Isolation of Notoamide E, a Key Precursor in the Biosynthesis of Prenylated Indole Alkaloids in a Marine-Derived Fungus, Aspergillus sp.

Isolation of Notoamide E, a Key Precursor in the Biosynthesis of Prenylated Indole Alkaloids in a Marine-Derived Fungus, <i>Aspergillus</i> sp. Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine‐Derived Fungus, <i>Aspergillus</i> sp. Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine‐Derived Fungus, <i>Aspergillus</i> sp. Notoamide O, a Structurally Unprecedented Prenylated Indole Alkaloid, and Notoamides P−R from a Marine-Derived Fungus, <i>Aspergillus</i> sp. Notoamide O, a Structurally Unprecedented Prenylated Indole Alkaloid, and Notoamides P−R from a Marine-Derived Fungus, Aspergillus sp. Notoamides F−K, Prenylated Indole Alkaloids Isolated from a Marine-Derived <i>Aspergillus</i> sp. Notoamides F−K, Prenylated Indole Alkaloids Isolated from a Marine-Derived <i>Aspergillus</i> sp. Isolation of Antipodal (−)-Versicolamide B and Notoamides L−N from a Marine-Derived <i>Aspergillus</i> sp. Isolation of amoenamide A and five antipodal prenylated alkaloids from Aspergillus amoenus NRRL 35600 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.