Taichunamides: Prenylated Indole Alkaloids from Aspergillus taichungensis (IBT 19404)

Isolation of Notoamide S and Enantiomeric 6-epi-Stephacidin A from the Fungus Aspergillus amoenus: Biogenetic Implications

(2015) Hikaru Kato et al.   ORGANIC LETTERS

Isolation and Photoinduced Conversion of 6-epi-Stephacidins from Aspergillus taichungensis

(2013) Shengxin Cai et al.   ORGANIC LETTERS

Comparative analysis of the biosynthetic systems for fungal bicyclo[2.2.2]diazaoctane indole alkaloids: the (+)/(−)-notoamide, paraherquamide and malbrancheamide pathways

(2012) Shengying Li et al.   MedChemComm

Notoamide O, a Structurally Unprecedented Prenylated Indole Alkaloid, and Notoamides P−R from a Marine-Derived Fungus,Aspergillussp.

(2010) Sachiko Tsukamoto et al.   JOURNAL OF NATURAL PRODUCTS

Asymmetric total syntheses of (+)- and (−)-versicolamide B and biosynthetic implications

(2009) Kenneth A. Miller et al.   Nature Chemistry

Isolation, Structure Elucidation, and Biomimetic Total Synthesis of Versicolamide B, and the Isolation of Antipodal (−)-Stephacidin A and (+)-Notoamide B fromAspergillus versicolor NRRL 35600

(2008) Thomas J. Greshock et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Notoamides F−K, Prenylated Indole Alkaloids Isolated from a Marine-DerivedAspergillussp.

(2008) Sachiko Tsukamoto et al.   JOURNAL OF NATURAL PRODUCTS