Birch, A. J. ; Subba Rao, G. S. R. (1970) Steroid hormones. XXII. Total syntheses of (±)-equilenin methyl ether and (±)-oestrone methyl ether Australian Journal of Chemistry, 23 (3). pp. 547-552. ISSN 0004-9425
Full text not available from this repository.
Official URL: http://www.publish.csiro.au/?paper=CH9700547
Related URL: http://dx.doi.org/10.1071/CH9700547
Abstract
Total syntheses of oestrone methyl ether and equilenin methyl ether are described, based on the Robinson intermediate (1). The key steps are a stereo-specific introduction of the 18-methyl group and the reduction of ring B of the equilenane skeleton, rendered possible by the presence of an 11-carbonyl.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Commonwealth Scientific and Industrial Research Organisation Publishing. |
| ID Code: | 55693 |
| Deposited On: | 19 Aug 2011 03:21 |
| Last Modified: | 19 Aug 2011 03:21 |
Repository Staff Only: item control page
