| Literature DB >> 7078164 |
Abstract
In the presence of dilute alkali at room temperature aldosterone undergoes rearrangement to form an isomeric compound identified as 11 beta, 18;18,21-diepoxy-20,21-dihydroxypregn-4-en-3-one. The presence of dissolved oxygen causes simultaneous degradation to form 11 beta, 18-epoxy-18-hydroxy-3-oxo-17(beta H)-androst-4-ene-17 alpha-carboxylic acid. Under similar alkaline conditions at reflux temperature in aqueous methanol aldosterone undergoes rearrangement to form (20S)-20,21-dihydroxy-3-oxo-pregn-4-eno-18,11 beta-lactone accompanied by an intramolecular aldol type condensation to form 11 beta, 21-dihydroxy-18,21-cyclopregna-4,18(21)-diene-3,20-dione. Identical products were formed from 17-isoaldosterone. The mechanisms of these reactions are discussed.Entities:
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Year: 1982 PMID: 7078164 DOI: 10.1016/0022-4731(82)90175-3
Source DB: PubMed Journal: J Steroid Biochem ISSN: 0022-4731 Impact factor: 4.292