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Synthetic studies toward natural chromenes with biological activity:
Asymmetric total synthesis of gonytolide C and blennolide C via spiro chromanone
- In: Poster Presentation
- At: Stockholm (Sweden) (2017)
- Type: Poster
- Poster code: P-A-021-Monday
- By: KUMAMOTO, Takuya (Musashino University, Faculty of Pharmaceutical Sciences, Nishitokyo, Japan)
- Co-author(s): Kanna Adachi: Faculty of Pharmaceutical Sciences, Musashino University, Nishitokyo, Japan
Kazuaki Katakawa: Faculty of Pharmaceutical Sciences, Musashino University, Nishitokyo, Japan
Takuya Kumamoto: Faculty of Pharmaceutical Sciences, Musashino University, Nishitokyo, Japan - Abstract:
Backgrounds
Naturally-occurring xanthones and their biogenetically related chromanones with δ-butyrolactones have been isolated from a wide range of plants, bacteria, and fungi. Secalonic acid B (1) was isolated as dimeric xanthones from ergot and the monomeric blennolide C (2) was isolated with 1 from fungus Blennoria sp. Gonytolide A (3), dimeric .. The access to the whole abstract and if available the presentation file is available to FIP members and to congress participants of that specific congress.
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Last update 28 September 2023