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handle: 10261/13281
A new sesterterpene, caminatal 1, containing a bicyclic terpenoid moiety with an aldehyde appendage in combination with an isolated isoprenic aromatic ring leading to a novel carbon skeleton has been obtained from the Antarctic sponge Suberites caminatus. Its structure and relative stereochemistry were established by spectroscopic evidence and biogenetic considerations.
This work was supported by Ministerio de Ciencia y Tecnología (MCYT), projects: REN2002-10485-E/ ANT and PPQ2002-02494), Instituto Antártico Chileno (INACH), and DGUI (Gobierno de Canarias: PI2002/044). A.R.D.-M. acknowledges an I3P grant from the CSIC and E.D. acknowledges a fellowship (FPI) from the CICYT.
The structure and relative stereochemistry of caminatal 1 are described.
4 pages, 2 figures, 1 table.-- Printed version published Jul 28, 2003.
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