DOI: 10.1039/A703141F
(Paper)
Reference Section for: J. Chem. Soc., Perkin Trans. 1, 1998, 149-156
Synthesis of a diastereoisomer of the C-15 ∼ C-26 segment of amphidinolide L
(Note: The full text of this document is currently only available in the PDF Version )
Masashi Tsuda, Akiko Hatakeyama and Jun’ichi Kobayashi
Abstract
In order to determine the absolute stereochemistry of amphidinolide L 1, a cytotoxic macrolide from a marine dinoflagellate, (16R, 18S, 20R, 22S, 23R, and 25R)-2, one of the eight possible diastereoisomers of the C(15)–C(26) segment has been synthesized, thus providing an authentic sample for degradation studies of 1.
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