Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5221552 | Tetrahedron | 2011 | 9 Pages |
Abstract
A general strategy for the synthesis of both trans/syn- and trans/anti-sphenolobane diterpenes has been developed, which utilizes an intramolecular ester enolate alkylation (IEEA) as a key step. A stereoselective total synthesis of (±)-tormesol (1), an unusual trans/syn-sphenolobane diterpene, was accomplished in 18 steps in 4.1% overall yield from readily available aldehyde 16.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hyoungsu Kim, Hoon Bae, Sanghee Kim, Deukjoon Kim, Dongjoo Lee, Robert S. Paton,