Prorocentin, a New Polyketide from the Marine Dinoflagellate Prorocentrum lima
Resource
Organic Letters 7 (18): 3893-3896
Journal
ChemInform
Journal Volume
7
Journal Issue
18
Pages
3893-3896
Date Issued
2005
Date
2005
Author(s)
Abstract
(Chemical Equation Presented) Prorocentin (1), isolated from an okadaic acid-producing organism, Prorocentrum lima, possessed all-trans trienes, an epoxide, as well as the 6/6/6-trans-fused/spiro-linked polyether ring moieties. The unique structure supports the proposed cyclization mechanism, polyene formation, epoxidation, and cyclization, of marine polyether toxins. The relative stereostructure was determined on the basis of spectral data. © 2005 American Chemical Society.
SDGs
Other Subjects
furan derivative; macrolide; okadaic acid; prorocentin; animal; article; chemical structure; chemistry; cyclization; Dinoflagellate; isolation and purification; metabolism; Animals; Cyclization; Dinoflagellida; Furans; Macrolides; Molecular Structure; Okadaic Acid
Type
journal article
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