(equation presented) An approach to the tricyclic core of phomactin A is described via the synthesis of a reduced furanochroman model. Key elements of this study include the use of a highly functionalized 1-oxadecalone derivative as a template for the stereoselective introduction of functionality and a tandem retro aldol-epoxide opening-cyclization sequence for elaboration of the dihydrofuran ring.
|Original language||English (US)|
|Number of pages||3|
|State||Published - Aug 10 2000|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry