Works matching AU Sasmal, Pradip K.

Results: 11
    1

    Studies toward the Synthesis of Azadirachtin, Part 2: Construction of Fully Functionalized ABCD Ring Frameworks and Unusual Intramolecular Reactions Induced by Close-Proximity EffectsWe 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 grants from the National Institutes of Health (USA) and the Skaggs Institute for Chemical Biology, a postdoctoral fellowship from the Alexander von Humboldt Foundation (to F.K.), and a predoctoral fellowship from the Division of Organic Chemistry of the American Chemical Society sponsored by Novartis (to A.J.R.).

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 22, p. 3447, doi. 10.1002/anie.200500217
    By:
    • K. C. Nicolaou;
    • Pradip K. Sasmal;
    • Theocharis V. Koftis;
    • Antonella Converso;
    • Eriketi Loizidou;
    • Florian Kaiser;
    • A. J. Roecker;
    • Constantinos C. Dellios;
    • Xiao-Wen Sun;
    • Goran Petrovic
    Publication type:
    Article
    2

    Studies toward the Synthesis of Azadirachtin, Part 1: Total Synthesis of a Fully Functionalized ABC Ring Framework and Coupling with a Norbornene DomainWe 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 grants from the National Institutes of Health (USA) and the Skaggs Institute for Chemical Biology, and a predoctoral fellowship from the Division of Organic Chemistry of the American Chemical Society sponsored by Novartis (to A.J.R.).

    Published in:
    Angewandte Chemie International Edition, 2005, v. 44, n. 22, p. 3443, doi. 10.1002/anie.200500216
    By:
    • K. C. Nicolaou;
    • Pradip K. Sasmal;
    • A. J. Roecker;
    • Xiao-Wen Sun;
    • Sunil Mandal;
    • Antonella Converso
    Publication type:
    Article
    3
    4

    Total Synthesis of 1-O-MethyllaterifloroneWe thank Dr. D H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively, and Dr. R. K. Chadha for X-ray crystallographic analysis. Financial support for this work was provided by The Skaggs Institute for Chemical Biology and the National Institutes of Health (USA).

    Published in:
    Angewandte Chemie International Edition, 2003, v. 42, n. 35, p. 4225, doi. 10.1002/anie.200351805
    By:
    • K. C. Nicolaou;
    • Pradip K. Sasmal;
    • Hao Xu;
    • Kenji Namoto;
    • Andreas Ritzén
    Publication type:
    Article
    5

    Design, Synthesis, and Biological Properties of Highly Potent Epothilone B Analogues ( 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), and Novartis Pharma. )

    Published in:
    Angewandte Chemie International Edition, 2003, v. 42, n. 30, p. 3515, doi. 10.1002/anie.200351819
    By:
    • K. C. Nicolaou;
    • Pradip K. Sasmal;
    • Gerasimos Rassias;
    • Mali Venkat Reddy;
    • Karl-Heinz Altmann;
    • Markus Wartmann;
    • Aurora O'Brate;
    • Paraskevi Giannakakou
    Publication type:
    Article
    6
    7

    Iodine as a New Deoximating Agent.

    Published in:
    Synthetic Communications, 1999, v. 29, n. 21, p. 3667, doi. 10.1080/00397919908086004
    By:
    • Yadav, J. S.;
    • Sasmal, Pradip K.;
    • Chand, Pratap K.
    Publication type:
    Article
    8

    Studies toward the Synthesis of Azadirachtin, Part 2: Construction of Fully Functionalized ABCD Ring Frameworks and Unusual Intramolecular Reactions Induced by Close-Proximity EffectsWe 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 grants from the National Institutes of Health (USA) and the Skaggs Institute for Chemical Biology, a postdoctoral fellowship from the Alexander von Humboldt Foundation (to F.K.), and a predoctoral fellowship from the Division of Organic Chemistry of the American Chemical Society sponsored by Novartis (to A.J.R.).

    Published in:
    Angewandte Chemie, 2005, v. 117, n. 22, p. 3513, doi. 10.1002/ange.200500217
    By:
    • K. C. Nicolaou;
    • Pradip K. Sasmal;
    • Theocharis V. Koftis;
    • Antonella Converso;
    • Eriketi Loizidou;
    • Florian Kaiser;
    • A. J. Roecker;
    • Constantinos C. Dellios;
    • Xiao-Wen Sun;
    • Goran Petrovic
    Publication type:
    Article
    9

    Studies toward the Synthesis of Azadirachtin, Part 1: Total Synthesis of a Fully Functionalized ABC Ring Framework and Coupling with a Norbornene DomainWe 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 grants from the National Institutes of Health (USA) and the Skaggs Institute for Chemical Biology, and a predoctoral fellowship from the Division of Organic Chemistry of the American Chemical Society sponsored by Novartis (to A.J.R.).

    Published in:
    Angewandte Chemie, 2005, v. 117, n. 22, p. 3509, doi. 10.1002/ange.200500216
    By:
    • K. C. Nicolaou;
    • Pradip K. Sasmal;
    • A. J. Roecker;
    • Xiao-Wen Sun;
    • Sunil Mandal;
    • Antonella Converso
    Publication type:
    Article
    10

    Total Synthesis of 1-O-MethyllaterifloroneWe thank Dr. D H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively, and Dr. R. K. Chadha for X-ray crystallographic analysis. Financial support for this work was provided by The Skaggs Institute for Chemical Biology and the National Institutes of Health (USA).

    Published in:
    Angewandte Chemie, 2003, v. 115, n. 35, p. 4357, doi. 10.1002/ange.200351805
    By:
    • K. C. Nicolaou;
    • Pradip K. Sasmal;
    • Hao Xu;
    • Kenji Namoto;
    • Andreas Ritzén
    Publication type:
    Article
    11

    Design, Synthesis, and Biological Properties of Highly Potent Epothilone B Analogues ( 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), and Novartis Pharma. )

    Published in:
    Angewandte Chemie, 2003, v. 115, n. 30, p. 3639, doi. 10.1002/ange.200351819
    By:
    • K. C. Nicolaou;
    • Pradip K. Sasmal;
    • Gerasimos Rassias;
    • Mali Venkat Reddy;
    • Karl-Heinz Altmann;
    • Markus Wartmann;
    • Aurora O'Brate;
    • Paraskevi Giannakakou
    Publication type:
    Article