Works matching IS 14337851 AND DT 2005 AND VI 44 AND IP 45
Results: 38
Thermodynamic Stability and Ultrasmall-Size Effect of NanodiamondsWe gratefully acknowledge support by the National Science Foundation of China (NSFC) under Grants No.50072022 & 10474140 and the National Natural Science Foundation of China (the Distinguished Creative Group Project).
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7414, doi. 10.1002/anie.200501495
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Synthesis of [all]-S,S-Dioxide Oligothiophenes Using HOF⋅CH3CNThis work was supported by the Israel Science Foundation (Jerusalem, Israel).
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7374, doi. 10.1002/anie.200501681
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Scaffolds for Microtubule Inhibition through Extensive Modification of the Epothilone TemplateThis research was supported by Novartis Pharma AG (postdoctoral fellowships to F.C. and T.I.). We also thank Dr. Peter Ertl, Novartis Institute for Biomedical Research, Basel, for calculating the Tanimoto coefficients.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7469, doi. 10.1002/anie.200501760
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Highly Enantioselective Thiourea-Catalyzed Nitro-Mannich Reactions.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7327, doi. 10.1002/anie.200590151
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Preview: Angew. Chem. Int. Ed. 45/2005.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7483, doi. 10.1002/anie.200590152
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Cover Picture: Molecular Wires from Contorted Aromatic Compounds (Angew. Chem. Int. Ed. 45/2005).
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7315, doi. 10.1002/anie.200590149
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The Elements of Murder. A History of Poison. Von John Emsley.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7332, doi. 10.1002/anie.200585343
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Graphical Abstract: Angew. Chem. Int. Ed. 45/2005.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7318, doi. 10.1002/anie.200590150
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A Powerful Brønsted Acid Catalyst for the Organocatalytic Asymmetric Transfer Hydrogenation of IminesGenerous support by the DFG (Priority Program 1179, Organocatalysis) is gratefully acknowledged. We thank Jayasree Seayad and Sonja Mayer for catalyst preparations.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7424, doi. 10.1002/anie.200503062
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Combinatorial Chemistry: P. Seeberger Recognized / Medicinal Chemistry: R. Metternich on Board / Pharmaceutical Chemistry: G. Wess Directs GSF.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7330, doi. 10.1002/anie.200503723
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Preparation of a Magnetically Switchable Bio-electrocatalytic System Employing Cross-linked Enzyme Aggregates in Magnetic Mesocellular Carbon FoamT.H. thanks the Korean Ministry of Science and Technology for financial support through the National Creative Research Initiative Program. H.K. thanks the Nano Measurement Technology Project of the Ministry of Science and Technology and the BK21 Program of the Ministry of Education for financial support. J.K. thanks the US Department of Energy (DOE) LDRD for funds administered by the Pacific Northwest National Laboratory, the DOE Office of Biological and Environmental Research under the Environmental Management Science Program, and the Microsystems Technology Office of the US.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7427, doi. 10.1002/anie.200502995
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Cationic Yttrium Methyl Complexes as Functional Models for Polymerization Catalysts of 1,3-DienesThis work was supported by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie. We thank Prof. Dr. U. Englert for recording the crystallographic data.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7473, doi. 10.1002/anie.200502915
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Crown Ether Ligation: An Approach to Low-Oxidation-State Indium CompoundsFunding of this work by the Natural Sciences and Engineering Research Council (Canada), the Canada Foundation for Innovation, the Ontario Innovation Trust, and the Ontario Research and Development Challenge Fund (University of Windsor Centre for Catalysis and Materials Research) is gratefully acknowledged.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7453, doi. 10.1002/anie.200502901
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Small-Molecule Diversification from Iterated Branching Reaction Pathways Enabled by DNA-Templated SynthesisThis work was supported by the NIH/NIGMS (R01GM065865), the Office of Naval Research (No. N00014-03-1-0749), and an ACS Division of Organic Chemistry Graduate Research Fellowship to C.T.C. We thank Thomas M. Snyder for assistance with codon design.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7383
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Efficient Mono- and Bifunctionalization of Polyolefin Dendrimers by Olefin MetathesisWe are grateful to the Institut Universitaire de France (IUF; D.A.), Fundaçao para a Ciência e a Tecnologia (FCT), Portugal (PhD grant to C.O.), MRT (PhD grant to D.M.), CNRS, University Bordeaux I, and University Paris VI for financial support.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7399, doi. 10.1002/anie.200502848
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Ordered Multistep Synthesis in a Single Solution Directed by DNA TemplatesFunding was generously provided by the NIH/NIGMS (R01 M065865), the Office of Naval Research (N00014-03-1-0749), and an NSF Graduate Research Fellowship to T.M.S.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7379, doi. 10.1002/anie.200502879
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Difluoroallenyl Bromide as a Wide-Ranging Difluoromethylene Cation Equivalent: SN2 Substitution of Difluoropropargyl Bromide through Sequential SE2′ and SN2′ ReactionsSupport of our work by the National Science Foundation (CHE-0513483) is gratefully acknowledged. The authors are also grateful to Professor Richard W. Fitch (Indiana State University) for his helpful advice on nitrogen nucleophiles and to the University of Kentucky for the use of its supercomputing facilities.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7404, doi. 10.1002/anie.200502807
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Smooth Anodic TiO2 NanotubesWe thank A. Friedrich and H. Hildebrand for SEM investigations and Hans Rollig and Martin Kolacyak for valuable technical help with the experiments.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7463, doi. 10.1002/anie.200502781
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Pd-Catalyzed Stereoselective Oxidation of Methyl Groups by Inexpensive Oxidants under Mild Conditions: A Dual Role for Carboxylic Anhydrides in Catalytic C—H Bond OxidationWe wish to thank Brandeis University for financial support and the Camille and Henry Dreyfus Foundation for a New Faculty Award.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7420, doi. 10.1002/anie.200502767
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Rational Design and Synthesis of Highly Potent β-Glucocerebrosidase Inhibitors.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7450, doi. 10.1002/anie.200502662
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Synthesis of Borirenes by Photochemical Borylene Transfer from [(OC)5M=BN(SiMe3)2] (M=Cr, Mo) to AlkynesThis work was supported by the Deutsche Forschungsgemeinschaft. D.R. thanks the Alexander von Humboldt Foundation for a postdoctoral fellowship.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7461, doi. 10.1002/anie.200502524
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Allenophane and Allenoacetylenic Macrocycles: A New Class of Chiral Cyclophanes.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7334, doi. 10.1002/anie.200502474
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Harder than Diamond: Determining the Cross-Sectional Area and Young's Modulus of Molecular Rods.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7432, doi. 10.1002/anie.200502448
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Aluminum–Magnesium Complexes with Linearly Bridging Carbon DioxideThis work was supported by the National Science Council of Taiwan (NSC 93-2113M-110-005 to C.C.C.). We are greatly indebted to Analytische Laboratorien Prof. Dr. H. Malissa und G. Reuter GmbH (Germany) for elemental analysis, and to Prof. Dr. Michael Y. Chiang at the National Sun Yat-Sen University for constructive discussions.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7418, doi. 10.1002/anie.200502400
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Controlling Molecular Assembly in Two Dimensions: The Concentration Dependence of Thermally Induced 2D Aggregation of Molecules on a Metal SurfaceFinancial Support from the Swiss National Science Foundation and the National Center of Competence in Research (NCCR) “Nanoscale Science” as well as from the Fonds der Chemischen Industrie (Germany) is gratefully acknowledged. M.S. acknowledges support from the German Academy of Natural Scientists Leopoldina under the grant number BMBF-LPD 9901/8-86.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7394, doi. 10.1002/anie.200502316
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Anion-Induced Synthesis and Combinatorial Selection of Polypyrrolic MacrocyclesFinancial support from the U.S. Department of Energy Office of Science (grant no. DE-FG02-04ER63741 to J.L.S.), the National Science Foundation (CHE-0515670 to J.L.S.), and the Russian Foundation for Basic Research (grant nos. 05-03-32684 and 05-03-08017 to Y.A.U.) is acknowledged. This project is part of an ongoing collaboration involving the groups of Dr. Bruce Moyer at the Oak Ridge National Laboratory and Prof. Kristin Bowman-James at the University of Kansas.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7386, doi. 10.1002/anie.200502393
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Cationic Terminal Borylene Complexes: A Synthetic and Mechanistic Investigation of M=B Metathesis ChemistryWe thank the EPSRC for funding and access to the National Mass Spectrometry facility and Prof. C. Jones (Cardiff) for help in modeling crystallographic disorder.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7457, doi. 10.1002/anie.200502343
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“Hexacarboxytrindanes”: Benzene Rings with Homotopic Faces as Scaffolds for the Construction of D3 Chiral ArchitecturesThis work was cofounded by MURST within the national project “Stereoselezione in Sintesi Organica: Metodologie e Applicazioni”.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7435, doi. 10.1002/anie.200502262
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Complexation-Initiated Intramolecular [4+2] Cycloaddition: Construction of Bridged-Type CycloadductsThis research was partly supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan. We are grateful to the Tosoh Finechem Corporation for a generous gift of MeAlCl2.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7447, doi. 10.1002/anie.200502313
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Nanoparticle Assemblies with Molecular Springs: A Nanoscale ThermometerThis work was supported in part by an NSF-CAREER award (N.A.K.), NSF-Biophotonics (N.A.K.), AFOSR (N.A.K.), the University of Michigan (N.A.K.), and Ohio University (A.O.G.).
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7439, doi. 10.1002/anie.200501264
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Rate Enhancement by Ethylene in the Ru-Catalyzed Ring-Closing Metathesis of Enynes: Evidence for an “Ene-then-Yne” Pathway that Diverts through a Second Catalytic CycleWe thank C. Henry, M. D. Weller, and Dr. N. S. Hodnett for expert technical assistance in the early phases of this work and DSM Research, Life Sciences-Advanced Synthesis, Catalysis & Development for generous funding.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7442, doi. 10.1002/anie.200502243
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Molecular Wires from Contorted Aromatic CompoundsWe acknowledge primary financial support from the Nanoscale Science and Engineering Initiative of the National Science Foundation (NSF Award Number CHE-0117752); the New York State Office of Science, Technology, and Academic Research (NYSTAR); and the Department of Energy, Nanoscience Initiative (NSET 04ER46118). C.N. thanks the US National Science Foundation (CAREER award DMR-02-37860), the American Chemical Society (PRF type G 39263-G7), the Camille Dreyfus Teacher Scholar Program (2004), and the Alfred P. Sloan Fellowship Program (2004). We thank the MRSEC Program of the National Science Foundation (Award Number DMR-0213574) and the New York State Office of Science, Technology, and Academic Research (NYSTAR) for financial support for M.L.S. and the shared instrument facility. S.S. acknowledges financial support from the Centre Microélectronique de Provence—Georges Charpak.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7390, doi. 10.1002/anie.200502142
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Hexaarylbenzenes—Prospects for Toroidal Delocalization of Charge and Energy.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7337, doi. 10.1002/anie.200502105
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One-Pot Tandem 1,4–1,2-Addition of Phosphites to α,β-Unsaturated Imines for the Synthesis of Glutamic Acid AnaloguesWe thank the Fund for Scientific Research Flanders and Ghent University for financial support of this research.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7407, doi. 10.1002/anie.200501830
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Kinetic Resolution of Oxazinones: An Organocatalytic Approach to Enantiomerically Pure β-Amino AcidsThis work was supported by the Fonds der Chemischen Industrie, particularly through a doctoral fellowship to F.C. The authors thank Degussa AG, Hanau, for generous gifts of amino acids.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7466, doi. 10.1002/anie.200502003
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Protein Posttranslational Modifications: The Chemistry of Proteome Diversifications.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7342, doi. 10.1002/anie.200501023
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Large-Scale Nonhydrolytic Sol–Gel Synthesis of Uniform-Sized Ceria Nanocrystals with Spherical, Wire, and Tadpole ShapesThis work was supported by the National Creative Research Initiative Program of the Korean Ministry of Science and Technology.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7411, doi. 10.1002/anie.200500992
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Practical Interpretation of P-31 NMR Spectra and Computer Assisted Structure Verification. Von Louis D. Quin und Antony J. Williams.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 45, p. 7331, doi. 10.1002/anie.200485333
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