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Berichtigung: Asymmetric Total Synthesis of Brasilicardins.
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- Angewandte Chemie, 2021, v. 133, n. 44, p. 23679, doi. 10.1002/ange.202111499
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Asymmetric Total Synthesis of Brasilicardins.
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- Angewandte Chemie, 2018, v. 130, n. 52, p. 17407, doi. 10.1002/ange.201811403
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Asymmetric Total Synthesis of Brasilicardins.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 52, p. 17161, doi. 10.1002/anie.201811403
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- Article
Lipid Droplet Formation Is Regulated by Ser/Thr Phosphatase PPM1D via Dephosphorylation of Perilipin 1.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 19, p. 12046, doi. 10.3390/ijms231912046
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- Article
Synthetic Studies of the Zoanthamine Alkaloids: Total Synthesis of Zoanthenol Based on an Isoaromatization Strategy.
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- Chemistry - An Asian Journal, 2011, v. 6, n. 3, p. 922, doi. 10.1002/asia.201000552
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Total Synthesis of Isosilybin B.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 30, p. 1, doi. 10.1002/ejoc.202200653
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Pactamycin and Its Derivatives: Improved Synthesis Route.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 4, p. 488, doi. 10.1002/ejoc.201901747
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Corrigendum: Asymmetric Total Synthesis of Brasilicardins.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 44, p. 23487, doi. 10.1002/anie.202111499
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- Article
Inhibition of Ser/Thr phosphatase PPM1D induces neutrophil differentiation in HL-60 cells.
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- Journal of Biochemistry, 2017, v. 162, n. 4, p. 303, doi. 10.1093/jb/mvx032
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- Article
Synthetic study of andrastins: stereoselective construction of the BCD-ring system.
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- Journal of Antibiotics, 2019, v. 72, n. 6, p. 384, doi. 10.1038/s41429-018-0136-x
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- Article
Synthetic Studies of the Zoanthamine Alkaloids: The Total Syntheses of Norzoanthamine and Zoanthamine.
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- Chemistry - A European Journal, 2009, v. 15, n. 27, p. 6626, doi. 10.1002/chem.200900310
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Spin Trapping of 13C-Labeled p-Benzynes Generated by Masamune–Bergman Cyclization of Bicyclic Nine-Membered EnediynesThis work was supported by CREST (Core Research for Evolutional Science and Technology), the Japan Science and Technology Agency (postdoctoral fellowship to P.D.), and the Ministry of Education, Culture, Sports, Science and Technology. We are grateful for three Research Fellowships for Young Scientists (T.U., T.M., and F.Y.) from the Japanese Society for the Promotion of Science. We thank Dr. Jonathan Hobley, Tohoku University, for many insightful comments and fruitful discussions.
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- Angewandte Chemie, 2004, v. 116, n. 39, p. 5361, doi. 10.1002/ange.200454133
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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. )
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- Angewandte Chemie, 2003, v. 115, n. 39, p. 4910, doi. 10.1002/ange.200352361
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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. )
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- Angewandte Chemie, 2003, v. 115, n. 22, p. 2622, doi. 10.1002/ange.200351407
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- Article
Spin Trapping of 13C-Labeled p-Benzynes Generated by Masamune–Bergman Cyclization of Bicyclic Nine-Membered EnediynesThis work was supported by CREST (Core Research for Evolutional Science and Technology), the Japan Science and Technology Agency (postdoctoral fellowship to P.D.), and the Ministry of Education, Culture, Sports, Science and Technology. We are grateful for three Research Fellowships for Young Scientists (T.U., T.M., and F.Y.) from the Japanese Society for the Promotion of Science. We thank Dr. Jonathan Hobley, Tohoku University, for many insightful comments and fruitful discussions.
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- Angewandte Chemie International Edition, 2004, v. 43, n. 39, p. 5249, doi. 10.1002/anie.200454133
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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. )
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- Angewandte Chemie International Edition, 2003, v. 42, n. 39, p. 4762, doi. 10.1002/anie.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 International Edition, 2003, v. 42, n. 22, p. 2518, doi. 10.1002/anie.200351407
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- Article
A Direct and Efficient α-Selective Glycosylation Protocol for the Kedarcidin Sugar,.
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- Angewandte Chemie International Edition, 2001, v. 40, n. 5, p. 946, doi. 10.1002/1521-3773(20010302)40:5<946::AID-ANIE946>3.0.CO;2-G
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Inhibition of lipid droplet formation by Ser/Thr protein phosphatase PPM1D inhibitor, SL-176.
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- PLoS ONE, 2019, v. 14, n. 2, p. 1, doi. 10.1371/journal.pone.0212682
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Total Synthesis of Zoanthenol.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 47, p. 8905, doi. 10.1002/anie.200904537
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Palladium-Catalyzed Stereospecific Substitution of α,β-Unsaturated γ,δ-Epoxy Esters by Alcohols with Double Inversion of Configuration: Synthesis of 4-Alkoxy-5-hydroxy-2-pentenoates.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 4, p. 750, doi. 10.1002/anie.200703889
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- Article