Abstract
For a construction of potential scaffold of antitumor agents andrastins, intramolecular Diels-Alder reaction of the triene composed of trans-fused AB ring with tethered D ring was examined. The reaction in refluxing toluene afforded a desired cis-fused hydrindane skeleton, the relative stereochemistries of which were unambiguously determined by X-ray crystallographic analysis.
Original language | English |
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Pages (from-to) | 187-199 |
Number of pages | 13 |
Journal | Heterocycles |
Volume | 95 |
Issue number | 1 |
DOIs | |
State | Published - 2017 |
ASJC Scopus subject areas
- Analytical Chemistry
- Pharmacology
- Organic Chemistry