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 |
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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