Works matching Eli Lilly %26 Co.

Results: 1491
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    Gold(I)-Catalyzed Cyclizations of Silyl Enol Ethers: Application to the Synthesis of (+)-Lycopladine AWe gratefully acknowledge the University of California, Berkeley, NIHGMS (R01 GM073932-01), Merck Research Laboratories, Bristol-Myers Squibb, Amgen Inc., DuPont, GlaxoSmithKline, Eli Lilly & Co., Pfizer, AstraZeneca, and Roche for financial support. J.J.K.-S. thanks Eli Lilly & Co. for a graduate fellowship. We thank Lauren A. Young for the preparation of tributylallenylstannane.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 36, p. 6137, doi. 10.1002/ange.200602035
    By:
    • Steven T. Staben;
    • Joshua J. Kennedy-Smith;
    • David Huang;
    • Britton K. Corkey;
    • Rebecca L. LaLonde;
    • F. Dean Toste
    Publication type:
    Article
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    Gold(I)-Catalyzed Cyclizations of Silyl Enol Ethers: Application to the Synthesis of (+)-Lycopladine AWe gratefully acknowledge the University of California, Berkeley, NIHGMS (R01 GM073932-01), Merck Research Laboratories, Bristol-Myers Squibb, Amgen Inc., DuPont, GlaxoSmithKline, Eli Lilly & Co., Pfizer, AstraZeneca, and Roche for financial support. J.J.K.-S. thanks Eli Lilly & Co. for a graduate fellowship. We thank Lauren A. Young for the preparation of tributylallenylstannane.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 36, p. 5991, doi. 10.1002/anie.200602035
    By:
    • Steven T. Staben;
    • Joshua J. Kennedy-Smith;
    • David Huang;
    • Britton K. Corkey;
    • Rebecca L. LaLonde;
    • F. Dean Toste
    Publication type:
    Article
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    Enantioselective Synthesis of Cyclic Ethers through a Vanadium-Catalyzed Resolution/Oxidative CyclizationWe gratefully acknowledge the University of California (Berkeley), Merck Research Laboratories, Bristol-Myers Squibb, Amgen Inc., DuPont, GlaxoSmithKline, Eli Lilly & Co., Abbott, and Pfizer for financial support. A.B. thanks the Swiss National Science Foundation for a postdoctoral fellowship.

    Published in:
    Angewandte Chemie, 2006, v. 118, n. 13, p. 2150, doi. 10.1002/ange.200503852
    By:
    • Aurélien Blanc;
    • F. Dean Toste
    Publication type:
    Article
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    Total Synthesis of Avrainvillamide (CJ-17,665) and Stephacidin BWe are deeply grateful to Professor William Fenical (Scripps Institution of Oceanography) for his invaluable advice and support, and for generously providing samples of the crude extracts of Aspergillus sp. (CNC358). We are indebted to Professor Axel Zeeck, Dr. Jennifer Qian-Cutrone of BMS, and Pfizer for authentic samples of avrainvillamide, stephacidin B, and CJ-17,665, respectively. Ms. Sarah Siegel of the Kelly group is acknowledged for expertise in obtaining CD spectra. We thank Dr. D.-H. Huang and Dr. L. Pasternak for assistance with NMR spectroscopic studies, and Dr. G. Suizdak for assistance with mass spectrometry measurements. We thank Biotage for a generous donation of process vials that were used extensively during these studies. Financial support for this work was provided by The Scripps Research Institute, Eli Lilly & Co, GlaxoSmithKline, the Searle Scholarship fund, and the NIH (predoctoral fellowship to C.A.

    Published in:
    Angewandte Chemie, 2005, v. 117, n. 25, p. 3960, doi. 10.1002/ange.200500655
    By:
    • Phil S. Baran;
    • Carlos A. Guerrero;
    • Benjamin D. Hafensteiner;
    • Narendra B. Ambhaikar
    Publication type:
    Article
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    A Remarkable Ring Contraction En Route to the Chartelline AlkaloidsSteven Nguyen is gratefully acknowledged for his technical contributions. We thank Dr. D. H. Huang and Dr. L. Pasternak for assistance with the NMR spectroscopic analysis, and Dr. G. Suizdak and Dr. R. Chadha for assistance with the mass-spectrometric and X-ray crystallographic analysis, respectively. We are grateful to Biotage for their generous donation of the microwave process vials used extensively during these studies. Financial support for this work was provided by The Scripps Research Institute, the Department of Defense (predoctoral fellowship to R. A. S.), Eli Lilly & Co, GlaxoSmithKline, and the Searle Scholarship Fund.

    Published in:
    Angewandte Chemie, 2005, v. 117, n. 24, p. 3780, doi. 10.1002/ange.200500522
    By:
    • Phil S. Baran;
    • Ryan A. Shenvi;
    • Christos A. Mitsos
    Publication type:
    Article
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    Gold(I)-Catalyzed 5-endo-dig Carbocyclization of Acetylenic Dicarbonyl CompoundsWe gratefully acknowledge the University of California, Berkeley, Merck Research Laboratories, and Amgen Inc. for financial support. J.J.K.-S. thanks Eli Lilly & Co. for a graduate fellowship. The Center for New Directions in Organic Synthesis is supported by Bristol-Myers Squibb as a Sponsoring Member and Novartis Pharma as a Supporting Member.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 40, p. 5464, doi. 10.1002/ange.200460844
    By:
    • Steven T. Staben;
    • Joshua J. Kennedy-Smith;
    • F. Dean Toste
    Publication type:
    Article
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    Intermolecular Dienyl Pauson–Khand ReactionThis research was supported by a grant (CHE-9800445) from the National Science Foundation. High-resolution mass spectra were provided by the University of California, San Francisco. X-ray crystallographic data was collected at the University of California, Berkeley (CHEXRAY). Fellowship assistance from Eli Lilly and Co. (N.M.D. and T.J.W.) is gratefully acknowledged.

    Published in:
    Angewandte Chemie, 2004, v. 116, n. 23, p. 3138, doi. 10.1002/ange.200454117
    By:
    • Paul A. Wender;
    • Nicole M. Deschamps;
    • Travis J. Williams
    Publication type:
    Article
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    Enantioselective Synthesis of Cyclic Ethers through a Vanadium-Catalyzed Resolution/Oxidative CyclizationWe gratefully acknowledge the University of California (Berkeley), Merck Research Laboratories, Bristol-Myers Squibb, Amgen Inc., DuPont, GlaxoSmithKline, Eli Lilly & Co., Abbott, and Pfizer for financial support. A.B. thanks the Swiss National Science Foundation for a postdoctoral fellowship.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 13, p. 2096, doi. 10.1002/anie.200503852
    By:
    • Aurélien Blanc;
    • F. Dean Toste
    Publication type:
    Article
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    Total Synthesis of Avrainvillamide (CJ-17,665) and Stephacidin BWe are deeply grateful to Professor William Fenical (Scripps Institution of Oceanography) for his invaluable advice and support, and for generously providing samples of the crude extracts of Aspergillus sp. (CNC358). We are indebted to Professor Axel Zeeck, Dr. Jennifer Qian-Cutrone of BMS, and Pfizer for authentic samples of avrainvillamide, stephacidin B, and CJ-17,665, respectively. Ms. Sarah Siegel of the Kelly group is acknowledged for expertise in obtaining CD spectra. We thank Dr. D.-H. Huang and Dr. L. Pasternak for assistance with NMR spectroscopic studies, and Dr. G. Suizdak for assistance with mass spectrometry measurements. We thank Biotage for a generous donation of process vials that were used extensively during these studies. Financial support for this work was provided by The Scripps Research Institute, Eli Lilly & Co, GlaxoSmithKline, the Searle Scholarship fund, and the NIH (predoctoral fellowship to C.A.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 25, p. 3892, doi. 10.1002/anie.200500655
    By:
    • Phil S. Baran;
    • Carlos A. Guerrero;
    • Benjamin D. Hafensteiner;
    • Narendra B. Ambhaikar
    Publication type:
    Article
    17

    A Remarkable Ring Contraction En Route to the Chartelline AlkaloidsSteven Nguyen is gratefully acknowledged for his technical contributions. We thank Dr. D. H. Huang and Dr. L. Pasternak for assistance with the NMR spectroscopic analysis, and Dr. G. Suizdak and Dr. R. Chadha for assistance with the mass-spectrometric and X-ray crystallographic analysis, respectively. We are grateful to Biotage for their generous donation of the microwave process vials used extensively during these studies. Financial support for this work was provided by The Scripps Research Institute, the Department of Defense (predoctoral fellowship to R. A. S.), Eli Lilly & Co, GlaxoSmithKline, and the Searle Scholarship Fund.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 24, p. 3714, doi. 10.1002/anie.200500522
    By:
    • Phil S. Baran;
    • Ryan A. Shenvi;
    • Christos A. Mitsos
    Publication type:
    Article
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    Effect of growth hormone treatment on adult height in peripubertal children with idiopathic short stature: a randomized, double-blind, placebo-controlled trial.

    Published in:
    2004
    By:
    • Leschek, Ellen Werber;
    • Rose, Susan R;
    • Yanovski, Jack A;
    • Troendle, James F;
    • Quigley, Charmian A;
    • Chipman, John J;
    • Crowe, Brenda J;
    • Ross, Judith L;
    • Cassorla, Fernando G;
    • Blum, Werner F;
    • Cutler, Gordon B Jr;
    • Baron, Jeffrey;
    • National Institute of Child Health and Human Development-Eli Lilly & Co. Growth Hormone Collaborative Group
    Publication type:
    journal article
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    Patent watch.

    Published in:
    Nature Reviews Drug Discovery, 2010, v. 9, n. 10, p. 756, doi. 10.1038/nrd3291
    By:
    • Harrison, Charlotte
    Publication type:
    Article
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    TRENDS & TECHNOLOGY.

    Published in:
    Anaesthesia, Pain & Intensive Care, 2011, v. 15, n. 3, p. 195
    Publication type:
    Article
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    New indication.

    Published in:
    Formulary, 2008, v. 43, n. 7, p. 234
    Publication type:
    Article
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    New indication.

    Published in:
    Formulary, 2007, v. 42, n. 11, p. 626
    Publication type:
    Article
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    SCIENCE.

    Published in:
    Bulletin of the Atomic Scientists, 1960, v. 16, n. 5, p. 192
    Publication type:
    Article
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    Bridges, not barriers.

    Published in:
    Nature, 2010, v. 463, n. 7284, p. 999, doi. 10.1038/463999b
    Publication type:
    Article
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    Eli Lilly.

    Published in:
    Business & Society Review (00453609), 1994, n. 88, p. 70
    By:
    • Moskowitz, Milton R.
    Publication type:
    Article
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