Tetrahedron Letters p. 329 - 332 (1992)
Update date:2022-08-05
Topics:
Takano, Seiichi
Moriya, Minoru
Ogasawara, Kunio
Enantiocontrolled syntheses of the Cuparene sesquiterpenes, (-)-herbertene, (+)-cuparenone, (-)-debromoaplysin, and (-)-aplysin, have been achieved starting from the optically active tricyclic dienone by employing a Fischer indolization reaction under non-acidic conditions as the key step.
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