A stereoselective total synthesis of (−)-seychellene
Data(s) |
10/03/2008
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Resumo |
A stereoselective total synthesis of the tricyclic sesquiterpene (−)-seychellene, starting from (R)-carvone via (R)-3-methylcarvone has been accomplished, employing a combination of intermolecular Michael addition–intramolecular Michael addition sequence, a stereoselective hydrogenation, and an intramolecular alkylation reaction. |
Formato |
application/pdf |
Identificador |
Srikrishna, A and Ravi, G (2008) A stereoselective total synthesis of (−)-seychellene. In: Tetrahedron Letters, 64 (11). pp. 2565-2571. |
Publicador |
Elsevier Science |
Relação |
http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6THR-4RK5JYY-3&_user=512776&_coverDate=03%2F10%2F2008&_rdoc=1&_fmt=high&_orig=search&_sort=d&_docanchor=&view=c&_searchStrId=1230581757&_rerunOrigin=google&_acct=C000025298&_version=1&_urlVersion=0 http://eprints.iisc.ernet.in/25936/ |
Palavras-Chave | #Organic Chemistry |
Tipo |
Journal Article PeerReviewed |