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 *

219 related articles for article (PubMed ID: 11241609)

  • 41. New Synthetic Technology for the Construction of N-Containing Quinones and Derivatives Thereof: Total Synthesis of Epoxyquinomycin B We thank Dr. D. H. Huang, Dr. G. Siuzdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from the National Science Foundation (P.B.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.
    Nicolaou KC; Sugita K; Baran PS; Zhong YL
    Angew Chem Int Ed Engl; 2001 Jan; 40(1):207-210. PubMed ID: 11169714
    [No Abstract]   [Full Text] [Related]  

  • 42. New Synthetic Technology for the Construction of N-Containing Quinones and Derivatives Thereof: Total Synthesis of Epoxyquinomycin B We thank Dr. D. H. Huang, Dr. G. Siuzdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from the National Science Foundation (P.B.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.
    Nicolaou KC; Sugita K; Baran PS; Zhong YL
    Angew Chem Int Ed Engl; 2001 May; 40(9):1573. PubMed ID: 11353465
    [No Abstract]   [Full Text] [Related]  

  • 43. First Catalytic Asymmetric Aldol-Tishchenko Reaction-Insight into the Catalyst Structure and Reaction Mechanism J.P.M. gratefully acknowledges receipt of an NSF Career Award (CHE-9875488), a David and Lucile Packard Fellowship and a DuPont Young Professor Grant. Support from Amoco Chemicals is also appreciated. The authors thank Prof. Joseph Templeton for helpful discussions and Andrew Larsen of the Gagné research group for assistance with vapor pressure osmometry experiments.
    Mascarenhas CM; Miller SP; White PS; Morken JP
    Angew Chem Int Ed Engl; 2001 Feb; 40(3):601-603. PubMed ID: 11180384
    [No Abstract]   [Full Text] [Related]  

  • 44. The Zipper-Mode Domino Intramolecular Diels-Alder Reaction: A New 0-->ABCD Strategy for Steroids and Related Compounds We thank Dr. Simon Fielder (HortResearch New Zealand) and Mr. Leon Wong (University of Sydney) for preliminary experiments, Dr. Kelvin Picker (University of Sydney) for assistance with HPLC and GC analyses, and Dr. Ian Luck (University of Sydney) for 2D NMR experiments. This work was supported by The Australian Research Council and The University of Sydney.
    Nörret M; Sherburn MS
    Angew Chem Int Ed Engl; 2001 Nov; 40(21):4074-4076. PubMed ID: 12404497
    [No Abstract]   [Full Text] [Related]  

  • 45. 1,2-Seleno Migrations in Carbohydrate Chemistry: Solution and Solid-Phase Synthesis of 2-Deoxy Glycosides, Orthoesters, and Allyl Orthoesters We thank Drs. D. H. Huang and G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. We gratefully thank Nicolas Winssinger for helpful discussions and preparation of the selenium bromide resin. This work was financially supported by the Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), postdoctoral fellowships from M.E.C., Spain (R.M.R., Fullbright), the Japan Society for the Promotion of Science (H.S.), the George Hewitt Foundation (K.C.F.), and grants from Schering Plough, Pfizer, Glaxo, Merck, Hoffmann - La Roche, DuPont, Abbott Laboratories, and Boehringer - Ingelheim.
    Nicolaou KC; Mitchell HJ; Fylaktakidou KC; Suzuki H; Rodríguez RM
    Angew Chem Int Ed Engl; 2000 Mar; 39(6):1089-1093. PubMed ID: 10760930
    [No Abstract]   [Full Text] [Related]  

  • 46. Redox-Induced "Zipper" Action in Rb(2)Bi(4)Se(7) and Cs(2)Bi(4)Se(7): Coupling of Slabs to a Three-Dimensional Framework through Single-Crystal to Single-Crystal Conversion Financial support from the Office of Naval Research (contract No. N00014-98-1-0443) is gratefully acknowledged. The work made use of the SEM facilities of the Center for Electron Optics at Michigan State University (MSU). The Siemens SMART CCD diffractometer at MSU was purchased with funds from the National Science Foundation (CHE-9634638). We thank Victor G. Young and the X-ray Crystallographic Laboratory of the University of Minnesota for collecting the data set of RbBi(4)Se(7).
    Iordanidis L; Kanatzidis MG
    Angew Chem Int Ed Engl; 2000 Jun; 39(11):1927-1930. PubMed ID: 10940983
    [No Abstract]   [Full Text] [Related]  

  • 47. Preparation, Structure, and Redox Reactions of Nine-Membered Cyclic Peroxides: A Novel Electrochromic System Undergoing Reversible Extrusion and Trapping of O(2) This work was supported by the Ministry of Education, Science, and Culture, Japan (No. 10146101). Financial support by the Izumi Science and Technology Foundation and by a Research Grant from the Iwatani Naoji Foundation (T.S.) are gratefully acknowledged. J.N. thanks JSPS Research Fellowships for Young Scientists. We thank Prof. Tamotsu Inabe (Hokkaido University) for the use of facilities to analyze the X-ray structures. Technical support by Mr. Kenji Watanabe and Dr. Eri Fukushi (GC-MS & NMR Laboratory, Faculty of Agriculture, Hokkaido University) is gratefully acknowledged.
    Suzuki T; Nishida Ji; Ohkita M; Tsuji T
    Angew Chem Int Ed Engl; 2000 May; 39(10):1804-1806. PubMed ID: 10934368
    [No Abstract]   [Full Text] [Related]  

  • 48. An Atom-Economic Three-Carbon Chain Extension to Give Enamides We thank the National Science Foundation and the National Institutes of Health, General Medical Sciences, for their generous support of our programs and Rhône-Poulenc for partial financial support for J.P.S. Mass spectra were provided by the Mass Spectrometry Facility of the University of California, San Francisco, supported by the NIH Division of Research Resources.
    Trost BM; Surivet JP
    Angew Chem Int Ed Engl; 2001 Apr; 40(8):1468-1471. PubMed ID: 11317305
    [No Abstract]   [Full Text] [Related]  

  • 49. NSCl(2)(-): Thiazyl Dichloride-An Aza Analogue of Thionyl Dichloride A.S. thanks Prof. Dr. T. M. Klapötke (LMU München) for his generous support and Prof. Dr. R. D. Harcourt (Melbourne University) for many helpful discussions. We thank Prof. Dr. W. Schnick and S. Schmidt (LMU München) for carrying out the powder diffraction experiments, Dr. K. Karaghiosoff and Dr. J. Senker (MAS) for carrying out the NMR experiments.
    Keßenich E; Kopp F; Mayer P; Schulz A
    Angew Chem Int Ed Engl; 2001 May; 40(10):1904-1907. PubMed ID: 11385668
    [No Abstract]   [Full Text] [Related]  

  • 50. Resolution of the non-steady-state kinetics of the two-step mechanism for the Diels-Alder reaction between anthracene and tetracyanoethylene in acetonitrile.
    Handoo KL; Lu Y; Parker VD
    J Am Chem Soc; 2003 Aug; 125(31):9381-7. PubMed ID: 12889968
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Diels-Alder reactions of 4-triflyloxy-2,6,6-trimethyl-2,4-cyclohexadienone. An expedient methodology for the synthesis of bicyclo[2.2.2]oct-5-en-2-ones and bicyclo[2.2.2]octa-5,7-dien-2-ones.
    Lin YS; Chang SY; Yang MS; Rao CP; Peddinti RK; Tsai YF; Liao CC
    J Org Chem; 2004 Jan; 69(2):447-58. PubMed ID: 14725459
    [TBL] [Abstract][Full Text] [Related]  

  • 52. An Analytical Approach for a Comprehensive Study of Organic Aerosols The financial support by the Bundesministerium für Bildung und Forschung and the Senatsverwaltung für Wissenschaft, Forschung und Kultur des Landes Berlin (ISAS Berlin), and the Ministerium für Schule, Wissenschaft und Forschung NRW (ISAS Dortmund) is gratefully acknowledged. The authors want to thank U. Marggraff and W. Nigge (Dortmund) for assistence during MS measurements and Dr. R. Köppe (Univ. Karlsruhe) and Dr. H. Sievers (GSG Karlsruhe) for assistance in FT-ICR-MS measurements.
    Schrader W; Geiger J; Godejohann M; Warscheid B; Hoffmann T
    Angew Chem Int Ed Engl; 2001 Nov; 40(21):3998-4001. PubMed ID: 12404473
    [No Abstract]   [Full Text] [Related]  

  • 53. Immunosensing by a Synthetic Ligand-Gated Ion Channel Financial support from the board of the Swiss Federal Institutes of Technology (SPP Minast, 7.06) is acknowledged. We thank G. Corradin for numerous discussions and J. Lakey for critical reading of the manuscript.
    Terrettaz S; Ulrich WP; Guerrini R; Verdini A; Vogel H
    Angew Chem Int Ed Engl; 2001 May; 40(9):1740-1743. PubMed ID: 11353496
    [No Abstract]   [Full Text] [Related]  

  • 54. Novel Reactions Initiated by Titanocene Methylidenes: Deoxygenation of Sulfoxides, N-Oxides, and Selenoxides We thank Drs. D. H. Huang and G. Suizdak for NMR spectroscopic and mass spectroscopic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), fellowships from the National Science Foundation (S.A.S.) and the Alfred Benzons Foundation (K.B.S.), and grants from Abbott, Amgen, Boehringer-Ingelheim, GlaxoWellcome, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.
    Nicolaou KC; Koumbis AE; Snyder SA; Simonsen KB
    Angew Chem Int Ed Engl; 2000 Jul; 39(14):2529-2533. PubMed ID: 10941126
    [No Abstract]   [Full Text] [Related]  

  • 55. The Oxidative Power of Protonated Hydrogen Peroxide The work was supported by NFR (The Norwegian Research Council). The authors thank Drs. Gustav Bojesen and Steen Hammerum (University of Copenhagen) for generous cooperation, and Prof. H. Bernhard Schlegel (Wayne State University) for computer time and the use of a development version of Gaussian 98. Helpful suggestions from Profs. Terry B. McMahon (Waterloo University) and Michael T. Bowers (UC, Santa Barbara) are acknowledged.
    Leere Øiestad ÅM ÅM; Petersen AC; Bakken V; Vedde J; Uggerud E
    Angew Chem Int Ed Engl; 2001 Apr; 40(7):1305-1309. PubMed ID: 11301461
    [No Abstract]   [Full Text] [Related]  

  • 56. Highly Enantioselective Regiodivergent and Catalytic Parallel Kinetic Resolution This work was supported by the Ministero dell'Università e della Ricerca Scientifica e Tecnologica (MURST, Roma) and by the University of Pisa. We gratefully acknowledge Merck for the generous financial support derived from the 2000 ADP Chemistry Award.
    Bertozzi F; Crotti P; Macchia F; Pineschi M; Feringa BL
    Angew Chem Int Ed Engl; 2001 Mar; 40(5):930-932. PubMed ID: 11241649
    [No Abstract]   [Full Text] [Related]  

  • 57. The First Dendrimer-Based Enantioselective Fluorescent Sensor for the Recognition of Chiral Amino Alcohols The support of this work by the National Institute of Health (1R01GM58454) is gratefully acknowledged. We also thank the partial support from the donors of the Petroleum Research Fund-administered by the American Chemical Society.
    Pugh VJ; Hu QS; Pu L
    Angew Chem Int Ed Engl; 2000 Oct; 39(20):3638-3641. PubMed ID: 11091423
    [No Abstract]   [Full Text] [Related]  

  • 58. Unprecedented Detection of Distinct Barriers Involving Formally Enantiotopic Substituents: Phenyl Rotation in Solid Diphenyl Sulfoxide Conformational Studies by Dynamic NMR. Part 82. For Part 80 see ref. 1a, for Part 81 see ref. 1b. We thank J. E. Anderson (University College, London, UK), S. E. Biali (Hebrew University, Jerusalem, Israel), R. K. Harris (University of Durham, UK), W. B. Jennings (University College, Cork, Ireland), A. Rassat (École Normale Superieure, Paris, France) for critical reading of the manuscript, and I.Co.C.E.A., CNR, Bologna for access to the 400-MHz and solid-state NMR spectroscopy facilities. Financial support was received from MURST (national project "Stereoselection in Organic Synthesis") and from the University of Bologna (Funds for selected research topics 1999-2001).
    Casarini D; Lunazzi L; Mazzanti A
    Angew Chem Int Ed Engl; 2001 Jul; 40(13):2536-2540. PubMed ID: 11443692
    [No Abstract]   [Full Text] [Related]  

  • 59. Solution and Solid-Phase Synthesis of Functionalized 3-Arylbenzofurans by a Novel Cyclofragmentation - Release Pathway Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), doctoral fellowships from the National Science Foundation (S.A.S.) and the Department of Defense (J.A.P.), and grants from Abbott, Amgen, Boehringer - Ingelheim, Glaxo, Hoffmann - La Roche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.
    Nicolaou KC; Snyder SA; Bigot A; Pfefferkorn JA
    Angew Chem Int Ed Engl; 2000 Mar; 39(6):1093-1096. PubMed ID: 10760931
    [No Abstract]   [Full Text] [Related]  

  • 60. Reconstitution of Channel Proteins in (Polymerized) ABA Triblock Copolymer Membranes This work was supported by the Swiss National Science Foundation. We thank Dr. T. Hirt and Dr. J. Leukel for the synthesis of the triblock copolymer, Dr. P. Van Gelder and Dr. F. Dumas for bright and helpful discussions, and T. Haefele for his contribution to the experimental part.
    Meier W; Nardin C; Winterhalter M
    Angew Chem Int Ed Engl; 2000 Dec; 39(24):4599-4602. PubMed ID: 11169683
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.