Srikrishna, A. ; Satyanarayana, G. (2004) Enantioselective total synthesis of valeriananoids AC Organic Letters, 6 (14). pp. 2337-2339. ISSN 1523-7060
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Official URL: http://pubs.acs.org/doi/abs/10.1021/ol049341y
Related URL: http://dx.doi.org/10.1021/ol049341y
Abstract
The first enantioselective total synthesis of valeriananoids A-C (−)-1-3 is reported starting from the readily available monoterpene (R)-carvone, employing a tandem intermolecular Michael addition-intramolecular Michael addition-alkylation sequence and an electron-transfer-mediated 6-endo-trig cyclization as key steps.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to American Chemical Society. |
| ID Code: | 48685 |
| Deposited On: | 15 Jul 2011 11:45 |
| Last Modified: | 15 Jul 2011 11:45 |
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