Mehta, Goverdhan ; Srinivas, K. (1999) A stereoselective total synthesis of the novel sesquiterpene kelsoene Tetrahedron Letters, 40 (26). pp. 4877-4880. ISSN 0040-4039
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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...
Related URL: http://dx.doi.org/10.1016/S0040-4039(99)00901-6
Abstract
Employing commercially available 1,5-cyclooctadiene 5 as the starting material, the first total synthesis of the tricyclic sesquiterpene hydrocarbon kelsoene 3 has been accomplished, which also reaffirms its assigned structure. The basic strategy delineated here for the construction of the tricyclo [6.2.0.02,6]decane framework is eminently suitable for the synthesis of other members of this class.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Terpenes; Cyclobutene; Homologation; Wittig Reaction |
| ID Code: | 28938 |
| Deposited On: | 18 Dec 2010 05:47 |
| Last Modified: | 18 Dec 2010 05:47 |
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