Pramod, Kakumanu ; Subba Rao, G. S. R. (1982) Zizaene and cedrene sesquiterpenes. Novel synthesis of tricyclic intermediates for their preparation Journal of the Chemical Society, Chemical Communications (13). pp. 762-763. ISSN 0022-4936
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Official URL: http://pubs.rsc.org/en/content/articlelanding/1982...
Related URL: http://dx.doi.org/10.1039/C39820000762
Abstract
The tricyclic enone (8), conveniently prepared from the diene (5)via the adduct (7), afforded the endo-and exo-alcohols (9) whose toluene-p-sulphonates (10) were readily converted into the tricyclic ketones (11) and (12), thus paving the way for a new total synthesis of racemic zizaene (1) and of racemic cedrene (2) respectively.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Royal Society of Chemistry. |
| ID Code: | 55743 |
| Deposited On: | 19 Aug 2011 03:23 |
| Last Modified: | 19 Aug 2011 03:23 |
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