Birch, A. J. ; Corrie, J. E. T. ; Subba Rao, G. S. R. (1970) A non-stereospecific synthesis of (±)-davanone Australian Journal of Chemistry, 23 (9). pp. 1811-1817. ISSN 0004-9425
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Official URL: http://www.publish.csiro.au/?paper=CH9701811
Related URL: http://dx.doi.org/10.1071/CH9701811
Abstract
A synthesis of the optically inactive form of the natural sesquiterpene davanone(1) together with three stereoisomers has been carried out as in Scheme. Although not subject to steric control, the synthesis confirms the structure of davanone, and leads to the suggestion that the relative stereochemistry may be that shown in (16). The preparation and some reactions with carboxylic acids of 3-methylbut-2-enyllithium are described.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Commonwealth Scientific and Industrial Research Organisation Publishing. |
| ID Code: | 55694 |
| Deposited On: | 19 Aug 2011 03:21 |
| Last Modified: | 19 Aug 2011 03:21 |
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