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Convergent synthesis of diptoindonesin G
- Singh, Dileep Kumar, Kim, Ikyon
- Tetrahedron letters 2019 v.60 no.3 pp. 300-301
- Suzuki reaction, acylation, chemical structure, organic compounds
- 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.