Works matching IS 00448249 AND DT 2006 AND VI 118 AND IP 22

Results: 37
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    AuI-Catalyzed Tandem [3,3] Rearrangement–Intramolecular Hydroarylation: Mild and Efficient Formation of Substituted IndenesThe National Science Foundation is gratefully acknowledged for financial support of this work. S.D.G. thanks the Education, Research, and Universities Department of the Basque Government (Spain) for a postdoctoral fellowship. We also thank the Department of Chemistry of the University of Ottawa, and more specifically Prof. Deryn Fogg, for hosting our group while the University of New Orleans was recovering from Hurricane Katrina. Degussa AG, Umicore AG, and Strem are also gratefully acknowledged.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3729, doi. 10.1002/ange.200600571
    By:
    • Nicolas Marion;
    • Silvia Díez-González;
    • Pierre de Frémont;
    • April R. Noble;
    • Steven P. Nolan
    Publication type:
    Article
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    Controlled Self-Assembly Behavior of an Amphiphilic Bisporphyrin–Bipyridinium–Palladium Complex: From Multibilayer Vesicles to Hollow CapsulesThis work was supported by the National Natural Science Foundation of China (20531060, 10474101, 20418001, 20571078, and 20421101), and the Major State Basic Research Development Program (2005CB623602). This project is partly supported by National Center for Nanoscience and Technology, China.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3721, doi. 10.1002/ange.200600554
    By:
    • Yongjun Li;
    • Xiaofang Li;
    • Yuliang Li;
    • Huibiao Liu;
    • Shu Wang;
    • Haiyang Gan;
    • Junbo Li;
    • Ning Wang;
    • Xiaorong He;
    • Daoben Zhu
    Publication type:
    Article
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    Short Synthesis of Skeletally and Stereochemically Diverse Small Molecules by Coupling Petasis Condensation Reactions to Cyclization ReactionsThe NIGMS-sponsored Center of Excellence in Chemical Methodology and Library Design (Broad Institute CMLD) enabled this research. We thank Nilesh Kumar and Drs. Paul Clemons, Ryan Looper, Xiang Wang, and Damian Young for helpful discussions. G.M. is a visiting PhD student from the Dipartimento Farmacochimico, University of Bari (Italy). S.L.S. is an Investigator with the Howard Hughes Medical Institute.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3717, doi. 10.1002/ange.200600497
    By:
    • Naoya Kumagai;
    • Giovanni Muncipinto;
    • Stuart L. Schreiber
    Publication type:
    Article
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    Designed CO2-Philes Stabilize Water-in-Carbon Dioxide MicroemulsionsS.G., A.G., and S.R. thank the University of Bristol DTA, CNPq Brazil, and EPSRC (EP/C523105/1) for studentships and a post-doctoral fellowship, respectively. CCLRC are thanked for beam time and consumables/travel grants. Alan Pitt (Kodak (UK)) is thanked for stimulating discussions. The University of Pittsburgh would like to express its appreciation to the US DOE NETL for supporting this research through contract DE-FG26-04NT-15533.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3757, doi. 10.1002/ange.200600397
    By:
    • Julian Eastoe;
    • Sarah Gold;
    • Sarah Rogers;
    • Paul Wyatt;
    • David C. Steytler;
    • Alexandre Gurgel;
    • Richard K. Heenan;
    • Xin Fan;
    • Eric J. Beckman;
    • Robert M. Enick
    Publication type:
    Article
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    Surface Plasmon Resonances of Free-Standing Gold Nanowires Fabricated by NanoskivingThis research was supported by the NIH (GM065364), by DARPA (sub-award to G.M.W. from the Center for Optofluidic Integration at the California Institute of Technology), and by a MURI AFOSR sub-award to F.C. MRSEC and NSEC shared facilities supported by the NSF under awards DMR-0213805 (MRSEC) and PHY-0117795 (NSEC) were utilized. We thank Ertugrul Cubukcu, Dr. Marko Loncar, Dr. Brian Mayers, and Prof. Kenneth Crozier for helpful discussions.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3713, doi. 10.1002/ange.200600394
    By:
    • Qiaobing Xu;
    • Jiming Bao;
    • Federico Capasso;
    • George M. Whitesides
    Publication type:
    Article
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    A Nickel–Alkyl Bond in an Inactivated State of the Enzyme Catalyzing Methane FormationWe thank the Swiss National Science Foundation (SNF) and the Fonds der Chemischen Industrie for financial support. D.H. gratefully acknowledges a research scholarship (HI 1094/1-1) from the Deutsche Forschungsgemeinschaft (DFG). We are grateful to Brian M. Hoffman (Northwestern Univ.) for helpful discussions.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3684, doi. 10.1002/ange.200600366
    By:
    • Dariush Hinderberger;
    • Rafal P. Piskorski;
    • Meike Goenrich;
    • Rudolf K. Thauer;
    • Arthur Schweiger;
    • Jeffrey Harmer;
    • Bernhard Jaun
    Publication type:
    Article
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    A General Synthesis of C6-Azolyl Purine NucleosidesThis work was supported by a National Institutes of Health grant (no.: S06 GM008168-24S1), partially by a National Science Foundation (NSF) grant (no.: CHE-0314326), and by a PSC-CUNY 36 award. Acquisition of a 500 MHz NMR spectrometer and a mass spectrometer was funded by NSF grants (nos.: CHE-0210295 and CHE-0520963, respectively). Dr. P. Pradhan is thanked for his assistance.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3742, doi. 10.1002/ange.200504565
    By:
    • Pallavi Lagisetty;
    • Larry M. Russon;
    • Mahesh K. Lakshman
    Publication type:
    Article
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    Total Synthesis of (+)-Machaeriol D with a Key Regio- and Stereoselective SN2′ ReactionWe are grateful for the financial support of the NSFC (No. 20572036, QT program), the Special Doctorial Program Funds of the Ministry of Education of China (20040730008), GanSu Science Foundation (No. 3ZS051A25-004), and the Key Grant Project of the Ministry of Education of China (No.105169).

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3733, doi. 10.1002/ange.200600006
    By:
    • Qiaoling Wang;
    • Qinggang Huang;
    • Bo Chen;
    • Jiangping Lu;
    • Hui Wang;
    • Xuegong She;
    • Xinfu Pan
    Publication type:
    Article
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    Protected 32P-Labels in Deoxyribonucleotides: Investigation of Sequence Selectivity of DNA Photocleavage by Enediyne–, Fulvene–, and Acetylene–Lysine ConjugatesI.A. is grateful to the National Science Foundation (grant no.: CHE-0316598) for partial support of this research and to the 3M Company for an Untenured Faculty Award. N.L.G. thanks the National Science Foundation (grant no.: MCB 0316494) and the National Institutes of Health (grant no.: RO1 GM54008) for their support. We are also grateful for technical support from Dr. L. Keller (Florida State University Biology Department).

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3748, doi. 10.1002/ange.200504479
    By:
    • Boris Breiner;
    • Jörg C. Schlatterer;
    • Serguei V. Kovalenko;
    • Nancy L. Greenbaum;
    • Igor V. Alabugin
    Publication type:
    Article
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    A New Reaction Pathway in Organophosphorus Chemistry: Competing SN2 and AE′ Pathways for Nucleophilic Attack at a Phosphorus–Carbon Cage CompoundWe acknowledge the EPSRC (R.J.K., D.A.P., C.E.W.), the Universities of Bristol (M.G., C.A.R., C.F.) and York (C.E.W., J.M.L.), and The Royal Society (University Research Fellowship for C.A.R.) for financial assistance. We thank Dr. Craig Butts (Bristol) for helpful comments in preparing this manuscript.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3710, doi. 10.1002/ange.200504546
    By:
    • Cheryl Fish;
    • Michael Green;
    • Richard J. Kilby;
    • Jason M. Lynam;
    • John E. McGrady;
    • Dimitrios A. Pantazis;
    • Christopher A. Russell;
    • Adrian C. Whitwood;
    • Charlotte E. Willans
    Publication type:
    Article
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    Cyclophanes within Cyclophanes: The Synthesis of a Pyromellitic Diimide-Based Macrocycle as a Structural Unit in a Molecular Tube and Its Inclusion PhenomenaMolecular Tubes and Capsules, Part 1. We gratefully acknowledge the financial support by a Theme Project of Molecular Architecture of Organic Compounds for Functional Design (Prof. Tahsin J. Chow) from the Institute of Chemistry, Academia Sinica, Taiwan R.O.C. We are also grateful for partial financial support by the Joint Project of Chemical Synthesis Core Research Institutions, Research and Education for Inter-University Research Project, MEXT, Japan.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3725, doi. 10.1002/ange.200504499
    By:
    • Tetsuo Iwanaga;
    • Ryoma Nakamoto;
    • Mikio Yasutake;
    • Hiroyuki Takemura;
    • Katsuya Sako;
    • Teruo Shinmyozu
    Publication type:
    Article
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    Watson–Crick Base-Pairing Properties of Nucleic Acid Analogues with Stereocontrolled α and β Torsion Angles (α,β-D-CNAs)We thank the Centre Informatique National de l'Enseignement Supérieur (CINES) and the Centre Interuniversitaire de Calcul de Toulouse (CALMIP) for the generous allocation of computer time and Dr. M. Erard for assistance with the CD experiments. D-CNAs=constrained nucleic acids with dioxaphosphorinane ring.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3705, doi. 10.1002/ange.200504475
    By:
    • Christelle Dupouy;
    • Nathalie Iché-Tarrat;
    • Marie-Pierre Durrieu;
    • Frédéric Rodriguez;
    • Jean-Marc Escudier;
    • Alain Vigroux
    Publication type:
    Article
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    Enhanced Signals and Fast Nucleic Acid Hybridization By Microfluidic Chaotic MixingThis research was supported by the NIH Director's Pioneer Award (7DP1 0D000251-02) and NIH 1R01 HG002644-01A1. We thank Yanxia Hao and Dr. Christopher S. Baker of the Genomics Core Laboratory, Gladstone Institutes for providing mouse-printed oligoarrays (17 K) and Frederick Balagadde of Caltech for technical assistance.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3700, doi. 10.1002/ange.200503830
    By:
    • Jian Liu;
    • Brian A. Williams;
    • Richele M. Gwirtz;
    • Barbara J. Wold;
    • Stephen Quake
    Publication type:
    Article
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    Ultrastable Gold Nanocatalyst Supported by Nanosized Non-Oxide SubstrateThis work was conducted at the Oak Ridge National Laboratory and supported by the Division of Chemical Sciences, Office of Basic Energy Sciences, US Department of Energy, under contract no. DE-AC05-00OR22725 with UT-Battelle, LLC. We thank the SHARE Facility at ORNL for the transmission electron microscopy. This research was supported in part by an appointment for W.F.Y. to the ORNL Postdoctoral Research Associates Program, administered jointly by the Oak Ridge Institute for Science and Education and ORNL.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3696, doi. 10.1002/ange.200503808
    By:
    • Wenfu Yan;
    • Suree Brown;
    • Zhengwei Pan;
    • Shannon M. Mahurin;
    • Steven H. Overbury;
    • Sheng Dai
    Publication type:
    Article
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    Epitaxial Growth of Peptide Nanofilaments on Inorganic Surfaces: Effects of Interfacial Hydrophobicity/HydrophilicityWe thank Dr. Bin Li, Xing-Fei Zhou, Yun-Chang Guo, and Hai Li for valuable discussions and Miss Stefanie Maerz for the helpful revisions. This work was supported by grants from the Shanghai Institute of Applied Physics, the National Natural Science Foundation of China (No. 10335070, 10404032, and 30400064), and the Science and Technology Commission of Shanghai Municipality (No. 04qmx1466 and 0552nm033).

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 22, p. 3693, doi. 10.1002/ange.200503636
    By:
    • Feng Zhang;
    • Hai-Ning Du;
    • Zhi-Xiang Zhang;
    • Li-Na Ji;
    • Hong-Tao Li;
    • Lin Tang;
    • Hua-Bin Wang;
    • Chun-Hai Fan;
    • Hong-Jie Xu;
    • Yi Zhang;
    • Jun Hu;
    • Hong-Yu Hu;
    • Jian-Hua He
    Publication type:
    Article