Works matching IS 00448249 AND DT 2004 AND VI 116 AND IP 33

Results: 31
    1
    2
    3

    Stereoselective Total Synthesis of the Ionophore Antibiotic ZincophorinFinancial support from the Ministry of Education, Culture, Sports, Science, and Technology, Japan (a Grant-in-Aid for Scientific Research (A) (No. 12304042) and a Grant-in-Aid for Scientific Research on Priority Areas (A): “Exploitation of Multi-Element Cyclic Molecules” (No. 13029003)) is gratefully acknowledged.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4441, doi. 10.1002/ange.200460434
    By:
    • Kei Komatsu;
    • Keiji Tanino;
    • Masaaki Miyashita
    Publication type:
    Article
    4
    5
    6
    7

    Rh-Catalyzed Amination of Ethereal Cα—H Bonds: A Versatile Strategy for the Synthesis of Complex AminesWe thank the National Institutes of Health (NINDS, R01 NS045684), Abbott Laboratories, Amgen, Boehringer Ingelheim, Bristol-Myers Squibb, Eli Lilly, GlaxoSmithKline, Merck, Pfizer, and Roche for support of our program. K.W.F. is the recipient of a National Science Foundation Predoctoral Fellowship. J.J.F. is grateful to Amgen for a Graduate Fellowship Award.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4449, doi. 10.1002/ange.200460791
    By:
    • Kristin Williams Fiori;
    • James J. Fleming;
    • Justin Du Bois
    Publication type:
    Article
    8
    9
    10

    A Lotus-Leaf-like Superhydrophobic Surface: A Porous Microsphere/Nanofiber Composite Film Prepared by ElectrohydrodynamicsThe authors thank the State Key Project for Fundamental Research (G1999064504) and the Special Research Foundation of the National Nature Science Foundation of China (29992530) for continuing financial support. The Chinese Academy of Sciences is gratefully acknowledged.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4438, doi. 10.1002/ange.200460333
    By:
    • Lei Jiang;
    • Yong Zhao;
    • Jin Zhai
    Publication type:
    Article
    11

    Fully Stereocontrolled Total Syntheses of (−)-Cylindricine C and (−)-2-Epicylindricine C: A Departure in Sulfonamide ChemistryWe thank the MENRT (doctoral fellowship to S.C.), the CNRS, and the Région Rhône-Alpes for support of our research. We are grateful to Ms. Laurence Rousset for the mass spectral data, to Professor Monique Perrin for the X-ray crystallographic studies, and to Prof. Adrian J. Blackman for 1H NMR spectra. M.A.C. is the recipient of a Merck & Co. Academic Development Award.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4436, doi. 10.1002/ange.200460178
    By:
    • Sylvain Canesi;
    • Denis Bouchu;
    • Marco A. Ciufolini
    Publication type:
    Article
    12
    13

    Probing the Mechanism of the Baylis–Hillman Reaction by Electrospray Ionization Mass and Tandem Mass SpectrometryWe thank the São Paulo State Research Foundation (FAPESP) and the Brazilian National Research Council (CNPq) for financial support. F.C. and M.N.E. thank CNPq, and C.H.P. and L.S.S. thank FAPESP for research fellowships.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4430, doi. 10.1002/ange.200460059
    By:
    • Leonardo Silva Santos;
    • Cesar Henrique Pavam;
    • Wanda P. Almeida;
    • Fernando Coelho;
    • Marcos N. Eberlin
    Publication type:
    Article
    14

    Stereocontrolled Total Synthesis of (+)-Streptazolin by a Palladium-Catalyzed Reductive Diyne CyclizationWe thank Professor D. L. Comins for kindly providing us with the spectroscopic data for 1, and the National Institutes of Health (GM 033 049) and the National Science Foundation for their generous financial support. C.K.C. is a Stanford Graduate Fellow. Mass spectra were measured by the Mass Spectrometry Facility, University of San Francisco, supported by the NIH Division of Research Resources.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4427, doi. 10.1002/ange.200460058
    By:
    • Barry M. Trost;
    • Cheol K. Chung;
    • Anthony B. Pinkerton
    Publication type:
    Article
    15
    16

    Structural Revision and Total Synthesis of Azaspiracid-1, Part 2: Definition of the ABCD Domain and Total SynthesisWe thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. Financial support for this work was provided by grants from the National Institutes of Health (USA) and the Skaggs Institute for Chemical Biology, and fellowships from the Ernst Schering AG Foundation (to S.V.), the National Science Foundation (to M.O.F.), and the Japanese Society for the Advancement of Science (to Y.M.A.Y.).

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4418, doi. 10.1002/ange.200460696
    By:
    • K. C. Nicolaou;
    • Theocharis V. Koftis;
    • Stepan Vyskocil;
    • Goran Petrovic;
    • Taotao Ling;
    • Yoichi M. A. Yamada;
    • Wenjun Tang;
    • Michael O. Frederick
    Publication type:
    Article
    17

    Structural Revision and Total Synthesis of Azaspiracid-1, Part 1: Intelligence Gathering and Tentative ProposalWe thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. Financial support for this work was provided by grants from the National Institutes of Health (USA) and the Skaggs Institute for Chemical Biology, and fellowships from the Ernst Schering AG Foundation (to S.V.), the Japanese Society for the Advancement of Science (to Y.M.A.Y.), the National Science Foundation (to M.O.F.), and Eli Lilly (to Y.L.).

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4412, doi. 10.1002/ange.200460695
    By:
    • K. C. Nicolaou;
    • Stepan Vyskocil;
    • Theocharis V. Koftis;
    • Yoichi M. A. Yamada;
    • Taotao Ling;
    • David Y.-K. Chen;
    • Wenjun Tang;
    • Goran Petrovic;
    • Michael O. Frederick;
    • Yiwei Li;
    • Masayuki Satake
    Publication type:
    Article
    18

    Binding Mode Determination of Benzimidazole Inhibitors of the Hepatitis C Virus RNA Polymerase by a Structure and Dynamics StrategyWe are grateful to Dr. Michael Bös, Dr. Michael Cordingley, and Dr. Paul Anderson for encouragement and support. We also thank Dr. Timothy Stammers, Dr. Nathalie Goudreau, Dr. Marc-André Poupart, Dr. Dale Cameron, and Mr. Jeff O'Meara for comments or critical reading of the manuscript, as well as Ginette McKercher for determining inhibition constants.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4406, doi. 10.1002/ange.200460326
    By:
    • Steven R. LaPlante;
    • Araz Jakalian;
    • Norman Aubry;
    • Yves Bousquet;
    • Jean-Marie Ferland;
    • James Gillard;
    • Sylvain Lefebvre;
    • Martin Poirier;
    • Youla S. Tsantrizos;
    • George Kukolj;
    • Pierre L. Beaulieu
    Publication type:
    Article
    19

    Nanoengineering of a Magnetically Separable Hydrogenation CatalystA.-H. Lu, acknowledges the Alexander von Humboldt Foundation for a scholarship. The authors would like to thank the Leibniz-Program and the FCI for support in addition to the basic funding provided by the Institute.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4403, doi. 10.1002/ange.200454222
    By:
    • An-Hui Lu;
    • Wolfgang Schmidt;
    • Nina Matoussevitch;
    • Helmut Bönnemann;
    • Bernd Spliethoff;
    • Bernd Tesche;
    • Eckhard Bill;
    • Wolfgang Kiefer;
    • Ferdi Schüth
    Publication type:
    Article
    20
    21

    Strain-Induced Formation of Subsurface Species in Transition MetalsJ.G. acknowledges partial financial support from an NSF predoctoral fellowship. This work was supported through an NSF-CAREER Award (CTS-0134561) and a DOE-BES Catalysis Science Grant (DE-FG02-03ER15469). We thank DOE-NERSC and NSF-NPACI for supercomputing time. Fruitful discussions on the atomic-scale aspects of defects on metal surfaces with Professor Joost Wintterlin are gratefully acknowledged.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4396, doi. 10.1002/ange.200454062
    By:
    • Jeff Greeley;
    • William P. Krekelberg;
    • Manos Mavrikakis
    Publication type:
    Article
    22

    Host–Guest Compounds in the Family of Tellurium–Nickel OxohalogenidesWe thank Mr. Marian Mikus at Sandvik Coromant AB for the microsond analyses and Dr. Javier Garcia-Garcia at Stockholm University for the TEM study. This work has been carried out in part through financial support from the Swedish Research Council and the European Union (HPHN-CT-2002-00193).

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 33, p. 4392, doi. 10.1002/ange.200460001
    By:
    • Mats Johnsson;
    • Sven Lidin;
    • Karl W. Törnroos;
    • Hans-Beat Bürgi;
    • Patrice Millet
    Publication type:
    Article
    23
    24
    25
    26
    27
    28
    29
    30
    31