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Design and Total Synthesis of a Superior Family of Epothilone Analogues, which Eliminate Xenograft Tumors to a Nonrelapsable State ( This work was supported by the National Institutes of Health (CA-28824). F.Y. is a Uehara Memorial Foundation Fellow. A.R. is a NIH Cancer Pharmacology Fellow (T32-CA62948). A.E.G. is a MSKCC Experimental Therapeutics Center Fellow. We thank Sylvi Rusli (NMR Core Facility, CA-02848) and Anna Dudkina for mass-spectral analyses. We thank Dr. Klaus Gerth and Dr. Rolf Müller of GBF, Germany for the picture of Sorangium cellulos that is part of the frontispiece design. )
- Published in:
- Angewandte Chemie, 2003, v. 115, n. 39, p. 4910, doi. 10.1002/ange.200352361
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- Publication type:
- Article
Synthesis and Conformational Analysis of (E)-9,10-Dehydroepothilone B: A Suggestive Link between the Chemistry and Biology of Epothilones ( This work was supported by the National Institutes of Health (CA-28824). F.Y. is a Uehara Memorial Foundation Fellow. A.R. is a NIH Cancer Pharmacology Fellow (T32-CA62948). A.E.G. is a MSKCC Experimental Therapeutics Center Fellow. We thank Ms. Sylvi Rusli (NMR Core Facility, CA-02848) and Mrs. Anna Dudkina for mass spectral analyses. )
- Published in:
- Angewandte Chemie, 2003, v. 115, n. 22, p. 2622, doi. 10.1002/ange.200351407
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- Publication type:
- Article
Novel 2-Substituted Quinolin-4-yl-benzenesulfonate Derivatives: Synthesis, Antiproliferative Activity, and Inhibition of Cellular Tubulin Polymerization.
- Published in:
- ChemMedChem, 2011, v. 6, n. 6, p. 1119, doi. 10.1002/cmdc.201100121
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- Publication type:
- Article
Design and Total Synthesis of a Superior Family of Epothilone Analogues, which Eliminate Xenograft Tumors to a Nonrelapsable State ( This work was supported by the National Institutes of Health (CA-28824). F.Y. is a Uehara Memorial Foundation Fellow. A.R. is a NIH Cancer Pharmacology Fellow (T32-CA62948). A.E.G. is a MSKCC Experimental Therapeutics Center Fellow. We thank Sylvi Rusli (NMR Core Facility, CA-02848) and Anna Dudkina for mass-spectral analyses. We thank Dr. Klaus Gerth and Dr. Rolf Müller of GBF, Germany for the picture of Sorangium cellulos that is part of the frontispiece design. )
- Published in:
- Angewandte Chemie International Edition, 2003, v. 42, n. 39, p. 4762, doi. 10.1002/anie.200352361
- By:
- Publication type:
- Article
Synthesis and Conformational Analysis of (E)-9,10-Dehydroepothilone B: A Suggestive Link between the Chemistry and Biology of Epothilones ( This work was supported by the National Institutes of Health (CA-28824). F.Y. is a Uehara Memorial Foundation Fellow. A.R. is a NIH Cancer Pharmacology Fellow (T32-CA62948). A.E.G. is a MSKCC Experimental Therapeutics Center Fellow. We thank Ms. Sylvi Rusli (NMR Core Facility, CA-02848) and Mrs. Anna Dudkina for mass spectral analyses. )
- Published in:
- Angewandte Chemie International Edition, 2003, v. 42, n. 22, p. 2518, doi. 10.1002/anie.200351407
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- Publication type:
- Article