Abstract

The absolute stereochemistry of 14 naturally occurring sesquiterpenecoumarin ethers is discussed. In 13 cases the coumarin moiety is isofraxidin (7-hydroxy-6,8-dimethoxycoumarin), in one case scopoletin (7-hydroxy-6-methoxycoumarin). The sesquiterpene moieties belong either to the bicyclic drimenole series or to its consecutive products (methyl migration, ring opening). The CD spectra of all compounds are given. The assignments of the absolute configurations are based on the method ofHoreau, chemical correlation by degradation reactions, extensive comparison of CD data, and biogenetic considerations.

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