Issue 13, 1976

The absolute configuration of avarol, a rearranged sesquiterpenoid hydroquinone from a marine sponge

Abstract

With the aid of circular dichroism, n.m.r. shift reagents, and 13C n.m.r. spectroscopy the absolute stereochemistry has been assigned to avarol {2-[(1R)-1,2,3,4,4a,7,8,8aα-octahydro-1β,2β,4aβ,5-tetramethyl-1-naphthylmethyl]-hydroquinone}, obtained from the marine sponge Disidea avara. Avarol is the first naturally occurring sesquiter-penoid of the 9,4-friedodrimane type to be isolated.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1976, 1408-1414

The absolute configuration of avarol, a rearranged sesquiterpenoid hydroquinone from a marine sponge

S. de Rosa, L. Minale, R. Riccio and G. Sodano, J. Chem. Soc., Perkin Trans. 1, 1976, 1408 DOI: 10.1039/P19760001408

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