The novel pentacyclic compound cyclotokinolide B was obtained from the natural phthalide tokinolide B under basic conditions, via the chemoselective g-enol lactone opening followed by a Michael addition of the generated carbanion to the enone and subsequent equilibration. This result confirms that s
✦ LIBER ✦
Base-catalyzed intramolecular condensations of diligustilide
✍ Scribed by María Yolanda Rios; Guillermo Delgado; Georgina Espinosa-Pérez
- Book ID
- 104259771
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 227 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Treatment of diligustilide (I) with base afforded the pentacyclic compounds 2 -4 with novel carbon-carbon connectivities via lactone-ring opening, intramolecutar condensations and competitive equilibrations. This reaction provides a useful entry to modified dimeric phthalides.
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