A convergent and scalable synthetic route to a tetracyclic oligostilbenoid natural product, diptoindonesin G, is described where Suzuki-Miyaura cross-coupling and intramolecular Friedel-Crafts acylation were employed to construct the central C ring of diptoindonesin G. Two fragments for cross-coupling reaction were readily synthesized with similar efficiency.
Bibliographical notePublisher Copyright:
© 2018 Elsevier Ltd
All Science Journal Classification (ASJC) codes
- Drug Discovery
- Organic Chemistry