These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 10941065)

  • 1. A New Gold-Catalyzed C-C Bond Formation This work was supported by the Deutsche Forschungsgemeinschaft (Ha 1932/5-1, Ha 1932/6-1) and the Fonds der Chemischen Industrie. Gold salts were donated by Degussa-Hüls AG. A.S.K.H. is indebted to Prof. M. Göbel for laboratory space.
    Hashmi AS; Schwarz L; Choi JH; Frost TM
    Angew Chem Int Ed Engl; 2000 Jul; 39(13):2285-2288. PubMed ID: 10941065
    [No Abstract]   [Full Text] [Related]  

  • 2. New Chiral Auxiliaries for the Construction of Quaternary Stereocenters by Copper-Catalyzed Michael Reactions This work was supported by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie. We are also grateful to the Degussa-Hüls AG for gifts of amino acids and to Prof. Dr. S. Blechert for his support.
    Christoffers J; Mann A
    Angew Chem Int Ed Engl; 2000 Aug; 39(15):2752-2754. PubMed ID: 10934415
    [No Abstract]   [Full Text] [Related]  

  • 3. Substituted Diazadibenzoperylenes: New Functional Building Blocks for Supramolecular Chemistry This work was supported by the Ulmer Universitätsgesellschaft, the Fonds der Chemischen Industrie (Liebig grant for F. W.), and the Deutsche Forschungsgemeinschaft (Habilitandenstipendium for F. W.). We are indebted to Dr. J. Schilling for the crystal structure determination and to Dr. E. Mena-Osteritz for helpful discussions about fluorescence measurements. We thank BASF AG and Degussa-Hüls AG for the donation of chemicals and Prof. P. Bäuerle for his support.
    Würthner F; Sautter A; Thalacker C
    Angew Chem Int Ed Engl; 2000 Apr; 39(7):1243-1245. PubMed ID: 10767019
    [No Abstract]   [Full Text] [Related]  

  • 4. Domino Michael Aldol and Domino Michael Mannich Reactions: Highly Stereoselective Synthesis of Functionalized Cyclohexanes This work has been supported by the Deutsche Forschungsgemeinschaft (Schn 441/1-2), the Fonds der Chemischen Industrie (doctoral fellowship to O. R.) and Degussa Hüls AG. We thank Prof. L. Tietze for constant support.
    Schneider C; Reese O
    Angew Chem Int Ed Engl; 2000 Aug; 39(16):2948-2950. PubMed ID: 11028020
    [No Abstract]   [Full Text] [Related]  

  • 5. A Neutral Three-Coordinate Alkylrhodium(I) Complex: Stabilization of a 14-Electron Species by gamma-C-H Agostic Interactions with a Saturated Hydrocarbon Group This work was supported by the Deutsche Forschungsgemeinschaft (SFB 247, Graduate College Fellowship to H.U.), by the BASF AG, by the Degussa-Hüls AG, by the Fonds der Chemischen Industrie, and by the EU.
    Urtel H; Meier C; Eisenträger F; Rominger F; Joschek JP; Hofmann P
    Angew Chem Int Ed Engl; 2001 Feb; 40(4):781-784. PubMed ID: 11241623
    [No Abstract]   [Full Text] [Related]  

  • 6. The First Stable Diazonium Ion on Solid Support-Investigations on Stability and Usage as Linker and Scavenger in Solid-Phase Organic Synthesis Nitrogen-Based Linkers, Part 8. This work was supported by the Fonds der Chemischen Industrie (Liebig-Stipend to S.B.) and the Deutsche Forschungsgemeinschaft (BR1750-1). We thank Prof. Dr. D. Enders for the generous support of our work. The companies BASF AG, Bayer AG, Degussa-Hüls AG, and Calbiochem-Novabiochem AG are acknowledged for donations of chemicals and Grünenthal GmbH for financial support. For DSC measurements we also thank Prof. Dr. Franz-Josef Wortmann and Dr. Numan Özgün at the Deutsches Wollforschungsinstitut (DWI) at the RWTH Aachen. Part 7: M. Lormann, S. Dahmen, S. Bräse, Tetrahedron Lett. 2000, 41, 3813-3816.
    Dahmen S; Bräse S
    Angew Chem Int Ed Engl; 2000 Oct; 39(20):3681-3683. PubMed ID: 11091438
    [No Abstract]   [Full Text] [Related]  

  • 7. C-H Activation by Direct Borane-Hydrocarbon Dehydrogenation: Kinetic and Thermodynamic Aspects This work was supported by the Fonds der Chemische Industrie (Sachbeihilfe and Liebig-Stipendium for B.G.), the Deutsche Forschungsgemeinschaft (GO 930/1-1 and Habilitationsstipendium for B.G.), the Research Pool Foundation of the University Heidelberg, Degussa-Hüls AG, and BASF AG. B.G. is grateful to Prof. P. Hofmann for support at Heidelberg and thanks Prof. A. Berndt (Marburg), Prof. G. Frenking (Marburg), and Prof. H. Mayr (München) for fruitful suggestions.
    Goldfuss B; Knochel P; Bromm LO; Knapp K
    Angew Chem Int Ed Engl; 2000 Nov; 39(22):4136-4139. PubMed ID: 11093231
    [No Abstract]   [Full Text] [Related]  

  • 8. Insertion Reactions of Nitriles into the P-C Bond of [(eta(1)-C(5)Me(5))P{W(CO)(5)}(2)]-A Novel Approach to Phosphorus-Containing Heterocycles This work was supported by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie. M. Schiffer thanks the Fonds der Chemischen Industrie for a PhD fellowship.
    Schiffer M; Scheer M
    Angew Chem Int Ed Engl; 2001 Sep; 40(18):3413-3416. PubMed ID: 11592156
    [No Abstract]   [Full Text] [Related]  

  • 9. In situ Transfer of Parahydrogen-Induced Nuclear Spin Polarization-Structural Characterization of Hydrogenation Intermediates This work was supported by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie. P. Hübler thanks the Fonds der Chemischen Industrie for a graduate fellowship. We thank Prof. Dr. S. J. Glaser (Technische Universität München, Germany) for valuable discussions.
    Hübler P; Bargon J
    Angew Chem Int Ed Engl; 2000 Oct; 39(20):3701-3703. PubMed ID: 11091446
    [No Abstract]   [Full Text] [Related]  

  • 10. Nickel-Catalyzed Cross-Coupling of Aryl Chlorides with Aryl Grignard Reagents N-Heterocyclic Carbenes, Part 27. This work was supported by Aventis R&T, the Deutsche Forschungsgemeinschaft (DFG), the Bayerischer Forschungsverbund Katalyse (FORKAT), Degussa-Hüls AG, and the Fonds der Chemischen Industrie (studentships for V.P.W.B. and T.W.). We thank C. Brossmer, K. Denk, R. W. Eckl, M. G. Gardiner, J. Schwarz, and C.-P. Reisinger for preparation of commercially unavailable ligands used in the screening assay and T. Boussie from Symyx Technologies for helpful discussions. Part 26: V. P. W. Böhm, C. W. K. Gstöttmayr, T. Weskamp, W. A. Herrmann, J. Organomet. Chem. 2000, 595, 186-190.
    Böhm VP; Weskamp T; Gstöttmayr CW; Herrmann WA
    Angew Chem Int Ed Engl; 2000 May; 39(9):1602-1604. PubMed ID: 10820447
    [No Abstract]   [Full Text] [Related]  

  • 11. Unusually Stable Vinyl Cations This work was supported by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie (Ulm). The Frankfurt group thanks Prof. N. Auner for support. We are indebted to Prof. Mark Fink, Tulane University, New Orleans, for carefully reading our manuscript. We thank Thomas Nau, Computer Center Universität Ulm, for adaptation of the Gaussian Program Suite.
    Müller T; Meyer R; Lennartz D; Siehl HU
    Angew Chem Int Ed Engl; 2000 Sep; 39(17):3074-3077. PubMed ID: 11028036
    [No Abstract]   [Full Text] [Related]  

  • 12. Chirally Modified n-Butyllithium: Tuning the Composition, Structure, and Enantioselectivity with Modular Fencholates This work was supported by the Fonds der Chemische Industrie (Sachbeihilfe and Liebig-Stipend for B.G.), the Deutsche Forschungsgemeinschaft (GO 930/1-1 and Habilitationsstipendium), the Research Pool Foundation (University Heidelberg), the Degussa-Hüls AG, and the BASF AG. B.G. is grateful to Prof. P. Hofmann for support at Heidelberg and thanks Prof. G. Boche (Marburg), Prof. D. Hoppe (Münster), and Prof. D. Seebach (Zürich) for fruitful suggestions. Parts of this work were presented at the 37th IUPAC Congress/ 27th GDCh General Meeting in Berlin (1999) and at the SFB-424 Symposium in Münster (2000).
    Goldfuss B; Steigelmann M; Rominger F
    Angew Chem Int Ed Engl; 2000 Nov; 39(22):4133-4136. PubMed ID: 11093230
    [No Abstract]   [Full Text] [Related]  

  • 13. Isolation of the Phenyl Cation in a Solid Argon Matrix This work was financially supported by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie. M.W. thanks the Fonds der Chemischen Industrie for a stipend.
    Winkler M; Sander W
    Angew Chem Int Ed Engl; 2000 Jun; 39(11):2014-2016. PubMed ID: 10941014
    [No Abstract]   [Full Text] [Related]  

  • 14. Gold Nanoparticles with Covalently Attached Polymer Chains This work was supported by the Deutsche Forschungsgemeinschaft and by the Fonds der Chemischen Industrie. We are grateful to Prof. Dr. H. Weller, Institut für Physikalische Chemie der Universität Hamburg, for the transmission electron microscopy pictures and to Prof. Dr. M. Möller and Dipl.-Chem. Bernd Tartsch, Abteilung Organische Chemie III der Universität Ulm, for the scanning forcce microscopy investigations.
    Nuss S; Böttcher H; Wurm H; Hallensleben ML
    Angew Chem Int Ed Engl; 2001 Nov; 40(21):4016-4018. PubMed ID: 12404478
    [No Abstract]   [Full Text] [Related]  

  • 15. Fluorinated Bis(enyl) Ligands by Metal-Induced Dimerization of Fluorinated Allenes This work was supported by the Fonds der Chemischen Industrie and the Deutsche Forschungsgemeinschaft. We are indebted to the Hoechst AG (Frankfurt/Main) and DUPONT (Wilmington, DE) for some starting materials. We thank Dr. Dieter Zobel for the collection of X-ray data at 20 K.
    Lentz D; Willemsen S
    Angew Chem Int Ed Engl; 2001 Jun; 40(11):2087-2091. PubMed ID: 11433452
    [No Abstract]   [Full Text] [Related]  

  • 16. DNA-Directed Functionalization of Colloidal Gold with Proteins This work was supported by Deutsche Forschungsgemeinschaft and Fonds der Chemischen Industrie. We thank Prof. D. Blohm for helpful discussions and generous support.
    Niemeyer CM; Ceyhan B
    Angew Chem Int Ed Engl; 2001 Oct; 40(19):3685-3688. PubMed ID: 11592222
    [No Abstract]   [Full Text] [Related]  

  • 17. Asymmetric Synthesis of alpha-Substituted beta-Nitrophosphonic Acids by Phospha-Analogous Michael Addition to Aromatic Nitroalkenes This work was supported by the Deutsche Forschungsgemeinschaft (Sonderforschungsbereich 380) and by the Fonds der Chemischen Industrie. We thank Jens Hasenjäger for his contribution to the experimental part of this work and the companies Degussa AG, BASF AG, and Bayer AG for the donation of chemicals.
    Enders D; Tedeschi L; Bats JW
    Angew Chem Int Ed Engl; 2000 Dec; 39(24):4605-4607. PubMed ID: 11169685
    [No Abstract]   [Full Text] [Related]  

  • 18. The Catalytic Enantioselective Claisen Rearrangement of an Allyl Vinyl Ether This work was financially supported by the Deutsche Forschungsgemeinschaft, the Fonds der Chemischen Industrie, and the Dr. Otto Röhm Gedächtnisstiftung. M.H. thanks Prof. P. Metz and Prof. H.-U. Reissig for their support.
    Abraham L; Czerwonka R; Hiersemann M
    Angew Chem Int Ed Engl; 2001 Dec; 40(24):4700-4703. PubMed ID: 12404389
    [No Abstract]   [Full Text] [Related]  

  • 19. Domino Hydroformylation/Knoevenagel/Hydrogenation Reactions This work was supported by the Fonds der Chemischen Industrie (Fellowship to S.K.Z.) and the Deutsche Forschungsgemeinschaft, as well as an Alfried Krupp Award for Young University Teachers from the Krupp foundation. We thank the companies BASF and Degussa for their gift of chemicals.
    Breit B; Zahn SK
    Angew Chem Int Ed Engl; 2001 May; 40(10):1910-1913. PubMed ID: 11385670
    [No Abstract]   [Full Text] [Related]  

  • 20. Enantioselective Synthesis of Functionalized 1,5-Cyclononadienes by Intramolecular Cycloalkylation under alpha,alpha'-Diallyl Coupling This work was supported by the Deutsche Forschungsgemeinschaft (Sonderforschungsbereich 424) and the Fonds der Chemischen Industrie. A.D. gratefully acknowledges a fellowship from the Fonds der Chemischen Industrie. We thank Mrs. C. Weitkamp for her outstanding experimental assistance and Mr. J. Müller for his skillful work during a laboratory course.
    Deiters A; Fröhlich R; Hoppe D
    Angew Chem Int Ed Engl; 2000 Jun; 39(12):2105-2107. PubMed ID: 10941029
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.