Abstract
The tricycle (5) with two trans-fused angular methyl groups is constructed from tiglic aldehyde and (S)-carvone involving a stereocontrolled aldol reaction and an endo-selective intramolecular Diels-Alder (IMDA) reaction; the stereochemistry was established by an X-ray study.
| Original language | English |
|---|---|
| Pages (from-to) | 1294-1295 |
| Number of pages | 2 |
| Journal | Journal of the Chemical Society, Chemical Communications |
| Issue number | 17 |
| DOIs | |
| Publication status | Published - 1989 Jan 1 |
ASJC Scopus subject areas
- Molecular Medicine
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Cite this
Shing, T. K. M., Tang, Y., & Malone, J. F. (1989). An expeditious and enantioselective entry to the ABC ring of the quassinoid skeleton. Journal of the Chemical Society, Chemical Communications, (17), 1294-1295. https://doi.org/10.1039/C39890001294