Expeditious synthetic route to B-ring functionalised 2-oxa-steroids: Synthesis of 17-ethylenedioxy-6α-hydroxy-2-oxa-4-androsten-3-one as key synthon
Expeditious synthetic route to B-ring functionalised 2-oxa-steroids: Synthesis of 17-ethylenedioxy-6α-hydroxy-2-oxa-4-androsten-3-one as key synthon
| dc.contributor.author | Nangia, Ashwini | |
| dc.contributor.author | Anthony, A. | |
| dc.date.accessioned | 2022-03-27T09:34:56Z | |
| dc.date.available | 2022-03-27T09:34:56Z | |
| dc.date.issued | 1997-12-01 | |
| dc.description.abstract | The easily prepared 17-ethylenedioxy-4-androsten-3,6-dione 8 is transformed to 17-ethylenedioxy-6α-hydroxy-2-oxa-4-androsten-3-one 15 in a few steps with complete stereo- and regio-control. The hydroxylactone 15 provides an easy entry to B-ring functionalised 2-oxa-androgens for evaluation as potential aromatase inhibitors and anabolic agents. | |
| dc.identifier.citation | Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. v.36(12) | |
| dc.identifier.issn | 03764699 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/13078 | |
| dc.title | Expeditious synthetic route to B-ring functionalised 2-oxa-steroids: Synthesis of 17-ethylenedioxy-6α-hydroxy-2-oxa-4-androsten-3-one as key synthon | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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