Works matching IS 00448249 AND DT 2006 AND VI 118 AND IP 4
Results: 37
Vorschau: Angew. Chem. 4/2006.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 689, doi. 10.1002/ange.200690015
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Ruthenium-Catalyzed Asymmetric Propargylic Substitution Reactions of Propargylic Alcohols with Acetone.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 547, doi. 10.1002/ange.200690014
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Graphisches Inhaltsverzeichnis: Angew. Chem. 4/2006.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 538, doi. 10.1002/ange.200690013
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Titelbild: Evidence from NMR and EXAFS Studies of a Dynamically Uniform Mononuclear Single-Site Zeolite-Supported Rhodium Catalyst (Angew. Chem. 4/2006).
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 535, doi. 10.1002/ange.200690012
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Elegant Solutions. Ten Beautiful Experiments in Chemistry. Von Philip Ball.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 555, doi. 10.1002/ange.200585368
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Quaternary Stereocenters. Challenges and Solutions for Organic Synthesis. Herausgegeben von Jens Christoffers und Angelika Baro.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 554, doi. 10.1002/ange.200585353
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Nicht nur Antibiotika!“9th International Conference on the Chemistry of Antibiotics and other Bioactive Compounds” vom 25. bis 29. September in Arcachon.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 550, doi. 10.1002/ange.200504256
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Experimental and Theoretical Characterization of Superoxide Complexes [W2O6(O2−)] and [W3O9(O2−)]: Models for the Interaction of O2 with Reduced W Sites on Tungsten Oxide SurfacesThis work was supported by the Chemical Sciences, Geosciences, and Biosciences Division, Office of Basic Energy Sciences, US Department of Energy (DOE) under grant No. DE-FG02-03ER15481 (catalysis center program) and was performed at the W. R. Wiley Environmental Molecular Sciences Laboratory (EMSL), a national scientific user facility sponsored by the DOE Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory, operated for the DOE by Battelle. Calculations were performed at the EMSL Molecular Science Computing Facility.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 673, doi. 10.1002/ange.200503652
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Separation of Hydrocarbons with a Microporous Metal–Organic FrameworkAcknowledgement is made to the donors of The Petroleum Research Fund, administrated by the ACS, for support of this research. The authors are grateful to the National Science Foundation for partial support through Grant No. DMR-0422932.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 632, doi. 10.1002/ange.200503503
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Synthese von 2,4,6-Trimethylphenylcalciumiodid und Zersetzung in THF-LösungWir danken der Deutschen Forschungsgemeinschaft für finanzielle Unterstützung.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 624, doi. 10.1002/ange.200503452
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Carbon Nanotubes as Intracellular Transporters for Proteins and DNA: An Investigation of the Uptake Mechanism and PathwayThis work was supported by a Stanford Interdisciplinary Translational Research Grant.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 591, doi. 10.1002/ange.200503389
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Formation of Cyclic Sulfinates and Sulfinamides through Homolytic Substitution at the Sulfur AtomWe thank Rhodia for financial support (PhD grant to J.C., postdoctoral grant to V.C.), and Dr. J.-P. Corbet and Dr. G. Mignani (Rhodia) for helpful discussions.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 649, doi. 10.1002/ange.200503369
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Epitope Mapping of the Protective Antigen of B. Anthracis by Using Nanoclusters Presenting Conformational Peptide EpitopesThis research was funded in part by a Vanderbilt Institute of Chemical Biology fellowship (A.E. Gerdon), the Chemical Biology Interface training grant (AE Gerdon, T32 GM065086), and the Vanderbilt Institute of Nanoscale Science and Engineering (A.E. Gerdon). DWW acknowledges support from the SouthEast Regional Center of Excellence for Biodefense (NIH U54 AI57157-03).
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 608, doi. 10.1002/ange.200503328
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A Copper(II)-Catalyzed Aza-Friedel–Crafts Reaction of N-(2-Pyridyl)sulfonyl Aldimines: Synthesis of Unsymmetrical Diaryl Amines and Triaryl MethanesThis work was supported by the Ministerio de Educación y Ciencia (MEC, project BQU2003-0508) and the Consejería de Educación de la Comunidad Autónoma de Madrid (Project GR/MAT/0016/2004). J.E. and R.G.A. thank the MEC for a predoctoral fellowship and for a Ramón y Cajal contract, respectively.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 645, doi. 10.1002/ange.200503305
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Label-Free, Real-Time Glycosyltransferase Assay Based on a Fluorescent Artificial ChemosensorJ.W. is grateful to the Inoue Foundation for Science.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 681
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A Synthetic Small Molecule That Induces Neuronal Differentiation of Adult Hippocampal Neural Progenitor CellsThis work was supported by the Novartis Research Foundation and the Skaggs Institute for Chemical Biology (P.G.S.), and partially by the Postdoctoral Fellowship Program of the Korea Science and Engineering Foundation (K.H.M). This is manuscript 17710-CH of the Scripps Research Institute.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 605, doi. 10.1002/ange.200503089
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Toward the Isolation of Functional Organic NanotubesWe thank the NSF for financial support.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 584, doi. 10.1002/ange.200503035
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Computational Design of a Human Butyrylcholinesterase Mutant for Accelerating Cocaine Hydrolysis Based on the Transition-State SimulationThis work was supported by a research grant from the National Institutes of Health/National Institute of Drug Abuse (grant no.: R01 DA013930 to C.-G.Z.). The authors also acknowledge the Center for Computational Sciences (CCS) at University of Kentucky for supercomputing time on Superdome (a shared-memory supercomputer with 256 processors).
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 669, doi. 10.1002/ange.200503025
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Total Synthesis of (−)- and ent-(+)-Vindorosine: Tandem Intramolecular Diels–Alder/1,3-Dipolar Cycloaddition of 1,3,4-OxadiazolesWe gratefully acknowledge the financial support of the National Institutes of Health (CA42056) and the Skaggs Institute for Chemical Biology.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 636, doi. 10.1002/ange.200503024
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Synthesis and Conformational Study of Water-Soluble, Rigid, Rodlike OligopiperidinesThis work was supported by the NIH (Grant GM30367). V.S. acknowledges La Ligue contre le Cancer for a postdoctoral fellowship. Initial design of this project was carried out by Dr. Val Martichonok.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 602, doi. 10.1002/ange.200502991
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Ordered Nanostructures from the Self-Assembly of Reactive Coil–Rod–Coil MoleculesThis work was supported by the Creative Research Initiative Program of the Ministry of Science and Technology, Korea, and Pohang Accelerator Laboratory, Korea (for using synchrotron radiation). J.B. thanks the Seoul Science Fellowship Program
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 666, doi. 10.1002/ange.200502911
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Mechanistic Studies on the Conversion of Arylamines into Arylnitro Compounds by Aminopyrrolnitrin Oxygenase: Identification of Intermediates and Kinetic StudiesThis research was supported by a grant from the Office of Naval Research (N00014–02-1-0725). We thank Ee Lui Ang for his help in homology modeling. J.L. was partially supported by the Korea Research Foundation Grant funded by the Korean Government (Basic Research Promotion Fund, M01-2004-000-10159-0).
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 638, doi. 10.1002/ange.200502903
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Hydrophob orientierte organische Synthesen.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 562, doi. 10.1002/ange.200502882
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Evidence from NMR and EXAFS Studies of a Dynamically Uniform Mononuclear Single-Site Zeolite-Supported Rhodium CatalystThis work was supported by the Department of Energy (DE-FG02-04ER15598, DE-FG02-04ER15600). We are grateful to the USC Center for High Performance Computing for granting computer time.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 588, doi. 10.1002/ange.200502864
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A Highly Active, Heterogeneous Catalyst for Alkyne MetathesisThis work is supported by the National Science Foundation (Grant No. 0345254) and the US Department of Energy, Division of Materials Sciences (Award No. DEFG02-91ER45439), through the Frederick Seitz Materials Research Laboratory at the University of Illinois at Urbana. We thank Wei Zhang for fruitful discussions and Dr. Paul Molitor for his help recording the 13C-MAS NMR spectra. We would also like to thank Richard Haasch for help with the X-ray photoelectron spectroscopy (XPS) measurements, which were performed in the Center for Microanalysis and Materials, University of Illinois, which is partially supported by the US Department of Energy Award No. DEFG02-91ER45439.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 599, doi. 10.1002/ange.200502840
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Biocatalytic Synthesis of Poly(L-Lactide) by Native and Recombinant Forms of the Silicatein EnzymesWe thank Dr T. Mates for his expert assistance with the collection and analysis of XPS data. This work was supported in part by grants from the U.S. Dept. of Energy (DE-FG03-02ER46006), the Institute for Collaborative Biotechnologies through grant DAAD19-03-D-0004 from the U.S. Army Research Office, NASA (University Research, Engineering and Technology Institute on Bio Inspired Materials (BIMat) under award No. NCC-1-02037 and NAG1-01-003), the NOAA National Sea Grant College Program, U.S. Department of Commerce (NA36RG0537, Project R/MP-92) through the California Sea Grant College System, and the MRSEC Program of the National Science Foundation under award No. DMR00-80034 to the UCSB Materials Research Laboratory. The U.S. Government is authorized to reproduce and distribute copies for governmental purposes.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 629, doi. 10.1002/ange.200502738
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Fluoromorphic Substrates for Fatty Acid Metabolism: Highly Sensitive Probes for Mammalian Medium-Chain Acyl-CoA DehydrogenaseThe authors thank Professor Horst Schulz, Wenfeng Yu, and Lina Nie (City University of New York) for assistance with rat homogenates and supplying the rMCAD enzyme; Professor Jung-Ja Kim (Medical College of Wisconsin) for supplying the pSCAD, pMCAD, and hLCAD enzymes; and Dominic Yee for intellectual contributions. This work was generously supported by The G. Harold & Leila Y. Mathers Charitable Foundation. M.K.F. is the recipient of a NSF Predoctoral Fellowship.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 653, doi. 10.1002/ange.200502675
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Ungewöhnliche freie Elektronenpaare in Tellur und ihre Bedeutung für die SupraleitfähigkeitDie Autoren danken Dr. O. Gunnarsson für hilfreiche Diskussionen.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 613, doi. 10.1002/ange.200502673
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Nonmechanical Protein Can Have Significant Mechanical StabilityThis work was supported by the Natural Sciences and Engineering Research Council of Canada, Canada Research Chair program, and the start-up fund from the University of British Columbia. Y.C. is partially supported by the Laird Fellowship.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 658, doi. 10.1002/ange.200502623
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The Importance of Inter- and Intramolecular van der Waals Interactions in Organic Reactions: the Dimerization of Anthracene RevisitedThis work was supported by the Deutsche Forschungsgemeinschaft in the framework of the SFB 424 (“Molekulare Orientierung als Funktionskriterium in chemischen Systemen”). The authors thank C. Mück-Lichtenfeld for technical assistance.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 641, doi. 10.1002/ange.200502440
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Enantioselektive α-Fluorierung von Carbonylverbindungen: Organo- oder Metallkatalyse?
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 558, doi. 10.1002/ange.200502425
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Serinoctamere: Clusterbildung, Reaktionen und Auswirkungen auf die Homochiralität von BiomolekülenDie beiden Enantiomere der Aminosäure Serin bilden den Ausgangspunkt für eine Reihe chemischer Vorgänge, die –...
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 568, doi. 10.1002/ange.200501328
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Reversible cis-trans-Isomerisierung eines einzelnen Azobenzol-MolekülsWir bedanken uns für finanzielle Unterstützung seitens der VolkswagenStiftung im Rahmen des Schwerpunkts “Physik, Chemie und Biologie mit...
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 617, doi. 10.1002/ange.200502229
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Derivatives of Octaethynylphenazine and HexaethynylquinoxalineWe thank the Petroleum Research Funds for support and Prof. Christoph Fahrni (School of Chemistry and Biochemistry, Georgia Institute of Technology) for the analysis of the binding constants of 4, 7, and 8 with metal ions.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 677, doi. 10.1002/ange.200502067
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Synthese funktionalisierter Benzylmagnesiumreagentien unter Verwendung einer S/Mg-AustauschreaktionWir danken dem Fonds der Chemischen Industrie, der Deutschen Forschungsgemeinschaft und den Merck Forschungslaboratorien für finanzielle...
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 621, doi. 10.1002/ange.200501882
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In Situ Deposition and Patterning of Single-Walled Carbon Nanotubes by Laminar Flow and Controlled Flocculation in Microfluidic ChannelsThe authors thank the Center for Nanoscale Chemical Electrical Mechanical Manufacturing Systems at the University of Illinois (funded by the National Science Foundation under grant DMI-0328162) and the Center for Microanalysis of Materials at the University of Illinois (partially supported by the U.S. Department of Energy under grant DEFG02-91-ER45439). M.S.S. acknowledges funding from the U.S. National Science Foundation Career award CTS-0449147.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 595, doi. 10.1002/ange.200501799
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Heteroditopic Rebek's Imide Directs the Reactivity of Homoditopic Olefins within Desolvated Quaternary Assemblies in the Solid StateWe are grateful to the National Science Foundation (CAREER Award, L.R.M., DMR-0133138) for funding. Acknowledgement is also made to the Research Corporation (Research Innovation Award) for financial support.
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- Angewandte Chemie, 2006, v. 118, n. 4, p. 662, doi. 10.1002/ange.200502294
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