Abstract
The synthesis of a number of β‐northiadiaza steroid analogs has been described. Suitable o‐aminonitriles were acylated with γ‐chlorobutyryl chloride. These amidonitriles were cyclized to substituted γ‐lactams and subsequently to the tetracyclic products. To functionalize the “17‐position” in these steroids, the intermediate γ‐lactams were converted to arylidene derivatives before cyclization to the tetracyclic derivatives.
Original language | English (US) |
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Pages (from-to) | 821-824 |
Number of pages | 4 |
Journal | Journal of Heterocyclic Chemistry |
Volume | 13 |
Issue number | 4 |
DOIs | |
State | Published - Aug 1976 |
All Science Journal Classification (ASJC) codes
- Organic Chemistry