Acyl migration in the Reformatsky reaction of 21-acyloxy-5-pregnen-20-one derivatives with ethyl bromoacetate
Reformatsky reaction of 3β, 21-diacyloxy- and 3β-methoxy-21-acyloxy-5-pregnen-20-one with ethyl bromoacetate yields, through an intramolecular 1,2-acyl migration, 3β, 20ξ-diacyloxy- and 3β-methoxy-20ξ-acyloxy-14α-card-5-enolide respectively. The 20ξ-acyloxy-14α-card-5-enolides were converted into th...
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| Autores principales: | , |
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| Formato: | JOUR |
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| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_0039128X_v39_n2_p181_Seldes |
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| Sumario: | Reformatsky reaction of 3β, 21-diacyloxy- and 3β-methoxy-21-acyloxy-5-pregnen-20-one with ethyl bromoacetate yields, through an intramolecular 1,2-acyl migration, 3β, 20ξ-diacyloxy- and 3β-methoxy-20ξ-acyloxy-14α-card-5-enolide respectively. The 20ξ-acyloxy-14α-card-5-enolides were converted into the respective 20ξ-hydroxy-14α-card-5-enolides and the 14α-carda-5,20(22)-dienolides. Experimental support to the proposed intramolecular 1,2-acyl migration is provided by the use of labelled compounds. © 1982. |
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