Abstract
The enolates generated by the conjugate addition of 1-(phenylthio)-2-octenyllithium to 4-tert-butoxycyclopent-2-en-1-one and <-crotonolactone react with methyl 7-halohept-5-ynoates in the presence of Ph3SnCl to deliver products which may be converted into prostaglandin precursors.
| Original language | English |
|---|---|
| Pages (from-to) | 3385-3388 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 26 |
| Issue number | 28 |
| DOIs | |
| Publication status | Published - 1985 |
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