Works matching AU Fokin, A. V.

Results: 147
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    SuFEx-Based Synthesis of Polysulfates.

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    Angewandte Chemie, 2014, v. 126, n. 36, p. 9620, doi. 10.1002/ange.201403758
    By:
    • Dong, Jiajia;
    • Sharpless, K. Barry;
    • Kwisnek, Luke;
    • Oakdale, James S.;
    • Fokin, Valery V.
    Publication type:
    Article
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    Hydrogenation of the YFe alloy.

    Published in:
    Inorganic Materials, 2015, v. 51, n. 6, p. 578, doi. 10.1134/S0020168515060047
    By:
    • Fokin, V.;
    • Fokina, E.;
    • Tarasov, B.
    Publication type:
    Article
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    Iterative In Situ Click Chemistry Creates Antibody-like Protein-Capture Agents.

    Published in:
    Angewandte Chemie International Edition, 2009, v. 48, n. 27, p. 4944, doi. 10.1002/anie.200900488
    By:
    • Agnew, Heather D.;
    • Rohde, Rosemary D.;
    • Millward, Steven W.;
    • Nag, Arundhati;
    • Yeo, Woon-Seok;
    • Hein, Jason E.;
    • Pitram, Suresh M.;
    • Tariq, Abdul Ahad;
    • Burns, Vanessa M.;
    • Krom, Russell J.;
    • Fokin, Valery V.;
    • Sharpless, K. Barry;
    • Heath, James R.
    Publication type:
    Article
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    Copper-Catalyzed Reaction Cascade: Direct Conversion of Alkynes into N-Sulfonylazetidin-2-iminesWe thank the National Institutes of Health, the National Institute of General Medical Sciences (GM28384), the Skaggs Institute for Chemical Biology, and Pfizer, Inc. for financial support. We also thank Prof. K. B. Sharpless for valuable advice and stimulating discussions.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 19, p. 3157, doi. 10.1002/anie.200503936
    By:
    • Matthew Whiting;
    • Valery V. Fokin
    Publication type:
    Article
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    Practical Synthesis of Amides from In Situ Generated Copper(I) Acetylides and Sulfonyl AzidesWe thank the National Institutes of Health, the National Institute of General Medical Sciences (GM28384), the Skaggs Institute for Chemical Biology, and Pfizer, Inc. for financial support. We also thank Prof. K. B. Sharpless, Prof. M. G. Finn, and Dr. M. Whiting for valuable advice and stimulating discussions.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 19, p. 3154, doi. 10.1002/anie.200503805
    By:
    • Michael P. Cassidy;
    • Jessica Raushel;
    • Valery V. Fokin
    Publication type:
    Article
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    Inhibitors of HIV-1 Protease by Using In Situ Click ChemistryWe thank the National Institute of General Medical Sciences, the National Institutes of Health (GM048870), the Skaggs Institute for Chemical Biology, and the W. M. Keck Foundation (K.B.S.) for financial support.

    Published in:
    Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1435, doi. 10.1002/anie.200502161
    By:
    • Matthew Whiting;
    • John Muldoon;
    • Ying-Chuan Lin;
    • Steven M. Silverman;
    • William Lindstrom;
    • Arthur J. Olson;
    • Hartmuth C. Kolb;
    • M. G. Finn;
    • K. Barry Sharpless;
    • John H. Elder;
    • Valery V. Fokin
    Publication type:
    Article
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    “On Water”: Unique Reactivity of Organic Compounds in Aqueous SuspensionWe thank Dr. Vladislav Litosh for carrying out preliminary work. Support from the National Institutes of Health, National Institute of General Medical Sciences (GM 28384), the National Science Foundation (CHE9985553), the Skaggs Institute for Chemical Biology, and the W. M. Keck Foundation is gratefully acknowledged. S.N. thanks the Skaggs Institute for a postdoctoral fellowship. We also thank Dr. Suresh Suri, Edwards Air Force Base, California, for a generous gift of quadricyclane. We urge our fellow chemists to float their problematic reactions on water and to send observations of success or failure to us at onwater@scripps.edu for public dissemination with attribution.

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 21, p. 3275, doi. 10.1002/anie.200462883
    By:
    • Sridhar Narayan;
    • John Muldoon;
    • M. G. Finn;
    • Valery V. Fokin;
    • Hartmuth C. Kolb;
    • K. Barry Sharpless
    Publication type:
    Article
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    Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and AlkynesWe thank the National Institute of General Medical Sciences, the National Institutes of Health (GM 28284), the National Science Foundation (CHE-9985553), the W. M. Keck Foundation, the Skaggs Institute for Chemical Biology, the MRSEC Program of the National Science Foundation (award no. DMR-0213618 for the Center for Polymeric Interfaces and Macromolecular Assemblies), the NIRT Program of the National Science Foundation (grant no. 0210247), IBM Corporation, DOE-BES, and NSF International/DAAD for financial support. We are also grateful to Prof. M. G. Finn for helpful discussions.

    Published in:
    Angewandte Chemie International Edition, 2004, v. 43, n. 30, p. 3928, doi. 10.1002/anie.200454078
    By:
    • Peng Wu;
    • Alina K. Feldman;
    • Anne K. Nugent;
    • Craig J. Hawker;
    • Arnulf Scheel;
    • Brigitte Voit;
    • Jeffrey Pyun;
    • Jean M. J. Fréchet;
    • K. Barry Sharpless;
    • Valery V. Fokin
    Publication type:
    Article
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