The Synthesis of Δ 5 -Cholestene-3β,19-diol via the 3,5-Cyclosterol Rearrangement. A Novel Route to 19-Nor Sterols
✍ Scribed by Moriarty, Robert M.; D'Silva, T. D.
- Book ID
- 126407809
- Publisher
- American Chemical Society
- Year
- 1963
- Tongue
- English
- Weight
- 302 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A Concise Route to 19-Nor-10-azasteroids, a New Class of Steroid 5α-Reductase Inhibitors. Part 3. Synthesis of (+)-19-Nor-10azatestosterone and (+)-17β-(Acetyloxy)-(5β)-10-azaestr-1-en-3-one. -The title compounds are of interest, since 5α-reductase inhibitors (by reducing the level of dihydrotesto
## Abstract Photocyclization of 3‐chloro‐N‐(3‐phenanthryl)thieno[2,3‐__b__]thiophene‐2‐carboxamide (5) yielded only one of the two possible structural isomers, thieno[3′,2′:4,5]thieno[2,3‐__c__]naphtho[1,2‐__f__]quinolin‐6(5__H__)‐one (6), which was further elaborated to afford the unsubstituted ri