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A Core–Corona Hierarchical Manganese Oxide and its Formation by an Aqueous Soft Chemistry MechanismPortehault, David / Cassaignon, Sophie / Nassif, Nadine / Baudrin, Emmanuel / Jolivet, Jean‐Pierre et al. | 2008
- 6541
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A Core-Corona Hierarchical Manganese Oxide and its Formation by an Aqueous Soft Chemistry Mechanism The authors acknowledge Sophia Khan for experimental support, Dr. Patricia Beaunier (University of Paris 6) for TEM measurements, Annie Richard and Dominique Jalabert (University of Orléans) for FESEM and HRTEM measurements, and Anny Anglo (University of Paris 6) for performing the ultrathin sections.Portehault, David et al. | 2008
- 6545
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Complete Deracemization by Attrition‐Enhanced Ostwald Ripening ElucidatedNoorduin, Wim L. / Meekes, Hugo / van Enckevort, Willem J. P. / Millemaggi, Alessia / Leeman, Michel / Kaptein, Bernard / Kellogg, Richard M. / Vlieg, Elias et al. | 2008
- 6545
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Complete Deracemization by Attrition-Enhanced Ostwald Ripening Elucidated We acknowledge Prof. D. G. Blackmond for the stimulating discussions. The SNN agency (Cooperation Northern Netherlands) and the European Fund for Regional Development (EFRO) are acknowledged for financial support.Noorduin, Wim L et al. | 2008
- 6548
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A Chiral Lewis Acid Strategy for Enantioselective Allylic CH OxidationCovell, Dustin J. / White, M. Christina et al. | 2008
- 6548
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A Chiral Lewis Acid Strategy for Enantioselective Allylic C&bond;H Oxidation Financial support was provided by NIH-NIGMS (grant no. GM076153) and kind gifts were received from Eli Lilly, Bristol-Myers Squibb, Pfizer, Amgen, and Merck Research Laboratories. D.J.C. is a recipient of a Roger Adams and a C.S. Marvel graduate fellowship. We thank the Aldrich Chemical Company for a generous gift of commercial bis(sulfoxide)-Pd(OAc)2 catalyst 1. We thank A. Young for checking the experimental procedure outlined in Table 2, entry 4. We thank Dr. N. Prabagaran for preliminary experiments.Covell, Dustin J et al. | 2008
- 6552
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Synthesis of Indolines and Tetrahydroisoquinolines from Arylethylamines by PdII‐Catalyzed CH Activation ReactionsLi, Jiao‐Jie / Mei, Tian‐Sheng / Yu, Jin‐Quan et al. | 2008
- 6552
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Synthesis of Indolines and Tetrahydroisoquinolines from Arylethylamines by PdII-Catalyzed C&bond;H Activation Reactions We wish to thank The Scripps Research Institute, Brandeis University, and the U.S. National Science Foundation (NSF CHE-0615716) for financial support and the A. P. Sloan Foundation for a fellowship (J.-Q.Y.).Li, Jiao-Jie et al. | 2008
- 6556
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Surface‐Enhanced Raman Spectroscopy for Trace Arsenic Detection in Contaminated WaterMulvihill, Martin / Tao, Andrea / Benjauthrit, Kanokraj / Arnold, John / Yang, Peidong et al. | 2008
- 6556
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Surface-Enhanced Raman Spectroscopy for Trace Arsenic Detection in Contaminated Water The authors would like to thank David Okawa and Prof. Alex Zettl for granting use of their multiple wavelength Renishaw MicroRaman instrument. We would like to thank Allan Smith for helpful discussions and Craig Steinmaus for providing the well-water samples and AFS data. Additionally, we would like to acknowledge the NIEHS Superfund Basic Research Program and the U.S. Department of Energy under Contract No. DE-AC02-05CH11231 for funding.Mulvihill, Martin et al. | 2008
- 6561
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Selenirenium‐ und TellurireniumionenPoleschner, Helmut / Seppelt, Konrad et al. | 2008
- 6561
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Selenirenium- und Tellurireniumionen Wir danken der Deutschen Forschungsgemeinschaft und dem Fonds der Chemischen Industrie für die Förderung dieser Arbeit.Poleschner, Helmut et al. | 2008
- 6565
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Ein kationisches cyclisches Phosphor(III)-azid Wir danken der Deutschen Forschungsgemeinschaft (SCHU 1170-4-1) für finanzielle Unterstützung. Des Weiteren danken wir LANXESS Deutschland GmbH (Leverkusen) für großzügige Chemikalienspenden.Michalik, Dirk et al. | 2008
- 6565
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Ein kationisches cyclisches Phosphor(III)‐azidMichalik, Dirk / Schulz, Axel / Villinger, Alexander / Weding, Nico et al. | 2008
- 6569
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Bismetallocene – Lanthanoid‐Übergangsmetall‐Bindungen durch AlkaneliminierungButovskii, M. V. / Tok, O. L. / Wagner, F. R. / Kempe, Rhett et al. | 2008
- 6569
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Bismetallocene - Lanthanoid-Ubergangsmetall-Bindungen durch AlkaneliminierungButovskii, M. V. / Tok, O. L. / Wagner, F. R. / Kempe, R. et al. | 2008
- 6569
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Bismetallocene - Lanthanoid-Übergangsmetall-Bindungen durch Alkaneliminierung Wir danken der Deutschen Forschungsgemeinschaft (SPP 1166 "Lanthanoid-spezifische Funktionalitäten in Molekül und Material") für finanzielle Unterstützung und Jacinta Bakker für das Wiederholen der Synthese von [(thf)Cp2Lu-RuCp(CO)2].Butovskii, M. V et al. | 2008
- 6573
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Totalsynthese von Chondramid C und Bindung an F‐AktinWaldmann, Herbert / Hu, Tai‐Shan / Renner, Steffen / Menninger, Sascha / Tannert, René / Oda, Toshiro / Arndt, Hans‐Dieter et al. | 2008
- 6573
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Totalsynthese von Chondramid C und Bindung an F-Aktin Diese Arbeit wurde von der Max-Planck-Gesellschaft (H.W.), der Deutschen Forschungsgemeinschaft (Emmy-Noether-Stipendium an H.D.A.), dem Land Nordrhein-Westfalen und der Europäischen Union (ZACG Dortmund) gefördert. T.S.H. dankt der Alexander-von-Humboldt-Stiftung für ein Forschungsstipendium. Wir danken Prof. Dr. M. Kalesse für Diskussionen und die Bereitstellung einer Probe von natürlichem Chondramid C.Waldmann, Herbert et al. | 2008
- 6578
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Chondramid C: Synthese, Strukturaufklarung und Struktur-Aktivitats-BeziehungenEggert, U. / Diestel, R. / Sasse, F. / Jansen, R. / Kunze, B. / Kalesse, M. et al. | 2008
- 6578
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Chondramid C: Synthese, Strukturaufklärung und Struktur‐Aktivitäts‐BeziehungenEggert, Ulrike / Diestel, Randi / Sasse, Florenz / Jansen, Rolf / Kunze, Brigitte / Kalesse, Markus et al. | 2008
- 6578
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Chondramid C: Synthese, Strukturaufklärung und Struktur-Aktivitäts-Beziehungen Diese Arbeit wurde von der DFG (Ka 913-11-1) unterstützt. Wir danken Bettina Hinkelmann und Birte Engelhardt für technische Unterstützung bei den Zelltests.Eggert, Ulrike et al. | 2008
- 6583
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Synthese und biologische Aktivitat von Largazol und DerivatenSeiser, T. / Kamena, F. / Cramer, N. et al. | 2008
- 6583
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Synthese und biologische Aktivität von Largazol und Derivaten N.C. wird vom Fonds der Chemischen Industrie durch ein Liebig-Stipendium gefördert. Wir danken Prof. Dr. Peter H. Seeberger für die großzügige finanzielle Unterstützung und Prof. Dr. Dieter Seebach für hilfreiche Diskussionen.Seiser, Tobias et al. | 2008
- 6583
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Synthese und biologische Aktivität von Largazol und DerivatenSeiser, Tobias / Kamena, Faustin / Cramer, Nicolai et al. | 2008
- 6586
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Echtzeitnachweis von Änderungen im Protein‐Wassernetzwerk während der Proteinfaltung mit Terahertz‐AbsorptionsspektroskopieKim, Seung Joong / Born, Benjamin / Havenith, Martina / Gruebele, Martin et al. | 2008
- 6586
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Echtzeitnachweis von Änderungen im Protein-Wassernetzwerk während der Proteinfaltung mit Terahertz-Absorptionsspektroskopie Wir danken J. D. McDonald für die Leihgabe eines Photovervielfachers und M. Krüger für die Programmierung der Software zur Erfassung der THz-Daten. Diese Arbeit wurde durch das Human Frontier Science Program (M.H. und M.G.) und die National Science Foundation (MCB-0613643) (M.G.) unterstützt. B.B. dankt dem DAAD und der Research School der Ruhr-Universität Bochum für finanzielle Unterstützung.Kim, Seung Joong et al. | 2008
- 6586
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Echtzeitnachweis von Anderungen im Protein-Wassernetzwerk wahrend der Proteinfaltung mit Terahertz-AbsorptionsspektroskopieKim, S. J. / Born, B. / Havenith, M. / Gruebele, M. et al. | 2008
- 6593
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Vorschau: Angew. Chem. 35/2008| 2008