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Enantiospecific approach to the tricyclic core structure of tricycloillicinone, ialibinones, and takaneones via ring-closing metathesis reaction
- Source :
- Tetrahedron. 65:2649-2654
- Publication Year :
- 2009
- Publisher :
- Elsevier BV, 2009.
-
Abstract
- Enantiospecific synthesis of the tricyclic core structure present in the biologically active natural products tricycloillicinone, ialibinones, and takaneones, starting from the readily available campholenaldehyde employing a transannular RCM reaction as the key step, has been accomplished.
Details
- ISSN :
- 00404020
- Volume :
- 65
- Database :
- OpenAIRE
- Journal :
- Tetrahedron
- Accession number :
- edsair.doi...........2e74e695faccfe185993af75c76324b6