| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5272535 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
The enantioselective synthesis of oxylipin-3 has been carried out. The synthetic strategy was started from commercially available n-decanal. The chiral source was based on Sharpless asymmetric dihydroxylation and CBS reduction.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Stereoselective synthesis of oxylipin-3: [(6R,9R,10R,7E)-6,9,10-trihydroxyoctadec-7-enoic acid]](/preview/png/5272535.png "First Page Preview: Stereoselective synthesis of oxylipin-3: [(6R,9R,10R,7E)-6,9,10-trihydroxyoctadec-7-enoic acid]")
Authors
Sachin B. Wadavrao, Ramesh S. Ghogare, A. Venkat Narsaiah,