Enantioselective Palladium-Catalyzed Trimethylenemethane [3+2] Cycloadditions (Englisch)
- Neue Suche nach: Le Marquand, P.
- Neue Suche nach: Tam, W.
- Neue Suche nach: Le Marquand, P.
- Neue Suche nach: Tam, W.
In:
ANGEWANDTE CHEMIE -INTERNATIONAL EDITION IN ENGLISH-
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47
, 16
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2926-2928
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2008
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ISSN:
- Aufsatz (Zeitschrift) / Print
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Titel:Enantioselective Palladium-Catalyzed Trimethylenemethane [3+2] Cycloadditions
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Beteiligte:Le Marquand, P. ( Autor:in ) / Tam, W. ( Autor:in )
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Erschienen in:ANGEWANDTE CHEMIE -INTERNATIONAL EDITION IN ENGLISH- ; 47, 16 ; 2926-2928
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Verlag:
- Neue Suche nach: John Wiley & Sons, Ltd
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Erscheinungsdatum:01.01.2008
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Format / Umfang:3 pages
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ISSN:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Print
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Sprache:Englisch
- Neue Suche nach: 540.5 / 540
- Weitere Informationen zu Dewey Decimal Classification
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Klassifikation:
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Cover Picture: Mixed Spin-State [HS-LS] Pairs in a Dinuclear Spin-Transition Complex: Confirmation by Variable-Temperature 57Fe Mossbauer Spectroscopy (Angew. Chem. Int. Ed. 16/2008)Grunert, C. M. / Reiman, S. / Spiering, H. / Kitchen, J. A. / Brooker, S. / Gutlich, P. et al. | 2008
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Enantioselective Palladium‐Catalyzed Trimethylenemethane [3+2] CycloadditionsLe Marquand, Paul / Tam, William et al. | 2008
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Enantioselective Palladium-Catalyzed Trimethylenemethane [3+2] CycloadditionsFNR HREF="nss"> FN ID="nss"> This work was supported by the Merck Frosst Centre for Therapeutic Research and the Natural Sciences and Engineering Research Council (NSERC) of Canada.Le Marquand, Paul et al. | 2008
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An Atomistic Branching Mechanism for Carbon Nanotubes: Sulfur as the Triggering AgentFNR HREF="nss"> FN ID="nss"> This work was supported by CONACYT-México grants: 56787 (Laboratory for Nanoscience and Nanotechnology Research-LINAN), 45762 (H.T.), 45772 (M.T.), 48300 S-3907, 41464-Inter American Collaboration (M.T.), 42428-Inter American Collaboration (H.T.), 2004-01-013-SALUD-CONACYT (M.T.), PUE-2004-CO2-9 Fondo Mixto de Puebla (M.T.) and PhD. Scholarships (E.C.S. and J.M.R.H.) as well as NSF-DMR Grant-0303429. We are very thankful to Daniel Ramírez and Grisel Ramírez for technical support. The work was also supported by the Center for Nanophase Materials Sciences (CNMS), sponsored by the Division of Scientific User Facilities, U.S. Department of Energy and by the Division of Materials Science and Engineering, U.S. Department of Energy under Contract No. DEAC05-00OR22725 with UT-Battelle, LLC at Oak Ridge National Laboratory (ORNL). The extensive computations were performed using the resources of the National Center for Computational Sciences at ORNL. We acknowledge use of facilities in the John M. Cowley Center for High ResolutRomo-Herrera, José M et al. | 2008
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Evolution of Chemical Bonding during HCN&rlarr2;HNC Isomerization as Revealed through Nuclear Quadrupole Hyperfine StructureFNR HREF="nss"> FN ID="nss"> This work was supported by the Office of Basic Energy Sciences of the US Department of Energy (DE-FG0287ER13671) and the Donors of the American Chemical Society Petroleum Research Fund.Bechtel, Hans A et al. | 2008
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- 2997
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Mixed Spin-State [HS-LS] Pairs in a Dinuclear Spin-Transition Complex: Confirmation by Variable-Temperature 57Fe Mössbauer SpectroscopyFNR HREF="nss"> FN ID="nss"> We are grateful for financial support from: the DFG (Priority Program 1137 "Molecular Magnetism"), the Fonds der Chemischen Industrie, and the University of Mainz (C.M.G., S.R., P.G.); and from the TEC (Bright Futures Top Achiever Doctoral scholarship to J.A.K.), the Marsden Fund (RSNZ), the CFN (Karlsruhe), the MacDiarmid Institute for Advanced Materials and Nanotechnology (NZ), the University of Otago (J.A.K., S.B.) and to Michael Crawford (Dunedin) for generating the front cover image. [HS-LS]=high-spin-low-spin.Grunert, C. Matthias et al. | 2008
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- 3021
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Total Synthesis of Spirastrellolide A Methyl Ester-Part 2: Subunit Union and Completion of the SynthesisFNR HREF="nss"> FN ID="nss"> This work was supported by the EPSRC (GR-C541677-1), Merck Research Laboratories, Homerton College, Cambridge (E.A.A.), SK Corporation (J.H.L.), and the German Academic Exchange Service (C.M.). We thank Prof. R. J. Andersen (University of British Columbia) for an authentic sample of spirastrellolide A methyl ester and for helpful discussions, as well as Dr. J. Davies (Cambridge) for solving the X-ray crystal structure of pentaol 12.Paterson, Ian et al. | 2008
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A Nitrido-Centered Uranium Azido Cluster Obtained from a Uranium AzideFNR HREF="nss"> FN ID="nss"> This work was supported by the Commissariat à l'Energie Atomique, Direction de l'Energie Nucléaire. We thank Jean-François Jacquot for the magnetic measurements.Nocton, Grégory et al. | 2008
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Asymmetric Iminium Ion Catalysis: An Efficient Enantioselective Synthesis of Pyranonaphthoquinones and β-LapachonesFNR HREF="nss"> FN ID="nss"> The authors acknowledge Degussa GmbH and the DFG (Priority Programme Organocatalysis) for financial support as well the Ministerio de Educacion y Ciencia, Spain, for a stipend given to E.M. and Dr. M. Bolte for the X-ray crystal structure analysis.Rueping, Magnus et al. | 2008
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A Concise Approach to VinigrolFNR HREF="nss"> FN ID="nss"> We thank Dr. D.-H. Huang and Dr. L. Pasternack for NMR spectroscopic assistance, Dr. G. Siuzdak for mass spectrometric and Dr. Arnold Rheingold (UCSD) for X-ray crystallographic assistance. Financial support for this work was provided by Bristol-Myers Squibb (predoctoral fellowship to T. J. M.), Merck, and Roche.Maimone, Thomas J et al. | 2008
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Chlorophyll Breakdown by a Biomimetic RouteFNR HREF="nss"> FN ID="nss"> We thank K. Breuker, K.-H. Ongania, and S. Gschösser for spectroscopic measurements and acknowledge financial support from the Austrian Science Funds (FWF P-16097 and P-19596).Oberhuber, Michael et al. | 2008
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Preview: Angew. Chem. Int. Ed. 17/2008| 2008