Biologisch aktive Moleküle mit "Lichtschalter" (Deutsch)
- Neue Suche nach: Mayer, Günter
- Neue Suche nach: Heckel, Alexander
- Neue Suche nach: Mayer, Günter
- Neue Suche nach: Heckel, Alexander
In:
Angewandte Chemie
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118
, 30
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5020-5042
;
2006
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ISSN:
- Aufsatz (Zeitschrift) / Print
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Titel:Biologisch aktive Moleküle mit "Lichtschalter"
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Weitere Titelangaben:Biologically active molecules with light switches
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Beteiligte:Mayer, Günter ( Autor:in ) / Heckel, Alexander ( Autor:in )
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Erschienen in:Angewandte Chemie ; 118, 30 ; 5020-5042
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Verlag:
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Erscheinungsdatum:2006
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Format / Umfang:23 Seiten, 1 Bild, Quellen
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ISSN:
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Coden:
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DOI:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Print
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Sprache:Deutsch
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Schlagwörter:
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Datenquelle:
Inhaltsverzeichnis – Band 118, Ausgabe 30
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Titelbild: A Ferromagnetically Coupled Mn19 Aggregate with a Record S=83/2 Ground Spin State (Angew. Chem. 30/2006)Ako, Ayuk M. / Hewitt, Ian J. / Mereacre, Valeriu / Clérac, Rodolphe / Wernsdorfer, Wolfgang / Anson, Christopher E. / Powell, Annie K. et al. | 2006
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Supramolekulare Chemie: Echegoyen leitet NSF‐Chemie / Organische Chemie: Curran ausgezeichnet / Organische Chemie: Huisgen geehrt| 2006
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Drug Discovery Handbook. Herausgegeben von Shayne C. Gad.Hölzemann, Günter et al. | 2006
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Nitric Oxide Donors. For Pharmaceutical and Biological Applications. Herausgegeben von Peng G. Wang, Tingwei B. Cai und Naoyuki Taniguchi.Lehmann, Jochen et al. | 2006
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Oberflächenreaktionen “nach Bedarf”: elektrochemische Steuerung von Reaktionen an selbstorganisierten MonoschichtenChoi, Insung S. / Chi, Young Shik et al. | 2006
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Oberflächenreaktionen "nach Bedarf": elektrochemische Steuerung von Reaktionen an selbstorganisierten Monoschichten. Abbildung 1 und Schema 2b wurden freundlicherweise von Prof. Langer und Prof. Kwak zur Verfügung gestellt.Choi, Insung S. et al. | 2006
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Oberflachenreaktionen "nach Bedarf": elektrochemische Steuerung von Reaktionen an selbstorganisierten MonoschichtenChoi, I. S. / Chi, Y. S. et al. | 2006
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Biologisch aktive Moleküle mit “Lichtschalter”Mayer, Günter / Heckel, Alexander et al. | 2006
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Biologisch aktive Molekule mit "Lichtschalter"Mayer, G. / Heckel, A. et al. | 2006
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Formation of Crystalline SrAl2O4 Nanotubes by a Roll‐Up and Post‐Annealing ApproachYe, Changhui / Bando, Yoshio / Shen, Guozhen / Golberg, Dmitri et al. | 2006
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Formation of Crystalline SrAl2O4 Nanotubes by a Roll-Up and Post-Annealing Approach. This work was supported by the Japan Society for the Promotion of Science (JSPS), in the form of a fellowship tenable at the National Institute for Materials Science, Tsukuba, Japan (C.Y.).Ye, Changhui et al. | 2006
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A Ferromagnetically Coupled Mn19 Aggregate with a Record S=83/2 Ground Spin StateAko, Ayuk M. / Hewitt, Ian J. / Mereacre, Valeriu / Clérac, Rodolphe / Wernsdorfer, Wolfgang / Anson, Christopher E. / Powell, Annie K. et al. | 2006
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A Ferromagnetically Coupled Mn19 Aggregate with a Record S=83-2 Ground Spin State. This work was supported by Bordeaux 1 University, the CNRS, the Region Aquitaine, the DFG (SPP 1137 and the Center for Functional Nanostructures), QuEMolNa (MRTN-CT2003-504880), MAGMANet (NMP3-CT-2005-515767), and the Alexander von Humboldt Foundation.Ako, Ayuk M. et al. | 2006
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Efficient Construction of the Clerodane Decalin Core by an Asymmetric Morita-Baylis-Hillman Reaction-Lewis Acid Promoted Annulation Strategy. The authors acknowledge Dr. J. P. Lee (Boston University) for assistance with key NMR experiments and Dr. E. B. Lobkovsky (Cornell University) for X-ray crystallographic analysis. This research was supported by a NSF CAREER grant (CHE-0349206) and Amgen, Inc.Rodgen, Stacy A. et al. | 2006
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Efficient Construction of the Clerodane Decalin Core by an Asymmetric Morita–Baylis–Hillman Reaction/Lewis Acid Promoted Annulation StrategyRodgen, Stacy A. / Schaus, Scott E. et al. | 2006
- 5054
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Metastable Sorption State of a Metal-Organic Porous Material Determined by In Situ Synchrotron Powder Diffraction. This study was supported by CREST-JST and JASRI-SPring-8 Nanotechnology Support Project of the Ministry of Education, Culture, Sports, Science and Technology of Japan. This study was also supported by a Grant-In-Aid for Science Research in a Priority Area "Chemistry of Coordination Space" from the Ministry of Education, Culture, Sports, Science and Technology of Japan. The authors thank Dr. K. Kato for the kind advice and support in data collection and Dr. H. Tanaka for the computer program ENIGMA for the MEM analysis.Kubota, Yoshiki et al. | 2006
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Metastable Sorption State of a Metal–Organic Porous Material Determined by In Situ Synchrotron Powder DiffractionKubota, Yoshiki / Takata, Masaki / Matsuda, Ryotaro / Kitaura, Ryo / Kitagawa, Susumu / Kobayashi, Tatsuo C. et al. | 2006
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HaloTag Protein‐Mediated Site‐Specific Conjugation of Bioluminescent Proteins to Quantum DotsZhang, Yan / So, Min‐kyung / Loening, Andreas M. / Yao, Hequan / Gambhir, Sanjiv S. / Rao, Jianghong et al. | 2006
- 5058
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HaloTag Protein-Mediated Site-Specific Conjugation of Bioluminescent Proteins to Quantum Dots. This work was supported by the Burroughs Wellcome Fund (to J.R.), a Stanford School of Medicine Dean's Fellowship (to Y.Z.), the Korea Research Foundation Grant M07-2004-000-10234-0 (to M.K.S.), a Stanford Bio-X Graduate Fellowship (to A.M.L.), and the National Cancer Institute Centers of Cancer Nanotechnology Excellence (CCNE) U54.Zhang, Yan et al. | 2006
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Switchable Chiral Architectures Containing PrIII Ions: An Example of Solvent‐Induced Adaptive BehaviorMamula, Olimpia / Lama, Marco / Stoeckli‐Evans, Helen / Shova, Sergiu et al. | 2006
- 5062
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Switchable Chiral Architectures Containing PrIII Ions: An Example of Solvent-Induced Adaptive Behavior. This work was supported by the Swiss National Science Foundation (grant no. 200020-105320). We thank Dr. R. Scopelliti for collecting the X-ray data for the compound rac-1, as well as S. Canarelli and F. Nyddegger for the ES-MS measurements.Mamula, Olimpia et al. | 2006
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A Spiropyran‐Based Ensemble for Visual Recognition and Quantification of Cysteine and Homocysteine at Physiological LevelsShao, Na / Jin, Jian Yu / Cheung, Sin Man / Yang, Rong Hua / Chan, Wing Hong / Mo, Tian et al. | 2006
- 5066
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A Spiropyran-Based Ensemble for Visual Recognition and Quantification of Cysteine and Homocysteine at Physiological Levels. This research was supported by the National Outstanding Youth Science Foundation of China (grant no. 20525518) and the National Natural Foundation of China (grant no. 20475005).Shao, Na et al. | 2006
- 5070
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A Simple Strategy for Prompt Visual Sensing by Gold Nanoparticles: General Applications of Interparticle Hydrogen BondsLin, Shu‐Yi / Wu, Sung‐Hsun / Chen, Chun‐hsien et al. | 2006
- 5070
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A Simple Strategy for Prompt Visual Sensing by Gold Nanoparticles: General Applications of Interparticle Hydrogen Bonds. We thank Dr. M.-S. Huang and Ms. S.-F. A. Chan at ITRI (Chutong, Hsinchu) for access to the zeta potential analyzer. The authors acknowledge the National Science Council and National Tsing Hua University for financial and research support.Lin, Shu-Yi et al. | 2006
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The Structure of a Designed Diiron(III) Protein: Implications for Cofactor Stabilization and CatalysisWade, Herschel / Stayrook, Steven E. / DeGrado, William F. et al. | 2006
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The Structure of a Designed Diiron(III) Protein: Implications for Cofactor Stabilization and Catalysis. We thank the National Institutes of Health (GM65416) and the NSF (DMR-05 20020 and 0425780).Wade, Herschel et al. | 2006
- 5077
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Enhancement of Pt Utilization in Electrocatalysts by Using Gold NanoparticlesZhao, Dan / Xu, Bo‐Qing et al. | 2006
- 5077
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Enhancement of Pt Utilization in Electrocatalysts by Using Gold Nanoparticles. The authors wish to thank Dr. Gang Wu for his help with the electrochemical measurements. This work was supported financially by the National Natural Science Foundation of China (20573062, 20590362 and 20125310).Zhao, Dan et al. | 2006
- 5081
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Formation of Complex Micelles with Double‐Responsive Channels from Self‐Assembly of Two Diblock CopolymersLi, Guiying / Shi, Linqi / Ma, Rujiang / An, Yingli / Huang, Nan et al. | 2006
- 5081
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Formation of Complex Micelles with Double-Responsive Channels from Self-Assembly of Two Diblock Copolymers. This work is supported by the National Natural Science Foundation of China (grant nos.: 50273015, 20474032, and 23030407) and the Program for New Century Talents in Universities.Li, Guiying et al. | 2006
- 5084
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Ionothermal Materials Synthesis Using Unstable Deep‐Eutectic Solvents as Template‐Delivery AgentsParnham, Emily R. / Drylie, Ewan A. / Wheatley, Paul S. / Slawin, Alexandra M. Z. / Morris, Russell E. et al. | 2006
- 5084
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Ionothermal Materials Synthesis Using Unstable Deep-Eutectic Solvents as Template-Delivery Agents. The authors thank Prof. George Ferguson and Dr. Philip Wormald of the University of St Andrews for interesting discussions and R.E.M. thanks the Royal Society for the provision of a University Research Fellowship. We thank the CCLRC and John Warren for access to the Synchrotron Radiation Source (Daresbury) and the EPSRC and David Apperley for access to solid-state NMR spectroscopy.Parnham, Emily R. et al. | 2006
- 5088
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Organocatalytic Asymmetric Conjugate Addition of 1,3-Dicarbonyl Compounds to Maleimides. This research was carried out within the framework of the National Project "Stereoselezione in Sintesi Organica. Metodologie e Applicazioni" with the financial support of the MIUR (Rome) and the FIRB National Project "Progettazione, preparazione e valutazione biologica e farmacologica di nuove molecole organiche quali potenziali farmaci innovativi".Bartoli, Giuseppe et al. | 2006
- 5088
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Organocatalytic Asymmetric Conjugate Addition of 1,3‐Dicarbonyl Compounds to MaleimidesBartoli, Giuseppe / Bosco, Marcella / Carlone, Armando / Cavalli, Andrea / Locatelli, Manuela / Mazzanti, Andrea / Ricci, Paolo / Sambri, Letizia / Melchiorre, Paolo et al. | 2006
- 5092
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Rhodium‐Catalyzed Propargylic Substitution: A Divergent Approach to Propargylic and Allenyl SulfonamidesEvans, P. Andrew / Lawler, Michael J. et al. | 2006
- 5092
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Rhodium-Catalyzed Propargylic Substitution: A Divergent Approach to Propargylic and Allenyl Sulfonamides. We sincerely thank the National Science Foundation (CHE-0316689) for generous financial support. We also thank Johnson and Johnson for a Focused Giving Award.Evans, P.Andrew et al. | 2006
- 5095
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Fluorobis(phenylsulfonyl)methane: A Fluoromethide Equivalent and Palladium‐Catalyzed Enantioselective Allylic MonofluoromethylationFukuzumi, Takeo / Shibata, Norio / Sugiura, Masayoshi / Yasui, Hiroyuki / Nakamura, Shuichi / Toru, Takeshi et al. | 2006
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Fluorobis(phenylsulfonyl)methane: A Fluoromethide Equivalent and Palladium-Catalyzed Enantioselective Allylic Monofluoromethylation. This research was supported in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan (17350047, 17590087) and by Japan Science & Technology (JST) Agency, Innovation Plaza Tokai. T.F. is grateful for research fellowships from JSPS. We thank Dr. Jon Bordner, Shin-ichi Sakemi, and Dr. Masami Nakane, Pfizer Inc., for X-ray crystallographic analysis.Fukuzumi, Takeo et al. | 2006
- 5099
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A Versatile Hexadiene Synthesis by Decarboxylative sp3–sp3 Coupling/Cope RearrangementWaetzig, Shelli R. / Rayabarapu, Dinesh K. / Weaver, Jimmie D. / Tunge, Jon A. et al. | 2006
- 5103
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Oxygen‐Balanced Energetic Ionic LiquidJones, C. Bigler / Haiges, Ralf / Schroer, Thorsten / Christe, Karl O. et al. | 2006
- 5103
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Oxygen-Balanced Energetic Ionic Liquid. This work was funded by the Office of Naval Research, the Lawrence Livermore National Laboratory, and the National Science Foundation. We thank Dr. J. A. Boatz and Dr. J. Mills for the theoretical calculations, and Prof. G. A. Olah and Dr. J. Goldwasser, Dr. C. Bedford, Dr. M. Berman, Dr. J. Gilje, and Dr. J. Satcher for their steady support, and Prof. Dr. R. Bau and Dr. S. Schneider, Dr. W. W. Wilson, and Dr. R. Wagner for their help and stimulating discussions.Jones, C.Bigler et al. | 2006
- 5106
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The Heat of Formation of Cyclobutadiene. We are grateful to the National Science Foundation, the donors of the Petroleum Research Foundation, as administered by the American Chemical Society, and the Minnesota Supercomputer Institute for support of this research. Fruitful discussions with Professor Thomas Bally also are acknowledged.Fattahi, Alireza et al. | 2006
- 5106
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The Heat of Formation of CyclobutadieneFattahi, Alireza / Lis, Lev / Tian, Zhixin / Kass, Steven R. et al. | 2006
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Formation of Seven-Membered Carbocycles by the Use of Cyclopropyl Silyl Ethers as Homoenols. This work was supported by NSF (CHE02-09321) and NIH (GM 35956).Epstein, Oleg L. et al. | 2006
- 5110
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Formation of Seven‐Membered Carbocycles by the Use of Cyclopropyl Silyl Ethers as HomoenolsEpstein, Oleg L. / Lee, Sejin / Cha, Jin Kun et al. | 2006
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Silver‐Catalyzed Hydroamination of Siloxy AlkynesSun, Jianwei / Kozmin, Sergey A. et al. | 2006
- 5113
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Silver-Catalyzed Hydroamination of Siloxy Alkynes. This work was supported by the NSF CAREER (CHE-0447751). S.A.K. thanks the Sloan Foundation, the Dreyfus Foundation, Amgen, and GlaxoSmithKline for additional funding.Sun, Jianwei et al. | 2006
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The Roles of Hydrogen Bonding and Sterics in RNA InterferenceSomoza, Alvaro / Chelliserrykattil, Jijumon / Kool, Eric T. et al. | 2006
- 5116
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The Roles of Hydrogen Bonding and Sterics in RNA Interference. This work was supported by the US National Institutes of Health (GM072705), and by a Marie Curie OIF Fellowship (6th Framework Program, UE) to A.S.Somoza, Alvaro et al. | 2006
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[Pd(Ar‐BIAN)(alkene)]‐Catalyzed Highly Chemo‐, Regio‐, and Stereoselective Semihydrogenation of 1,2‐Allenyl Phosphonates and Related CompoundsGuo, Hao / Zheng, Zilong / Yu, Fei / Ma, Shengming / Holuigue, Alexandre / Tromp, Dorette S. / Elsevier, Cornelis J. / Yu, Yihua et al. | 2006
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[Pd(Ar-BIAN)(alkene)]-Catalyzed Highly Chemo-, Regio-, and Stereoselective Semihydrogenation of 1,2-Allenyl Phosphonates and Related Compounds. The Chinese authors acknowledge financial support from the International Program of the National Natural Science Foundation of China. This research has also been partially funded by the National Research School Combination Catalysis (project number: 2000-14) and by the Universiteit van Amsterdam (grant SAP 2255). We thank Mr. Tao Bai of this group for independently reproducing representative examples of the work reported herein. Ar-BIAN=bis(arylimino)acenaphthene.Guo, Hao et al. | 2006
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Asymmetric Aza-Wittig Reactions: Enantioselective Synthesis of b-Quaternary Azacycles. We thank the Royal Thai Government for Ph.D. support (D.L.) and the University of Almeria, Spain for research leave (I.R.-G.).Lertpibulpanya, Duanpen et al. | 2006
- 5122
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Asymmetric Aza‐Wittig Reactions: Enantioselective Synthesis of β‐Quaternary AzacyclesLertpibulpanya, Duanpen / Marsden, Stephen P. / Rodriguez‐Garcia, Ignacio / Kilner, Colin A. et al. | 2006
- 5122
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Asymmetric Aza-Wittig Reactions: Enantioselective Synthesis of b-Quaternary AzacyclesLertpibulpanya, D. / Marsden, S. P. / Rodriguez-Garcia, I. / Kilner, C. A. et al. | 2006
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Substituted Allyl Diphenylphosphine Oxides as Radical Allylating AgentsOuvry, Gilles / Quiclet‐Sire, Béatrice / Zard, Samir Z. et al. | 2006
- 5124
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Substituted Allyl Diphenylphosphine Oxides as Radical Allylating Agents. G.O. thanks the Ecole Polytechnique for a fellowship.Ouvry, Gilles et al. | 2006
- 5129
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Antrieb eines oberflächengebundenen DNA‐Schalters mit einem chemischen OszillatorLiedl, Tim / Olapinski, Michael / Simmel, Friedrich C. et al. | 2006
- 5129
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Antrieb eines oberflachengebundenen DNA-Schalters mit einem chemischen OszillatorLiedl, T. / Olapinski, M. / Simmel, F. C. et al. | 2006
- 5129
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Antrieb eines oberflächengebundenen DNA-Schalters mit einem chemischen Oszillator. Diese Arbeit wurde von der Deutschen Forschungsgemeinschaft gefördert (Emmy Noether-Projekt DFG SI 761-2-2). T.L. und M.O. werden durch die LMU International Graduate School "Nanobiotechnology" unterstützt.Liedl, Tim et al. | 2006
- 5132
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Übergangsmetall‐freie Homokupplungen von OrganomagnesiumverbindungenKrasovskiy, Arkady / Tishkov, Alexander / del Amo, Vicente / Mayr, Herbert / Knochel, Paul et al. | 2006
- 5132
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Ubergangsmetall-freie Homokupplungen von OrganomagnesiumverbindungenKrasovskiy, A. / Tishkov, A. / del Amo, V. / Mayr, H. / Knochel, P. et al. | 2006
- 5132
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Übergangsmetall-freie Homokupplungen von Organomagnesiumverbindungen. Wir danken dem Fonds der Chemischen Industrie und den Merck Research Laboratories (MSD) für finanzielle Unterstützung. Außerdem gilt unser Dank V. Malakhov für die Durchführung einiger Vorversuche sowie der Chemetall GmbH und der BASF AG für großzügige Chemikalienspenden. V. del Amo dankt der Alexander von Humboldt-Stiftung für finanzielle Unterstützung.Krasovskiy, Arkady et al. | 2006
- 5137
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Multiple Pd‐katalysierte Reaktionen zur Synthese von Analoga des hochpotenten Insektizids Spinosyn ATietze, Lutz F. / Brasche, Gordon / Stadler, Christian / Grube, Alexander / Böhnke, Niels et al. | 2006
- 5137
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Multiple Pd-katalysierte Reaktionen zur Synthese von Analoga des hochpotenten Insektizids Spinosyn A. Die Untersuchungen wurden von der deutschen Forschungsgemeinschaft (SFB 416) und dem Fonds der chemischen Industrie unterstützt. Wir danken den Firmen BASF, Bayer und Wacker-Chemie für Chemikalien-Spenden.Tietze, Lutz F. et al. | 2006
- 5147
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Vorschau: Angew. Chem. 30/2006| 2006