Enol ethers: preparation and synthetic applications

J. B. Ousset, C. Mioskowski, Y. L. Yang, J R Falck

Research output: Contribution to journalArticle

62 Citations (Scopus)

Abstract

A versatile preparation of α-alkoxyphosphonium bromides leading to enol ethers by Wittig coupling was exploited for the convergent synthesis of pheromones from the Douglas-fir tussock moth and the olive fly Dacus oleae as well as an oxaspirolactone and C-glycoside.

Original languageEnglish (US)
Pages (from-to)5903-5906
Number of pages4
JournalTetrahedron Letters
Volume25
Issue number51
DOIs
StatePublished - 1984

Fingerprint

Pseudotsuga
Psychodidae
Ethers
Pheromones
Olea
Bromides
C-glycoside

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Enol ethers : preparation and synthetic applications. / Ousset, J. B.; Mioskowski, C.; Yang, Y. L.; Falck, J R.

In: Tetrahedron Letters, Vol. 25, No. 51, 1984, p. 5903-5906.

Research output: Contribution to journalArticle

Ousset, J. B. ; Mioskowski, C. ; Yang, Y. L. ; Falck, J R. / Enol ethers : preparation and synthetic applications. In: Tetrahedron Letters. 1984 ; Vol. 25, No. 51. pp. 5903-5906.
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