
Synthesis p. 863 - 870 (1996)
Update date:2022-07-30
Topics:
Eicher, Theophil
Servet, Frank
Speicher, Andreas
Efficient total syntheses are described for the racemic sesquiterpenes herbertenolide (2), α-herbertenol (3) and β-herbertenol (4) from Herberta adunca. ent-Herbertenolide [(+)-2] was prepared from enantiopure (-)-ethyl (1R)-1-methyl-2-oxocyclopentanecarboxylate (9) obtained from ethyl 2-oxocyclopentanecarboxylate (19) via reduction with baker's yeast.
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