Enantiospecific synthesis of the tricyclic core structure of lippifolianes
| Data(s) |
08/04/2010
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|---|---|
| Resumo |
An enantiospecific synthesis of the [6.6.3]-tricyclic carbon framework, 2,6,6,9-tetra-methyltricyclo[5.4.0.02,4]undecane, present in the sesquiterpenes lippifolianes and the diterpenes cyclosclareol, metasequoic acids and parguerols, starting from the readily available monoterpene (R)-carvone, is described. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/29185/1/Tric.pdf Srikrishna, Adusumilli and Babu, Ramesh R and Beeraiah, Baire (2010) Enantiospecific synthesis of the tricyclic core structure of lippifolianes. In: Tetrahedron: Asymmetry, 21 (6). pp. 719-724. |
| Publicador |
Elsevier Science |
| Relação |
http://dx.doi.org/10.1016/j.tetasy.2010.04.001 http://eprints.iisc.ernet.in/29185/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
