Journal
TETRAHEDRON LETTERS
Volume 44, Issue 51, Pages 9103-9106Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2003.10.039
Keywords
triterpenes; sesterterpenes; diatoms; Rhizosolenia setigera; hydrocarbons; NMR spectroscopy; rhizenes
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The structures of two polyunsaturated monocyclic triterpenes have been elucidated using NMR spectroscopy following their isolation from the common marine diatom, Rhizosolenia setigera. The structure of a related monocyclic sesterterpene is proposed on the basis of mass spectral comparisons with the two monocyclic triterpenes. (C) 2003 Elsevier Ltd. All rights reserved.
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