Synthesis of Notoamide J: A Potentially Pivotal Intermediate in the Biosynthesis of Several Prenylated Indole Alkaloids

Synthesis of Notoamide J: A Potentially Pivotal Intermediate in the Biosynthesis of Several Prenylated Indole Alkaloids Isolation of Notoamide E, a Key Precursor in the Biosynthesis of Prenylated Indole Alkaloids in a Marine-Derived Fungus, <i>Aspergillus</i> sp. Total synthesis of the indole alkaloids henrycinol A and B Total Synthesis of Nortopsentin D via a Late-Stage Pinacol-like Rearrangement Notoamide O, a Structurally Unprecedented Prenylated Indole Alkaloid, and Notoamides P−R from a Marine-Derived Fungus, Aspergillus sp. Notoamide O, a Structurally Unprecedented Prenylated Indole Alkaloid, and Notoamides P−R from a Marine-Derived Fungus, <i>Aspergillus</i> sp. Flavin‐Dependent Monooxygenases NotI and NotI′ Mediate Spiro‐Oxindole Formation in Biosynthesis of the Notoamides Stereoselective Synthesis of the Indole Alkaloids Nitrarine, Nitramidine, and Isomers. A Biomimetic Approach Synthesis of Indole Alkaloid Analogues:  Novel Domino Stereoselective Electrophile Addition−Cyclizations of Tryptophan-Derived α-Amino Nitriles Total Synthesis of a Pyrroloindoloquinazoline Alkaloid