Marine Terpenes and Terpenoids. XIV. Absolute Configuration and Acid-Catalyzed Transformation of (-)-12, 13-Didehydrofurospongin-1 Isolated from an Arabian Sea Sponge, Fasciospongia cavernosa SCHMIDT

Abstract

Three furanoterpenes, one having a furanocyclohexane ring (1) and two methyl ethers (2 and 3), and 12, 13-didehydrofurospongin-1 (4a) were isolated from the lipid extract of the sponge, Fasciospongia cavernosa SCHMIDT. The absolute configuration of 4a at C-11 was shown to be (S), opposite to that reported for furospongin-1 (5). Compound 4a was found to be quite labile in acidic media and was converted, at room temperature, to 1 (HClO₄ in dioxane) or to a mixture of 1, 2 and 3 (HClO₄ in MeOH). These results suggest that 1, 2 and 3 are at least partly artefacts formed from 4a during the isolation process.