Synthesis of a marine polyether toxin, okadaic acid [1] — strategy and synthesis of segment a
- 1 January 1987
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 43 (20), 4737-4748
- https://doi.org/10.1016/s0040-4020(01)86915-5
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Acyclic stereocontrol by heteroconjugate addition—4Tetrahedron, 1986
- Synthetic studies toward marine toxic polyethers (4) synthesis of segment -A of okadaic acid viaTetrahedron Letters, 1985
- Synthetic studies toward marine toxic polyethers (3) stereocontrol for segment-A1 of okadaic acid by means of oxymercuration and epoxydationTetrahedron Letters, 1985
- Diarrhetic shellfish toxinsTetrahedron, 1985
- Identification of okadaic acid as a toxic component of a marine dinoflagellate Prorocentrum lima.NIPPON SUISAN GAKKAISHI, 1982
- 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
- Acanthifolicin, a new episulfide-containing polyether carboxylic acid from extracts of the marine sponge Pandaros acanthifoliumJournal of the American Chemical Society, 1981
- Synthetic studies on insect hormones. VIII. Stereospecific synthesis of trisubstituted olefins from organocopper reagents and acetylenesJournal of the American Chemical Society, 1969
- Stereospecific synthesis of trisubstituted and tetrasubstituted olefins. Conjugate addition of dialkylcopper-lithium reagents to .alpha.,.beta.-acetylenic estersJournal of the American Chemical Society, 1969