| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5216410 | Tetrahedron | 2014 | 5 Pages |
Abstract
Three diprenylated indole alkaloids, mangrovamides A–C (1–3), featured a bicyclo [2.2.2] diazaoctane core and possessed a novel γ-methyl proline and isoprene derived dimethyl γ-pyrone functionalities hitherto unknown among the family of paraherquamides, were isolated from the fungus Penicillium sp., which was separated from a mangrove soil sample. The structures were elucidated based on NMR, X-ray, and CD methods. The possible biosynthetic pathway of these compounds is proposed.
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