Enol ethers: preparation and synthetic applications

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

doi:10.1016/S0040-4039(01)81716-0

Enol ethers: preparation and synthetic applications

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

Biochemistry

Research output: Contribution to journal › Article › peer-review

65 Scopus citations

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 language	English (US)
Pages (from-to)	5903-5906
Number of pages	4
Journal	Tetrahedron Letters
Volume	25
Issue number	51
DOIs	https://doi.org/10.1016/S0040-4039(01)81716-0
State	Published - 1984

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(01)81716-0

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title = "Enol ethers: preparation and synthetic applications",

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.",

author = "Ousset, {J. B.} and C. Mioskowski and Yang, {Y. L.} and Falck, {J R}",

year = "1984",

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journal = "Tetrahedron Letters",

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TY - JOUR

T1 - Enol ethers

T2 - preparation and synthetic applications

AU - Ousset, J. B.

AU - Mioskowski, C.

AU - Yang, Y. L.

AU - Falck, J R

PY - 1984

Y1 - 1984

N2 - 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.

AB - 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.

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U2 - 10.1016/S0040-4039(01)81716-0

DO - 10.1016/S0040-4039(01)81716-0

M3 - Article

AN - SCOPUS:0001080909

SN - 0040-4039

VL - 25

SP - 5903

EP - 5906

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 51

ER -

Enol ethers: preparation and synthetic applications

Abstract

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