Abstract
Advancing alkaloid synthesis: (+)-Haplophytine (see structure) was the target of a total synthesis featuring a highly stereoselective intramolecular Mannich reaction, Friedel-Crafts alkylation, oxidative rearrangement, and Fischer indole synthesis.
| Original language | English |
|---|---|
| Pages (from-to) | 7600-7603 |
| Number of pages | 4 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 48 |
| Issue number | 41 |
| DOIs | |
| Publication status | Published - 2009 Sep 28 |
Keywords
- Alkaloids
- Mannich reaction
- Natural products
- Rearrangement
- Total synthesis
ASJC Scopus subject areas
- Catalysis
- Chemistry(all)
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Cite this
Ueda, H., Satoh, H., Matsumoto, K., Sugimoto, K., Fukuyama, T., & Tokuyama, H. (2009). Total synthesis of (+)-haplophytine. Angewandte Chemie - International Edition, 48(41), 7600-7603. https://doi.org/10.1002/anie.200902192