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 *

296 related articles for article (PubMed ID: 11169652)

  • 1. The Synthesis of CP-263,114 and CP-225,917: Striking Long-Range Stereocontrol in the Fashioning of C7 Financial support was provided by the National Institutes of Health (Grant nos. CA-28824 and HL-25848 for S.J.D., CA-08748 for the Sloan-Kettering Institute Core Facility). Q.T. gratefully acknowledges the US Department of Defense for a postdoctoral fellowship (U.S. Army grant no. DAMD-17-99-1-9373). We thank the Pfizer Corporation, particularly Dr. T. Kaneko and Dr. T. T. Dabrah for discussions and for providing valuable CP samples from fermentation broth. We are grateful to Dr. Dongfang Meng for his major contributions to this work. We also thank George Sukenick of the Sloan-Kettering Institute Core Facility for mass spectral analyses and assistance in NMR spectroscopic and HPLC analyses, and Sylvi Rusli for mass spectral analyses.
    Tan Q; Danishefsky SJ
    Angew Chem Int Ed Engl; 2000 Dec; 39(24):4509-4511. PubMed ID: 11169652
    [No Abstract]   [Full Text] [Related]  

  • 2. The Synthesis of CP-263,114 and CP-225,917: Striking Long-Range Stereocontrol in the Fashioning of C7 Financial support was provided by the National Institutes of Health (Grant nos. CA-28824 and HL-25848 for S.J.D., CA-08748 for the Sloan-Kettering Institute Core Facility). Q.T. gratefully acknowledges the US Department of Defense for a postdoctoral fellowship (U.S. Army grant no. DAMD-17-99-1-9373). We thank the Pfizer Corporation, particularly Dr. T. Kaneko and Dr. T. T. Dabrah for discussions and for providing valuable CP samples from fermentation broth. We are grateful to Dr. Dongfang Meng for his major contributions to this work. We also thank George Sukenick of the Sloan-Kettering Institute Core Facility for mass spectral analyses and assistance in NMR spectroscopic and HPLC analyses, and Sylvi Rusli for mass spectral analyses.
    Tan Q; Danishefsky SJ
    Angew Chem Int Ed Engl; 2001 Feb; 40(4):647. PubMed ID: 11241592
    [No Abstract]   [Full Text] [Related]  

  • 3. Toward Fully Synthetic Homogeneous Glycoproteins: A High Mannose Core Containing Glycopeptide Carrying Full H-Type 2 Human Blood Group Specificity This work was supported by the National Institutes of Health (Grant nos.: HL-25848 and CA-28824 (to S.J.D.), and CA-710506 (to K.O.L.)). Postdoctoral fellowship support is gratefully acknowledged by Z.-G.W. (US Army breast cancer grant no.: DAMD17-97-1-7119) and M.V. (NIH grant no.: CA-62948-04). We gratefully acknowledge Dr. George Sukenick of the Sloan-Kettering Institute's NMR core facility for mass spectral and NMR spectroscopic analyses (SKI core grant no.: CA-08748).
    Wang ZG; Zhang X; Visser M; Live D; Zatorski A; Iserloh U; Lloyd KO; Danishefsky SJ
    Angew Chem Int Ed Engl; 2001 May; 40(9):1728-1732. PubMed ID: 11353493
    [No Abstract]   [Full Text] [Related]  

  • 4. Thermal Intermolecular Hetero Diels-Alder Cycloadditions of Aldehydes and Imines via o-Quinone Dimethides This work was supported by the National Institutes of Health (AI 16943/CA 28824). Postdoctoral Fellowship support is gratefully acknowledged by M.F.H. (5T32 CA62948-05) and J.G.A (NIH, CA-80356). We are grateful to Dr. George Sukenick (NMR Core Facility, Sloan-Kettering Institute) for NMR and mass spectral analyses.
    Hentemann MF; Allen JG; Danishefsky SJ
    Angew Chem Int Ed Engl; 2000 Jun; 39(11):1937-1940. PubMed ID: 10940987
    [No Abstract]   [Full Text] [Related]  

  • 5. Synthesis of the Functionalized Macrocyclic Core of Proteasome Inhibitors TMC-95A and B This work was supported by grants from the National Institutes of Health (grant CA28824). We thank Dr. George Sukenick and Sylvi Rusli of the MSKCC NMR Core Facility for NMR and mass spectral analyses (NIH Grant CA08748).
    Lin S; Danishefsky SJ
    Angew Chem Int Ed Engl; 2001 May; 40(10):1967-1970. PubMed ID: 11385688
    [No Abstract]   [Full Text] [Related]  

  • 6. The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2 Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, a NIH Postdoctoral Fellowship to C.S.B., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the Tanabe Seiyaku Co., Ltd for financial support. Finally we thank Dr George T. Furst, Dr. Patrick J. Carroll, and Dr. Rakesh Kohli of the University of Pennsylvania Spectroscopic Service Center for assistance in securing and interpreting high-field NMR spectra, X-ray crystal structures, and mass spectra, respectively.
    Smith III AB; Lin Q; Doughty VA; Zhuang L; McBriar MD; Kerns JK; Brook CS; Murase N; Nakayama K
    Angew Chem Int Ed Engl; 2001 Jan; 40(1):196-199. PubMed ID: 11169711
    [No Abstract]   [Full Text] [Related]  

  • 7. The Spongistatins: Architecturally Complex Natural Products-Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, NIH Postdoctoral Fellowships to A.M.B. and W.H.M., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the Tanabe Seiyaku Co., Ltd for financial support. Finally we thank Dr. George T. Furst, Dr. Patrick J. Carroll, Dr. Rakesh Kohli, and Mr John Dykins of the University of Pennsylvania Spectroscopic Service Center for assistance in securing and interpreting high-field NMR spectra, X-ray crystal structures, and mass spectra.
    Smith III AB; Doughty VA; Lin Q; Zhuang L; McBriar MD; Boldi AM; Moser WH; Murase N; Nakayama K; Sobukawa M
    Angew Chem Int Ed Engl; 2001 Jan; 40(1):191-195. PubMed ID: 11169710
    [No Abstract]   [Full Text] [Related]  

  • 8. From Glycals to Glycopeptides: A Convergent and Stereoselective Total Synthesis of a High Mannose N-Linked Glycopeptide This work was supported by the National Institutes of Health (Grant Numbers AI16943/CA28824). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses (NIH Grant Number: CA08748).
    Wang ZG; Zhang X; Live D; Danishefsky SJ
    Angew Chem Int Ed Engl; 2001 Feb; 40(4):647. PubMed ID: 11241590
    [No Abstract]   [Full Text] [Related]  

  • 9. Mechanistic Studies of Periodinane-Mediated Reactions of Anilides and Related Systems Professors M. G. Finn, A. Eschenmoser, and M. E. Newcomb are gratefully acknowledged for valuable discussions and suggestions. We thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. We would also like to thank Dr. G. Vasilikogiannakis for helpful discussions and an anonymous referee for critical suggestions. 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.), postdoctoral fellowships from ArrayBiopharma (N.Z.) and Bayer AG (R.K.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.
    Nicolaou KC; Baran PS; Kranich R; Zhong YL; Sugita K; Zou N
    Angew Chem Int Ed Engl; 2001 Jan; 40(1):202-206. PubMed ID: 11169713
    [No Abstract]   [Full Text] [Related]  

  • 10. Total Synthesis and Proof of Stereochemistry of Natural and Unnatural Pinnaic Acids: A Remarkable Long-Range Stereochemical Effect in the Reduction of 17-Oxo Precursors of the Pinnaic Acids This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses. We would like to thank professor Nakanishi for his supportive interest in the project.
    Carson MW; Kim G; Danishefsky SJ
    Angew Chem Int Ed Engl; 2001 Dec; 40(23):4453-4456. PubMed ID: 12404443
    [No Abstract]   [Full Text] [Related]  

  • 11. Concise Stereoselective Routes to Advanced Intermediates Related to Natural and Unnatural Pinnaic Acid This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154), M.F.H. (5T32 CA62948-05), and D.T. (Schering Research Foundation, Berlin). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses.
    Carson MW; Kim G; Hentemann MF; Trauner D; Danishefsky SJ
    Angew Chem Int Ed Engl; 2001 Dec; 40(23):4450-4452. PubMed ID: 12404442
    [No Abstract]   [Full Text] [Related]  

  • 12. Total Synthesis of Apoptolidin: Part 2. Coupling of Key Building Blocks and Completion of the Synthesis We thank Dr. C. Khosla and Dr. Y. Hayakawa for generous gifts of apoptolidin, and Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. This work was financially supported by the National Institutes of Health (USA), the Skaggs Institute for Chemical Biology, American Biosciences, a predoctoral fellowship from Boehringer Ingelheim (to Y.L.), a postdoctoral fellowship the George Hewitt Foundation (to K.C.F.), and grants from Abbott Laboratories, ArrayBiopharma, Bayer, Boehringer Ingelheim, DuPont, Glaxo, Hoffmann-LaRoche, Merck, Novartis, Pfizer, and Schering Plough.
    Nicolaou KC; Li Y; Fylaktakidou KC; Mitchell HJ; Sugita K
    Angew Chem Int Ed Engl; 2001 Oct; 40(20):3854-3857. PubMed ID: 11668554
    [No Abstract]   [Full Text] [Related]  

  • 13. Total Synthesis of Apoptolidin: Part 1. Retrosynthetic Analysis and Construction of Building Blocks We thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. This work was financially supported by the National Institutes of Health (USA), the Skaggs Institute for Chemical Biology, American Biosciences, a pre-doctoral fellowship from Boehringer Ingelheim (Y.L.), a postdoctoral fellowship the George Hewitt Foundation (K.C.F.), and grants from Abbott Laboratories, ArrayBiopharma, Bayer, Boehringer Ingelheim, DuPont, Glaxo, Hoffmann-LaRoche, Merck, Novartis, Pfizer, and Schering Plough.
    Nicolaou KC; Li Y; Fylaktakidou KC; Mitchell HJ; Wei HX; Weyershausen B
    Angew Chem Int Ed Engl; 2001 Oct; 40(20):3849-3854. PubMed ID: 11668553
    [No Abstract]   [Full Text] [Related]  

  • 14. Synthesis of the FGHI Ring System of Azaspiracid We thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric 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 Bristol-Myers Squibb (F.B.), postdoctoral fellowships from the Academy of Finland, the Ella and Georg Ehrnrooth Foundation, and the Tauno Tönning Foundation (all to P.M.P.), ArrayBiopharma (N.Z.), and Bayer AG (N.D.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.
    Nicolaou KC; Pihko PM; Diedrichs N; Zou N; Bernal F
    Angew Chem Int Ed Engl; 2001 May; 40(9):1573. PubMed ID: 11353466
    [No Abstract]   [Full Text] [Related]  

  • 15. Synthesis of the FGHI Ring System of Azaspiracid We thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric 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 Bristol-Myers Squibb (F.B.), postdoctoral fellowships from the Academy of Finland, the Ella and Georg Ehrnrooth Foundation, and the Tauno Tönning Foundation (all to P.M.P.), ArrayBiopharma (N.Z.), and Bayer AG (N.D.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.
    Nicolaou KC; Pihko PM; Diedrichs N; Zou N; Bernal F
    Angew Chem Int Ed Engl; 2001 Apr; 40(7):1262-1265. PubMed ID: 11301444
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1 Financial support was provided by the EPSRC (GR/L41646), Cambridge Commonwealth Trust (Scholarship to M.J.C.), EC (Marie Curie Postdoctoral Fellowship to J.L.A.), DFG (Postdoctoral Fellowship to T.T.), NSERC-Canada (Postdoctoral Fellowship to R.M.O.), Churchill College (Research Fellowship to D.J.W.), Kingapos;s College and Sims Fund, Cambridge (Scholarship to D.Y.K.C.). We also thank Merck and AstraZeneca Pharmaceuticals for generous support, and Dr. Anne Butlin (AZ) and Dr. Nick Bampos (Cambridge) for valuable assistance.
    Paterson I; Chen DY; Coster MJ; Aceña JL; Bach J; Gibson KR; Keown LE; Oballa RM; Trieselmann T; Wallace DJ; Hodgson AP; Norcross RD
    Angew Chem Int Ed Engl; 2001 Nov; 40(21):4055-4060. PubMed ID: 12404491
    [No Abstract]   [Full Text] [Related]  

  • 19. Total Synthesis of Hybocarpone We thank Dr. D. H. Huang, Dr. G. Siuzdak and Dr. I. Ioannou for NMR spectroscopic, mass spectrometric and computational assistance, respectively. Financial support for this work was provided by the Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-La Roche, DuPont, Merck, Novartis, Pfizer, CaPCURE, and Schering Plough.
    Nicolaou KC; Gray D
    Angew Chem Int Ed Engl; 2001 Feb; 40(4):761-763. PubMed ID: 11241615
    [No Abstract]   [Full Text] [Related]  

  • 20. Isolation and Characterization of the Osmium(V)-Imido Complex [Os(V)(Tp)(Cl)(2)(NH)] We are grateful to the National Science Foundation under Grant number CHE-9503738, the Los Alamos National Laboratory (DOE) under Grant Number 10730-001-00-2C, and the Laboratory Directed Research and Development Program for support of this research. M. H. V. Huynh gratefully acknowledges postdoctoral fellowship support from the Directorapos;s Office of Los Alamos National Laboratory. Los Alamos National Laboratory is operated by the University of California for the U.S. Department of Energy under Contract W-7405-ENG-36. We also thank Dr. Paul R. Sharp (Professor of Chemistry, University of Missouri, Columbia, MO, 65211) for the information on transition metal parent imido complexes.
    Huynh MH; White PS; John KD; Meyer TJ
    Angew Chem Int Ed Engl; 2001 Nov; 40(21):4049-4051. PubMed ID: 12404489
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 15.