Skip to main navigation Skip to search Skip to main content

A route to prostaglandin precursors from 1-(phenylthio)-2-octenyllithium.

  • The University of Sydney

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Pages (from-to)3385-3388
Number of pages4
JournalTetrahedron Letters
Volume26
Issue number28
DOIs
Publication statusPublished - 1985

Fingerprint

Dive into the research topics of 'A route to prostaglandin precursors from 1-(phenylthio)-2-octenyllithium.'. Together they form a unique fingerprint.

Cite this