Base-catalyzed intramolecular condensation of tokinolide B.
Author
Summary, in English
The novel pentacyclic compound cyclotokinolide B was obtained from the natural phthalide tokinolide B under basic conditions, via the chemoselective -enol lactone opening followed by a Michael addition of the generated carbanion to the enone and subsequent equilibration. This result confirms that some dimeric phthalides undergo intramolecular cyclizations in basic media.
Department/s
Publishing year
2003
Language
English
Pages
2509-2512
Publication/Series
Tetrahedron Letters
Volume
44
Issue
12
Document type
Journal article
Publisher
Elsevier
Topic
- Organic Chemistry
Status
Published
ISBN/ISSN/Other
- ISSN: 0040-4039