Enantioselective formal total syntheses of Clavukerin A and isoclavukerin A via a ring-closing metathesis reaction
| Data(s) |
08/04/2010
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|---|---|
| Resumo |
Enantioselective formal total syntheses of the marine trisnorsesquiterpenes clavukerin A and isoclavukerin A, starting from (R)-limonene employing an RCM reaction as the key step, are described. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/29186/1/Clav.pdf Srikrishna, Adusumilli and Pardeshi, Vijendra H and Satyanarayana, Gedu (2010) Enantioselective formal total syntheses of Clavukerin A and isoclavukerin A via a ring-closing metathesis reaction. In: Tetrahedron: Asymmetry, 21 (6). pp. 746-750. |
| Publicador |
Elsevier Science |
| Relação |
http://dx.doi.org/10.1016/j.tetasy.2010.04.003 http://eprints.iisc.ernet.in/29186/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
