Reaction of trimethylsilylimidazole with 5,10 beta-epoxy-3-ketosteroids: enolization and aromatization of the A-ring.
S Kulkarni, S Abdel-Baky, P W Le Quesne, P Vouros
Index: Steroids 53(1-2) , 131-47, (1989)
Full Text: HTML
Abstract
The reaction of trimethylsilylimidazole (TSIM) and 3-keto-5,10-epoxy-nor-19-methylandrostanone 3 and its 17-acetate analog 4 was examined at two different temperatures. In both compounds, reaction at 90 degrees C gave predominantly a delta 3-silyl-enol ether plus a minor product as a result of the epoxide ring opening. Under reflux conditions, besides the aforementioned products, aromatization of the A-ring was observed as a major process. The results suggest the potential use of silylation reactions with epoxyketones towards the synthesis of aromatic compounds.
Related Compounds
Related Articles:
2014-06-01
[J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 960 , 8-13, (2014)]
2015-06-01
[J. Exp. Bot. 66 , 3085-97, (2015)]
2015-09-01
[Planta 242 , 613-29, (2015)]
2015-03-15
[Food Chem. 171 , 40-9, (2014)]
2015-02-01
[Biomarkers 20(1) , 71-6, (2015)]