Synthesis of 6α-Methyl-16α,17α-cyclohexanoprogesterone via γ-Methylenation of 16α,17. alpha.-Cyclohexanopregn-4-ene-3,20-dione. -An improved synthetic way to the title cyclohexanoprogesterone (IV) is presented. The introduction of the 6α-methyl group is achieved by regioselective γ-methylenation of
✦ LIBER ✦
Synthesis and Structure of 4′,4′-Dimethyl[16α,17α]spiropentanopregn-4-ene-3,20-dione.
✍ Scribed by I. S. Levina; L. E. Kulikova; E. V. Shulishov; I. P. Klimenko; A. V. Kamernitskii; Yu. V. Tomilov
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 24 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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