Title of article
Short total synthesis of the spiro[4.5]decane sesquiterpene (−)-gleenol
Author/Authors
Kai Oesterreich، نويسنده , , Dietrich Spitzner، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2002
Pages
4
From page
4331
To page
4334
Abstract
The spirocyclic sesquiterpene (−)-gleenol was prepared in five steps starting from (−)-methone via a di-olefin. The final spiro-ring system was made using the olefin metathesis reaction. The resulting ketone was selectively reduced to the natural product.
Keywords
Reduction , Olefin metathesis , Michael addition , sesquiterpene
Journal title
Tetrahedron
Serial Year
2002
Journal title
Tetrahedron
Record number
1083120
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