The Beckmann rearrangement of the oxime of 11-oxo-⍺, 20-dihydroxy-C-nor pregnane (54) provided the corresponding lactam (56). Oxidation of the latter with Jones reagent furnished the 3-keto-alcohol (57), which upon its conversion to the acetate derivative (58) followed by bromination and dehydrobromination yielded ll-aza-20-acetoxy-pregn-4-ene-3,12-dione (60). Hydrolysis of the latter to the ∆⁴ -3-keto alcohol (62) followed by oxidation furnished the desired ll-aza-pregn-4-ene-3,12,20-trione (63). The synthetic sequence provides the first examples of ll-aza steroid analogues in which ring C is a six membered and ring A possesses the ∆⁴-3-keto moiety. / Science, Faculty of / Chemistry, Department of / Graduate
| Identifer | oai:union.ndltd.org:UBC/oai:circle.library.ubc.ca:2429/36007 |
| Date | January 1967 |
| Creators | Sood, Rattan Sagar |
| Publisher | University of British Columbia |
| Source Sets | University of British Columbia |
| Language | English |
| Detected Language | English |
| Type | Text, Thesis/Dissertation |
| Rights | For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use. |
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