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.
Table of contents
1169
Titelbild: Aeruginosine: Chemie und Biologie der Serinprotease‐Inhibitoren (Angew. Chem. 7/2008)
Ersmark, Karolina
/ Del Valle, Juan R.
/ Hanessian, Stephenet al.
| 2008
Innentitelbild: Oxidative Cross‐Coupling of Arenes Induced by Single‐Electron Transfer Leading to Biaryls by Use of Organoiodine(III) Oxidants (Angew. Chem. 7/2008)
Die vielseitige Chemie von Bodipy-FluoreszenzfarbstoffenFNR HREF="nss"> FN ID="nss"> Bodipy, abgeleitet von Bordipyrromethen, steht für Dipyrromethenbordifluorid, 4,4-Difluoro-4-borata-3a-azonia-4a-aza-s-indacen.
Structure of the Tyrosyl Biradical in Mouse R2 Ribonucleotide Reductase from High-Field PELDORFNR HREF="nss"> FN ID="nss"> We thank P. P. Schmidt for helping with the sample preparation and Prof. Lars Thelander (Umeå, Sweden) for supplying us with E. coli cells that overexpress mouse R2 protein. M.B. would like to acknowledge the Max Planck Society and the IRTG 1422 for financial support. PELDOR=pulse electron-electron double resonance.
Reversible Electron Transfer Coupled to Spin Crossover in an Iron Coordination Salt in the Solid StateFNR HREF="nss"> FN ID="nss"> A. Göbels, H. Schucht, and B. Mienert are acknowledged for their high skill in measurements of sensitive compounds. M.M.K. is grateful to the Max Planck Society for a postdoctoral fellowship.
Evolution of Homochiral Helical Dye Assemblies: Involvement of Autocatalysis in the "Majority-Rules" EffectFNR HREF="nss"> FN ID="nss"> This work was supported by the Deutsche Forschungsgemeinschaft (Wu 317-1-5) and the Fonds der Chemischen Industrie. We thank S. Geschwentner and S. Gruss for help with mathematical questions and Dr. M. Knoll for performing AFM measurements.
Photoisomerization of cis,cis- and cis,trans-1,4-Di-o-tolyl-1,3-butadiene in Glassy Media at 77 K: One-Bond-Twist and Bicycle-Pedal MechanismsFNR HREF="nss"> FN ID="nss"> J.S. thanks the National Science Foundation (Grant No. CHE-0314784) for partial support of this research
Nanofibers and Lyotropic Liquid Crystals from a Class of Self-Assembling β-PeptidesFNR HREF="nss"> FN ID="nss"> This research was supported by University of Wisconsin-Madison Nanoscale Science and Engineering Center (NSF grant DMR-0425880). V.M.Y. was supported by the Welch Foundation research grant C-1557. Authors kindly thank PepTech for a generous supply of several β-amino acids at a discounted price and Arun Yethiraj for helpful conversations during the preparation of this manuscript.
Self-Assembly of a Homochiral Nanoscale Metallacycle from a Metallosalen Complex for Enantioselective SeparationFNR HREF="nss"> FN ID="nss"> This work was supported by NSFC-20671062, NCET-05-0395, Key Project of Basic Research of Shanghai (05JC14020), Shanghai Pujiang Program (B4727A), Shuguang Program (06SG12), and the State Key Laboratory of Structural Chemistry. We also thank the "Instrumental Analysis Center" of Jiao Tong University for the use of the spectrometers.
Antibacterial and Hemolytic Activities of Pyridinium Polymers as a Function of the Spatial Relationship between the Positive Charge and the Pendant Alkyl Tail
Sambhy, Varun
/ Peterson, Blake R.
/ Sen, Ayusmanet al.
| 2008
Antibacterial and Hemolytic Activities of Pyridinium Polymers as a Function of the Spatial Relationship between the Positive Charge and the Pendant Alkyl TailFNR HREF="nss"> FN ID="nss"> This work was supported by the Huck Institutes of the Life Sciences and the Materials Research Institute of the Pennsylvania State University.
Synthesis and Lithographic Patterning of FePt Nanoparticles Using a Bimetallic Metallopolyyne PrecursorFNR HREF="nss"> FN ID="nss"> I.M. and H.E.R. are grateful to the NSERC AGENO program for supporting this research, and I.M. thanks the Canadian Government for a Canada Research Chair. W.-Y.W. thanks the Hong Kong Research Grants Council for a CERG grant (project no. HKBU2021-06P) and the Hong Kong Baptist University (FRG-05-06-I-63) for financial support. We also thank Prof. P. D. Harvey for assistance in GPC measurements and H. Wang for DLS measurements.
Virion-Mimicking Nanocapsules from pH-Controlled Hierarchical Self-Assembly for Gene DeliveryFNR HREF="nss"> FN ID="nss"> This work was supported by the National Science Foundation (DMR-0705298), American Cancer Society (RSG-06-118-01-CDD), and National Institutes of Health (RR-016474).
Differentiation between Structurally Homologous Shiga 1 and Shiga 2 Toxins by Using Synthetic GlycoconjugatesFNR HREF="nss"> FN ID="nss"> Financial support for this work was provided by the Center for Chemical and Biosensors, Department of Chemistry, University of Cincinnati (SSI), UC Research Council and Nanotechnology Institute (A.A.W. and S.S.I.), NIAID (RO1 AI064893 A.A.W.) and NIAID (U01-AI075498 A.A.W. and S.S.I.). S.S.I. thanks Dr. Stephan Macha for mass spectral analysis.
A Selective Instant Synthesis of a Coordination Network and Its Ab Initio Powder Structure DeterminationFNR HREF="nss"> FN ID="nss"> We thank Prof. Y. Ohashi and Dr. K. Miura (JASRI) for helpful discussions and their support during the PXRD measurements at SPring-8 (proposal nos. 2006A1824 and 2006B1740).
Total Synthesis of Ouabagenin and OuabainFNR HREF="nss"> FN ID="nss"> We thank Dr. Vijay Kumar for his assistance in providing starting materials. We also thank NSERCC (Ottawa) for financial support.
Dissociation Behavior of Clathrate Hydrates to Ice and Dependence on Guest MoleculesFNR HREF="nss"> FN ID="nss"> We thank Drs. M. Sergey, H. Lu, K. Udachin, and D. D. Klug of NRC for their discussions and assistance on sample synthesis. S.T. also thanks Drs. R. Ohmura of Keio University and J. Nagao of AIST for their discussions.
Palladium-(S,pR)-FerroNPS-Catalyzed Asymmetric Allylic Etherification: Electronic Effect of Nonconjugated Substituents on Benzylic Alcohols on EnantioselectivityFNR HREF="nss"> FN ID="nss"> We thank the University Grants Committee Area of Excellence Scheme (AoE-P-10-01) and The Hong Kong Polytechnic University (Area of Strategic Development) for financial support of this study. FerroNPS refers to a series of P,S ligands with a ferrocenyl motif and an amine linkage.
Palladium–(S,pR)‐FerroNPS‐Catalyzed Asymmetric Allylic Etherification: Electronic Effect of Nonconjugated Substituents on Benzylic Alcohols on Enantioselectivity
Lam, Fuk Loi
/ Au‐Yeung, Terry Tin‐Lok
/ Kwong, Fuk Yeeet al.
| 2008
Enantioselective Synthesis of (+)-Monobromophakellin and (+)-Phakellin: A Concise Phakellin Annulation Strategy Applicable to Palau'amineFNR HREF="nss"> FN ID="nss"> We thank the NIH (GM52964) and the Welch Foundation for generous support. We also thank Dr. Joe Reibenspies for X-ray structural analysis, Francisco M. Torres for early studies in this project, and Prof. Justin Du Bois for helpful discussions.
Structural Aspects of Nucleation Inhibitors for Diastereomeric Resolutions and the Relationship to Dutch ResolutionFNR HREF="nss"> FN ID="nss"> We are grateful to the Samenwerkingsverband Noord- Nederland (Cooperation Northern Netherlands) and the European Fund for Regional Development (EFRO) for partial support of this work.
Use of Sodium Iodide as the Precursor to the Control Agent in Ab Initio Emulsion PolymerizationFNR HREF="nss"> FN ID="nss"> Frédéric Delolme (CNRS-SCA Vernaison) is acknowledged for performing MALDI-TOF analyses.
[2+1] Cycloaddition of Nitrene onto C60 Revisited: Interconversion between an Aziridinofullerene and an AzafulleroidFNR HREF="nss"> FN ID="nss"> We thank Dr. H. Sawa for his experimental help at the Photon Factory. We also thank T. Wakahara for interesting discussions. This work was supported in part by a Grant-in-Aid and the 21st Century COE Program, Nanotechnology Support Project, The Next Generation Super Computing Project (Nanoscience Project), and Scientific Research on Priority Area from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.
Oxidative Cross-Coupling of Arenes Induced by Single-Electron Transfer Leading to Biaryls by Use of Organoiodine(III) OxidantsFNR HREF="nss"> FN ID="nss"> This work was supported by a Grant-in-Aid for Scientific Research (A) and for Encouragement of Young Scientists, and by a Grant-in-Aid for Scientific Research on Priority Areas "Advanced Molecular Transformations of Carbon Resources" from the Ministry of Education Culture, Sports, Science, and Technology (Japan). T.D. also thanks the Industrial Technology Research Grant Program from the New Energy and Industrial Technology Development Organization (NEDO) of Japan. We are grateful to Dr. S. Obika for his help with X-ray analysis.
Iron-Catalyzed Desulfinylative C&bond;C Cross-Coupling Reactions of Sulfonyl Chlorides with Grignard ReagentsFNR HREF="nss"> FN ID="nss"> We are grateful to the Swiss National Science Foundation (Bern) and the Roche Research Foundation (Basel). We also thank F. Sepulveda, M. Rey, and A. Razaname for their technical help, as well as A. Yella and Dr. S. R. Dubbaka for helpful discussions.
An N,N′‐Dioxide/In(OTf)3 Catalyst for the Asymmetric Hetero‐Diels–Alder Reaction Between Danishefsky's Dienes and Aldehydes: Application in the Total Synthesis of Triketide
An N,N'-Dioxide-In(OTf)3 Catalyst for the Asymmetric Hetero-Diels-Alder Reaction Between Danishefsky's Dienes and Aldehydes: Application in the Total Synthesis of TriketideFNR HREF="nss"> FN ID="nss"> We are grateful to the National Natural Science Foundation of China (grant Nos. 20732003 and 20472056) for financial support. We also thank the Sichuan University Analytical & Testing Center for performing the NMR analysis.
An N,Nprime-Dioxide/In(OTf)3 Catalyst for the Asymmetric Hetero-Diels-Alder Reaction Between Danishefskys Dienes and Aldehydes: Application in the Total Synthesis of Triketide
Highly Regio-, Diastereo-, and Enantioselective [2+2+2] Cycloaddition of 1,6-Enynes with Electron-Deficient Ketones Catalyzed by a Cationic RhI-H8-binap ComplexFNR HREF="nss"> FN ID="nss"> This research was partly supported by a Grant-in-Aid for Scientific Research on Priority Areas (No. 19028015, Chemistry of Concerto Catalysis) from the Ministry of Education, Culture, Sports, Science and Technology (Japan). We thank Yusuke Aida (TUAT) for his experimental assistance and Takasago International Corporation for the gift of modified binap ligands. H8-binap=2,2'-bis(diphenylphosphanyl)-5,5',6,6',7,7- ',8,8'-octahydro-1,1'-binaphthyl.
Highly Regio‐, Diastereo‐, and Enantioselective [2+2+2] Cycloaddition of 1,6‐Enynes with Electron‐Deficient Ketones Catalyzed by a Cationic RhI/H8‐binap Complex
Katalytische enantioselektive Reformatsky-Reaktionen mit AldehydenFNR HREF="nss"> FN ID="nss"> Diese Forschungsarbeit wurde finanziell unterstützt vom Niederländischen Ministerium für Wirtschaft. M.A.F.-I. bedankt sich beim spanischen Ministerium für Bildung und Forschung für ein Postdoktorandenstipendium.
Eine Halbleiterhybrid-Elektrode zum wellenlängengesteuerten Schalten der PhotostromrichtungFNR HREF="nss"> FN ID="nss"> Wir danken W. Macyk und K. Szacilowski für wertvolle Diskussionen, A. Friedrich für SEM- und EDX-Analysen sowie M. Weller für die Konstruktion der photoelektrochemischen Zelle.
Vesikelbildung aus reaktiven TensidenFNR HREF="nss"> FN ID="nss"> Diese Arbeit wurde von der EU COST action D27 "Prebiotic Chemistry and Early Evolution" unterstützt.
Synthesen und Kristallstrukturen der ligandenstabilisierten Silberchalkogenidcluster [Ag154Se77(dppxy)18], [Ag320(StBu)60S130(dppp)12], [Ag352S128(StC5H11)96] und [Ag490S188(StC5H11)114]FNR HREF="nss"> FN ID="nss"> Diese Arbeit wurde von der DFG (Centrum für Funktionelle Nanostrukturen) und dem Fonds der Chemischen Industrie gefördert. Wir danken Dr. H. Rösner (Institut für Nanotechnologie, Forschungszentrum Karlsruhe) für die Anfertigung der TEM-Aufnahmen und Dr. G. Buth (Institut für Synchrotronstrahlung, Forschungszentrum Karlsruhe) für die Unterstützung bei der Röntgenbeugungsmessung von 4 am ANKA-Synchrotron Karlsruhe. dppxy = 1,4-Bis(diphenylphosphanylmethyl)benzol; dppp = 1,3-Bis(diphenylphosphanyl)propan.
Synthesen und Kristallstrukturen der ligandenstabilisierten Silberchalkogenidcluster [Ag154Se77(dppxy)18], [Ag320(StBu)60S130(dppp)12], [Ag352S128(StC5H11)96] und [Ag490S188(StC5H11)114]
Anson, Christopher E.
/ Eichhöfer, Andreas
/ Issac, Ibrahimet al.
| 2008
Allosterische Aktivierung der HtrA-Protease DegP durch Stress-Signale während der bakteriellen ProteinqualitätskontrolleFNR HREF="nss"> FN ID="nss"> Diese Arbeit wurde von der Deutschen Forschungsgemeinschaft, dem Fonds der Chemischen Industrie (M.E.), dem Österreichischen Wissenschaftsfonds (FWF P17881-B10, T.K.) und dem BBSRC (D.J., M.E.) unterstützt.