A stereoselective total synthesis of (−)-seychellene


Autoria(s): Srikrishna, A; Ravi, G
Data(s)

10/03/2008

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

http://eprints.iisc.ernet.in/25936/1/http___www.sciencedirect.com_science__ob%3DMImg%26_imagekey%3DB6THR-4RK5JYY-3-1%26_cdi%3D5289%26_user%3D512776%26_pii%3DS0040402008000720%26_orig%3Dsearch%26_coverDate%3D03%252F10%25.pdf

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