Works matching IS 14337851 AND DT 2006 AND VI 45 AND IP 17

Results: 39
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    Control of Amyloid β-Peptide Protofibril Formation by a Designed Template AssemblyWe thank Dr. Serge Perez for access to an electron microscope and Isabelle Paintrand for performing the study. This work was supported by grants from AFM-INSERM GIS “maladies rares amyloses héréditaires” (no. AE02013 KSA), IUF, and ACI.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2699, doi. 10.1002/anie.200600395
    By:
    • Gunnar T. Dolphin;
    • Pascal Dumy;
    • Julian Garcia
    Publication type:
    Article
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    Flattened Cone 2,8,14,20-Tetrakis(L-valinamido)[4]resorcinarene: An Enantioselective Allosteric Receptor in the Gas PhaseThis work was supported by the Ministero dell'Istruzione dell'Università e della Ricerca (MIUR, COFIN), the Consiglio Nazionale delle Ricerche (CNR), and the Istituto Pasteur Fondazione Cenci Bolognetti. B.B. and A.T. gratefully acknowledge Project “FIRB 2003” from MIUR (Ministero della Università e della Ricerca). We are grateful to F. Angelelli for technical assistance.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2717, doi. 10.1002/anie.200503987
    By:
    • Bruno Botta;
    • Fabiana Caporuscio;
    • Deborah Subissati;
    • Andrea Tafi;
    • Maurizio Botta;
    • Antonello Filippi;
    • Maurizio Speranza
    Publication type:
    Article
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    A Genetically Encoded Photocaged TyrosineA.D. gratefully acknowledges a postdoctoral fellowship from the Deutsche Forschungsgemeinschaft. This work was supported by funding from the National Institutes of Health (GM62159) and the Department of Energy (ER46051). This is manuscript 17952-CH of The Scripps Research Institute.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2728, doi. 10.1002/anie.200600264
    By:
    • Alexander Deiters;
    • Dan Groff;
    • Youngha Ryu;
    • Jianming Xie;
    • Peter G. Schultz
    Publication type:
    Article
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    Total Synthesis of (+)-β-ErythroidineThis work was partly supported by a Grant-in-Aid for Scientific Research on Priority Areas (16073213) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT). We thank Prof. Takanori Suzuki (Graduate School of Science, Hokkaido University) for the X-ray analysis of 16.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2731, doi. 10.1002/anie.200600210
    By:
    • Hironori Fukumoto;
    • Keisuke Takahashi;
    • Jun Ishihara;
    • Susumi Hatakeyama
    Publication type:
    Article
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    Cleavage of the N2 Triple Bond by the Ti Dimer: A Route to Molecular Materials for Dinitrogen Activation?H.-J.H. gratefully acknowledges financial support by the Deutsche Forschungsgemeinschaft (DFG) and the German Academic Exchange Service (DAAD PROCOPE grant). W.K. acknowledges support by the DFG through the Center for Functional Nanostructures (CFN, Project No. C3.3). L.M. acknowledges support by the Centre National de la Recherche Scientifique (PICS3032) and Ministère des Affaires Etrangères (PROCOPE09643SG).

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2799, doi. 10.1002/anie.200503709
    By:
    • Hans-Jörg Himmel;
    • Olaf Hübner;
    • Wim Klopper;
    • Laurent Manceron
    Publication type:
    Article
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    Highly Enantioselective Conjugate Reduction of β,β-Disubstituted α,β-Unsaturated NitrilesThis work was supported by a Korea Research Foundation grant funded by the Korean Government (R08-2004-000-10429-0). The LC and GC equipment was supported by the Faculty Research Fund 2005, Sungkyunkwan University. Prof. C. Song and E. Kwon at SKKU are acknowledged for valuable advice and assistance with the chiral analysis.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2785, doi. 10.1002/anie.200600184
    By:
    • Daehyung Lee;
    • Daesung Kim;
    • Jaesook Yun
    Publication type:
    Article
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    Highly Active, Productive, and Syndiospecific Yttrium Initiators for the Polymerization of Racemic β-ButyrolactoneThis research was financially supported in part by the Region Bretagne (grant-in-aid COPOBIO to A.A.). We thank A. Bondon (University of Rennes 1) for NMR experiments.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2782, doi. 10.1002/anie.200600058
    By:
    • Abderramane Amgoune;
    • Christophe M. Thomas;
    • Simona Ilinca;
    • Thierry Roisnel;
    • Jean-François Carpentier
    Publication type:
    Article
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    Oxidative De-aromatization of para-Alkyl Phenols into para-Peroxyquinols and para-Quinols Mediated by Oxone as a Source of Singlet OxygenWe thank the Ministerio de Ciencia y Tecnología (Grants BQU2002-03371 and CTQ2005-02095/BQU) and the Comunidad Autónoma de Madrid (Grant GR/MAT/0152/2004) for financial support. M.G.-L. thanks the Comunidad Autónoma de Madrid for a fellowship.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2737
    By:
    • M. Carmen Carreño;
    • Marcos González-López;
    • Antonio Urbano
    Publication type:
    Article
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    Oxidative De-aromatization of para-Alkyl Phenols into para-Peroxyquinols and para-Quinols Mediated by Oxone as a Source of Singlet OxygenWe thank the Ministerio de Ciencia y Tecnología (Grants BQU2002-03371 and CTQ2005-02095/BQU) and the Comunidad Autónoma de Madrid (Grant GR/MAT/0152/2004) for financial support. M.G.-L. thanks the Comunidad Autónoma de Madrid for a fellowship.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2737
    By:
    • M. Carmen Carreño;
    • Marcos González-López;
    • Antonio Urbano
    Publication type:
    Article
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    An Organic Photoelectrode Working in the Water Phase: Visible-Light-Induced Dioxygen Evolution by a Perylene Derivative/Cobalt Phthalocyanine BilayerThis work was partially supported by Grant-in-Aid for Scientific Research (No. 15750110 (T.A.)) and for Scientific Research in Priority Areas (Fundamental Science and Technology of Photofunctional Interfaces, No. 417 (T.A., K.N., and M.K.)) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2778, doi. 10.1002/anie.200504454
    By:
    • Toshiyuki Abe;
    • Keiji Nagai;
    • Satoko Kabutomori;
    • Masao Kaneko;
    • Akio Tajiri;
    • Takayoshi Norimatsu
    Publication type:
    Article
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    A Hexanuclear Iron(III) Carboxylate with an [Fe6(μ3-O)3(μ2-OH)]11+ Core as an Efficient Catalyst for Cycloalkane OxidationThis work was supported by DSM Fine Chemicals Austria and the University of Vienna. Mr. B. Mienert (Max-Planck-Institute for Bioinorganic Chemistry, Mülheim an der Ruhr (Germany)) is kindly acknowledged for carrying out the Mössbauer spectra measurements. We also thank Prof. Ya. D. Lampeka, Dr. S. Shova and Mr. N. A. Sheddan for valuable discussions.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2794, doi. 10.1002/anie.200504406
    By:
    • Günter Trettenhahn;
    • Michael Nagl;
    • Norbert Neuwirth;
    • Vladimir B. Arion;
    • Walther Jary;
    • Peter Pöchlauer;
    • Walther Schmid
    Publication type:
    Article
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    A Ligand-Library Approach to the Highly Efficient Rhodium/Phosphoramidite-Catalyzed Asymmetric Arylation of N,N-Dimethylsulfamoyl-Protected AldiminesFinancial support from DSM, the Ministry of Economic Affairs, and the Dutch Science Foundation NWO/CW, administered through the CW/Combichem program, is gratefully acknowledged. We thank E. P. Schudde and T. D. Tiemersma-Wegman for technical support.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2789, doi. 10.1002/anie.200504309
    By:
    • Richard B. C. Jagt;
    • Patrick Y. Toullec;
    • Danny Geerdink;
    • Johannes G. de Vries;
    • Ben L. Feringa;
    • Adriaan J. Minnaard
    Publication type:
    Article
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    Cyclic Dimethylsiloxanes as Pseudo Crown Ethers: Syntheses and Characterization of Li(Me2SiO)5[Al{OC(CF3)3}4], Li(Me2SiO)6[Al{OC(CF3)3}4], and Li(Me2SiO)6[Al{OC(CF3)2Ph}4]Acknowledgement is made to NSERC (Canada) for financial support of this research, Mikko Rautiainen for help with calculations, and Dr. Carsten Knapp for his helpful suggestions.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2773, doi. 10.1002/anie.200504262
    By:
    • Andreas Decken;
    • Jack Passmore;
    • Xinping Wang
    Publication type:
    Article
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    Reactivity-Based One-Pot Synthesis of the Tumor-Associated Antigen N3 Minor Octasaccharide for the Development of a Photocleavable DIOS-MS Sugar ArrayJ.-C.L. and C.-Y.W. contributed equally. This work was supported by the NIH. C.-Y.W. thanks the National Science Council of Taiwan and the Genomics Research Center, Academia Sinica for financial support. DIOS-MS=desorption/ionization on silicon mass spectrometry.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2753, doi. 10.1002/anie.200504067
    By:
    • Jinq-Chyi Lee;
    • Chung-Yi Wu;
    • Junefredo V. Apon;
    • Gary Siuzdak;
    • Chi-Huey Wong
    Publication type:
    Article
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    Construction of a Ball-and-Spike Protein SupramoleculeWe are grateful to T. Douglas for a gift of the LisDps clone. A part of this work was supported by the Nanotechnology Support Project of the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan, at the Research Center for Ultrahigh Voltage Electron Microscopy, Osaka University.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2725, doi. 10.1002/anie.200504018
    By:
    • Kenji Sugimoto;
    • Shuji Kanamaru;
    • Kenji Iwasaki;
    • Fumio Arisaka;
    • Ichiro Yamashita
    Publication type:
    Article
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    Structural and Spectroscopic Characterization of Active Sites in a Family of Light-Emitting Sodium Lanthanide TetrafluoridesWe thank Prof. R. B. Neder for help with the DISCUS software and D. Biner for assistance in the syntheses. This work was financially supported by the Swiss National Science Foundation.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2802, doi. 10.1002/anie.200503966
    By:
    • Annina Aebischer;
    • Marc Hostettler;
    • Jürg Hauser;
    • Karl Krämer;
    • Thomas Weber;
    • Hans Ulrich Güdel;
    • Hans-Beat Bürgi
    Publication type:
    Article
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    Rhenium- and Aniline-Catalyzed One-Pot Annulation of Aromatic Ketones and α,β-Unsaturated Esters Initiated by C—H Bond ActivationFinancial support by a Grant-in-Aid for Scientific Research on Priority Areas (No. 14 078 219, “Reaction Control of Dynamic Complexes”) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2766, doi. 10.1002/anie.200503627
    By:
    • Yoichiro Kuninobu;
    • Yuta Nishina;
    • Makoto Shouho;
    • Kazuhiko Takai
    Publication type:
    Article
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    Catalysis in Capillaries by Pd Thin Films Using Microwave-Assisted Continuous-Flow Organic Synthesis (MACOS)This work was funded by the Ontario Research and Development Challenge Fund (ORDCF), Canada Foundation for Innovation (CFI), the Ontario Innovation Trust (OIT), NSERC, and York University. The authors are grateful to Biotage Inc. for the donation of a Smith Creator Synthesizer to develop this new methodology. We acknowledge Ross Davidson at Surface Science Western, University of Western Ontario, London, ON, for the SEM and EDX measurements.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2761, doi. 10.1002/anie.200503600
    By:
    • Gjergji Shore;
    • Sylvie Morin;
    • Michael G. Organ
    Publication type:
    Article
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    Substrate Specificity of the Macrolide-Glycosylating Enzyme Pair DesVII/DesVIII: Opportunities, Limitations, and Mechanistic HypothesesThis work was supported in part by the National Institutes of Health (grants GM 35 906 and GM 54 346 (H.-w.L.) and AI 52 218, CA 84 374 and GM 70 637) and an NCDDG grant (U19 CA 113 297) from the National Cancer Institute (J.S.T.).

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    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2748, doi. 10.1002/anie.200503195
    By:
    • Svetlana A. Borisova;
    • Changsheng Zhang;
    • Haruko Takahashi;
    • Hua Zhang;
    • Alexander W. Wong;
    • Jon S. Thorson;
    • Hung-wen Liu
    Publication type:
    Article
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    DNA Recognition with Large Calixarene DimersWe are indebted to the Carell group (Munich) for a sample of fluorescein-labeled triadenosine, as well as to the Marahiel group (Marburg) for 45-bp DNA samples. Valuable advice came from Dr. Mohamad Mofid. We also thank the Pingoud group (Giessen) for the measurements of CD spectra. Funding by the Deutsche Forschungsgemeinschaft is gratefully acknowledged.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 17, p. 2703, doi. 10.1002/anie.200502946
    By:
    • Reza Zadmard;
    • Thomas Schrader
    Publication type:
    Article
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