Sabitha, Gowravaram ; Bhaskar, V. ; Yadav, J. S. (2006) The first asymmetric total synthesis of (R)-tuberolactone, (S)-jasmine lactone and (R)-δ-decalactone Tetrahedron Letters, 47 (46). pp. 8179-8181. ISSN 0040-4039
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2006.08.135
Abstract
A general synthetic approach has been developed for the first asymmetric total synthesis of tuberolactone 1, jasmine lactone 2 and δ-decalactone 3. The key step is the selective hydrogenation of triple and endocyclic double bonds in the key intermediate 4.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Natural Products; Chiral Lactones; Hydrogenation; Flavour; Fragrance; Asymmetric Synthesis |
| ID Code: | 59564 |
| Deposited On: | 07 Sep 2011 05:42 |
| Last Modified: | 07 Sep 2011 05:42 |
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