Srikrishna, Adusumilli ; Satyanarayana, Gedu (2005) An enantiospecific total synthesis of (−)-patchouli alcohol Tetrahedron: Asymmetry, 16 (24). pp. 3992-3997. ISSN 0957-4166
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetasy.2005.11.012
Abstract
An enantiospecific total synthesis of patchouli alcohol, starting from the readily available monoterpene (R)-carvone, has been accomplished. A tandem double Michael reaction-alkylation sequence and single electron mediated 6-endo trig cyclisation reaction have been employed as key steps.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 48715 |
| Deposited On: | 15 Jul 2011 11:47 |
| Last Modified: | 15 Jul 2011 11:47 |
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