Abstract
The pentacyclic quassinoid skeleton 3 is constructed from (S)-carvone involving a 1,3-sigmatropic rearrangement and an intramolecular Diels-Alder reaction as the key steps.
| Original language | English |
|---|---|
| Pages (from-to) | 2369-2370 |
| Number of pages | 2 |
| Journal | Chemical Communications |
| Issue number | 20 |
| DOIs | |
| Publication status | Published - 1996 Jan 1 |
ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Chemistry(all)
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry
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Shing, T. K. M., Zhu, X. Y., & Mak, T. C. W. (1996). Expeditious and enantiospecific avenue to pentacyclic quassinoid skeleton. Chemical Communications, (20), 2369-2370. https://doi.org/10.1039/cc9960002369