Blue-Green Up-Conversion: Noncoherent Excitation by NIR Light (English)
- New search for: Baluschev, S.
- New search for: Yakutkin, V.
- New search for: Miteva, T.
- New search for: Avlasevich, Y.
- New search for: Chernov, S.
- New search for: Aleshchenkov, S.
- New search for: Nelles, G.
- New search for: Cheprakov, A.
- New search for: Yasuda, A.
- New search for: Mullen, K.
- New search for: Baluschev, S.
- New search for: Yakutkin, V.
- New search for: Miteva, T.
- New search for: Avlasevich, Y.
- New search for: Chernov, S.
- New search for: Aleshchenkov, S.
- New search for: Nelles, G.
- New search for: Cheprakov, A.
- New search for: Yasuda, A.
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In:
ANGEWANDTE CHEMIE -INTERNATIONAL EDITION IN ENGLISH-
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46
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7693-7696
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2007
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ISSN:
- Article (Journal) / Print
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Title:Blue-Green Up-Conversion: Noncoherent Excitation by NIR Light
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Contributors:Baluschev, S. ( author ) / Yakutkin, V. ( author ) / Miteva, T. ( author ) / Avlasevich, Y. ( author ) / Chernov, S. ( author ) / Aleshchenkov, S. ( author ) / Nelles, G. ( author ) / Cheprakov, A. ( author ) / Yasuda, A. ( author ) / Mullen, K. ( author )
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Published in:ANGEWANDTE CHEMIE -INTERNATIONAL EDITION IN ENGLISH- ; 46, 40 ; 7693-7696
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Publisher:
- New search for: John Wiley & Sons, Ltd
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Publication date:2007-01-01
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Size:4 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 540.5 / 540
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Table of contents – Volume 46, Issue 40
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 7519
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Cover Picture: Synthesis of Azadirachtin: A Long but Successful Journey (Angew. Chem. Int. Ed. 40/2007)Veitch, Gemma E. / Beckmann, Edith / Burke, Brenda J. / Boyer, Alistair / Maslen, Sarah L. / Ley, Steven V. et al. | 2007
- 7520
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Inside Cover: Molecular Switches Flipped by Oxygen (Angew. Chem. Int. Ed. 40/2007)Zehm, Daniel / Fudickar, Werner / Linker, Torsten et al. | 2007
- 7523
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Graphical Abstract: Angew. Chem. Int. Ed. 40/2007| 2007
- 7536
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Spotlights on our sister journals: Angew. Chem. Int. Ed. 40/2007| 2007
- 7538
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Makoto Kumada (1920–2007)Tamao, Kohei et al. | 2007
- 7540
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Calculated Risks. The Toxicity and Human Health Risk of Chemicals in our Environment. 2nd ed. Edited by Joseph V. Rodricks.Greim, Helmut et al. | 2007
- 7541
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Collidal Particles at Liquid Interfaces. Edited by Bernard P. Binks and Tommy S. Horozov.Hellweg, Thomas et al. | 2007
- 7544
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Heterodimerization of Olefins: A Highly Promising Strategy for the Selective Synthesis of Functionalized AlkenesGooßen, Lukas J. / Rodríguez, Nuria et al. | 2007
- 7548
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Mesoporous Materials for Drug DeliveryVallet‐Regí, María / Balas, Francisco / Arcos, Daniel et al. | 2007
- 7560
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Hierarchical Nanomanufacturing: From Shaped Zeolite Nanoparticles to High‐Performance Separation MembranesSnyder, Mark A. / Tsapatsis, Michael et al. | 2007
- 7574
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Self-Assembly of Polyoxo Clusters and Extended Frameworks by Controlled Hydrolysis of Low-Valent UraniumFNR 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. | 2007
- 7574
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Self‐Assembly of Polyoxo Clusters and Extended Frameworks by Controlled Hydrolysis of Low‐Valent UraniumNocton, Grégory / Burdet, Fabien / Pécaut, Jacques / Mazzanti, Marinella et al. | 2007
- 7579
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Modular Assembly of a Functional Polyoxometalate-Based Open Framework Constructed from Unsupported AgIsssAgI InteractionsStreb, C. / Ritchie, C. / Long, D. L. / Kogerler, P. / Cronin, L. et al. | 2007
- 7579
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Modular Assembly of a Functional Polyoxometalate‐Based Open Framework Constructed from Unsupported AgI⋅⋅⋅AgI InteractionsStreb, Carsten / Ritchie, Chris / Long, De‐Liang / Kögerler, Paul / Cronin, Leroy et al. | 2007
- 7579
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Modular Assembly of a Functional Polyoxometalate-Based Open Framework Constructed from Unsupported AgI···AgI InteractionsFNR HREF="nss"> FN ID="nss"> We thank the EPSRC, WestCHEM and the University of Glasgow for supporting this work.Streb, Carsten et al. | 2007
- 7583
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Allosteric Control of Self-Assembly: Modulating the Formation of Guanine Quadruplexes through Orthogonal Aromatic InteractionsFNR HREF="nss"> FN ID="nss"> This study has been partially supported by the National Science Foundation and the National Institutes of Health (GM 35208).Jayawickramarajah, Janarthanan et al. | 2007
- 7583
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Allosteric Control of Self‐Assembly: Modulating the Formation of Guanine Quadruplexes through Orthogonal Aromatic InteractionsJayawickramarajah, Janarthanan / Tagore, Debarati M. / Tsou, Lun K. / Hamilton, Andrew D. et al. | 2007
- 7587
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Rational Design of “Turn‐On” Allosteric DNAzyme Catalytic Beacons for Aqueous Mercury Ions with Ultrahigh Sensitivity and SelectivityLiu, Juewen / Lu, Yi et al. | 2007
- 7587
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Rational Design of "Turn-On" Allosteric DNAzyme Catalytic Beacons for Aqueous Mercury Ions with Ultrahigh Sensitivity and SelectivityFNR HREF="nss"> FN ID="nss"> This material is based upon work supported by the U.S. Department of Energy (DE-FG02-01-ER63179), the National Science Foundation (DMI-0328162 and CTS-0120978), and by the Illinois Waste Management and Research Center.Liu, Juewen et al. | 2007
- 7591
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Neutral Desorption Sampling of Living Objects for Rapid Analysis by Extractive Electrospray Ionization Mass SpectrometryChen, Huanwen / Yang, Shuiping / Wortmann, Arno / Zenobi, Renato et al. | 2007
- 7591
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Neutral Desorption Sampling of Living Objects for Rapid Analysis by Extractive Electrospray Ionization Mass SpectrometryFNR HREF="nss"> FN ID="nss"> This work is partly supported by a grant from NNSFC (No.20505003). H.W.C. sincerely acknowledges support from a Wilheem Simon Fellowship from the CEAC at ETH Zurich.Chen, Huanwen et al. | 2007
- 7595
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Cyclic Luciferase for Real‐Time Sensing of Caspase‐3 Activities in Living MammalsKanno, Akira / Yamanaka, Yuko / Hirano, Hisashi / Umezawa, Yoshio / Ozawa, Takeaki et al. | 2007
- 7595
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Cyclic Luciferase for Real-Time Sensing of Caspase-3 Activities in Living MammalsFNR HREF="nss"> FN ID="nss"> This work was supported by grants from the Japan Science and Technology Agency (JST), the Japan Society for the Promotion of Science (JSPS), and the New Energy and Industrial Technology Development Organization (NEDO) of Japan.Kanno, Akira et al. | 2007
- 7600
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Optically Triggered Release of DNA from Multivalent Dendrons by Degrading and Charge-Switching MultivalencyFNR HREF="nss"> FN ID="nss"> This work was supported by the Finnish National Graduate School in Nanoscience (M.A.K.) and partly carried out in the Centre of Excellence of Academy of Finland (Bio- and Nanopolymers Research Group, 77317). The Research Foundation of Orion Corporation is gratefully acknowledged for a study grant. We acknowledge Dr. Markus Linder and Samuli Hirsjärvi for discussions and support.Kostiainen, Mauri A et al. | 2007
- 7600
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Optically Triggered Release of DNA from Multivalent Dendrons by Degrading and Charge‐Switching MultivalencyKostiainen, Mauri A. / Smith, David K. / Ikkala, Olli et al. | 2007
- 7605
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Two‐Dimensional Helix‐Bundle Formation of a Dynamic Helical Poly(phenylacetylene) with Achiral Pendant Groups on GraphiteSakurai, Shin‐ichiro / Ohsawa, Sousuke / Nagai, Kanji / Okoshi, Kento / Kumaki, Jiro / Yashima, Eiji et al. | 2007
- 7609
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χ(4) Raman Spectroscopy for Buried Water InterfacesYamaguchi, Shoichi / Tahara, Tahei et al. | 2007
- 7609
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chi(4) Raman spectroscopy for buried water interfacesYamaguchi, Shoichi / Tahara, Tahei et al. | 2007
- 7613
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Direct Visualization of Enantiospecific Substitution of Chiral Guest Molecules into Heterochiral Molecular Assemblies at SurfacesLiu, Ning / Haq, Sam / Darling, George R. / Raval, Rasmita et al. | 2007
- 7613
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Direct Visualization of Enantiospecific Substitution of Chiral Guest Molecules into Heterochiral Molecular Assemblies at SurfacesFNR HREF="nss"> FN ID="nss"> We are thankful for grants from EPSRC and BBSRC and EU Marie-Curie CHEXTAN network MRTN-CT-2004-512161. The authors declare no competing financial interests.Liu, Ning et al. | 2007
- 7617
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1:1 Cross‐Assembly of Two β‐Diketonate Complexes through Arene–Perfluoroarene InteractionsHori, Akiko / Shinohe, Ayaka / Yamasaki, Mikio / Nishibori, Eiji / Aoyagi, Shinobu / Sakata, Makoto et al. | 2007
- 7617
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1:1 Cross-Assembly of Two β-Diketonate Complexes through Arene-Perfluoroarene InteractionsFNR HREF="nss"> FN ID="nss"> This work was supported by a Grant-in-Aid for Young Scientists Start-Up (no. 18850022) from the JSPS (A.H.) and a Grant-in-Aid for Young Scientists A (no. 17686003) from MEXT (E.N.). A.H. and A.S. thank Prof. Dr. Takeshi Miyamoto of Kitasato University for valuable suggestions. Thanks are also due to Professors Makoto Fujita and Masaki Kawano of the University of Tokyo for the opportunity to carry out solid-state luminescence and UV-Vis measurements. The synchrotron radiation experiments were performed at beamline BL02B2 at SPring-8 with the approval of JASRI.Hori, Akiko et al. | 2007
- 7617
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1:1 Cross-Assembly of Two b-Diketonate Complexes through Arene-Perfluoroarene InteractionsHori, A. / Shinohe, A. / Yamasaki, M. / Nishibori, E. / Aoyagi, S. / Sakata, M. et al. | 2007
- 7617
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1:1 cross-assembly of two beta-diketonate complexes through arene-perfluoroarene interactionsHori, Akiko / Shinohe, Ayaka / Yamasaki, Mikio / Nishibori, Eiji / Aoyagi, Shinobu / Sakata, Makoto et al. | 2007
- 7621
-
A Selective Chemical Probe for Coenzyme A‐Requiring EnzymesHwang, Yousang / Thompson, Paul R. / Wang, Ling / Jiang, Lihua / Kelleher, Neil L. / Cole, Philip A. et al. | 2007
- 7621
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A Selective Chemical Probe for Coenzyme A-Requiring EnzymesFNR HREF="nss"> FN ID="nss"> We are grateful for financial support from the NIH, the Kaufman Foundation, and to Cole laboratory members for advice and discussion.Hwang, Yousang et al. | 2007
- 7625
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Water-Tolerant, Highly Active Solid Acid Catalysts Composed of the Keggin-Type Polyoxometalate H3PW12O40 Immobilized in Hydrophobic Nanospaces of Organomodified Mesoporous SilicaFNR HREF="nss"> FN ID="nss"> This work was partly supported by a CREST project from the Japan Science and Technology Agency (JST), by Grant-in-Aid on Priority Areas (417) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), and by Grant-in-Aid for Scientific Research (S, B) and for Creative Scientific Research from the Japan Society for the Promotion of Science (JSPS).Inumaru, Kei et al. | 2007
- 7625
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Water‐Tolerant, Highly Active Solid Acid Catalysts Composed of the Keggin‐Type Polyoxometalate H3PW12O40 Immobilized in Hydrophobic Nanospaces of Organomodified Mesoporous SilicaInumaru, Kei / Ishihara, Toru / Kamiya, Yuichi / Okuhara, Toshio / Yamanaka, Shoji et al. | 2007
- 7629
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Synthesis of Azadirachtin: A Long but Successful JourneyVeitch, Gemma E. / Beckmann, Edith / Burke, Brenda J. / Boyer, Alistair / Maslen, Sarah L. / Ley, Steven V. et al. | 2007
- 7629
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Synthesis of Azadirachtin: A Long but Successful JourneyFNR HREF="nss"> FN ID="nss"> We gratefully acknowledge the many co-workers who have worked on this project and the EPSRC (G.E.V. and A.B.), Alexander von Humboldt Foundation (E.B.), and Novartis (S.V.L.) for generous funding.Veitch, Gemma E et al. | 2007
- 7633
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A Relay Route for the Synthesis of AzadirachtinVeitch, Gemma E. / Beckmann, Edith / Burke, Brenda J. / Boyer, Alistair / Ayats, Carles / Ley, Steven V. et al. | 2007
- 7633
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A Relay Route for the Synthesis of AzadirachtinFNR HREF="nss"> FN ID="nss"> We gratefully acknowledge the many co-workers who have worked on this project and the EPSRC (G.E.V. and A.B.), Alexander von Humboldt Foundation (E.B.), and Novartis (S.V. L.) for generous funding.Veitch, Gemma E et al. | 2007
- 7636
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Cellulose Conversion into Polyols Catalyzed by Reversibly Formed Acids and Supported Ruthenium Clusters in Hot WaterLuo, Chen / Wang, Shuai / Liu, Haichao et al. | 2007
- 7636
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Cellulose Conversion into Polyols Catalyzed by Reversibly Formed Acids and Supported Ruthenium Clusters in Hot WaterFNR HREF="nss"> FN ID="nss"> This work was supported by the National Basic Research Project of China (No. 2006CB806100) and NSFC (Grant Nos. 20673005 and 20573004). This work was also supported in part by the Program for New Century Excellent Talents in University,(NECT-05-0010), State Education Ministry.Luo, Chen et al. | 2007
- 7640
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Towards Molecular Magnetic Switching with an Electric BiasDiefenbach, Martin / Kim, Kwang S. et al. | 2007
- 7640
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Towards Molecular Magnetic Switching with an Electric BiasFNR HREF="nss"> FN ID="nss"> Financial support by the Global Research Laboratory (GRL) project of KOSEF and BK21 is acknowledged. Computations were carried out at the Korea Supercomputing Centre (KSC) and at the Samsung Corporate R&D Headquarters (Samsung Adv. Inst. Tech.).Diefenbach, Martin et al. | 2007
- 7644
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Push-Pull Molybdenum Trisdithiolenes Allow Rapid Nonconventional Binding of Ethylene at Ligand Sulfur AtomsFNR HREF="nss"> FN ID="nss"> This work was supported by the Natural Sciences and Engineering Research Council (NSERC) of Canada, the Canadian Foundation for Innovation, the Ontario Research Fund, and the University of Toronto.Harrison, Daniel J et al. | 2007
- 7644
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Push–Pull Molybdenum Trisdithiolenes Allow Rapid Nonconventional Binding of Ethylene at Ligand Sulfur AtomsHarrison, Daniel J. / Lough, Alan J. / Nguyen, Neilson / Fekl, Ulrich et al. | 2007
- 7648
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Highly Enantioselective Reactions of α‐Sulfonyl Carbanions of Trifluoromethyl SulfonesNakamura, Shuichi / Hirata, Norimune / Kita, Takeshi / Yamada, Ryusuke / Nakane, Daisuke / Shibata, Norio / Toru, Takeshi et al. | 2007
- 7648
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Highly Enantioselective Reactions of a-Sulfonyl Carbanions of Trifluoromethyl SulfonesNakamura, S. / Hirata, N. / Kita, T. / Yamada, R. / Nakane, D. / Shibata, N. / Toru, T. et al. | 2007
- 7648
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Highly Enantioselective Reactions of α-Sulfonyl Carbanions of Trifluoromethyl SulfonesFNR HREF="nss"> FN ID="nss"> We thank Dr. Jon Bordner, Shin-ichi Sakemi, and Dr. Masami Nakane, Pfizer Inc., for X-ray crystallographic analysis. This work was partly supported by the Asahi Glass Foundation.Nakamura, Shuichi et al. | 2007
- 7651
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Highly Diastereoselective Formation of Ruthenium Complexes for Efficient Catalytic Asymmetric Transfer HydrogenationFNR HREF="nss"> FN ID="nss"> This work was supported by the Ministero dell'Università e della Ricerca (MUR). We thank Johnson-Matthey-Alfa Aesar for a generous loan of ruthenium, and Stephan D. Hoffmann (TU München) for his help during the course of the X-ray measurements.Baratta, Walter et al. | 2007
- 7651
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Highly Diastereoselective Formation of Ruthenium Complexes for Efficient Catalytic Asymmetric Transfer HydrogenationBaratta, Walter / Chelucci, Giorgio / Herdtweck, Eberhardt / Magnolia, Santo / Siega, Katia / Rigo, Pierluigi et al. | 2007
- 7655
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Alkyl Radical Generation in Water under Ambient Conditions- A New Look at the Guareschi Reaction of 1897FNR HREF="nss"> FN ID="nss"> We thank the EU for award of a Marie Curie Host Fellowship (HPMT-CT-2001-00317) for supporting the exchange of M.P. from the University of Florence, 2005. B.N. acknowledges the award of Clarendon and ORS Scholarships from Oxford. We thank Prof. Tito Scaiano (Ottawa) and Prof. Allen Hill (Oxford) for very useful discussions. A.S.D. is indebted to the Russian Science Support Foundation for a postgraduate scholarship in 2007. For X-ray structures we thank Dr. Andrew Cowley and Dr. Amber Thompson.Nguyen, Bao et al. | 2007
- 7655
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Alkyl Radical Generation in Water under Ambient Conditions— A New Look at the Guareschi Reaction of 1897Nguyen, Bao / Chernous, Katya / Endlar, Daniel / Odell, Barbara / Piacenti, Michela / Brown, John M. / Dorofeev, Alexander S. / Burasov, Alexander V. et al. | 2007
- 7659
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Facile Shape-Controlled Synthesis of Well-Aligned Nanowire Architectures in Binary Aqueous SolutionFNR HREF="nss"> FN ID="nss"> This work was supported by the National Basic Research Program of China (2006CB705703).Shen, Xiao-Fang et al. | 2007
- 7659
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Facile Shape‐Controlled Synthesis of Well‐Aligned Nanowire Architectures in Binary Aqueous SolutionShen, Xiao‐Fang / Yan, Xiu‐Ping et al. | 2007
- 7664
-
An Alkyne Strategy for the Asymmetric Synthesis of Natural Products: Application to (+)-Spirolaxine Methyl EtherFNR HREF="nss"> FN ID="nss"> We thank NIH (GM 13598) and the National Science Foundation for the generous support of our programs. A.H.W. thanks GlaxoSmithKline (ACS Division of Organic Chemistry Fellowship) and Bristol-Myers Squibb (for a graduate fellowship). Mass spectra were provided by the Mass Spectrometry Regional Center of the University of California, San Francisco, which is supported by the NIH Division of Research Resources. Palladium salts were generously supplied by Johnson-Matthey.Trost, Barry M et al. | 2007
- 7664
-
An Alkyne Strategy for the Asymmetric Synthesis of Natural Products: Application to (+)‐Spirolaxine Methyl EtherTrost, Barry M. / Weiss, Andrew H. et al. | 2007
- 7667
-
Enantioselective 1,3‐Dipolar Cycloaddition of Cyclic Enones Catalyzed by Multifunctional Primary Amines: Beneficial Effects of Hydrogen BondingChen, Wei / Du, Wei / Duan, Yong‐Zheng / Wu, Yong / Yang, Sheng‐Yong / Chen, Ying‐Chun et al. | 2007
- 7667
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Enantioselective 1,3-Dipolar Cycloaddition of Cyclic Enones Catalyzed by Multifunctional Primary Amines: Beneficial Effects of Hydrogen BondingFNR HREF="nss"> FN ID="nss"> We are grateful for the financial support from the NSFC (20502018), Ministry of Education (NCET-05-0781), Fok Ying Tung Education Foundation (101037), and Sichuan Province Government (07ZQ026-027).Chen, Wei et al. | 2007
- 7671
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Total Synthesis of (+)-FawcettimineFNR HREF="nss"> FN ID="nss"> We gratefully acknowledge the University of California, Berkeley, NIHGMS (R01 GM073932-01), Merck Research Laboratories, Bristol-Myers Squibb, Amgen Inc., DuPont, GlaxoSmithKline, Eli Lilly & Co., Pfizer, AstraZeneca, and Roche for financial support.Linghu, Xin et al. | 2007
- 7671
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Total Synthesis of (+)‐FawcettimineLinghu, Xin / Kennedy‐Smith, Joshua J. / Toste, F. Dean et al. | 2007
- 7674
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Reductive Elimination of Ether from T-Shaped, Monomeric Arylpalladium AlkoxidesFNR HREF="nss"> FN ID="nss"> We are grateful to the NIH-NIGMS (GM-55382) for support of this work and Johnson-Matthey for palladium.Stambuli, James P et al. | 2007
- 7674
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Reductive Elimination of Ether from T‐Shaped, Monomeric Arylpalladium AlkoxidesStambuli, James P. / Weng, Zhiqiang / Incarvito, Christopher D. / Hartwig, John F. et al. | 2007
- 7678
-
Electrochemical Sensor with Record Performance CharacteristicsKaryakin, Arkady A. / Puganova, Elena A. / Bolshakov, Ivan A. / Karyakina, Elena E. et al. | 2007
- 7681
-
Direct Magnesiation of Polyfunctionalized Arenes and Heteroarenes Using (tmp)2Mg⋅2 LiClClososki, Giuliano C. / Rohbogner, Christoph J. / Knochel, Paul et al. | 2007
- 7681
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Direct Magnesiation of Polyfunctionalized Arenes and Heteroarenes Using (tmp)2Mg·2 LiClFNR HREF="nss"> FN ID="nss"> We thank the Fonds der Chemischen Industrie and the Deutsche Forschungsgemeinschaft (DFG) for financial support. G.C.C. thanks the Humboldt Foundation for a fellowship. We also thank Chemetall GmbH (Frankfurt), Degussa GmbH (Hanau), and BASF AG (Ludwigshafen) for generous gifts of chemicals.Clososki, Giuliano C et al. | 2007
- 7681
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Direct Magnesiation of Polyfunctionalized Arenes and Heteroarenes Using (tmp)2Mgs2 LiClClososki, G. C. / Rohbogner, C. J. / Knochel, P. et al. | 2007
- 7685
-
(tmp)2Zns2 MgCl2s2 LiCl: A Chemoselective Base for the Directed Zincation of Sensitive Arenes and HeteroarenesWunderlich, S. H. / Knochel, P. et al. | 2007
- 7685
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(tmp)2Zn·2 MgCl2·2 LiCl: A Chemoselective Base for the Directed Zincation of Sensitive Arenes and HeteroarenesFNR HREF="nss"> FN ID="nss"> We thank the Fonds der Chemischen Industrie, Merck Research Laboratories (MSD) and the Deutsche Forschungsgemeinschaft (DFG) for financial support. We also thank Degussa GmbH, BASF AG and Chemetall GmbH for the generous gift of chemicals. tmp=2,2,6,6-tetramethylpiperidide.Wunderlich, Stefan H et al. | 2007
- 7685
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(tmp)2Zn⋅2 MgCl2⋅2 LiCl: A Chemoselective Base for the Directed Zincation of Sensitive Arenes and HeteroarenesWunderlich, Stefan H. / Knochel, Paul et al. | 2007
- 7689
-
Molecular Switches Flipped by OxygenZehm, Daniel / Fudickar, Werner / Linker, Torsten et al. | 2007
- 7689
-
Molecular Switches Flipped by OxygenFNR HREF="nss"> FN ID="nss"> This work was generously supported by the DFG.Zehm, Daniel et al. | 2007
- 7693
-
Blue-Green Up-Conversion: Noncoherent Excitation by NIR LightFNR HREF="nss"> FN ID="nss"> S.C., S.A., and A.C. thank the Russian Foundation of Basic Research for the support through grants RFBR-04-03-32650-a and RFBR-07-03-01121-a.Baluschev, Stanislav et al. | 2007
- 7693
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Blue‐Green Up‐Conversion: Noncoherent Excitation by NIR LightBaluschev, Stanislav / Yakutkin, Vladimir / Miteva, Tzenka / Avlasevich, Yuri / Chernov, Sergei / Aleshchenkov, Sergei / Nelles, Gabriele / Cheprakov, Andrei / Yasuda, Akio / Müllen, Klaus et al. | 2007
- 7697
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Saccharin Inhibits Carbonic Anhydrases: Possible Explanation for its Unpleasant Metallic AftertasteKöhler, Karen / Hillebrecht, Alexander / Schulze Wischeler, Johannes / Innocenti, Alessio / Heine, Andreas / Supuran, Claudiu T. / Klebe, Gerhard et al. | 2007
- 7700
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A Microarray Strategy for Mapping the Substrate Specificity of Protein Tyrosine PhosphataseKöhn, Maja / Gutierrez‐Rodriguez, Marta / Jonkheijm, Pascal / Wetzel, Stefan / Wacker, Ron / Schroeder, Hendrik / Prinz, Heino / Niemeyer, Christof M. / Breinbauer, Rolf / Szedlacsek, Stefan E. et al. | 2007
- 7700
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A Microarray Strategy for Mapping the Substrate Specificity of Protein Tyrosine PhosphataseFNR HREF="nss"> FN ID="nss"> This work was supported by the Max-Planck Gesellschaft, the research program "Molecular Basics of Biosciences" of the University of Dortmund, the Fonds der Chemischen Industrie, and the Zentrum für Angewandte Chemische Genomik. P.J. thanks the Alexander von Humboldt Stiftung and S.W. thanks Novartis for a scholarship.Köhn, Maja et al. | 2007
- 7704
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Asymmetric Formation of Allylic Amines with N‐Substituted Quaternary Stereocenters by PdII‐Catalyzed Aza‐Claisen RearrangementsFischer, Daniel F. / Xin, Zhuo‐qun / Peters, René et al. | 2007
- 7704
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Asymmetric Formation of Allylic Amines with N-Substituted Quaternary Stereocenters by PdII-Catalyzed Aza-Claisen RearrangementsFNR HREF="nss"> FN ID="nss"> This work was financially supported by ETH Research Grant TH-30-04-2, Novartis (Ph.D. fellowship to Z.-q.X.) and F. Hoffmann-La Roche.Fischer, Daniel F et al. | 2007
- 7713
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Preview: Angew. Chem. Int. Ed. 41/2007| 2007