@article{oai:kumadai.repo.nii.ac.jp:00031909,
 author = {Sugimoto, Kayo and Sadahiro, Yusaku and Kagiyama, Ippei and Kato, Hikaru and David H., Sherman and Williams, Robert M., and Tsukamoto, Sachiko},
 issue = {29},
 journal = {Tetrrahedron Lettters},
 month = {Jul},
 note = {A new prenylated alkaloid, Amoenamide A (6), was isolated from the fungus Aspergillus amoenus NRRL 35600. Previously, 6 was postulated to be a precursor of Notoamide E4 (21) converted from Notoamide E (16), which was a key precursor of the prenylated indole alkaloids in the fungi of the genus Aspergillus. We previously succeeded in the isolation of two pairs of antipodes, Stephacidin A (1) and Notoamide B (2), from A. amoenus and A. protuberus MF297-2 and expected the presence of other antipodes in the culture of A. amoenus. We here report five new antipodes (7–11) along with a new metabolite (12), which was isolated as a natural compound for the first time, from A. amoenus.},
 pages = {2297--2800},
 title = {Isolation of amoenamide A and five antipodal prenylated alkaloids from Aspergillus amoenus NRRL 35600},
 volume = {58},
 year = {2017}
}