Works matching IS 14337851 AND DT 2005 AND VI 44 AND IP 40

Results: 39
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    The Aromaticity of the Stannole DianionThis work was partially supported by Grants-in-Aid for Young Scientists (B) No. 17750032 (M.S.) and the Nanotechnology Support Project from the Ministry of Education, Culture, Sports, Science, and Technology of Japan. M.S. acknowledges a research grant from Toray Science Foundation. R.H. thanks 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. 40, p. 6553, doi. 10.1002/anie.200501632
    By:
    • Masaichi Saito;
    • Ryuta Haga;
    • Michikazu Yoshioka;
    • Kazuya Ishimura;
    • Shigeru Nagase
    Publication type:
    Article
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    Straightforward Access to a Structurally Diverse Set of Oxacyclic Scaffolds through a Four-Component ReactionThis work was supported by DGICYT (Spain, project BQU 2003-00089) and Almirall-Prodesfarma (Barcelona). We also thank Inés Carranco, Prof. F. Albericio, Dr. Miriam Royo, and Marc Vendrell for their assistance with syntheses and analyses.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6521, doi. 10.1002/anie.200501548
    By:
    • Oscar Jiménez;
    • Guillermo de la Rosa;
    • Rodolfo Lavilla
    Publication type:
    Article
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    Finding Adiabatically Bound Anions of Guanine through a Combinatorial Computational ApproachThis work was supported by the U.S. DOE Office of Biological and Environmental Research, Low Dose Radiation Research Program (M.G.), and the Polish State Committee for Scientific Research (KBN, grant 4 T09A 012 24 for M.H.). Computing resources were available through a Computational Grand Challenge Application grant from the Molecular Sciences Computing Facility in the Environmental Molecular Sciences Laboratory, the National Energy Research Scientific Computing Center (NERSC), and the Academic Computer Center in Gdańsk (TASK). PNNL is operated by Battelle for the U.S. DOE under contract DE-AC06-76RLO 1830.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6585
    By:
    • Maciej Harańczyk;
    • Maciej Gutowski
    Publication type:
    Article
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    Essential NMR. By Bernhard Blümich.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6445, doi. 10.1002/anie.200585322
    By:
    • Arne Lützen
    Publication type:
    Article
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    Linking Rings through Diamines and Clusters: Exploring Synthetic Methods for Making Magnetic Quantum GatesThis work was supported by the EPSRC (UK), the EC-RTN “QueMolNa” (contract no. MRTN-CT-2003-504880), and INTAS.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6496, doi. 10.1002/anie.200502505
    By:
    • Marco Affronte;
    • Ian Casson;
    • Marco Evangelisti;
    • Andrea Candini;
    • Stefano Carretta;
    • Christopher A. Muryn;
    • Simon J. Teat;
    • Grigore A. Timco;
    • Wolfgang Wernsdorfer;
    • Richard E. P. Winpenny
    Publication type:
    Article
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    Synthesis, Intermolecular Interaction, and Semiconductive Behavior of a Delocalized Singlet Biradical HydrocarbonThis work was supported by a Grant-in-Aid for Scientific Research on Priority Areas (No. 17550034, and Area No. 769, Proposal No. 15087202) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6564, doi. 10.1002/anie.200502303
    By:
    • Takashi Kubo;
    • Akihiro Shimizu;
    • Maki Sakamoto;
    • Mikio Uruichi;
    • Kyuya Yakushi;
    • Masayoshi Nakano;
    • Daisuke Shiomi;
    • Kazunobu Sato;
    • Takeji Takui;
    • Yasushi Morita;
    • Kazuhiro Nakasuji
    Publication type:
    Article
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    Two-Step Spin Conversion in a Cyanide-Bridged Ferrous SquareThis work was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports, and Culture, Japan, and by the COE and TARA projects at the University of Tsukuba.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6484, doi. 10.1002/anie.200502216
    By:
    • Masayuki Nihei;
    • Mayumi Ui;
    • Mizuho Yokota;
    • Lingqin Han;
    • Atsushi Maeda;
    • Hideo Kishida;
    • Hiroshi Okamoto;
    • Hiroki Oshio
    Publication type:
    Article
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    Fabrication of Random Assemblies of Metal Nanobands: A General MethodThe authors thank the EPSRC for studentships for T.J.D. and M.E.H. We further thank Roger Bowler for his expertise in the preparation of the highly ordered pyrolytic-graphite (HOPG) electrode housing, Robert M. J. Jacobs for his help with the metal deposition, and Andrew J. Wain for his assistance with the sodium sulfite experiments. T.J.D. thanks Lincoln College and the Lord Crewe's Society for a scholarship (2004–2005) and Abi Smith for all her support.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6491, doi. 10.1002/anie.200502128
    By:
    • Michael E. Hyde;
    • Trevor J. Davies;
    • Richard G. Compton
    Publication type:
    Article
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    A Diels–Alder Macrocyclization Enables an Efficient Asymmetric Synthesis of the Antibacterial Natural Product Abyssomicin CThis work was supported by Princeton University, a Bristol-Myers Squibb unrestricted research grant in synthetic organic chemistry (E.J.S.), the National Institute of General Medical Sciences (GM065483), Merck Research Laboratories (E.J.S.), a NRSA fellowship (1 F32 GM070235) from the National Institutes of Health (USA; B.A.H.), and a National Science Foundation (USA) Predoctoral Fellowship (C.D.). We thank Prof. Robert Pascal, Jr. for the conformational analysis of compound 5 and Dr. István Pelczer for assistance with the NMR spectroscopic analysis.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6533, doi. 10.1002/anie.200502119
    By:
    • Christoph W. Zapf;
    • Bryce A. Harrison;
    • Carmen Drahl;
    • Erik J. Sorensen
    Publication type:
    Article
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    Highly Enantioselective Pd-Catalyzed Allylic Alkylations of Acyclic KetonesFinancially supported by the Major Basic Research Development Program (Grant G 200077506), National Nature Science Foundation of China, Chinese Academy of Sciences, Shanghai Committee of Science and Technology, and the Croucher Foundation of Hong Kong.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6544, doi. 10.1002/anie.200502020
    By:
    • Xiao-Xia Yan;
    • Chun-Gen Liang;
    • Yan Zhang;
    • Wei Hong;
    • Bo-Xun Cao;
    • Li-Xin Dai;
    • Xue-Long Hou
    Publication type:
    Article
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    Saccharide–Peptide Hybrid Copolymers as BiomaterialsWe thank the Arnold and Mabel Beckman Foundation and the University of California at Irvine (UCI) for partial financial support. We thank Professor Ken Longmuir and Sherry Haynes for generous help with cell culturing and gene transfection studies, Professor Gregory Weiss and Sara Avrantinis for assistance in DNA electrophoresis study, and Jane Z. Bai and Derek Weisel for the AFM study.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6529, doi. 10.1002/anie.200501944
    By:
    • Mark Metzke;
    • Naphtali O'Connor;
    • Soumen Maiti;
    • Edward Nelson;
    • Zhibin Guan
    Publication type:
    Article
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    Synthetic Macrocyclic Peptidomimetics as Tunable pH Probes for the Fluorescence Imaging of Acidic Organelles in Live CellsThis work was supported by the Spanish Ministerio de Ciencia y Tecnología (Project BQU-2003-0915-C03-02), Fundació Caixa Castelló-Bancaixa and Universitat Jaume I (Project 04I007.25/1 to F.G.), and The Wellcome Trust (Showcase award to D.A.R. and J.G.). F.G. thanks the Spanish MEC for financial support (Ramón y Cajal Program).

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6504, doi. 10.1002/anie.200501920
    By:
    • Francisco Galindo;
    • M. Isabel Burguete;
    • Laura Vigara;
    • Santiago V. Luis;
    • Nurul Kabir;
    • Jelena Gavrilovic;
    • David A. Russell
    Publication type:
    Article
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    Uncatalyzed Mukaiyama–Michael Reaction: Rapid Access to Simple and Complex Enantiopure γ-ButenolidesThis research was partially supported by the Spain and Principado de Asturias Governments (BQU-2001–3853 and GE-EXP01–11). A.P. acknowledges the F.I.C.Y.T (Principado de Asturias) for a fellowship. We are also grateful to Dr. A. L. Suárez-Sobrino (Universidad de Oviedo) for his assistance in the X-ray crystallogaphic analysis and Dr. A. C. Valdés (Universidad de Oviedo) for ab initio calculations.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6583, doi. 10.1002/anie.200501746
    By:
    • José Barluenga;
    • Ana de Prado;
    • Javier Santamaría;
    • Miguel Tomás
    Publication type:
    Article
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    Enhanced Metabolic Stability and Protein-Binding Properties of Artificial α Helices Derived from a Hydrogen-Bond Surrogate: Application to Bcl-xLWe thank Prof. Neville Kallenbach for insightful comments. P.S.A. is grateful for financial support from the NIH (GM073943), the American Chemical Society Petroleum Research Fund, Research Corporation (Cottrell Scholar Award), and the New York State Office of Science, Technology, and Academic Research (James D. Watson investigator). We thank the National Science Foundation for equipment grants for the NMR spectrometer (MRI-0116222) and the capillary LC–ion-trap mass spectrometer (CHE-0234863).

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6525, doi. 10.1002/anie.200501603
    By:
    • Deyun Wang;
    • Wei Liao;
    • Paramjit S. Arora
    Publication type:
    Article
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    The Internal Structure of Helical Pores Self-Assembled from Dendritic Dipeptides is Stereochemically Programmed and Allosterically RegulatedFinancial support by the National Science Foundation (DMR-9996288 and DMR-0102459) and the Office of Naval Research is gratefully acknowledged.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6516, doi. 10.1002/anie.200501331
    By:
    • Virgil Percec;
    • Andrés E. Dulcey;
    • Mihai Peterca;
    • Monica Ilies;
    • Janine Ladislaw;
    • Brad M. Rosen;
    • Ulrica Edlund;
    • Paul A. Heiney
    Publication type:
    Article
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    Rapid Synthesis in Ionic Liquids of Room-Temperature-Conducting Solid Microsilica SpheresWe thank Dr. Yakov Langsam for SEM analyses, Michael Riboch for AFM measurements, and Dr. Boris Markovsky for conductivity measurements.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6560, doi. 10.1002/anie.200501446
    By:
    • David S. Jacob;
    • Augustine Joseph;
    • Somashekarappa P. Mallenahalli;
    • Sangaraju Shanmugam;
    • Shirly Makhluf;
    • Jose Calderon-Moreno;
    • Yuri Koltypin;
    • Aharon Gedanken
    Publication type:
    Article
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    The Hierarchical Architecture of Nacre and Its Mimetic MaterialThis work was supported by a Grant-in-Aid for Scientific Research (No. 15560587) and the 21st Century COE program “KEIO Life Conjugated Chemistry” from the Ministry of Education, Culture, Sports, Science, and Technology, Japan. We thank Mikimoto Pearl Museum for kindly providing nacre samples. Y. O. is grateful for a JSPS research fellowship for young scientists.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6571, doi. 10.1002/anie.200500338
    By:
    • Yuya Oaki;
    • Hiroaki Imai
    Publication type:
    Article
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    Catalytic Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea OrganocatalystWe acknowledge financial support by the “Progetti FIRB”, by the National Project “Stereoselezione in Sintesi Organica Metodologie ed Applicazioni, 2003”, and by the EC-RTN project “Design, Analysis and Computation for Catalytic Organic Reactions”, contract HPRN-CT-2001-00172.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 40, p. 6576, doi. 10.1002/anie.200500227
    By:
    • Raquel P. Herrera;
    • Valentina Sgarzani;
    • Luca Bernardi;
    • Alfredo Ricci
    Publication type:
    Article
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