Synthesis and stereochemistry of the terminal spiroketal domain of the phosphatase inhibitor dinophysistoxin-2
- 15 May 2008
- journal article
- research article
- Published by Elsevier BV in Bioorganic & Medicinal Chemistry Letters
- Vol. 18 (10), 3043-3046
- https://doi.org/10.1016/j.bmcl.2008.01.002
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Clarification of the C-35 Stereochemistries of Dinophysistoxin-1 and Dinophysistoxin-2 and Its Consequences for Binding to Protein PhosphataseChemical Research in Toxicology, 2007
- Importance of the C28–C38 hydrophobic domain of okadaic acid for potent inhibition of protein serine-threonine phosphatases 1 and 2ABioorganic & Medicinal Chemistry Letters, 2001
- Expedient Access to the Okadaic Acid Architecture: A Novel Synthesis of the C1−C27 DomainThe Journal of Organic Chemistry, 2001
- An Efficient Total Synthesis of Okadaic AcidJournal of the American Chemical Society, 1997
- Dinophysistoxin-2: The predominant diarrhoetic shellfish toxin in IrelandToxicon, 1996
- Isolation of a new diarrhetic shellfish poison from Irish musselsJournal of the Chemical Society, Chemical Communications, 1992
- Diarrhetic shellfish toxinsTetrahedron, 1985
- Isolation and structural elucidation of the causative toxin of the diarrhetic shellfish poisoning.NIPPON SUISAN GAKKAISHI, 1982
- Okadaic acid, a cytotoxic polyether from two marine sponges of the genus HalichondriaJournal of the American Chemical Society, 1981
- Identification of Dinophysis fortii as the causative organism of diarrhetic shellfish poisoning.NIPPON SUISAN GAKKAISHI, 1980