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Inhaltsverzeichnis
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Titelbild: Templated Ligand Environments for the Selective Incorporation of Different Metals into DNA (Angew. Chem. 52/2009)
Yang, Hua
/ Rys, Andrzej Z.
/ McLaughlin, Christopher K.et al.
| 2009
Momentaufnahmen bei der Bildung einer Al-Al-σ-Bindung aus {AlR2}-Einheiten - experimentelle und quantenchemische Befunde Wir danken der Deutschen Forschungsgemeinschaft (CFN) und dem Fonds der Chemischen Industrie für finanzielle Unterstützung.
Produktion der Isochromanon-Antimykotika AjudazolA und B in Chondromyces crocatus Cmc5: Biosynthesemaschinerie und Cytochrom-P450-Modifikationen Wir danken Dr. Josef Zapp vom Institut für Pharmazeutische Biologie für die Aufnahme der NMR-Spektren. Diese Arbeit wurde von der Deutschen Forschungsgemeinschaft (DFG) finanziell unterstützt.
Lineare Energiebeziehungen und rechnergestütztes Design selektiver Hydrierungs-/Dehydrierungskatalysatoren Der Autor dankt Prof. G.A. Somorjai und seiner Arbeitsgruppe an der U.C. Berkeley für die Gastfreundschaft. Das Center for Atomic-scale Materials Design wird von der Lundbeck-Stiftung finanziell unterstützt.
Photoredoxkatalyse mit sichtbarem Licht Dem Fonds der Chemischen Industrie und der Dr. Otto Röhm-Gedächtnisstiftung wird für ihre Unterstützung gedankt.
Direct Assessment of Electron Delocalization Using NMR Chemical Shifts The Sandoz family foundation, the Swiss NSF Grant 200021121577/1, and EPFL are acknowledged for financial support.
Asymmetric Organocatalytic Relay Cascades: Catalyst-Controlled Stereoisomer Selection in the Synthesis of Functionalized Cyclohexanes We are grateful for the financial support of "973" project (2009CB626604) from MOST, the foundation (20772051) from NSFC, the "111" program from MOE of P. R. China, the EPSRC for a Leadership fellowship to D.J.D.
Non-Metal-Mediated Homogeneous Hydrogenation of CO2 to CH3OH We thank the EPSRC for support, Balliol College, Oxford for a Junior Research Fellowship (A.E.A.), and Dr. Nick Rees (CRL, Oxford) for NMR support.
Abnormal Reactivity of an N-Heterocyclic Carbene (NHC) with a Phosphaalkene: A Route to a 4-Phosphino-Substituted NHC We gratefully acknowledge the following funding bodies: The Natural Sciences and Engineering Research Council of Canada (Discovery Grants, and Research Tools and Instruments Grants to P.K. and D.P.G., and a PGS D scholarship to J.I.B.), the Canada Foundation for Innovation, and the B.C. Knowledge Development Fund.
anti-Selective Asymmetric Michael Reactions of Aldehydes and Nitroolefins Catalyzed by a Primary Amine/Thiourea We thank the Skaggs Institute for Chemical Biology for funding.
Photo-Thermal Haptotropism in Cyclopentadienylcobalt Complexes of Linear Phenylenes: Intercyclobutadiene Metal Migration This work was supported by the NSF (CHE 0451241, 0907800 (K.P.C.V.) and CHE 0832622 (T.V.T.)) and the Welch Foundation (E-075 (T.A.A.)). We thank Prof. A.D. Bond, University of Southern Denmark, for obtaining synchrotron diffraction data on 2. We appreciate constructive comments from Prof. R.G. Bergman.
Highly Stereoselective Synthesis of Monofluoroalkenes from α-Fluorosulfoximines and Nitrones We thank the National Natural Science Foundation of China (20772144, 20825209, 20832008) and the Chinese Academy of Sciences (Hundreds-Talent Program and Knowledge Innovation Program) for financial support.
Phospholipid-Coated Carbon Nanotubes as Sensitive Electrochemical Labels with Controlled-Assembly-Mediated Signal Transduction for Magnetic Separation Immunoassay This work was supported by "973" National Key Basic Research Program (2007CB310500), NSFC (20875027, 20775023) and NSF of Hunan province (07JJ1002).
Phospholipid‐Coated Carbon Nanotubes as Sensitive Electrochemical Labels with Controlled‐Assembly‐Mediated Signal Transduction for Magnetic Separation Immunoassay
Metalloorganic Polymerization Catalysis as a Tool To Probe Crystallization Properties of Polymers: The Case of Isotactic Poly(1-butene) Financial support from Basell Polyolefins (Italy) and MIUR (PRIN 2007) are gratefully acknowledged.
Intramolecular Alkynylcyclopropanation of Olefins Catalyzed by Bi(OTf)3: Stereoselective Synthesis of 1-Alkynyl-3-azabicyclo[3.1.0]hexanes We thank H. Fukuoka for X-ray analysis. This work was partially supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT). K.K. acknowledges financial support from the Electric Technology Research Foundation of Chugoku.
Analysis and Optimization of Copper-Catalyzed Azide-Alkyne Cycloaddition for Bioconjugation This work was supported by The Skaggs Institue for Chemical Biology, Pfizer, Inc., and the NIH (RR021886). We are grateful to Matthias Park for assistance with the synthesis of 3.
Diversification of RTH-Type Zeolite and Its Catalytic Application We thank Mr. Mikio Hayashi and Dr. Tooru Setoyama (Mitsubishi Chemical Group, Science and Technology Research Center) for helpful discussion. This work was supported by Research and Development in a New Interdisciplinary Field based on Nanotechnology and Materials Science Program of the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT). This work was also partly supported by Grant-in-Aid for Scientific Research (S) (No. 19106015) of MEXT.
Efficient Catalytic Synthesis of Tertiary and Secondary Amines from Alcohols and Urea This work was supported in part by the Global COE Program (Chemistry Innovation through Cooperation of Science and Engineering), the Core Research for Evolutional Science and Technology (CREST) program of the Japan Science and Technology Agency (JST), and Grants-in-Aid for Scientific Researches from Ministry of Education, Culture, Sports, Science, and Technology.
Gold-Silane and Gold-Stannane Complexes: Saturated Molecules as σ-Acceptor Ligands Financial support from the Centre National de la Recherche Scientifique, the Université de Toulouse, the Agence Nationale de la Recherche (ANR-06-BLAN-0034), the National Science Foundation (CHE-0646916), and the Welch Foundation (A-1423) is gratefully acknowledged. We thank: the Unidade de RaiosX of the Universidade de Santiago de Compostela for the X-ray diffraction analyses of 4 and 5; Christopher Cummins (MIT) for useful discussions regarding the use of the Dgrid program; the Laboratory for Molecular Simulation at Texas A&M University for providing software and computation resources. L.M. thanks the Institut Universitaire de France and D.B. thanks the COST action CM0802 PhoSciNet for supporting this work.
Surface Passivation and Transfer Doping of Silicon Nanowires This work was supported by grants from the Research Grants Council of Hong Kong SAR [Project No. CityU 103907, CityU5/CRF/08, NCityU 108/08].
Iodinated Nanoscale Coordination Polymers as Potential Contrast Agents for Computed Tomography We acknowledge financial support from the NIH (U54-CA119343) and the NSF (DMR-0906662).
Freeze Drying Significantly Increases Permanent Porosity and Hydrogen Uptake in 4,4-Connected Metal-Organic Frameworks We acknowledge financial support from NSF.
Photoresponsive Supramolecular Organometallic Nanosheets Induced by PtII···PtII and CH···π Interactions This work was supported by the "Nanotechnology Research Program" of the University Development Fund of The University of Hong Kong, and the Hong Kong Research Grants Council (HKU 7011/07P and 7008/09P). Y.C. thanks The University of Hong Kong for a Postdoctoral Fellowship. Thanks go to Dr. Zong-Xiang Xu, Frankie Yu-Fee Chan, and Amy Sui-Ling Wong for assistance in device fabrication and TEM/SEM observations. We thank Dr. Nianyong Zhu for solving the crystal structure of complex 7.
Reversibly Stabilized Multifunctional Dextran Nanoparticles Efficiently Deliver Doxorubicin into the Nuclei of Cancer Cells This work was financially supported by research grants from the National Natural Science Foundation of China (NSFC 50703028, 50973078, 20874070, and 20974073), the Natural Science Foundation of the Jiangsu Higher Education Institutions of China (08KJB150016), and the Program of Innovative Research Team of Soochow University.
Templated Ligand Environments for the Selective Incorporation of Different Metals into DNA We thank the NSERC, CFI, CSACS, and CIFAR for financial support. H.F.S. is a Cottrell Scholar of the Research Cooperation.
Probing the Photothermal Effect of Gold-Based Nanocages with Surface-Enhanced Raman Scattering (SERS) This work was supported in part by a 2006 Director's Pioneer Award from the NIH (DP1 OD000798-05), a research grant from the NSF (DMR-0804088), and start-up funds from Washington University in St. Louis.
A Calix[4]arene 3d/4f Magnetic Cooler We thank the EPSRC and Heriot-Watt University for financial support of this work. M.E. acknowledges grants MAT2009-13977-C03 and CSD2007-00010, and funding from the RyC program, all from the Spanish Ministry for Science and Innovation.
Direct Evidence of High Spatial Localization of Hot Spots in Surface-Enhanced Raman Scattering C.C. thanks the SBA for a scholarship, P.V.D. thanks the FWO for a fellowship.
Pentiptycene-Derived Oligo(p-phenyleneethynylene)s: Conformational Control, Chain-Length Effects, Localization of Excitation, and Intrachain Resonance Energy Transfer We thank the National Science Council of Taiwan and Academia Sinica, ROC for financial support.
Pentiptycene‐Derived Oligo(p‐phenyleneethynylene)s: Conformational Control, Chain‐Length Effects, Localization of Excitation, and Intrachain Resonance Energy Transfer
Total Synthesis of SpirastrellolideF Methyl Ester-Part1: Strategic Considerations and Revised Approach to the Southern Hemisphere Generous financial support by the MPG, the Chemical Genomics Center (CGC) of the MPG, the Fonds der Chemischen Industrie (Kekulé-stipend to S.B.), the Alexander-von-Humboldt Foundation (fellowship to G.O'N.), and F. Hoffmann-LaRoche, Basel, is gratefully acknowledged. We sincerely thank the NMR, X-ray, and chromatography departments of our Institute for excellent support over the entire duration of this project.
Total Synthesis of SpirastrellolideF Methyl Ester-Part2: Macrocyclization and Completion of the Synthesis Generous financial support by the MPG, the Chemical Genomics Center (CGC) of the MPG, the Fonds der Chemischen Industrie (Kekulé-stipend to S.B.), the Alexander-von-Humboldt Foundation (fellowships to G.O'N. and M.D.B.F.), the Fonds de Recherche sur la Nature et les Technologies Québec (fellowship to C.G.), and F. Hoffmann-LaRoche, Basel, is gratefully acknowledged. We sincerely thank the NMR, X-ray, and chromatography departments of our Institute for excellent support over the entire duration of this project, the ANKA Angstroemquelle, Karlsruhe, for the provision of beamtime, and Prof. R.J. Andersen, University of British Columbia, Vancouver, for an exchange of information.
Eine Dilithium-1,4-butandiid-Struktur mit einem chlorzentrierten Li12-Ikosaeder Die Deutsche Forschungsgemeinschaft (DFG, Bonn) unterstützte diese Forschung großzügig. Wir danken ebenfalls dem Fonds der Chemischen Industrie (Frankfurt/Main) für die Förderung. Wir sind auch Dr. R. Wyrwa (Innovent Jena) für hilfreiche Diskussionsbeiträge und R. Suxdorf für ihre Unterstützung dankbar.
Eisencarbonyle: effiziente Katalysatoren für die lichtgetriebene Wasserstofferzeugung aus Wasser Diese Arbeit wurde vom Land Mecklenburg-Vorpommern, dem BMBF und der DFG (Leibniz-Preis) unterstützt. F.G. dankt dem Fonds der chemischen Industrie für die Unterstützung durch ein Kekulé-Stipendium.
Einzelne molekulare Drähte verbinden metallische und isolierende Oberflächenbereiche Diese Arbeit wurde vom EU-Projekt "pico inside", dem Förderprogramm "Functional materials at the nanoscale" (FU Berlin) und der DFG (SFB 658) finanziell gefördert. Wir danken Christian Roth für die technische Unterstützung, und L.G. dankt Gerhard Meyer für hilfreiche Diskussionen.
Eine katalytische asymmetrische 6π-Elektrocyclisierung: enantioselektive Synthese von 2-Pyrazolinen Wir danken der Röntgen-Abteilung unseres Instituts, D. Bock für Kristallstrukturanalysen sowie H. vanThienen und Dr. V. Wakchaure für Unterstützung. Weiterer Dank gilt der Max-Planck-Gesellschaft, der Deutschen Forschungsgemeinschaft (SPP 1179, Organokatalyse) und dem Fonds der Chemischen Industrie (Auszeichnung an B.L. und Stipendium an S.M.) für großzügige finanzielle Unterstützung.
Catalytic Asymmetric 6π Electrocyclization: Enantioselective Synthesis of Functionalized Indolines We acknowledge funding from the Royal Society (MDS), GSK and the EPSRC (E.E.M. and S.T.), the University of Oxford John Fell Fund and AstraZeneca. We thank Dr. John Ward (GSK) and Dr. Andrew Cridland (GSK) for useful discussions, Dr. Amber Thompson for assistance with X-ray crystallography, and Prof. Ian Fleming FRS for insightful comments.