Works matching IS 14337851 AND DT 2005 AND VI 44 AND IP 39

Results: 37
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    Regiospecific Side-Chain Functionalization of Linear Low-Density Polyethylene with Polar GroupsWe thank the National Science Foundation (CHE-0301907) and Frontier Scientific Co. for a gift of B2pin2. C.B. thanks the UNLV Office of Research and Graduate Studies for support through the New Investigator Award, and Professor Byron L. Bennett for use of laboratory instrumentation.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6410, doi. 10.1002/anie.200501837
    By:
    • Chulsung Bae;
    • John F. Hartwig;
    • Hoyong Chung;
    • Nicole K. Harris;
    • Karen A. Switek;
    • Marc A. Hillmyer
    Publication type:
    Article
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    N-Methylhydroxylamido(1−)- and Nitrosomethaneruthenium Complexes Derived from Nitrosyl Complexes: Reversible N-Protonation of an N-Coordinated NitrosoalkaneThis work was supported by a Grant-in-Aid for Scientific Research on Priority Areas (no. 14078209, “Reaction Control of Dynamic Complexes”) from the Ministry of Education, Culture, Sports, Science, and Technology, Japan.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6406, doi. 10.1002/anie.200501916
    By:
    • Satoshi Kura;
    • Shigeki Kuwata;
    • Takao Ikariya
    Publication type:
    Article
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    SiGe2 and Ge3: Cyclic Digermenes that Undergo Unexpected Ring-Expansion ReactionsThis work was supported by Grants-in-Aid for Scientific Research (Nos. 14078204, 16205008, 17655014) from the Ministry of Education, Culture, Sports, Science, and Technology, and the COE (Center of Excellence) program.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6378, doi. 10.1002/anie.200501885
    By:
    • Vladimir Ya. Lee;
    • Hiroyuki Yasuda;
    • Masaaki Ichinohe;
    • Akira Sekiguchi
    Publication type:
    Article
    9

    Total Synthesis of Antigen Bacillus Anthracis Tetrasaccharide—Creation of an Anthrax Vaccine CandidateThis research was supported by the ETH Zürich, by a Feodor Lynen Research Fellowship of the Alexander von Humboldt Foundation, and by an Emmy Noether Fellowship of the Deutsche Forschungsgemeinschaft (to D.B.W.). We thank Prof. Dr. B. Jaun and B. Brandenberg for NMR measurements.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6315, doi. 10.1002/anie.200502615
    By:
    • Daniel B. Werz;
    • Peter H. Seeberger
    Publication type:
    Article
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    Effect of C-Terminal Amidation on Folding and Disulfide-Pairing of α-Conotoxin ImIThis work is supported by the Biomedical Research Council, Agency for Science, Technology, and Research, Singapore. T.S.K. acknowledges the Singapore Millennium Foundation for granting the research scholarship. The authors thank the Sophisticated Instrument Facility at the Indian Institute of Science and the Chemical and Molecular Analysis Center, Department of Chemistry at the National University of Singapore for allowing the use of their NMR spectrometers.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6333, doi. 10.1002/anie.200502300
    By:
    • Tse Siang Kang;
    • Subramanian Vivekanandan;
    • Seetharama D. S. Jois;
    • R. Manjunatha Kini
    Publication type:
    Article
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    A Helical Molecule That Exhibits Two Lengths in Response to an Applied PotentialThis work is partly supported by a Grant-in-Aid for Scientific Research B (15350068) from the Ministry of Education, Culture, Sports, Science, and Technology, Japan. K.K. acknowledges the Research Fellowships of the Japan Society for the Promotion of Science for Young Scientists.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6330, doi. 10.1002/anie.200502240
    By:
    • Kazuya Kitagawa;
    • Tomoyuki Morita;
    • Shunsaku Kimura
    Publication type:
    Article
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    One-Pot Reaction Cascades Using Star Polymers with Core-Confined CatalystsThis work was funded through the National Science Foundation (NSF-DMR0317514) and the Department of Energy (DE-AC03-76SF00098). Dr. Jeffrey Pyun contributed to early exploratory work on this project.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6384, doi. 10.1002/anie.200502095
    By:
    • Brett Helms;
    • Steven J. Guillaudeu;
    • Yu Xie;
    • Meredith McMurdo;
    • Craig J. Hawker;
    • Jean M. J. Fréchet
    Publication type:
    Article
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    Ion-Coordinating Sensitizer in Solid-State Hybrid Solar CellsThis work was funded by the MOLYCELL European project. We thank Jacques E. Moser for the introduction and use of the transient photovoltage equipment and Michel Schaer and Libero Zuppiroli from the Laboratory of Optoelectronics of Molecular Materials at the EPFL for discussions, assistance with, and use of a low-temperature testing rig.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6413, doi. 10.1002/anie.200502009
    By:
    • Henry J. Snaith;
    • Shaik M. Zakeeruddin;
    • Lukas Schmidt-Mende;
    • Cédric Klein;
    • Michael Grätzel
    Publication type:
    Article
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    Highly Enantioselective sec-Alkyl Sulfatase Activity of the Marine Planctomycete Rhodopirellula baltica Shows Retention of ConfigurationThis study was performed within the Research Centre for Applied Biocatalysis. Financial support by the FFG, the City of Graz, and the Province of Styria is gratefully acknowledged. L. Arbanas, T. Glieder, W. Kroutil, and U. Wagner (Graz) are thanked for their valuable contributions in sequence analysis.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6381, doi. 10.1002/anie.200501955
    By:
    • Sabine R. Wallner;
    • Marga Bauer;
    • Chris Würdemann;
    • Patricia Wecker;
    • Frank O. Glöckner;
    • Kurt Faber
    Publication type:
    Article
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    Urea- and Thiourea-Substituted Cinchona Alkaloid Derivatives as Highly Efficient Bifunctional Organocatalysts for the Asymmetric Addition of Malonate to Nitroalkenes: Inversion of Configuration at C9 Dramatically Improves Catalyst Performance.Financial support from the Irish Research Council for Science Engineering and Technology is gratefully acknowledged. We would like to thank TopChem Laboratories Ltd. and the Gunnlaugsson group (TCD) for the use of their equipment.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6367, doi. 10.1002/anie.200501721
    By:
    • Séamus H. McCooey;
    • Stephen J. Connon
    Publication type:
    Article
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    A De Novo Designed Inhibitor of D-Ala–D-Ala Ligase from E. coli.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6403, doi. 10.1002/anie.200501662
    By:
    • Gilbert E. Besong;
    • Julieanne M. Bostock;
    • Will Stubbings;
    • Ian Chopra;
    • David I. Roper;
    • Adrian J. Lloyd;
    • Colin W. G. Fishwick;
    • A. Peter Johnson
    Publication type:
    Article
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    Heterogenization of Shibasaki's Binol/La Catalyst for Enantioselective Epoxidation of α,β-Unsaturated Ketones with Multitopic Binol Ligands: The Impact of Bridging SpacersFinancial support from the National Natural Science Foundation of China, the Chinese Academy of Sciences, the Major Basic Research Development Program of China (Grant no. G2000077506), and the Ministry of Science and Technology of Shanghai Municipality is gratefully acknowledged. Binol=2,2′-dihydroxy-1,1′-binaphthyl.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6362, doi. 10.1002/anie.200501676
    By:
    • Xingwang Wang;
    • Lei Shi;
    • Mingxing Li;
    • Kuiling Ding
    Publication type:
    Article
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    The Internuclear Potential, Electronic Structure, and Chemical Bond of Tellurium SelenideWe would like to thank the Deutscher Akademischer Austauschdienst (PPP D/0246239) as well as the Spanish ministry of education (Acciones Integradas HA-2002-0014) for funding a bilateral exchange program. M.S. thanks the Fonds der Chemischen Industrie (FCI) for support. J.-U.G. thanks the Deutsche Forschungsgemeinschaft (DFG) and th eLand Niedersachsen, A.L. and J.L.A. thank the Spanish Ministry of Science and Technology (BQU2003-03275). We are indepted to R. LeRoy, Waterloo, and S. Cooke, Vancouver, for fruitful discussions.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6311, doi. 10.1002/anie.200501658
    By:
    • Deike Banser;
    • Melanie Schnell;
    • Jens-Uwe Grabow;
    • Emilio J. Cocinero;
    • Alberto Lesarri;
    • José L. Alonso
    Publication type:
    Article
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    Targeted Delivery of Amphotericin B to Cells by Using Functionalized Carbon NanotubesThis work was financially supported by the CNRS, the University of Trieste, and the MIUR (PRIN 2004, prot. 2004035502). W.W. and G.P. are grateful to the French Ministry for Research and New Technologies for a post doctoral fellowship. The authors wish to thank Sylvie Fournel for critical reading of this manuscript.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6358, doi. 10.1002/anie.200501613
    By:
    • Wei Wu;
    • Sébastien Wieckowski;
    • Giorgia Pastorin;
    • Monica Benincasa;
    • Cédric Klumpp;
    • Jean-Paul Briand;
    • Renato Gennaro;
    • Maurizio Prato;
    • Alberto Bianco
    Publication type:
    Article
    24

    Facile Disulfide Bond Cleavage in Gaseous Peptide and Protein Cations by Ultraviolet Photodissociation at 157 nmThis work was supported by the Swedish Research Council and KAW Foundation (to R.Z.) as well as by the CUHK Postgraduate Student Grants for Overseas Academic Activities (grant no. 0680026 to Y.M.E.F.).

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6399, doi. 10.1002/anie.200501533
    By:
    • Y. M. Eva Fung;
    • Frank Kjeldsen;
    • Oleg A. Silivra;
    • T. W. Dominic Chan;
    • Roman A. Zubarev
    Publication type:
    Article
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    Pushing the Synthetic Limit: Polyphenylene Dendrimers with “Exploded” Branching Units—22-nm-Diameter, Monodisperse, Stiff MacromoleculesThe research was supported by the Deutsche Forschungsgemeinschaft (DFG) in the frame of the Sonderforschungsbereich (SFB) 625. C.G.C. is greatful for financial support from a US National Science Foundation MPS Distinguished International Postdoctoral Research Fellowship (MPS-DRF; Award: DMR-0207086). We would like to thank M. Wagner for NMR results and A. Rouhanipour and H.-J. Räder for mass spectrometric results and helpful discussions.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6348
    By:
    • Ekaterina V. Andreitchenko;
    • Christopher G. Clark;
    • Roland E. Bauer;
    • Günter Lieser;
    • Klaus Müllen
    Publication type:
    Article
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    Interfacing Capillary Electrophoresis and Electrothermal Atomic Absorption Spectroscopy To Study Metal Speciation and Metal–Biomolecule InteractionsThis work was supported by the National Basic Research Program of China (No. 2003CB415001), the National Natural Science Foundation of China (No. 20475028, 20437020), and the National Key Technologies R&D Program (2002A906A28-2).

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6387, doi. 10.1002/anie.200501245
    By:
    • Yan Li;
    • Xiu-Ping Yan;
    • Yan Jiang
    Publication type:
    Article
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    Differential Receptors Create Patterns That Distinguish Various ProteinsWe gratefully acknowledge support for this work from the U.S. NIH (EB00549-5). We thank Dr. Lara Mahal for her advice and insight. Thanks also to Dr. Klaus Linse and Michelle Gadush for their assistance in sequencing beads.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6375, doi. 10.1002/anie.200501137
    By:
    • Aaron T. Wright;
    • Michael J. Griffin;
    • Zhenlin Zhong;
    • Shawn C. McCleskey;
    • Eric V. Anslyn;
    • John T. McDevitt
    Publication type:
    Article
    31

    Catalytic Enantioselective 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylides and Alkenes: The Direct Strategy To Prepare Enantioenriched Highly Substituted Proline DerivativesWe thank the Spanish Ministerio de Ciencia y Tecnología (BQU2001-0724-C02 and CTQ 2004-00808/BQU), the Generalitat Valenciana (CTIOIB/2002/320 and GRUPOS 03/134), and the University of Alicante for financial support.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6272, doi. 10.1002/anie.200501074
    By:
    • Carmen Nájera;
    • José M. Sansano
    Publication type:
    Article
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