Correction to “Isolation of Notoamide S and Enantiomeric 6-epi-Stephacidin A from the Terrestrial Fungus Aspergillus amoenus: Biogenetic Implications”

Correction to “Isolation of Notoamide S and Enantiomeric 6-<i>epi</i>-Stephacidin A from the Terrestrial Fungus <i>Aspergillus amoenus</i>: Biogenetic Implications” Isolation of Notoamide S and Enantiomeric 6-<i>epi</i>-Stephacidin A from the Fungus <i>Aspergillus amoenus</i>: Biogenetic Implications Isolation of amoenamide A and five antipodal prenylated alkaloids from Aspergillus amoenus NRRL 35600 X-Ray Structure of Two Stephacidins, Heptacyclic Alkaloids from the Marine-Derived Fungus Aspergillus ostianus Isolation of Notoamide E, a Key Precursor in the Biosynthesis of Prenylated Indole Alkaloids in a Marine-Derived Fungus, <i>Aspergillus</i> sp. Genome-Based Characterization of Two Prenylation Steps in the Assembly of the Stephacidin and Notoamide Anticancer Agents in a Marine-Derived <i>Aspergillus</i> sp. Isolation of amoenamide A and five antipodal prenylated alkaloids from Aspergillus amoenus NRRL 35600 Isolation, Structure Elucidation, and Biomimetic Total Synthesis of Versicolamide B, and the Isolation of Antipodal (−)‐Stephacidin A and (+)‐Notoamide B from <i>Aspergillus versicolor</i> NRRL 35600 Isolation of a new indoxyl alkaloid, Amoenamide B, from Aspergillus amoenus NRRL 35600: Biosynthetic implications and correction of the structure of Speramide B Isolation and Photoinduced Conversion of 6-<i>epi</i>-Stephacidins from <i>Aspergillus taichungensis</i>