| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269143 | Tetrahedron Letters | 2011 | 5 Pages |
Abstract
An enantioselective synthesis of cyclopropyl δ-lactonealdehydes and dodecyl-5-ene-1-yne-3-ol is accomplished via organocatalytic and asymmetric transfer hydrogenation reactions as genesis of chirality. These precursors would envision culminating the synthesis of every representative member of the oxylipin class of natural products such as solandelactone A and B.
Related Topics
Physical Sciences and Engineering
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Organic Chemistry
Authors
Gullapalli Kumaraswamy, Gajula Ramakrishna, Balasubramanian Sridhar,