“Targeted Metabolomics” in der Biomarkerforschung (Deutsch)
- Neue Suche nach: Griffiths, William J.
- Neue Suche nach: Koal, Therese
- Neue Suche nach: Wang, Yuqin
- Neue Suche nach: Kohl, Matthias
- Neue Suche nach: Enot, David P.
- Neue Suche nach: Deigner, Hans‐Peter
- Neue Suche nach: Griffiths, William J.
- Neue Suche nach: Koal, Therese
- Neue Suche nach: Wang, Yuqin
- Neue Suche nach: Kohl, Matthias
- Neue Suche nach: Enot, David P.
- Neue Suche nach: Deigner, Hans‐Peter
In:
Angewandte Chemie
;
122
, 32
;
5554-5575
;
2010
- Aufsatz (Zeitschrift) / Elektronische Ressource
-
Titel:“Targeted Metabolomics” in der Biomarkerforschung
-
Beteiligte:Griffiths, William J. ( Autor:in ) / Koal, Therese ( Autor:in ) / Wang, Yuqin ( Autor:in ) / Kohl, Matthias ( Autor:in ) / Enot, David P. ( Autor:in ) / Deigner, Hans‐Peter ( Autor:in )
-
Erschienen in:Angewandte Chemie ; 122, 32 ; 5554-5575
-
Verlag:
- Neue Suche nach: WILEY‐VCH Verlag
-
Erscheinungsdatum:26.07.2010
-
Format / Umfang:22 pages
-
ISSN:
-
DOI:
-
Medientyp:Aufsatz (Zeitschrift)
-
Format:Elektronische Ressource
-
Sprache:Deutsch
-
Schlagwörter:
-
Datenquelle:
Inhaltsverzeichnis – Band 122, Ausgabe 32
Zeige alle Jahrgänge und Ausgaben
Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
- 5517
-
Titelbild: Design and Folding of [GluA4(OβThrB30)]Insulin (“Ester Insulin”): A Minimal Proinsulin Surrogate that Can Be Chemically Converted into Human Insulin (Angew. Chem. 32/2010)Sohma, Youhei / Hua, Qing‐Xin / Whittaker, Jonathan / Weiss, Michael A. / Kent, Stephen B. H. et al. | 2010
- 5517
-
Titelbild: Design and Folding of [GluA4(ObThrB30)]Insulin ("Ester Insulin"): A Minimal Proinsulin Surrogate that Can Be Chemically Converted into Human Insulin (Angew. Chem. 32/2010)Sohma, Y. / Hua, Q. X. / Whittaker, J. / Weiss, M. A. / Kent, S. B. et al. | 2010
- 5518
-
Innentitelbild: Supported Gold and Silver Nanoparticles for Catalytic Deoxygenation of Epoxides into Alkenes (Angew. Chem. 32/2010)Mitsudome, Takato / Noujima, Akifumi / Mikami, Yusuke / Mizugaki, Tomoo / Jitsukawa, Koichiro / Kaneda, Kiyotomi et al. | 2010
- 5521
-
Graphisches Inhaltsverzeichnis: Angew. Chem. 32/2010| 2010
- 5530
-
Vor 50 Jahren in der Angewandten Chemie| 2010
- 5532
-
Top‐Beiträge aus unseren Schwesterzeitschriften: Angew. Chem. 32/2010| 2010
- 5532
-
Top-Beitrage aus unseren Schwesterzeitschriften: Angew. Chem. 32/2010| 2010
- 5536
-
Kim Renée Dunbar| 2010
- 5536
-
Kim Renee Dunbar| 2010
- 5537
-
On Solar Hydrogen & Nanotechnology. Herausgegeben von Lionel Vayssieres.Nann, Thomas et al. | 2010
- 5538
-
Der molekulare Mechanismus der Bildung von SpinnenseideSilvers, Robert / Buhr, Florian / Schwalbe, Harald et al. | 2010
- 5538
-
Der molekulare Mechanismus der Bildung von Spinnenseide Unsere Arbeit wird gefördert vom DFG Cluster of Excellence: Macromolecular Complexes. R.S. wird von der Stiftung Polytechnische Gesellschaft und F.B. vom Fonds der Chemischen Industrie gefördert.Silvers, Robert et al. | 2010
- 5541
-
Eine goldene Episode in der farbenfrohen Geschichte des Fenton-Reagens Ich danke Prof. F. Scholz und Prof. S. Fletcher für ihre sorgfältigen Korrekturen und konstruktiven Anmerkungen.Chen, GeorgeZ. et al. | 2010
- 5541
-
Eine goldene Episode in der farbenfrohen Geschichte des Fenton‐ReagensChen, George Z. et al. | 2010
- 5544
-
Dünner, kleiner, schneller – wie die IR‐Spektroskopie zur Aufklärung des Funktionsmechanismus biologischer und biomimetischer Systeme beiträgtAtaka, Kenichi / Kottke, Tilman / Heberle, Joachim et al. | 2010
- 5544
-
Dunner, kleiner, schneller - wie die IR-Spektroskopie zur Aufklarung des Funktionsmechanismus biologischer und biomimetischer Systeme beitragtAtaka, K. / Kottke, T. / Heberle, J. et al. | 2010
- 5554
-
“Targeted Metabolomics” in der BiomarkerforschungGriffiths, William J. / Koal, Therese / Wang, Yuqin / Kohl, Matthias / Enot, David P. / Deigner, Hans‐Peter et al. | 2010
- 5576
-
Doppelte und dreifache In‐vivo‐Funktionalisierung von Proteinen mit synthetischen AminosäurenLepthien, Sandra / Merkel, Lars / Budisa, Nediljko et al. | 2010
- 5576
-
Doppelte und dreifache In-vivo-Funktionalisierung von Proteinen mit synthetischen Aminosäuren Prof. Luis Moroder danken wir für hilfreiche Diskussionen und seinen Rat, Elisabeth Weyher-Stingl und der Microchemistry Core Facility für exzellente Unterstützung in der Analytik und Waltraud Wenger für hervorragende technische Assistenz. Dem National BioResource Project (Japan) verdanken wir die Bereitstellung der Bakterienstämme. Diese Arbeit wurde durch das BioFuture-Programm des Bundesministeriums für Bildung und Forschung finanziert.Lepthien, Sandra et al. | 2010
- 5576
-
Doppelte und dreifache In-vivo-Funktionalisierung von Proteinen mit synthetischen AminosaurenLepthien, S. / Merkel, L. / Budisa, N. et al. | 2010
- 5582
-
Hoch selektive Metallierungen von Pyridinen und verwandten Heterocyclen mithilfe frustrierter Lewis-Paare sowie tmp-Zink- und tmp-Magnesium-Basen mit BF3sOEt2Jaric, M. / Haag, B. A. / Unsinn, A. / Karaghiosoff, K. / Knochel, P. et al. | 2010
- 5582
-
Hoch selektive Metallierungen von Pyridinen und verwandten Heterocyclen mithilfe frustrierter Lewis-Paare sowie tmp-Zink- und tmp-Magnesium-Basen mit BF3·OEt2 Wir danken dem Fonds der Chemischen Industrie, dem European Research Council, der Deutschen Forschungsgemeinschaft und dem SFB749 für finanzielle Unterstützung. Wir danken auch der BASFAG (Ludwigshafen), W.C. Heraeus (Hanau) und der Chemetall GmbH (Frankfurt) für großzügige Chemikalienspenden. tmp=2,2,6,6-Tetramethylpiperidyl.Jaric, Milica et al. | 2010
- 5582
-
Hoch selektive Metallierungen von Pyridinen und verwandten Heterocyclen mithilfe frustrierter Lewis‐Paare sowie tmp‐Zink‐ und tmp‐Magnesium‐Basen mit BF3⋅OEt2Jaric, Milica / Haag, Benjamin A. / Unsinn, Andreas / Karaghiosoff, Konstantin / Knochel, Paul et al. | 2010
- 5587
-
Zugang zu photochromen und fluoreszierenden Biliproteinen über fusionierte Gene H.S. und K.H.Z. wurden vor der Volkswagen-Stiftung (I/77900) gefördert, H.S. von der Deutschen Forschungsgemeinschaft (SFB 533, TPA1), K.H.Z. und M.Z. von der National Natural Science Foundation of China (30870541 und 30870519). Wir danken R.J. Porra für die kritische Durchsicht des Manuskripts sowie K. Cang, H.H. Hua, J.P. Li, Y.F. Sun und J.G. Xu für technische Assistenz.Zhang, Juan et al. | 2010
- 5587
-
Zugang zu photochromen und fluoreszierenden Biliproteinen über fusionierte GeneZhang, Juan / Wu, Xian‐Jun / Wang, Zhi‐Bin / Chen, Yu / Wang, Xing / Zhou, Ming / Scheer, Hugo / Zhao, Kai‐Hong et al. | 2010
- 5587
-
Zugang zu photochromen und fluoreszierenden Biliproteinen uber fusionierte GeneZhang, J. / Wu, X. J. / Wang, Z. B. / Chen, Y. / Wang, X. / Zhou, M. / Scheer, H. / Zhao, K. H. et al. | 2010
- 5591
-
Isolation of the Triplet Ground State Aminyl Diradical We thank the National Science Foundation for support of this work through grant CHE-0718117.Boratynski, PrzemyslawJ. et al. | 2010
- 5591
-
Isolation of the Triplet Ground State Aminyl DiradicalBoratyński, Przemysław J. / Pink, Maren / Rajca, Suchada / Rajca, Andrzej et al. | 2010
- 5595
-
Amidinium Carboxylate Salt Bridges as a Recognition Motif for Mechanically Interlocked Molecules: Synthesis of an Optically Active [2]Catenane and Control of Its Structure This work was supported in part by Grants-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (JSPS) and for Scientific Research on Innovative Areas, "Emergence in Chemistry" (21111508) from the MEXT. We thank Dr. Masato Ikeda for his preliminary work.Nakatani, Yuji et al. | 2010
- 5595
-
Amidinium Carboxylate Salt Bridges as a Recognition Motif for Mechanically Interlocked Molecules: Synthesis of an Optically Active [2]Catenane and Control of Its StructureNakatani, Yuji / Furusho, Yoshio / Yashima, Eiji et al. | 2010
- 5600
-
Monomeric Organoantimony(I) and Organobismuth(I) Compounds Stabilized by an NCN Chelating Ligand: Syntheses and StructuresŠimon, Petr / de Proft, Frank / Jambor, Roman / Růžička, Aleš / Dostál, Libor et al. | 2010
- 5600
-
Monomeric Organoantimony(I) and Organobismuth(I) Compounds Stabilized by an NCN Chelating Ligand: Syntheses and Structures The authors thank the GACR (P207/10/0130) and the Ministry of Education of the Czech Republic (MSM0021627501) for financial support. F.D.P. wishes to acknowledge the Fund for Scientific Research Flanders (Belgium) FWO and the Vrije Universiteit Brussel for financial support.Simon, Petr et al. | 2010
- 5604
-
Side-by-Side and End-to-End Gold Nanorod Assemblies for Environmental Toxin Sensing The authors thank the following institutions for support of this work: The National Science Foundation (NSF) (ECS-0601345, R8112-G1, 0932823, 0933384, 0938019), the Air Force Office of Scientific Research (AFOSR) (GRT00008581/RF60012388, 444286-P061716, FA9550-08-1-0382), the Department of Energy (DOE) EFRC program (DE-SC0000957), the National Natural Science Foundation of China (20675035, 20871060, 20835006), and the 11th Five Years Key Programs for Science and Technology Development of China (200810099, 200810219, 2008ZX08012-001).Wang, Libing et al. | 2010
- 5604
-
Side‐by‐Side and End‐to‐End Gold Nanorod Assemblies for Environmental Toxin SensingWang, Libing / Zhu, Yingyue / Xu, Liguang / Chen, Wei / Kuang, Hua / Liu, Liqiang / Agarwal, Ashish / Xu, Chuanlai / Kotov, Nicholas A. et al. | 2010
- 5608
-
Label‐Free, Real‐Time Monitoring of Biomass Processing with Stimulated Raman Scattering MicroscopySaar, Brian G. / Zeng, Yining / Freudiger, Christian W. / Liu, Yu‐San / Himmel, Michael E. / Xie, X. Sunney / Ding, Shi‐You et al. | 2010
- 5608
-
Label-Free, Real-Time Monitoring of Biomass Processing with Stimulated Raman Scattering Microscopy We thank G.R. Holtom and M.B.J. Roeffaers for helpful discussions. B.G.S. was supported by the Army Research Office through an NDSEG fellowship. C.W.F. was supported by a Boehringer Ingelheim Fonds Ph.D. fellowship. This work is also supported by the US Department of Energy: the instrumentation and data analysis is funded under grant DE-FG02-07ER64500, and the BioEnergy Science Center is a U.S. Department of Energy Bioenergy Research Center supported by the Office of Biological & Environmental Research in the DOE Office of Science; the delignification process is funded by the Office of the Biomass Program.Saar, BrianG. et al. | 2010
- 5612
-
Phosphorus Ligand Imaging with Two‐Photon Fluorescence Spectroscopy: Towards Rational Catalyst ImmobilizationMarras, Fabrizio / Kluwer, Alexander M. / Siekierzycka, Joanna R. / Vozza, Alessandro / Brouwer, Albert M. / Reek, Joost N. H. et al. | 2010
- 5612
-
Phosphorus Ligand Imaging with Two-Photon Fluorescence Spectroscopy: Towards Rational Catalyst Immobilization This research is supported by the National Research School Combination-Catalysis (NRSC-C), The Netherlands Organisation for Scientific Research (NWO)-STW and NanoNed (AMM, 6980), a national nanotechnology program coordinated by the Dutch Ministry of Economic Affairs. We acknowledge H.J. vanRamesdonk for technical assistance with the confocal microscope setup and Dr. E.R.H. vanEck of the solid-state NMR facility for advanced materials science, jointly supported by the Netherlands Organisation for Scientific Research (NWO) and Radboud University Nijmegen, for acquiring the solid-state NMR spectra.Marras, Fabrizio et al. | 2010
- 5617
-
Synthesis, Structure, and Reactivity of a Stabilized Phosphiranylium SaltJansen, Helen / Läng, Florian B. / Slootweg, J. Chris / Ehlers, Andreas W. / Lutz, Martin / Lammertsma, Koop / Grützmacher, Hansjörg et al. | 2010
- 5617
-
Synthesis, Structure, and Reactivity of a Stabilized Phosphiranylium Salt This work was supported by the Council for Chemical Sciences of the Netherlands Organization for Scientific Research (NWO/CW), the ETH Zürich, and the Swiss National Science Foundation. We acknowledge the National Center for Computing Facilities (SARA) and NWO/NCF for computer time and the VU University Amsterdam for a travel grant (H.J.). We thank Dr. M. Smoluch for the exact mass determination.Jansen, Helen et al. | 2010
- 5621
-
Design and Folding of [GluA4(OβThrB30)]Insulin (“Ester Insulin”): A Minimal Proinsulin Surrogate that Can Be Chemically Converted into Human InsulinSohma, Youhei / Hua, Qing‐Xin / Whittaker, Jonathan / Weiss, Michael A. / Kent, Stephen B. H. et al. | 2010
- 5621
-
Design and Folding of [GluA4(ObThrB30)]Insulin ("Ester Insulin"): A Minimal Proinsulin Surrogate that Can Be Chemically Converted into Human InsulinSohma, Y. / Hua, Q. X. / Whittaker, J. / Weiss, M. A. / Kent, S. B. et al. | 2010
- 5621
-
Design and Folding of [GluA4(OβThrB30)]Insulin ("Ester Insulin"): A Minimal Proinsulin Surrogate that Can Be Chemically Converted into Human Insulin This research was supported by the NIH grant RO1 GM075993 to S.B.H.K, and in part by grants from the American Diabetes Association (1-08-RA-218) and the NIH (DK040949 and DK074176) to M.A.W. Y.S. is grateful for a JSPS Postdoctoral Fellowship for Research Abroad. We thank Salih Özcubukcu (University of Chicago) for NMR characterization of new compounds.Sohma, Youhei et al. | 2010
- 5626
-
Assessment of Tumor Metastasis by the Direct Determination of Cell‐Membrane Sialic Acid ExpressionMatsumoto, Akira / Cabral, Horacio / Sato, Naoko / Kataoka, Kazunori / Miyahara, Yuji et al. | 2010
- 5626
-
Assessment of Tumor Metastasis by the Direct Determination of Cell-Membrane Sialic Acid Expression This research was supported in part by the JST, CREST.Matsumoto, Akira et al. | 2010
- 5630
-
Ultrasensitive Detection of microRNAs by Exponential Isothermal AmplificationJia, Hongxia / Li, Zhengping / Liu, Chenghui / Cheng, Yongqiang et al. | 2010
- 5630
-
Ultrasensitive Detection of microRNAs by Exponential Isothermal Amplification This project was supported by the National Natural Science Foundation of China (20925519, 20875021) and the National Science Foundation of Hebei Province (B2009001525).Jia, Hongxia et al. | 2010
- 5634
-
Coherent Quenching of a Fluorophore for the Design of a Highly Sensitive In‐Stem Molecular BeaconHara, Yuichi / Fujii, Taiga / Kashida, Hiromu / Sekiguchi, Koji / Liang, Xingguo / Niwa, Kosuke / Takase, Tomokazu / Yoshida, Yasuko / Asanuma, Hiroyuki et al. | 2010
- 5634
-
Coherent Quenching of a Fluorophore for the Design of a Highly Sensitive In-Stem Molecular Beacon This work was supported by the Core Research for Evolution Science and Technology (CREST) (Japan) Science and Technology Agency (JST). Partial support by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology (Japan) is also acknowledged.Hara, Yuichi et al. | 2010
- 5639
-
The Catalytic Z to E Isomerization of Stilbenes in a Photosensitizing Porous Coordination NetworkOhara, Kazuaki / Inokuma, Yasuhide / Fujita, Makoto et al. | 2010
- 5639
-
The Catalytic Z to E Isomerization of Stilbenes in a Photosensitizing Porous Coordination Network This research was supported by the CREST project of the Japan Science and Technology Agency (JST), for which M.F. is the principal investigator, and also in part by KAKENHI (20044006), JSPS, and Global COE Program (Chemistry Innovation through Cooperation of Science and Engineering), MEXT (Japan).Ohara, Kazuaki et al. | 2010
- 5642
-
Selective and Flexible Transformation of Biomass‐Derived Platform Chemicals by a Multifunctional Catalytic SystemGeilen, Frank M. A. / Engendahl, Barthel / Harwardt, Andreas / Marquardt, Wolfgang / Klankermayer, Jürgen / Leitner, Walter et al. | 2010
- 5642
-
Selective and Flexible Transformation of Biomass-Derived Platform Chemicals by a Multifunctional Catalytic System This work was performed as part of the Cluster of Excellence "Tailor-Made Fuels from Biomass" (TMFB), which is funded by the Excellence Initiative of the German federal and state governments to promote science and research at German universities.Geilen, FrankM.A. et al. | 2010
- 5647
-
Combining Metallasupramolecular Chemistry with Dynamic Covalent Chemistry: Synthesis of Large Molecular CagesGranzhan, Anton / Riis‐Johannessen, Thomas / Scopelliti, Rosario / Severin, Kay et al. | 2010
- 5647
-
Combining Metallasupramolecular Chemistry with Dynamic Covalent Chemistry: Synthesis of Large Molecular Cages This work was supported by funding from the Swiss National Science Foundation and by the EPFL. We thank Dr. Laura Menin (EPFL) for help with mass spectrometry and Dr. Antonia Neels (CSEM, Neuchâtel) for powder XRD measurements.Granzhan, Anton et al. | 2010
- 5651
-
Gold‐Catalyzed Intramolecular Aminoarylation of Alkenes: CC Bond Formation through Bimolecular Reductive EliminationBrenzovich, William E. Jr. / Benitez, Diego / Lackner, Aaron D. / Shunatona, Hunter P. / Tkatchouk, Ekaterina / Goddard, William A. III / Toste, F. Dean et al. | 2010
- 5651
-
Gold-Catalyzed Intramolecular Aminoarylation of Alkenes: CC Bond Formation through Bimolecular Reductive Elimination F.D.T. gratefully acknowledges NIHGMS (R01 GM073932-04S1), Novartis, and Amgen for funding and Johnson Matthey for a generous donation of AuCl3. The MSC computational facilities were funded by grants from ARO-DURIP and ONR-DURIP.Brenzovich, William E. et al. | 2010
- 5655
-
Fused Pyrene-Diporphyrins: Shifting Near-Infrared Absorption to 1.5 mm and BeyondDiev, V. V. / Hanson, K. / Zimmerman, J. D. / Forrest, S. R. / Thompson, M. E. et al. | 2010
- 5655
-
Fused Pyrene-Diporphyrins: Shifting Near-Infrared Absorption to 1.5µm and Beyond We thank the Defense Advanced Research Projects Agency HARDI Program and Universal Display Corp. for their partial financial support. The views, opinions, and/or findings contained in this article/presentation are those of the author/presenter and should not be interpreted as representing the official views or policies, either expressed or implied, of the Defense Advanced Research Projects Agency or the Department of Defense.Diev, VyacheslavV. et al. | 2010
- 5655
-
Fused Pyrene–Diporphyrins: Shifting Near‐Infrared Absorption to 1.5 μm and BeyondDiev, Vyacheslav V. / Hanson, Kenneth / Zimmerman, Jeramy D. / Forrest, Stephen R. / Thompson, Mark E. et al. | 2010
- 5659
-
Stereoselective Total Synthsis of (±)-UrechitolA We are grateful to Dr. L.M. Peña-Rodríguez for providing NMR spectra of natural urechitolA.Sumiya, Tatsunobu et al. | 2010
- 5659
-
Stereoselective Total Synthsis of (±)‐Urechitol ASumiya, Tatsunobu / Ishigami, Ken / Watanabe, Hidenori et al. | 2010
- 5661
-
Modular Synthesis of 1,2-Diamine Derivatives by Palladium-Catalyzed Aerobic Oxidative Cyclization of Allylic Sulfamides We thank Dr. ChristopherC. Scarborough for helpful discussions, Dr. I.A. Guzei and L.C. Spencer for X-ray crystallographic assistance, and Dr. C.G. Fry for NMR spectroscopic assistance. We are grateful for financial support from the NIH (R01 GM67163) and Abbott Laboratories (graduate fellowship for R.I.M.).McDonald, RichardI. et al. | 2010
- 5661
-
Modular Synthesis of 1,2‐Diamine Derivatives by Palladium‐Catalyzed Aerobic Oxidative Cyclization of Allylic SulfamidesMcDonald, Richard I. / Stahl, Shannon S. et al. | 2010
- 5665
-
Probing the Mechanism of Olefin Metathesis in Grubbs–Hoveyda and Grela Type ComplexesVorfalt, Tim / Wannowius, Klaus‐Jürgen / Plenio, Herbert et al. | 2010
- 5665
-
Probing the Mechanism of Olefin Metathesis in Grubbs-Hoveyda and Grela Type Complexes This work was supported by the DFG via Pl 178/8-3.Vorfalt, Tim et al. | 2010
- 5669
-
Selective Discharge of Electrostatic Charges on Electrets Using a Patterned Hydrogel Stamp This research was supported by the National Science Foundation of China under grant Nos. 20674096, 20733001, and 50773092.Ma, Xinlei et al. | 2010
- 5669
-
Selective Discharge of Electrostatic Charges on Electrets Using a Patterned Hydrogel StampMa, Xinlei / Zhao, Dan / Xue, Mianqi / Wang, Hai / Cao, Tingbing et al. | 2010
- 5673
-
Synthesis of Polyarylated Methanes through Cross-Coupling of Tricarbonylchromium-Activated Benzyllithiums This research was supported by the National Institutes of Health, General Medical Sciences (GM058101), and National Science Foundation (CHE-0848467). J.T. is a Vagelos Scholar.McGrew, GenetteI. et al. | 2010
- 5673
-
Synthesis of Polyarylated Methanes through Cross‐Coupling of Tricarbonylchromium‐Activated BenzyllithiumsMcGrew, Genette I. / Temaismithi, Jesada / Carroll, Patrick J. / Walsh, Patrick J. et al. | 2010
- 5677
-
Supported Gold and Silver Nanoparticles for Catalytic Deoxygenation of Epoxides into Alkenes This work was supported by a Grant-in-Aid for Scientific Research on Priority Areas (No.18065016, "Chemistry of Concerto Catalysis") from the Ministry of Education, Culture, Sports, Science and Technology (Japan). Y.M. thanks the JSPS Research Fellowships for Young Scientists, and extends his special thanks to The Global COE (center of excellence) Program "Global Education and Research Center for Bio-Environmental Chemistry" of Osaka University. Some of the experiments were carried out at the Research Center for Ultrahigh Voltage Electron Microscopy, Osaka University. We thank Drs. Uruga, Tanida, Honma, Taniguchi, and Hirayama (SPring-8) for X-ray absorption fine structure (XAFS) measurements.Mitsudome, Takato et al. | 2010
- 5677
-
Supported Gold and Silver Nanoparticles for Catalytic Deoxygenation of Epoxides into AlkenesMitsudome, Takato / Noujima, Akifumi / Mikami, Yusuke / Mizugaki, Tomoo / Jitsukawa, Koichiro / Kaneda, Kiyotomi et al. | 2010
- 5681
-
Hydrodeoxygenation of Lignin-Derived Phenols into Alkanes by Using Nanoparticle Catalysts Combined with Brønsted Acidic Ionic Liquids This research was performed in the framework of Sino-Swiss Science & Technology Cooperation Program (No. 2010DFA42110).Yan, Ning et al. | 2010
- 5681
-
Hydrodeoxygenation of Lignin-Derived Phenols into Alkanes by Using Nanoparticle Catalysts Combined with Bronsted Acidic Ionic LiquidsYan, N. / Yuan, Y. / Dykeman, R. / Kou, Y. / Dyson, P. J. et al. | 2010
- 5681
-
Hydrodeoxygenation of Lignin‐Derived Phenols into Alkanes by Using Nanoparticle Catalysts Combined with Brønsted Acidic Ionic LiquidsYan, Ning / Yuan, Yuan / Dykeman, Ryan / Kou, Yuan / Dyson, Paul J. et al. | 2010
- 5686
-
Artificial Genetic Systems: Self-Avoiding DNA in PCR and Multiplexed PCR This research was supported by a grant from Nucleic Acids Licensing LLC and by the National Human Genome Research Institute under 1R01 HG004831 and the Defense Threat Reduction Agency under its basic research program (HDTRA-08-1-0052).Hoshika, Shuichi et al. | 2010
- 5686
-
Artificial Genetic Systems: Self‐Avoiding DNA in PCR and Multiplexed PCRHoshika, Shuichi / Chen, Fei / Leal, Nicole A. / Benner, Steven A. et al. | 2010
- 5690
-
Enantioselective Oxidative Cross‐Coupling Reaction of 3‐Indolylmethyl CH Bonds with 1,3‐Dicarbonyls Using a Chiral Lewis Acid‐Bonded Nucleophile to Control StereochemistryGuo, Chang / Song, Jin / Luo, Shi‐Wei / Gong, Liu‐Zhu et al. | 2010
- 5690
-
Enantioselective Oxidative Cross-Coupling Reaction of 3-Indolylmethyl CH Bonds with 1,3-Dicarbonyls Using a Chiral Lewis Acid-Bonded Nucleophile to Control Stereochemistry We are grateful for financial support from MOST (973 project 2009CB825300) and the Ministry of Education.Guo, Chang et al. | 2010
- 5695
-
Preparation and Regioselective Diels–Alder Reactions of Borylbenzynes: Synthesis of Functionalized ArylboronatesIkawa, Takashi / Takagi, Akira / Kurita, Yurio / Saito, Kozumo / Azechi, Kenji / Egi, Masahiro / Kakiguchi, Keisuke / Kita, Yasuyuki / Akai, Shuji et al. | 2010
- 5695
-
Preparation and Regioselective Diels-Alder Reactions of Borylbenzynes: Synthesis of Functionalized Arylboronates This work was supported by KAKENHI (No. 19890182) and a Grant-in-Aid for the Global COE Program from MEXT. T.I. is also grateful for receiving the Daicel Chemical Industry Award in Synthetic Organic Chemistry (Japan). Prof.Dr. Philip Hawke is acknowledged for assistance in preparation of this manuscript.Ikawa, Takashi et al. | 2010
- 5699
-
Chiral Ammonium Betaines as Ionic Nucleophilic Catalysts This work has been supported by the Sumitomo Foundation, the Global COE program in Chemistry of Nagoya University, and the Tatematsu Foundation.Uraguchi, Daisuke et al. | 2010
- 5699
-
Chiral Ammonium Betaines as Ionic Nucleophilic CatalystsUraguchi, Daisuke / Koshimoto, Kyohei / Miyake, Shuhei / Ooi, Takashi et al. | 2010
- 5702
-
A Monomeric Dilithio Methandiide with a Distorted trans-Planar Four-Coordinate Carbon We thank the Royal Society, the EPSRC, the European Research Council, and the University of Nottingham for generously supporting this work.Cooper, OliverJ. et al. | 2010
- 5702
-
A Monomeric Dilithio Methandiide with a Distorted trans‐Planar Four‐Coordinate CarbonCooper, Oliver J. / Wooles, Ashley J. / McMaster, Jonathan / Lewis, William / Blake, Alexander J. / Liddle, Stephen T. et al. | 2010
- 5706
-
Total Synthesis and Structural Reassignment of (+)-Dictyosphaeric AcidA: A Tandem Intramolecular Michael Addition/Alkene Migration Approach We thank the BBSRC for studentship funding (A.R.B.), GlaxoSmithKline for CASE support, and the University of York for post-doctoral funding (G.D.M.). We are also grateful to Dr. A.C. Whitwood and R. Thatcher (University of York) for X-ray crystallography studies and to Dr. T. Dransfield (University of York) for invaluable assistance with mass spectrometry. We would also like to thank Prof. C.M. Ireland (University of Utah) for providing us with copies of 1H and 13CNMR spectra for compounds 1 and 2, and for helpful discussions. We also thank Dr. C.W. Barfoot for carrying out relevant model studies (to be reported in a full paper) and Archimica for a kind gift of T3P.Burns, AlanR. et al. | 2010
- 5706
-
Total Synthesis and Structural Reassignment of (+)‐Dictyosphaeric Acid A: A Tandem Intramolecular Michael Addition/Alkene Migration ApproachBurns, Alan R. / McAllister, Graeme D. / Shanahan, Stephen E. / Taylor, Richard J. K. et al. | 2010
- 5713
-
Vorschau: Angew. Chem. 33/2010| 2010