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Total syntheses of (±)-α-acorenol, β-acorenol, α-epi-acorenol and β-epi-acorenol via an Ireland ester Claisen rearrangement and RCM reaction sequence
- Source :
- Tetrahedron Letters. 48:6916-6919
- Publication Year :
- 2007
- Publisher :
- Elsevier BV, 2007.
-
Abstract
- Total syntheses of (±)-α- and β-acorenols and (±)-α- and β- epi -acorenols, spiro[4.5]decane sesquiterpenes, isolated from the western Australian sandalwood oil, have been accomplished employing a combination of Ireland ester Claisen rearrangement and RCM reactions for an efficient construction of the spiro[4.5]decane present in acoranes.
Details
- ISSN :
- 00404039
- Volume :
- 48
- Database :
- OpenAIRE
- Journal :
- Tetrahedron Letters
- Accession number :
- edsair.doi...........e856e787db14bb43bad79f2bd5859ea4