Abstract
The neutral form of the spirocation intermediate in the dienone-phenol rearrangement of a steroidal p-quinol has been isolated, providing a direct prove of the accepted mechanism. Changing acidic conditions, phenolic products were obtained.
| Original language | English |
|---|---|
| Pages (from-to) | 471-474 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 28 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 1987 |
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